- Staat
- -
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 31.07.2023
- Impfdatum
- 20.10.2022
- Beginn
- 23.04.2023
- Tage bis Beginn
- 185,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute respiratory failure
Chronic obstructive pulmonary disease
Condition aggravated
Symptomtext
J96.01 ACUTE HYPOXEMIC RESPIRATORY FAILURE 4/23/2023 ACUTE EXACERBATION OF COPD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 19.07.2023
- Impfdatum
- 06.10.2022
- Beginn
- 02.03.2023
- Tage bis Beginn
- 147,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Hypoxia
Symptomtext
ACUTE HYPOXEMIC RESPIRATORY FAILURE HYPOXEMIA
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 18.07.2023
- Impfdatum
- 08.10.2022
- Beginn
- 15.03.2023
- Tage bis Beginn
- 158,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Symptomtext
ACUTE HYPOXEMIC RESPIRATORY FAILURE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 18.07.2023
- Impfdatum
- 11.10.2022
- Beginn
- 04.02.2023
- Tage bis Beginn
- 116,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Cardiogenic shock
Symptom recurrence
Symptomtext
ACUTE RESPIRATORY FAILURE CARDIOGENIC SHOCK 2/20/2023 -- RECURRENCE OF HOSPITALIZATION WITH SAME SYMPTOMS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 17.07.2023
- Impfdatum
- 13.10.2022
- Beginn
- 31.12.2022
- Tage bis Beginn
- 79,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Symptomtext
ACUTE HYPOXEMIC RESPIRATORY FAILURE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 17.07.2023
- Impfdatum
- 13.10.2022
- Beginn
- 08.03.2023
- Tage bis Beginn
- 146,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Symptomtext
ACUTE HYPOXEMIC RESPIRATORY FAILURE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 14.07.2023
- Impfdatum
- 26.10.2022
- Beginn
- 17.04.2023
- Tage bis Beginn
- 173,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cerebrovascular accident
Hemiparesis
Hemiplegia
Ischaemic stroke
Symptomtext
ACUTE STROKE, UNSPECIFIED TYPE AND ARTERY 4/29/2023 HEMIPLEGIA & HEMIPARESIS, RIGHT DOMINANT SIDE, LATE EFFECT OF ISCHEMIC STROKE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 90,0
- Geschlecht
- F
- Eingang
- 13.07.2023
- Impfdatum
- 22.10.2022
- Beginn
- 08.01.2023
- Tage bis Beginn
- 78,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Respiratory failure
Symptomtext
ACUTE ON CHRONIC HYPOXEMIC 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
- 71,0
- Geschlecht
- F
- Eingang
- 12.07.2023
- Impfdatum
- 26.10.2022
- Beginn
- 01.03.2023
- Tage bis Beginn
- 126,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Symptomtext
ACUTE HYPOXEMIC RESPIRATORY FAILURE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 84,0
- Geschlecht
- M
- Eingang
- 11.07.2023
- Impfdatum
- 28.10.2022
- Beginn
- 07.02.2023
- Tage bis Beginn
- 102,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute myocardial infarction
Symptom recurrence
Symptomtext
ACUTE NON ST ELEVATION MI 2/1/2023 -- 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
- 91,0
- Geschlecht
- M
- Eingang
- 11.07.2023
- Impfdatum
- 31.10.2022
- Beginn
- 15.02.2023
- Tage bis Beginn
- 107,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute myocardial infarction
Symptomtext
ACUTE NON ST ELEVATION MI
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 07.07.2023
- Impfdatum
- 10.11.2022
- Beginn
- 13.01.2023
- Tage bis Beginn
- 64,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Pulmonary embolism
Symptomtext
ACUTE PULMONARY EMBOLISM
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary embolism
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 07.07.2023
- Impfdatum
- 14.11.2022
- Beginn
