- Staat
- TN
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 01.09.2023
- Impfdatum
- 01.07.2022
- Beginn
- 01.06.2023
- Tage bis Beginn
- 335,0
- Dosis
- 3
- Route/Site
- UN / UN
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Computerised tomogram thorax abnormal
Death
Hypervolaemia
Positive airway pressure therapy
Urine output decreased
Symptomtext
Pt was admitted with slowly increasing O2 requirement and volume retention as DC PO dose of lasix may have been inadequate. Pt was re-initiated on diamox within a few days of admission in an attempt to improve UOP, but this was inadequate. Despite multiple attempts to get pt to wear CPAP or BIPAP she would not. Repeat evaluation with CT chest showed slowly worsening volume overload and/or possible pneumonitis presumed related to her decitabine. On 7/10/23 she precipitously declined in the afternoon and family requested her goals of care be moved to comfort. Comfort measures were initiated and pt passed peacefully with family at bedside early on 7/13/2023.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Myeloproliferative neoplasm Hypertension A-fib Arthritis Hyperlipidemia Diverticulitis Partial colectomy 2002 Hysterectomy Bilateral knee replacements Cardiac ablation May 2022
- Andere Medikamente
- -
- Allergien
- Prednisone Tetracycline Levalbuterol Azithromycin
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 94,0
- Geschlecht
- F
- Eingang
- 02.08.2023
- Impfdatum
- 08.05.2022
- Beginn
- 09.06.2022
- Tage bis Beginn
- 32,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Cerebrovascular accident
Hypoxia
Symptomtext
ACUTE STROKE, UNSPECIFIED TYPE AND ARTERY HYPOXIA
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 02.08.2023
- Impfdatum
- 20.05.2022
- Beginn
- 16.03.2023
- Tage bis Beginn
- 300,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Respiratory failure
Symptomtext
ACUTE RESPIRATORY FAILURE RESPIRATORY FAILURE, UNSPECIFIED ACUITY
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 85,0
- Geschlecht
- M
- Eingang
- 06.06.2023
- Impfdatum
- 20.05.2022
- Beginn
- 17.06.2022
- Tage bis Beginn
- 28,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute myocardial infarction
Symptom recurrence
Symptomtext
ACUTE ST ELEVATION MI, UNSPECIFIED ACUTE NON ST ELEVATION MI 6/20/2022 -- RECURRENCE OF HOSPITALIZATION WITH SAME SYMPTOMS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 31.05.2023
- Impfdatum
- 26.05.2022
- Beginn
- 02.11.2022
- Tage bis Beginn
- 160,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute respiratory failure
Aortic arteriosclerosis
Chronic respiratory failure
Hypoxia
Respiratory failure
Symptomtext
ACUTE HYPOXEMIC RESPIRATORY FAILURE 11/8/2022 CHRONIC HYPOXEMIC RESPIRATORY FAILURE ACUTE ON CHRONIC RESPIRATORY FAILURE 11/8/2022 CHRONIC HYPOXEMIC RESPIRATORY FAILURE ACUTE ON CHRONIC HYPOXEMIC RESPIRATORY FAILURE 2/6/2023 CHRONIC HYPOXEMIC RESPIRATORY FAILURE RESPIRATORY FAILURE, UNSPECIFIED ACUITY 2/11/2023 CHRONIC HYPOXEMIC RESPIRATORY FAILURE ACUTE HYPOXEMIC RESPIRATORY FAILURE 11/8/2022 ACUTE ON CHRONIC HYPOXEMIC RESPIRATORY FAILURE ACUTE ON CHRONIC RESPIRATORY FAILURE 11/8/2022 ACUTE ON CHRONIC HYPOXEMIC RESPIRATORY FAILURE ACUTE ON CHRONIC HYPOXEMIC RESPIRATORY FAILURE 2/6/2023 ACUTE ON CHRONIC HYPOXEMIC RESPIRATORY FAILURE RESPIRATORY FAILURE, UNSPECIFIED ACUITY 2/11/2023 ACUTE ON CHRONIC HYPOXEMIC RESPIRATORY FAILURE ACUTE HYPOXEMIC RESPIRATORY FAILURE 11/8/2022 ATHEROSCLEROSIS OF AORTA ACUTE ON CHRONIC RESPIRATORY FAILURE 11/8/2022 ATHEROSCLEROSIS OF AORTA ACUTE ON CHRONIC HYPOXEMIC RESPIRATORY FAILURE 2/6/2023 ATHEROSCLEROSIS OF AORTA RESPIRATORY FAILURE, UNSPECIFIED ACUITY 2/11/2023 ATHEROSCLEROSIS OF AORTA ACUTE HYPOXEMIC RESPIRATORY FAILURE 11/8/2022 HYPOXIA ACUTE ON CHRONIC RESPIRATORY FAILURE 11/8/2022 HYPOXIA ACUTE ON CHRONIC HYPOXEMIC RESPIRATORY FAILURE 2/6/2023 HYPOXIA RESPIRATORY FAILURE, UNSPECIFIED ACUITY 2/11/2023 HYPOXIA ACUTE HYPOXEMIC RESPIRATORY FAILURE 11/8/2022 AMBULATORY OXYGEN THERAPY DEPENDENCE ACUTE ON CHRONIC RESPIRATORY FAILURE 11/8/2022 AMBULATORY OXYGEN THERAPY DEPENDENCE ACUTE ON CHRONIC HYPOXEMIC RESPIRATORY FAILURE 2/6/2023 AMBULATORY OXYGEN THERAPY DEPENDENCE RESPIRATORY FAILURE, UNSPECIFIED ACUITY 2/11/2023 AMBULATORY OXYGEN THERAPY DEPENDENCE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 23.05.2023
- Impfdatum
- 20.05.2022
- Beginn
- 08.08.2022
- Tage bis Beginn
- 80,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute myocardial infarction
Symptom recurrence
Symptomtext
PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ACUTE NON ST ELEVATION MI 8/10/2022 & 2/13/2023 -- RECURRENCE OF SAME SYMPTOMS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 04.05.2023
- Impfdatum
- 19.05.2022
- Beginn
- 17.10.2022
- Tage bis Beginn
- 151,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Symptomtext
PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ACUTE RESPIRATORY FAILURE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 24.04.2023
- Impfdatum
- 09.06.2022
- Beginn
- 18.03.2023
- Tage bis Beginn
- 282,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Asthma
COVID-19
Condition aggravated
SARS-CoV-2 test positive
Symptomtext
Hospitalization: 3/17/2023 - 3/20/2023 (3 days) Presentation to the ED: acute hypoxic respiratory failure from acute asthma exacerbation COVID + date: 3/18/2023 Treatment: high dose steroids Discharge to: HOME. 013L20A 2/3/2021 039K20A 3/1/2021 038A22A 6/9/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- ASTHMA, RA, HLD, ANXIETY
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 27.03.2023
- Impfdatum
- 17.05.2022
- Beginn
- 20.03.2023
- Tage bis Beginn
- 307,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Acute respiratory failure
Bladder catheterisation
COVID-19
Chest X-ray abnormal
Complication associated with device
Condition aggravated
Decubitus ulcer
Haematuria
Hyperlipidaemia
Hyponatraemia
Infection
Influenza A virus test negative
Influenza B virus test
Legionella test
Mental status changes
Pneumonia
Pneumonia bacterial
Pyrexia
Symptomtext
Admission Date: 3/20/2023 Discharge Date: 3/23/2023 PRESENTING PROBLEM: Sepsis Bacterial lobar pneumonia Urinary tract infection with hematuria, site unspecified Altered mental status, unspecified altered mental status type Sepsis, due to unspecified organism, unspecified whether acute organ dysfunction present COVID-19 HOSPITAL COURSE: Patient is a 68 y.o. man with DM2, HTN, hyperlipidemia, and metastatic RCC (with metastases to the bones, skin, likely lungs) receiving treatment with axitinib/nivolumab now admitted with altered mental status likely in the setting of infection. In the ED was found to be febrile, altered mental status, hyponatremia, hyperlipidemia, AHRF and be COVID positive. Furthermore he was found to be tachycardic tachypneic with no leukocytosis. CXR significant for R lower lobe pneumonia. He was started on Zosyn and vancomycin in the emergency department. During his hospital course his infectious workup was negative for MRSA, strep, Legionella, influenza A/B and respiratory panel film array. His sepsis and altered mental status had resolved after 2 L of IV fluids. Per his CAP, the abx was switched to ceftriaxone for targeted coverage. He was transitioned to Augmentin prior to SAR discharge to complete 5 day course. Per patient's COVID status he remained asymptomatic and satting 100% on room air. He was treated with remdesivir for 3 days. On his arrival to the medicine floor patient was found to have pressure injuries. Type 1 to coccyx and patient offloading of pressure was prioritized. Type 2 to urethra likely secondary to chronic foley. Photos were uploaded to media tab. Patient denied any pain to these locations. Patient discharged in stable condition back to his SAR facility. With plan for close PCP follow up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Essential (primary) hypertension Hyperlipidemia, unspecified DM type 1 (diabetes mellitus, type 1) (HCC) Back pain Hypertrophy of prostate without urinary obstruction and other lower urinary tract symptoms (LUTS) Type 2 diabetes mellitus with hyperglycemia (HCC) Primary osteoarthritis of both knees Secondary malignant neoplasm of bone (HCC) Renal cell carcinoma of right kidney (HCC) Lumbar spinal stenosis Spinal cord compression due to malignant neoplasm metastatic to spine (HCC) Weakness Hyponatremia Cancer related pain Opiate analgesic use agreement exists Constipation due to opioid therapy Neoplastic (malignant) related fatigue Mood insomnia (HCC) Anorexia Hallucinations Closed right hip fracture, initial encounter (HCC) Acute low back pain due to spinal disorder Anemia Chronic pain syndrome Gastro-esophageal reflux disease without esophagitis History of falling Type 2 diabetes mellitus without complications (HCC) Generalized weakness Depression
- Andere Medikamente
- acetaminophen (TYLENOL) 500 MG tablet aspirin 81 MG tablet bisacodyl (DULCOLAX) 10 MG suppository cetirizine (ZYRTEC) 10 MG tablet Glucagon, rDNA, (GLUCAGON EMERGENCY) 1 MG KIT HYDROcodone-acetaminophen (NORCO) 5-325 mg per tablet (Expired)
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 24.03.2023
- Impfdatum
- 28.07.2022
- Beginn
- 15.03.2023
- Tage bis Beginn
- 230,0
- Dosis
- 3
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain upper
Acute respiratory failure
Aortic stenosis
Barrett's oesophagus
Bile duct stone
Biliary dilatation
Biliary sphincterotomy
Blood potassium decreased
COVID-19
Cholecystectomy
Cholelithotomy
Computerised tomogram abdomen abnormal
Echocardiogram abnormal
Encephalopathy
Endoscopic retrograde cholangiopancreatography
Endotracheal intubation
Gallbladder disorder
Hiatus hernia
Symptomtext
Discharge summary: "Brief Summary of Hospital Stay: patient is a 74 YO female a past medical history of hypertension, hyperlipidemia, who presented to the emergency department with acute onset of nausea, vomiting, and RUQ abdominal pain shortly after meal. On arrival, the patient was hemodynamically stable but she was found to have elevated LFTs with cholestatic pattern as well as potassium 2.6. CT abdomen and pelvis was obtained which showed gallbladder and cystic duct distention, mild intrahepatic and extrahepatic biliary dilatation, radiographic findings suggestive of choledocholithiasis. Gastroenterology was consulted who recommended ERCP. Potassium was replaced. The patient initially underwent EGD given limited anesthesia availability, which was negative for Zenker's diverticulum, but did show esophageal mucosa consistent with short-segment Barrett's esophagus as well as a large hiatal hernia, otherwise unrevealing. Patient then underwent ERCP on 3/17/2023 with Dr., where biliary sphincterotomy was performed, the common bile duct was dilated, the biliary tree was swept, and choledocholithiasis was visualized and removed. Patient tolerated the procedure well. General surgery was consulted for cholecystectomy evaluation given her presentation. She underwent robotic assisted laparoscopic cholecystectomy on 3/18/2023 with another Dr. which she tolerated without immediate complicatinon. In the interim, she was receiving maintenance IV fluids. She initially tolerated the surgery well. However, postoperatively on 3/18, she began exhibiting acute encephalopathy and respiratory distress, becoming acutely hypoxic. Attempt was made to place her on BiPAP, however she acutely developed nausea and vomiting. Given her respiratory distress and aspiration risk, ICU was consulted and the patient was intubated for airway protection. The patient was diuresed and started on antibiotics given concern for aspiration pneumonia. She would improvement in her oxygen requirements and was able to be extubated on 3/19 without postextubation complication. She was transferred to floor status. Antibiotics were discontinued given low suspicion for aspiration pneumonia. Suspect that her acute respiratory decompensation was due to volume overload in setting of perioperative IV fluids and is supported chest imaging and physical exam. Echo was obtained which showed EF 50% and mild aortic stenosis and mild-moderate MR. Diuresis was continued, after which the patient demonstrated improvement in her oxygen requirements and respiratory effort, being able to wean down to room air this admission. She had resolution of her abdominal pain in her liver function testing had normalized, she otherwise remained hemodynamically stable. Patient will be discharged home with PRN Lasix to treat volume overload with close PCP follow-up. Patient will follow-up with General surgery. She was discharged home in good condition."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 7,0
- Labordaten
- COVID PCR positive test on 3/18/23
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 93,0
- Geschlecht
- F
- Eingang
- 19.01.2023
- Impfdatum
- 03.11.2022
- Beginn
- 08.11.2022
- Tage bis Beginn
- 5,0
- Dosis
- 4
- Route/Site
- UN / UN
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
COVID-19
COVID-19 pneumonia
Chronic obstructive pulmonary disease
Confusional state
Death
Hypoxia
Pneumonia
Respiratory failure
SARS-CoV-2 test positive
Superinfection
Symptomtext
Patient brought to the ED on 11/8 for evaluation of confusion. Patient lives independently, and for the past 3 days her son has noticed that she has been confused. Patient was brough in by EMS, and on arrival to the scene she was notably hypoxic to 75-85%. She continued to have hypoxia in the ED and required supplemental oxygen. Patient had a COVID-19 PCR test done in the ED which resulted positive. Ultimately, she was admitted 11/8 with acute hypoxic/hypercapnic respiratory failure, suspected COVID-19 pneumonia with superimposed pneumonia, and chronic COPD with possible acute exacerbation, among other diagnoses. Patient was transitioned to comfort cares, and passed away on 11/11.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 95,0
- Geschlecht
- M
- Eingang
- 02.12.2022
- Impfdatum
- 26.05.2022
- Beginn
- 30.10.2022
- Tage bis Beginn
- 157,0
- Dosis
- 4
- Route/Site
- UN / UN
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Acute myocardial infarction
Aspiration
Asthenia
Bladder irrigation
COVID-19
Chest X-ray
Computerised tomogram head
Computerised tomogram thorax
Death
Echocardiogram
Electrocardiogram
Fall
General physical health deterioration
Haemorrhage
Haemothorax
Laboratory test
Malaise
Mobility decreased
Symptomtext
Information provided in this adverse event note, is per web report received by Health Department from submitting facility. Covid-19 vaccination information is provided by information that is in Immunization Registry. Pfizer 02/04/2021 EL9264 / public; Pfizer 2/25/2021 EL9267 / public; Moderna 12/01/2021 013F21A / public; Moderna 5/16/2022 038A22A / public PER WEB REPORT RECEIVED: Patient brought into the ED on 10/30/2022 following a fall at home. He fell on 10/29/2022, was able to get up with assistance, but then throughout the next few hours became very weak and was unable to get out of bed. Had COVID symptoms since 10/28/2022. Patient tested positive for COVID-19. Hospital stay was complicated by worsening COVID symptoms, pneumonia, aspiration, NSTEMI, bleeding, need for CBI, and worsening restlessness. Family agreed to hospice care. Patient to go to Hospice when possible. Admitted Hospice In-House awaiting bed. Patient?s condition worsened and patient was admitted at 15:10 to Inpatient Hospice ---- Patient died @ 2140 on 11/4/22. Death abstracted received. Death Certificated listed Covid-19 as a contributing cause of death.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- 5,0
- Labordaten
- Lab work, EKG, CT-head, C-XR, CT- chest, Echo Cardiogram, Pelvis-XR
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- Dementia, recurrent falls c/b rib fractures and hemothorax (9/2022), severe aortic stenosis, HLD, and HTN
- Andere Medikamente
- unknown
- Allergien
- unknown, no information received.
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 22.08.2022
- Impfdatum
- 27.05.2022
- Beginn
- 18.08.2022
- Tage bis Beginn
- 83,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient admitted as inpatient on 08/18/2022 due to Acute respiratory failure with hypoxia (*) 2/2 covid. Patient was tested for COVID-19 and was positive on 08/18/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 20.06.2023
- Impfdatum
- 09.06.2022
- Beginn
- 24.11.2022
- Tage bis Beginn
- 168,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Computerised tomogram
Generalised tonic-clonic seizure
Loss of consciousness
Magnetic resonance imaging
Seizure
Symptomtext
I had a Grand mal seizure after my COVID-19 Moderna vaccine on 25NOV2022 and previous to that I was having black out seizures.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Generalised tonic-clonic seizure
- Hospital-Tage
- -
- Labordaten
- MRI; blood profile and CT scan no results known.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension; Obesity; COPD; Diabetes
- Andere Medikamente
- Lisinopril; simvistatin; omeprazole; ropinirole; meloxicam; trazadone; metformin; loratadine; XANAX; insulin
- Allergien
- KEFLEX; ZOFRAN; codeine; VICODIN; REGLAN
- Vorherige Impfungen
- Age 46 Tachycardia was diagnosed post this vaccine; Dose 2 Pfizer 13JUL2021.
