- Staat
- WI
- Alter
- 90,0
- Geschlecht
- M
- Eingang
- 02.12.2022
- Impfdatum
- 17.06.2021
- Beginn
- 20.10.2022
- Tage bis Beginn
- 490,0
- Dosis
- 2
- Route/Site
- UN / UN
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Anticoagulant therapy
Asthenia
Atrial fibrillation
Brain natriuretic peptide increased
COVID-19
Chest X-ray abnormal
Computerised tomogram head normal
Confusional state
Cough
Death
Diuretic therapy
Dyspnoea
Electrocardiogram abnormal
Fall
Fatigue
General physical health deterioration
Hypervolaemia
Hypoxia
Symptomtext
Adverse event information provided in this submission, is per a report received by Public Health Department from a submitting facility. Covid-19 vaccination information is from Immunization Registry. Moderna 5/20/2021 Lot number: 017C21A, Moderna 6/17/2021 Lot number 039C21A Admitted to Hospital 10/20/2022. Acute hypoxemia secondary to COVID-19/pneumonia/multiple rib fractures: New onset atrial fibrillation and Elevated troponin and Elevated brain natriuretic peptide (BNP) level. Patient had been recently admitted on 10/1-10/7/2022 after a fall. On that admission he was fluid overloaded and diuresed. When he was medically stable, he was discharged to rehab. At rehab, he developed fatigue, cough, and shortness of breath. He tested positive for COVID and was symptomatically treated as an outpatient and the facility had him in isolation. 10/20/2022 the patient had worsening shortness of breath and was sent to Hospital for further evaluation. Patient required 2 L oxygen to keep O2 sats above 90%. No oxygen requirement noted at rehab facility. Chest x-ray showed pneumonia. IV Rocephin and azithromycin ordered in ER. Per submitted note; He did not meet sepsis protocol. X-ray of patient?s ribs showed multiple rib fractures. Lidoderm patch, Tylenol, and tramadol provided for pain control. PT/OT ordered. COVID-19 inflammatory markers elevated, will monitor intermittently. Steroids and vitamins ordered. EKG showed new onset A. fib with rate control of 55. Patient was anticoagulated on warfarin, PT/INR was supratherapeutic, rechecked and Pharmacy to dose. Troponin elevated. Patient denies any chest pain. EKG shows new onset A. fib, but no acute ischemic changes, lab work-up was unremarkable. Patient denied any chest pain, nausea, vomiting, lightheadedness, dizziness, fever, chills, dysuria, constipation, diarrhea, or abdominal pain. 2nd report received: (unknown length of stay of prior 10/20/2022 admission) Patient was recently admitted on 10/20/2022 for hypoxia secondary to pneumonia, COVI D-19, and rib fractures. Patient was found to be in new onset A. fib. Cardiology adjusted medication and patient was discharged on Augmentin for pneumonia. Patient was discharged in stable condition and was sent back to his facility. Family noticed over the last week that at times he was more confused and weaker. They noticed a cough again over the last few days as well. 11/5/2022, patient was so weak that he was unable to get out of bed and family had him sent back to the ER for further evaluation. Chest x-ray showed worsening pneumonia. He is not requiring any oxygen at this time. CT of head was negative. BNP improved from baseline. Patient appeared dry, despite leg edema. Gentle IV hydration was ordered. Compression stockings were ordered. The rest of his lab work-up was unremarkable. Patient denies any chest pain, shortness of breath, nausea, vomiting, lightheadedness, dizziness, fever, dysuria, diarrhea, or abdominal pain. Unfortunately, after hospitalization and treatment in the hospital patient continued to decline. On 11/8/2022 patient took started experiencing worsening of his mentation, prolonged pauses of his heartbeat. The trajectory of patient disease was discussed with the family, Patient?s family agreed on further management of comfort measures. Patient was transferred to hospice. On 11/8/2022 patient was pronounced dead at 1420. County Public Health has no further information. Please contact providers for additional information.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- Tests: IMAGING: 10/20/22 CXR: "IMPRESSION: 1. Bibasilar airspace disease left worse than right likely pneumonia. 2. 2 cm soft tissue density left suprahilar region which could be site of pneumonia though neoplastic nodule not excludable by this study. 3. Small bilateral pleural effusions. 10/20/22 left ribs XR: IMPRESSION: Multiple left rib fractures, acute appearing. Tiny left pleural effusion. No pneumothorax.? Labs, EKG and Chest-XR, Left rib-XR
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- Venous thrombosis and embolism Lupus anticoagulant with hypercoagulable state Hypercholesterolemia Chronic anticoagulation - coumadin. CKD (chronic kidney disease) stage 4, Anemia in chronic kidney disease (CKD) Iron deficiency
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 93,0
- Geschlecht
- F
- Eingang
- 02.04.2022
- Impfdatum
- 22.06.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 176,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Death
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Patient had breakthrough infection and passed away.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- 2,0
- Labordaten
- First positive CVOID test on 12/6/2021 and second positive on 12/13/2021.
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Dementia
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 93,0
- Geschlecht
- F
- Eingang
- 02.04.2022
- Impfdatum
- 22.06.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 176,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Death
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Patient had breakthrough infection and passed away.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- 2,0
- Labordaten
- First positive CVOID test on 12/6/2021 and second positive on 12/13/2021.
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Dementia
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 14.02.2022
- Impfdatum
- 17.08.2021
- Beginn
- 13.02.2022
- Tage bis Beginn
- 180,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Anticoagulant therapy
Aspiration
COVID-19 pneumonia
Cerebrovascular accident
Computerised tomogram head normal
COVID-19
Death
SARS-CoV-2 test positive
Hemiparesis
Hypoxia
Symptomtext
Client passed away on 2/13/2022 while positive with covid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 14.12.2021
- Impfdatum
- 18.06.2021
- Beginn
- 30.11.2021
- Tage bis Beginn
- 165,0
- Dosis
- 2
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute respiratory failure
COVID-19
COVID-19 pneumonia
Chest X-ray abnormal
Chronic obstructive pulmonary disease
Computerised tomogram thorax normal
Condition aggravated
Cough
Dyspnoea
Fatigue
Hypoxia
Incentive spirometry
Lung consolidation
Lung infiltration
Malaise
Prone position
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
Hospitalized 12/6/2021-still admitted currently; COVID-19 positive 11/30/2021; fully vaccinated History of Present Illness Patient is a 82 y.o. female who presents to the hospital with shortness of breath. The patient began having symptoms approximately 8 days ago. She was seen in the walk-in clinic on 11/30 for symptoms of cough and congestion. She was diagnosed with upper respiratory infection but also had a COVID test ordered which subsequently came back positive. Throughout the course of the next several days she became increasingly fatigued with progressive cough and worsening shortness of breath. Patient was seen in the emergency department. She was afebrile but tachypneic in the 20s. While there she required 6 L of oxygen to maintain sats above 90%. Chest x-ray showed bilateral infiltrates consistent with possible COVID. Due to her worsening hypoxemia she was transferred to the hospital for further evaluation care. Acute respiratory failure with hypoxemia Assessment & Plan Likely related to COVID pneumonia in setting of mild chronic obstructive pulmonary disease Current required 4 L of oxygen Supportive care, wean as tolerated Instructed in incentive spirometry, flutter and proning * Pneumonia due to COVID-19 virus Assessment & Plan Patient was symptom onset 8 days ago Vaccination status-vaccinated in April, no booster Patient with increasing cough shortness of breath and fatigue Positive test 11/30/2021 Admission 12/06/2021 Planned steroids, remdesivir and supportive care Note from 12/13/2021: Acute respiratory failure with hypoxemia Assessment & Plan Likely related to COVID pneumonia in setting of mild chronic obstructive pulmonary disease More hypoxic this morning, CXR yesterday showing some disease progression IV lasix today Supportive care, wean as tolerated Instructed in incentive spirometry, flutter and proning Currently on 60% HFNC * Pneumonia due to COVID-19 virus Assessment & Plan Patient with symptom onset 11/29 Vaccination status-vaccinated in April, no booster Patient with increasing cough shortness of breath and fatigue Positive test 11/30/2021 Admission 12/06/2021 Dexamethasone 8/10 Remdesivir 5/5 Worsening hypoxia, CT negative for PE but does show basilar consolidative changes Check sputum culture, start empiric antibiotics Rocephin/azithro day 1/5
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 8,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Pneumonia due to COVID-19 virus Acute respiratory failure with hypoxemia Acquired hypothyroidism Type 2 diabetes mellitus without complication Hypertension Atrial fibrillation, unspecified type Chronic obstructive pulmonary disease with acute exacerbation Chronic kidney disease (CKD) stage G3a/A1, moderately decreased glomerular filtration rate (GFR) between 45-59 mL/min/1.73 square meter and albuminuria creatinine ratio less than 30 mg/g Hyperlipidemia Lichen sclerosus of female genitalia Abdominal aortic aneurysm (AAA) without rupture Tobacco abuse, in remission History of bladder cancer PAD (peripheral artery disease) Pulmonary nodule Depression, recurrent H/O malignant neoplasm of endometrium
- Andere Medikamente
- amLODIPine (NORVASC) 10 MG tablet apixaban (ELIQUIS) 5 MG tablet aspirin 81 MG tablet atorvastatin (LIPITOR) 80 MG tablet betamethasone dipropionate 0.05 % cream busPIRone (BUSPAR) 5 MG tablet fluticasone (FLONASE) 50 MCG/ACT nasal spray gl
- Allergien
- Amoxicillin Augmentin Sulfa Tape Moderna
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 03.10.2021
- Impfdatum
- 12.06.2021
- Beginn
- 26.09.2021
- Tage bis Beginn
- 106,0
- Dosis
- 2
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: ja
ER: ja
Erholt: ja
Activated partial thromboplastin time shortened
Basophil count decreased
Basophil percentage
Coronary artery thrombosis
Electrocardiogram
Eosinophil count decreased
Eosinophil percentage
Haematocrit normal
Haemoglobin normal
Immature granulocyte count
International normalised ratio normal
Lymphocyte count normal
Lymphocyte percentage
Mean cell haemoglobin concentration normal
Mean cell haemoglobin normal
Mean cell volume normal
Mean platelet volume normal
Monocyte count
Symptomtext
I had a sudden unexpected heart attach caused by a blood clot in left atrial descending (LAD). I cannot say for certain the event was related to the vaccine but I had been otherwise healthy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocardial infarction
- Hospital-Tage
- 5,0
- Labordaten
- 9/26/2021 5:25 PM - ECG 12-LEAD -This test result has been released by an automatic process. 09/26/2021 5:57 PM - CBC W/ AUTO DIFFERENTIAL - Component Results Component Your Value Standard Range WBC 8.86 K/mcL 4.50 - 11.00 K/mcL RBC 5.39 M/mcL 4.50 - 5.90 M/mcL Hemoglobin 15.1 g/dL 13.5 - 17.5 g/dL Hematocrit 46.3 % 41.0 - 53.0 % MCV 85.9 fL 80.0 - 100.0 fL MCH 28.0 pg 26.0 - 34.0 pg MCHC 32.6 g/dL 31.0 - 37.0 g/dL Platelets 336 K/mcL 150 - 400 K/mcL RDW - CV 13.3 % 11.6 - 14.8 % MPV 9.3 fL 9.4 - 12.4 fL Neutrophils 55.4 % %% Lymphocytes 33.1 % %% Monocytes 9.4 % %% Eosinophils 1.1 % %% Basophils 0.5 % %% IG Percent 0.50 % %% The IG parameter is the percentage of metamyelocytes, myelocytes and promyelocytes. An immature granulocyte count (IG) of 1% or more suggests the possibility of infection, an IG count of 3% is very likely related to an infection. Neutrophils Abs 4.92 K/mcL 1.70 - 7.00 K/mcL Lymphocytes Abs 2.93 K/mcL 0.90 - 4.00 K/mcL Monocytes Abs 0.83 K/mcL 0.30 - 0.90 K/mcL Eosinophils Abs 0.10 K/mcL 0.00 - 0.50 K/mcL Basophils Abs 0.04 K/mcL 0.00 - 0.30 K/mcL IG Absolute 0.04 K/mcL 0.00 - 0.30 K/mcL Nucleated RBC 0.0 % %% Nucleated RBC Abs 0.00 K/mcL 0.00 - 0.00 K/mcL 09/26/2021 6:08 PM - APTT - Component Your Value Standard Range APTT 27 seconds 23 - 34 seconds 09/26/2021 6:08 PM - PROTIME-INR - Component Your Value Standard Range Protime (PT) 12.0 seconds 11.8 - 14.3 seconds INR 0.9 0.8 - 1.1 09/26/2021 6:08 PM - TROPONIN - Component Your Value Standard Range Troponin T 10 ng/L <=22 ng/L<=22 ng/L Troponin T Interpretation Normal
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Daily multi-vitamin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 29.09.2021
- Impfdatum
- 23.07.2021
- Beginn
- 29.07.2021
- Tage bis Beginn
- 6,0
- Dosis
- 1
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: ja
ER: unbekannt
Erholt: nein
Cerebrovascular accident
Dysphagia
Hemiparesis
Symptomtext
Pt sustained a CVA. Pt was hospitalized and discharged home with left sided hemiparesis and inability to swallow.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- -
- Labordaten
- Not available
- Aktuelle Erkrankungen
- Hypertension CHF Morbid Obesity Lymphedema
- Vorgeschichte
- Hypertension CHF Morbid Obesity Lymphedema
- Andere Medikamente
- Losartan Escitalopram Carvedilol Tamsulosin Finasteride Mirtazapine Tramadol Atorvastatin Aspirin
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 83,0
- Geschlecht
- F
- Eingang
- 06.07.2021
- Impfdatum
- 01.07.2021
- Beginn
- 02.07.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Cardioversion
Death
Dyspnoea
Oxygen saturation decreased
Respiratory tract congestion
Resuscitation
Unresponsive to stimuli
Symptomtext
Pt received vaccine 07/01/2021 in the afternoon and patient felt fine with no complaints that day. The following day the patient complained of SOB and the nursing staff found her O2 sat in the 50 so she was brought to the hospital. She was evaluated at the Hospital and discharged back to nursing facility the same day. Patients daughter brought patient back to facility from hospital. On 07/03 patient complained of congestion but "breathing better". On 07/04, patient stayed in bed all day. RN at facility administered tylenol and a soda and right after administration found the patient unresponsive. Nurse started CPR and 911 was called. EMS used defibrillator until the staff alerted EMS that patient was DNR. Patient passed away in room between 3-4pm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- ANORO INHALER, CRESTOR, ESOMEPRAZOLE, LEVOTHYROXINE, FOLIC ACID, DILTIAZEM, CARVEDILOL, ASPIRIN, LASIX, MIRTAZAPINE, ALBUTEROL NEBS, FLOVENT INHALER, TYLENOL
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 29.06.2021
- Impfdatum
- 11.06.2021
- Beginn
- 15.06.2021
- Tage bis Beginn
- 4,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Axillary vein thrombosis
Pain in extremity
Peripheral swelling
Pulmonary embolism
Subclavian vein thrombosis
Symptomtext
Swelling and pain in right upper extremity on 6/15/2021
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary embolism
- Hospital-Tage
- 1,0
- Labordaten
- Urgent care and ER visit resulting in hospitalization. Acute right subclavian and axillary vein DVT noted along with bilateral lower lobe pulmonary embolism
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Obesity
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 17.11.2021
- Impfdatum
- 28.10.2021
- Beginn
- 28.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Flushing
Pharyngeal paraesthesia
Presyncope
Symptomtext
1345 - Vaccine Given 1400 - 15 minutes of observation time should of ended, but patient reported feeling "flushed", vasovagal-like symptoms, so increased observation time to monitor and given juice and crackers. 1406 - Patient now reports "tingling in throat". Reviewed body systems. No difficulty breathing. Offered and given 25 mL Benadryl, which is consistent with vaccine clinic practice for patient's driving home and patient agreed as she "routinely takes Benadryl for anxiety". 1409 - Patient declined staying any longer and says "feels better". Advised of concerns to stay, but 1 of patient's 2 kids has to go to the bathroom and none acceptable on-site to patient. Advised of s/s to warrant urgent or emergent medical care, including but not limited to s/s of anaphylaxis. Patient left site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- N/A.
- Aktuelle Erkrankungen
- Unknown.
- Vorgeschichte
- Anxiety.
- Andere Medikamente
- Unknown.
- Allergien
- Unknown.