- 01.02.2023
- Tage bis Beginn
- 79,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute myocardial infarction
Angioedema
Symptomtext
ACUTE NON ST ELEVATION MI ANGIOEDEMA, INIT
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
- 29.06.2023
- Impfdatum
- 23.12.2022
- Beginn
- 31.01.2023
- Tage bis Beginn
- 39,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Pulmonary embolism
Symptomtext
ACUTE PULMONARY EMBOLISM
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary embolism
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 29.06.2023
- Impfdatum
- 27.12.2022
- Beginn
- 03.02.2023
- Tage bis Beginn
- 38,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Chronic respiratory failure
Respiratory failure
Symptomtext
ACUTE HYPOXEMIC RESPIRATORY FAILURE CHRONIC HYPOXEMIC RESPIRATORY FAILURE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 23.06.2023
- Impfdatum
- 21.10.2022
- Beginn
- 14.12.2022
- Tage bis Beginn
- 54,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute myocardial infarction
Epilepsy
Symptomtext
EPILEPSY, UNSPECIFIED ACUTE NON ST ELEVATION MI
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 22.06.2023
- Impfdatum
- 29.10.2022
- Beginn
- 17.04.2023
- Tage bis Beginn
- 170,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute myocardial infarction
Cerebrovascular accident
Symptomtext
ACUTE ST ELEVATION MI, UNSPECIFIED 4/18/2023 ACUTE MI ACUTE MI 4/17/2023 ACUTE MI ACUTE STROKE, UNSPECIFIED TYPE AND ARTERY 4/18/2023 ACUTE MI
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 20.06.2023
- Impfdatum
- 10.10.2022
- Beginn
- 22.03.2023
- Tage bis Beginn
- 163,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Dementia
Dyspnoea
Lung infiltration
Pyrexia
SARS-CoV-2 test positive
Septic shock
Symptomtext
The patient has a history of Down's syndrome and Alzheimer's. He was brought to the ED by EMS from his adult foster care home on 3/22/23 with a fever and shortness of breath. On EMS arrival, the patient had O2 saturations of 85% on room air; this improved to 100% after the patient was placed on 10L O2 by non-rebreater. A COVID-19 rapid PCR test performed in the ED resulted positive. Ultimately the patient was admitted 3/22/23 - 3/24/23. Discharge diagnoses include end stage dementia, left lower lobe infiltrate, septic shock, and COVID-19. Of note, the patient has received the primary COVID vaccine series and three boosters.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Septic shock
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 13.06.2023
- Impfdatum
- 02.11.2022
- Beginn
- 31.03.2023
- Tage bis Beginn
- 149,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute respiratory failure
Asthma-chronic obstructive pulmonary disease overlap syndrome
Symptomtext
J96.00 ACUTE RESPIRATORY FAILURE 3/31/2023 ASTHMA COPD OVERLAP SYNDROME (ASTHMA W COPD) J96.00 ACUTE RESPIRATORY FAILURE 3/31/2023 ACUTE RESPIRATORY FAILURE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 08.06.2023
- Impfdatum
- 12.10.2022
- Beginn
- 09.12.2022
- Tage bis Beginn
- 58,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Symptomtext
ACUTE HYPOXEMIC RESPIRATORY FAILURE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 07.06.2023
- Impfdatum
- 14.10.2022
- Beginn
- 13.04.2023
- Tage bis Beginn
- 181,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute myocardial infarction
Cirrhosis alcoholic
Hypotension
Symptomtext
ACUTE NON ST ELEVATION MI 4/13/2023 ALCOHOLIC CIRRHOSIS HYPOTENSION 4/21/2023 ALCOHOLIC CIRRHOSIS ACUTE NON ST ELEVATION MI 4/13/2023 ALCOHOLIC CIRRHOSIS HYPOTENSION 4/21/2023 ALCOHOLIC CIRRHOSIS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 94,0