- Staat
- -
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 01.06.2023
- Impfdatum
- 03.06.2022
- Beginn
- 12.07.2022
- Tage bis Beginn
- 39,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Epilepsy
Ischaemic stroke
Partial seizures
Symptomtext
PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE FOCAL MOTOR SEIZURE EPILEPSY, UNSPECIFIED ACUTE STROKE DUE TO ISCHEMIA, UNSPECIFIED TYPE AND ARTERY
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ischaemic stroke
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 31.08.2022
- Impfdatum
- 12.05.2022
- Beginn
- 13.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Cough
Face and mouth X-ray abnormal
Face injury
Facial bones fracture
Fall
Jaw fracture
Loss of consciousness
Pyrexia
Syncope
Symptomtext
Patient received the vaccine on 05/12/2022 at 5 pm. Felt fine until the following day when she woke up and stood out of bed around 11 am. At that time, patient lost consciousness and fell forward. She hit her face on the ground resulting in a facial fracture. She was taken by ambulance to a hospital where they triaged her. She was told she had a fracture on her upper jaw between front teeth. They could not find a specific reason as to why the she fainted. She also experienced a slight fever, which lasted a few days after the vaccine, as well as, a cough that lingered up to 35 days after the vaccine. Patient still has a lingering cough.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- Patient received an x-ray and bloodwork in the hospital the day after the vaccine. Besides the fracture in the jaw, they could not find any specific results.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 90,0
- Geschlecht
- F
- Eingang
- 23.06.2022
- Impfdatum
- 21.06.2022
- Beginn
- 22.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Acute kidney injury
Acute leukaemia
Asthenia
Blast cells present
Blood creatinine increased
Blood urea increased
Dehydration
Dizziness
Headache
Laboratory test abnormal
Lymphadenopathy
Lymphocyte count
Platelet count decreased
Presyncope
Urinary tract infection
White blood cell count increased
Symptomtext
RIGHT AXILLARY LYMPH NODE SWELLING APPROX SIZE OF GOLF BALL, DIZZINESS, ABNORMAL LABS PT PRESENTED TO ER WITH C/O OF FEELING WEAK AND DIZZY X 1 WK, WORSE TODAY, LEFT SIDED HEADACHE, ADMITTED TO HOSPITAL FOR INPT DUE TO AKI, NEAR SYNCOPE , DEHYDRATION, ACUTE LEUKEMIA, UTI GIVEN FLUIDS AND ANTIBIOTICS STARTED
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- WBC-55, PLATLET- 88, BLAST CELLS 34%- LYMPHOBLASTS, LYMPH-45, BUN- 35, CREAT- 2.49 ON INITIAL ER PRESENTATION 06/22/22 WBC-44.13, PLATLET- 85, BLAST CELLS - NONE, LYMPH- 71, BUN-34, CREAT- 2.36 06/23/22
- Aktuelle Erkrankungen
- UTI, NEAR SYNCOPE
- Vorgeschichte
- CHRONIC KIDNEY DISEASE LONG TERM USE OF ANTICOAGULANTS SPONDYLOSIS WITHOUT MYELOPATHY HYPERLIPIDEMIA DEMENTIA HYPERTENSION GERD
- Andere Medikamente
- AMLODIPINE ELIQUIS ASPIRIN LISINOPRIL MEMANTINE PROTONIX RIVASTIGMINE TARTRATE SIMVASTATIN
- Allergien
- CODEINE, MEPIVCAINE
- Vorherige Impfungen
- -
- Staat
- WY
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 20.06.2022
- Impfdatum
- 02.06.2022
- Beginn
- 02.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood glucose normal
Blood test normal
Computerised tomogram normal
Laboratory test normal
Loss of consciousness
Malaise
Urine analysis normal
Symptomtext
Client states that she "passed out approx 4.5 hours after vaccination" She states that she passed out while taking the trash out and woke up about 1 hour later. Also, states that she has not felt well since. Also states that when she checked her blood sugar after she woke up, it was 97.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- 06/03/2022- Multiple labs done, blood urine and CT scan all returned unremarkable except blood glucose which was slightly elevated.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Diabetes Type 2, Chronic Fatigue syndrome
- Andere Medikamente
- -
- Allergien
- Sulfa antibiotics
- Vorherige Impfungen
- Client states that in 1988 she received a Td and Flu vaccine at the same visit. Sh believes that this combination of vaccines t
- Staat
- MN
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 06.06.2022
- Impfdatum
- 19.05.2022
- Beginn
- 01.06.2022
- Tage bis Beginn
- 13,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anaphylactic reaction
Condition aggravated
Food allergy
Pruritus
Urticaria
Symptomtext
My current peanut allergy got way worse than it initially was. When I walked pass my neighbors who were cooking with peanuts, I only smelled it. And when i got back to my apt I started itching on my back and I got hives on my front chest area. I was only able to calm it down when in my apartment that was bleached and ventilated and that was after 30 minutes. It was way worse than I just ate peanuts and had an antiphallic reaction. Technically this response to breathing in peanuts and not being able to even in a room with the smell of peanuts started at the Moderna Covid 2nd dose. This never happened before- and this is the only adverse reaction I've been having. And I almost died from having COVID in 2020 Nov. I've had the anaphallitic reaction to peanuts since I was three years old (which is very severe to the point that I'm not able to have a allergy test because I could have a anaphallic reaction to the actual test), never had an airborne reaction to peanuts until after Moderna dose 2.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anaphylactic reaction
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- asthma, diabetes
- Andere Medikamente
- VIT D3 2000iu, Intuiniv 4mg, Alamzapine, Topamax 50mg, Colace 100mg, omega 3 - 2mg, zytec 10mg, multivitamin, pepsid,
- Allergien
- peanuts, sulfur, droperadol, lorazapam, perxyotine, methylapentine, rasparadone, lamotrigen, declomethosone, zenlasaxine anaogoues
- Vorherige Impfungen
- 2nd dose moderna vaccine- peanut allergy got worse, first airborne reaction to peanut smell. I couldn't eat anything with it or
- Staat
- TX
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 05.06.2022
- Impfdatum
- 20.05.2022
- Beginn
- 21.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Depressed level of consciousness
Electric shock sensation
Headache
Hypersomnia
Mobility decreased
Pain
Symptomtext
All of my joints, muscles and nerves felt like they were connected to an electric switch in the on position. I had a very severe headache, couldn?t control my hands to hold phone or push buttons to call an ambulance, could not control my legs to get on my feet, could not completely wake up, it was as though I had been drugged an would go back to sleep, was confused when I would wake up because the pains were so severe. When I did wake up after about 24 hrs all of the pains were completely gone as though the electric switch was turned off.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Electric shock sensation
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Diabetics, Chronic kidney disease stage 2,
- Andere Medikamente
- Metoprolol, Olmesartan, Hydrochlorothiazide, Rosuvastatin, Risedronate, Vascepa, Vitamin D3, Aspirin, Victoza
- Allergien
- Yellow dye, metformin, januvia, jardiance
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 03.06.2022
- Impfdatum
- 03.06.2022
- Beginn
- 03.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoaesthesia
Pain in extremity
Syncope
Wrong product administered
Symptomtext
PT GIVEN BOOSTRIX VACCINE DUE TO INCORRECT ENTRY TO PHARMACY SYSTEM. PT CONFIRMED DESIRE TO RECEIVE BOOSTRIX DURING PRE-ADMINISTRATION PERIOD WITH PHARMACIST, BUT REALIZED THIS IS NOT WHAT SHE WANTED AFTER ADMINISTRATION. ROUGHLY 2 HOURS AFTER VACCINATION, PT REPORTED LEFT ARM SHOULDER-TO-WRIST PAIN/FAINT NUMBNESS. PT CALLED HER DOCTOR AND TOOK 2 TYLENOL AS ADVISED BY DOCTOR. VACCINES WERE APPROPRIATELY SPACED IN LEFT ARM DURING ADMINISTRATION BY PHARMACIST.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- Shingrix dose 1, body aches, 50 years old, shot given april 2022
- Staat
- WA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 27.05.2022
- Impfdatum
- 23.05.2022
- Beginn
- 24.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Incoherent
Loss of consciousness
Seizure like phenomena
Symptomtext
Patient states approximately 16 hours post vaccination she experienced dizziness which caused her to pass out. She described herself as incoherent and having seizing like reactions. Patient said that symptoms resolved about an hour after onset. Patient states to not have any reaction to previous doses.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hyperlipidemia
- Andere Medikamente
- Lovastatin 10mg
- Allergien
- No known drug allergies
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 18.08.2023
- Impfdatum
- 23.09.2022
- Beginn
- 17.06.2023
- Tage bis Beginn
- 267,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dyspnoea
Symptomtext
2/7/2021 031L20A 3/7/2021 031M0A 10/27/2021 939905 5/19/2022 038A22A 9/23/2022 AS7163B Moderna BiValent 6/17/2023 - 6/19/2023 (2 days) Presents to the emergency department for shortness of breath dexamethasone and remdesivir.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 04.05.2023
- Impfdatum
- 26.05.2022
- Beginn
- 01.10.2022
- Tage bis Beginn
- 128,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Drainage
Fatigue
Pain
Pharyngeal paraesthesia
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
I tested positive for COVID-19 in October 2022. I had congestion, body aches, fatigue, cough, fever, tingling in my throat and drainage. I contacted my doctor but was not prescribed medications. I did take TYLENOL, and TYLENOL PM. I was sick for about four days after that I still had fatigue, but no other symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pharyngeal paraesthesia
- Hospital-Tage
- -
- Labordaten
- OCT2022 COVID-19 test positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Dorzolamide; timolol; multivitamin; vitamin C; vitamin B12
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 21.04.2023
- Impfdatum
- 01.03.2021
- Beginn
- 01.05.2021
- Tage bis Beginn
- 61,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Cardiac stress test
Catheterisation cardiac
Computerised tomogram thorax
Dyspnoea
Dyspnoea exertional
Echocardiogram
Electrocardiogram
Heart rate increased
Pulmonary function test
Sinus tachycardia
Symptomtext
Inappropriate sinus tachycardia. Heart rate increased withstanding or any activity. Extremely elevated after few minutes of exercise. Shortness of breath with any activity due to elevated heart rate
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Heart cath, ekg, echocardiogram, respiratory function tests, CT scan to check for pulmonary thrombosis, metabolic stress test. All tests feb between June 2021 and November 2021
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Diastolic heart failure Asthma Gerd CVID CKD stage 3
- Andere Medikamente
- Bystolic, Bumex, Aldactone, Potassium, Singulair, Synthroid, Prilosec, Symbicort, Dupixent ,
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 07.03.2023
- Impfdatum
- 03.11.2022
- Beginn
- 05.03.2023
- Tage bis Beginn
- 122,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Dyspnoea
Fatigue
Heart rate increased
Pneumonia
SARS-CoV-2 test positive
Symptomtext
Pt transferred from a local Hospital due to fatigue and increased heart rate and shortness of breath. Pt tested positive for COVID and was found to have pneumonia and was transferred. He has a PMH of CAD s/p multiple cardiovascular stents, CHF, and liver cirrhosis.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 03.01.2023
- Impfdatum
- 20.05.2022
- Beginn
- 15.06.2022
- Tage bis Beginn
- 26,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Electrocardiogram
Palpitations
Symptomtext
About 3 weeks after getting vaccine on 5-20-2022, started having heart palpitations. This was a new condition.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- EKG, Blood work and blood pressure in ER in October 2022; EKG, bloodwork and blood pressure.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Acid Reflux
- Andere Medikamente
- Pantoprazole
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 23.12.2022
- Impfdatum
- 02.06.2022
- Beginn
- 16.06.2022
- Tage bis Beginn
- 14,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Injected limb mobility decreased
Injection site pain
Magnetic resonance imaging
Magnetic resonance imaging head
Magnetic resonance imaging spinal
Scan with contrast
Tremor
X-ray limb
Symptomtext
1. Repeat episodes of extreme pain in upper left arm and left shoulder which lasted for ca. 30 minutes for a period of a week. 2. Tremor in left hand while using a mobile phone for photos. 3. Inability to raise left arm beyond waist level. 4. Multiple Post-event Physical Therapy Sessions
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- MR Brachial Plexus with + without IV Contrast - Left Jul 5, 2022 MR Cervical Spine with + without IV Contrast Jul 5, 2022 XR Shoulder 2-View with Axillary (True AP, Axil) - Left Jun 23, 2022 MRI BRAIN WO CONTRAST June 22, 2022
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hyphosphatemic Osteomalacia
- Andere Medikamente
- Phospha 250, Ramipril, Atorvatatin, Ergocalciferol, Tamsulosin, Calcitriol
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 21.12.2022
- Impfdatum
- 21.06.2022
- Beginn
- 01.10.2022
- Tage bis Beginn
- 102,0
- Dosis
- 4
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Dyspnoea
Fatigue
Headache
SARS-CoV-2 test positive
Symptomtext
Starting 10/01/2022, I developed severe coughing to the point where I was having a hard time catching my breath. I tested myself for COVID at home and it was positive. The coughing was severe that weekend and on monday, 10/03/2022, I had a telehealth visit, where I was prescribed Paxlovid and an inhaler and something for the headaches. I started the Paxlovid the same day and it worked wonders. After 5 days, I felt very close to normal just a little tired. I had just gotten back from a trip at the end of September. (returned 09/21/2022). We stayed for 4 days upon arrival before heading home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- At-home COVID-19 test (10/01/2022): Positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypothyroidism
- Andere Medikamente
- Levothyroxine
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 28.11.2022
- Impfdatum
- 25.05.2022
- Beginn
- 08.11.2022
- Tage bis Beginn
- 167,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Dyspnoea
Exposure to SARS-CoV-2
Fatigue
Feeling abnormal
Insomnia
SARS-CoV-2 test positive
Sneezing
Symptomtext
We were at the store on Nov 8th and I got out there and I kept sneezing which was very odd. Next day I woke up well rested, but I felt like I had a cold just generally miserable that was Nov 9th. This night which was the 9th and 10th I had a horrible tome sleeping which consistence of difficulty's breathing and nonstop coughing. By November 10 friends of ours gave us COVID-19 test and it was positive. That same day I called my doctor and she said because I'm over 65 with asthma she prescribed me PAXLOVID on the 11th. I took the medication as she instructed, and it started working right away. The doctor said it would take five days. The first night I was able to sleep in my bed but the only issue that I am still having fatigue. I thought it was the rebound COVID-19 but its lingering fatigue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Asthma
- Andere Medikamente
- Levothyroxine; pravastatin; losartan; inhaler
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 09.11.2022
- Impfdatum
- 06.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- 5
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anxiety
Arthralgia
Asthenia
Chills
Confusional state
Crying
Diarrhoea
Emotional distress
Fatigue
Fear
Food intolerance
Headache
Hyperacusis
Hyperaesthesia
Lacrimation increased
Nasal congestion
Nausea
Pain
Symptomtext
histamine overload, chills, nausea, vomiting, diarrhea, joint pain - knees, hip, shoulders, elbows, thumbs, pains come and go, parathesia, overall pain, severe pain in right knee - comes and goes, emotional volatility, anxiety, fear, itching, tearing, stuffy nose, reactions to otherwise tolerated foods, headache, weakness, exhaustion , hyper-sensitivity to light, sound, touch, confusion.... mostly pain so bad it makes me cry...... able to do many many things I had before. resting, going on low-histamine diet, drinking extra water, mild moving around, going outside, taking tylenol
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- none ... was in OT but could not continue because of the pain in moving.
- Aktuelle Erkrankungen
- Central nervous injury from withdrawal from Klonopin and Trazodone. Last does of Klonopin was 6/1/2020; last does of trazodone was 12/1/2020. I tapered off these meds that I had taken as prescribed but nevertheless went into tolerance withdrawal
- Vorgeschichte
- heart rhythm
- Andere Medikamente
- eloquis, spironolactone, furosemide, carvidolol, entresto
- Allergien
- advil, lisinopril
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 04.11.2022
- Impfdatum
- 16.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Blood test
Frustration tolerance decreased
Impaired quality of life
Injected limb mobility decreased
Injection site erythema
Injection site swelling
Injection site warmth
Loss of personal independence in daily activities
Neuralgia
Pain in extremity
Symptomtext
Within 24 hours of receiving 2nd Booster of Moderna, the injection site (left arm) swelled up. It was red, hot and swollen for at least 3 weeks. Very slowly, over time, I noticed generalized pain in my left arm and restricted range of motion in my left arm. On Aug 1st, I had a medical physical with my physician and I described my problems with my arm that had appeared since I received my 2nd booster. She said it sounded like my shoulder and prescribed PT. From Aug-Sept 2022, I received 16 sessions of PT and did my required exercises daily. Instead of improving, my ROM and pain increased from Level 1 to Level 4-5. They discharged me due to limits of my PT sessions and they recommended Acupuncture. In Oct, I started Acupuncture to try to improve my condition. It has been slow going and I have increased nerve pain throughout my upper left arm. This impacts on my ability to dress without pain, put on my seatbelt, reach for objects on the side and high up, lift heavy objects, etc.... It is very debilitating, and I'm upset that it impacts on my quality of life. Moreover, I just turned 65 and retired and Medicare doesn't cover Acupuncture so I'm paying for it out of pocket. I don't know if Acupuncture will work or not and if not, what is my next step? Its frustrating because I'm pro Covid vaccination and I had 3 Pfizer shots and no issues at all. I feel that this condition is totally under reported and that is why I'm reporting it myself. I have heard other people have had shoulder issues too since getting the vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- Blood Test on Aug 1 2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hypothyroidism Osteoporosis
- Andere Medikamente
- Levotyhroxine 75mcg; Zyrtec 5mg; Melatonin 5mg; Vitamin D3
- Allergien
- Allergic to Anti Inflammatories (swell up in face/mouth area) - Severe Autoimmune Urticaria
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 04.11.2022
- Impfdatum
- 23.05.2022
- Beginn
- 06.06.2022
- Tage bis Beginn
- 14,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test abnormal
Blood thyroid stimulating hormone
Differential white blood cell count
Dyspnoea
Fatigue
Full blood count
Glycosylated haemoglobin
Human chorionic gonadotropin
Hyperthyroidism
Metabolic function test
Tachycardia
Thyroxine free
Tri-iodothyronine free
Symptomtext
fatigue, shortness of breath; went to doctor; tachycardia (suggest my be due to booster advise no more booster) prescribed 25 mg Atenolol; follow up blood work indicated hyperthyroidism; referred to endocrinologist; prescribed Methimazole 5 mg (two tabs once day; been playing with dosage as per follow up blood work
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 6/30/2022 T4Free, T3Free CBC Differential, Comprehensive Metabolic, TSHThyroid stimulating Hormne; Hemoglobin A1C 07/05/2022 TSH, T4Free, T3Free, Thyrotropin Receptor, 08/15/2022 Thyrotropin Receptor, Comprehensive Metabolic, CBC with Differential, T3FREE, T4FREE, TSH, 10/11/2022 HCG QUANTITIVE PREGNANCY, T3FREE, T4FREE, TSH
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 28.10.2022
- Impfdatum
- 25.05.2022
- Beginn
- 28.05.2022
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Anxiety
Cardiac monitoring abnormal
Chest pain
Head titubation
Musculoskeletal stiffness
Sinus tachycardia
Tremor
Symptomtext
After my 4th vaccine I had noticed my leg would quiver when I was doing physical therapy. I spoke with my neurologist and they stated it may be due to an old injury. I noticed my hand would tremor as well when trying to drink water or coffee, and my neurologist notated that my head was also showing signs of tremors. After dinner in July, my smart watch had alerted me that my heart rate was over 120. I started to then feel a stiff arm and chest pain. I went to the emergency room and they had diagnosed me with a sinus ventral tachycardia. Now I feel fine except the episode has given me anxiety.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Heart monitor for 10 days
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Chronic Back Pain
- Andere Medikamente
- CELEBREX; gabapentin; alfuzosin; multivitamin; REPATHA injections
- Allergien
- Codeine; statins; oxycodone; ibuprofen; diclofenac; doxycycline; propranolol
- Vorherige Impfungen
- 1st: Moderna 2/14/2021; 2nd: Moderna 03/14/2021 Lot: 044A21A; #3: Moderna 10/27/2021 Lot: 939905 I may have had my tremors begin
- Staat
- CA
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 26.08.2022
- Impfdatum
- 25.05.2022
- Beginn
- 27.05.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypertension
Laboratory test
Symptomtext
Continued High Blood pressure. Following first booster my normal 100/70 blood pressure raised to 158/95. It eventually settled to 123/80. Following the second booster it went high again but has remained high. BP checks this week 147/90 and booster was received 3 months ago. Do not know if this will reamain or eventually go back.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- Blood Pressure, Inflammation tests
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Vitamin D, Children Multi Vitamin
- Allergien
- -
- Vorherige Impfungen
- Moderna 9/28/2022
- Staat
- WA
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 25.08.2022
- Impfdatum
- 25.05.2022
- Beginn
- 17.07.2022
- Tage bis Beginn
- 53,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chest X-ray
Cough
Dizziness
Electrocardiogram
Fatigue
Feeling abnormal
Laboratory test
Malaise
Pain
Postural orthostatic tachycardia syndrome
Pyrexia
Symptomtext
Got Covid on July 19; quite sick with cough, fever, aches and pains, severe fatigue. Cough and severe fatigue took quite awhile to resolve. 3 weeks later was very dizzy, light-headed and brain fog. Diagnosed wit POTS (postural orthostatic tachycardia syndrome whic i am still suffering with.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Postural orthostatic tachycardia syndrome
- Hospital-Tage
- -
- Labordaten
- ECG, chest x-ray, stand up from lying down position(similar to tilt table test)
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- calcium, tumeric, B-12, CoQ10, fish oil, magnesium, Cymbalta
- Allergien
- hay fever
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 23.08.2022
- Impfdatum
- 23.05.2022
- Beginn
- 01.06.2022
- Tage bis Beginn
- 9,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthma
Blood iron
Condition aggravated
Cough
Dysphonia
Dyspnoea
Fatigue
Full blood count abnormal
Laboratory test
Night sweats
Symptomtext
Started in June Asthma with shortness of breath with coughing and hoarseness, low blood count with fatigue, also experienced nightly sweats.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- BBC testing for low blood count and also iron test
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Asthma, High Blood pressure
- Andere Medikamente
- Breo Inhaler, Omeprazole, Metoprolol, Hctz, Potassium,
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 19.08.2022
- Impfdatum
- 18.05.2022
- Beginn
- 28.07.2022
- Tage bis Beginn
- 71,0
- Dosis
- 5
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Atrial fibrillation
COVID-19
Condition aggravated
Cough
Fatigue
Myalgia
SARS-CoV-2 test positive
Symptomtext
I had COVID-19 and it started with a cough. My son had it so I tested myself and it was positive. I had mild muscle ache and was tired. No symptoms were severe. My Doctor gave me Paxlovid for 5 days. Two weeks after that my heart went into Affib which didn't suprised me because I have a history of this but it stayed for a while so I went to my Cardiologist who said sometimes ppl with COVID sometimes have gone back into Affib, and it's been a year and a half since I was in Affib.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- COVID-19 at home test in July - positive, and another one the other day and it was negative
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Affib
- Andere Medikamente
- Metformin; Picacin (for heart); Warfarin; Isosorbide; Prozac; Magnesium; Vitamin B
- Allergien
- Sulfur; Amoxicillin; Statins
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 16.08.2022
- Impfdatum
- 27.05.2022
- Beginn
- 30.05.2022
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Contusion
Electrocardiogram normal
Impaired work ability
Mobility decreased
Pain
Pain in extremity
Pyrexia
Symptomtext
She got her vaccine, she had pain, slight fever. She woke up to go to work and she was not able to due to pain in her arms, not able to lift her arm and pain. She continues to have the pain, has been taking Tylenol which helps a little bit, but still not able to work due to the reaction. She went to an UC on 7/5/22 and had an EKG because the pain was in her left arm and she thought that she may have been having a heart attack, they said her EKG was fine. She had a very red bruise on my right arm, and it went away. She was prescribed OTC medication but she did not get it as she did not want to take so much medication when she is already taking prescription medication. She has an APT to see her PCP on 9/21/2022. She believes her reaction is to the shingles shot as she did not hit herself or fall or do anything to her arm, just has the pain and not able to fold sheets or do much of anything.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- EKG and blood work.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- High blood pressure.
- Andere Medikamente
- Fish oil, Centrum multivitamin, Vitamin D, Vitamin C. Atorvastatin, Olanzapine, Amlodipine, Chlorthalidone.
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 20.07.2022
- Impfdatum
- 24.06.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- 7,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Paraesthesia
Pruritus
Symptomtext
Itching that turned to tingling(pins and needles) and now burning in hands
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 11.07.2022
- Impfdatum
- 27.05.2022
- Beginn
- 28.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anticoagulant therapy
Chest pain
Symptomtext
The next day there were sharp pains in my chest area. I felt like a heart attack. The pan lasted about a hour. I took a baby aspirin, Gas-ex and Pepcid. This has happened after every shot of the Moderna vaccine. The pain went away after applying the medications each time .
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypothyroidism
- Andere Medikamente
- Synthroid; Calcium; Vitamin D
- Allergien
- Sulfa drugs; Penicillin
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 01.07.2022
- Impfdatum
- -
- Beginn
- 24.05.2022
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Computerised tomogram abnormal
Computerised tomogram spine
Condition aggravated
Gait inability
Laboratory test
Mobility decreased
Pain
Peripheral swelling
Polymyalgia rheumatica
Scan with contrast abnormal
Ultrasound Doppler normal
Ultrasound scan
Symptomtext
Monday, June 20, 2022, I called my doctor and he prescribed Prednisone. I couldn't get out of bed or even walk, I was in so much pain from the PMR. We had driven, stopping on the way. Coming back I noticed my right leg started swelling. I was worried I was getting a DVT. My daughter said I had to get to the ER. They did tests and it was not a DVT. I was admitted to the hospital on Wednesday morning. I had CT Scan and saw an orthopedic surgeon. The imaging showed a 14 cm place on my leg, the inside, back side. The surgeon did an ultrasound and thought the radiologist could send the fluid off from my leg but he could not. We also had blood samples sent off in case it was a staff infection. Two have come back, negative. We are still waiting on another blood sample to come back. The neurologist said I could take Prednisone and an antibiotic. They started Prednisone yesterday and changed my pain meds. I was having 10/10 pain and now I am a 5/10. They think the flare up was from the Moderna.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- 3,0
- Labordaten
- CT Scan; Ultrasound; CT Scan of neck with contrast; CT Scan of leg with contrast; will have MRI today; blood tests
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Diabetes; Osteoporosis; Osteoarthritis
- Andere Medikamente
- Metformin; Iron
- Allergien
- N/A
- Vorherige Impfungen
- Moderna Doses 1, 2, 3 had chills, vomiting
- Staat
- CA
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 28.06.2022
- Impfdatum
- 11.05.2022
- Beginn
- 18.06.2022
- Tage bis Beginn
- 38,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Cough
Dysgeusia
Dyspnoea exertional
Fatigue
Laboratory test abnormal
Mobility decreased
Pain
Pyrexia
Respiratory tract congestion
Sensitive skin
Wheezing
Symptomtext
Starting 06/18/2022, I had congestion which worsened and then included coughing, wheezing and a fever of 101 for a few days and body aches. I tested positive on 06/18/2022. The body aches were the worst around Tuesday 06/21/2022 to the point where I didn't want to move and my joints hurt a lot as well. My congestion gradually got better up until yesterday. My aches are becoming more infrequent. My fever has resolved. I still have coughing spells and have only needed to use my inhaler 1x or 2x. I have been taking mucinex to help with congestion and staying hydrated. On day 5, I still tested positive. I will go back this coming Tuesday (07/05/2022) and I am still experiencing fatigue, feeling out of breath if I exert myself and coughing spells. I am continuing mucinex to keep the mucous thin so that I don't have trouble breathing. My congestion is not fully resolved but its getting better and the mucinex is helping that. Also, all the food I ate tasted metallic and as of today its better but still present. Also, my face was very sensitive and my normal face wash bothered my skin.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea exertional
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Exercise induced allergies and seasonal allergies
- Vorherige Impfungen
- 2nd Covid Vaccine: I had flu-like symptoms
- Staat
- WY
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 28.06.2022
- Impfdatum
- 01.05.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Mobility decreased
Underdose
Symptomtext
The event was: He got .25 mg for his first dose (5-31-22)instead of the .5mg. Stated he had a strong reaction. "laid up for a few days" Today (6-28-22) he got .5 mg as his true first dose. Called our health Department, they stated his first dose is invalid and we informed him that he would need to come back and get another .5 mg dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 27.06.2022
- Impfdatum
- 25.05.2022
- Beginn
- 28.05.2022
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Paraesthesia
Symptomtext
Sudden onset of paresthesia, knee to foot, bilaterally and no improvement after 4 weeks
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Adverse reaction to Ciprofloxacin (tendon pain)
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 21.06.2022
- Impfdatum
- 15.05.2022
- Beginn
- 16.06.2022
- Tage bis Beginn
- 32,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Disorientation
Dizziness
Dyspnoea
Fatigue
Feeling abnormal
Headache
Oropharyngeal pain
Respiratory tract congestion
SARS-CoV-2 test positive
Sneezing
Symptomtext
I came back from my cruise I had a sore throat, was a little dizzy, had a mild headache, a little tired, sneezing, disoriented, no fever, slight congestion. I thought I had jet lag from my vacation. I took a home COVID 19 test on June 16, 2022 it was very light pink so I thought I got a false positive. I took a second test on the morning of June 17, 2022 and this test came back dark pink and positive very fast. They did prescribe me PAXLOVID but unfortunately I did not receive the call to pick it up it the time frame to take it. I am feelin better, I can breathe better but I do not feel one hundred percent myself yet.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Home COVID 19 test
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- High Blood Pressure
- Andere Medikamente
- Losartan HCTZ; LUNESTA
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 16.06.2022
- Impfdatum
- 28.05.2022
- Beginn
- 07.06.2022
- Tage bis Beginn
- 10,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dyspnoea
Fatigue
Pain in extremity
Symptomtext
She got her vaccine, had an intense arm pain and feeling of fatigue for the first 24 hours, that was getting better gradually and then 48 hours was gone. Then she started feeling more tired than normal and very quickly getting short of breath. She dismissed this at first, but did not feel it was related to the vaccine and it has continued. She told her husband and he is also experiencing the same thing, which he got the vaccine as well on 5/7/22. She has not contacted her doctor for the symptoms as they are mild but are unpleasant. She is a healthcare provider and in pretty good condition. She was going to contact her person in charge of infectious disease where she works.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- Pepcid and Pantoprazole.
- Allergien
- Nitrofurantoin.
- Vorherige Impfungen
- The first vaccine she had throat itchiness which they have been observing but nothing severe other than arm pain.