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 05.11.2021
- Impfdatum
- 21.07.2021
- Beginn
- 21.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Anxiety
Dizziness
Nausea
Syncope
Vomiting
Symptomtext
Anxiety, caused dizziness, nausea, vomiting, and fainting. She was taken to the nearest hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 01.10.2021
- Impfdatum
- 20.08.2021
- Beginn
- 18.09.2021
- Tage bis Beginn
- 29,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal discomfort
Asthenia
Chills
Dysphonia
Fatigue
Injection site discolouration
Insomnia
Limb discomfort
Loss of consciousness
Lung disorder
Neuralgia
Pyrexia
Symptomtext
voice sounds congested but not congested; lungs and stomach out of normal; no energy; lungs and stomach out of normal; so tired; Temp high again; chills only at night; passed out; huge mark on arm at injection site; nerve pain; couldn't sleep; legs could not be still; This spontaneous case was reported by a consumer and describes the occurrence of LOSS OF CONSCIOUSNESS (passed out) in a 59-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 036C21A and 039C21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 20-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 17-Sep-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 18-Sep-2021, the patient experienced INJECTION SITE DISCOLOURATION (huge mark on arm at injection site), NEURALGIA (nerve pain), INSOMNIA (couldn't sleep) and LIMB DISCOMFORT (legs could not be still). On 19-Sep-2021, the patient experienced LOSS OF CONSCIOUSNESS (passed out) (seriousness criterion medically significant). On an unknown date, the patient experienced DYSPHONIA (voice sounds congested but not congested), LUNG DISORDER (lungs and stomach out of normal), ASTHENIA (no energy), ABDOMINAL DISCOMFORT (lungs and stomach out of normal), FATIGUE (so tired), PYREXIA (Temp high again) and CHILLS (chills only at night). At the time of the report, LOSS OF CONSCIOUSNESS (passed out) had resolved, INJECTION SITE DISCOLOURATION (huge mark on arm at injection site) had not resolved and NEURALGIA (nerve pain), INSOMNIA (couldn't sleep), LIMB DISCOMFORT (legs could not be still), DYSPHONIA (voice sounds congested but not congested), LUNG DISORDER (lungs and stomach out of normal), ASTHENIA (no energy), ABDOMINAL DISCOMFORT (lungs and stomach out of normal), FATIGUE (so tired), PYREXIA (Temp high again) and CHILLS (chills only at night) outcome was unknown. Concomitant medications were not provided. Treatment medications were not provided. Company comment: This case concerns a 59 year-old female who experienced the unexpected events of Loss of Consciousness with Injection site discolouration, Neuralgia, Insomnia, and Limb discomfort. The event of Injection site discolouration occurred one day after receiving the second dose of Moderna COVID-19 Vaccine. The event of Loss of Consciousness occurred 2 days after the second dose.The benefit-risk relationship of Moderna COVID-19 Vaccine is not affected by this report. Most recent FOLLOW-UP information incorporated above includes: On 23-Sep-2021: Follow up contains no new information.; Sender's Comments: This case concerns a 59 year-old female who experienced the unexpected events of Loss of Consciousness with Injection site discolouration, Neuralgia, Insomnia, and Limb discomfort. The event of Injection site discolouration occurred one day after receiving the second dose of Moderna COVID-19 Vaccine. The event of Loss of Consciousness occurred 2 days after the second dose.The benefit-risk relationship of Moderna COVID-19 Vaccine is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 30.09.2021
- Impfdatum
- 20.08.2021
- Beginn
- 23.08.2021
- Tage bis Beginn
- 3,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal pain
Chest pain
Diarrhoea
Dyspnoea
Electrocardiogram abnormal
Nausea
Pericarditis
Troponin normal
Vomiting
Symptomtext
Chest pain, SOB, N/V/D and abd pain. No fever, cough or sore throat. Worsen over the next 2 days prompting ED visit. Dx Pericarditis
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pericarditis
- Hospital-Tage
- -
- Labordaten
- Trop nml. EKG- suggestive of pericarditis
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 18.09.2021
- Impfdatum
- -
- Beginn
- 01.08.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest discomfort
Chromaturia
Dyspepsia
Renal pain
Thrombosis
Vaccination site rash
Symptomtext
Discomfort in chest area; Rusty colored urine for 3 days; Mild heartburn for 8 days; 3 small red dots on lower left arm; Possible blood clots on lower arm; Soreness in the kidney area; This spontaneous case was reported by a consumer and describes the occurrence of THROMBOSIS (Possible blood clots on lower arm), RENAL PAIN (Soreness in the kidney area), CHEST DISCOMFORT (Discomfort in chest area), CHROMATURIA (Rusty colored urine for 3 days) and DYSPEPSIA (Mild heartburn for 8 days) in a 61-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 039c21a) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On an unknown date, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. In August 2021, the patient experienced THROMBOSIS (Possible blood clots on lower arm) and RENAL PAIN (Soreness in the kidney area). On 18-Aug-2021, the patient experienced CHEST DISCOMFORT (Discomfort in chest area), CHROMATURIA (Rusty colored urine for 3 days), DYSPEPSIA (Mild heartburn for 8 days) and VACCINATION SITE RASH (3 small red dots on lower left arm). On 28-Aug-2021, CHROMATURIA (Rusty colored urine for 3 days), DYSPEPSIA (Mild heartburn for 8 days) and VACCINATION SITE RASH (3 small red dots on lower left arm) had resolved. At the time of the report, THROMBOSIS (Possible blood clots on lower arm), RENAL PAIN (Soreness in the kidney area) and CHEST DISCOMFORT (Discomfort in chest area) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Concomitant product use was not provided by the reporter. No treatment information was provided.; Sender's Comments: This case concerns a 61-year-old male patient with no details on previous medical history, who experienced the unexpected events of Thrombosis (reported as possible blood clots on lower arm) after Spikevax (mRNA- 1273 vaccine / Moderna COVID-19 Vaccine). The event occurred after the first dose of Spikevax, temporal relationship is unknown. The rechallenge was not applicable since only information about one dose was disclosed. The benefit-risk relationship of Spikevax vaccine is not affected by this report. Thrombosis was automatically upgraded as serious as per Regulatory authority list. However, based on information available and due to the lack of evidence of seriousness from a regulatory or clinical standpoint, it was assessed as non-serious. Medical confirmation has been requested.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Thrombosis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 26.08.2021
- Impfdatum
- 13.08.2021
- Beginn
- 16.08.2021
- Tage bis Beginn
- 3,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Angiogram
Angiogram normal
C-reactive protein normal
Chest pain
Condition aggravated
Dyspnoea
Electrocardiogram ST-T change
Full blood count normal
Herpes zoster
Myocardial necrosis marker normal
Pericarditis
Troponin normal
Upper respiratory tract infection
Symptomtext
Patient developed chest pain and shortness of breath 3 days after his 2nd moderna vaccine. Was diagnosised and treated for acute pericarditis. Cardiac enzymes were normal so no myocarditis. He did have a viral URI illness 1-3 weeks before his 2nd vaccine and also developed shingles 3 days after the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pericarditis
- Hospital-Tage
- -
- Labordaten
- CBC, troponin, crp all normal. EKG w/ diffuse ST changes, CT PE angio normal
- Aktuelle Erkrankungen
- had cold like illness 1-3 weeks before, shingles outbreak after onset of pericarditis symptoms
- Vorgeschichte
- none
- Andere Medikamente
- nothing
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 22.07.2021
- Impfdatum
- 25.06.2021
- Beginn
- 26.06.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Adverse reaction
Asthenia
Balance disorder
Blood test normal
Chest X-ray normal
Computerised tomogram normal
Confusional state
Dehydration
Dysphemia
Feeling abnormal
Gait disturbance
Headache
Heart rate increased
Hypoaesthesia
Impaired work ability
Magnetic resonance imaging normal
Memory impairment
Mobility decreased
Symptomtext
Developed numbness in arms/hands that spread within minutes to both legs. High fever, high heartrate and low oxygen levels, Couldn't talk normally (stuttering) confusion at about 10 am. Was driving at the time for work and pulled into a customers yard and collapsed. They called 911 and I was transported to Hospital. They tested for stroke since that's what the symptoms pointed to. Performed Cat Scan, X-rays, and multiple blood and urine tests. They could find nothing that would have caused it. They concluded it was an adverse reaction to the Moderna Vaccine I received the day before. I was released and then was walking out of hospital my DR. stopped me and readmitted me because he
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- 2,0
- Labordaten
- Cat Scan, MRI, Chest X-ray, blood and urine tests. All tests came back negative for stroke. Dehydration from fever all performed on June 26-27th 2021
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 09.07.2021
- Impfdatum
- 09.07.2021
- Beginn
- 09.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Anaphylactic reaction
Anxiety
Chest discomfort
Dyspnoea
Hypopnoea
Palpitations
Tachycardia
Throat tightness
Symptomtext
Patient received the Covid-19 vaccine. She reports symptoms of Anaphylaxis - chest discomfort, palpitations, tachycardia, shortness of breath, feeling of tightness in the throat. I have observed patient was mildy anxious, with shallow rapid respirations. Patient then disclosed having similar reaction after previous covid vaccination. Per the vaccinator patient had stated having an "issue" with her first vaccination, but that she had spoke with her primary and was told it would be ok to proceed" . No report of allergic reaction was reported at this vaccination. Patient described previous reaction as tightness in the chest "menthol feeling" with some shortness of approximately 40 minutes post initial vaccination lasting 7 hours. This reaction remained mild initially. Approximately 20 minutes into observation time patient reported having increased s/sx - chest tightness and rapid heart rate, some shortness of breath and throat/tongue swelling. Patient then reported having hx of anaphylaxis to bee stings. Patient reported this reaction was consistent with previous allergic reactions. Patient advised epi would be best choice - patient refused. MED TEAM called. Patient agreed to PO benadryl, however, as medication was prepped did agree to IM benadryl and 50mg was given to patient in the R deltoid as team arrived on scene. Patient transferred to ED via wheelchair.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anaphylactic reaction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- -
- Andere Medikamente
- meloxicam (MOBIC) 15 MG tablet Take 1 tablet by mouth daily. acetaminophen (TYLENOL) 325 MG tablet Take 650 mg by mouth every 4 hours as needed for Pain. albuterol 108 (90 Base) MCG/ACT inhaler Inhale 2 puffs into the lungs every 4 hours as
- Allergien
- Bee Stings Hydrocodone/apap
- Vorherige Impfungen
- SEE NOTES IN ITEM 18
- Staat
- FL
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 05.07.2021
- Impfdatum
- 02.07.2021
- Beginn
- 05.07.2021
- Tage bis Beginn
- 3,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal discomfort
Dizziness
Headache
Nausea
Pain
Syncope
Symptomtext
Patient called to let us know that about 12 hours after receiving the Moderna vaccine she had stomach upset and felt like vomiting. As she was walking to the bathroom she became very dizzy and fainted . Her husband was home and was able to bring her to . She is okay except for body pain from the fall and a headache. She is going to go to the doctor to get checked just to be on the safe side.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Arthritis Anxiety Depression Cholesterol
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 30.06.2021
- Impfdatum
- 30.06.2021
- Beginn
- 30.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Hypotonia
Loss of consciousness
Snoring
Symptomtext
Patient reported history of syncope with shots/blood draws in the past. After shot was given, patient stated that she felt light headed and bent over on the chair with her head between her knees. She began to snore and so I rubbed her back to wake her up and she came to almost immediately. She then alternated between sitting upright and hunched over on the chair while I continued to fan her as she was feeling warm. After 15 minutes she started feeling better and was able to call a friend to come pick her up at the pharmacy. She also asked for some water. At this point, she was sitting upright and was on her phone for another 15-20 minutes before her friend arrived and she left on her own strength
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None reported
- Vorgeschichte
- Patient mentioned fainting from other vaccines and blood draws in the past
- Andere Medikamente
- -
- Allergien
- None Reported
- Vorherige Impfungen
- patient stated fainting from shots and blood draws in the past
- Staat
- NC
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 18.06.2021
- Impfdatum
- 18.06.2021
- Beginn
- 18.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Balance disorder
Hyperhidrosis
Seizure
Syncope
Yawning
Symptomtext
Approximately seven minutes after the vaccine was given, the patient fainted and had a seizure. The paramedics came and took her to the hospital. Patient was still sweating, unsteady, yawning, and kept her eyes closed as they were examining her and when she left in the ambulance.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma
- Andere Medikamente
- -
- Allergien
- Amoxicillin
- Vorherige Impfungen
- The patient stated she had fainted when given a vaccine a long time ago.
- Staat
- NM
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 18.06.2021
- Impfdatum
- 17.06.2021
- Beginn
- 17.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dyspnoea
Flushing
Hyperhidrosis
Loss of consciousness
Seizure like phenomena
Syncope
Symptomtext
PATIENT RECEIVED VACCINE AND SAT DOWN TO BE MONITORED, SHE THEN FAINTED AND APPEARED TO BE SEIZING, VACCINATOR MONITORED PATIENTS BREATHING WHILE STAFF CALLED 911. PATIENT HAD SEIZURE LIKE ACTIVITY FOR 10-15 SECONDS, WAS UNCONSCIOUS FOR 30-45 SECONDS, MADE LABOR BREATHING SOUNDS WHILE UNCONSCIOUS, APPEARED FLUSHED AND SWEATING. AMBULANCE TRANSPORTED HER TO THE HOSPITAL, SHE WAS AWAKE AND ALERT WHEN SHE LEFT OUR FACILITY.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- NOT KNOWN
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NONE
- Andere Medikamente
- NA
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 11.03.2022
- Impfdatum
- 27.01.2021
- Beginn
- 10.02.2021
- Tage bis Beginn
- 14,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Dyspnoea
Fatigue
Malaise
Oxygen saturation decreased
SARS-CoV-2 test positive
Secretion discharge
Symptomtext
After receiving my first dose I had a blood oxygen problem. My oxygen would go from 97 to 85. It lasted for a week and my oxygen went back to normal range. 13 days later I woke up feeling extremely tired and feeling ill. I made the decision to go the doctor's office and get tested for COVID-19 due to the fatigue feeling. I tested positive for COVID-19. The fatigue feeling lasted for a week, and I started feeling better. After receiving my second dose I experienced a lot of pf mucus and was struggling to breathe. I only experienced the mucus and breathing problem for a week, and I felt better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- COVID-19
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Cancer
- Andere Medikamente
- Mucinex Tylenol
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 03.03.2022
- Impfdatum
- 10.09.2021
- Beginn
- 10.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Ageusia
Amenorrhoea
Condition aggravated
Dizziness
Electrocardiogram
Laboratory test
Migraine
Muscle spasms
Palpitations
Systemic lupus erythematosus
Ultrasound pelvis
Vision blurred
X-ray
Symptomtext
Bet 2-2:30pm day of 2nd shot: cramping in legs spread throughout entire body, pounding migraine, loss of taste, dizziness, blurred vision, lasted until Sunday late morning until around 11am, 9/12/21. Sunday pm felt a little better then debilitating migraine Monday am. 10/13: racing heart beat for 10 minutes twice in the day. 10/14 racing heartbeat would not stop. Went to ER. All lupus symptoms inflammatory issues have gotten worse since 2nd shot and have not subsided including menstruations stopped suddenly.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Tests is ER for rapid heartbeat. EKG/ECG. DX X-Ray, LABs Pelvic Ultrasound, various labwork, seeing a cardiologist now and also integrative doctor for inflamation issues
- Aktuelle Erkrankungen
- mild lupus symptoms
- Vorgeschichte
- mild chronic body aches from lupus, low immune
- Andere Medikamente
- none
- Allergien
- sesame, penicillin, nsaid's, macrobid, cephalexin
- Vorherige Impfungen
- flu
- Staat
- VA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 26.02.2022
- Impfdatum
- 30.06.2021
- Beginn
- 30.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Asthenia
Body temperature
Chills
Dehydration
Dizziness
Dry eye
Dyspnoea
Erythema
Eye irritation
Fatigue
Feeling hot
Headache
Hyperhidrosis
Mobility decreased
Myalgia
Nausea
Ocular hyperaemia
Symptomtext
Eyes are burning; W eakness; Dizziness; Fever of 102 F; Pouring sweat; Joints in her body started hurting really bad; Nausea; Headache; Feel extreme fatigue,couldn't even lift up her head,exhausting/felt so fatigue; Eyes were dry, had to pour water into them; Eyes were blood shot and red; Felt thirsty, thirsty, drank like a gallon and a half of water.; Severe dehydration,dehydrated for 24 hrs; She couldn't walk 3-4 stairs; Walking a short distance, I would feel out of breath; Arm got red; Arm got warm,/Arm got hot; pain in my arm", and like "someone was punching my arm". It never stopped, it kept getting worse; chills; This spontaneous case was reported by a nurse and describes the occurrence of ERYTHEMA (Arm got red), FEELING HOT (Arm got warm,/Arm got hot), DRY EYE (Eyes were dry, had to pour water into them), EYE IRRITATION (Eyes are burning) and MOBILITY DECREASED (She couldn't walk 3-4 stairs) in a 51-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 039C21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 30-Jun-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 30-Jun-2021, the patient experienced ERYTHEMA (Arm got red), FEELING HOT (Arm got warm,/Arm got hot), MYALGIA (pain in my arm", and like "someone was punching my arm". It never stopped, it kept getting worse) and CHILLS (chills). On 01-Jul-2021, the patient experienced DRY EYE (Eyes were dry, had to pour water into them), MOBILITY DECREASED (She couldn't walk 3-4 stairs), DYSPNOEA (Walking a short distance, I would feel out of breath), OCULAR HYPERAEMIA (Eyes were blood shot and red), THIRST (Felt thirsty, thirsty, drank like a gallon and a half of water.) and DEHYDRATION (Severe dehydration,dehydrated for 24 hrs). On 01-Jul-2021 at 6:00 AM, the patient experienced FATIGUE (Feel extreme fatigue,couldn't even lift up her head,exhausting/felt so fatigue) and HEADACHE (Headache). On 01-Jul-2021 at 11:00 AM, the patient experienced NAUSEA (Nausea). On 01-Jul-2021 at 2:00 PM, the patient experienced ARTHRALGIA (Joints in her body started hurting really bad). On 02-Jul-2021, the patient experienced HYPERHIDROSIS (Pouring sweat). On 02-Jul-2021 at 2:00 AM, the patient experienced PYREXIA (Fever of 102 F). On an unknown date, the patient experienced EYE IRRITATION (Eyes are burning), DIZZINESS (Dizziness) and ASTHENIA (W eakness). The patient was treated with ONDANSETRON (ZOFRAN [ONDANSETRON]) at a dose of 8 mg and IBUPROFEN (ADVIL [IBUPROFEN]) from 01-Jul-2021 to 02-Jul-2021 at a dose of four times since patient got the injection 800 mg.. On 01-Jul-2021, THIRST (Felt thirsty, thirsty, drank like a gallon and a half of water.), DEHYDRATION (Severe dehydration,dehydrated for 24 hrs) and CHILLS (chills) had resolved. On 02-Jul-2021 at 11:00 AM, PYREXIA (Fever of 102 F) had resolved. At the time of the report, ERYTHEMA (Arm got red), FEELING HOT (Arm got warm,/Arm got hot), DRY EYE (Eyes were dry, had to pour water into them), EYE IRRITATION (Eyes are burning), FATIGUE (Feel extreme fatigue,couldn't even lift up her head,exhausting/felt so fatigue), MYALGIA (pain in my arm", and like "someone was punching my arm". It never stopped, it kept getting worse), HEADACHE (Headache) and NAUSEA (Nausea) had not resolved and MOBILITY DECREASED (She couldn't walk 3-4 stairs), DYSPNOEA (Walking a short distance, I would feel out of breath), DIZZINESS (Dizziness), HYPERHIDROSIS (Pouring sweat), ASTHENIA (W eakness), OCULAR HYPERAEMIA (Eyes were blood shot and red) and ARTHRALGIA (Joints in her body started hurting really bad) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 02-Jul-2021, Body temperature: 102 f (High) Fever 102 F. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No relevant concomitant medications were reported. On 1-Jul-2021, patient used heating pad in arm three times This case was linked to MOD-2021-245599 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 16-Jul-2021: Follow up received on 16-JUL-2021, it contains no significant information. The contact info updated and qualification corrected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dehydration
- Hospital-Tage
- -
- Labordaten
- Test Date: 20210702; Test Name: Body temperature; Result Unstructured Data: Fever 102 F
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- F
- Eingang
- 26.02.2022
- Impfdatum
- 26.06.2021
- Beginn
- 26.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Dizziness
Tremor
Symptomtext
Shakiness in legs; Dizziness; Weakness; This spontaneous case was reported by a consumer and describes the occurrence of DIZZINESS (Dizziness), ASTHENIA (Weakness) and TREMOR (Shakiness in legs) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 039C21A) for COVID-19 vaccination. No Medical History information was reported. On 26-Jun-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 26-Jun-2021, the patient experienced DIZZINESS (Dizziness) and ASTHENIA (Weakness). On 01-Jul-2021, the patient experienced TREMOR (Shakiness in legs). At the time of the report, DIZZINESS (Dizziness) and ASTHENIA (Weakness) had not resolved and TREMOR (Shakiness in legs) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No relevant Concomitant Medications were reported. No Treatment Information Provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 28.01.2022
- Impfdatum
- 10.06.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 203,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Anticoagulant therapy
Arachnoid cyst
COVID-19
COVID-19 pneumonia
Chest pain
Computerised tomogram head abnormal
Computerised tomogram thorax normal
Fibrin D dimer increased
Headache
Hypoxia
Lung infiltration
Neurological examination normal
Normocytic anaemia
SARS-CoV-2 test positive
Symptomtext
Patient is fully vaccinated. COVID positive 12/31/2021 at admission to hospital. 51-year-old female who presented to the hospital with headaches, in the setting of an arachnoid cyst history. Arachnoid cyst was seen once again on CT of the head without contrast. She was evaluated by neurology, who deemed her stable for discharge with outpatient follow-up with neurosurgery. She had a normal neurological exam and a stable CT of the head, and her headaches seem to be controlled with Tylenol. She also had some slight hypoxia, and was found to be covid positive with covid 19 pneumonia. Positive for chest pain. She did exhibit a left lower lobe patchy infiltrate on the CT of the chest. D dimer elevated. Lovenox given. Negative for PE. Normocytic anemia. She was given some breathing treatmentsand decadron, and remained on room air for the rest of her admission. Stable for discharge. Will follow up with neurosurgery.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19 pneumonia
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 11.10.2021
- Impfdatum
- 03.08.2021
- Beginn
- 11.08.2021
- Tage bis Beginn
- 8,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Blood pressure abnormal
Cardiac flutter
Condition aggravated
Dizziness
Nausea
Symptomtext
Within the first week of receiving the 1st dose of Moderna, out of the blue I would start feeling pressure in my forehead -around my eyes and then my heart would start fluttering and feel like it was up in my throat and I would feel dizzy and nauseous. This happened several times within the 2 weeks after getting the shot. All my life I have had low blood pressure - but these episodes made me think my blood pressure was spiking! After I received the 2nd dose 28 days later - within days, the "blood pressure" episodes started happening daily and several times a day. Sometimes I feel like I am going to faint when this happens. This is when I looked up "heart fluttering/blood pressure" to figure out what was going wrong as I have always had low blood pressure! That's when I saw that heart inflammation was a side effect of the Moderna vaccine! All the symptoms described was what I was experiencing!! After 2 weeks of the 2nd dose, it seemed like the episodes had dwindled... but last week - October 6-8 - I started experiencing these symptoms again and I really hate the feeling of my heart fluttering and like it is in my throat and the feelings of weakness & nausea that follow. These episodes lasted for half an hour or so!!! I thought these symptoms would go away after a couple of weeks after the vaccine but now 6 weeks later, I am still experiencing them!
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- I have not yet gone to the doctor about this because I was hoping it would subside but now i will probably make an appointment with my family doctor to check into this further as I don't want to develop high blood pressure and heart problems when I had neither prior to August 3 and August 30, 2021 - when I got the 2 Moderna vaccines.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None - I have always had low blood pressure.