- Geschlecht
- F
- Eingang
- 02.06.2023
- Impfdatum
- 12.10.2022
- Beginn
- 06.11.2022
- Tage bis Beginn
- 25,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute respiratory failure
Hyperkalaemia
Hypernatraemia
Respiratory failure
Symptomtext
ACUTE HYPERCAPNIC RESPIRATORY FAILURE 11/6/2022 HYPERNATREMIA RESPIRATORY FAILURE, UNSPECIFIED ACUITY 11/30/2022 HYPERNATREMIA ACUTE HYPERCAPNIC RESPIRATORY FAILURE 11/6/2022 HYPERKALEMIA RESPIRATORY FAILURE, UNSPECIFIED ACUITY 11/30/2022 HYPERKALEMIA
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
- 02.06.2023
- Impfdatum
- 23.01.2023
- Beginn
- 14.02.2023
- Tage bis Beginn
- 22,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Symptomtext
ACUTE HYPOXEMIC RESPIRATORY FAILURE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 23.05.2023
- Impfdatum
- 15.10.2022
- Beginn
- 30.10.2022
- Tage bis Beginn
- 15,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute myocardial infarction
Symptomtext
ACUTE NON ST ELEVATION MI
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 13.12.2022
- Impfdatum
- 08.10.2022
- Beginn
- 11.12.2022
- Tage bis Beginn
- 64,0
- Dosis
- 5
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Alanine aminotransferase increased
Anion gap
Antidepressant drug level
Aspartate aminotransferase increased
Bacterial test positive
Barbiturates negative
Basophil count decreased
Basophil percentage decreased
Benzodiazepine drug level
Bilirubin urine
Bladder scan
Blood albumin normal
Blood alkaline phosphatase normal
Blood bilirubin normal
Blood calcium normal
Blood cannabinoids
Blood chloride normal
Blood creatinine normal
Symptomtext
Document Type: History and Physical Document Subject: History & Physical Note Performed By: DO on December 12, 2022 00:58 EST Verified By: DO on December 12, 2022 00:58 EST Encounter Info: Hospital, Observation, 12/11/22 - * Final Report * Chief Complaint vomiting History of Present Illness/Subjective Patient presented to hospital ED due to vomiting that began today. Patient is concerned that the vomitus appeared to be mixed with dark red material and given that she has also been dealing with chronic lower gi bleeding with a c-scope scheduled with Dr. next month she was concerned enough to come in. She also endorses SOB, dizziness. She denies CP, syncope, abd pain, dysuria. Denies blood thinners or history of upper GI bleeding prior. Add'l medical hx includes: HTN, HLD, psoriatic arthritis, IBS, Gilberts syndrome, hypothyroid, breast ca Social hx: former smoker In the ED patient met sirs criteria for sepsis cultures sent and abx started, patient incidentally tested positive for covid though other than some transient hypoxia is asymptomatic, she also had a UA positive for uti. She improved with ivf, We will place her in obs and transition to oral abx tomorrow if improving. Will also obtain gi consultation from Dr. in the am Note, per chart review, patient has a hx of pyelnephritis. Review of Systems A complete, 13-system review was performed and was negative except for as noted in the HPI. Physical Exam/Objective Vital Signs (most recent and range for last 24 hours) Temp (CEL) 37.2 (36.3-37.2) Temp (FAHR) 99.0 (97.3-99.0), BP 140/65 (140-173)/(65-92), HR 89 (84-111), RR 18 (18-24), O2Sat 90 (90-90) Neurologic (most recent and range for last 24 hours) GCS 15(15-15) Patient Weight Current Daily Weight: 76 kg 12/11/22 Previous Daily Weight: 76 kg 12/11/22 BMI: 27.9 12/11/22 Overweight (BMI 25-29.9) Patient Height Current Height: 165.1 cm 12/11/22 Constitutional: No acute distress, well-nourished Eyes: PERRL, EOMI, normal conjunctiva, no scleral icterus ENMT: Moist