- Staat
- PA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 14.06.2022
- Impfdatum
- 29.05.2022
- Beginn
- 29.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Chills
Fatigue
Headache
Laboratory test
Migraine
Myalgia
Nausea
Pain
Vitreous floaters
Symptomtext
The day of the vaccination I started getting headaches and body aches. I was very tired and got chills. And it was pretty bad for 48 hrs. Then I started feeling better. Then not the day after but the following Monday I got a really bad migraine headache. The Wednesday following that I got a floater in my left eye. I have muscle aches in my back and I'm nauseous, and I'm still tired. Last Wed I saw the Dr. and she said if the headache doesn't go away as of yesterday I should call her and I did. Now I have a follow up appointment with her next week. I also saw an eye Dr. for the floater in my left eye.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- Eye Dr. did some tests - said it wasn't a retinal test or detachment.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- High blood pressure; high cholesterol; GERD
- Andere Medikamente
- Losartan; simvastatin; omeprazole; fish oil; vitamin D; ibuprofen
- Allergien
- No
- Vorherige Impfungen
- 1st Covid vaccine I had arm pain and was tired. the 2nd Covid vaccine I was sick to my stomach and slept for 14 hrs. and had hea
- Staat
- TX
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 14.06.2022
- Impfdatum
- 31.05.2022
- Beginn
- 01.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Electromyogram
Hypoaesthesia
Paraesthesia
Symptomtext
Patient reported left arm numbness and tingling after one month. EMG ordered, awaiting results;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 07.06.2022
- Impfdatum
- 20.05.2022
- Beginn
- 23.05.2022
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dehydration
Diarrhoea
Dysmenorrhoea
Flatulence
Gastrointestinal pain
Heavy menstrual bleeding
Laboratory test normal
Menstruation irregular
Migraine
Nausea
Symptomtext
Bad gas pains- 1 week Menses arrived 9 days earlier than expected- heavier flow, much more painful After that, 2 days of migraines Followed by perpetual nausea(even with ZOFRAN), diarrhea- unable to remain hydrated Ended up going to the ER to get fluids, more meds
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dehydration
- Hospital-Tage
- -
- Labordaten
- Nothing really came up on the medical tests
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- IBS
- Andere Medikamente
- Prevacid, immodium, zyrtec
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 06.06.2022
- Impfdatum
- 24.05.2022
- Beginn
- 03.06.2022
- Tage bis Beginn
- 10,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Chills
Condition aggravated
Dizziness
Dry skin
Fatigue
Headache
Migraine
Myalgia
Nausea
Pain in extremity
Pruritus
Retching
Skin fissures
Vertigo
Vomiting
Symptomtext
Severe Chills. Arthralgia. Severe muscle aches - all extremities and lumbar and cervical. 6/3 ( about 10days post injection) Awoke with very severe vertigo and dizziness. Severe nausea and vomiting and retching and migraine and chills and severe fatigue.- Lasting 12 hours. Treated with compazine and zofran po and imetrex. Left arm ache for 3 days post injection and couple days with severe fatigue, headaches. Remain intermittent itching of extremities with cracked dry skin hands.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Migraine.
- Vorgeschichte
- DJD. Scoliosis. Spina stenosis multiple levels. LBP with sciatica. Migraine . Osteopenia. Aneurysm heart. Asthma. Cervical and Lumbar pain. Hiatal hernia. Iron def. anemia. IBS. Insomnia. OAB. Reflux esophagitis. Chronic and intermittent acute frontal sinusitis. Vasomotor rhinitis.
- Andere Medikamente
- Cytotec. Omega 3. CoQ10. Senoket S. Halcion. Tylenol. Gaviscon. Tums Magnesium. Vit D . Sumitriptan Flovent. Flonase Estradiol cream. Biofreeze. Voltaren cream.
- Allergien
- Bactrim. ASA. Lisinopril. Inderal. Advair. Diary. Lanolin .
- Vorherige Impfungen
- Pfzer Covid first booster 9/2021 ( 72) Achey muscles, arthragia. fatigue, Headache. Chills
- Staat
- CA
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 03.06.2022
- Impfdatum
- 28.05.2022
- Beginn
- 29.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cardiac flutter
Chills
Dyspnoea
Fatigue
Pyrexia
Symptomtext
Patient said after she got moderna she started experiencing fewer a few hours later and the she had shivers, heart fluttering , tires and shortness of breath.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- VT
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 03.06.2022
- Impfdatum
- 01.06.2022
- Beginn
- 02.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Chills
Decreased appetite
Feeling abnormal
Headache
Insomnia
Mobility decreased
Muscle discomfort
Nausea
Vomiting
Symptomtext
Chills started around 1:30am, very bad headache (I never get headaches), some muscle discomfort, was unable to sleep. The following day, very weak, no appetite, nauseous and did vomit several times. Had to stay in bed pretty much the whole day. Following day -today- feel better but still not 100%- some brain fog.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- elevated cholesterol treated by medication
- Andere Medikamente
- simvastatin, calcium. vitamin d, multi vitamin
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 02.06.2022
- Impfdatum
- 19.05.2022
- Beginn
- 22.05.2022
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injected limb mobility decreased
Pain in extremity
Symptomtext
Patient reported having arm pain and a hard time raising her arm/moving her shoulder about 2-3 days after receiving 2nd Moderna booster. She said she was applying heat and went to her doctor and was prescribed prednisone, but said that it didn't help and she is still having issues weeks after receiving. Advised patient to contact dr again and to apply ice to help with the pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 24.05.2022
- Impfdatum
- 20.05.2022
- Beginn
- 21.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Glomerulonephritis
Haematuria
Hypertension
Protein urine present
Red blood cells urine positive
Urine analysis
Symptomtext
Received immunization at Pharmacy, was treated at the Hospital. Developed Glomerulonephritic, self resolving after 49 hours. Initial gross hematuria and proteinurea.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- 5/21/2022 hypertension 168/95. UA: protein30mg/ml, RBC 2438.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- HTN, Graves Disease, seasonal allergic rhinitis, Polycystic Kidney Disease, renal calculi
- Andere Medikamente
- Synthroid, Losartan , Zyrtec, Allegra, acetaminophen
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 05.06.2023
- Impfdatum
- 04.06.2022
- Beginn
- 10.02.2023
- Tage bis Beginn
- 251,0
- Dosis
- 4
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Fatigue
Glossodynia
Oropharyngeal pain
SARS-CoV-2 test positive
Somnolence
Symptomtext
On 02/10/2023, I had a bit of a soreness at the base of my tongue. I have food allergy reactions, so I thought it was that. The next morning, it was on the other side which was strange. I took an at home COVID-19 test and it was positive. I went to the doctor the next day, they gave me PAXLOVID. Aside from the sore throat, I felt a little tired, but I didn't have any extraordinary cough or anything. I had a bit of a dry cough, but it didn't last. My biggest thing was feeling a little tired. The first day or so of the medication, I just felt like I wanted to sleep. I was still able to work virtually.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 10FEB2023 at home COVID-19 test positive; 11FEB2023 COVID-19 test positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension; Obesity
- Andere Medikamente
- MOVANTIK; esomeprazole; trazadone; aspirin; hydrochlorothiazide; XIIDRA; biotin; calcium; FLINTSTONES vitamins; triamcinolone
- Allergien
- Azithromycin; SKELAXIN; tramadol; citrus
- Vorherige Impfungen
- Third Moderna, vaginal irritation 11/04/2021 age 67
- Staat
- FL
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 27.04.2023
- Impfdatum
- 01.06.2022
- Beginn
- 29.09.2022
- Tage bis Beginn
- 120,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Arthralgia
Arthritis
Carpal tunnel syndrome
Electromyogram abnormal
Hypoaesthesia
Joint swelling
Pain in extremity
Peripheral swelling
Swelling
Swelling face
Symptomtext
Severe arthritic issues developed Sept. 29, 2022 in both hands and wrists, including swelling, numbness, and pain that ibuprofen, ice, heat, and massage could not manage. I had mild arthritis in my fingers prior to that. The same symptoms would stop after 3-4 days, and reappear in another joint...ankle, knee, toes, or jaw. Dr. prescribed Prednisone on Oct. 26, 2022 and sent a referral for an EMG.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- Dec. 5, 2022 - EMG on both wrists for Carpal Tunnel Sydrome as a probably cause of issues. Both wrists were considered Moderate with no need for surgery. Dec. 6, 2022 - Both wrists became inflamed 10 hours after EMG, Dr. administered Cortisone injections in both wrists
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Osteo-penia Calcification in Cervical Spine
- Andere Medikamente
- Levothyroxine 25 mcg
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 06.04.2023
- Impfdatum
- 24.05.2022
- Beginn
- 30.03.2023
- Tage bis Beginn
- 310,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Fatigue
Headache
Nasopharyngitis
Oropharyngeal pain
Pyrexia
SARS-CoV-2 test positive
Sinus congestion
Symptomtext
It felt like the worst cold I ever had. My sinuses were totally congested. I had a sore throat, headache, fever, and a cough. I feel better now but I'm fatigue with a little bit of congestion.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 01APR2023 COVID-19 test positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Diabetes
- Andere Medikamente
- Cabergoline; simvastatin; losartan; JANUMET; aspirin
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 15.01.2023
- Impfdatum
- 27.06.2022
- Beginn
- 21.12.2022
- Tage bis Beginn
- 177,0
- Dosis
- 1
- Route/Site
- JET / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Pain in extremity
SARS-CoV-2 test
Symptomtext
Sore arm and tired for a day
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Covid home test
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Synthroid, losartan, metoprolol, focus select eye
- Allergien
- codeine - itchy
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 29.12.2022
- Impfdatum
- 28.06.2022
- Beginn
- 06.12.2022
- Tage bis Beginn
- 161,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Fatigue
Influenza like illness
Oropharyngeal discomfort
Pain
SARS-CoV-2 test positive
Symptomtext
On 12/6/22 I started feeling like I had a little tickle in my throat. I just felt like I had the flu, fatigue, mild cough, no fever, body aches. I took home COVID-19 test on 12/9/22 that came back positive, I called my doctor. His nurse called me back, we discussed my symptoms, and he advised me to quarantine until I was negative. I am feeling better now as if I had never been sick.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Home COVID-19 test
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Chronic pain
- Andere Medikamente
- Omeprazole; anastrozole; calcium; garlic; vitamin D; vitamin C; vitamin E; alprazolam
- Allergien
- Diphenhydramine
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 28.12.2022
- Impfdatum
- 28.06.2022
- Beginn
- 23.11.2022
- Tage bis Beginn
- 148,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Malaise
Oropharyngeal pain
Pain
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test negative
SARS-CoV-2 test positive
Symptomtext
I started having a sore throat, with a slight fever, achy. I did a home COVID-19 test, the first one was negative the second came back positive. I called my doctor's office, had a telehealth visit, they had me come in for an antigen COVID-19 test that came back positive. I was prescribed PAXLOVID for three days. I felt a little rough for a couple days but day five I was testing negative. I am still experiencing the stuffy of a head in the morning but by afternoon it is gone.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- Home COVID19 test; antigen COVID-19 test
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Rheumatoid Arthritis; High Blood Pressure
- Andere Medikamente
- Amlodipine; aspirin; atorvastatin; BYSTOLIC; CENTRUM SILVER for men 50 plus; vitamin D; folic acid; hydrochlorothiazide; losartan; methotrexate; PAXIL
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 05.12.2022
- Impfdatum
- 03.06.2022
- Beginn
- 22.09.2022
- Tage bis Beginn
- 111,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Bronchospasm
COVID-19
Cough
Dysphonia
Exposure to SARS-CoV-2
Fatigue
Oropharyngeal pain
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Upper-airway cough syndrome
Symptomtext
09/22/2022 Woke up congested, post-natal drip, 99 degree temperature, sore throat, fatigued and hoarse. I took TYLENOL and SUDAFED because I thought it was hay fever. I took a home COVID test before meeting friends, it was negative, but my husbands was positive. I called my doctor and told me to hydrate and take MUCINEX. It took 2 days for my test to showed positive. My symptoms were the same as my husband, he had the same symptoms. I had fever 9/22/22 through 9/26/22. On 9/26/22 my fever was normal and I just had post nasal drip. 10/01/22 I was coughing so bad with broncho spasms. I took over the counter medication for my cough, not sure which one. 10/4/22 I did a tele visit with my physician and he put me on promethazine DM, methyl prednisone pack and saline nasal spray. Retested on 10/03/22 and I was negative. I felt better from 10/10/22 through 10/15/22. On 10/16/22 I began having the respiratory issues. On 10/17/22 with my physician and he put me on a Z PAK. Once I finished the antibiotic, I continued to test negative for COVID. I have pretty much recovered now.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- At home COVID test, both negative and positive.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Multivitamin
- Allergien
- Penicillin; codeine; sulfa; chocolate; coconut; seasonal
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 30.11.2022
- Impfdatum
- 13.05.2022
- Beginn
- 20.10.2022
- Tage bis Beginn
- 160,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Bed sharing
Cough
Headache
Laryngitis
Malaise
Oropharyngeal pain
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
I contracted COVID-19 on 10/20/22 with symptoms of headache, sore throat, laryngitis, fever, cough, and congestion. I was prescribed PAXLOVID on 10/22/22. I was ill for 5 days before my symptoms began to abate. I am still experiencing a lingering cough and sore throat.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- COVID-19 rapid nasal swab was positive 10/22/22.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypertension; Type II Diabetes
- Andere Medikamente
- Vitamin D3; OZEMPIC; JARDIANCE; COZAAR; hydrochlorothiazide; aspirin; LEXAPRO
- Allergien
- KEFLEX
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 21.11.2022
- Impfdatum
- 21.05.2022
- Beginn
- 11.10.2022
- Tage bis Beginn
- 143,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Headache
Malaise
Pain
Pyrexia
SARS-CoV-2 test positive
Sneezing
Upper-airway cough syndrome
Symptomtext
On 10/11/2022 I started feeling COVID-19 symptoms. I developed body aches; headache; nasal drip; sneezing; and 102.0 fever for 2 -3 days. Tested positive on 10/12/2022 and was prescribed a 5 day course of PAXLOVID. I also noticed that once I completed the medication I started getting light headaches.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- PCR test positive for COVID-19
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Osteoporosis
- Andere Medikamente
- Atorvastatin; vitamin C; fish oil
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 21.11.2022
- Impfdatum
- 20.05.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 140,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Pain
Pyrexia
Respiratory tract congestion
Symptomtext
I experienced Covid-19 on October 07, 2022 my symptoms were body aches, fever, cough, congestion. I was prescribed PAXLOVID.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Lisinopril; LIPITOR; aspirin
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 27.10.2022
- Impfdatum
- 03.06.2022
- Beginn
- 25.09.2022
- Tage bis Beginn
- 114,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Bed sharing
Cough
Dry throat
Fatigue
Malaise
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test negative
Symptomtext
I had traveled. I started feeling ill (dry throat, and tired) as I waited for a connecting flight. I took a rapid test when I arrived home, the morning of September 25th, testing positive. I called my health care provider and described my symptoms to a nurse, and received a phone call back about 2 hours from a Doctor. I had a fever of 103.7 by this time and was coughing and congested, and the Doctor prescribed Paxlovid for me. My wife picked up the prescription for me about an hour later, and I started the 5 day regimen of the prescription. After about 2 days, I started feeling much better, while isolating. On the 6th day after starting the prescription, I tested negative using a rapid test. No further symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Only took 2 Rapid tests at home
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High Cholesterol
- Andere Medikamente
- Atorvistatin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 17.10.2022
- Impfdatum
- 21.06.2022
- Beginn
- 19.08.2022
- Tage bis Beginn
- 59,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Chills
Lymphadenopathy
Oropharyngeal pain
Pain
Pyrexia
Quarantine
SARS-CoV-2 test positive
Upper respiratory tract congestion
Symptomtext
On 8/19/2022, I had a fever of 101 and I had a lot of body aches, chills, and a lot of upper respiratory congestion, swollen glands and sore throat. On 8/20/2022, I went to the urgent care, and they did a PCR COVID-19 test and a quick COVID-19 test and the result was negative. The PCR test came back on 8/21/2022 as positive. The doctor told me to quarantine and to take acetaminophen, and prescribed me a cough medicine, BROMPHEN-PSE-DM. My symptoms resolved in about 6 to 7 days and we quarantined for 10 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- 8/20/2022 PCR COVID-19 test positive.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Scoliosis
- Andere Medikamente
- Atorvastatin; HRT; estrogen patches; progesterone pills; fish oils, glucosamine; multivitamin, flaxseed oil, vitamin D3; vitamin C; biotin; L-arginine; vitamin E; selenium; zinc; calcium
- Allergien
- N/A
- Vorherige Impfungen
- Pfizer Dose 1, 2, 3 and the Moderna dose 4- 6 to 8 hours after the COVID-19, I have severe pain at the site of the injection an
- Staat
- CA
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 12.09.2022
- Impfdatum
- 11.06.2022
- Beginn
- 04.09.2022
- Tage bis Beginn
- 85,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chills
Cough
Exposure to SARS-CoV-2
Myalgia
Nasal congestion
Oropharyngeal pain
SARS-CoV-2 test positive
Symptomtext
On 06/11/2022 I had my second booster shot. On 09/04/2022 I started to experience a severe sore throat and nasal congestion. My son had tested COVID-19 positive earlier in the week. I had chills muscle aches and has settled into my chest the following Sunday with a severe cough. I tested COVID-19 positive on 09/07/2022. They did offer medication but I declined due to my blood pressure issues. This is the second time I have had COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- 09/07/2022 I had PCR test which was COVID-19 positive.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Hydrochlorothiazide; Losartan
- Allergien
- Penicillin; Ibuprofen
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 06.09.2022
- Impfdatum
- 14.05.2022
- Beginn
- 15.07.2022
- Tage bis Beginn
- 62,0
- Dosis
- 4
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Chills
Cough
SARS-CoV-2 test positive
Throat irritation
Symptomtext
On 07/15/2022 around 05:30AM in the morning I had a raspy throat. I went to work I thought It was nothing for me. In the evening around 05:00PM I started feeling chills and slight cough. I felt like something was off so I took the COVID-19 test that day and It was positive. I called my doctor and they called in a prescription for me for PAXLOVID I took it for 5 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- COVID-19 home test positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypothyroidism
- Andere Medikamente
- Levothyroxine; omeprazole; fish oil; multivitamins; B12; MOVE FREE ultra; calcium; hair, skin & nails gummy; SINGULAIR inhaler
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 24.08.2022
- Impfdatum
- 23.05.2022
- Beginn
- 08.07.2022
- Tage bis Beginn
- 46,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Decreased appetite
Fatigue
Oropharyngeal pain
Pain
Pyrexia
SARS-CoV-2 test positive
Symptomtext
Covid-19, I tested positive for Covid 19 on July 8, 2022 I experienced a terrible cough, sore throat, fever of 100.0 and body aches, with loss of appetite & fatigue. I was prescribed PAXLOVID and was taking a prescription for the cough.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypothyroidism; High Cholesterol
- Andere Medikamente
- Levothyroxine; liothyronine; CRESTOR
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 23.08.2022
- Impfdatum
- 23.05.2022
- Beginn
- 17.08.2022
- Tage bis Beginn
- 86,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Fatigue
Nasal discomfort
Oropharyngeal pain
Pain
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
The morning before I tested positive for COVID-19. I have a low grade fever, sore throat, burning in nose, terrible congestion, and body aches. I called my doctors office and they prescribed me Paxlovid. I am just now finishing it and I feel a little better. I still have body aches and a little throat issues and fatigue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19-08/17/2022
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypothyroid
- Andere Medikamente
- Multivitamin; Fyavolv
- Allergien
- Seasonal allergies
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 23.08.2022
- Impfdatum
- 17.05.2022
- Beginn
- 11.07.2022
- Tage bis Beginn
- 55,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Headache
Symptomtext
head aches, tiredness
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Penicillin, sulfa drugs, bees, stone fruits
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 87,0
- Geschlecht
- F
- Eingang
- 18.08.2022
- Impfdatum
- 09.08.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood pressure increased
Injection site erythema
Injection site pruritus
Symptomtext
She claims her BP went up to 215, on 8/15/22 and she took it herself on the wrist. On the 8/16 it was 160 and she also got itchiness on the arm and redness where the shot was given. She called me and I told her to take a Benadryl and she should see a doctor. ON 8/16 she told me the itchiness is almost gone that the Benadryl helped her. She told me her BP was always normal.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Leaky Gut
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 18.08.2022
- Impfdatum
- 18.05.2022
- Beginn
- 19.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Eyelid rash
Headache
Pain
Peripheral swelling
Pyrexia
Rash
SARS-CoV-2 test negative
Symptomtext
12 hours after vaccine I got fever, body ache, this time I got swelling in my fingers, feet and hands, for 5 days I have terrible headache and fever, no higher than 101. As the weeks went by, I got rash on my head, forehead and my eyes. I will see the doctor on August 30th, 2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Eyelid rash
- Hospital-Tage
- -
- Labordaten
- N/A, AUG2022 - COVID-19 test negative.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Vitamin D
- Allergien
- N/A
- Vorherige Impfungen
- Flu vaccine, blood clot in my arms, 55 years old. COVID-19 vaccines, 1st dose, 2nd dose, 3 dose, low fever, lasted 24 hours.
- Staat
- MT
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 15.08.2022
- Impfdatum
- 13.05.2022
- Beginn
- 21.07.2022
- Tage bis Beginn
- 69,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood sodium decreased
COVID-19
Feeling abnormal
Oropharyngeal pain
SARS-CoV-2 test positive
Symptomtext
05/13/2022 I had vaccination. On 07/21/2022 I started to experience a sore throat. I have a history of low sodium which I was worried as it can be dangerous. I went to the doctor for my brain fog the blood panel showed my sodium levels were fine. He contributed the brain fog to COVID-19. I was not put on any medication.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- COVID-19
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Lisinopril; amlodipine; simvastatin; baby aspirin; multivitamin; I may not have had the over counter medication with me as I had lost luggage when traveling.
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 15.08.2022
- Impfdatum
- 14.05.2022
- Beginn
- 03.08.2022
- Tage bis Beginn
- 81,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Productive cough
SARS-CoV-2 test positive
Sinus headache
Symptomtext
05/14/2022 I had my second booster. On 08/03/2022 I started experience I was getting a really bad sinus headache. I thought I had a cold. Tested COVID negative that Tuesday night on 08/02/2022. On the morning of 08/03/2022 I tested positive. I was put on 3 pills 2 times a day PAXLOVID. Physically I feel fine but my lung capacity I am still working on and producing phlegm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Sinus headache
- Hospital-Tage
- -
- Labordaten
- COVID-19 positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- COVID-19 1st vaccination
- Staat
- OH
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 08.08.2022
- Impfdatum
- 06.05.2022
- Beginn
- 16.06.2022
- Tage bis Beginn
- 41,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Fatigue
Feeling cold
Oropharyngeal pain
Pain
Rhinorrhoea
SARS-CoV-2 test
Vaccine breakthrough infection
Symptomtext
I experienced a breakthrough case of COVID-19 with runny nose, sore throat, mild cough, chills, body aches and fatigue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 Test
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypertension; Arthritis; Reflux disease
- Andere Medikamente
- Lexapro; Verapamil; Primpro.
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 05.08.2022
- Impfdatum
- 31.05.2022
- Beginn
- 22.07.2022
- Tage bis Beginn
- 52,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Fatigue
Headache
Oropharyngeal pain
Pain
Pyrexia
SARS-CoV-2 test positive
Symptomtext
I tested positive for COVID-19 at home on July 22 I had headache, sore throat, low-grade fever (99.5 was highest reading), body aches, fatigue, and dry cough. My fever and sore throat lasted two days. Dry cough and fatigue lasted about five or six days total.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- I only used at home tests. I tested positive July 22, again on July 31 and August 2.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Zyrtec, Flucatisone, Vitamin D, Vitamin B12, Folic Acid, Fish Oil, CoQ10, Magnesium, Women's Multivitamin, Estroven (over the counter menopause supplement)
- Allergien
- Sulfa drugs
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 01.08.2022
- Impfdatum
- 01.07.2022
- Beginn
- 02.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Fatigue
Induration
Pain
Pruritus
Swelling
Symptomtext
I experienced tremendous pain and swelling and had terrible itching on my arm with redness, hardness of my arm. That was pretty much killed for me on getting any future COVID-19 vaccinations. I was taking antihistamines to help with the itching in my arm. It lasted about a week and the fatigue is still a factor. I did not see a doctor for this.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Celiac Disease; Rosacea; Light Sensitivity to pollutants
- Andere Medikamente
- NYSTATIN; vitamin EMERGEN-C; vitamin B5; omega 3 with fish oil; calcium; vitamin D3
- Allergien
- Gluten; lactose intolerant; night shade plants; corn; AVELOX; cefaloram; doxycycline; KEFLEX; morphine; sulfa; TYLENOL 3; shell fish; hay fever
- Vorherige Impfungen
- Flu headache, nausea, fatigue, Yellow fever nausea, headache Summer of 2009.