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 09.09.2021
- Impfdatum
- 09.09.2021
- Beginn
- 09.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest discomfort
Diabetes mellitus
Dyspnoea
Throat irritation
Symptomtext
chest tightness, scratchy throat, shortness of breath, diaphoresis
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- morbid obesity, HTN
- Andere Medikamente
- diltiazem, simvastatin, aspirin, clonidine, montelukast, tizandidine, cetirizine
- Allergien
- Flu vaccine, amoxicillin, Hepatitis vaccines, Lexapro, Toradol, Lisinopril, Tree nuts, Cymbalta, Pregabalin
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 20.08.2021
- Impfdatum
- 09.06.2021
- Beginn
- 12.06.2021
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Activated partial thromboplastin time
Blood thyroid stimulating hormone
C-reactive protein increased
Chest X-ray normal
Dyspnoea
Electrocardiogram abnormal
Fatigue
Full blood count
Metabolic function test
Palpitations
Prothrombin time
Red blood cell sedimentation rate
Supraventricular extrasystoles
Supraventricular tachycardia
Troponin
Ventricular extrasystoles
Symptomtext
Heart palpitations, shortness of breathe, fatigue
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- normal chest X-ray, CMP, CBC with auto diff, TSH, PT/PTT, troponin, ESR EKGx2 showed PVCs and PACs 4-hour holter monitor showed PACs, PVCs, and SVT C-Reactive Protein slightly elevated at 8.7 (however I couldn?t get this test ordered until 7/13/21)
- Aktuelle Erkrankungen
- No other illnesses
- Vorgeschichte
- No chronic conditions
- Andere Medikamente
- Velivet (birth control) Iron Vitamin D Biotin Adrenal support supplements
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- ND
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 11.08.2021
- Impfdatum
- 29.06.2021
- Beginn
- 02.07.2021
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Disturbance in attention
Fatigue
Feeling abnormal
Heart rate increased
Incomplete course of vaccination
Lymphadenopathy
Pain in extremity
Palpitations
Sensory disturbance
Sleep disorder
Symptomtext
On July 30, I was so fatigued I slept 19 of 24 hours. The next day I slept 14 hours. I had severe brain fog and was exhausted. My arm was also so sore it hurt to move it. Starting on July 2nd, three days after my second Moderna shot, I woke up in the early AM hours with my heart beating strongly and at a very high rate. I had a pulsing in my face around my eyes that was also very distracting and my entire body felt like it was vibrating. I took my heart rate and it was 110 beat/minute. I am a very fit individual, I am not overweight, I exercise regularly and eat healthy. I do not abuse drugs or alcohol and get 9 hours of rest per night. I was very alarmed and went to my local Urgent Med at 8AM. My heart rate did decrease to 80 beats/minute but it was still very strong - I could FEEL my heart beating. The doctor sent me home to self monitor. A few days later the lymph notes on my right side, where I had the shot, became extremely enlarged. I took Ibuprofen. My throat was also sore. These symptoms lasted three days. Of the course of the next 5 weeks my heart continued to pound no matter what I was doing and the pulsing in my face also continued to the point where these symptoms would wake me up. I also had a lot of brain fog and had trouble concentrating. I am writing this now on August 11 and this is the first week I feel normal. I will NOT be getting a booster shot. This was one of the scariest health developments I have ever had and this shot did something to my heart and entire system that I do not want to ever experience again. I am going to go to the doctor to have an EKG to ensure that my heart is functioning normally.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- You will have to contact my doctor for the results of my tests.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Valtrex
- Allergien
- Sulfa, Green Tea, Fish
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 28.07.2021
- Impfdatum
- 19.07.2021
- Beginn
- 23.07.2021
- Tage bis Beginn
- 4,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Chest pain
Electrocardiogram normal
Magnetic resonance imaging normal
Ultrasound scan normal
Symptomtext
Severe chest pains
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- 1,0
- Labordaten
- Negative EKG/Ultrasound/MRI for heart attack and/or stroke...
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Though my AC1 has never been over 6.5 they say diabetes. I am currently 6.1 Hypertension (Lisinopril) Both of these conditions are under control
- Andere Medikamente
- Lisinopril 25mg Multi-vitamin Biotin
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 27.07.2021
- Impfdatum
- 23.06.2021
- Beginn
- 25.06.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Arthritis
Chills
Cough
Dyspnoea
Nasopharyngitis
Pain
Symptomtext
After 2nd dose of vaccine, had coughing and cold for 2 days and cleared up. Then after 4 days of vaccine, started with joint pain and inflammation. All major joints experiencing severe pain periodically. Also will experience chills. Pain is severe, that is not experienced before vaccine. Also, feeling short of breath.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- not yet, will be contacting doctor.
- Aktuelle Erkrankungen
- myasthenia gravis, diabetes, asthma, fibromyelgia
- Vorgeschichte
- myasthenia gravis, diabetes, asthma, fibromyelgia
- Andere Medikamente
- yes, multiple on same meds.
- Allergien
- penicillin, codeine, aspirin, gentamicin, flagyl, skelaxin, macrolide
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 26.07.2021
- Impfdatum
- 08.07.2021
- Beginn
- 11.07.2021
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Atrial fibrillation
Cardiac flutter
Decreased appetite
Dyspnoea
Laboratory test normal
Rhinorrhoea
Tachycardia
Tremor
Symptomtext
Tachycardia, Afib, Pounding, Flutter (Heart) Short of Breath, runnier nose, Weak & Shaky, no Apatite.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- ER visit bloodwork within normal range.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- B50 Complex, Tylenol, carvedilol 6.25mg, flecainide 50mg, glucosamine-chondroitin-msn 50-40-167, Magnesium PO, multi-vitamin, vitamin c, warfarin 5mg,
- Allergien
- Haldol, Prolia, Timolol,
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 22.07.2021
- Impfdatum
- 13.07.2021
- Beginn
- 13.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Dizziness
Dyspnoea
Fatigue
Headache
Injection site pain
Symptomtext
Symptoms after and until now are injection site pain, tiredness, headache, shortness of breath when I move around and I have a habit of running every morning. Since the vaccine I lack of more air. I have dizziness and before I didn't have any, also I have slight chest pains and tiredness which previously I didn't have.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Before filling out this document. NO
- Vorgeschichte
- No sickness
- Andere Medikamente
- No medication prescribe.
- Allergien
- None before the mandatory vaccine that my boss make take by the University.
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 12.07.2021
- Impfdatum
- 08.06.2021
- Beginn
- 01.06.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Mobility decreased
Musculoskeletal stiffness
Myalgia
Pain in extremity
Symptomtext
Arm was sore for 2 weeks then became stiff and unable to raise my arm. I can now raise my arm but my muscle is still extremely painful
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- No tests were done. I was prescribed Ibuprofen
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- diabetes 2, high blood pressure, high cholesterol
- Andere Medikamente
- Xigduo, Lisinopril, Amlodipine, Atorvastatin, Vitamin D
- Allergien
- allergic to sulphur
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 12.07.2021
- Impfdatum
- 21.06.2021
- Beginn
- 23.06.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest pain
Computerised tomogram normal
Fibrin D dimer increased
Symptomtext
Chest pain starting on the second day after the second dose. Still occurring as of this submission. Presumed pericarditis after my last appointment with Cardiologist. Colchicine and ibuprofen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Ddimmer was high on June 27 2021. Went to ED for CT scan, as blood clots were concerned. Scan of Lungs clear. Echocardiogram pending for the 19th of July.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Ocycodine
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 11.07.2021
- Impfdatum
- 13.06.2021
- Beginn
- 15.06.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site pain
Mobility decreased
Pain
Symptomtext
The patient reported to the pharmacist on duty on 07/11/2021 that two days after receiving the second dose of the moderna COVID19 vaccine she began experiencing "excruciating pain" in the left arm where the injection was given: described as a sharp, shooting pain like knives. The patient reported a loss of use of the affected (left) arm and suffered immobility of the arm due to the pain for 6 days post-onset. The condition resolved spontaneously and she did not seek medical care.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- ND
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 02.07.2021
- Impfdatum
- 01.07.2021
- Beginn
- 02.07.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Erythema
Joint swelling
Migraine
Nausea
Pain in extremity
Symptomtext
Pain in right and left arm, redness, swelling in wrists, migraine, nausea,
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- Covid arm
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High blood pressure
- Andere Medikamente
- Lisinopril Cymbalta spironolactone birth control, tylenol, advil, and benadryl allergy
- Allergien
- Flu shot
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 29.06.2021
- Impfdatum
- 07.06.2021
- Beginn
- 06.06.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Chest X-ray
Chest discomfort
Dyspnoea
Electrocardiogram
Exercise tolerance decreased
Fatigue
Gastrooesophageal reflux disease
Hyperhidrosis
Palpitations
Vaccination complication
Symptomtext
immediate heart palpitations and sweating. 2 days later tighteness of the chest and trouble breathing. trouble breathing for 7 days after vaccine along with fatigue and inability to tolerate exercise. up every single night trying to catch breath along with acid reflux. needed IV treatment, nebulizer, and supplements.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- ekg, CXR, blood work June 13ths. 2021, reuslts normal at Medical Center. D/C diagnosis: Covid-19 vaccine reaction
- Aktuelle Erkrankungen
- mold illness
- Vorgeschichte
- mold toxicity
- Andere Medikamente
- -
- Allergien
- erythromycin & cephalexin
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 28.06.2021
- Impfdatum
- 27.06.2021
- Beginn
- 28.06.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest discomfort
Chest pain
Symptomtext
CHEST PAIN AND DISCOMFORT, HEAVINESS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 28.06.2021
- Impfdatum
- 22.06.2021
- Beginn
- 27.06.2021
- Tage bis Beginn
- 5,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test normal
Chest pain
Dizziness
Electrocardiogram
Troponin
Symptomtext
Chest pain and lightheaded. Resolved prior to arrival in ED
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Troponon, EKG and blood work negative for acute cardiac condition
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Wellbutrin 150mg daily Bit B2 Daily Omega 3 BID
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 24.06.2021
- Impfdatum
- 18.06.2021
- Beginn
- 19.06.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dyspnoea
Headache
Pain
Pyrexia
SARS-CoV-2 test negative
Symptomtext
PT WOKE UP OM 6/19/21 WITH 102.6 DEGREE FEVER. FEVER LASTED FOR ABOUT 2-3 DAYS. PT ALSO REPORTS SOB, HA, BODY ACHES. PT TOOK TYLENOL AND IBUPROFEN PRIOR TO BEING SEEN IN CLINIC 6/24/21. SHE WAS GIVEN 30 MG OF TORODOL IM AT THIS VISIT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- RAPID COVID TEST WAS PERFORMED WITH NEGATIVE RESULT AT TIME OF VISIT 6/24/21
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- ANXIETY, DEPRESSION
- Andere Medikamente
- FLUOXETINE, KLONOPIN
- Allergien
- REGLAN
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 22.06.2021
- Impfdatum
- 11.06.2021
- Beginn
- 12.06.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest X-ray normal
Chills
Dyspnoea
Erythema
Headache
Limb discomfort
Lung disorder
Peripheral swelling
Pyrexia
Tenderness
Symptomtext
On Saturday the 12th she experienced fever, chills and a slight headache. And her arm was tender and felt heavy. It was swollen and slightly red. On Sunday she started having trouble breathing. She went to a Medical Center and they checked her vitals. They gave her an inhaler (Albuterol). She used that on Sunday. She still was having issues on Monday. She took a Benadryl hoping that would help. Tuesday she was still having breathing issues. She then went to her PCP, who ordered a chest X ray. It came back normal. Her doctor was concerned it may be a pulmonary issue. The doctor told her to continue to take her inhaler. She tried taking a shower to get steam. She then took a medicine she was prescribed for her allergies to tree pollen called Montelukast 10 MG 1x daily. She also tried a daytime allergy medicine taken during pollen season. She started feeling better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Chest X ray
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Junel Fe 1/20 1xdaily; Spironolactone 50mg 1xdaily
- Allergien
- Pine trees; Pollen; Amoxicillin
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 13.06.2021
- Impfdatum
- 10.06.2021
- Beginn
- 10.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest discomfort
Chest pain
Chills
Dizziness
Nausea
Pharyngeal swelling
Sensation of foreign body
Symptomtext
Dizziness, nausea, chills lasting 20-30 minutes tightness in chest / light pain near heart, lump/swelling in throat lasting 5-6 hours then tapering down for the next 4 hours
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 12.06.2021
- Impfdatum
- 12.06.2021
- Beginn
- 12.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Lip swelling
Paraesthesia oral
Symptomtext
tingling in lips and he states he feels swelling in lips, but no visible swelling noted
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia oral
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- rash on forearm and redness
- Staat
- PR
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 06.12.2022
- Impfdatum
- 05.12.2022
- Beginn
- 05.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Formication
Hypoaesthesia
Pruritus
Rash
Rash erythematous
Spider vein
Symptomtext
I was not observed after the shot. About 7 minutes later I got a sudden and severe itch on my left lower jaw with a bright red rash, my left nostril felt like ants crawling over it, the rash then spread a lighter red up my cheeks, over my chin, and to the right side of my face. Once it spread the itch went away, the itch lasted about 7 minutes. The rash then turned brighter and no longer spread, the brightest spots were along my jawline and followed a line to the other side of my jaw and was very dense (it looked like a severe sunburn) the rash on my cheeks and chin were not as bright (it looked like I got slapped repeatedly on both cheeks) it also showed what appeared to be spider veins on my cheeks that were bright red. We were stuck in traffic and couldn?t get to ER the rash lasted an hour and complete disappeared, it left a numb internal feeling on my right cheek, I took a Benadryl and this feeling went away in 5 minutes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- Stuck in traffic
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- CRPS/RSD and Dystonia in left hand which affects left arm for 11 years. Diagnosed with MS 11 years ago, then told a year later that the brain lesions didn?t change and I don?t have MS, doctors attribute my neurological issues of Dystonia with the radiation injury to my hand which affects my walking at sporadic times.
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 27.04.2022
- Impfdatum
- 26.10.2021
- Beginn
- 10.04.2022
- Tage bis Beginn
- 166,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
COVID-19
Cough
Fatigue
Rhinorrhoea
SARS-CoV-2 test positive
Sinus congestion
Vaccine breakthrough infection
Symptomtext
Breakthrough covid. No fever. Cough, sinus congestion, runny nose, weakness, fatigue for about 5 times. Lingering weakness and fatigue continuing to date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Positive PCR 4/10/22
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Hashimoto's, PCOS
- Andere Medikamente
- Synthroid, Atenolol, Fluoxetine, Metformin, multivitamin, vitamin D, zyrtec, aspirin, iron
- Allergien
- aleve
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 28.03.2022
- Impfdatum
- 19.08.2021
- Beginn
- 10.02.2022
- Tage bis Beginn
- 175,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Urticaria
Symptomtext
Body broke out into hives from head to toe
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Effexor
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 12.03.2022
- Impfdatum
- 31.07.2021
- Beginn
- 31.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Symptomtext
Headache onset each time after shot. Last for about a month or so; did not seek treatment. I filled out the VSAFE questionnaire and someone called suggested I fill out this form.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Diagnosed with 6.5 A1C diabetes 12/22/21 Diagnosed with 6.4 A1C Pre-diabetes 6/16/2021
- Vorgeschichte
- Hypothyroidism, anemia
- Andere Medikamente
- None
- Allergien
- Biaxin, Septra
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 26.02.2022
- Impfdatum
- 19.08.2021
- Beginn
- 20.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Headache
Myalgia
Tinnitus
Symptomtext
Ringing in her ears; Headache; sore arm; This spontaneous case was reported by a consumer and describes the occurrence of MYALGIA (sore arm), HEADACHE (headache) and TINNITUS (ringing in her ears) in a 66-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 039C21A) for COVID-19 vaccination. No Medical History information was reported. On 19-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 20-Aug-2021, the patient experienced MYALGIA (sore arm), HEADACHE (headache) and TINNITUS (ringing in her ears). On 21-Aug-2021, MYALGIA (sore arm), HEADACHE (headache) and TINNITUS (ringing in her ears) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 26.02.2022
- Impfdatum
- 19.06.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Fatigue
Product dose omission issue
Symptomtext
couldn't get warm/had chills; felt tired; More than 35 days after the first dose without receiving the second dose; This spontaneous case was reported by a consumer and describes the occurrence of CHILLS (couldn't get warm/had chills), FATIGUE (felt tired) and PRODUCT DOSE OMISSION ISSUE (More than 35 days after the first dose without receiving the second dose) in a 58-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 039C21A) for COVID-19 vaccination. No medical history information was reported. Concomitant products included AMLODIPINE and LISINOPRIL for an unknown indication. On 19-Jun-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced CHILLS (couldn't get warm/had chills), FATIGUE (felt tired) and PRODUCT DOSE OMISSION ISSUE (More than 35 days after the first dose without receiving the second dose). At the time of the report, CHILLS (couldn't get warm/had chills) and FATIGUE (felt tired) outcome was unknown and PRODUCT DOSE OMISSION ISSUE (More than 35 days after the first dose without receiving the second dose) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Treatment information was not provided. Patient missed appointment for the second dose on 17-jul-2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: No medical history information was reported.
- Andere Medikamente
- AMLODIPINE; LISINOPRIL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- F
- Eingang
- 26.02.2022
- Impfdatum
- 08.07.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Malaise
Pain
Pyrexia
Symptomtext
Generally didn't feel well; Aches; Chills; Fever; This spontaneous case was reported by a nurse and describes the occurrence of MALAISE (Generally didn't feel well), PAIN (Aches), CHILLS (Chills) and PYREXIA (Fever) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 039C21A) for COVID-19 vaccination. The patient's past medical history included COVID-19 (The patient was hospitalized for Covid-19 the last week of May and was treated with monoclonal antibody therapy.). Previously administered products included for an unreported indication: BAMLANIVIMAB and REMDESIVIR. On 08-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced MALAISE (Generally didn't feel well), PAIN (Aches), CHILLS (Chills) and PYREXIA (Fever). The patient was treated with PARACETAMOL (TYLENOL) at an unspecified dose and frequency. At the time of the report, MALAISE (Generally didn't feel well), PAIN (Aches), CHILLS (Chills) and PYREXIA (Fever) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Concomitant product use was not provided by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19 (The patient was hospitalized for Covid-19 the last week of May and was treated with monoclonal antibody therapy.)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 26.02.2022
- Impfdatum
- 22.06.2021
- Beginn
- 23.06.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Erythema
Fatigue
Headache
Skin warm
Vomiting
Symptomtext
This spontaneous case was reported by a consumer and describes the occurrence of SKIN WARM (Hot to the touch), ASTHENIA (Doesn?t have the energy as it used too), ERYTHEMA (Redness started to go up the arm), HEADACHE (More frequent head aches) and FATIGUE (Feeling more tired) in a 39-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 039C21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 22-Jun-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 23-Jun-2021, the patient experienced HEADACHE (More frequent head aches), FATIGUE (Feeling more tired) and VOMITING (Felt like going to throw up). On an unknown date, the patient experienced SKIN WARM (Hot to the touch), ASTHENIA (Doesn?t have the energy as it used too) and ERYTHEMA (Redness started to go up the arm). At the time of the report, SKIN WARM (Hot to the touch), ASTHENIA (Doesn?t have the energy as it used too), ERYTHEMA (Redness started to go up the arm), HEADACHE (More frequent head aches), FATIGUE (Feeling more tired) and VOMITING (Felt like going to throw up) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Concomitant product use was not provided. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 27.07.2021
- Beginn
- 27.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Lymphadenopathy
Pain
Pharyngeal swelling
Swelling
Tenderness
Symptomtext
Approx 45 minutes after vaccine, throat swelling that started to decrease after about 3 hours. Mild swelling, no wheezing noted, but noticeable when swallowing and eating. The next day, approx 12 hours later, supraclavicular lymph node enlargement, pain, and tenderness on left side (the side of vaccine). Tenderness and swelling lasted approx 1.5-2 weeks, gradually decreasing. Reported results to online site that checks in on pt after COVID 19 vaccine, symptoms checker
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- None Seen ER physician at work about lymph node enlargement and tenderness, thinks it was a reaction to vaccine
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypothyroidism (Hashimoto?s) Acne Pemphigus Folicaeous Seasonal Allergies GERD
- Andere Medikamente
- Synthroid Spironolactone Depo-Provera IM injection every 3 months (last in June 22/2021) Multivitamin
- Allergien
- Demerol IV
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 14.05.2021
- Beginn
- 01.07.2021
- Tage bis Beginn
- 48,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Eczema
Rash
Symptomtext
Eczema all over my body. Saw primary MD in August 2021, prescribed cortisone cream. Cream used but eczema rash continues to develop in new areas.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- N/a
- Vorgeschichte
- History of immune issues (low IGG) , these issues were not present when vaccinated.
- Andere Medikamente
- Fluoxetine 40 mg Singular 10 mg Xyzal 5 mg Prilosec 40 mg Cytomel 5 mcg Synthroid 75 mcg Ambien 10 mg
- Allergien
- Clindamycin
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 06.01.2022
- Impfdatum
- 20.08.2021
- Beginn
- 05.01.2022
- Tage bis Beginn
- 138,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Abdominal pain
COVID-19
Rectal haemorrhage
SARS-CoV-2 test positive
Symptomtext
ABDOMINAL PAIN AND RECTAL BLEEDING
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- POSITIVE COVID-19 PCR 1/5/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Rheumatoid arthritis, hypertension, GERD, mesenteric vein thrombosis on apixaban
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 18.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 9,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Extra dose administered
Injection site pain
Injection site pruritus
Pruritus
Symptomtext
Itching and burning at injection site, then spread throughout body, worse at hairlines, chest, arms, and stomach
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Daily multi -vitamins, fish oil
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 15.11.2021
- Impfdatum
- 23.10.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Lymphadenopathy
Myalgia
Pruritus
Pyrexia
Splenomegaly
Vaccination site erythema
Vaccination site swelling
Symptomtext
patient's spleen enlarged 6 times the normal size; has had itching from head to toe; left arm pit is also swollen.; had fever,; arm of the injection has been red from her shoulder to her elbow; arm of the injection has been swollen from her shoulder to her elbow.; aches; joint pain; This spontaneous case was reported by a pharmacist and describes the occurrence of SPLENOMEGALY (patient's spleen enlarged 6 times the normal size), PRURITUS (has had itching from head to toe), LYMPHADENOPATHY (left arm pit is also swollen.), PYREXIA (had fever,) and VACCINATION SITE ERYTHEMA (arm of the injection has been red from her shoulder to her elbow) in a 67-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 039C21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 23-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. In 2021, the patient experienced SPLENOMEGALY (patient's spleen enlarged 6 times the normal size), PRURITUS (has had itching from head to toe), LYMPHADENOPATHY (left arm pit is also swollen.), PYREXIA (had fever,), VACCINATION SITE ERYTHEMA (arm of the injection has been red from her shoulder to her elbow), VACCINATION SITE SWELLING (arm of the injection has been swollen from her shoulder to her elbow.), MYALGIA (aches) and ARTHRALGIA (joint pain). At the time of the report, SPLENOMEGALY (patient's spleen enlarged 6 times the normal size), LYMPHADENOPATHY (left arm pit is also swollen.), PYREXIA (had fever,), VACCINATION SITE ERYTHEMA (arm of the injection has been red from her shoulder to her elbow), VACCINATION SITE SWELLING (arm of the injection has been swollen from her shoulder to her elbow.), MYALGIA (aches) and ARTHRALGIA (joint pain) outcome was unknown and PRURITUS (has had itching from head to toe) had not resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medications were reported. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 05.11.2021
- Impfdatum
- 23.10.2021
- Beginn
- 23.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Erythema
Pain
Pain in extremity
Peripheral swelling
Pruritus
Pyrexia
Splenomegaly
Symptomtext
Spleen enlarged up to six times normal size, itchy from head to toe, fever of 99.4 (treated with tylenol), aches, joint pain, arms red, swollen and sore from shoulder to elbow.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- Originally diagnosed with cellulitis at injection site; treated with antibiotics. Oncologist later stated it wasn't cellulitis just normal immune response to booster.