oral mucosa Neck: Supple, non-tender, intact range of motion Respiratory: Lungs have scattered crackles b/l in bases no wheezes, sat 93% on RA while in bed Cardiovascular: Regular rate and rhythm, no murmurs appreciated Gastrointestinal: Soft, non-tender, non-distended, rectal exam declined Musculoskeletal: No joint swelling, no deformity, intact ROM Integumentary: Intact, warm, dry no rashes Neurologic: Alert & Oriented x 3, no cognitive impairment, no focal deficits Psychiatric: Cooperative, appropriate mood and affect Assessment/Plan 1. Nausea & vomiting R11.2 zofran prn monitor qtc possibly 2/2 uti vs covid vs dyspepsia vs other given patient noted some dark red material in her vomit will obtain gi consultation in the am and start pantoprazole 40mg iv bid and keep on cld 2. Sepsis A41.9 likely 2/2 uti vs covid component, bacterial pna less likely sepsis now resolved after iv fluid admin, dehydration more likely culprit of initial tachycardia follow cultures, trend lactate until normalized 3. UTI (urinary tract infection) N39.0 follow culture rocephin monitor urine output due to hx of nephrolithiasis and pyelonephritis, will obtain a renal/bladder us however nothing to suggest obstructive uropathy or pyelonephritis at present time 4. COVID-19 U07.1 mild remdesivir resp eval and svns prn fluticasone inhaler 5. Dehydration E86.0 cont iv fluids 6. Chronic lower GI bleeding K92.2 see plan for #1 patient was scheduled for c-scope in january, will see if Dr. would like to do c-scope while here 7. Hyperglycemia R73.9 cont to monitor with accuchecks q12 hx of prediabetes will obtain a1c 8. Chronic GERD K21.9 see above 9. Hyperlipidemia E78.5 10. Hypothyroidism E03.9 11. Irritable bowel syndrome with diarrhea K58.0 12. Nephrolithiasis N20.0 13. Psoriatic arthritis L40.50 14. Gilbert's syndrome E80.4 noted. cont home medications as appropriate Orders: acetaminophen, 650 mg, Orally, Tablet, Q6H, PRN, Fever/Pain, Mild (1-3 out of 10), 12/12/22 0:03:00 EST albuterol-ipratropium, 3 mL, Neb Inhal, Inhalation SOLN, Aerosol Treatment, Q6H, PRN, Shortness of Breath/Wheezing, 12/12/22 0:02:00 EST ceftRIAXone, 1 GM, IVPB, Injection, Q24H, 12/12/22 19:00:00 EST, 12/12/22 19:00:00 EST, 100 mL/hr, Infuse Over 30 minutes, Total Volume (mL) = 50 fluticasone, 2 Puff, Inhalation, Aerosol, MDI/DPI Inhaler Treatment, BID, 12/12/22 9:00:00 EST, for 7 Days, 12/18/22 21:00:00 EST Lactated Ringers 1,000 mL, Total Volume (mL) = 1,000, IV, 12/12/22 0:02:00 EST, 100 mL/hr, Clinical Weight morphine, 2 mg, IV Push, Injection, Q4H, PRN, Pain Severe IV (7-10 out of 10), 12/12/22 0:02:00 EST ondansetron, 4 mg, IV Push, Injection, Q6H, PRN, Nausea/Vomiting IV - Use First, 12/12/22 0:02:00 EST pantoprazole, 40 mg, IV Push, Injection, BID, 12/12/22 9:00:00 EST remdesivir, 100 mg, IVPB, Injection, At Bedtime, 12/12/22 21:00:00 EST, for 4 Doses, 12/15/22 21:00:00 EST, 500 mL/hr, Infuse Over 30 minutes, Total Volume (mL) = 250 remdesivir, 200 mg, IVPB, Injection, ONCE, 12/12/22 1:00:00 EST, 12/12/22 1:00:00 EST, 500 mL/hr, Infuse Over 30 minutes, Total Volume (mL) = 250 Assign To Auto Diff Bladder Scan Call Blood Glucose Call Diastolic Blood Pressure Call Heart Rate Call Mental Status Changes Call O2 Saturation Call Oxygen Need Greater Than Call Respiratory Distress Call Respiratory Rate Call Systolic Blood Pressure Call Temperature Call Urine Output CBC w/Differential CBC w/Differential Clear Liquid no Red or Purple Diet Comp Metabolic Panel Comp Metabolic Panel DC SIRS Alert and Sepsis Screen Do Not (Specify) Gluc-Strip POC Hgb A1C HPLC Bld QN Initiate IV Care Protocols As Appropriate Initiate Mobility Protocol Initiate