- Staat
- NY
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 25.07.2022
- Impfdatum
- 15.10.1942
- Beginn
- 19.07.2022
- Tage bis Beginn
- 29.132,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Nasal congestion
Nasopharyngitis
Pain
Pyrexia
SARS-CoV-2 test positive
Symptomtext
Covid 19 A bad cold- stuffy nose cough fevers body aches
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- Rapid Home Test confirmed covid 19 telehealth meeting with doctor monoclonal antibody infusion
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- heart failure thyroidectomy
- Andere Medikamente
- lipitor carvediliol Entresto synthroid
- Allergien
- penicillin
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 20.07.2022
- Impfdatum
- 24.05.2022
- Beginn
- 24.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Injection site swelling
Symptomtext
The site had localized swelling, about 1cm diameter. No erythema, no edema. The pt denied dyspnea or feelings of throat closing. No stridor, no wheezes. Medical provider evaluated patient, placed an ice pack on the injection site. He evaluated 10 minutes later w/ similar, stabilized results. Discharged pt w/ instructions to take an antihistamine if itchiness or swelling worsens. If dyspnea develops, instructed pt to call 911 or go to the ED immediately.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site swelling
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 18.07.2022
- Impfdatum
- 03.06.2022
- Beginn
- 04.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Headache
Pyrexia
SARS-CoV-2 test negative
Symptomtext
I had a fever that went up to 101.6 and it stayed there from 3pm on Sat for about 36 hours (sun the 5th around 3 or 4pm). I was really out of it. I had chills and a headache. That was pretty much it.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- COVID-19 test - negative at the end of Jun
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Diabetes; Hypertension; Asthma; Sleep apnea; Depression; Anxiety; ADD; Osteoarthritis; Non seasonal allergies; Hypothyroid
- Andere Medikamente
- Adderall; Ibuprofen; Levothyroxine; Actose; Spironolactone; Potassium; Lexapro; Aspirin; Advair; Glimepiride; Zetia; Rosuvastatin; Montelukast; Pantoprazole; Doxepin; Zyrtec; Demister; Centrum Silver Women's; Niacin; Vit B3
- Allergien
- Iodine; IVP contrast; Shellfish; Topical iodine; Dexmethylphenidate; Animal dander; Mold; Dust; Pollen
- Vorherige Impfungen
- I had the same kind of responses to the 2nd dose moderna and my moderna boster
- Staat
- IL
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 12.07.2022
- Impfdatum
- 20.05.2022
- Beginn
- 26.05.2022
- Tage bis Beginn
- 6,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Skin reaction
Symptomtext
un-control Itching those spreads all over the body and when scratched skin tuns read. Took OTC Cetirizine medicine, which provided relief for itching.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Heartburn
- Vorgeschichte
- Post-Polio
- Andere Medikamente
- Tums
- Allergien
- non that i am aware of
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 08.07.2022
- Impfdatum
- 02.06.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- 29,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Cough
Dysphagia
Headache
Lymphadenopathy
Pain
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Throat irritation
Symptomtext
I started to have symptoms on Friday afternoon. My symptoms included body aches, scratchy throat, swollen glands, and a headache. Friday evening, they symptoms continued. I took a home COVID-19 test, and it was negative. I developed a terrible cough. The symptoms continued to get worse. My throat especially. I couldn't swallow. I had terrible congestion a runny nose. I had to continuously blow it and was coughing. On Sunday morning, I took another COVID-19 test and tested positive. That afternoon we went to an immediate care clinic. We were given another COVID-19 test that was positive. The doctor prescribed antivirals. Today, I finished my last dose of Paxlovid and tested negative for COVID-19 yesterday. I've progressively been feeling a little bit better each day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- 07/01/2022 At Home COVID-19 Test - Negative; 07/03/2022 At Home COVID-19 Test - Positive; 07/03/2022 COVID-19 Test at Clinic - Positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Lisinopril/HCTC
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 07.07.2022
- Impfdatum
- 25.05.2022
- Beginn
- 29.06.2022
- Tage bis Beginn
- 35,0
- Dosis
- 4
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Fatigue
Nasopharyngitis
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Sneezing
Symptomtext
6/29/2022 I started feeling like I was getting a cold that night. The next day, I started having a cough, runny nose and sneezing. On 7/1/2022 I was not feeling much better. That night I had a low grade fever. The next morning, I still had a cough and was sneezing, but did not have a fever. I took a home COVID test and it was positive. I went to a doctor associated with my doctor in their clinic. He prescribed Paxlovid at my request. I started taking it on 07/02/2022. The next day I started to feel better. On 7/4/2022 I felt a little tired. The coughing, sneezing and runny nose had gone away. Today, I feel really good. I do not feel tired and have no lingering symptoms. I feel I have recovered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID Home test , positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Zoloft; Omeprazole; Occuvite; Biotin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 06.07.2022
- Impfdatum
- 31.05.2022
- Beginn
- 29.06.2022
- Tage bis Beginn
- 29,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Exposure to SARS-CoV-2
Fatigue
Lower respiratory tract congestion
Malaise
Nasal congestion
Pain
Pyrexia
SARS-CoV-2 test positive
Symptomtext
We had a family gathering. My son-in-law had a business trip out of country and he as well as a majority in my family got COVID-19. There were no flight restrictions anymore. I developed a fever, nasal congestion, chest congestion, tiredness, and body aches. I took an at home COVID-19 test and also went to a clinic and had a rapid and PCR test which were all positive. I did a telehealth visit and was prescribed Paxlovid. I had 2 doses and I could not tolerate it due to hurting my stomach and I felt worse with it. I am still experiencing symptoms except for the fever. I have been advised by my doctor to take Mucinex and Advil.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 test - positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- N/A
- Allergien
- Penicillin; Sulfa
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 05.07.2022
- Impfdatum
- 20.05.2022
- Beginn
- 24.06.2022
- Tage bis Beginn
- 35,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Decreased appetite
Eye irritation
Eye pruritus
Feeling abnormal
Headache
Malaise
Nasopharyngitis
Oropharyngeal pain
Pyrexia
SARS-CoV-2 test positive
Sneezing
Symptomtext
06/24/2022 that afternoon, I had what felt like a bad cold. I had a sore throat, sneezing, coughing, headache, a low grade fever and loss of appetite. I tested for COVID twice on 6/24/2022 and the next day that came back negative. 0n 06/26/2022 I tested positive for COVID. I continued to have the symptoms. I had a telehealth with my doctor on 6/27/2022. I started feeling better around 6/28/2022 or 6/29/2022 and am still having symptoms. I continue to have a cough, feel a little foggy and am having some burning and itching in my eyes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Eye pruritus
- Hospital-Tage
- -
- Labordaten
- COVID tests, 2 negative and 3 positive tests.
- Aktuelle Erkrankungen
- Upper respiratory infection; stomach bug
- Vorgeschichte
- High cholesterol
- Andere Medikamente
- Crestor; low dose aspirin; nebivolol; XANAX; calcium; vitamin D
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 01.07.2022
- Impfdatum
- 19.05.2022
- Beginn
- 26.06.2022
- Tage bis Beginn
- 38,0
- Dosis
- 4
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abnormal behaviour
COVID-19
Diarrhoea
Exposure to SARS-CoV-2
Feeling abnormal
Head discomfort
Headache
SARS-CoV-2 test positive
Thinking abnormal
Symptomtext
4 weeks after receiving my vaccine shot, I was exposed to my son's family who was COVID-19 positive. Four days later I tested positive. I contacted my doctor and was prescribed PAXLOVID. My COVID-19 was a very mild case. I had diarrhea earlier in the week, it lasted about five to six days. It came back a few days later. I had foggy brain, I was not thinking clearly, and I was doing ignorant things. Like placing objects in weird places. It was stupid and not typical of me. It was dementia type behavior. I just could not think clearly it was pressure in my head. This lasted, about a five days. I had headache associated with the fogginess, it went away even before I was tested during the brain fog. I never get headaches, I did not have fever.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- No
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Allergies
- Andere Medikamente
- Rosuvastatin; atenolol; estradiol; vitamins; PROAIR inhaler; zolpidem
- Allergien
- Hydrocodone; tramadol
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 30.06.2022
- Impfdatum
- 16.06.2022
- Beginn
- 16.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Chills
Extra dose administered
Lip swelling
Loss of personal independence in daily activities
Malaise
Monoplegia
Muscular weakness
Musculoskeletal pain
Pain
Pain in extremity
Pyrexia
Quality of life decreased
Symptomtext
I received the Modera half dose. I started feeling sick around 3pm. I had fever, chills, pain so severe n my left arm shooting down to my finger tips. I felt like my left arm was paralyzed just like my right arm in April 2021. I also with this vaccine, my lips swelled for several days. Two to three days after that I now have pain in both arm, from my shoulders across my clavicles to my shoulder blades. I can not sleep from 2am to 6am because of this pain and the only helps me is coffee. I also take OTC Advil the generic form for pain. My doctor put me on Prednisone medication. I am living in pain, in my shoulders since April 06, 2021 and present. The shots have changed my life forever. I just hope they can find an answer for me as what I need to do. I also do not know if this is permanent, my quality of life has changed since receiving the vaccines. I am scared to have permanent damage and this pain does not go away. I can no do my activities as I used to and also have weakness in my arms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- No tests performed
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Haschimoto Disease
- Andere Medikamente
- Synthroid; Vitamin D3
- Allergien
- Penicillin; Ciprofloxacin; Monohydrate-macro tabs
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 29.06.2022
- Impfdatum
- 22.06.2022
- Beginn
- 28.06.2022
- Tage bis Beginn
- 6,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Dysphonia
Exposure to SARS-CoV-2
Oropharyngeal pain
SARS-CoV-2 test positive
Symptomtext
Initially I had a sore throat and raspy voice, the sore throat lasted about a half day and the raspy voice was gone after my second dose of Paxlovid. I was home testing since my husband had tested positive. I took three home COVID-19 test that came back negative even the day before my positive test. I called my doctor on Tuesday June 28, 2022 after my home COVID-19 test came back positive. She prescribed the Paxlovid that I started last night. As of this morning June 28, 2022 I am feeling much better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- Home COVID-19 Test
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Thyroid
- Andere Medikamente
- Vitamin D3, Prozac, Synthroid, Methylphenidate
- Allergien
- No Known Allergies
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 29.06.2022
- Impfdatum
- 24.05.2022
- Beginn
- 28.06.2022
- Tage bis Beginn
- 35,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Oropharyngeal pain
Pain
SARS-CoV-2 test positive
Symptomtext
I had a mild cough that turned more serious yesterday morning. I also have a sore throat and general body ache. I took a COVID-19 rapid antigen test that turned positive. I was prescribed PAXLOVID by my doctor.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- COVID-19 Antigen test- positive.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Major depression; Acid reflux; Herpes; Benign prostatic hyperplasia
- Andere Medikamente
- Simvastatin; fluoxetine; omeprazole; valacyclovir; vitamin D; iron
- Allergien
- Pollen
- Vorherige Impfungen
- 1975 Typhus Vaccine, 22 years old. I got ill afterwards.
- Staat
- GA
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 29.06.2022
- Impfdatum
- 17.05.2022
- Beginn
- 18.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blister
Erythema
Rash
Rash macular
Symptomtext
The day after my 4th dose, I had a rash on my arm, face, legs. My arm was red and I had blotches and a blister on my face. I immediately took BENADRL and within a few days it went away.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Blood clots
- Andere Medikamente
- SYNTHROID; XARELTO; iron; multivitamins
- Allergien
- Seasonal allergies
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 28.06.2022
- Impfdatum
- 23.05.2022
- Beginn
- 07.06.2022
- Tage bis Beginn
- 15,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Skin reaction
Urticaria
Symptomtext
I woke up at like 3 am itchy everywhere I stayed up. I made an appointment with my allergist, and we went through all the stuff I ate and I hadn?t taken any medication that was different. The doctor said I had a delayed skin reaction. The doctor prescribed me Pepcid Zyrtec which helped but it didn?t stop all the reaction all together. I still have hives that pop up randomly. The doctor told me that sometimes it takes a few weeks to clear up completely. I still have some itchiness its just not as bad as it was before.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- no
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 27.06.2022
- Impfdatum
- 16.05.2022
- Beginn
- 24.05.2022
- Tage bis Beginn
- 8,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Feeling abnormal
Malaise
SARS-CoV-2 test positive
Symptomtext
I got the booster on 5/16/22, I started coming down with symptoms the morning of 05/24/22. I did an at home covid test and it was positive. I called my primary care doctor and got a telemedicine visit the next day and was able to talk with the doctor. The doctor prescribed cough syrup and Paxlovid. I took those as prescribed. I'm not sure of the date I called the doctor back, after finishing Paxlovid I started to feel better but then the next week on 06/08/22 I started to feel bad again. I was still coughing and still testing positive for covid. My doctor prescribed Amoxicillin and waited it out. I finally tested negative on 06/13/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Arthritis, overweight
- Andere Medikamente
- Lexapro, Naprosyn
- Allergien
- none
- Vorherige Impfungen
- COVID 2nd dose, flu like symptoms.
- Staat
- OR
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 27.06.2022
- Impfdatum
- 23.06.2022
- Beginn
- 24.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Cough
Dizziness
Fatigue
Nausea
Pain
Peripheral swelling
Pyrexia
Rhinorrhoea
Symptomtext
Swollen arm, chills, fever, nausea, lightheaded, dizziness, aches, coughing, running nose, fatigue
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Zyrtec, vitamins B, D, E, C, Zinc, Calcium, Glucosamine, Cranberry
- Allergien
- Hay fever, shellfish
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 27.06.2022
- Impfdatum
- 13.05.2022
- Beginn
- 18.06.2022
- Tage bis Beginn
- 36,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Disturbance in attention
Dizziness
Fatigue
Headache
SARS-CoV-2 test positive
Symptomtext
When I got back on June 18, 2022 I felt tired. I thought it was just from traveling and getting up extra early to catch our flights. We had the test and I took it and it was positive. then I took another test on the 19th from the Urgent Care and it was positive as well. I felt lightheaded not able to focus and occasionally I would get headaches. The Urgent Care doctor prescribed Paxlovic and I took it as directed. I took the entire 5 day course and I actually tested negative on day 3 but I took the medication until it was all gone.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- COVID Test
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Tadalafil
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 26.06.2022
- Impfdatum
- 15.06.2022
- Beginn
- 18.06.2022
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Chills
Fatigue
Injection site erythema
Injection site pain
Injection site swelling
Lymphadenopathy
Pyrexia
Symptomtext
After my usual reaction to shot (swelling, redness, tenderness at inj site and fatigue, fever,chills) lasing 3 days, I woke up 6/18 with my left axilla filled with large, soft lymph nodes filling the entire axilla. I was worried about plague( there are prairie dogs around communal pond but neither me nor my cats have had direct contact, no nodes on cats) but the nodes filled only left axilla- I had small hard nodes in other places (R axilla and groin due to gardening). NP at Urgent care felt the lymph node enlargement was due to the vax and found no cellulitis at inj site. Since that time I have not had fever, or other such nodes appear- the nodes have diminished over time(not reddened ever) and are pretty much resolved today
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None except exam
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- osteoporosis, osteoarthritis
- Andere Medikamente
- Areds 2, Restasis, Retaine, Ca++ and vit D3 supplements, Omega 3, Vit B12
- Allergien
- gluten and yeast sensitive
- Vorherige Impfungen
- earlier moderna shots gave brain fog, fatigue, fever chills tinnitus, headache with redness swelling and tenderness at inj site
- Staat
- WA
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 24.06.2022
- Impfdatum
- 02.06.2022
- Beginn
- 03.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chills
Pruritus
Pyrexia
SARS-CoV-2 test negative
Urticaria
Symptomtext
Severe fever, chills, 3 days straight-right foot big toe and second started itching with hives. Started 4 days ago.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Covid test negative.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 11,0
- Geschlecht
- F
- Eingang
- 22.06.2022
- Impfdatum
- 08.06.2022
- Beginn
- 08.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Fatigue
Hypersomnia
Product administered to patient of inappropriate age
Pyrexia
Wrong product administered
Symptomtext
Patient was given a 0.25mL booster of Moderna instead of the age appropriate booster for Pfizer 5-11 year-old vaccine. We did not have any Pfizer in stock, and mother was insistent on the patient getting the vaccine that day. She did not have a reaction immediately after receiving the vaccine. For the next two days mother reported that she was very tired and slept for almost 2 days, was dizzy, and slightly feverish. Since then she has not reported any side-effects and seems to be doing fine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 21.06.2022
- Impfdatum
- 21.05.2022
- Beginn
- 01.05.2022
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood chloride decreased
Blood electrolytes decreased
Blood potassium decreased
Blood sodium decreased
Erythema
Laboratory test
Limb mass
Magnetic resonance imaging
Pain in extremity
Peripheral swelling
Scan with contrast
Symptomtext
Routine lab work on June 9, 2022, showed that my electrolytes were low: sodium, potassium, and chloride. Needed to take potassium chloride er 10 meq for 7 days. I will have another blood test on June 22, 2022, to recheck my values. I also noticed while taking off my sock on my left leg that I felt a lump on my lower leg. I am usure of the exact date that I felt the lump. I thought I must have just bumped my leg. However, the lump became painful, red, and swollen. Then my left lower leg became shiny, swollen, and red thus making me concerned enough to see an orthopedist on June 8, 2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- I had an MRI with and without contrast on my left lower tib/fib on June 16, 2022. Will repeat blood test on June 22, 2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Vertigo Balance Issues
- Andere Medikamente
- Clonazepam Zyrtec Vitamin D Calcium
- Allergien
- KNA
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 21.06.2022
- Impfdatum
- 18.05.2022
- Beginn
- 18.06.2022
- Tage bis Beginn
- 31,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Injection site pain
Lymphadenopathy
Pain in extremity
Pyrexia
SARS-CoV-2 test positive
Symptomtext
I felt feverish the next day but only slightly and not for more than an hour or two. I had worse pain around the injection site and hand sore and swollen lymph nodes under my arm on the right side for a few days afterward. Tested Positive for COVID-19 on 6/18/2022 I attended a Conference the previous week, I'm pretty sure I got it there.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- Two positive tests one 6/18 another 6/21
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Pantoprazole
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 21.06.2022
- Impfdatum
- 17.05.2022
- Beginn
- 11.06.2022
- Tage bis Beginn
- 25,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Fatigue
SARS-CoV-2 test positive
Somnolence
Symptomtext
I went camping with some friends on Thursday 06/09/22. I didn't feel or notice any symptoms until Saturday, 06/11/2022 in the evening around 6pm. I needed a nap which is unusual for me. I went in to take a nap, but ended up sleeping all night. I drove home the next day and was extremely fatigued. I almost fell asleep 3 times while driving. I thought it was just allergies so I took a ZYRTEC. When I returned home I tested myself for Covid and was positive. I called the on call doctor and was prescribed PAXLOVID that same day. My symptoms began to improve by the following Tuesday. I am still experiencing fatigue but it is much better than before.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- At home Covid test- 06/12/2022-positive.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Diabetes; Non alcoholic fatty liver disease.
- Andere Medikamente
- Metformin; ZYRTEC; fenofibrate; RYBELSUS.
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 15.06.2022
- Impfdatum
- 17.05.2022
- Beginn
- 09.06.2022
- Tage bis Beginn
- 23,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Fatigue
Feeling abnormal
Nausea
Pruritus
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
On Tuesday June 7, 2022, I felt very tired , run down and nauseous, the next day I had a runny nose, chest congestion, I also had very itchy skin. I took a home COVID 19 test it came back negative. On June 9th I woke up feeling even worse, I went to Urgent Care to have PCR COVID 19 test that came back positive. I was prescribed medication for my itchy skin, Hydroxyzine HCL. I am still tired but I am starting to feel better, I have that post cold tired feeling.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Home COVID 19 Test PCR COVID 19 Test
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Vitamin D3, Ofphena, Xyygal
- Allergien
- Sulfa, Cipro, Malaron,
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 15.06.2022
- Impfdatum
- 27.05.2022
- Beginn
- 01.06.2022
- Tage bis Beginn
- 5,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 15.06.2022
- Impfdatum
- 10.05.2022
- Beginn
- 12.06.2022
- Tage bis Beginn
- 33,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Fatigue
Nasal congestion
Oropharyngeal pain
Pyrexia
SARS-CoV-2 test positive
Symptomtext
On Sunday I started having a stuffy nose, sore throat, and a cough so I took a COVID-19 test the next day which came back positive. I called the afterhours clinic connected to my Doctors office and they gave me Paxlovid for treatment. Since then I have had a slight fever and am very fatigued. I am still having these symptoms and have not recovered yet.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 Home Test
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Blood Pressure
- Andere Medikamente
- Lisinopril, Amlodipine, Sertraline, Gabapentin, Zyrtec, Multivitamin, Calcium, Turmeric, Vitamin D
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 13.06.2022
- Impfdatum
- 20.05.2022
- Beginn
- 21.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pain in extremity
Peripheral swelling
Pyrexia
Symptomtext
My arm became sore and swollen that evening after the vaccine and I ran a very high fever.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- One month before vaccination, from 4/19/2022 through 04/22/2022 I had a virus of some kind. I had bad cramps and diarrhea.
- Vorgeschichte
- Asthma, Eczema
- Andere Medikamente
- Combivent, Breo Ellipta, Singular, Rosuvastatin, Zoloft
- Allergien
- Whey milk, Antihistimines, Drixoral, Navcon A Eye drops
- Vorherige Impfungen
- I ran a fever when I got my Shingles vaccine last fall.
- Staat
- PA
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 13.06.2022
- Impfdatum
- 28.05.2022
- Beginn
- 06.06.2022
- Tage bis Beginn
- 9,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Pyrexia
SARS-CoV-2 test positive
Symptomtext
On June 4, 2022 I had cough and slightly elevated temperature, I took a home test and it was negative. On 06/05/2022 my symptoms got worse and I had an appointment to be at on 06/06/2022 so I tested and it was immediately positive. I contacted my doctor on 06/06/2022 and received a prescription for Paxlovid from her. I have now finished my medication and having no muscle aches or fever still having a little bit of cough. I did test this morning and it was a faint positive line.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- Home COVID-19 Test 06/06/2022 Positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Crestor
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 12.06.2022
- Impfdatum
- 10.06.2022
- Beginn
- 11.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Dizziness
Fatigue
Headache
Hypoaesthesia
Myalgia
Neuralgia
Oedema peripheral
Peripheral swelling
Pyrexia
Swelling
Tinnitus
Symptomtext
Extreme muscle and nerve pain, fever of 102 degrees, dizziness, fatigue, headache, tinnitus, swelling and numbness of hands, arm and armpit pain, swelling of arm and armpit area spreading to the ribs and hand.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Hypothyroidism Arthritis
- Andere Medikamente
- Lunesta 2 mg Synthroid .75
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 12.06.2022
- Impfdatum
- 10.06.2022
- Beginn
- 10.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Myalgia
Sleep disorder
Symptomtext
general fatigue and diffuse muscle aching that interfered with sleep. All resolved by 10/12/2022 at 7 AM
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- hypertension, diabetes, diffuse heart disease, gout, bronchiectasis (mild)
- Andere Medikamente
- Lipitor, Losartan, amlodipine, metoprolol, febuxostat, metformin, magnesium supplement, fish oil caps
- Allergien
- shellfish
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 11.06.2022
- Impfdatum
- 20.05.2022
- Beginn
- 04.06.2022
- Tage bis Beginn
- 15,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Chest X-ray normal
Fibrin D dimer normal
Pleurisy
Pleuritic pain
SARS-CoV-2 antibody test negative
SARS-CoV-2 test negative
White blood cell count increased
Symptomtext
Patient developed pleuritic left sided chest pain worse with laying back and better with leaning forward. Patient diagnosed with pleurisy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pleuritic pain
- Hospital-Tage
- -
- Labordaten
- CXR normal 6-4-22, WBC 12,000 6-4-22, DDimer normal 6-4-22, daily COVID antigen negative 6-4-22 to 6-9-22. SARS CoV2 IgM Spike antibody negative 6-9-22, SARS CoV 2 IgG nucleocapsid negative 6-9-22
- Aktuelle Erkrankungen
- TIAs for 1 month prior
- Vorgeschichte
- History of breast cancer, patent foramen ovale, migraine, TIA, postural orthostatic tachycardia, hyperlipidemia
- Andere Medikamente
- Aspirin 81 mg 1, magnesium 400 mg, crestor 20 mg, Repatha 140 mg, Ubrevely 100 mg as needed, Excedrin as needed.