- Aktuelle Erkrankungen
- Splenic marginal Zone stage 4 lymphoma
- Vorgeschichte
- splenic marginal zone stage 4 lymphoma
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- HI
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 01.11.2021
- Impfdatum
- 28.10.2021
- Beginn
- 29.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal discomfort
Chills
Diarrhoea
Fatigue
Pain
Pyrexia
Symptomtext
Vax administered Thursday at noon Thursday evening, chills, slight fever (99.9), body aches Friday morning at wakeup (530am), woke up with fatigue, body aches. Continued through bedtime (9pm) Friday night Saturday morning, fever, body aches were better, but stomach was upset (not nausea, but unsettled.) Diarrhea started at 930 am. Sunday, unsettled stomach, diarrhea. Monday, unsettled stomach, diarrhea, and body aches are back. No fever or chills. Treating with fluids (water, tea and gatorade), soup, crackers, bananas, Aleve for the body aches.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- COPD
- Andere Medikamente
- Rovustatin, 10 mg, twice a day Wixcela inhaler, twice a day
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 29.10.2021
- Impfdatum
- 25.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Burning sensation
Clumsiness
Confusional state
Dizziness
Fatigue
Swelling
Tenderness
Symptomtext
Burning fatigue swelling clumsiness dizzy sore to touch 4 days later aching in every joint confusion
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Dystonia heart anomaly diabetes
- Andere Medikamente
- Levetiracetam 1400 mg a day carbedidol isosorbide mon er30 2 x per day lisinapril 2.5 daily medium 1 x daily junevia metformin 500 mg baclofen 10 mg 3 x aday b-12 vit e zinc
- Allergien
- Latex tape erothromiacin augmenton
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 27.10.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Nausea
Pruritus
Symptomtext
Approximately 14-15minutes after receiving Moderna vaccine (dose 1), patient c/o itching to scalp, ears, arms, legs and nausea. MD evaluated patient who recommended transferring of patients to ER. Patient transferred to ER.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- HTN
- Andere Medikamente
- None
- Allergien
- PCN
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 13.10.2021
- Impfdatum
- 02.07.2021
- Beginn
- 02.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Symptomtext
Patient allergic to everything, after 20 minutes reports feeling itching on arm. Situation was evaluated and she will go to emergency.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Shellfish
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 06.10.2021
- Impfdatum
- 17.09.2021
- Beginn
- 17.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Nausea
Pyrexia
Vaccination site induration
Vaccination site warmth
Symptomtext
injection site gets warm to the touch/ injection site especially gets hot with sun exposure; There is a kind of hardness in his arm at the injection site; also experienced fever; chills; nausea; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE WARMTH (injection site gets warm to the touch/ injection site especially gets hot with sun exposure), VACCINATION SITE INDURATION (There is a kind of hardness in his arm at the injection site), PYREXIA (also experienced fever), CHILLS (chills) and NAUSEA (nausea) in a 44-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 039C21A) for COVID-19 vaccination. Concurrent medical conditions included Blood pressure management (Blood pressure) and Blood cholesterol abnormal (Cholesterol). On 17-Sep-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 17-Sep-2021, the patient experienced PYREXIA (also experienced fever), CHILLS (chills) and NAUSEA (nausea). On an unknown date, the patient experienced VACCINATION SITE WARMTH (injection site gets warm to the touch/ injection site especially gets hot with sun exposure) and VACCINATION SITE INDURATION (There is a kind of hardness in his arm at the injection site). The patient was treated with IBUPROFEN for Adverse event, at an unspecified dose and frequency. On 20-Sep-2021, PYREXIA (also experienced fever), CHILLS (chills) and NAUSEA (nausea) had resolved. At the time of the report, VACCINATION SITE WARMTH (injection site gets warm to the touch/ injection site especially gets hot with sun exposure) and VACCINATION SITE INDURATION (There is a kind of hardness in his arm at the injection site) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Concomitant medications reported for indication Blood Pressure and Cholesterol with unknown medications This case was linked to MOD-2021-333268 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Blood cholesterol abnormal (Cholesterol); Blood pressure management (Blood pressure)
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 06.10.2021
- Impfdatum
- 17.09.2021
- Beginn
- 17.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Nausea
Pyrexia
Vaccination site bruising
Vaccination site discolouration
Vaccination site mass
Vaccination site swelling
Vaccination site warmth
Symptomtext
Area is warm to touch; Really swollen, it got to the size of nickle; Pretty good sized bump; Discolored where bump is; It bruised right away; It's feverish on and off/it's feverish on and off; Dizziness; Nausea; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE BRUISING (It bruised right away), VACCINATION SITE MASS (Pretty good sized bump), VACCINATION SITE DISCOLOURATION (Discolored where bump is), VACCINATION SITE WARMTH (Area is warm to touch) and VACCINATION SITE SWELLING (Really swollen, it got to the size of nickle) in a 28-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 039C21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No medical history was provided by the reporter. Concomitant products included MULTIVITAMINS [VITAMINS NOS] for an unknown indication. On 17-Sep-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 17-Sep-2021, the patient experienced VACCINATION SITE BRUISING (It bruised right away), PYREXIA (It's feverish on and off/it's feverish on and off), DIZZINESS (Dizziness) and NAUSEA (Nausea). On 27-Sep-2021, the patient experienced VACCINATION SITE DISCOLOURATION (Discolored where bump is). On an unknown date, the patient experienced VACCINATION SITE MASS (Pretty good sized bump), VACCINATION SITE WARMTH (Area is warm to touch) and VACCINATION SITE SWELLING (Really swollen, it got to the size of nickle). The patient was treated with IBUPROFEN at an unspecified dose and frequency. On 23-Sep-2021, PYREXIA (It's feverish on and off/it's feverish on and off), DIZZINESS (Dizziness) and NAUSEA (Nausea) had resolved. At the time of the report, VACCINATION SITE BRUISING (It bruised right away), VACCINATION SITE MASS (Pretty good sized bump), VACCINATION SITE DISCOLOURATION (Discolored where bump is), VACCINATION SITE WARMTH (Area is warm to touch) and VACCINATION SITE SWELLING (Really swollen, it got to the size of nickle) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. This case was linked to MOD-2021-333519 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: No medical history was provided by the reporter.
- Andere Medikamente
- MULTIVITAMINS [VITAMINS NOS]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 22.09.2021
- Impfdatum
- 15.06.2021
- Beginn
- 30.06.2021
- Tage bis Beginn
- 15,0
- Dosis
- 2
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Pain
Skin discolouration
Swelling
Ultrasound scan
Symptomtext
Onset of swelling, pain, color change to right lower extremity on 6/30/2021. Presented to office for evaluation and to establish care on 9/13/2021
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- Ultra sound of LLE
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- SD
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 17.09.2021
- Impfdatum
- 14.07.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Headache
Illness
Vomiting
Weight decreased
Symptomtext
sick as a dog/still sick a month later/made me sick; lost 20 pounds/She's lost 18 pounds; can't hold anything down; can't get rid of my headache/ plagued with headaches; can't quit throwing up/throwing up water and bile; This spontaneous case was reported by a consumer and describes the occurrence of ILLNESS (sick as a dog/still sick a month later/made me sick), WEIGHT DECREASED (lost 20 pounds/She's lost 18 pounds), ASTHENIA (can't hold anything down), HEADACHE (can't get rid of my headache/ plagued with headaches) and VOMITING (can't quit throwing up/throwing up water and bile) in a 61-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 006D21A and 039C21A) for COVID-19 vaccination. No Medical History information was reported. On 14-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 11-Aug-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient experienced ILLNESS (sick as a dog/still sick a month later/made me sick), WEIGHT DECREASED (lost 20 pounds/She's lost 18 pounds), ASTHENIA (can't hold anything down), HEADACHE (can't get rid of my headache/ plagued with headaches) and VOMITING (can't quit throwing up/throwing up water and bile). The patient was treated with ACETYLSALICYLIC ACID, CAFFEINE, PARACETAMOL (EXCEDRIN [ACETYLSALICYLIC ACID;CAFFEINE;PARACETAMOL]) for Headache, at a dose of 6-8 Excedrin a day. At the time of the report, ILLNESS (sick as a dog/still sick a month later/made me sick), WEIGHT DECREASED (lost 20 pounds/She's lost 18 pounds), ASTHENIA (can't hold anything down), HEADACHE (can't get rid of my headache/ plagued with headaches) and VOMITING (can't quit throwing up/throwing up water and bile) had not resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Patient has stated that she underwent MRI scan to her brain but can't found anything No concomitant medications were reported. Patient has stated that it hits her hard and felt angry and she felt plagued with headache and had headache prior to the vaccine. Most recent FOLLOW-UP information incorporated above includes: On 08-Sep-2021: Updated Reporter information, Updated patient details, Updated treatment partial frequency, Added patient lab details, Added suspect start dates and lot numbers, Added events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 16.09.2021
- Impfdatum
- 29.08.2021
- Beginn
- 01.09.2021
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site pain
Injection site rash
Injection site warmth
Lymphadenopathy
Symptomtext
Patient reported to Pharmacy injection site rash, with tenderness on 9/08/2021. Rash around injection site was about 6 inches in diameter and warm to the touch at the time patient presented to pharmacy. The right arm lymph nodes were enlarged.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none reported
- Vorgeschichte
- none reported
- Andere Medikamente
- none reported
- Allergien
- none reported
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 13.09.2021
- Impfdatum
- 03.08.2021
- Beginn
- 31.08.2021
- Tage bis Beginn
- 28,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Fatigue
Myalgia
Pyrexia
Symptomtext
Fatigue; Body aches / Muscle Pain; Chills; Fever; This spontaneous case was reported by a consumer and describes the occurrence of FATIGUE (Fatigue), MYALGIA (Body aches / Muscle Pain), CHILLS (Chills) and PYREXIA (Fever) in a 65-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 017E21A and 039C21A) for COVID-19 vaccination. No Medical History information was reported. On 03-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 31-Aug-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 31-Aug-2021, the patient experienced FATIGUE (Fatigue), MYALGIA (Body aches / Muscle Pain), CHILLS (Chills) and PYREXIA (Fever). On 31-Aug-2021, PYREXIA (Fever) had resolved. At the time of the report, FATIGUE (Fatigue), MYALGIA (Body aches / Muscle Pain) and CHILLS (Chills) outcome was unknown. patient stated fever occurred only last night and does not have fever that day. Concomitant medications were not provided. Treatment includes intake of lot of fluids.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 13.09.2021
- Impfdatum
- 10.06.2021
- Beginn
- 18.06.2021
- Tage bis Beginn
- 8,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Blood test
Burning sensation
Chronic obstructive pulmonary disease
Dizziness
Headache
Middle ear effusion
Rhinorrhoea
X-ray
Symptomtext
My lungs felt like it was burning. I had a headache. I a running Nosie. My ears was fluid. I felt dizzy. I went to the ER. They did x-rays and blood work. They said I had COPD.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- x-ray blood work
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- sleep apnea
- Andere Medikamente
- Complete Vitamin, Eye care vitamin
- Allergien
- amoxicillin, Narcan
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 11.09.2021
- Impfdatum
- 06.07.2021
- Beginn
- 17.08.2021
- Tage bis Beginn
- 42,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Headache
Inappropriate schedule of product administration
Malaise
Nausea
Symptomtext
Feeling unwell; Fatigue; Headache; Nausea; first dose of the Moderna COVID-19 vaccine on 06Jul2021 and the second on 17Aug2021; This spontaneous case was reported by a consumer and describes the occurrence of MALAISE (Feeling unwell), FATIGUE (Fatigue), HEADACHE (Headache), NAUSEA (Nausea) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (first dose of the Moderna COVID-19 vaccine on 06Jul2021 and the second on 17Aug2021) in a 67-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 039C21A and 040C21A) for COVID-19 vaccination. Concurrent medical conditions included Nerve pain and Rheumatoid arthritis. Concomitant products included GABAPENTIN for Nerve pain, SALICYLIC ACID (SALVAX) for Rheumatoid arthritis. On 06-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 17-Aug-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 17-Aug-2021, the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (first dose of the Moderna COVID-19 vaccine on 06Jul2021 and the second on 17Aug2021). On an unknown date, the patient experienced MALAISE (Feeling unwell), FATIGUE (Fatigue), HEADACHE (Headache) and NAUSEA (Nausea). The patient was treated with PARACETAMOL (TYLENOL) for Adverse event, at an unspecified dose and frequency. On 17-Aug-2021, INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (first dose of the Moderna COVID-19 vaccine on 06Jul2021 and the second on 17Aug2021) had resolved. At the time of the report, MALAISE (Feeling unwell), FATIGUE (Fatigue), HEADACHE (Headache) and NAUSEA (Nausea) outcome was unknown. Patient didn't feel well, was fatigued, had a headache, all around didn't feel good at all, had nausea, was tired. Side effects started that afternoon.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Nerve pain; Rheumatoid arthritis
- Vorgeschichte
- -
- Andere Medikamente
- GABAPENTIN; SALVAX
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 10.09.2021
- Impfdatum
- 23.07.2021
- Beginn
- 23.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Dry eye
Eye pain
Photopsia
Vision blurred
Symptomtext
For three nights after the first vaccine shot I had flashes of lights in my right eye when I closed them. After three days my right eye became very dry. Since that time my right eye is blurry off and on. After the second vaccine shot both eyes Ache all the time and I se flashes of light off to the sides of my eyes when they are closed. I have waited to get them checked to see if they would recover. This has not happened.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Eye pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 09.09.2021
- Impfdatum
- 28.08.2021
- Beginn
- 30.08.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Headache
Injection site pain
Symptomtext
I had a little bit of a headache and my right arm where the injection is - was kind of hurting a little bit (which is a normal reaction to the vaccine). Also, I had a little bit of fatigue. Those symptoms lasted a day or two. Those symptoms did come back - came and went - but they are not doing that anymore. I just let it pass - as far as letting symptoms run it's course- no treatment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- no
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- arthritis; high blood pressure
- Andere Medikamente
- High blood pressure medicine Lisinopril; Ciprilapram - for anxiety and depression; Prednisone for arthritis
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 08.09.2021
- Impfdatum
- 22.06.2021
- Beginn
- 01.07.2021
- Tage bis Beginn
- 9,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Feeling abnormal
Pain in extremity
Symptomtext
This spontaneous case was reported by a patient and describes the occurrence of PAIN IN EXTREMITY (Sore arm), DIZZINESS (Lightheadedness) and FEELING ABNORMAL (It is still sore, know exactly where receive the shot, can feel it exactly) in a 63-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 040C21A and 039C21A) for COVID-19 vaccination. No Medical History information was reported.On 22-Jun-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 20-Jul-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. In July 2021, the patient experienced PAIN IN EXTREMITY (Sore arm), DIZZINESS (Lightheadedness) and FEELING ABNORMAL (It is still sore, know exactly where receive the shot, can feel it exactly). At the time of the report, PAIN IN EXTREMITY (Sore arm), DIZZINESS (Lightheadedness) and FEELING ABNORMAL (It is still sore, know exactly where receive the shot, can feel it exactly) had not resolved. Concomitant product use was not provided. Treatment information was not provided. Patient received both doses of the Moderna COVID-19 Vaccine and called to report a sore arm still today and a lightheadedness that is ongoing.The patient said that thought the lightheadedness was going to pass but has been going on. The symptoms started between 4 to 6 days after the second dose and have been having it since. He is going to see the doctor next Friday.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 07.09.2021
- Impfdatum
- 01.09.2021
- Beginn
- 02.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Dizziness
Gait disturbance
Headache
Joint swelling
Musculoskeletal stiffness
Nausea
Pain in extremity
Pyrexia
Stomatitis
Tongue blistering
Symptomtext
High fever 103.5 , chills for 6-8 hours, unable to hold objects without dropping them, very dizzy, stiff, unsteady walking, Nausea, and extreme headache for 4 days and off and on continuing today 9/7/21, Mouth sores started day 4 with extreme nausea. Blister on tongue., swollen joints in hand/ pain. Headache.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Did not go to doctor. Thought it would go away. Should I go to doctor.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asthma, allergies, NSVT , migraines, degenerative disease, ruptured disc, fibromyalgia.