Protocol Initiate Skin and Wound Care Protocol Intake + Output Strict L pneumophila Ag Ur QL Lactate Pl Venous QN Level of Care Lipid Panel SerPl QN Magnesium SerPl QN Magnesium SerPl QN Medical Service Peripheral IV Insertion Procalcitonin Reason for Not Ordering Medication Prophylaxis Resp Evaluation or Assessment Resuscitation Status Sequential Compression Device Single Oxygen Saturation Strep pneumoniae Ag Urine Telemetry Class III 24hr Recommendation TSH w FreeT4 reflex Urine CX US Renal and Bladder Vital Signs Vital Signs Weight Weight Code Status Resuscitation Status - Ordered -- 12/12/22 0:02:00 EST, Full Code Chronic Problem List Breast cancer Chronic GERD Degenerative arthritis of ankle Depressive disorder Diarrhea Diverticulosis Gilbert's syndrome Hyperlipidemia Hypothyroidism Irritable bowel syndrome with diarrhea Multiple joint pain Nephrolithiasis PA (psoriatic arthritis) Prehypertension Rectal bleeding Trochanteric bursitis Weight gain Procedure/Surgical History ?Kidney Stone Removal (09/27/2020) ?colonoscopy (11/07/2017) ?egd (11/07/2017) ?Lumpectomy (07/01/2015) ?uterine ablation (2014) ?EGD and Colonoscopy w/ antrum and colon polyp from sigmoid bx (01/23/2007) ?Colonoscopy (2004) ?Dilation and Curettage (2002) ?Carpal Tunnel Repair (1992) ?back surgery for scoliosis and low grade spinal bifida (1979) ?ovaries removed ?Removal of both fallopian tubes ?Sling procedure of bladder neck ?oophorectomy-left Surgical History Internal 09/03/2020 Ureteroscopy. (Right) MD 08/27/2020 Cystoscopy Insert Ureteral Stent or Cath (Right) MD 08/05/2015 Breast Axillary Excision Biopsy (Left) MD 07/07/2015 Breast Excision Biopsy (Left) MD Medications Home Medications (17) Active alendronate 35 mg oral tablet 35 mg = 1 Tablet, Orally, Weekly, with 6-8 oz plain water, at least 30 minutes before first food, beverage, or medication of the day. aripiprazole 5 mg oral tablet See Instructions, 1/2 Tablet Orally Daily Calcium 500+D 1 Tablet, Orally, QAM chromium picolinate 1 Tablet, Orally, QAM Colestid 1 g oral tablet 1 GM = 1 Tablet, PRN, Orally, BID, Take 1 tablet 1 to 2 times daily desvenlafaxine 100 mg oral tablet, extended release 100 mg = 1 Tablet, Orally, QAM Fish Oil 1,000 mg, Orally, QAM folic acid 1 mg oral tablet 1 mg = 1 Tablet, Orally, QAM GaviLyte-G oral powder for reconstitution See Instructions, as directed letrozole 2.5 mg oral tablet 1 Tablet, Orally, Daily levothyroxine 100 mCg (0.1 mg) oral tablet 100 mCg = 1 Tablet, Orally, QAM metoPROLOL succinate 50 mg oral tablet, extended release 50 mg = 1 Tablet, Orally, QAM nitroGLYCerin 0.4 mg sublingual tablet 0.4 mg = 1 Tablet, PRN, Sublingually, Q5min prazosin 2 mg oral capsule 4 mg = 2 Capsule, Orally, QHS Viberzi 100 mg oral tablet 100 mg, Orally, BID Vitamin B-12 500 mCg, Orally vitamin E 400 intl units oral capsule 400 IntlUnits = 1 Capsule, Orally, Daily Active Scheduled Inpatient Medications ceftRIAXone, Injection, 1 GM, IVPB, Q24H, Start: 12/12/22 19:00:00 fluticasone (fluticasone HFA 220 mCg/inh), Aerosol, 2 Puff, Inhalation, BID, Start: 12/12/22 09:00:00 pantoprazole, Injection, 40 mg, IV Push, BID, Start: 12/12/22 09:00:00 remdesivir, Injection, 200 mg, IVPB, ONCE, Start: 12/12/22 01:00:00 remdesivir, Injection, 100 mg, IVPB, At Bedtime, Start: 12/12/22 21:00:00 Lactated Ringers 1,000 mL IV 100 mL/hr One-Time Medications Given 12/11/22 00:00:00 TO 12/12/22 00:36:33 ceftRIAXone, Injection, 1 GM, IV Push, ONCE, (1 DOSE 12/11/22 19:17:00) droperidol, Injection, 1.25 mg, IV Push, ONCE, (1 DOSE 12/11/22 21:34:00) ondansetron, Injection, 4 mg, IV Push, ONCE, prn, Nausea/Vomiting IV - Use First, (1 DOSE 12/11/22 