- Allergien
- Penicillin, sulfa, codeine, ferrlecit
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 11.06.2022
- Impfdatum
- 08.06.2022
- Beginn
- 09.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypersensitivity
Injection site pain
Injection site pruritus
Injection site swelling
Injection site warmth
Symptomtext
Patient had received first vaccine of Moderna. She reports itchiness on injection site, warm/hot to touch, soreness, and very swollen. She had seen another pharmacist at another pharmacy and they had told her that it looked like an allergic reaction. Patient cannot take tylenol or ibuprofen. She had placed an ice pack on injected arm. Swelling has gone down a little, patient still reports itchiness and warmth on injection site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- no (per patient)
- Vorgeschichte
- grand mal seizures
- Andere Medikamente
- gabapentin, ambien, seroquel, fioricet, soma, metoprolol
- Allergien
- codeine (itch), something for migraines but patient could not remember name of medication (was given long time ago)
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 11.06.2022
- Impfdatum
- 07.06.2022
- Beginn
- 08.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 7+
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Fatigue
Joint swelling
Lip pruritus
Lip swelling
Peripheral swelling
Productive cough
Respiratory tract congestion
Skin fissures
Swelling
Swelling face
Urticaria
Symptomtext
Night of vaccine, some aching of joints and fatigue. Next day, hives and swelling on back of neck and all over head, throughout next day after shot and that evening itchy swelling lips. Took Benadryl and itchiness calmed down Next day forehead, lips, itching and swelling of hands and wrists, took more Benadryl Next Day still having swelling of wrists and cracking of skin on wrists Congestion and phelgm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- No test yet
- Aktuelle Erkrankungen
- Seasonal Allergies
- Vorgeschichte
- Pop up hives
- Andere Medikamente
- Alegra Zyrtec Flonaise
- Allergien
- Walnuts, hazelnuts
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 08.06.2022
- Impfdatum
- 31.05.2022
- Beginn
- 31.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Blood glucose normal
Decreased appetite
Dizziness
Feeling abnormal
Pain in extremity
Symptomtext
When she got her vaccine, she felt fine that day. About 8:00 PM her arm started hurting so she iced it down twice. Then about 10:00 PM she started feeling dizzy, weak slightly but not too bad. She sat down and decided to relax. She got back up in about 15 minutes trying to get her phone charger, and if she had not had the AC she would have passed out. Her blood sugar was fine, was not hungry and tried to figure out why she was feeling bad. She called her sister and told she got her booster. She woke up the next morning and read her side effects and realized that this is what was happening, and had not had one with any other vaccine. This effect then passed and she is doing fine now.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- Vitamin D3 1000 IU daily, 81 mg aspirin.
- Allergien
- Sulfa.
- Vorherige Impfungen
- Flu shot was sick for a week many years ago (10 years ago). Now gets them without any difficulties.
- Staat
- FL
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 06.06.2022
- Impfdatum
- 20.05.2022
- Beginn
- 30.05.2022
- Tage bis Beginn
- 10,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Fatigue
Headache
Nasal congestion
Oropharyngeal pain
SARS-CoV-2 test positive
Symptomtext
I received my Covid vaccine on 05/20/2022. On the afternoon of 05/30/2022 I started feeling sore throat nasal congestion, fatigue, and mild headache. I then took an home Covid test and was diagnosed for Covid on 06/01/2022. I then reached out to my doctor and was prescribed PAXLOVID. I took the PAXLOVID for 5 days and the symptoms went down. I retested 06/06/2022 and was negative. I had then accumulated sides effects from the medication PAXLOVID.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Covid testing
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Skeletal muscular injuries
- Andere Medikamente
- Zyrtec; calcium supplement
- Allergien
- Codeine
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 06.06.2022
- Impfdatum
- 20.05.2022
- Beginn
- 21.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Erythema
Pruritus
Symptomtext
Large red circle over 2 inches and itching. Redness was approximately 4 inch in diameter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Allergies/seasonal
- Andere Medikamente
- Claritin Serevent Advair Singulair Vit. A/D/multi/D Omega 3 Probiotic
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 06.06.2022
- Impfdatum
- 31.05.2022
- Beginn
- 01.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Aphonia
Feeling cold
Headache
Laryngitis
Pain
Pain in extremity
Secretion discharge
Symptomtext
On 5/31, I just had pain in my arm. On Wednesday, I was still experiencing arm pain but also was having some body aches. My temperature was 99. something but I was feeling cold, so I stayed home to rest under a blanket all day. Thursday, I was having a headache and body aches, but nothing too severe. On Saturday morning 06/04, I started to experiencing laryngitis and began to lose my voice. I spoke with a friend who also has experienced this after a vaccine, so I wasn't too concerned until I noticed some mucus build up. So I intended to see a doctor on 06/05, but I woke up that morning on 06/05 and my symptoms had begun to improve and this morning on 06/06 the mucus had broken up so I decided to not go to see a doctor.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- High blood pressure (controlled)
- Andere Medikamente
- HCTZ 10mg, Lisinopril 20mg, Metoprolol Time released 50mg, Vitamin D, Nexium, Ambien as needed
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 03.06.2022
- Impfdatum
- 16.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Atrial fibrillation
Body temperature increased
Cardiac monitoring abnormal
Fatigue
Headache
Ventricular extrasystoles
Symptomtext
Day after: ached in every joint, bad headache, fatigued, temperature of about 100. Two days after: fatigued and bad headache. Then, Just after midnight on the 3rd day I went into atrial fibrillation (I have a Kardia Mobil unit that can detect heart arrhythmias). I had two more readings of afib over the next hour or so and then fell asleep reading. When I awoke a couple of hrs. later had a "normal" reading but, after falling back asleep, I awoke about 9 am and had a reading of "normal sinus rhythm with premature ventricular contractions (pvc)". I have been having either pvc's or "sinus rhythm with supraventricular ectopy" readings on and off daily ever since (two and a half weeks). I contacted my cardiologist and he said continue on the same medications as see what happens. I have an appointment on June 14 to discuss this. Could it be related to this second booster?
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- I have been on medications since December of 2017, flecainide (heart rythmn), metoprolol (heart rate) and eliquis (blood thinner) for the treatment of paroxysmal atrial fibrillation (which had generally worked well until after this second booster).
- Andere Medikamente
- famotidine, metoprolol, flecainide, eliquis, glucosimine/msm, magnesium.
- Allergien
- -
- Vorherige Impfungen
- Just felt a achy and headachy after second original shots.
- Staat
- IL
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 03.06.2022
- Impfdatum
- 31.05.2022
- Beginn
- 01.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Decreased appetite
Dizziness
Fatigue
Feeling cold
Headache
Hyperhidrosis
Nasopharyngitis
Pyrexia
Rhinorrhoea
Symptomtext
06/01/2022 In the early afternoon started to feel feverish, dizzy, and very fatigued. I did not have any other symptoms other than sweating and freezing of and on. At night I had no appetite and slept for a while and was still extremely cold after falling asleep. 06/02/2022 Additionally my nose started running, I developed a terrible cough, low grade fever that is still continuing, and overall fatigue. 06/03/2022 met with my doctor today and was given prescription for PAXLOVID. The cough and cold like symptoms gone away however my headache is still present.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Wellbutrin 150mg
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 02.06.2022
- Impfdatum
- 23.04.2022
- Beginn
- 23.05.2022
- Tage bis Beginn
- 30,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Diarrhoea
Fatigue
Nasal congestion
Nasopharyngitis
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
I received my vaccine on 04/23/2022. On 05/23/2022 I started having runny, stuffed nose, fatigue, diarrhea and I felt as if I had a cold. On 05/25/2022 I was tested positive for Covid. Spoke to doc and had a telehealth on 05/26/2022. I was prescribed Paxlovid. After taking the Paxlovid the symptoms went away.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Ulcerative colitis; hyperthyroid
- Andere Medikamente
- Mesalamine; levothyroxine; atorvastatin; fluticasone; cyanocobalamin; fish oil; calcium citrate; magnesium zinc; Osteo Bi-Flex; Preservision; aspirin
- Allergien
- Demerol; tetracycline; azolidine; seldane
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 01.06.2022
- Impfdatum
- 26.05.2022
- Beginn
- 27.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Fatigue
Immunisation reaction
Myalgia
Nasal congestion
Oropharyngeal pain
Pain
Pyrexia
SARS-CoV-2 test negative
Throat irritation
Symptomtext
Potential COVID breakthrough. I had the vaccine on May 26th at 5PM and then went home. Felt fine that day. Also had the Hep B same time. Woke up in the morning with muscle soreness, tired and achy. I ran a couple of errands with my brother and came home. Later that day/Saturday I got a potential exposure notification from the previous week. I rode the commuter bus and only came in contact with 3 people from my office that day. Must have been someone on the commuter bus. Called the nurse on 5/29 for advice. Both of my at home COVID Tests were negative. Nurse stated my symptoms were probably not COVID but instead just reactions to both vaccines. Fevers and chills and nasal congestion continues as well as tickle in the back of my throat. I had a very sore throat for the first 36 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Two nasal swab at home COVID tests
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Non-allergic rhinitis
- Andere Medikamente
- Ipratropium Bromide; Azelastine HCL; Budesonide inhalation suspension; NETI bottle; vitamin; fiber supplement daily; green tea; turmeric
- Allergien
- Doxycycline
- Vorherige Impfungen
- 4th dose of Anthrax vaccine - 1999, swelling, tingling
- Staat
- WI
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 01.06.2022
- Impfdatum
- 27.05.2022
- Beginn
- 28.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Injection site erythema
Injection site pain
Injection site swelling
Injection site warmth
Symptomtext
She reported having a red blotch about 2.5 inches in diameter on her arm below injection site. It was tender, swollen and warm to the touch. It only lasted a bout two days
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 30.05.2022
- Impfdatum
- 26.05.2022
- Beginn
- 27.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site rash
Pruritus
Symptomtext
pt had a skin rash around injection site. patient used oral benadryl and benadryl skin cream to decrease itching
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 28.05.2022
- Impfdatum
- 28.04.2022
- Beginn
- 27.05.2022
- Tage bis Beginn
- 29,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Diarrhoea
Fatigue
Symptomtext
Severe all over pain in joints and muscles. Severe diarrhea. Overall tiredness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Migraine, hashimotos disease, high cholesterol
- Andere Medikamente
- Lipitor, synthroid, zegerid, nadolol
- Allergien
- Penicillin
- Vorherige Impfungen
- J&J 4/12/21 fever headache light sensitivity, Moderna 11/16/21 fever headache malaise
- Staat
- FL
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 26.05.2022
- Impfdatum
- 23.05.2022
- Beginn
- 23.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Injection site pain
Injection site rash
Injection site swelling
Injection site warmth
Pruritus
Rash erythematous
Vaccination site reaction
Symptomtext
The second dose caused headache, low grade fever, chills began 8 hours after vaccination and lasted 12 hours; took Tylenol and side effect dissipated The fourth dose 5/23/22 caused soreness and minor swelling at injection site began 8 hours later; swelling continued to enlarge over the course of the next day (5/24/22); swelling on 5/25/22 became the size of a large egg, became itchy, red and sore and rash appeared (flat, red dots) at injection site confined in a circular pattern the size of a small round teacup; 5/26/22 the site is warm to the touch, decreased in swelling slightly, reddened and rash remains. Cortisone cream applied to the injection site once with no relief
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Sneezing, Itchy eyes related to pollen x 1 week one month prior to vaccination
- Vorgeschichte
- Bladder spasms Depression Anxiety
- Andere Medikamente
- Vitamin D 10,000 mg qd Trazadone 150 mg QHS Xanax PRN
- Allergien
- Penicillin Macrobid Sulfa
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 25.05.2022
- Impfdatum
- 19.05.2022
- Beginn
- 19.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Rash
Symptomtext
moderna 2nd booster from a store caused rashes in arm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Breast Cancer, Hep B
- Andere Medikamente
- Medications: Medication Sig ? ALAWAY 0.025 % (0.035 %) ophthalmic solution ? amLODIPine (NORVASC) 2.5 MG tablet Take 2.5 mg by mouth daily. ? calcium carbonate (CALCIUM CARBONATE) 300 mg (750 mg) Chew Take 1 tablet by mouth 2 (two) times
- Allergien
- Allergies: Latex
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- -
- Geschlecht
- F
- Eingang
- 24.05.2022
- Impfdatum
- 19.05.2022
- Beginn
- 20.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Nausea
Symptomtext
dizziness; Nauseous; This spontaneous case was reported by a patient and describes the occurrence of DIZZINESS (dizziness) and NAUSEA (Nauseous) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038A22A) for COVID-19 vaccination. Previously administered products included for Product used for unknown indication: Pfizer (1st dose), Pfizer (1st booster) and Pfizer (2nd dose). Past adverse reactions to the above products included No adverse event with Pfizer, Pfizer and Pfizer. On 19-May-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 20-May-2022, the patient experienced DIZZINESS (dizziness) and NAUSEA (Nauseous). At the time of the report, DIZZINESS (dizziness) and NAUSEA (Nauseous) had not resolved. No concomitant medication was reported. The allergies (medications, food and other products) included as unknown. It was unknown that the patient had COVID positive test or diagnosis. Medical History relating to mentioned AE and both Acute and Chronic illnesses at the time of vaccination was unknown. Recent change in status such as improvement or worsening was unknown. Other vaccines given within 1 month prior to Moderna COVID-19 vaccine was unknown. The AE did not cause the patient to seek medical care (office visit, Urgent care, ER, hospitalized). It was unknown the patient experienced a similar event n past. The symptoms was worsened. No treatment medication was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 23.05.2022
- Impfdatum
- 21.05.2022
- Beginn
- 21.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Erythema
Nausea
Symptomtext
chills, naseau,eurythmia
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- itp
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 23.05.2022
- Impfdatum
- 20.05.2022
- Beginn
- 20.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Adverse drug reaction
Injection site hypertrophy
Injection site pain
Injection site reaction
Injection site warmth
Skin hypertrophy
Skin texture abnormal
Symptomtext
Hot to touch, very painful, skin is thickening and feels gelatinous in area of injection. It has been three days since injection but side effect has barely subsided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site hypertrophy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 23.05.2022
- Impfdatum
- 08.05.2022
- Beginn
- 16.05.2022
- Tage bis Beginn
- 8,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Dysphonia
Oropharyngeal pain
Pain
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
On 5/16, I started to get a sore throat. when I woke up on 5/17, I also had fever, achiness, and congestion so I took an at home covid test which was positive. I called my doctor right away and was prescribed antibiotics and a steroid. My symptoms have been getting progressively better. The only symptom I am really still suffering from is the raspy throat.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- 05/17-at home Covid test-positive, 05/20-at home Covid test- positive.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- Oxybutynin, Omeprazole, Vitamin D3, Florastor (probiotic supplement)
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 94,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 19.05.2022
- Beginn
- 19.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Nausea
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- Moderna
- Staat
- SD
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 19.05.2022
- Impfdatum
- 16.05.2022
- Beginn
- 16.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site erythema
Injection site pruritus
Injection site swelling
Symptomtext
Itching, local swelling, and redness around the injection area for 1 day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 19.05.2022
- Impfdatum
- 18.05.2022
- Beginn
- 19.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain
Chills
Diarrhoea
Headache
Pyrexia
Symptomtext
Approximately the next day after my 2nd booster (Dose 4) I experienced the following symptoms: Headache, Diarrhea, Abdominal Pain, Low grade fever and Chills. I am currently taking Tylenol to help ease my symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Asthma; Migraine
- Andere Medikamente
- Topiramate
- Allergien
- Penicillin; codeine; Benadryl; latex; peanuts
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 17.05.2022
- Impfdatum
- 10.05.2022
- Beginn
- 13.05.2022
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Fatigue
Feeling abnormal
Headache
Loss of personal independence in daily activities
Nausea
Oropharyngeal pain
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
05/13/2022 I had nausea, diarrhea, headache and congestion that evening. The next morning, I had a terrible sore throat, coughing like crazy and general fatigue. I could not do much of anything. The nurse practitioner referred me to the state. I received the monoclonal antibody infusion. Since then, I am still lying around feeling bad.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID, positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Dilated cardia myopathy; Asthma; Hypertension; Hypothyroidism; AFIB; Bilateral Achilles tendon ruptures
- Andere Medikamente
- COREG; Spironolactone; SYNTHROID; Lansoprazole; Gabapentin; CRESTOR; Finasteride; ADVAIR; SINGULAIR; Omega 3; Vitamin B12; Vitamin E; METAMUCIL; Naproxen; TIGAN; Estradiol; Extra Strength TYLENOL; ETRESTO; ELIQUIA; Fenofibrate
- Allergien
- LEVAQUIN; Ace inhibitors
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 27.10.2023
- Impfdatum
- 14.06.2022
- Beginn
- 14.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Vaccine adminstered after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 27.10.2023
- Impfdatum
- 27.06.2022
- Beginn
- 27.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Vaccine administered after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 27.10.2023
- Impfdatum
- 22.06.2022
- Beginn
- 22.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Vaccine adminstered after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 27.10.2023
- Impfdatum
- 07.06.2022
- Beginn
- 07.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Poor quality product administered
Product temperature excursion issue
Symptomtext
Vaccine adminstered after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 20.10.2023
- Impfdatum
- 09.05.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Immunisation reaction
Symptomtext
She also had some of these after her previous vaccines; This spontaneous case was reported by a patient and describes the occurrence of IMMUNISATION REACTION (She also had some of these after her previous vaccines) in a 76-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038A22A) for COVID-19 prophylaxis. Previously administered products included for Product used for unknown indication: Pfizer vaccine (Dose 1) on 04-Feb-2021 and Pfizer vaccine (Dose 2) on 25-Feb-2021. Past adverse reactions to the above products included No adverse event with Pfizer vaccine and Pfizer vaccine. On 09-May-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced IMMUNISATION REACTION (She also had some of these after her previous vaccines). At the time of the report, IMMUNISATION REACTION (She also had some of these after her previous vaccines) outcome was unknown. Concomitant medication not reported. The patient had Pfizer booster on 11 Oct 2022. Treatment medication not reported. This case was linked to US-MODERNATX, INC.-MOD-2023-745708.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Immunisation reaction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 07.10.2023
- Impfdatum
- 23.05.2023
- Beginn
- 26.05.2023
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dysphagia
Swollen tongue
Symptomtext
Swollen tongue - difficulty talking and swallowing
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dysphagia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- gluten
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 02.08.2023
- Impfdatum
- 23.05.2022
- Beginn
- 11.09.2022
- Tage bis Beginn
- 111,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Breakthrough COVID-19
SARS-CoV-2 test positive
Symptomtext
Breakthrough case admission after 4 vaccines Moderna 2/5/21 lot# 007M20A; Moderna 3/5/21 lot# 023M20A; Moderna 10/31/21 lot# 939904; MOderna 5/23/22 lot# 038A22A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Breakthrough COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 01.08.2023
- Impfdatum
- 22.05.2022
- Beginn
- 17.03.2023
- Tage bis Beginn
- 299,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Reversible ischaemic neurological deficit
Symptomtext
REVERSIBLE ISCHEMIC NEUROLOGIC DEFICIT SYNDROME
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Reversible ischaemic neurological deficit
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 25.05.2023
- Impfdatum
- 24.05.2022
- Beginn
- 03.01.2023
- Tage bis Beginn
- 224,0
- Dosis
- 4
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Nasopharyngitis
SARS-CoV-2 test positive
Symptomtext
My symptoms were like a very bad cold. The outcome is that symptoms resolved after three or four days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- 03JAN2023 COVID-19 Test-Positive.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Lisinopril
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 12.05.2023
- Impfdatum
- 11.05.2022
- Beginn
- 22.06.2022
- Tage bis Beginn
- 42,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Atrial fibrillation
Cardiac ablation
Symptomtext
Afib flare requiring cardiac ablation after booster covid vax.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Atrial fibrillation
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hypothyroidism, senile osteomalacia, mild intermittent asthma, Pure Hypercholesterolemia, nonrheumatic mitral
- Andere Medikamente
- See attach
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 08.05.2023
- Impfdatum
- 07.05.2022
- Beginn
- 01.12.2022
- Tage bis Beginn
- 208,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Biopsy lymph gland
Invasive ductal breast carcinoma
Lymphadenectomy
Mammogram abnormal
Radiotherapy
Symptomtext
I went in for a routine mammogram where they found something on my right breast. My doctor ordered an MRI of my breast to get a better look at what had been seen on the mammogram. The MRI came back showing DCIF, grade 1 invasive, I had biopsies, my lymph nodes under my right arm have been removed, and two weeks of radiation. At this point in time, I do not need chemotherapy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Biopsy lymph gland
- Hospital-Tage
- -
- Labordaten
- 00DEC2022 Mammogram - positive for unknown on right breast; 00DEC2022 MRI - positive DCIF, grade 1 invasive
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Duloxetine; Levothyroxine; Lipitor; Prinivil; Valacyclovir; Multivitamin
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 19.04.2023
- Impfdatum
- 26.05.2022
- Beginn
- 12.04.2023
- Tage bis Beginn
- 321,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 3 vaccines Moderna 3/31/21 Lot# 010A21A; Moderna 4/30/21 Lot# 043B21A; Moderna 5/26/22 Lot# 038A22A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 06.04.2023
- Impfdatum
- 24.10.2021
- Beginn
- 04.04.2023
- Tage bis Beginn
- 527,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Symptomtext
patient hospitalized
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 27.03.2023
- Impfdatum
- 13.05.2022
- Beginn
- 20.05.2022
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Deafness
Frustration tolerance decreased
Hypoacusis
Symptomtext
Began to have problems with muffled hearing in both ears shortly after receiving this shot (my first booster). Reported it to my primary care doctor in early July 2022 when I saw her for my regular checkup. She prescribed Azelastaine nose spray, which did not help. Have also taken Sudafed with little impact. Finally saw my Ear, Nose and Throat doctor on 2/9/2023. He prescribed steroids, which did not help. Neither doctor has related my hearing problems to the vaccination, but I have since heard other people report that they are experiencing the same hearing problems I am. All say that their problems began after receiving the Moderna booster. So while I have no proof that my hearing problems are related to the vaccine, I want to register this adverse effect as a possibility. My muffled hearing has not responded to any treatment and I am very frustrated. I have tried to look at your adverse effect database to see how many others have reporting hearing loss, but it is very difficult to use.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Deafness
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Synthoid Timolol Dorzolamide
- Allergien
- Levaquin
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 20.03.2023
- Impfdatum
- 15.05.2022
- Beginn
- 05.11.2022
- Tage bis Beginn
- 174,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 4 vaccines Moderna 3/17/21 Lot# 040A21A; Moderna 4/14/21 Lot# 037A21B; Moderna 1/11/22 Lot# 032H21A; Moderna 5/15/22 Lot# 038A22A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 41,0
- Geschlecht
- U
- Eingang
- 28.02.2023
- Impfdatum
- 24.02.2023
- Beginn
- 24.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; 7 doses of Moderna monovalent lot number 038A22A, expiration date 10.30.2022, was administered to patients/Date(s) of administration of vaccine*: 24Feb2023; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (7 doses of Moderna monovalent lot number 038A22A, expiration date 10.30.2022, was administered to patients/Date(s) of administration of vaccine*: 24Feb2023) and NO ADVERSE EVENT (No adverse event) in a 41-year-old patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 038A22A) for COVID-19 prophylaxis. No Medical History information was reported. On 24-Feb-2023, the patient received first dose of mRNA-1273 (Spikevax) (Intramuscular) .5 milliliter. On 24-Feb-2023, the patient experienced EXPIRED PRODUCT ADMINISTERED (7 doses of Moderna monovalent lot number 038A22A, expiration date 10.30.2022, was administered to patients/Date(s) of administration of vaccine*: 24Feb2023). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (7 doses of Moderna monovalent lot number 038A22A, expiration date 10.30.2022, was administered to patients/Date(s) of administration of vaccine*: 24Feb2023) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (7 doses of Moderna monovalent lot number 038A22A, expiration date 10.30.2022, was administered to patients/Date(s) of administration of vaccine*: 24Feb2023). Concomitant medication was not reported. The patient received vaccine at 12:11 PM. Patient received expired Moderna monovalent dose. The vaccine had been frozen with no known temperature excursion before being thawed today for administration. Vial was initially stored in the refrigerator on 24-Feb-2023. Vial did not undergo any temperature excursions. Treatment medication was not reported. This case was linked to US-MODERNATX, INC.-MOD-2023-712705, US-MODERNATX, INC.-MOD-2023-712698 (E2B Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 24-Feb-2023: Live non significant follow up received.; Sender's Comments: US-MODERNATX, INC.-MOD-2023-712705: US-MODERNATX, INC.-MOD-2023-712698:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 43,0
- Geschlecht
- U
- Eingang
- 28.02.2023
- Impfdatum
- 24.02.2023
- Beginn