- Andere Medikamente
- None
- Allergien
- Tomatoes, corn, walnuts And environmental allergies
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 04.09.2021
- Impfdatum
- 09.08.2021
- Beginn
- 10.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Rash
Symptomtext
Pretty bad looking rash on both of my legs; This spontaneous case was reported by a consumer and describes the occurrence of RASH (Pretty bad looking rash on both of my legs) in a 77-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 039C21A) for COVID-19 vaccination. The patient's past medical history included Angioedema (angioedema/anaphylaxis when patient took a sulfa medication.). On 09-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 10-Aug-2021, the patient experienced RASH (Pretty bad looking rash on both of my legs). In August 2021, RASH (Pretty bad looking rash on both of my legs) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Concomitant medications were not reported. Treatment medications were not reported. It was stated that the patient experienced the same rash when patient took INH in the 70s for a positive PPD.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Angioedema (angioedema/anaphylaxis when patient took a sulfa medication.)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 02.09.2021
- Impfdatum
- 29.08.2021
- Beginn
- 29.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Pain
Pain in extremity
Symptomtext
Dose was administered from vial that was initially punctured 2 days prior, therefor expired. Patient did not experience any reaction aside from expected side effects of vaccine. Patient did report sore arm the night of injection, and body aches the day following.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 02.09.2021
- Impfdatum
- 16.06.2021
- Beginn
- 14.08.2021
- Tage bis Beginn
- 59,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Headache
Hot flush
Inappropriate schedule of product administration
Limb discomfort
Symptomtext
1st dose June 16 2021/ 2nd dose 13August 2021; Hot flushes; felt like his arm was gonna fall out; Headache; This spontaneous case was reported by a patient and describes the occurrence of HOT FLUSH (Hot flushes), LIMB DISCOMFORT (felt like his arm was gonna fall out), INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (1st dose June 16 2021/ 2nd dose 13August 2021) and HEADACHE (Headache) in a 25-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 039C21A and 039C21A) for COVID-19 vaccination. Concomitant products included CLONIDINE and LORAZEPAM (ATIVAN) for an unknown indication. On 16-Jun-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 13-Aug-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 14-Aug-2021, the patient experienced HOT FLUSH (Hot flushes), LIMB DISCOMFORT (felt like his arm was gonna fall out) and HEADACHE (Headache). On an unknown date, the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (1st dose June 16 2021/ 2nd dose 13August 2021). At the time of the report, HOT FLUSH (Hot flushes), LIMB DISCOMFORT (felt like his arm was gonna fall out) and HEADACHE (Headache) outcome was unknown and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (1st dose June 16 2021/ 2nd dose 13August 2021) had resolved. No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- CLONIDINE; ATIVAN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 30.08.2021
- Impfdatum
- 20.07.2021
- Beginn
- 20.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pain
Injection site swelling
Injection site warmth
Symptomtext
Large raised, red area at site of injection. Area had fever and was very sore
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 28.08.2021
- Impfdatum
- 28.07.2021
- Beginn
- 28.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Ageusia
Anosmia
Body temperature
Chills
Dizziness
Fatigue
Headache
Pain
Peripheral swelling
Pyrexia
Throat irritation
Symptomtext
Throat felt like burning; Body temperature raised; Dizzy; Loss of taste; Loss of smell; Chills are so strong felt they're killing patient; Body aches; Tired of speaking; Headache; Arm swelled a little; This spontaneous case was reported by a consumer and describes the occurrence of PERIPHERAL SWELLING (Arm swelled a little), THROAT IRRITATION (Throat felt like burning), PYREXIA (Body temperature raised), DIZZINESS (Dizzy) and AGEUSIA (Loss of taste) in a 51-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 039C21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 28-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 28-Jul-2021, the patient experienced PERIPHERAL SWELLING (Arm swelled a little). On 07-Aug-2021, the patient experienced THROAT IRRITATION (Throat felt like burning), PYREXIA (Body temperature raised), DIZZINESS (Dizzy), AGEUSIA (Loss of taste), ANOSMIA (Loss of smell), CHILLS (Chills are so strong felt they're killing patient), PAIN (Body aches), FATIGUE (Tired of speaking) and HEADACHE (Headache). On 30-Jul-2021, PERIPHERAL SWELLING (Arm swelled a little) had resolved. At the time of the report, THROAT IRRITATION (Throat felt like burning), PYREXIA (Body temperature raised), DIZZINESS (Dizzy), AGEUSIA (Loss of taste), ANOSMIA (Loss of smell), CHILLS (Chills are so strong felt they're killing patient), PAIN (Body aches), FATIGUE (Tired of speaking) and HEADACHE (Headache) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Body temperature: high (High) high. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No concomitant medications were provided by the reporter No treatment medication were provided by the reporter
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Test Name: Body temperature; Result Unstructured Data: high
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 28.08.2021
- Impfdatum
- 20.07.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blister
Burning sensation
Chills
Dry mouth
Dry throat
Dysphagia
Erythema
Feeling hot
Nausea
Night sweats
Pyrexia
Skin exfoliation
Vaccination site reaction
Symptomtext
covid arm that is not going away down to her elbow; Red; Hot; Peeling; Burning; Night sweats; Throat dry; Can't really eat; Mouth dry; feels like there are blisters in her mouth; Nauseous; Mild fever; Chills; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE REACTION (covid arm that is not going away down to her elbow), ERYTHEMA (Red), FEELING HOT (Hot), SKIN EXFOLIATION (Peeling) and BURNING SENSATION (Burning) in a 67-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 039C21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 20-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced VACCINATION SITE REACTION (covid arm that is not going away down to her elbow), ERYTHEMA (Red), FEELING HOT (Hot), SKIN EXFOLIATION (Peeling), BURNING SENSATION (Burning), NIGHT SWEATS (Night sweats), DRY THROAT (Throat dry), DYSPHAGIA (Can't really eat), DRY MOUTH (Mouth dry), BLISTER (feels like there are blisters in her mouth), NAUSEA (Nauseous), PYREXIA (Mild fever) and CHILLS (Chills). At the time of the report, VACCINATION SITE REACTION (covid arm that is not going away down to her elbow), ERYTHEMA (Red), FEELING HOT (Hot), SKIN EXFOLIATION (Peeling), BURNING SENSATION (Burning), NIGHT SWEATS (Night sweats), DRY THROAT (Throat dry), DYSPHAGIA (Can't really eat), DRY MOUTH (Mouth dry), BLISTER (feels like there are blisters in her mouth), NAUSEA (Nauseous), PYREXIA (Mild fever) and CHILLS (Chills) had not resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Concomitant product information was not provided. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 27.08.2021
- Impfdatum
- 23.04.2021
- Beginn
- 23.04.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain in extremity
Pyrexia
Symptomtext
This spontaneous case reported by a patient, describes the occurrence of pain in extremity (pain in the left arm) and pyrexia (a little bit of fever) in a 48-year-old male patient who received mRNA-1273 (Moderna COVID-19 vaccine, batch# 039B21A and 039C21A) for COVID-19 immunization. No medical history reported. On Apr 23, 2021, patient received the first dose of mRNA-1273 (Moderna COVID-19 vaccine), unknown route; 1 dosage form. On Jun 14, 2021, patient received the second dose of mRNA-1273 (Moderna COVID-19 vaccine), unknown route; 1 dosage form. On Apr 23, 2021, patient experienced pain in extremity (pain in the left arm) and pyrexia (a little bit of fever). Patient treated with Tylenol (paracetamol); unspecified dose and frequency. At the time of the report, pain in extremity (pain in the left arm) and pyrexia (a little bit of fever) outcome: unknown. Concomitant product use not provided. Patient did not receive any treatment after first dose of vaccine until second dose administration. This case linked to MOD-2021-225658 (patient link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 92,0
- Geschlecht
- F
- Eingang
- 27.08.2021
- Impfdatum
- 15.06.2021
- Beginn
- 15.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Headache
Myalgia
Pyrexia
Symptomtext
Vaccine administered after it was stored at room temperature for 18 hours; Headache; Muscle aches; Fever; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine administered after it was stored at room temperature for 18 hours), HEADACHE (Headache), MYALGIA (Muscle aches) and PYREXIA (Fever) in a 92-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 039C21A) for COVID-19 vaccination. No medical history information was provided. Concomitant products included LISINOPRIL, FUROSEMIDE, METOPROLOL and WARFARIN for an unknown indication. On 15-Jun-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On an unknown date, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 15-Jun-2021, the patient experienced HEADACHE (Headache), MYALGIA (Muscle aches) and PYREXIA (Fever). On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine administered after it was stored at room temperature for 18 hours). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine administered after it was stored at room temperature for 18 hours), HEADACHE (Headache), MYALGIA (Muscle aches) and PYREXIA (Fever) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Treatment information not reported. Most recent FOLLOW-UP information incorporated above includes: On 15-Jul-2021: Follow up received and new events were added.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: No medical history information was provided.
- Andere Medikamente
- LISINOPRIL; FUROSEMIDE; METOPROLOL; WARFARIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VI
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 17.08.2021
- Impfdatum
- 13.08.2021
- Beginn
- 13.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Decreased appetite
Diarrhoea
Dizziness
Eye pain
Headache
Injection site pain
Injection site swelling
Lethargy
Malaise
Pain
Photophobia
Pyrexia
Visual impairment
Symptomtext
1st Dose: Injections site pain, tenderness and swelling by the afternoon; slight light-headed/dizziness in the evening into the next day. Took two dose of Tylenol on the second day for the pain in the arm. The light-headed/dizziness was gone by the fourth day. 2nd Dose: Injection site swelling tenderness and body ache by the afternoon; fever, intense head ache, dizziness, light sensitivity eye pain vision impaired, lost of appetite lethargic state of not feeling well lasted for three days after the injection. Symptoms were treated with Tylenol every 4-hours, intake as much water, bush tea and home-made fish and onion soups that I could and slept/rest. On the third day the fever subsided about midday, but the headaches, eye sensitivity, lost of appetite, and lethargy continued, which continued to be treated with Tylenol, bush tea and soup. By the fourth day the head aches subsided, appetite still light, slight light-headed, some diarrhea and tenderness at the injection site continues. Symptoms were treated with bush tea and rest. Body achy feeling, eye sensitivity are not apparent.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- None taken
- Aktuelle Erkrankungen
- None known
- Vorgeschichte
- Sciatic nerve pain and herniated disc
- Andere Medikamente
- Standard Process Immune System Health Pack (Vegetarian) and Cod Liver Oil dietary supplements.
- Allergien
- Penicillin and environmental allergies
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 17.08.2021
- Impfdatum
- 12.07.2021
- Beginn
- 12.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Urticaria
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 12.08.2021
- Impfdatum
- 29.05.2021
- Beginn
- 30.05.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Breast pain
Fatigue
Symptomtext
PATIENT REPORTS SINCE VACCINATION TIREDNESS, JOINT PAIN AND BREST PAIN
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HYPERCHOLESTEROLEMIA, HIGH BLOOD PRESUURE
- Andere Medikamente
- -
- Allergien
- PENICCILLIN, LOBSTER, 14 TYPES OF FUNGUS
- Vorherige Impfungen
- -
- Staat
- HI
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 11.08.2021
- Impfdatum
- 21.05.2021
- Beginn
- 02.08.2021
- Tage bis Beginn
- 73,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Fatigue
Headache
Oropharyngeal pain
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
symptoms begin on 08/02/21 fatigue, headache, sore throat, congestion, runny nose
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Covid test done on 08/08/21, results on 08/10/21 positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- low back pain, ADHD, allergic rhinitis, hearing loss, GERD
- Andere Medikamente
- -Mouthwash: Magic Oral Solu
- Allergien
- -No known allergies
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 03.08.2021
- Impfdatum
- 15.07.2021
- Beginn
- 18.07.2021
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Activated partial thromboplastin time normal
Contusion
Fatigue
Injection site pain
Oral pruritus
Platelet count normal
Swelling
Urticaria
Wheezing
Symptomtext
Patient reports no immediate symptoms other than some mild pain at the site of the injection during the observation period. She noted after the observation period but within the first 24 hours, some mild fatigue and local swelling but no fever, chills or myalgias. The swelling resolved and was without symptoms until 3 days later on 18 June 2021.On that evening she noted hives on her face and itching around her mouth. She heard faint wheezing and noted a bruise on her L wrist. Symptoms were not severe enough to seek care and that evening hives subsided but the following day on 19 June 2021, the hives returned/persisted. She took Benadryl with some transient relief every 6 hours. The hives persisted off/on through the following day through 20 Jun 2021. Because the hives persisted and noted some mild wheezing, she went to a civilian urgent care on 21 June 2021. She was prescribed prednisone and an albuterol inhaler. The lesions and dyspnea resolved within a few hours and was discharged. Labs were drawn. of note PT/PTT and platelet count normal. She reports that the bruise on her wrist persisted for 2 weeks. She reports no other symptoms currently but a day or so ago noted a bruise on her R ankle.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- PT/PTT normal. Platelet count normal
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 01.08.2021
- Impfdatum
- 29.07.2021
- Beginn
- 29.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Rash
Urticaria
Symptomtext
Severe itching on trunk ( arms, chest, back) as well as neck and head, by 9 am the next day the hives / rash appeared as small bumps and then turned to raised spreading rash. Called pharmacist and doctor's office I was advised to treat with Zyrtec and topical steroid. Also applied Cer?ve anti itch cream every few hours. My husband showered and that provided temporary relief. Even the little bit of relief he gets from the Zyrtec doesn?t last more than 8 hours. Its has been 3 days and his symptoms are not resolving. I increased the Zyrtec to 10 mg every 12-15 hours yesterday. Also stopped myrbetriq since pharmacist indicated there is possible contraindications with the antihistamine. .
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Chronic COPD, incontinence, dementia, osteoporosis, arthritis
- Vorgeschichte
- Chronic COPD, incontinence, dementia, osteoporosis, arthritis
- Andere Medikamente
- Lamotrigine 200 mg, lexapro 10 mg, atorvastatin 80 mg, Myrbetriq er 50 mg, clopidogrel 75 mg, vit D3 5000 mg, vit E 400 mg, calcium 1200 mgs, omega 3 1000mg, potassium, abuteral, advair, spireava, B12, donepezil hcl
- Allergien
- Amoxicillin, dairy ( lactose intolerant)
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 29.07.2021
- Impfdatum
- 28.06.2021
- Beginn
- 06.07.2021
- Tage bis Beginn
- 8,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Rash
Symptomtext
She had rash on her arm, Neck after a week of the first dose
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- NO
- Vorgeschichte
- NO
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 29.07.2021
- Impfdatum
- 27.07.2021
- Beginn
- 27.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Pain in extremity
Symptomtext
Pt c/o L/arm & fingerpain 15 minutes after injection in R/arm. No swelling, redness or tenderness noted. Strong grip bilaterally. Also c/o congested nose. BP 122/78 Heart Rate 68, Resp 16. Rested 15 more minutes. translator relay to pt if pain continues or worsens, she should go to urgent care or ER. Husband & pt understood. Pt left w/o assistance with husband.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 26.07.2021
- Impfdatum
- 14.04.2021
- Beginn
- 01.04.2021
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Arthralgia
Menstruation irregular
Pain in extremity
Symptomtext
I did not get my menstrual cycle come on for seven weeks post the first vaccine.This is the longest time I have ever not got my period.(as a note, I also took three pregnancy tests that were all negative) Following my second vaccine I have still not gotten my period. Even more concerning I have been having severe joint pain in my hands that I have never had before in my entire life. Also some additional pain seems arthritic that I have never had before.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Gluten
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 23.07.2021
- Impfdatum
- 13.06.2021
- Beginn
- 18.07.2021
- Tage bis Beginn
- 35,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Chills
Computerised tomogram
Dizziness
Electrocardiogram
Headache
Hemiparesis
Laboratory test
Muscle twitching
Muscular weakness
Myalgia
Nausea
Pyrexia
Vaccination site pain
Vomiting
Symptomtext
left side weakness; muscle weakness; dizziness; arm site injection pain; nausea; chills; body ache; low grade fever; headache; vomiting; twitching; This spontaneous case was reported by a consumer and describes the occurrence of HEMIPARESIS (left side weakness) in a 26-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 040C21A and 039C21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 13-Jun-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 13-Jul-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 18-Jul-2021, the patient experienced MUSCLE TWITCHING (twitching). On an unknown date, the patient experienced HEMIPARESIS (left side weakness) (seriousness criterion medically significant), MUSCULAR WEAKNESS (muscle weakness), DIZZINESS (dizziness), VACCINATION SITE PAIN (arm site injection pain), NAUSEA (nausea), CHILLS (chills), MYALGIA (body ache), PYREXIA (low grade fever), HEADACHE (headache) and VOMITING (vomiting). The patient was treated with VALACICLOVIR HYDROCHLORIDE (VALTREX) for Herpes simplex type II, at an unspecified dose and frequency; PHENTERMINE HYDROCHLORIDE (ADIPEX-P) for Weight loss, at an unspecified dose and frequency and PARACETAMOL (TYLENOL) at an unspecified dose and frequency. At the time of the report, HEMIPARESIS (left side weakness), MUSCULAR WEAKNESS (muscle weakness), DIZZINESS (dizziness), MUSCLE TWITCHING (twitching), VACCINATION SITE PAIN (arm site injection pain), NAUSEA (nausea), CHILLS (chills), MYALGIA (body ache), PYREXIA (low grade fever), HEADACHE (headache) and VOMITING (vomiting) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In 2021, Blood test: normal (normal) normal. In 2021, Computerised tomogram: normal (normal) normal. In 2021, Electrocardiogram: normal (normal) normal. In 2021, Laboratory test: normal (normal) normal. Concomitant product was not provided. Based on the current available information and temporal association between the use of the product and the events, a causal relationship cannot be excluded.; Sender's Comments: Based on the current available information and temporal association between the use of the product and the events, a causal relationship cannot be excluded.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Test Date: 2021; Test Name: Blood test; Result Unstructured Data: normal; Test Date: 2021; Test Name: Computerised tomogram; Result Unstructured Data: normal; Test Date: 2021; Test Name: Electrocardiogram; Result Unstructured Data: normal; Test Date: 2021; Test Name: Laboratory test; Result Unstructured Data: normal
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ND
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 22.07.2021
- Impfdatum
- 08.07.2021
- Beginn
- 08.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site bruising
Injection site pain
Symptomtext
Pt states right upper arm hurt immediately upon 2nd COVID-19 vaccination on 7/9/21 and the pain has continued but has lessened in severity. Pt saw provider on 7/22/21 who recommended pt use acetaminophen to help with pain. Provider reviewed arm and noted there was still bruising to the area and noted that injection was done higher than normal. Discussed injection placement with vaccinator.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Diabetes, Hypertension, Hyperlipidemia, Coronary artery disease, Plantar fascitis
- Andere Medikamente
- Levemir, Novolog, Clopidogrel, Lisinopril, Alogliptin, Aspirin, Metformin, Simvastatin, Metoprolol, Carboxymethylcellulose
- Allergien
- Amoxicillin, Ibuprofen, Levaquin
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 16.07.2021
- Impfdatum
- 08.07.2021
- Beginn
- 08.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pain
Pyrexia
Symptomtext
Patient received the Moderna approximately 2 weeks before the 90 day period from her last Remdesivir that was given on 4/24/2021. Patient was called on Monday, 7/12/21 and she stated that she was doing fine and felt well. Patient stated that she had a low grade fever and body aches the day after the vaccine, but Tylenol controlled her symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 15.07.2021
- Impfdatum
- 06.07.2021
- Beginn
- 15.07.2021
- Tage bis Beginn
- 9,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Injection site erythema
Injection site pruritus
Injection site swelling
Symptomtext
Red lesion around injection site. Slightly raised and itchy
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Azithromycin
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 12.07.2021
- Impfdatum
- 08.07.2021
- Beginn
- 09.07.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Axillary pain
Dizziness
Fatigue
Headache
Oedema peripheral
Pain in extremity
Pyrexia
Rash
Rash erythematous
Skin warm
Symptomtext
Fever (40 degrees), headache, tiredness, weakness, dizziness. Arm area red with rash, hot to the touch, with pain. Swollen and sore armpit.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Elevated Blood Pressure
- Andere Medikamente
- Losartan; Metoprolol; Aspirin; Multivitamins
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 07.07.2021
- Impfdatum
- 29.06.2021
- Beginn
- 29.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Contusion
Headache
Lip swelling
Nausea
Pruritus
Pyrexia
Rash
Vomiting
Symptomtext
A 45-year-old female patient reports that 60 minutes after leaving the vaccination center, she presented the following symptoms: Nausea; Vomiting; Fever; Headache; Rash when scratching; Itching; Swelling on the lips; Small bruise on your left upper limb. After taking your second dose of MODERNA.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Diabetes, Hypertension.
- Andere Medikamente
- Enalapril 20mg Humulin 70/30
- Allergien
- Codeine, Meatballs
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 06.07.2021
- Impfdatum
- 30.06.2021
- Beginn
- 06.07.2021
- Tage bis Beginn
- 6,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dizziness
Symptomtext
A 68-year-old female patient oriented in time and space refers to the EMT feeling dizzy 26 minutes after her second dose of MODERNA. At 10:56a.m. we proceed to take the s/v are: B/P. 240/100 mmHg, P. 72 beats/min. and Sat. 98%. She is transported to the Hospital at 11:40a.m.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HBP Hypothyroidism Arrhythmias
- Andere Medikamente
- Losartan Cardol Synthroid
- Allergien
- Caffeine, Codeine, Acetaminophen, Bread, Pasta.
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 02.07.2021
- Impfdatum
- 02.07.2021
- Beginn
- 01.07.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Nausea
Vomiting
Symptomtext
20-YEAR-OLD FEMALE, REFERS THAT AT THE MOMENT SHE DOES NOT HAVE KNOWN ALLERGIES, NOR SUFFER FROM MEDICAL CONDITIONS. AFTER THE INOCULATION THE PATIENT REFERS FEELING Dizzy AND NAUSED. PRESENTS 3 TO 4 VOMITS CONTINUOUSLY. VITAL SIGNS ARE MEASURED EVERY 15 MINUTES.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NKDA
- Andere Medikamente
- NONE
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 30.06.2021
- Impfdatum
- 25.06.2021
- Beginn
- 25.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Product administered to patient of inappropriate age
Pyrexia
Symptomtext
Patient received Moderna vaccine on 6/25/2021 at age 14. She should have received Pfizer. The patient developed a high fever after vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- unknown
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- angelman syndrome, developmental delay
- Andere Medikamente
- unknown
- Allergien
- flavoring agents
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 30.06.2021
- Impfdatum
- 15.06.2021
- Beginn
- 15.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Rash
Symptomtext
I had a rash show up an hour after I got the vaccine. I have now had it for 2 weeks. I've been given 2 steroid shots in 10 days, prescription steroid cream, benadryl, and they now have me on Vistril.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Hashimoto thyroiditis, endometriosis, 2 bulging discs, and sleep apnea
- Vorgeschichte
- -
- Andere Medikamente
- Methoprolol, acyclivir, claritin
- Allergien
- Vancomycin, lamictal, buspar, and benadryl cream
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 29.06.2021
- Impfdatum
- 18.06.2021
- Beginn
- 18.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Hypersensitivity
Inflammation
Nausea
Pyrexia
Rash
Rash erythematous
Rash pruritic
Symptomtext
Patient reported allergic reaction such as red itchy bumps on her neck, shoulders, arms, chest and under the breast area. She also had fever, dizziness and nausea. The red inflamed bumps are still visible after more than 10 days but are improving gradually. She is concerned about the second dose and will be contacting her Doctor to confirm. She has already also reported her adverse effects to Moderna.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 29.06.2021
- Impfdatum
- 01.06.2021
- Beginn
- 01.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Exposure during pregnancy
Urticaria
Symptomtext
38 year old G3 P2 22 week *pregnant no complications. At approximately 11:33 the patient reported hives to upper arms and axilla, Denies SOB, swelling to lips, eyes, tongue and throat, diaphoresis, N/V chest pain or abdominal pain. Medicated with 25 mg of Benadryl. by mouth
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- *prenatal vitamins with 0.8 mg folic acid
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 28.06.2021
- Impfdatum
- 23.06.2021
- Beginn
- 28.06.2021
- Tage bis Beginn
- 5,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary mass
Axillary pain
Symptomtext
Pain in the armpit area. A mass or ball is felt in the armpit of the injected arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma
- Andere Medikamente
- None
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 25.06.2021
- Impfdatum
- 18.06.2021
- Beginn
- 19.06.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Injection site pain
Limb discomfort
Lymphadenopathy
Periorbital swelling
Peripheral swelling
Pyrexia
Swelling
Symptomtext
On 6/19 patient had had mild fever, sore arm (as expected at injection site), and general fatigue (as expected). On 6/20 both of his feet were swollen and it felt as if he was walking on marbles. 6/21 feet had gone down and were normal but later in the day lymph nodes in neck were swollen and he developed a lump on the back of his neck. On 6/22 the neck swelling went away but he then developed left hand and lower left arm swelling. On 6/23 the left hand/arm had gone down but the right hand/arm was swollen. On 6/24 patient experienced swelling around the eyes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 25.06.2021
- Impfdatum
- 15.06.2021
- Beginn
- 23.06.2021
- Tage bis Beginn
- 8,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arthralgia
Lymphadenopathy
Musculoskeletal discomfort
Neck pain
Streptococcus test
Swelling
X-ray
Symptomtext
The patient received her first Moderna vaccine 6/15/21. She started to feel pain and discomfort radiating from her shoulder toward her neck on 6/23/21. She stated that her shoulder also feels "a little swollen" but no redness or inflammation is visable on the skin. The patient was seen in the ER 6/24/21 . X-ray of shoulder, neck and chest and Strep test were done. Dr told pt her lymph node in neck was swollen. Dr told pt it was possible the vaccine cause the pain in should/neck and swollen lymph node. She was told to return to ER or see PCP if the pain did not resolve in 5 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- X-ray and Strep test 6/23/21
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 25.06.2021
- Impfdatum
- 23.06.2021
- Beginn
- 23.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Dizziness
Fatigue
Pain in extremity
Peripheral swelling
Vomiting
Symptomtext
Fatigue, vomiting, chills, dizzy, sore swollen arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Heart condition
- Andere Medikamente
- Aspirin, Lisinopril, Vitamin D, Calcium, Effient, Protonix, Singular, Fluticasone-umeclidin-vilanter, Flonase, Ipratropium-albuterol, Probiotics.