- 24.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; Dose of Moderna monovalent lot number 038A22A, expiration date 30-Oct-2022 was administered to patient; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Dose of Moderna monovalent lot number 038A22A, expiration date 30-Oct-2022 was administered to patient) and NO ADVERSE EVENT (No adverse event) in a 43-year-old patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 038A22A) for COVID-19 prophylaxis. No Medical History information was reported. On 24-Feb-2023 at 1:07 PM, the patient received first dose of mRNA-1273 (Spikevax) (Intramuscular) .5 milliliter. On 24-Feb-2023, after starting mRNA-1273 (Spikevax), the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose of Moderna monovalent lot number 038A22A, expiration date 30-Oct-2022 was administered to patient). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Dose of Moderna monovalent lot number 038A22A, expiration date 30-Oct-2022 was administered to patient) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Dose of Moderna monovalent lot number 038A22A, expiration date 30-Oct-2022 was administered to patient). It was unknown if patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. No concomitant medications was reported. The vaccine was frozen with no known temperature excursion before being thawed for administration. The vial was initially stored in the refrigerator on 24-Feb-2023. The vial had not undergone any temperature excursions. No treatment medications was reported. This case was linked to US-MODERNATX, INC.-MOD-2023-712705, US-MODERNATX, INC.-MOD-2023-712698 (E2B Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 24-Feb-2023: Follow-up received included no new information.; Sender's Comments: US-MODERNATX, INC.-MOD-2023-712705: US-MODERNATX, INC.-MOD-2023-712698:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 35,0
- Geschlecht
- U
- Eingang
- 28.02.2023
- Impfdatum
- 24.02.2023
- Beginn
- 24.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (7 doses of Moderna monovalent lot number 038A22A, expiration date 10.30.2022, was administered to patients/ Date(s) of administration of vaccine: 24Feb2023) and NO ADVERSE EVENT (No adverse event) in a 35-year-old patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 038A22A) for COVID-19 prophylaxis. No Medical History information was reported. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (7 doses of Moderna monovalent lot number 038A22A, expiration date 10.30.2022, was administered to patients/ Date(s) of administration of vaccine: 24Feb2023). Concomitant medication was not reported. T
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 53,0
- Geschlecht
- U
- Eingang
- 28.02.2023
- Impfdatum
- 24.02.2023
- Beginn
- 24.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; Dose administered after manufacturer date of expiry; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry) and NO ADVERSE EVENT (No adverse event) in a 53-year-old patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 038A22A) for COVID-19 prophylaxis. No Medical History information was reported. On 24-Feb-2023, the patient received first dose of mRNA-1273 (Spikevax) (unknown route) .5 milliliter. On 24-Feb-2023, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry). Concomitant medications were not reported. Patient received the vaccine at 12:28 pm. It was unknown if patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. The vaccine had been frozen with no known temperature excursion before being thawed for administration. Date the vial was initially stored in the refrigerator was 24-Feb-2023. The vial did not undergone any temperature excursions. Treatment information was not reported. This case was linked to US-MODERNATX, INC.-MOD-2023-712705, US-MODERNATX, INC.-MOD-2023-712700 (E2B Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 24-Feb-2023: Live follow up contains the administration time of suspect product.; Sender's Comments: US-MODERNATX, INC.-MOD-2023-712705: US-MODERNATX, INC.-MOD-2023-712698:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 38,0
- Geschlecht
- U
- Eingang
- 28.02.2023
- Impfdatum
- 24.02.2023
- Beginn
- 24.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event; 7 doses of Moderna monovalent lot number 038A22A, expiration date 30-Oct-2022, was administered to patients; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (7 doses of Moderna monovalent lot number 038A22A, expiration date 30-Oct-2022, was administered to patients) and NO ADVERSE EVENT (No adverse event) in a 38-year-old patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 038A22A) for COVID-19 prophylaxis. It was unknown if the patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. On 24-Feb-2023 at 1:02 PM, the patient received first dose of mRNA-1273 (Spikevax) (unknown route) .5 milliliter. On 24-Feb-2023 at 1:02 PM, after starting mRNA-1273 (Spikevax), the patient experienced EXPIRED PRODUCT ADMINISTERED (7 doses of Moderna monovalent lot number 038A22A, expiration date 30-Oct-2022, was administered to patients). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (7 doses of Moderna monovalent lot number 038A22A, expiration date 30-Oct-2022, was administered to patients) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (7 doses of Moderna monovalent lot number 038A22A, expiration date 30-Oct-2022, was administered to patients). Concomitant medication was not provided. It was reported that the vaccine was frozen with no known temperature excursion before being thawed. The vial was initially stored in refrigerator on 24-Feb-2023. The vial did not undergo any temperature excursion. Treatment information was not provided. This case was linked to C-INT-0002940, US-MODERNATX, INC.-MOD-2023-712705, US-MODERNATX, INC.-MOD-2023-712700, US-MODERNATX, INC.-MOD-2023-712708, US-MODERNATX, INC.-MOD-2023-712760, US-MODERNATX, INC.-MOD-2023-712765, US-MODERNATX, INC.-MOD-2023-712766, US-MODERNATX, INC.-MOD-2023-712708 (E2B Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 24-Feb-2023: Non significant live follow up received: Vaccination time added.; Sender's Comments: US-MODERNATX, INC.-MOD-2023-712705: US-MODERNATX, INC.-MOD-2023-712760: US-MODERNATX, INC.-MOD-2023-712765: US-MODERNATX, INC.-MOD-2023-712766:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: It was unknown if the patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 46,0
- Geschlecht
- U
- Eingang
- 28.02.2023
- Impfdatum
- 24.02.2023
- Beginn
- 24.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
Dose administered after manufacturer date of expiry; No adverse event; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry) and NO ADVERSE EVENT (No adverse event) in a 46-year-old patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 038A22A) for COVID-19 prophylaxis. No Medical History information was reported. On 24-Feb-2023, the patient received first dose of mRNA-1273 (Spikevax) (unknown route) .5 milliliter. On 24-Feb-2023, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry). Concomitant product use was not provided by the reporter. Patient received vaccine at 01:04 PM . It has been reported that vaccine had been frozen with no known temperature excursion before being thawed on 24-Feb-2023 for administration. Vial did not go any temperature excursions. Individual vials or unbroken cartons were 4. Vial size was 5. Date the vial was initially stored in the refrigerator was 24-Feb-2023. Treatment information was not provided. This case was linked to US-MODERNATX, INC.-MOD-2023-712705 (E2B Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 24-Feb-2023: Live follow up has been appended.; Sender's Comments: US-MODERNATX, INC.-MOD-2023-712705:Master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 24.02.2023
- Impfdatum
- 24.02.2023
- Beginn
- 24.02.2023
- 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
No adverse event
Symptomtext
PT RECEIVED EXPIRED IMMUNIZATION. PT DENIES ANY SIDE EFFECTS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 24.02.2023
- Impfdatum
- 24.02.2023
- Beginn
- 24.02.2023
- 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
PT RECEIVED EXPIRED MEDICATION- DENIES ANY REACTION
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 24.02.2023
- Impfdatum
- 24.02.2023
- Beginn
- 24.02.2023
- 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
pt received expired immunization. pt declines any negative/ unwanted signs or symptoms
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 24.02.2023
- Impfdatum
- 24.02.2023
- Beginn
- 24.02.2023
- 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
No adverse event
Symptomtext
patient received expired vaccine- no adverse reation
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 24.02.2023
- Impfdatum
- 24.02.2023
- Beginn
- 24.02.2023
- 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
No adverse event
Symptomtext
received expired vaccine- no reaction
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 24.02.2023
- Impfdatum
- 24.02.2023
- Beginn
- 24.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Pt received expired immunization. pt denies complaint.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 24.02.2023
- Impfdatum
- 24.02.2023
- Beginn
- 24.02.2023
- 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
No adverse event
Symptomtext
received expired immunization- no reation- no complaints.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 24.02.2023
- Impfdatum
- 24.02.2023
- Beginn
- 24.02.2023
- 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
7 PATIENTS RECEIVED EXPIRED DOSES BEFORE NURSING REALIZED THE LOT NUMBER WAS EXPIRED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 08.02.2023
- Impfdatum
- 14.11.2022
- Beginn
- 29.12.2022
- Tage bis Beginn
- 45,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Acute kidney injury
COVID-19
Encephalopathy
Hypernatraemia
Influenza
Mental status changes
SARS-CoV-2 test positive
Screaming
Sedation
Somnolence
Symptomtext
"Patient with history of COVID vaccines who admitted to hospital with COVID detected PCR. Provider d/c note: ""78-year-old female with dementia who presents with acute encephalopathy, somnolence. Suspect influenza with over-sedation. Wean down psychotropic medications. Her mental status improved although she did have outbreaks of yelling. Tamiflu x5 days. Hypernatremia and AKI resolved with IV fluids and was stable without IV fluids. Recommend outpatient neuropsych testing and psychiatric consultation. I suspect progression of patient's dementia is causing many of her symptoms. Incidentally tested positive for COVID on day of discharge, was negative on admission. Question if false positive as she had no change in her respiratory status."""
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute kidney injury
- Hospital-Tage
- 5,0
- Labordaten
- Covid PCR dectected on 01/03/2023
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Cardiovascular High blood pressure Hyperlipidemia Bilateral pulmonary embolism (HCC) Hypotension Endocrine Type 2 diabetes mellitus with stable proliferative retinopathy of both eyes, without long-term current use of insulin (HCC) Psychological Late onset Alzheimer's dementia with behavioral disturbance (HCC) Respiratory Influenza A Acute respiratory failure with hypoxia (HCC) Urinary AKI (acute kidney injury) (HCC) Other Retinopathy, hypertensive, right eye Obesity (BMI 30.0-34.9) Benign familial tremor Osteoporosis Weakness Chronic midline low back pain without sciatica Hypernatremia Viral sepsis (HCC) Toxic metabolic encephalopathy
- Andere Medikamente
- acetaminophen (TYLENOL) 500 MG tablet Take 1 tablet by mouth every 4 (four) hours as needed for Pain. aluminum-magnesium hydroxide-simethicone (MAALOX) 200-200-20 mg/5 mL suspension Take 30 mLs by mouth every 4 (four) hours as needed for I
- Allergien
- No Know Allergies
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 87,0
- Geschlecht
- F
- Eingang
- 13.01.2023
- Impfdatum
- 26.10.2022
- Beginn
- 08.01.2023
- Tage bis Beginn
- 74,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Dysarthria
Hemiparesis
Muscular weakness
SARS-CoV-2 test positive
Symptomtext
Hospitalization: 1/8/2023 - 1/10/2023 (2 days) Presentation to the ED: left-sided lower extremity weakness, dysarthria. COVID + date: 1/8/23 Treatment: no indication for therapy. Discharge to: Home. Moderna 031L20A 2/21/2021 Moderna 030A21A 3/15/2021 Moderna 013F21A 11/15/2021 Moderna 038A22A 5/19/2022 Moderna BiValent AS7163B 10/26/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HTN, HLD, GERD, SUBDURAL HEMORRHAGE.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 11.01.2023
- Impfdatum
- 12.07.2022
- Beginn
- 06.12.2022
- Tage bis Beginn
- 147,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Large granular lymphocytosis
White blood cell count decreased
Symptomtext
I had doctors appoint. and had blood work drawn on or around 12/06/2022. My nutrified/ white blood cell count was low. He referred me to a Hematologist, I went around 12/10/2022, and 10 days later I was diagnosed with T-cell Large Grain Leukemic Leukemia.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Large granular lymphocytosis
- Hospital-Tage
- -
- Labordaten
- 12Dec2022 blood work, abnormal low blood cell count
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Blood Pressure
- Andere Medikamente
- Simvastatin; olmesartan; atenolol; hydrochlorothiazide; multivitamin; vitamin C; B12; glucosamine
- Allergien
- Lisinopril
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 22.12.2022
- Impfdatum
- 16.05.2022
- Beginn
- 30.11.2022
- Tage bis Beginn
- 198,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Symptomtext
HOSPITALIZED WITH COVID
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 5,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 15.12.2022
- Impfdatum
- 15.06.2022
- Beginn
- 22.06.2022
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Bursitis
Feeling abnormal
X-ray
Symptomtext
I have Bursitis in upper left arm and it is prolonged. I also felt really bad after the vaccine for about 24 hours and it went away except the Bursitis.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood test
- Hospital-Tage
- -
- Labordaten
- X rays; blood work
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High Cholesterol; Chronic depression
- Andere Medikamente
- ZIPRONE; imipramine; trazodone; LIPITOR; metformin; finasteride; tadalafil
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 23.11.2022
- Impfdatum
- 24.05.2022
- Beginn
- 23.11.2022
- Tage bis Beginn
- 183,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against then tested positive for COVID-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 21.11.2022
- Impfdatum
- 25.05.2022
- Beginn
- 20.11.2022
- Tage bis Beginn
- 179,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against then tested positive for COVID-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 15.11.2022
- Impfdatum
- 11.07.2022
- Beginn
- 06.11.2022
- Tage bis Beginn
- 118,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after four vaccines Moderna 2/24/21 Lot# 010A21A; Moderna 3/24/21 Lot# 017B21A; Moderna 10/27/21 Lot# 041C21A; Moderna 7/11/22 Lot# 038A22A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 04.11.2022
- Impfdatum
- 15.03.2021
- Beginn
- 26.05.2022
- Tage bis Beginn
- 437,0
- Dosis
- 4
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood test abnormal
Carcinoembryonic antigen increased
Colectomy
Colonoscopy abnormal
Computerised tomogram normal
Large intestine polyp
Neoplasm malignant
Scan with contrast normal
Symptomtext
Routine colonoscopy screening on 05/ 26/2022 showed a 18 mm recto-sigmoid polyp invasive carcinoma. Subsequent resection 07/21/2022 partial colectomy showed no evidence of residual cancer
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood test abnormal
- Hospital-Tage
- 5,0
- Labordaten
- ? 06/14 /2022, blood tests showed CEA 3.1( normal range of lab up to 2.5) ? 6//2022 CAT scan with iv and oral contrast with no abnormality shown
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- chronic sinusitis, prediabetes
- Andere Medikamente
- ciclopirox 8% solution to toe nails fluticasone propionate 50 mcg/actuation nasal spray 2 sprays Multivitamin and glucosamine tab1 qd
- Allergien
- sulfamethoxazole-trimethoprim & sulfa drugs , Amoxicillin
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 02.11.2022
- Impfdatum
- 24.05.2022
- Beginn
- 02.06.2022
- Tage bis Beginn
- 9,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Exposure to SARS-CoV-2
SARS-CoV-2 test positive
Symptomtext
I went to a family reunion, the next day a family member called to let everyone know they tested positive for COVID-19. I did not have any symptoms but tested to be on the side of caution, it came back positive. Once I received the positive test result, I went to an urgent care, I was prescribed PAXLOVID and started taking it immediately. My case was mild, I recovered within twenty fours with no rebound.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Home COVID-19 test
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Thyroid Condition
- Andere Medikamente
- Levothyroxine: multivitamin
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 24.10.2022
- Impfdatum
- 17.03.2021
- Beginn
- 01.09.2022
- Tage bis Beginn
- 533,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Cough
SARS-CoV-2 test positive
Symptomtext
09/01/22 presents to EC ED for "cough". PMHx of "multiple sclerosis , COPD and bronchiectasis"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- 09/01/22 SARS-CoV-2 (COVID-19) by NAA detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 12.10.2022
- Impfdatum
- 25.05.2022
- Beginn
- 11.10.2022
- Tage bis Beginn
- 139,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against then tested positive for COVID-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 01.10.2022
- Impfdatum
- 22.09.2022
- Beginn
- 22.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
MODERNA MONVALENT COVID 19 VACCINE GIVEN MISTAKENLY AS 1ST BOOSTER.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE NOTED
- Vorgeschichte
- IN FORMATION NOT AVAILABLE
- Andere Medikamente
- information not available. She does not use our pharmacy.
- Allergien
- NO KNOWN ALLERGIES
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 01.10.2022
- Impfdatum
- 22.09.2022
- Beginn
- 22.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
MODERNA MONOVALENT COVID 19 VACCINE GIVEN MISTAKENLY AS 2ND BOOSTER.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE NOTED
- Vorgeschichte
- INFORMATION NOT AVAILABLE
- Andere Medikamente
- INFORMATION NOT AVAILABLE
- Allergien
- LATEX
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 26.09.2022
- Impfdatum
- 27.05.2022
- Beginn
- 28.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Mass
Symptomtext
Patient develop large round bump next day on shoulder and now has developed an even larger soft mass on the left elbow that is continuing to grow daily. Patient has been monitoring both masses, they are not red or warm to touch per my observation. Patient was instructed by myself to seek medical attention from a dermatologist or primary care physician for possible draining. Patient claims that neither area is painful, solely cumbersome.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mass
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- tizanidine 4 mg
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 16.09.2022
- Impfdatum
- 01.09.2022
- Beginn
- 01.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
Monovalent Booster was given
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 16.09.2022
- Impfdatum
- 01.09.2022
- Beginn
- 01.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
Monovalent Booster was given
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 14.09.2022
- Impfdatum
- 12.06.2022
- Beginn
- 12.08.2022
- Tage bis Beginn
- 61,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Extra dose administered
SARS-CoV-2 test positive
Symptomtext
Came down with Covid two months after receiving 4th moderna dose
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Covid 19 PCR test
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Zoloft, buspar, klonopin, singular, Flonase, multi vitamin
- Allergien
- Shellfish
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 89,0
- Geschlecht
- M
- Eingang
- 14.09.2022
- Impfdatum
- 28.05.2022
- Beginn
- 13.09.2022
- Tage bis Beginn
- 108,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Symptomtext
Fully vaccinated with 2 boosters
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 86,0
- Geschlecht
- M
- Eingang
- 09.09.2022
- Impfdatum
- 08.09.2022
- Beginn
- 08.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
The Monovalent COVID-19 vaccine was inadvertently given to the patient who was scheduled to receive the Bivalent COVID-19 vaccination as per the recent FDA approval of the Bivalent COVID-19 vaccines. The patient was notified of the error on the same day of the incident and written communication is being drafted and sent to all patients reiterating what was discussed over the phone with the patient. Further action is underway with the guidance of the CDC Interim Clinical Considerations for using COVID-19 Vaccines. All patients were instructed to follow up with their primary care physician and were offered the opportunity to receive a booster dosage in line with the recommendations of the FDA.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 96,0
- Geschlecht
- F
- Eingang
- 09.09.2022
- Impfdatum
- 08.09.2022
- Beginn
- 08.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
The Monovalent COVID-19 vaccine was inadvertently given to the patient who was scheduled to receive the Bivalent COVID-19 vaccination as per the recent FDA approval of the Bivalent COVID-19 vaccines. The patient was notified of the error on the same day of the incident and written communication is being drafted and sent to all patients reiterating what was discussed over the phone with the patient. Further action is underway with the guidance of the CDC Interim Clinical Considerations for using COVID-19 Vaccines. All patients were instructed to follow up with their primary care physician and were offered the opportunity to receive a booster dosage in line with the recommendations of the FDA.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 08.09.2022
- Impfdatum
- 07.09.2022
- Beginn
- 07.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
No adverse event
Symptomtext
9/7/2022 Moderna Monovalent was given not Bivalent. We advised patient in 2 months they can return for a Bivalent shot. Patient tolerated well. No Adverse reactions.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 08.09.2022
- Impfdatum
- 07.09.2022
- Beginn
- 07.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
No adverse event
Symptomtext
9/7/2022 Moderna monovalent given not bivalent. We advised patient in 2 months they can return for a bivalent shot. Patient tolerated well. No adverse reaction.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 08.09.2022
- Impfdatum
- 07.09.2022
- Beginn
- 07.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
No adverse event
Symptomtext
9/7/2022 Moderna monovalent given not bivalent. We advised patient in 2 months they can return for a bivalent shot. Patient tolerated well. No adverse reaction.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 08.09.2022
- Impfdatum
- 07.09.2022
- Beginn
- 07.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
No adverse event
Symptomtext
9/7/2022 Moderna monovalent given not bivalent. We advised patient in 2 months they can return for a bivalent shot. Patient tolerated well. No adverse reaction.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 08.09.2022
- Impfdatum
- 07.09.2022
- Beginn
- 07.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
9/7/2022 Moderna monovalent given not bivalent. We advised patient in 2 months they can return for a bivalent shot. Patient tolerated well. No adverse reaction.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 08.09.2022
- Impfdatum
- 08.09.2022
- Beginn
- 08.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
9/7/2022 Moderna Monovalent was given not Bivalent. We advised patient in 2 months they can return for a Bivalent shot. Patient tolerated well. No Adverse reactions
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 31.08.2022
- Impfdatum
- 31.05.2022
- Beginn
- 20.07.2022
- Tage bis Beginn
- 50,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Rhinorrhoea
SARS-CoV-2 test positive
Throat irritation
Symptomtext
I tested positive for COVID-19 and had a scratchy throat, running nose, and cough. I saw a doctor on a cruise and he prescribed me Paxlovid. My symptoms lasted 3 to 4 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID-19- Positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Isothermal fibrillation
- Andere Medikamente
- Fish oil; Niacin; Naproxen; Multivitamin; Metoprolol; Melatonin; Aspirin; Zolpidem
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 31.08.2022
- Impfdatum
- 02.06.2022
- Beginn
- 02.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Bronchitis
Cough
Ear infection
Feeling abnormal
Respiratory tract congestion
Symptomtext
Starting the evening of receiving the vaccine, I was really congested (but I hadn't been outside) so I didn't think it was an allergy issue. I started with a slight cough but over the next few days it got progressively worse. I normally cough from my asthma/allergies but by the 4th day the cough got so bad that I realized something more was going on. About 1 week after receiving the vaccine, I went and saw my doctor, He said I had Bronchitis and prescribed me Zithromax and Prednisone. I went home and started taking it. I started feeling better within a few days then I started feeling crummy again. I went back and saw him at the end of june (06/28/2022) and he prescribed me Pulmicort (nebulizer treatment), Promethazine and another round of Prednisone. He also told me to take the Albuterol 3 times daily. About 1 week after 06/28, I saw my allergist for a normal yearly exam and decided to bring up my issue there. The allergist said I had 2 ear infections and she put me on a different antibiotic. Then, on 07/14/2022, I went back to my doctor for a follow up, and he put me back on Prednisone, refilled my nebulizer prescription and gave me another antibiotic: Azithromycin. Once I finished this round of medicine, I felt better than I had in the past 6 weeks prior to this. The cough lingered for about a week or so then resolved.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bronchitis
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma; Allergies;
- Andere Medikamente
- Budesonide inhaler; Albuterol as needed; Zetia; Singulair; Aciphex; Azelastine; Flonase; Zyrtec; Allergy drops sublingually
- Allergien
- Penicillin; Lipitor
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 29.08.2022
- Impfdatum
- 14.06.2022
- Beginn
- 27.08.2022
- Tage bis Beginn
- 74,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Vaccine breakthrough infection
Symptomtext
Fully vaccinated and boosted twice. COVID breakthrough infection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 27.08.2022
- Impfdatum
- 20.05.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 65-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 06Mar2021 as dose 1, single (Lot number: EN 6199), in left arm, on 26Mar2021 as dose 2, single (Lot number: ER 8732), in left arm, on 29Oct2021 as dose 3 (booster), single (Lot number: FF2593), in left arm and on 20May2022 as dose 4 (booster), single (Lot number: 038A22A) at the age of 65 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Celiac disease" (unspecified if ongoing). Concomitant medication(s) included: VIT D3, start date: 01Jan2022; VIT B12, start date: 01Jan2022. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Positive; (Aug2022) Positive. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical Course: The patient had no known allergies. The patient received vaccine. The patient received Paxlovid for COVID 19 Treatment as other medication in 2weeks. The start date for paxlovid was 11Aug2022 and stop date was 16Aug2022. The patient took Multi vitamin (Vita fusion) as other medication in 2weeks; lot: YY20695090) with start date as 01Jan2022. The patient took Ibuprofen (lot: 2BE2284A) 200mg as needed as other medication in 2weeks product with start date as 01Aug2022 and stop date as 22Aug2022. The brand name for vit B12 was reported as Nature Made and brand name for Vit D3 was reported Vita fusion.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID-19 test; Test Result: Positive ; Test Date: 202208; Test Name: COVID-19 test; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Celiac disease
- Andere Medikamente
- VIT D3; VIT B12
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 20.08.2022
- Impfdatum
- 13.05.2022
- Beginn
- 15.06.2022
- Tage bis Beginn
- 33,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Diabetes mellitus
Glycosylated haemoglobin increased
Symptomtext
DIAGNOSED WITH DIABETES WITH HBA1C OF 8.5 in August 2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diabetes mellitus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- ESSENTIAL HYPERTENSION
- Andere Medikamente
- -
- Allergien
- NKDA
- Vorherige Impfungen
- significant arthralgia following COVID vaccine #2
- Staat
- -
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 18.08.2022
- Impfdatum
- 16.07.2022
- Beginn
- 16.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
No adverse event
Symptomtext
RECEIVED 4TH VACCINE (2ND BOOSTER) BEFORE ELIGIBLE. NO ADVERSE EFFECTS REPORTED
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 18.08.2022
- Impfdatum
- 16.07.2022
- Beginn
- 16.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
No adverse event
Product administered to patient of inappropriate age
Symptomtext
4TH DOSE (2ND BOOSTER) GIVEN BEFORE ELIGIBLE. PT REPORTS NO ADVERSE EFFECTS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 18.08.2022
- Impfdatum
- 02.08.2022
- Beginn
- 02.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product storage error
Symptomtext
vial was initially stored in the refrigerator on 02-Jun-2022 and administered on 02-Aug-2022; No adverse event; patient received moderna covid-19 vaccine past the 30 day beyond use date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (patient received moderna covid-19 vaccine past the 30 day beyond use date), PRODUCT STORAGE ERROR (vial was initially stored in the refrigerator on 02-Jun-2022 and administered on 02-Aug-2022) and NO ADVERSE EVENT (No adverse event) in a 64-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038A22A) for COVID-19 prophylaxis. Previously administered products included for Product used for unknown indication: Pfizer Covid-19 vaccine (Primary series), Pfizer Covid-19 vaccine (first booster dose) and Pfizer Covid-19 vaccine (Primary series). Past adverse reactions to the above products included No adverse event with Pfizer Covid-19 vaccine, Pfizer Covid-19 vaccine and Pfizer Covid-19 vaccine. On 02-Aug-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 02-Aug-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (patient received moderna covid-19 vaccine past the 30 day beyond use date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (vial was initially stored in the refrigerator on 02-Jun-2022 and administered on 02-Aug-2022) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (patient received moderna covid-19 vaccine past the 30 day beyond use date), PRODUCT STORAGE ERROR (vial was initially stored in the refrigerator on 02-Jun-2022 and administered on 02-Aug-2022) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (patient received moderna covid-19 vaccine past the 30 day beyond use date) and PRODUCT STORAGE ERROR (vial was initially stored in the refrigerator on 02-Jun-2022 and administered on 02-Aug-2022). No concomitant medications information was reported. The vial was initially stored in the refrigerator on 2-Jun-2022. Not the pharmacist aware of vial was undergo any temperature excursions. . It was reported that there were no known adverse events. No treatment medications were provided. This case was linked to MOD-2022-629202, MOD-2022-629210 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 17.08.2022
- Impfdatum
- 02.08.2022
- Beginn
- 02.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Upon trying to return some unused vaccine bottles to another store we realized that the vaccine was only good 30 days from the deep freeze. We thought is was good unitl 10-30-2022 according to the mfg website when kept in the fridge. We received this medication on 06-02-2022 from supplier and gave the vaccine on 08-02-2022. We contacted the manufacter which is going to do batch testing to see if we need to revaccinate
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- hypothyroid, migraines, pain
- Andere Medikamente
- Cyclobenzaprine, gabapentin, trazodone, doxepin
- Allergien
- sumatriptan
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 17.08.2022
- Impfdatum
- 02.08.2022
- Beginn
- 02.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Upon trying to return unused vaccine to another store we realized that the vaccine was only good 30 days from deep freeze. We thought is was good until 10-30-2022 according to the mfg website when kept in the fridge. We received this medication on 06-02-2022 and vaccinated on 08-02-2022. We reported this problem to the mfg and they are going to do batch testing to see if we need to revaccinate
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- hypertension, seasonal allergies
- Andere Medikamente
- losartan, fluticasone, azelastine nasal, hctz
- Allergien
- ace inhibitors
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 17.08.2022
- Impfdatum
- 02.08.2022
- Beginn
- 02.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Upon trying to return unused vaccine vials to another store we realized that it was only good 30 days from the deep freeze. We got the vaccine on 06-02-2022 and vaccinated on 08-02-2022. We thought that it was good until 10-30-2022 according to the mfg website when kept in the fridge. We created a report to Moderna and requested batch testing to see if we should revaccinate. Waiting for a reply.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- HYPERTENSION, SEASONAL ALLERGIES
- Andere Medikamente
- FLUTICASONE NASAL SPRAY, LISINOPRIL/HCTZ
- Allergien
- SALICYLATES
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- -
- Geschlecht
- M
- Eingang
- 17.08.2022
- Impfdatum
- 02.08.2022
- Beginn
- 17.08.2022
- Tage bis Beginn
- 15,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Upon returning the unused bottles of vaccine that we had left we realized that the vaccine was only good 30 days from the deep freeze. We thought it was 10-30-2022 the date on the manufacter website when kept in the fridge. We received this vaccine on 06-02-2022 and vaccinated on 08-02-2022. We contacted the mfg which is going to do batch testing to see if we need to revaccinate.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- unkown
- Vorgeschichte
- hypertension, diabetes, high blood pressure, high cholesterol. heart
- Andere Medikamente
- jardiance,metoprolol er, losartan, fluticasone, ozempic, metformin er, rosuvastatin, diclofenac, semglee, desipramine, omeprazole, verapamil er, montelukast
- Allergien
- ceftriaxone, rochephin, cephlasporin, quinolone
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 17.08.2022
- Impfdatum
- 02.08.2022
- Beginn
- 02.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Potentially sub therapeutic dose. When we were returning the vaccine to another store we realized that it was only good 30 days from the deep freeze. We thought is was good until 10-30-2022 when kept in the fridge. We got this medication from supplier on 06-02-2022 and vaccinated 08-02-2022. We contacted the mfg and they are going to do batch testing to see if we need to re-vaccinate.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- unkown
- Vorgeschichte
- unkown
- Andere Medikamente
- Upon returning the vaccine to another store we realized that it was only good 30 days from the deep freeze. We thought it was good until 10-30-2022 according to the mfg website. We got this vaccine on 06-02-2022 and vaccinated on 08-02-202
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 17.08.2022
- Impfdatum
- 02.08.2022
- Beginn
- 02.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Upon returning the vaccine to another store we reallized that it is only good 30 days from the deep freeze. We thought that it was good until 10-30-2022 according to the mfg website when kept at room temperature. We received this medication on 06-02-2022. We called the manufactor and gave them the information. They are going to do batch testing to see if we need to revaccinate.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- UNKOWN
- Andere Medikamente
- UNKOWN
- Allergien
- CODEINE,MEPERIDINE, MORPHINE, NALOXONE, OPIUM
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 17.08.2022
- Impfdatum
- 02.08.2022
- Beginn
- 02.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product storage error
Symptomtext
This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (6 patients received Moderna Covid-19 vaccine past the 30 day beyond use date.), PRODUCT STORAGE ERROR (Expired vial was not discarded after the use by date) and NO ADVERSE EVENT (No adverse event) in a 72-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038A22A) for COVID-19 prophylaxis. Previously administered products included for Product used for unknown indication: Pfizer vaccine (Dose 1 (primary series)), Pfizer vaccine (first booster) and Pfizer vaccine (Dose 2 (primary series)). Past adverse reactions to the above products included No adverse event with Pfizer vaccine, Pfizer vaccine and Pfizer vaccine. On 02-Aug-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 02-Aug-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (6 patients received Moderna Covid-19 vaccine past the 30 day beyond use date.). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Expired vial was not discarded after the use by date) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (6 patients received Moderna Covid-19 vaccine past the 30 day beyond use date.), PRODUCT STORAGE ERROR (Expired vial was not discarded after the use by date) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (6 patients received Moderna Covid-19 vaccine past the 30 day beyond use date.) and PRODUCT STORAGE ERROR (Expired vial was not discarded after the use by date). No concomitant medications information was reported. The vial was initially stored in the refrigerator on 2-JUN-2022. Pharmacist is aware of any temperature excursions undergone by the vial. It was reported that there were no known adverse events. No treatment medications were provided. This case was linked to MOD-2022-629202, MOD-2022-629207, MOD-2022-629208, MOD-2022-629210 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 86,0
- Geschlecht
- M
- Eingang
- 10.08.2022
- Impfdatum
- 27.05.2022
- Beginn
- 08.08.2022
- Tage bis Beginn
- 73,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asthenia
COVID-19
Fall
SARS-CoV-2 test positive
Symptomtext
Patient was admitted to observation level of care on 8-9 with weakness. Patient noted to have had a gradual fall on date of admission. Patient does have mild dementia. There is a HCPOA on file but is not currently activated. Patient did test positive for covid on 8-8.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asthenia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 87,0
- Geschlecht
- M
- Eingang
- 08.08.2022
- Impfdatum
- 20.05.2021
- Beginn
- 07.08.2022
- Tage bis Beginn
- 444,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Vaccine breakthrough infection
Symptomtext
Fully vaccinated with one booster. COVID breakthrough infection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 08.08.2022
- Impfdatum
- 03.06.2022
- Beginn
- 06.06.2022
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
patient covid positive on 6/6/22, 3 days after 4th booster dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 86,0
- Geschlecht
- F
- Eingang
- 30.07.2022
- Impfdatum
- 24.05.2022
- Beginn
- 24.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Dysstasia
Fall
Gait inability
Immobile
Wheelchair user
Symptomtext
Within hours of receiving the Covid-19 second booster injection the resident was not able to stand or ambulate. This immobility continued about 48 hours and then she became able to ambulate but only with strong assistance. Before the Covid injection she was fully ambulatory, used a rollator and rarely stumbled. She is now wheelchair bount and often falls from attempts to stand on her own.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dysstasia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Dementia with Lewey Bodies Asthma Hypertension Hypothyroidism GERD Edema in lower extremeties
- Andere Medikamente
- Cetirizine, Donepezil, Memantine, Fluticasone, Seroquel, Depakote, Furosemide
- Allergien
- Quinolones, Cephalosporins, Nitrofurantoin, Barbiturates
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 26.07.2022
- Impfdatum
- 25.05.2022
- Beginn
- 25.07.2022
- Tage bis Beginn
- 61,0
- Dosis
- 4
- 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+ 7/25/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- hypertension, TIA as well as COPD
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 25.07.2022
- Impfdatum
- 25.05.2022
- Beginn
- 28.06.2022
- Tage bis Beginn
- 34,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
SARS-CoV-2 test positive
Symptomtext
I did not have an adverse reaction to the vaccine. I started feeling symptoms on 06/28/2022 with mainly coughing. I tested positive for COVID-19 on 06/29/2022 with a home test. As I was traveling during this time I had a video conference with medical staff at a urgent care center in another location. I was given the prescription Paxlovid and started feeling better within 24 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Home test and it was positive for COVID-19 for 06/28/2022
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Diabetes
- Andere Medikamente
- Metformin; Tresiba; Trulicity; Losartan; Rosuvastatin; Vitamin D3 K2; fish oil
- Allergien
- Latex
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 23.07.2022
- Impfdatum
- 11.07.2022
- Beginn
- 11.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vial was initially stored in the refrigerator on 10-JUN-2022 and vaccine was administered on 11-Jul-2022; Booster dose administered to patients after use by date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Booster dose administered to patients after use by date) and PRODUCT STORAGE ERROR (Vial was initially stored in the refrigerator on 10-JUN-2022 and vaccine was administered on 11-Jul-2022) in a 28-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038A22A) for COVID-19 prophylaxis. Previously administered products included for Product used for unknown indication: Janssen COVID-19 Vaccine (Primary series). Past adverse reactions to the above products included No adverse event with Janssen COVID-19 Vaccine. On 11-Jul-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 11-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Booster dose administered to patients after use by date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vial was initially stored in the refrigerator on 10-JUN-2022 and vaccine was administered on 11-Jul-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Booster dose administered to patients after use by date) and PRODUCT STORAGE ERROR (Vial was initially stored in the refrigerator on 10-JUN-2022 and vaccine was administered on 11-Jul-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication was not provided. Patients had received their 1st booster dose of the Moderna COVID-19 vaccine after the use by date. The vial was initially stored in the refrigerator on 10-JUN-2022. The vial did not undergo any temperature excursions. BUD in refrigerator was on 10-Jul-2022 at 10am. Patients had not reported any adverse reactions post vaccination. 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
- WI
- Alter
- 87,0
- Geschlecht
- M
- Eingang
- 20.07.2022
- Impfdatum
- 20.07.2022
- Beginn
- 20.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
No adverse event
Symptomtext
Third booster of Moderna (0.25ml) given in error. Patient had no adverse events at time of injection or 2 hours after. Facility will monitor patient for side effects in accordance with regular facility protocol after vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 19.07.2022
- Impfdatum
- 16.07.2022
- Beginn
- 16.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
No adverse event
Symptomtext
PATIENT RECEIVED A FULL DOSE (0.5ML) WHEN THE PATIENT SHOULD HAVE RECEIVED A HALF DOSE (0.25ML) BOOSTER. PATIENT MADE AWARE. NO ADVERSE REACTION REPORTED BY PATIENT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 19.07.2022
- Impfdatum
- 16.07.2022
- Beginn
- 16.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
No adverse event
Symptomtext
Patient received a full dose (0.5ml) when she should have received a half dose (0.25ml) booster. Patient was informed. No adverse effects reported by patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 19.07.2022
- Impfdatum
- 11.07.2022
- Beginn
- 11.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
vial was initially stored in the refrigerator on 10-JUN-2022 and vaccine was administered on 11-Jul-2022; booster dose administered to patient after use by date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (booster dose administered to patient after use by date) and PRODUCT STORAGE ERROR (vial was initially stored in the refrigerator on 10-JUN-2022 and vaccine was administered on 11-Jul-2022) in a 28-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038A22A) for COVID-19 prophylaxis. Previously administered products included for Product used for unknown indication: Janssen COVID-19 VACCINE (primary series). Past adverse reactions to the above products included No adverse event with Janssen COVID-19 VACCINE. On 11-Jul-2022, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 11-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (booster dose administered to patient after use by date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (vial was initially stored in the refrigerator on 10-JUN-2022 and vaccine was administered on 11-Jul-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (booster dose administered to patient after use by date) and PRODUCT STORAGE ERROR (vial was initially stored in the refrigerator on 10-JUN-2022 and vaccine was administered on 11-Jul-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication was not provided. Patients had received their 1st booster dose of the Moderna COVID-19 vaccine after the use by date. The vial was initially stored in the refrigerator on 10-JUN-2022. The vial did not undergo any temperature excursions. BUD in refrigerator was on 10-Jul-2022 at 10am. Patients had not reported any adverse reactions post vaccination. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- F
- Eingang
- 12.07.2022
- Impfdatum
- 10.06.2022
- Beginn
- 10.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
They have remained in a refrigerated state this entire time within the temperature range required to maintain stability.; Expired Vaccine Administration; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired Vaccine Administration) and PRODUCT STORAGE ERROR (They have remained in a refrigerated state this entire time within the temperature range required to maintain stability.) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038A22A) for COVID-19 prophylaxis. No Medical History information was reported. On 10-Jun-2022 at 9:30 AM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 10-Jun-2022 at 9:30 AM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired Vaccine Administration). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They have remained in a refrigerated state this entire time within the temperature range required to maintain stability.). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired Vaccine Administration) and PRODUCT STORAGE ERROR (They have remained in a refrigerated state this entire time within the temperature range required to maintain stability.) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. It was reported that patient had taken booster dose. It was reported that reporter received vaccines on 05-MAY-2022. 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
- MD
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 07.07.2022
- Impfdatum
- 29.06.2022
- Beginn
- 30.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Blood pressure increased
Disorientation
Dysstasia
Gait disturbance
Transient ischaemic attack
Symptomtext
Had TIA, Increased Blood Pressure, Patient reported body weakness, Difficulty standing, Disorientation, Difficulty walking
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asthenia
- Hospital-Tage
- 1,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 07.07.2022
- Impfdatum
- 29.06.2022
- Beginn
- 30.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Blood pressure increased
Confusional state
Hemiparesis
Symptomtext
Increased blood pressure, Right sided weakness, Confusion, Patient complains of weakness. Patient still in Hospital
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asthenia
- Hospital-Tage
- 7,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 06.07.2022
- Impfdatum
- 23.05.2022
- Beginn
- 22.06.2022
- Tage bis Beginn
- 30,0
- Dosis
- 4
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Tested positive one month after vaccine. Took COVID-19 home test came up positive. Called my Dr. and they asked me to come in to officially test and it came back positive. Breakthrough case.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Home COVID-19 test and went to the Dr. and had another COVID-19 test run and it was positive. Was prescribed a cocktail of ZYRTEC; PEPCID; vitamin D3; vitamin C; zinc; quercetin; aspirin. Took for 14 days.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Past Diabetes; Arthritis
- Andere Medikamente
- Meloxicam; aspirin; vitamin C; magnesium; coQ10; nutritional yeast; B-12; calcium; cinnamon; turmeric; marine collagen; zinc; vitamin D; hair formula; loratadine.
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 05.07.2022
- Impfdatum
- 23.06.2022
- Beginn
- 23.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
The vial was punctured on 6/22/22 at 9:00 am. The punctured vial was left in the refrigerator for 24 hours before being accessed for the vaccine that I am reporting on. Thus, this vaccine was given 12 hours after the recommended time for the vial to be sterile. RN called manufacturer--Moderna reports that the vial and vaccine is viable from an efficacy standpoint and does not need to be re-given. However, there is a question of sterility as accessing the vial of vaccine after recommended time of 12 hours may cause introduction of bacteria. RN attempted to call patient, but is unable to get a hold of patient. Pt has not reported adverse event. RN will call patient tomorrow.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 53,0
- Geschlecht
- U
- Eingang
- 03.07.2022
- Impfdatum
- 24.06.2022
- Beginn
- 24.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vial was stored about 20 hours post puncture; Received expired Booster dose about 20 hours post puncture; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Received expired Booster dose about 20 hours post puncture) and PRODUCT STORAGE ERROR (Vial was stored about 20 hours post puncture) in a 53-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038A22A) for COVID-19 vaccination. No Medical History information was reported. On 24-Jun-2022 at 9:00 AM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 24-Jun-2022 at 9:00 AM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Received expired Booster dose about 20 hours post puncture). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vial was stored about 20 hours post puncture). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Received expired Booster dose about 20 hours post puncture) and PRODUCT STORAGE ERROR (Vial was stored about 20 hours post puncture) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications was reported. Number of doses/vials: 1 vial / 2 doses. The vial was initially stored in the refrigerator on 02-JUN-2022. The vial was first punctured on 23-JUN-2022 at 1:14PM. The vial was stored in Refrigerator post puncture. The vial does not undergone any temperature excursions. Post punctured the vial was stored in the refrigerator approximately for under 20 hours. The vial exposed to room temperature for >24 hours: Less than 24 hours. No treatment medications was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 64,0
- Geschlecht
- U
- Eingang
- 03.07.2022
- Impfdatum
- 24.06.2022
- Beginn
- 24.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Received expired Booster dose about 20 hours post puncture; Received expired Booster dose about 20 hours post puncture; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Received expired Booster dose about 20 hours post puncture) and PRODUCT STORAGE ERROR (Received expired Booster dose about 20 hours post puncture) in a 64-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038A22A) for COVID-19 vaccination. No Medical History information was reported. On 24-Jun-2022 at 9:00 AM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 24-Jun-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Received expired Booster dose about 20 hours post puncture). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Received expired Booster dose about 20 hours post puncture). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Received expired Booster dose about 20 hours post puncture) and PRODUCT STORAGE ERROR (Received expired Booster dose about 20 hours post puncture) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No relevant concomitant medications were reported. It was reported that number of doses/vials was 1 vial / 2 doses. On 02-JUN-2022 the vial was initially stored in the refrigerator. On 23JUN2022 at 1:14PM the vial was first punctured. Vial did not undergone any temperature excursions. Post punctured the vial was stored in the refrigerator approximately for under 20 hours. Treatment medication was not provided by the reporter. This case was linked to MOD-2022-596592.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- -
- Geschlecht
- U
- Eingang
- 03.07.2022
- Impfdatum
- 27.06.2022
- Beginn
- 27.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Refrigerator expiration date: 6/25/2022 (removed from freezer on 5/26/22), Administered to patient: 6/27/22; Vaccine that was administered after the refrigerator expiration date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine that was administered after the refrigerator expiration date) and PRODUCT STORAGE ERROR (Refrigerator expiration date: 6/25/2022 (removed from freezer on 5/26/22), Administered to patient: 6/27/22) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 038A22A) for COVID-19 prophylaxis. No Medical History information was reported. On 27-Jun-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 27-Jun-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine that was administered after the refrigerator expiration date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Refrigerator expiration date: 6/25/2022 (removed from freezer on 5/26/22), Administered to patient: 6/27/22). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine that was administered after the refrigerator expiration date) and PRODUCT STORAGE ERROR (Refrigerator expiration date: 6/25/2022 (removed from freezer on 5/26/22), Administered to patient: 6/27/22) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. Concomitant product use was not provided by the reporter. Vaccine was administered after the refrigerator expiration date. Refrigerator expiration date: 25-Jun-2022 (removed from freezer on 26-May-2022). 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
- UT
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 29.06.2022
- Impfdatum
- 31.05.2022
- Beginn
- 23.06.2022
- Tage bis Beginn
- 23,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Respiratory symptom
SARS-CoV-2 test positive
Symptomtext
On 6/23 I developed a dry cough overnight. 6/24 Tested with a home test negative. Dry cough continued through the day. The next day 6/25 I had upper respiratory symptoms. Tested positive with at home test on 6/26. Symptoms decreased by them. Reached out to physician on 6/27, who prescribed Paxlovid. Treated symptoms with Dayquil. Symptoms greatly diminished, but still persist. Stopped chronic medication to take the Paxlovid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- At home COVID test
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Lisinopril; Amlodipine; Atorvastatin; Ezetimibe
- Allergien
- Small Pox Vaccine
- Vorherige Impfungen
- Small pox vaccine as infant.
- Staat
- WA
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 28.06.2022
- Impfdatum
- 19.05.2022
- Beginn
- 19.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
We administered 0..25ml to the patient instead of the 0.5ml (additional dose for immunocompromised).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HYPOTHYROIDISM, HYPERTENSION, ANXIETY, AUTOIMMUNE HEPATITIS
- Andere Medikamente
- -
- Allergien
- NO KNOWN ALLERGIES
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 27.06.2022
- Impfdatum
- 24.06.2022
- Beginn
- 27.06.2022
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Tinnitus
Symptomtext
Tinnitus in my right ear
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tinnitus
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Sinusitis
- Vorgeschichte
- -
- Andere Medikamente
- Quetiapine, estrogen patch, lithium, milk thistle, multi-vitamin, l lysine
- Allergien
- Morphine
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 27.06.2022
- Impfdatum
- 25.06.2022
- Beginn
- 25.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Symptomtext
Customer is 16 yo. Father is a physician, Mother requested MODERNA for booster. Primary doses for Moderna recommendation approved few days ago. Pharmacist on duty didn't realize the booster was not approved. Provided booster dose number one (0.25 ml) which is indicated only for 18yo & up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none to report
- Vorgeschichte
- not available
- Andere Medikamente
- not available
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 25.06.2022
- Impfdatum
- 23.06.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product administered to patient of inappropriate age
Symptomtext
No adverse event - normal reaction to the immunization. Moderna booster not approved for teens, however received Pfizer as primary series. Confusing on CDC's web page.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 23.06.2022
- Impfdatum
- 08.06.2022
- Beginn
- 20.06.2022
- Tage bis Beginn
- 12,0
- Dosis
- 4
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
My husband had it so I quarantined with him, I decided to get tested myself when I went to my Dr. I tested positive on 6/21/2022. My Dr. prescribed Dexamethasone , and Cephalexin
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID test
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Thyroid Eye Disease, High Blood Pressure, Afib.