- Allergien
- Eggs
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 25.06.2021
- Impfdatum
- 24.06.2021
- Beginn
- 24.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Hyperhidrosis
Nausea
Vomiting
Symptomtext
Patient received the COVID19 Moderna vaccine dose 1. Patient began to get nauseous and vomited 7 minutes after the vaccine was administered. Additional symptoms included sweating and chill. The patient remained under observation and left with symptoms resolved after approximately 30 minutes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 24.06.2021
- Impfdatum
- 17.06.2021
- Beginn
- 01.06.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site erythema
Injection site pruritus
Symptomtext
Patient stated that a red itchy spot appeared on injection site after a few days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 17.06.2021
- Impfdatum
- 16.06.2021
- Beginn
- 16.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Gait disturbance
Malaise
Posture abnormal
Vomiting
Symptomtext
Pt said he didn't feel so well a couple of minutes after administering his first Covid Moderna vaccine at 2:10 PM on 6/16/2021. Pt then staggered toward a chair and slumped down in chair. Pharmacy called 911. Pt was given supportive care and became alert in about 15 seconds. Pt taken to counseling where he vomited for approximately 8 minutes. Squad arrived and patient cared for by EMS. Patient taken to hospital, fully responsive.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- not known
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Not available
- Andere Medikamente
- Information not available
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 16.06.2021
- Impfdatum
- 10.06.2021
- Beginn
- 10.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Insomnia
Vertigo
Symptomtext
Patient had insomnia for 24 hours could not sleep, she admits to having a bad headache and vertigo that have not resolved.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 15.06.2021
- Impfdatum
- 13.06.2021
- Beginn
- 14.06.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pain
Symptomtext
My first shot 033C21A left me with a small acceptable pain for about 3 hours. THE REASON I AM FILING THIS IS BECAUSE I HAVE DOUBTS ABOUT MY SECOND SHOT. I felt absolutely NOTHING AT ALL and both shots went into my left shoulder area. I AM WONDERING IF THE SECOND SHOT was somehow corrupted and not at the strength it should have been. I tried 5 times calling the Pharmacy but was never connected. It struck me that maybe you could provide me with the answer. I realize this is a somewhat backward report since you are looking for adverse reactions, BUT NO REACTION AT ALL left me wondering if something went wrong in the processing stage . The Pharmacy and the label on the first shot ONLY shows expiration of 10/27/21 but there is no comparable information about the second shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- n/.a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 14.06.2021
- Impfdatum
- 14.06.2021
- Beginn
- 14.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dizziness
Nausea
Symptomtext
pt got moderna shot, after about 20min she said she was nauseous and dizzy and requested us call 911 for ambulance which we did. took her blood pressure it was 132/90 heart rate 85.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- depression, anxiety, takes eliquis for blood
- Andere Medikamente
- fluoxetine 20mg, eliquis 5mg, buspirone 15mg
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 14.06.2021
- Impfdatum
- 01.06.2021
- Beginn
- 09.06.2021
- Tage bis Beginn
- 8,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abnormal dreams
Ageusia
Dizziness
Fatigue
Feeling of body temperature change
Hallucination
Headache
Hyperhidrosis
Injection site pain
Myalgia
Nausea
Pyrexia
Symptomtext
Fever, nausea, muscle aches and pains, sweating, cold/hot flashes, headache, no taste, fatigue, exhaustion, dizzy, pain in injection site, deep sleep, bizarre dreams, hallucinations when closing eyes (dots and eye spinning sensation)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 10.06.2021
- Impfdatum
- 12.05.2021
- Beginn
- 13.05.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Fatigue
Nausea
Pain
Pain in extremity
Posture abnormal
Pyrexia
Symptomtext
About 24 hours from vaccine administration patient reported onset of chills fever body aches and nausea she took tylenol but still was extremely fatigued and curled into a ball. Symptoms resolved at 48 hour mark from vaccination. Patient also reported extremely sore arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 01.11.2023
- Impfdatum
- 03.09.2021
- Beginn
- 27.08.2023
- Tage bis Beginn
- 723,0
- Dosis
- 2
- Route/Site
- - / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Breakthrough COVID-19
Symptomtext
Covid-19 Breakthrough Infection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Breakthrough COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- AFIB, T2DM, Glaucoma, Heart Failure, COPD
- Andere Medikamente
- Fluticasone, Furosemide, Gabapentin, Latanoprost, Losartan, Meloxicam, Metformin, Metoprolol, Multivitamins, Nortriptyline, Omeprazole, Rivaroxaban,
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 21.07.2023
- Impfdatum
- 18.06.2021
- Beginn
- 17.01.2022
- Tage bis Beginn
- 213,0
- Dosis
- 2
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Fall
Pneumothorax
Symptomtext
Presented to ED s/p ground level fall sustaining large left pneumothorax; incidental finding of COVID-19; asymptomatic
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 24.02.2023
- Impfdatum
- 07.05.2021
- Beginn
- 25.01.2023
- Tage bis Beginn
- 628,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Tinnitus
Symptomtext
Developed Tinnitus in the left ear , this condition happened after more than a year or so.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tinnitus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 07.12.2022
- Impfdatum
- 24.05.2021
- Beginn
- 26.04.2022
- Tage bis Beginn
- 337,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Patient had a breakthrough infection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Positive COVID test on 2/3/2022.
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 98,0
- Geschlecht
- M
- Eingang
- 07.07.2022
- Impfdatum
- 30.08.2021
- Beginn
- 07.06.2022
- Tage bis Beginn
- 281,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Symptomtext
Patient hospitalized with COVID while vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 15,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 22.05.2022
- Impfdatum
- 28.06.2021
- Beginn
- 28.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 22.05.2022
- Impfdatum
- 28.06.2021
- Beginn
- 28.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 22.05.2022
- Impfdatum
- 28.06.2021
- Beginn
- 28.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 22.05.2022
- Impfdatum
- 28.06.2021
- Beginn
- 28.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 22.05.2022
- Impfdatum
- 28.06.2021
- Beginn
- 28.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 22.05.2022
- Impfdatum
- 28.06.2021
- Beginn
- 28.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was a refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 22.05.2022
- Impfdatum
- 28.06.2021
- Beginn
- 28.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was a refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 22.05.2022
- Impfdatum
- 28.06.2021
- Beginn
- 28.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 22.05.2022
- Impfdatum
- 06.07.2021
- Beginn
- 06.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was a refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 89,0
- Geschlecht
- F
- Eingang
- 22.05.2022
- Impfdatum
- 06.07.2021
- Beginn
- 06.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 22.05.2022
- Impfdatum
- 06.07.2021
- Beginn
- 06.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 22.05.2022
- Impfdatum
- 06.07.2021
- Beginn
- 06.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 22.05.2022
- Impfdatum
- 06.07.2021
- Beginn
- 06.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 22.05.2022
- Impfdatum
- 06.07.2021
- Beginn
- 06.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 22.05.2022
- Impfdatum
- 06.07.2021
- Beginn
- 06.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 22.05.2022
- Impfdatum
- 29.06.2021
- Beginn
- 29.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 90,0
- Geschlecht
- F
- Eingang
- 22.05.2022
- Impfdatum
- 29.06.2021
- Beginn
- 29.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by Regulatory Authority for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 22.05.2022
- Impfdatum
- 29.06.2021
- Beginn
- 29.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 22.05.2022
- Impfdatum
- 29.06.2021
- Beginn
- 29.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 22.05.2022
- Impfdatum
- 29.06.2021
- Beginn
- 29.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was a refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 93,0
- Geschlecht
- M
- Eingang
- 22.05.2022
- Impfdatum
- 29.06.2021
- Beginn
- 29.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 22.05.2022
- Impfdatum
- 29.06.2021
- Beginn
- 29.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was a refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 66,0
- Geschlecht
- U
- Eingang
- 21.05.2022
- Impfdatum
- 28.06.2021
- Beginn
- 28.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 21.05.2022
- Impfdatum
- 28.06.2021
- Beginn
- 28.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 21.05.2022
- Impfdatum
- 28.06.2021
- Beginn
- 28.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by agency for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 21.05.2022
- Impfdatum
- 28.06.2021
- Beginn
- 28.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by agency for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 21.05.2022
- Impfdatum
- 28.06.2021
- Beginn
- 28.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID 19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 87,0
- Geschlecht
- F
- Eingang
- 21.05.2022
- Impfdatum
- 28.06.2021
- Beginn
- 28.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was a refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 21.05.2022
- Impfdatum
- 28.06.2021
- Beginn
- 28.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by Regulatory Authority for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 21.05.2022
- Impfdatum
- 18.06.2021
- Beginn
- 18.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 85,0
- Geschlecht
- M
- Eingang
- 21.05.2022
- Impfdatum
- 18.06.2021
- Beginn
- 18.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 21.05.2022
- Impfdatum
- 18.06.2021
- Beginn
- 18.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by agency for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 21.05.2022
- Impfdatum
- 18.06.2021
- Beginn
- 18.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by Regulatory Authority for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 21.05.2022
- Impfdatum
- 18.06.2021
- Beginn
- 18.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 21.05.2022
- Impfdatum
- 18.06.2021
- Beginn
- 18.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 20.05.2022
- Impfdatum
- 28.06.2021
- Beginn
- 28.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 18.06.2021
- Beginn
- 18.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 18.06.2021
- Beginn
- 18.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 20.05.2022
- Impfdatum
- 18.06.2021
- Beginn
- 18.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was a refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by the Regulatory Authority for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 20.05.2022
- Impfdatum
- 18.06.2021
- Beginn
- 18.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 10.06.2021
- Beginn
- 10.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 20.05.2022
- Impfdatum
- 10.06.2021
- Beginn
- 10.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 20.05.2022
- Impfdatum
- 10.06.2021
- Beginn
- 10.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was a refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 10.06.2021
- Beginn
- 10.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 10.06.2021
- Beginn
- 10.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 10.06.2021
- Beginn
- 10.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 10.06.2021
- Beginn
- 10.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 20.05.2022
- Impfdatum
- 18.06.2021
- Beginn
- 18.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 10.06.2021
- Beginn
- 10.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 87,0
- Geschlecht
- M
- Eingang
- 20.05.2022
- Impfdatum
- 18.06.2021
- Beginn
- 18.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 20.05.2022
- Impfdatum
- 18.06.2021
- Beginn
- 18.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 18.06.2021
- Beginn
- 18.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 18.06.2021
- Beginn
- 18.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 16.06.2021
- Beginn
- 16.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 20.05.2022
- Impfdatum
- 16.06.2021
- Beginn
- 16.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 20.05.2022
- Impfdatum
- 16.06.2021
- Beginn
- 16.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 20.05.2022
- Impfdatum
- 16.06.2021
- Beginn
- 16.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 16.06.2021
- Beginn
- 16.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 86,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 10.06.2021
- Beginn
- 10.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was a refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 16.06.2021
- Beginn
- 16.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 16.06.2021
- Beginn
- 16.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 10.06.2021
- Beginn
- 10.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 20.05.2022
- Impfdatum
- 08.06.2021
- Beginn
- 08.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 08.06.2021
- Beginn
- 08.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 08.06.2021
- Beginn
- 08.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was a refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 08.06.2021
- Beginn
- 08.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 08.06.2021
- Beginn
- 08.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was a refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by the Regulatory Authority for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 08.06.2021
- Beginn
- 08.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was a refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 08.06.2021
- Beginn
- 08.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was a refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 08.06.2021
- Beginn
- 08.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 08.06.2021
- Beginn
- 08.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was a refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 20.05.2022
- Impfdatum
- 08.06.2021
- Beginn
- 08.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 20.05.2022
- Impfdatum
- 08.06.2021
- Beginn
- 08.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 08.06.2021
- Beginn
- 08.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 08.06.2021
- Beginn
- 08.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 20.05.2022
- Impfdatum
- 08.06.2021
- Beginn
- 08.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 08.06.2021
- Beginn
- 08.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 08.06.2021
- Beginn
- 08.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was a refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 08.06.2021
- Beginn
- 08.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 08.06.2021
- Beginn
- 08.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 08.06.2021
- Beginn
- 08.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 08.06.2021
- Beginn
- 08.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was a refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 08.06.2021
- Beginn
- 08.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 08.06.2021
- Beginn
- 08.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 08.06.2021
- Beginn
- 08.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 20.05.2022
- Impfdatum
- 08.06.2021
- Beginn
- 08.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by state for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 20.05.2022
- Impfdatum
- 08.06.2021
- Beginn
- 08.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 08.06.2021
- Beginn
- 08.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 20.05.2022
- Impfdatum
- 08.06.2021
- Beginn
- 08.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 20.05.2022
- Impfdatum
- 08.06.2021
- Beginn
- 08.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 20.05.2022
- Impfdatum
- 08.06.2021
- Beginn
- 08.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 20.05.2022
- Impfdatum
- 08.06.2021
- Beginn
- 08.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was a refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 20.05.2022
- Impfdatum
- 08.06.2021
- Beginn
- 08.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was a refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 08.06.2021
- Beginn
- 08.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 08.06.2021
- Beginn
- 08.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was a refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 20.05.2022
- Impfdatum
- 08.06.2021
- Beginn
- 08.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was a refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 08.06.2021
- Beginn
- 08.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 08.06.2021
- Beginn
- 08.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was a refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 08.06.2021
- Beginn
- 08.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was a refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by State for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 08.06.2021
- Beginn
- 08.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was a refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved by the Regulatory Authority for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 08.06.2021
- Beginn
- 08.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
On the clinic day, the vaccine was transported out from the pharmacy to the facility without a digital data logger. The packing used for transport was a refrigerated packaging tote to maintain a temperature of 36 F - 46 F. However, that is not approved for COVID-19 vaccine transportation. The total time (from when vaccine left the pharmacy to the clinic completion) was less than 6 hours. There were no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 03.06.2021
- Beginn
- 10.06.2021
- Tage bis Beginn
- 7,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Skin irritation
Symptomtext
PER PATIENT, STATED BREAKING OUT ON ARMS AND BACK WITHIN A WEEK AFTER RECEIVING MODERNA, COULD HAVE BEEN REFERRING TO 6/3/21 DOSE, I DID NOT GIVE BOOSTER DOSE TODAY. PATIENT STATED HE ALREADY REPORTED TO CDC
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Skin irritation
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 11.04.2022
- Impfdatum
- 08.07.2021
- Beginn
- 13.07.2021
- Tage bis Beginn
- 5,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Lipase increased
Pancreatitis acute
Symptomtext
Acute pancreatitis - Plan to likely go home and return in one week for OP lap chole due to effient 07/16/21 lipase is 403, patient wants to go home and come back if we have to wait a week due to effient. Awaiting recs from GI and Cardiology. No longer any abdominal pain. Will stay on ASA through surgery per GI. Will restart effient or plavix a few days Post surgery. Cardio rec restart statin the night before surgery, restart zetia now, Dc home today and surgery planned for Wednesday. ED visit to hospital admission within 6 weeks of receiving the COVID vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lipase increased
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 26.02.2022
- Impfdatum
- 25.07.2021
- Beginn
- 25.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient was vaccinated with a vial that had been in the refrigerator past the 30 days; This spontaneous case was reported by a physician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient was vaccinated with a vial that had been in the refrigerator past the 30 days) in a 22-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 039C21A) for COVID-19 vaccination. No Medical History information was reported. On 25-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 25-Jul-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient was vaccinated with a vial that had been in the refrigerator past the 30 days). On 25-Jul-2021, EXPIRED PRODUCT ADMINISTERED (Patient was vaccinated with a vial that had been in the refrigerator past the 30 days) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were provided. No treatment drugs were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 26.02.2022
- Impfdatum
- 21.06.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymphadenopathy
Symptomtext
Enlargement of lymph nodes; This spontaneous case was reported by a pharmacist and describes the occurrence of LYMPHADENOPATHY (Enlargement of lymph nodes) in a 55-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 078C21A and 039C21A) for COVID-19 vaccination. No medical history was reported. Concomitant products included CITALOPRAM, CLONAZEPAM, LORATADINE, FISH OIL and IBUPROFEN for an unknown indication. On 21-Jun-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 19-Jul-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On an unknown date, the patient experienced LYMPHADENOPATHY (Enlargement of lymph nodes). At the time of the report, LYMPHADENOPATHY (Enlargement of lymph nodes) had not resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No treatment details were added.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymphadenopathy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: No medical history was reported
- Andere Medikamente
- CITALOPRAM; CLONAZEPAM; LORATADINE; FISH OIL; IBUPROFEN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 26.02.2022
- Impfdatum
- 30.06.2021
- Beginn
- 27.07.2021
- Tage bis Beginn
- 27,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
gave two Moderna vaccines that were expired by 14 hours; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (gave two Moderna vaccines that were expired by 14 hours) in a 58-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 040C21A and 039C21A) for COVID-19 vaccination. No Medical History information was reported. On 30-Jun-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 27-Jul-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 27-Jul-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (gave two Moderna vaccines that were expired by 14 hours). On 27-Jul-2021, EXPIRED PRODUCT ADMINISTERED (gave two Moderna vaccines that were expired by 14 hours) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No treatment information was provided. No concomitant medication was provided. Most recent FOLLOW-UP information incorporated above includes: On 27-Jul-2021: Non significant follow up added.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 26.02.2022
- Impfdatum
- 29.06.2021
- Beginn
- 27.07.2021
- Tage bis Beginn
- 28,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Vaccine given from a vial that had been punctured for more than 24 hours/gave two Moderna vaccines that were expired by 14; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine given from a vial that had been punctured for more than 24 hours/gave two Moderna vaccines that were expired by 14) in a 43-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 040C21A and 039C21A) for COVID-19 vaccination. No Medical History information was reported. On 29-Jun-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 27-Jul-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 27-Jul-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine given from a vial that had been punctured for more than 24 hours/gave two Moderna vaccines that were expired by 14). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine given from a vial that had been punctured for more than 24 hours/gave two Moderna vaccines that were expired by 14) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medication was provided. No treatment medication was provided. Reporter wants to know if there is a need to revaccinate their patients. Most recent FOLLOW-UP information incorporated above includes: On 27-Jul-2021: Follow up received contains No New Information
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 26.02.2022
- Impfdatum
- 21.07.2021
- Beginn
- 21.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product temperature excursion issue
Symptomtext
It was First Punctured at 10AM on 20JUL2021 and kept at 69 Fahrenheit; kept at room temp for 26 hours; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (It was First Punctured at 10AM on 20JUL2021 and kept at 69 Fahrenheit) and PRODUCT TEMPERATURE EXCURSION ISSUE (kept at room temp for 26 hours) in a 20-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 039C21A) for COVID-19 vaccination. No Medical History information was reported. On 21-Jul-2021 at 11:30 AM, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 21-Jul-2021 at 11:30 AM, the patient experienced EXPIRED PRODUCT ADMINISTERED (It was First Punctured at 10AM on 20JUL2021 and kept at 69 Fahrenheit) and PRODUCT TEMPERATURE EXCURSION ISSUE (kept at room temp for 26 hours). On 21-Jul-2021 at 11:30 AM, EXPIRED PRODUCT ADMINISTERED (It was First Punctured at 10AM on 20JUL2021 and kept at 69 Fahrenheit) and PRODUCT TEMPERATURE EXCURSION ISSUE (kept at room temp for 26 hours) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Reporter reported that patient has received vaccine from an expired vial. She stated that one punctured vial of Moderna COVID-19 vaccine was kept at room temp for 26 hours. The vial was moved from refrigerator to the room temperature on 20-JUL-2021 around 7:30AM and was first punctured at 10AM on 20-JUL-2021 and kept at 69 Fahrenheit. The vial was never exposed to temperature excursion in the past. No relevant 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
- NJ
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 26.02.2022
- Impfdatum
- 12.07.2021
- Beginn
- 12.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Symptomtext
16 years old patient received her 1st dose of the Moderna COVID 19 vaccine; This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (16 years old patient received her 1st dose of the Moderna COVID 19 vaccine) in a 16-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 039C21A) for COVID-19 vaccination. No Medical History information was reported. On 12-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 12-Jul-2021, the patient experienced PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (16 years old patient received her 1st dose of the Moderna COVID 19 vaccine). At the time of the report, PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (16 years old patient received her 1st dose of the Moderna COVID 19 vaccine) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 31.01.2022
- Impfdatum
- 17.07.2021
- Beginn
- 19.12.2021
- Tage bis Beginn
- 155,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Symptomtext
Vaccinated patient hospitalized with COVID-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- PCN
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 31.01.2022
- Impfdatum
- 17.07.2021
- Beginn
- 19.12.2021
- Tage bis Beginn
- 155,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Symptomtext
Vaccinated patient hospitalized with COVID-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- PCN
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 20.01.2022
- Impfdatum
- 13.07.2021
- Beginn
- 19.01.2022
- Tage bis Beginn
- 190,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
COVID BREAKTHROUGH CASE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID+ 1/19/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Acute exacerbation of CHF (congestive heart failure) Acute Hyperglycemia Closed T4 spinal fracture Hypoglycemia Obesity, Class I, BMI 30-34.9
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 83,0
- Geschlecht
- F
- Eingang
- 08.12.2021
- Impfdatum
- 26.04.2021
- Beginn
- 03.12.2021
- Tage bis Beginn
- 221,0
- Dosis
- UNK
- Route/Site
- IM / LA
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
- 79,0
- Geschlecht
- F
- Eingang
- 08.12.2021
- Impfdatum
- 04.01.2021
- Beginn
- 03.12.2021
- Tage bis Beginn
- 333,0
- Dosis
- UNK
- Route/Site
- IM / LA
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
- AL
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 13.11.2021
- Impfdatum
- 14.10.2021
- Beginn
- 14.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
expired moderna vaccine mistakenly administered; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered) in a 73-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 039C21A) for COVID-19 vaccination. No Medical History information was reported. On 14-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 ml. On 14-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered). On 14-Oct-2021, EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. This is a case of Expired Product Administered concerning a 73-year-old female patient with no relevant medical history, who experienced no other associated adverse events. The event occurred the same day after receiving the third dose number of mRNA-1273 (Moderna COVID-19 Vaccine). The rechallenge is unknown since no information on other doses were disclosed. The benefit-risk relationship of mRNA-1273 (Moderna COVID-19 Vaccine) is not affected by this report. Concomitant product use was not provided by the reporter. Treatment information was not provided by the reporter.; Sender's Comments: This is a case of Expired Product Administered concerning a 73-year-old female patient with no relevant medical history, who experienced no other associated adverse events. The event occurred the same day after receiving the third dose number of mRNA-1273 (Moderna COVID-19 Vaccine). The rechallenge is unknown since no information on other doses were disclosed. The benefit-risk relationship of mRNA-1273 (Moderna COVID-19 Vaccine) is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- -
- Geschlecht
- U
- Eingang
- 12.11.2021
- Impfdatum
- 02.11.2021
- Beginn
- 02.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
23 patients received expired dose of the vaccine; Based on the current case data, this case has been classified as invalid. This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (23 patients received expired dose of the vaccine) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 039C21A) for COVID-19 vaccination. No Medical History information was reported. On 02-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 02-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (23 patients received expired dose of the vaccine). On 02-Nov-2021, EXPIRED PRODUCT ADMINISTERED (23 patients received expired dose of the vaccine) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication details was reported. No treatment medication details was reported. The reporter believes the vail was initially stored in the refrigerator on 19 Oct 2021. the vial had not underwent any temperature excursions. This case was linked to MOD-2021-373198 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 05-Nov-2021: Follow-up received on contains non significant information
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 11.11.2021
- Impfdatum
- 02.11.2021
- Beginn
- 02.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Expired moderna vaccine mistakenly administered; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered) in a 55-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 039C21A) for COVID-19 vaccination. No Medical History information was reported. On 02-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 ml. On 02-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered). On 02-Nov-2021, EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication were reported. No treatment information was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 11.11.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
expired moderna vaccine mistakenly administered; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered) in a 69-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 039C21A) 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) .25 milliliter. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No information regarding first or second dose were provided. No concomitant medications were reported. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 11.11.2021
- Impfdatum
- 02.11.2021
- Beginn
- 02.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Expired moderna vaccine mistakenly administered; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired moderna vaccine mistakenly administered) in a 58-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 039C21A) for COVID-19 vaccination. No Medical History information was reported. On 02-Nov-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 02-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired moderna vaccine mistakenly administered). On 02-Nov-2021, EXPIRED PRODUCT ADMINISTERED (Expired moderna vaccine mistakenly administered) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported. No treatment medication was reported. The vaccine was removed from freezer on 14-Oct-2021 into refrigerator and never opened before the administration day and the temperature was never compromised.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 11.11.2021
- Impfdatum
- 14.10.2021
- Beginn
- 14.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
expired moderna vaccine mistakenly administered; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered) in a 78-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 039C21A) for COVID-19 vaccination. No Medical History information was reported. On 14-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 ml. On 14-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered). On 14-Oct-2021, EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported No treatment medications were reported. It was reported that on 14-Oct-2021, the vial was removed from refrigerator and was not opened before vaccination and temperature was not compromised.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 11.11.2021
- 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 moderna vaccine mistakenly administered; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered) in a 71-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. Unknown) 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) .25 ml. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was mentioned. No treatment medication was mentioned.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 11.11.2021
- Impfdatum
- 02.11.2021
- Beginn
- 02.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
expired moderna vaccine mistakenly administered; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered) in a 54-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 039C21A) for COVID-19 vaccination. No Medical History information was reported. On 02-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 02-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered). On 02-Nov-2021, EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant drugs were not reported. Treatment medications were not provided. It was reported that the vial was kept in refrigerator on 14-Oct-2021 and reported no temperature excursion. This case was linked to MOD-2021-372310 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 11.11.2021
- Impfdatum
- 02.11.2021
- Beginn
- 02.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
expired moderna vaccine mistakenly administered; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered) in a 74-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 039C21A) for COVID-19 vaccination. No Medical History information was reported. On 02-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 ml. On 02-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered). On 02-Nov-2021, EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications was reported. no treatment was reported. (removed from freezer 10-14-21 into refrigerator and never opened before today and temperature never compromised)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 11.11.2021
- Impfdatum
- 02.11.2021
- Beginn
- 02.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Expired product administered
Symptomtext
expired moderna vaccine mistakenly administered; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered) in a 70-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 039C21A) for COVID-19 vaccination. No Medical History information was reported. On 02-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 02-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered). On 02-Nov-2021, EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication was not provided. Treatment information was not provided. (removed from freezer 10-14-21 into refrigerator and never opened before today and temperature never compromised )
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 11.11.2021
- Impfdatum
- 02.11.2021
- Beginn
- 02.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Expired moderna vaccine mistakenly administered; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired moderna vaccine mistakenly administered) in a 62-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 039C21A) for COVID-19 vaccination. No Medical History information was reported. On 02-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 ml. On 02-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired moderna vaccine mistakenly administered). On 02-Nov-2021, EXPIRED PRODUCT ADMINISTERED (Expired moderna vaccine mistakenly administered) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. The reporter stated that they mistakenly administered expired vaccine today which was removed from freezer on 14-Oct-2021 into refrigerator and never opened before administration and temperature was never compromised. It was also reported that it was patient's third dose, and it was a 0.25-ml dose and no information regarding first or second dose were provided. 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
- AL
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 11.11.2021
- Impfdatum
- 02.11.2021
- Beginn
- 02.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Expired moderna vaccine mistakenly administered; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired moderna vaccine mistakenly administered) in a 61-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 039C21A) for COVID-19 vaccination. No Medical History information was reported. On 02-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 02-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired moderna vaccine mistakenly administered). On 02-Nov-2021, EXPIRED PRODUCT ADMINISTERED (Expired moderna vaccine mistakenly administered) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medications were not provided. Treatment information was not provided. On 14-Oct-2021, vial was removed from freezer into refrigerator. It was never opened before today and temperature was never compromised.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 11.11.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Expired moderna vaccine mistakenly administered; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired moderna vaccine mistakenly administered) in a 77-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 039C21A) 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) .25 milliliter. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired moderna vaccine mistakenly administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired moderna vaccine mistakenly administered) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medications were not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 11.11.2021
- Impfdatum
- 02.11.2021
- Beginn
- 02.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
14-Oct-21 into refrigerator and never opened before today; expired moderna vaccine mistakenly administered; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered) and PRODUCT STORAGE ERROR (14-Oct-21 into refrigerator and never opened before today) in a 67-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 039c21a) for COVID-19 vaccination. No Medical History information was reported. On 02-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 02-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (14-Oct-21 into refrigerator and never opened before today). On 02-Nov-2021, EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered) had resolved. At the time of the report, PRODUCT STORAGE ERROR (14-Oct-21 into refrigerator and never opened before today) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 11.11.2021
- Impfdatum
- 02.11.2021
- Beginn
- 02.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Expired moderna vaccine mistakenly administered; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired moderna vaccine mistakenly administered) in a 65-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 039C21A) for COVID-19 vaccination. No Medical History information was reported. On 02-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 02-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired moderna vaccine mistakenly administered). On 02-Nov-2021, EXPIRED PRODUCT ADMINISTERED (Expired moderna vaccine mistakenly administered) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications information was reported. No treatment medications were provided. Vial was removed from freezer on 14-Oct-2021 into refrigerator and never opened until the date of administration and temperature was never compromised.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 11.11.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
expired moderna vaccine mistakenly administered; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered) in an 80-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 039c21a) 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) .25 milliliter. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 11.11.2021
- Impfdatum
- 02.11.2021
- Beginn
- 02.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
expired moderna vaccine mistakenly administered; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered) in a male patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 039C21A) 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) .25 milliliter. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was provided by reporter. No treatment information was provided by reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 11.11.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
expired moderna vaccine mistakenly administered; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered) in a 54-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 039C21A) 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) .25 milliliter. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was provided by reporter. No treatment information was provided by reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 11.11.2021
- Impfdatum
- 02.11.2021
- Beginn
- 02.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Expired moderna vaccine mistakenly administered; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired moderna vaccine mistakenly administered) in a 73-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 039C21A) for COVID-19 vaccination. No Medical History information was reported. On 02-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 ml. On 02-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired moderna vaccine mistakenly administered). On 02-Nov-2021, EXPIRED PRODUCT ADMINISTERED (Expired moderna vaccine mistakenly administered) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication reported. No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 10.11.2021
- Impfdatum
- 14.10.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
expired moderna vaccine mistakenly administered; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered) in a 73-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 039C21A) for COVID-19 vaccination. No Medical History information was reported. On 14-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 ml. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication provided No treatment medication provided (removed from freezer 10-14-21 into refrigerator and never opened before today and temperature never compromised).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 10.11.2021
- Impfdatum
- 02.11.2021
- Beginn
- 02.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
expired moderna vaccine mistakenly administered; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered) in a 52-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 039C21A) for COVID-19 vaccination. No Medical History information was reported. On 02-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 02-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown Route), the reporter did not provide any causality assessments. Concomitant medication information was not provided by the reporter. Treatment information was not provided by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 10.11.2021
- Impfdatum
- 14.10.2021
- Beginn
- 14.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
expired moderna vaccine mistakenly administered; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered) in a 67-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 039C21A) for COVID-19 vaccination. No Medical History information was reported. On 14-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 ml. On 14-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered). On 14-Oct-2021, EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication provided No treatment medication provided
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 10.11.2021
- Impfdatum
- -
- Beginn
- 02.11.2021
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
expired moderna vaccine mistakenly administered; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered) in a 50-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 039C21A) 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) .25 ml. On 02-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered). On 02-Nov-2021, EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 10.11.2021
- Impfdatum
- 14.10.2021
- Beginn
- 14.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
expired moderna vaccine mistakenly administered; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered) in a 70-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 039C21A) for COVID-19 vaccination. No Medical History information was reported. On 14-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 ml. On 14-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered). On 14-Oct-2021, EXPIRED PRODUCT ADMINISTERED (expired moderna vaccine mistakenly administered) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No Concomitant medications were provided No treatment medications were provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 11.10.2021
- Impfdatum
- 21.06.2021
- Beginn
- 21.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood glucose normal
Erythema
Peripheral coldness
Somnolence
Symptomtext
Patient in area of observation had left arm cold, excessive sleepiness, right side neck red. P 75 Sat 99% BP 125/80 Dxt 109 was in observation for 1hr.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood glucose normal
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Gastritis
- Vorgeschichte
- N/A
- Andere Medikamente
- Unknown
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 08.10.2021
- Impfdatum
- 19.06.2021
- Beginn
- 19.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Balance disorder
Symptomtext
After patient was vaccinated, reports feeling unbalance, paramedic gives her alcohol and takes her vitals BP 130/90, sat 99, pulse 85. She waited 30 minutes for any adverse reaction to vaccine. After 30 minutes when patient was leaving she was feeling unbalance and reports not having breakfast that morning. She had water and her family brought her some breakfast. Paramedic called the ambulance.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Balance disorder
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 08.10.2021
- Impfdatum
- 16.06.2021
- Beginn
- 16.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cardiac monitoring normal
Catatonia
Movement disorder
Symptomtext
Epileptic patient presents in a catatonic state and movement difficulties. DX 145 R16 BP97/67 P66 Sat99. He was attended by medical personnel; staff who evaluated the patient, placed a normal rhythm heart monitor. The patient refuses to go to the hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cardiac monitoring normal
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Epileptic
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 30.09.2021
- Impfdatum
- 24.05.2021
- Beginn
- 27.09.2021
- Tage bis Beginn
- 126,0
- 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 work contact
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VI
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 16.09.2021
- Impfdatum
- 01.07.2021
- Beginn
- 01.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Recipient did not experience an adverse reaction. He inadvertently received the Moderna vaccine before 18 years old. He was 17 years 6 months at the time of vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none known
- Andere Medikamente
- -
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 14.09.2021
- Impfdatum
- 08.09.2021
- Beginn
- 08.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
No adverse event
Symptomtext
The client was transferred to this hospital from another hospital. The hospital did not have documentation of prior COVID-19 vaccination. The client received a Moderna COVID-19 vaccination at the facility on 9/8/21 at 4:43 pm in the right deltoid. Upon Database entry of immunization it was discovered that the client had already received 2 prior Moderna COVID-19 vaccinations on 12/31/20 and 1/28/21. The client, nurse, and provider were notified. The client was monitored for any adverse reactions to the 3rd Moderna COVID-19 vaccination received. Vitals remained at baseline with no fever documented. The client was administered one dose of acetaminophen 650 mg on 9/8 at 6:11 pm, 2 doses 9/9-9/12 and 1 dose on 9/13 for pain. No other treatment was necessary.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- Vital signs monitored.