- Andere Medikamente
- Eliquis 10mg, Simvastatin 20mg, Diltiazem 120mg, Flecainide 100mg, Multivitamin, Calcium, D3
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 22.06.2022
- Impfdatum
- 22.06.2022
- Beginn
- 22.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- 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
Patient came into our clinic and she had the primary series of Moderna in "private". She came for her booster with her parent who requested Moderna to complete the series. She was given the booster dose of 0.25mL and it was then identified that she was only 14 years old and not eligible for this vaccine. We will input the patient into system directly, since Moderna will not populate. We have also reeducated the vaccinating nurse and referenced the binders on site that have all the vaccine doses information, as well as provided remediation training and testing. Patient was monitored for 30 minutes and reported no side effects from the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 17.06.2022
- Impfdatum
- 13.06.2022
- Beginn
- 14.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
The morning after the vaccine was given the patient experienced a larger than expected adverse effect profile and noticed he was given a full 0.5ml dose. He then realized he should have received a booster dose and reported his symptoms to the pharmacy. His first two doses of the Covid vaccine were given at another location and the patient requested and reported needing a "second" dose. This was confirmed at the time of administration and according to all information that was presented we thought the patient was receiving the correct dose in the series. As we discussed his experience he acknowledged we had less than adequate communication. We checked in on him on 06/17 and he reported feeling 99% with resolution of nealry all vaccine related side effects.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- No Known Allergies
- Vorherige Impfungen
- Similar anticipated side effects including fever, chills, fatigue, aches
- Staat
- CA
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 17.06.2022
- Impfdatum
- 17.06.2022
- Beginn
- 17.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Product administered to patient of inappropriate age
Symptomtext
NA; 2nd dose 0.5 cc moderna; previous 2nd invalid received pediatric Orange top Pfizer.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- NA
- Allergien
- NA
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 15.06.2022
- Impfdatum
- 10.06.2022
- Beginn
- 10.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Puctured vial was left in the refrigerator overnight; Dose administered from a vial that was punctured for more than 24 hours; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Dose administered from a vial that was punctured for more than 24 hours) and PRODUCT STORAGE ERROR (Puctured vial was left in the refrigerator overnight) in an 83-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038A22A) for COVID-19 vaccination. No Medical History information was reported. On 10-Jun-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 10-Jun-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose administered from a vial that was punctured for more than 24 hours). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Puctured vial was left in the refrigerator overnight). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Dose administered from a vial that was punctured for more than 24 hours) and PRODUCT STORAGE ERROR (Puctured vial was left in the refrigerator overnight) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medications were reported. Time of administration of vaccine was 1:10-1:15 PM. Vial was initially stored in the refrigerator on 08-JUN-2022. Vial was first punctured on 9-JUN-2022 at 2:32 PM and 3 doses were administered at that time.Post punctured vial was stored in refrigerator. Vial did not undergo any temperature excursions. Total amount of time the vial was exposed to room temperature (8 to 25 degree Celsius= 46 to 77 degree Fahrenheit) was 15-20 minutes. No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 15.06.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Accidental exposure to product
Syringe issue
Wrong technique in device usage process
Symptomtext
pressure was high and squirted mostly in the air, but in her face and little got in her mouth; the syringe that come with the vaccines (she referred to them as not high-quality kind) leaked, pressure was high and squirted mostly in the air; the syringe that come with the vaccines (she referred to them as not high-quality kind) leaked; This spontaneous case was reported by a pharmacist and describes the occurrence of ACCIDENTAL EXPOSURE TO PRODUCT (pressure was high and squirted mostly in the air, but in her face and little got in her mouth), WRONG TECHNIQUE IN DEVICE USAGE PROCESS (the syringe that come with the vaccines (she referred to them as not high-quality kind) leaked, pressure was high and squirted mostly in the air) and SYRINGE ISSUE (the syringe that come with the vaccines (she referred to them as not high-quality kind) leaked) in a 32-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 038A22A) for COVID-19 prophylaxis. Previously administered products included for Drug use for unknown indication: Pfizer vaccine. Past adverse reactions to the above products included No adverse event with Pfizer vaccine. On an unknown date, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On an unknown date, the patient experienced ACCIDENTAL EXPOSURE TO PRODUCT (pressure was high and squirted mostly in the air, but in her face and little got in her mouth), WRONG TECHNIQUE IN DEVICE USAGE PROCESS (the syringe that come with the vaccines (she referred to them as not high-quality kind) leaked, pressure was high and squirted mostly in the air) and SYRINGE ISSUE (the syringe that come with the vaccines (she referred to them as not high-quality kind) leaked). At the time of the report, ACCIDENTAL EXPOSURE TO PRODUCT (pressure was high and squirted mostly in the air, but in her face and little got in her mouth), WRONG TECHNIQUE IN DEVICE USAGE PROCESS (the syringe that come with the vaccines (she referred to them as not high-quality kind) leaked, pressure was high and squirted mostly in the air) and SYRINGE ISSUE (the syringe that come with the vaccines (she referred to them as not high-quality kind) leaked) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant drug was reported. Pharmacist reported no symptoms. No treatment information was provided by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Accidental exposure to product
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 14.06.2022
- Impfdatum
- 13.06.2022
- Beginn
- 14.06.2022
- Tage bis Beginn
- 1,0
- 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
mRNA primary series dose administered prior to the recommended interval. Moderna was given at 21 days, instead of 28 days. Spoke with patient one day after, no adverse effects reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 14.06.2022
- Impfdatum
- 06.06.2022
- Beginn
- 06.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product administered to patient of inappropriate age
Symptomtext
No adverse reaction. Patient received 2nd booster and didn't meet the CDC requirements of being age 50+
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 14.06.2022
- Impfdatum
- 06.06.2022
- Beginn
- 06.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
No adverse event
Symptomtext
No adverse reaction. Patient received 2nd booster and didn't meet the CDC requirements of being age 50+
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 14.06.2022
- Impfdatum
- 06.06.2022
- Beginn
- 06.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
No adverse event
Symptomtext
No adverse reaction. patient received 2nd booster and did not meet the CDC requirements of being age 50+
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 13.06.2022
- Impfdatum
- 06.06.2022
- Beginn
- 06.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Symptomtext
No adverse effects just receive 2nd booster and did not meet CDC requirements
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 13.06.2022
- Impfdatum
- 17.05.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Symptomtext
Covid-19; This spontaneous case was reported by a physician and describes the occurrence of COVID-19 (Covid-19) in a 59-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 038A22A) for COVID-19 vaccination. Previously administered products included for Product used for unknown indication: Pfizer / BioNTech (Dose Number: 1 Batch/Lot No: EH9899 Location of injection: Arm Right) on 15-Dec-2020, Pfizer / BioNTech (Dose Number: 3 Batch/Lot No: 30145BA Location of injection: Arm Right) on 29-Sep-2021 and Pfizer / BioNTech (Dose Number: 2 Batch/Lot No: EJ1686 Location of injection: Arm Right) on 06-Jan-2022. Past adverse reactions to the above products included No adverse event with Pfizer / BioNTech, Pfizer / BioNTech and Pfizer / BioNTech. Concurrent medical conditions included Hypertension, Type 2 diabetes mellitus, Obesity (BMI 30) and Drug allergy (No drug was reported). Concomitant products included METFORMIN, HYDROCHLOROTHIAZIDE, VALSARTAN (VALSARTAN & HCTZ), TADALAFIL and AMLODIPINE for an unknown indication. On 17-May-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced COVID-19 (Covid-19). The patient was treated with NIRMATRELVIR, RITONAVIR (PAXLOVID) (oral) from 24-May-2022 to 28-May-2022 for COVID-19 treatment, at an unspecified dose and frequency. At the time of the report, COVID-19 (Covid-19) had resolved. Not provided. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Patient was taking other medications/products within 2 weeks of starting COVID-19 treatment. On 16-Jun-2022, patient had Rebound COVID symptoms with positive antigen test, 10 days after finishing Paxlovid. Company Comment: This is a spontaneous case concerning a 59-year-old, male patient with concurrent medical conditions of Hypertension, Type 2 diabetes mellitus, Obesity, who experienced the unexpected non-serious event of Covid-19. The event occurred on an unknown date day after the fourth dose of mRNA-1273 COVID 19 Vaccine, which was administered on May 17, 2022. Patient was treated with nirmatrelvir and ritonavir from 24-May-2022 to 28-May-2022 at an unspecified dose and frequency. Patient re-developed symptoms of Covid-19, 10 days after finishing course of nirmatrelvir and ritonavir (Paxlovid). The event was reported as resolved. The concurrent medical conditions of Hypertension, Type 2 diabetes mellitus, Obesity remains a confounder. The benefit-risk relationship of mRNA-1273 COVID 19 Vaccine, is not affected by this report.; Sender's Comments: This is a spontaneous case concerning a 59-year-old, male patient with concurrent medical conditions of Hypertension, Type 2 diabetes mellitus, Obesity, who experienced the unexpected non-serious event of Covid-19. The event occurred on an unknown date day after the fourth dose of mRNA-1273 COVID 19 Vaccine, which was administered on May 17, 2022. Patient was treated with nirmatrelvir and ritonavir from 24-May-2022 to 28-May-2022 at an unspecified dose and frequency. Patient re-developed symptoms of Covid-19, 10 days after finishing course of nirmatrelvir and ritonavir (Paxlovid). The event was reported as resolved. The concurrent medical conditions of Hypertension, Type 2 diabetes mellitus, Obesity remains a confounder. The benefit-risk relationship of mRNA-1273 COVID 19 Vaccine, is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Drug allergy (No drug was reported); Hypertension; Obesity (BMI 30); Type 2 diabetes mellitus.
- Vorgeschichte
- -
- Andere Medikamente
- METFORMIN; VALSARTAN & HCTZ; TADALAFIL; AMLODIPINE.
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 08.06.2022
- Impfdatum
- 15.05.2022
- Beginn
- 04.06.2022
- Tage bis Beginn
- 20,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Influenza
Nasopharyngitis
Rhinorrhoea
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
On 6-4-2022, I started having a runny nose and a mild cough. I started taking OTC daytime severe cold and flu symptom medication. On 6-5, I took a home Covid test and it was positive. I called my doctors office on 6-6 and he prescribed PAXLOVID. I am currently still taking this medication. I am feeling better today. I am reporting my breakthrough case of Covid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- 1 home Covid test on 6-5-2022 with positive result.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Finasteride 5mg daily; atorvastatin 10mg daily; aspirin 162mg daily; vit D3 125mcg daily; zinc 50mg daily; fish oil 1000mg daily; flaxseed oil 700mg daily; B6 vit 100mg daily; B complex 1 daily; AREDS vit 2 daily; loratadine 10mg daily
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 08.06.2022
- Impfdatum
- 05.06.2022
- Beginn
- 05.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
No adverse event
Symptomtext
Patient received booster about 6 weeks after their primary series. Patient was informed and had no other adverse events. (This was vaccine administration error)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 07.06.2022
- Impfdatum
- 04.06.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- 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
There were no, adverse events. Patient who is a minor (17yrs and 1month old) recieved a Moderna booster vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 06.06.2022
- Impfdatum
- 19.05.2022
- Beginn
- 21.05.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Tinnitus
Symptomtext
Tinnitus (in both ears) which began a couple days after the fourth shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tinnitus
- Hospital-Tage
- -
- Labordaten
- Doctor's office visit/ visual ear examination on 5/26. Verified that both ears appear clear (no wax) and healthy (no infections). To this point I have never had any issues with my ears. Appointment scheduled for an Audiologist on 6/16.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Finasteride (1mg) , Hydrochlorothorizide (25mg) , Losartan (potassium 25mg), Atorvastatin (10mg), COQ10, Turmeric. (Have not had any significant side effects or symptoms with any of these meds).
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 03.06.2022
- Impfdatum
- 03.06.2022
- Beginn
- 03.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- 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
no adverse event reported but patient asked for moderna and we gave patient moderna without realizing patient under 18 years old
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 01.06.2022
- Impfdatum
- 01.06.2022
- Beginn
- 01.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Wrong product administered
Symptomtext
Patient denied any adverse reactions. Patient was in the clinic with guardian for 15 mins and denied any adverse reactions. Patient guardian was informed by the community health nurse about the wrong brand vaccine administered and grandmother denied any adverse reactions.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- None was taken. Patient did not have an adverse reaction to the vaccine.
- Aktuelle Erkrankungen
- Patient denied.
- Vorgeschichte
- Patient denies. Past medical history in chart is depression .
- Andere Medikamente
- Birth control depo given in separate arm at the same time of covid vaccination. (covid vaccine and depo given in separate deltoids)
- Allergien
- Allergy to penicillin's
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 01.06.2022
- Impfdatum
- 06.05.2022
- Beginn
- 21.05.2022
- Tage bis Beginn
- 15,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Nasopharyngitis
Rhinorrhoea
SARS-CoV-2 test positive
Throat irritation
Symptomtext
I felt like I had a really bad head cold. It started with a scratchy throat on Saturday. By Thursday, I was feeling better enough so that I was able to clean the house on Friday. I just felt like for 2 and a half days, I felt constantly like I was going to sneeze. Felt like on the verge of sneezing and nothing happening. Felt like the head cold. I do have some residual drainage but feeling pretty good right now. Out of isolation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- 05/22/2022 at home COVID test possibly positive. 05/23/2022 Rapid COVID test at urgent care positive.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Vitamin D; fish oil
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 31.05.2022
- Impfdatum
- 17.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
Vaccine administered beyond 12 hour usage time frame, approximately 8 hours beyond the use time frame. no reports of adverse symptoms, reaction, or associated symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Hypertension; Diabetes mellitus type 2; Hypothyroidism; Hyperlipidemia; B12 deficiency; Pustule; Intertrigo.
- Vorgeschichte
- Hypertension; Diabetes mellitus type 2; Hypothyroidism; B12 deficiency.
- Andere Medikamente
- -
- Allergien
- Amitriptyline; Cefaclor; Hydrocodone; Nefazadone; Sertraline; Cephalexin; Ciporofloxacin; Sulfamethoxazole; Trimethoprin.
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 31.05.2022
- Impfdatum
- 17.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
Vaccine administered beyond 12 hour usage time frame, approximately 8 hours beyond the use time frame. No reports of adverse symptoms, reaction, or associated symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- hypertension, prediabetes, morbid obesity, hyperlipidemia
- Vorgeschichte
- hypertension, prediabetes, morbid obesity, hyperlipidemia
- Andere Medikamente
- -
- Allergien
- Tetracycline
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 87,0
- Geschlecht
- F
- Eingang
- 31.05.2022
- Impfdatum
- 17.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
vaccine administered beyond 12 hour usage time, approximately 8 hours beyond the time frame. no reports of adverse symptoms, reaction, or associated symptoms
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- atrial fibrillation, hyperlipidemia, secondary hypercoagulate state
- Vorgeschichte
- atrial fibrillation, hyperlipidemia, secondary hypercoagulate state
- Andere Medikamente
- -
- Allergien
- nitrofurantoin
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 31.05.2022
- Impfdatum
- 17.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
vaccine administered beyond 12 hour usage time frame, approximately 8 hours beyond the use time frame. no reports of adverse symptoms, reaction, or associated symptoms
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- adult ADHD
- Vorgeschichte
- adult ADHD
- Andere Medikamente
- -
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 31.05.2022
- Impfdatum
- 17.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product use issue
Symptomtext
vaccine administered beyond 12 hour usage time frame, approximately 8 hours beyond the use time frame. no reports of adverse symptoms , reaction, or associated symptoms
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- hypertension, hyperlipidemia, diabetes mellitus type 2
- Vorgeschichte
- hypertension, hyperlipidemia, diabetes mellitus type 2
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 29.05.2022
- Impfdatum
- 28.05.2022
- Beginn
- 28.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Moderna was given to patient 13 years of age, which is below the approved age of 18, mother was called, was fine with it, no adverse affects that we have been made aware of.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 28.05.2022
- Impfdatum
- 28.05.2022
- Beginn
- 28.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Photopsia
Symptomtext
The patient stated that they sat down to wait for 20 minutes after receiving the vaccine. They did not experience any symptoms. When they exited the building and entered the sunlight, they stated their "eyes began flashing." It was described as bright flashing spots. This continued for about 30 minutes before it stopped. They did not experience this before and they have not had symptoms after it stopped. No other symptoms were experienced. It was recommended the patient follow up with an eye doctor to ensure there are no issues. Whether the patient went to see a provider is not known.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Photopsia
- Hospital-Tage
- -
- Labordaten
- Not available.
- Aktuelle Erkrankungen
- Not known
- Vorgeschichte
- Not known
- Andere Medikamente
- No known
- Allergien
- Aztreonam, belladonna alkaloids, benztropine, benzyl benzoate, buzepide metiodide, carbapenems, cephalosporins, dibutoline sulfate, dicyclomine, diphemanil methylsulfate, glycopyrrolate, homatropine, isopropamide, macrolides and ketolides, mephenzolate, mepiperphenidol bromide, oxyphencyclimine, penicillins, penthienate bromide, pimecrolimus, poldine, propantheline, sirolimus, tacrolimus, tolterodine
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 26.05.2022
- Impfdatum
- 25.05.2022
- Beginn
- 25.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Underdose
Symptomtext
Pt was given the .25mg of Moderna covid vaccine booster . Pt was to have been given Moderna .5mg as her 1st covid vaccine in the series.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- tylenol 325 mg prn, ibuprofen 600mg prn, pre-natal vitamin 1 daily, trandate 100mg 1 BID
- Allergien
- no allergies
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 24.05.2022
- Impfdatum
- 20.05.2022
- Beginn
- 23.05.2022
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Atrial fibrillation
Cyanosis
General physical health deterioration
Pulse absent
Renal failure
Symptomtext
5/23/2022 2:51am Resident declining, BP 102/54, P 61, R 39, O2 Sats 83 % on 4 LPM of O2, no pedal pulse X 2, legs bluish purple to knees, Resident sent to Hospital. Resident admitted to hospital dx kidney failure and A FIB . resident currently on hospital at this time
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Atrial fibrillation
- Hospital-Tage
- 3,0
- Labordaten
- resident still in hospital
- Aktuelle Erkrankungen
- Chronic PNU
- Vorgeschichte
- CEREBRAL INFARCTION, UNSPECIFIED, DYSPHAGIA, OROPHARYNGEAL PHASE, PERIPHERAL VASCULAR DISEASE, UNSPECIFIED, CYST OF KIDNEY, ACQUIRED, ESSENTIAL (PRIMARY) HYPERTENSION, UNSPECIFIED ATRIAL FIBRILLATION, CHRONIC OBSTRUCTIVE PULMONARY DISEASE, UNSPECIFIED, HEART FAILURE, UNSPECIFIED
- Andere Medikamente
- Mirtazapine Tablet 30 MG, Pro-Stat Liquid, Lactulose Solution 10 GM/15ML, pratropium-Albuterol Solution 0.5-2.5 (3) MG/3ML, Metoprolol Tartrate Tablet, Guar Gum Packet, Reglan Tablet 5 MG, Aspirin Tablet Chewable 81 MG, Atorvastatin Calcium
- Allergien
- Doxycycline, Rocephin
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 24.05.2022
- Impfdatum
- 18.05.2022
- Beginn
- 18.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
A dose was administered from a vial that had been opened for more than 12 h; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (A dose was administered from a vial that had been opened for more than 12 h) in a 73-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 038A22A) for COVID-19 vaccination. No Medical History information was reported. On 18-May-2022 at 1:15 PM, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 18-May-2022 at 1:15 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (A dose was administered from a vial that had been opened for more than 12 h). At the time of the report, EXPIRED PRODUCT ADMINISTERED (A dose was administered from a vial that had been opened for more than 12 h) outcome was unknown. The action taken with mRNA-1273 (Spikevax) (Unknown) was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. Concomitant product use was not provided by the reporter. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 23.05.2022
- Impfdatum
- 23.05.2022
- Beginn
- 23.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Symptomtext
Patient had 3 Moderna vaccine and wanted to do 2nd booster with Pfizer, however I, Pharmacist, administered Moderna vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 23.05.2022
- Impfdatum
- 20.05.2022
- Beginn
- 20.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
Patient was given a 5th dose (3rd booster) of Moderna vaccine. Patient's vaccine card that was provided to the pharmacy only listed 3 doses, but when it was entered into the state registry, it was discovered the patient has already completed all recommended doses and this was an additional, unnecessary dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 23.05.2022
- Impfdatum
- 20.05.2022
- Beginn
- 20.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Circumstance or information capable of leading to medication error
Extra dose administered
Symptomtext
Patient was given a 5th dose (3rd booster) of Moderna vaccine. Patient's vaccine card that was provided to the pharmacy only listed 3 doses, but when it was entered into the state registry, it was discovered the patient has already completed all recommended doses and this was an additional, unnecessary dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Circumstance or information capable of leading to medication error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 85,0
- Geschlecht
- M
- Eingang
- 20.05.2022
- Impfdatum
- 19.05.2022
- Beginn
- 20.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoaesthesia
Muscular weakness
Symptomtext
Patient vaccinated without incident. Wife of patient phoned pharmacy at approximately 10:00am this morning reporting that her husband (patient) was having numbness and weakness in both legs, not allowing him to bear weight. Patient conscious and breathing normally. I advised her to immediately call EMS for evaluation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypoaesthesia
- Hospital-Tage
- -
- Labordaten
- unknown at this time. Patient referred to EMS.
- Aktuelle Erkrankungen
- none known
- Vorgeschichte
- none known
- Andere Medikamente
- unknown
- Allergien
- none known
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 19.05.2022
- Impfdatum
- 18.05.2022
- Beginn
- 18.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
Vaccine was administered after 12 hours of first puncture. Vaccine given after being at room temperature for 23 hours. Manufacturer of Moderna contacted and they stated that vaccine still effective if done within 24 hours of first puncture. No adverse event reported by patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Synthroid 75 and Pantoprazole 40mg
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 18.05.2022
- Impfdatum
- 18.05.2022
- Beginn
- 18.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Moderna booster was given to soon, pt was not due for it until 8/25/22, spoke to pts PCP that reassured that pt will be okay just to notify about the incident, called pt and informed her about incident, pt understood and had no questions
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- ferrous sulfate 325 mg (65 mg iron) tablet norgestrel-ethinyl estradioL (LO/OVRAL) 0.3-30 mg-mcg per tablet fluticasone propionate (FLONASE) 50 mcg/actuation nasal spray
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 16.05.2022
- Impfdatum
- 16.05.2022
- Beginn
- 16.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Sensory disturbance
Symptomtext
10-15 min after administration of her 2nd booster, she came up to me and told me that within 5 min of giving her the shot she felt a pinching feeling in her chest. She said that at that point it had started to subside. She took her BP on the HIGI machine and it was 126/62. I asked her if she wanted me to call anyone for her. she declined. I asked her to stay a little longer for further observation. at this point she said that the pinching feeling had almost completely subsided. She continued to sit in the waiting area until she came up to me and told me she was leaving and that she felt fine. I told her to call 911 if it came back or if there was an emergency. *I did ask her prior to immunization whether she had reacted to any of the previous 3 doses and she said no*
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Sensory disturbance
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 93,0
- Geschlecht
- F
- Eingang
- 15.05.2022
- Impfdatum
- 11.05.2022
- Beginn
- 11.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Inappropriate schedule of product administration
Symptomtext
Patient received 2 Moderna booster doses during the vaccine clinic as the patient had 2 different consent forms and went to both of the vaccinators so it was unknown to the vaccinators that the patient had already received a vaccine in that same day. The booster vaccine doses were given in different arms: 1 in the left deltoid and 1 in the right deltoid. When discovered, the information was given to the Long-Term Care facility and she was going to contact the primary physician. At the time which was 2 days later, the patient was doing fine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Acetaminophen, Levothyroxine, Loratadine, Polyvinyl ophth solution, Premarin Cream
- Allergien
- Penicillins, Sulfa, Enalapril,
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 11.05.2022
- Impfdatum
- 10.05.2022
- Beginn
- 10.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Symptomtext
Pt came in asking for second booster and received booster dose. However, patient is not eligible for second booster at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 10.05.2022
- Impfdatum
- 10.05.2022
- Beginn
- 10.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
Patient is 48 y/o and is not eligible for the second booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 16.04.2021
- Impfdatum
- 26.03.2021
- Beginn
- 06.04.2021
- Tage bis Beginn
- 11,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Tinnitus
Symptomtext
Tinnitus both ears 10 days after 2 vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tinnitus
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Common vitamin Probiotic Hair vitamin
- Allergien
- Slight allergy to more than 1 egg & more than 1 piece of bread in a day
- Vorherige Impfungen
- -