- Aktuelle Erkrankungen
- Left shoulder pain treated with methyl salicylate/menthol topical ointment
- Vorgeschichte
- Obesity, Asthma/COPD, Dementia, unspecified psychosis, insomnia, arthritis, overactive bladder, constipation, CAD, GERD, history of pressure ulcer
- Andere Medikamente
- Sertraline 150 mg in the morning for depression, risperidone 1 mg at bedtime for psychosis, omeprazole 20 mg in the morning for GERD, mirabegron 25 mg at bedtime for overactive bladder, meloxicam 7.5 mg once a day in the morning after meal
- Allergien
- Penicillin- severe unspecified reaction requiring hospitalization
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 13.09.2021
- Impfdatum
- 01.07.2021
- Beginn
- 29.08.2021
- Tage bis Beginn
- 59,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Administered Expired Vaccine to a patient; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Administered Expired Vaccine to a patient) in a 37-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 039C21A and 039C21A) for COVID-19 vaccination. No Medical History information was reported. In July 2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 29-Aug-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 29-Aug-2021, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced EXPIRED PRODUCT ADMINISTERED (Administered Expired Vaccine to a patient). On 29-Aug-2021, EXPIRED PRODUCT ADMINISTERED (Administered Expired Vaccine to a patient) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No Concomitant medication was 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
- NY
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 11.09.2021
- Impfdatum
- 17.06.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product dose omission issue
Symptomtext
it's been more than 42 days since he received his first vaccination. Has not received 2nd dose.; This spontaneous case was reported by a consumer and describes the occurrence of PRODUCT DOSE OMISSION ISSUE (it's been more than 42 days since he received his first vaccination. Has not received 2nd dose.) in a 24-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 039C21A) for COVID-19 vaccination. No Medical History information was reported. On 17-Jun-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced PRODUCT DOSE OMISSION ISSUE (it's been more than 42 days since he received his first vaccination. Has not received 2nd dose.). At the time of the report, PRODUCT DOSE OMISSION ISSUE (it's been more than 42 days since he received his first vaccination. Has not received 2nd dose.) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No concomitant medication was reported. No treatment history was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product dose omission issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 08.09.2021
- Impfdatum
- 03.09.2021
- Beginn
- 03.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Symptomtext
Patient under 18 yo
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 07.09.2021
- Impfdatum
- 13.08.2021
- Beginn
- 13.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Exposure during pregnancy
Symptomtext
Received the vaccine being pregnant; This spontaneous prospective pregnancy case was reported by a consumer and describes the occurrence of EXPOSURE DURING PREGNANCY in a 25-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 039C21A) for COVID-19 vaccination. No Medical History information was reported. On 13-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. The patient's last menstrual period was on 17-Feb-2021 and the estimated date of delivery was 24-Nov-2021. On 13-Aug-2021, the patient experienced EXPOSURE DURING PREGNANCY. The patient received mRNA-1273 (Moderna COVID-19 Vaccine) beginning around the twenty-fifth week of the pregnancy. On 13-Aug-2021, EXPOSURE DURING PREGNANCY (Received the vaccine being pregnant) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Concomitant product use was not provided by the reporter. Treatment information was not provided by the reporter. This is a case of product exposure during pregnancy with no associated AEs for this 25-year-old female. Further information has been requested.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Exposure during pregnancy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 04.09.2021
- Impfdatum
- 21.07.2021
- Beginn
- 21.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
Fourth vaccination on 21-JUL-2021/Four doses of moderna; This spontaneous case was reported by a consumer and describes the occurrence of EXTRA DOSE ADMINISTERED (Fourth vaccination on 21-JUL-2021/Four doses of moderna) in a 63-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 039C21A) for COVID-19 vaccination. No Medical History information was reported. On 21-Jul-2021, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 21-Jul-2021, the patient experienced EXTRA DOSE ADMINISTERED (Fourth vaccination on 21-JUL-2021/Four doses of moderna). At the time of the report, EXTRA DOSE ADMINISTERED (Fourth vaccination on 21-JUL-2021/Four doses of moderna) had resolved. Concomitant medication was not provided Treatment information was not reported This case was linked to MOD-2021-265485 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 02.09.2021
- Impfdatum
- 31.08.2021
- Beginn
- 31.08.2021
- 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
Patient was under 18, age 17 and 8 months and vaccine should have been administered at age 18 or >
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 28.08.2021
- Impfdatum
- 23.06.2021
- Beginn
- 23.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Device connection issue
Symptomtext
most of the vaccine went on the patient's arm; This spontaneous case was reported by a pharmacist and describes the occurrence of DEVICE CONNECTION ISSUE (most of the vaccine went on the patient's arm) in a 60-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 039C21A) for COVID-19 vaccination. No Medical History information was reported. On 23-Jun-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 23-Jun-2021, the patient experienced DEVICE CONNECTION ISSUE (most of the vaccine went on the patient's arm). On 23-Jun-2021, DEVICE CONNECTION ISSUE (most of the vaccine went on the patient's arm) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Device connection issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ND
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 27.08.2021
- Impfdatum
- 24.06.2021
- Beginn
- 02.08.2021
- Tage bis Beginn
- 39,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Inappropriate schedule of product administration
Interchange of vaccine products
Symptomtext
Pt presented for COVID-19 vaccine on 6/24/21 at community event. Pt filled out paperwork stating that this was his 1st COVID-19 Vaccine and he chose to get Moderna. Pt presented to the clinic on 8/2/21 for his 2nd dose of Moderna. Pharmacy staff received email from on 8/27/21 to look into pt as he may have received too many doses. Reviewed and noted that pt had also received the Pfizer COVID-19 Vaccine on 4/22/21 and 5/13/21 at another facility. Tried contacting pt to discuss if he had any side effects, however pt is currently incarcerated and I was unable to get ahold of him.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Hepatitis C, Psychotic disorder, Paranoid schizophrenia, depressive disorder, alcohol dependence
- Andere Medikamente
- Cetirizine, Hydroxyzine, Paliperidone inj, Sertraline, Trazodone, Naltrexone inj
- Allergien
- No known drug allergies
- Vorherige Impfungen
- -
- Staat
- ND
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 27.08.2021
- Impfdatum
- 24.06.2021
- Beginn
- 02.08.2021
- Tage bis Beginn
- 39,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Inappropriate schedule of product administration
Interchange of vaccine products
Symptomtext
Pt presented for COVID-19 vaccine on 6/24/21 at community event. Pt filled out paperwork stating that this was his 1st COVID-19 Vaccine and he chose to get Moderna. Pt presented to the clinic on 8/2/21 for his 2nd dose of Moderna. Pharmacy staff received email from on 8/27/21 to look into pt as he may have received too many doses. Reviewed and noted that pt had also received the Pfizer COVID-19 Vaccine on 4/22/21 and 5/13/21 at another facility. Tried contacting pt to discuss if he had any side effects, however pt is currently incarcerated and I was unable to get ahold of him.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Hepatitis C, Psychotic disorder, Paranoid schizophrenia, depressive disorder, alcohol dependence
- Andere Medikamente
- Cetirizine, Hydroxyzine, Paliperidone inj, Sertraline, Trazodone, Naltrexone inj
- Allergien
- No known drug allergies
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 27.08.2021
- Impfdatum
- 15.06.2021
- Beginn
- 15.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Vaccine administered after it was stored at room temperature for 18 hours; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine administered after it was stored at room temperature for 18 hours) in a 22-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 039C21A) for COVID-19 vaccination. No Medical History information was reported. On 15-Jun-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 15-Jun-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine administered after it was stored at room temperature for 18 hours). On 15-Jun-2021, EXPIRED PRODUCT ADMINISTERED (Vaccine administered after it was stored at room temperature for 18 hours) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medications were reported. No treatment medications were provided by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 26.08.2021
- Impfdatum
- 15.06.2021
- Beginn
- 15.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
Vaccine administered after it was stored at room temperature for 18 hours; Vaccine administered after it was stored at room temperature for 18 hours; This spontaneous case was reported by a pharmacist and describes the occurrence of PRODUCT STORAGE ERROR (Vaccine administered after it was stored at room temperature for 18 hours) and EXPIRED PRODUCT ADMINISTERED (Vaccine administered after it was stored at room temperature for 18 hours) in a 50-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 039C21A) for COVID-19 vaccination. No Medical History information was reported. On 15-Jun-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 15-Jun-2021, the patient experienced PRODUCT STORAGE ERROR (Vaccine administered after it was stored at room temperature for 18 hours) and EXPIRED PRODUCT ADMINISTERED (Vaccine administered after it was stored at room temperature for 18 hours). On 15-Jun-2021, PRODUCT STORAGE ERROR (Vaccine administered after it was stored at room temperature for 18 hours) and EXPIRED PRODUCT ADMINISTERED (Vaccine administered after it was stored at room temperature for 18 hours) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. 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
- NM
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 19.08.2021
- Impfdatum
- 16.07.2021
- Beginn
- 16.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthropod bite
Contusion
Skin discolouration
Symptomtext
about 20 minutes post ima, the patient noticed that her arm began to become discolored (dark grey in color) and continued to get darker over several days. the area in size was 3 inches by 6 inches. the spot lasted about 4 weeks long. a week after the shot the patient got a bug bite on her leg and then got a large bruise over the area that was approximately 4 inches by 5 inches. there is still a large bruise over the area. Recommended to patient to hold off on second shot until we have more information. the primary doctor said she needs to get it but should check with her pulmonary doctor, the pulmonary dr said she needs to get the shot but that she needs to ask more questions before doing so.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthropod bite
- Hospital-Tage
- -
- Labordaten
- na
- Aktuelle Erkrankungen
- asthma (copd) controlled
- Vorgeschichte
- asthma (copd) controlled
- Andere Medikamente
- na
- Allergien
- na
- Vorherige Impfungen
- flu shot lead to a blood infection
- Staat
- MN
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 11.08.2021
- Impfdatum
- 08.08.2021
- Beginn
- 08.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
No adverse event
Symptomtext
Due to error in name spelling in state immunization registry, we did not find the clients information in the system indicating he already received 2 prior doses of the Pfizer vaccine in April and May. This was his 3rd dose of the COVID-19 vaccine and a different one than he originally received. Called to verify information and after some questioning, patient knew was he was doing and thought a booster was fine. He had no adverse effects from his 3rd dose and feels just fine per his report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 11.08.2021
- Impfdatum
- 28.06.2021
- Beginn
- 06.07.2021
- Tage bis Beginn
- 8,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
Symptomtext
8/11/21 - PT IS HERE AT HEALTH CLINIC would like to get a 3rd dose of MODERNA vaccine. At this moment, pt doesn't complains of any symptoms. Writer consulted w/ provider hotline, to check if pt needs to have another Moderna vaccine since the 1st and the 2nd dose is 8 days apart. Per hotline, did checked and double checked w/ the vaccine team and both stated "No". Do not give the 3rd Moderna vaccine. Hotline operator requested writer to fill out the VAERS as there is an vaccine errors. Information is below. Covid-19 Provider Hotline
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 10.08.2021
- Impfdatum
- 25.07.2021
- Beginn
- 25.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient was given the first dose from a vial that was expired, from 30 days of date it was received. The Moderna Vaccine dose was inadvertently administration past the 30-day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 10.08.2021
- Impfdatum
- 06.08.2021
- Beginn
- 06.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Circumstance or information capable of leading to medication error
Extra dose administered
No adverse event
Symptomtext
Pt came to hospital's vaccine site on 8/6/21, filled out and signed a consent form stating that it was his 1st COVID vaccine dose. Pt got the vaccine, was observed for 15 minutes, and left. No reactions observed. Staff went to enter the vaccine into the state's database and saw that the pt had previously gotten 2 doses of the Moderna COVID vaccine, the dose given on 8/6/2021 was the patient's 3rd dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Circumstance or information capable of leading to medication error
- Hospital-Tage
- -
- Labordaten
- None. Pt was contacted 8/10/2021, confirmed that he lied to get a 3rd dose. Stated that he had no adverse reactions, but would call his provider if he felt any.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VI
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 09.08.2021
- Impfdatum
- 08.07.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product administered to patient of inappropriate age
Symptomtext
16 Y O MALE INADVERTANTLY RECEIVED MODERNA VACCINE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE KNOWN
- Vorgeschichte
- NONE KNOWN
- Andere Medikamente
- NONE KNOWN
- Allergien
- NONE KNOWN
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 06.08.2021
- Impfdatum
- 28.06.2021
- Beginn
- 06.08.2021
- Tage bis Beginn
- 39,0
- Dosis
- 1
- 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 didn't informed us she received J&J shot back in March, and received her first dose of Moderna from us back in June. She did not report any adverse event except for sore arms and tiredness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 31.07.2021
- Impfdatum
- 20.03.2021
- Beginn
- 31.07.2021
- Tage bis Beginn
- 133,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Wrong product administered
Symptomtext
Patient female 26 years old received a dose Janssen lot-1805018 in the associated medical facilities on March 20, 2021. Patient came in July 17, 2021 in the vaccination center of to receive her first Moderna vaccine lot 039C21A since she said she was worried of the effectness of Janssen and her health conditions of diabetes, hx of cancer thyroid and being a care giver of the elderly, It is for this reason that she agrees to have omitted the information from the previous vaccination of Janssen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- N.A
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- Diabetes; Hx Cancer thyroid surgery.
- Andere Medikamente
- N/A
- Allergien
- UNKNOWN
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 26.07.2021
- Impfdatum
- 19.07.2021
- Beginn
- 24.07.2021
- Tage bis Beginn
- 5,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anosmia
Symptomtext
Patient came to the pharmacy and asked if it was something usual to lose the sense of smell after receiving the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anosmia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- HI
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 23.07.2021
- Impfdatum
- 22.06.2021
- Beginn
- 22.07.2021
- Tage bis Beginn
- 30,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
+COVID after full vaccination
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- +COVID test on 7/22/21
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Mango
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 21.07.2021
- Impfdatum
- 12.07.2021
- Beginn
- 12.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product administered to patient of inappropriate age
Symptomtext
PATIENT IS UNDER THE RECOMMENDED AGE RANGE. THE PATIENT'S AGE IS 16 AND 4 MONTHS. THE VACCINE ERROR WAS FOUNDED BY THE PHARMACY THAT THE VACCINE IS PROVIDED BY AND ALSO DOES THE BILLING FOR THE VACCINE. THE PHARMACY NOTIFIED THE MEDICAL OFFICE THE SAME DAY THAT THE VACCINE WAS ADMINSTERED ON 07/12/2021. THE MEDICAL OFFICE NOTIFIED THE PATIENT THE FOLLOWING DAY 07/13/2021. ACCORDING TO THE MEDICAL OFFICE THE PATIENT DID NOT REPORT ANY SIDE EFFECTS AFTER THE VACCINE WAS ADMINSTERED. PHARMACY ALSO CALLED MODERNA COMPANY AND SPOKE WITH CUSTOMER SERVICE REPRESENTATIVE ADE. HE TOLD THE PHARMACY TO SUBMIT A VAERS ADVERSE EVENT. MODERNA COMPANY DOESNT HAVE ANY FURTHER INFORMATION REGARDING ANY ADVERSE EVENT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- NO
- Vorgeschichte
- NO
- Andere Medikamente
- N/A
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 21.07.2021
- Impfdatum
- 21.07.2021
- Beginn
- 21.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Moderna vaccine at room temperature for 25.5 hours inadvertently was administered to patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 19.07.2021
- Impfdatum
- 25.06.2021
- Beginn
- 25.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Symptomtext
No adverse events, no treatments, no negative outcomes
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 13.07.2021
- Impfdatum
- 10.06.2021
- Beginn
- 17.06.2021
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Tinnitus
Symptomtext
Patient reports abnormal ringing in her ears ~1 week after receiving first dose that has not gone away since. The patient's PCP has been notified.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tinnitus
- Hospital-Tage
- -
- Labordaten
- N/A - currently receiving follow-up
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypothyroidism Cardiovascular conditions Psoriasis on scalp
- Andere Medikamente
- Triamcinolone Cream PRN Montelukast 10 mg daily Levothyroxine 50 mcg daily Gabapentin 300 mg (1 capsule in the morning, 1 in the evening, and 2 at bedtime) Nortriptyline 50 mg at bedtime Hydroxyzine HCl 10 mg (1-2 tablets three times daily)
- Allergien
- Sulfonamide derivatives
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 13.07.2021
- Impfdatum
- 31.05.2021
- Beginn
- 31.05.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product administered to patient of inappropriate age
Symptomtext
*ADMINISTRATION ERROR - PATIENT UNDER 18 YEARS OLD* Patient received first dose of Moderna Covid vaccine on 05/31/21 with previous pharmacy manager. Patient filled out Prevaccination Checklist with no reported allergies, medical conditions, or adverse events with other vaccines. Patient came back to pharmacy on 06/28/2021 for second Moderna dose, accompanied by father. Because patient came in for second dose, new pharmacy manager focused on going over Prevaccination Checklist with patient without realizing patient age. Patient reported no adverse events or allergic reaction after getting first dose or second dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 13.07.2021
- Impfdatum
- 06.07.2021
- Beginn
- 06.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
Symptomtext
Moderna 2nd dose given too early. First dose was on 6/21/21 and second dose was given 7/6/21.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 13.07.2021
- Impfdatum
- 17.06.1921
- Beginn
- 21.06.2021
- Tage bis Beginn
- 36.529,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Platelet count decreased
Symptomtext
platelet count decreased to 30K on 6/21/21, then 7/9/21 15K, 7/12/21 20K, 7/13/21 21K started on dexamethasone on 7/21
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Platelet count decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- liver disease d/t alcohol Dx 11/17 tobacco abuse
- Vorgeschichte
- see above
- Andere Medikamente
- pepcid 20 mg prn, lasix 20 mg twice daily, lopressor 25 mg daily, viagra 50 mg prn
- Allergien
- no known drug allergies
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 09.07.2021
- Impfdatum
- 01.07.2021
- Beginn
- 01.07.2021
- 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
No adverse event
Symptomtext
Invalid 3rd dose administered. Patient is under nursing supervision in a skilled facility. Per nurses at the facility, patient has exhibited no adverse reactions to this dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 07.07.2021
- Impfdatum
- 06.07.2021
- Beginn
- 06.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Symptomtext
Pt, who was deaf, arrived for 2nd Moderna vaccine. Vaccine card showed she had received 1st Moderna vaccine on June 8. Nurse gave 2nd Moderna vaccine. Later, through software, found out she had also received both Pfizer vaccines in April, 2021. Pt, while in waiting area, nurse wrote a note asking about getting the Pfizer vaccine in April. She acknowledged that she had received both Pfizer vaccine in April.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 03.07.2021
- Impfdatum
- 03.07.2021
- Beginn
- 03.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fall
Symptomtext
After receiving her Moderna IMZ, pt stepped out of both and I was about to administer IMZ to her dad when she suddenly fell over in front of me. Her mom and I rushed to her aid, fortunately she did not hit her head when she went down. With her mom's assistance, she walked over to a waiting chair where I suggested pt be sitting on the floor instead of up high on a chair. I gave patient two ice packs - one for her forehead and one for the back of her neck, and a small bottle of water. Code white was immediately called, I asked pt and pt's mom and dad if they wanted me to call 911 to have emergency services to check her out, they all declined. I told them I would be happy to call if they change their mind. Employees stayed with her and began taking her report. Patient stayed for about 30 minutes, declined 911 emergency services, and patient left with her parents under her own strength.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fall
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- None listed on VAR
- Andere Medikamente
- Unknown
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 03.07.2021
- Impfdatum
- 25.06.2021
- Beginn
- 25.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blepharospasm
Dysgeusia
Hypoaesthesia
Vision blurred
Visual impairment
Symptomtext
1. Odd taste in mouth -metallic taste 5 minutes after the vaccine -still experiencing this symptom. No treatment has not call primary care provider. 2. Left eye started twitching and visual issues including blurry vision and seeing three images. Started 5 minutes after vaccine -still experiencing symptom. No treatment has not call primary care provider. 3. Left hand is numb, this started a couple days after the vaccine -not sure of date and is still experiencing this symptom. No treatment has not call primary care provider.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blepharospasm
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- 1. blood pressure 2. acid reflux
- Andere Medikamente
- 1. Lisinopril-HCTZ 20-12.5mg qd 2. Pantoprazole 40mg bid
- Allergien
- 1. Soma -blotchy red spots
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 01.07.2021
- Impfdatum
- 29.06.2021
- Beginn
- 29.06.2021
- 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
No adverse event
Symptomtext
The patient did not have a reaction he just received the vaccine 20 days after the 1st dose
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- None
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 30.06.2021
- Impfdatum
- 25.06.2021
- Beginn
- 25.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
Patient was given Moderna vaccine at age 14. She should have received Pfizer vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- unknown
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- Developmental delay, angelman syndrome, chromosome deletion
- Andere Medikamente
- unknown
- Allergien
- no known allergies
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 29.06.2021
- Impfdatum
- 24.06.2021
- Beginn
- 24.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Symptomtext
Unknown - Unable to reach patient's guardian or patient himself to inquire. Unable to confirm whether or not patient has experienced an adverse event at this time. Patient or his guardian have not been in contact to report an adverse event.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Class I Obesity
- Andere Medikamente
- None
- Allergien
- No Known Allergies
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 28.06.2021
- Impfdatum
- 28.06.2021
- Beginn
- 28.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
Noticed after I gave vaccine that his first one was on 6/14/21. I called patient because he had left before his 15 minute waiting period was done. He said he thought that it was 2 weeks from the first one. I said that according to the informatin on the CDC web site, he does not need to repeat the dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None known
- Vorgeschichte
- None stated on Vaccine contraindications
- Andere Medikamente
- Not known
- Allergien
- None Known
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 22.06.2021
- Impfdatum
- 15.06.2021
- Beginn
- 15.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Interchange of vaccine products
No adverse event
Symptomtext
Patient was mistakenly given Moderna as a 2nd dose instead of Pfizer. Patient was observed for 30 minutes with no apparent signs, symptoms or adverse reaction.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ND
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 21.06.2021
- Impfdatum
- 15.06.2021
- Beginn
- 15.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient was given expired dose by 1 hour. No treatment needed. Patient was notified. Patient reported no signs/symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 20.06.2021
- Impfdatum
- 11.06.2021
- Beginn
- 12.06.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test normal
Hemiplegia
Sensory processing disorder
Symptomtext
Intermittent paralysis on right side of body at extremities. Pleasurable feelings on right side of body. No pain at all. Happens when standing from sitting position, or bending at the waist while standing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood test normal
- Hospital-Tage
- -
- Labordaten
- Sensory disorder Blood tests normal 06/18/2021
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Amoxicillin
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 15.06.2021
- Impfdatum
- 15.06.2021
- Beginn
- 15.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Patient was given vaccine that was past 12 hours of viability but less than 18 hours since first puncture. We called moderna and they directed us to the state. The state directed back to us as whether to re administer. Currently we are consulting with our company as to the best course of action.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 92,0
- Geschlecht
- F
- Eingang
- 15.06.2021
- Impfdatum
- 15.06.2021
- Beginn
- 15.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Patient was given vaccine that was past 12 hours of viability but less than 18 hours since first puncture. We called moderna and they directed us to the state. The state directed back to us as whether to re administer. Currently we are consulting with our company as to the best course of action.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 15.06.2021
- Impfdatum
- 15.06.2021
- Beginn
- 15.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Patient was given vaccine that was past 12 hours of viability but less than 18 hours since first puncture. We called moderna and they directed us to the state. The state directed back to us as whether to re administer. Currently we are consulting with our company as to the best course of action.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 14.06.2021
- Impfdatum
- 11.06.2021
- Beginn
- 11.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Patient was a 17 year old that received the Moderna vaccine in error. No adverse events reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 11.06.2021
- Impfdatum
- 11.06.2021
- Beginn
- 11.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
Product preparation issue
Symptomtext
With everything going on in the pharmacy, I neglected to draw up medication into the syringe. I had to stick patient twice so she could get the dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 10.06.2021
- Impfdatum
- 10.06.2021
- Beginn
- 10.06.2021
- 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
No adverse event
Symptomtext
Was given 2nd dose of Moderna Vaccine 20 days after 1st dose.No apparent injury, patient was monitored for 30 min in the COVID vaccine clinic in the gym no adverse reactions noted
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 10.06.2021
- Impfdatum
- 10.06.2021
- Beginn
- 10.06.2021
- 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
No adverse event
Symptomtext
Was given 2nd dose of Moderna Vaccine 20 days after 1st dose.No apparent injury, patient was monitored for 30 min in the COVID vaccine clinic in the gym no adverse reactions noted
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 10.06.2021
- Impfdatum
- 10.06.2021
- Beginn
- 10.06.2021
- 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
No adverse event
Symptomtext
Was given 2nd dose of Moderna Vaccine 20 days after 1st dose.No apparent injury, patient was monitored for 30 min in the COVID vaccine clinic in the gym no adverse reactions noted
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 10.06.2021
- Impfdatum
- 10.06.2021
- Beginn
- 10.06.2021
- 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
No adverse event
Symptomtext
Was given 2nd dose of Moderna Vaccine 20 days after 1st dose.No apparent injury, patient was monitored for 30 min in the COVID vaccine clinic in the gym no adverse reactions noted
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 10.06.2021
- Impfdatum
- 10.06.2021
- Beginn
- 10.06.2021
- 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
No adverse event
Symptomtext
Was given 2nd dose of Moderna Vaccine 20 days after 1st dose.No apparent injury, patient was monitored for 30 min in the COVID vaccine clinic in the gym no adverse reactions noted
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 10.06.2021
- Impfdatum
- 10.06.2021
- Beginn
- 10.06.2021
- 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
No adverse event
Symptomtext
Was given 2nd dose of Moderna Vaccine 20 days after 1st dose.No apparent injury, patient was monitored for 30 min in the COVID vaccine clinic in the gym no adverse reactions noted
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 10.06.2021
- Impfdatum
- 10.06.2021
- Beginn
- 10.06.2021
- 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
Symptomtext
Was given 2nd dose of Moderna Vaccine 20 days after 1st dose.No apparent injury, patient was monitored for 30 min in the COVID vaccine clinic in the gym no adverse reactions noted
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 10.06.2021
- Impfdatum
- 10.06.2021
- Beginn
- 10.06.2021
- 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
No adverse event
Symptomtext
Was given 2nd dose of Moderna Vaccine 20 days after 1st dose.No apparent injury, patient was monitored for 30 min in the COVID vaccine clinic in the gym no adverse reactions noted
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 10.06.2021
- Impfdatum
- 10.06.2021
- Beginn
- 10.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Symptomtext
No apparent injury, patient was monitored for 30 min in the COVID vaccine clinic in the gym no adverse reactions noted
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 10.06.2021
- Impfdatum
- 10.06.2021
- Beginn
- 10.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Symptomtext
No apparent injury, patient was monitored for 30 min in the COVID vaccine clinic in the gym no adverse reactions noted
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 04.06.2021
- Impfdatum
- 04.06.2021
- Beginn
- 04.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Symptomtext
No adverse reactions noted. Patient came in for her second dose of the Moderna vaccine. Vial was punctured 1:55PM on 06/03/2021. Vaccine was administered from the same vial at 08:55AM 06/04/2021
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- anxiety
- Andere Medikamente
- sertraline 100mg daily
- Allergien
- NKDA
- Vorherige Impfungen
- -