17:46:00) ondansetron, Injection, 4 mg, IV Push, ONCE, (1 DOSE 12/11/22 20:57:00) promethazine, Injection, 25 mg, IVPB, ONCE, (1 DOSE 12/11/22 19:17:00) Sodium Chloride 0.9% (Sodium Chloride 0.9% - ED Bolus), Infusion, 1,000 mL, IVPB, ONCE, (1 DOSE 12/11/22 19:17:00) Sodium Chloride 0.9% (Sodium Chloride 0.9% - ED Bolus), Infusion, 1,000 mL, IVPB, ONCE, (1 DOSE 12/11/22 20:57:00) PRN Medications (0600 - 0559) from 12/11 - 12/12 acetaminophen, 650 mg, Orally, Q6H, 0 Dose(s) albuterol-ipratropium, 3 mL, Neb Inhal, Q6H, 0 Dose(s) morphine, 2 mg, IV Push, Q4H, 0 Dose(s) ondansetron, 4 mg, IV Push, Q6H, 1 Dose(s) Allergies Duragesic (unknown) tricyclic antidepressants (unknown) Butrans (Unknown) CeleBREX (Unknown) Cymbalta (Weight Gain, Anxiety) Ibu (Unknown) Suboxone (Unknown) Vicodin (Unknown) Voltaren (Unknown) Wellbutrin (Anxiety) carisoprodol (Unknown) codeine (Unknown) cyclobenzaprine (Unknown) fentaNYL (Unknown) meloxicam (Unknown) meperidine (Unknown) methadone (Unknown) methotrexate (Rash and vomiting) naltrexone (Unknown) oxyCODONE (Unknown) sulfa drugs (Nausea) tetracyclic antidepressants (Unknown) traMADol (Unknown) Social History Alcohol Current, 1-2 times per week Electronic Cigarette/Vaping E-Cigarette Use Never. Substance Abuse Denies Tobacco Tobacco Use: Former smoker, quit more than 30 days ago. Family History Cancer involving organ by direct extension from uterine cervix: Mother. Cancer of colon: Father. Lung cancer..: Grandmother. Throat: Aunt. Thyroid: Brother. Thyroid cancer: Brother. Lab Results All Labs Last 24 hours (No Micro or Pathology) Hematology: WBC: 9.4 k/cumm (12/11/22 17:45:00) RBC: 5.27 million/cumm High (12/11/22 17:45:00) Hgb: 17.4 GM/dL High (12/11/22 17:45:00) Hct: 50.8 % High (12/11/22 17:45:00) MCV: 97 fL (12/11/22 17:45:00) MCH: 33 pg (12/11/22 17:45:00) MCHC: 34.2 GM/dL (12/11/22 17:45:00) RDW: 13.4 % (12/11/22 17:45:00) Platelet: 295 k/cumm (12/11/22 17:45:00) MPV: 7.8 fL (12/11/22 17:45:00) Neutrophils %: 60 % (12/11/22 17:45:00) Lymphocytes %: 34 % (12/11/22 17:45:00) Monocytes %: 6 % (12/11/22 17:45:00) Eosinophils %: 0 % (12/11/22 17:45:00) Basophils %: 0 % (12/11/22 17:45:00) Absolute Neutrophil: 5.7 k/cumm (12/11/22 17:45:00) Absolute Lymphocyte: 3.2 k/cumm (12/11/22 17:45:00) Absolute Monocyte: 0.6 k/cumm (12/11/22 17:45:00) Absolute Eosinophil: 0 k/cumm (12/11/22 17:45:00) Absolute Basophil: 0 k/cumm (12/11/22 17:45:00) Chemistry: Sodium SerPl QN: 139 mmol/L (12/11/22 17:45:00) Potassium SerPl QN: 4.2 mmol/L (12/11/22 17:45:00) Chloride SerPl QN: 100 mmol/L (12/11/22 17:45:00) Carbon Dioxide SerPl QN: 20 mmol/L Low (12/11/22 17:45:00) Anion Gap: 19 mmol/L High (12/11/22 17:45:00) BUN SerPl QN: 23 mg/dL High (12/11/22 17:45:00) Creatinine SerPl QN: 0.93 mg/dL (12/11/22 17:45:00) Estimated GFR (CKD-EPI, no race): 73 mL/min/1.73m2 (12/11/22 17:45:00) Estimated CRCL (CG): 70 mL/min (12/11/22 17:45:00) Glucose SerPl QN: 141 mg/dL High (12/11/22 17:45:00) Calcium Total SerPl QN: 9.1 mg/dL (12/11/22 17:45:00) Alkaline Phos SerPl QN: 101 Units/L (12/11/22 17:45:00) ALT SerPl QN: 72 Units/L High (12/11/22 17:45:00) AST SerPl QN: 58 Units/L High (12/11/22 17:45:00) Bilirubin Total SerPl QN: 1 mg/dL (12/11/22 17:45:00) Total Protein SerPl QN: 6.9 GM/dL (12/11/22 17:45:00) Albumin SerPl QN: 4.5 GM/dL (12/11/22 17:45:00) Lipase SerPl QN: 76 Units/L High (12/11/22 17:45:00) Troponin-I High Sensitivity: 7 ng/L (12/11/22 19:32:00) BNP Pl QN: 14 pg/mL (12/11/22 18:51:00) Lactate Venous Pl QN: 3.5 mmol/L High (12/11/22 21:20:00) Coagulation: PT: 13.4 seconds (12/11/22 17:45:00) INR: 1.17 (12/11/22 17:45:00) D-Dimer Pl QN: <200 (12/11/22 18:51:00) Urine Studies: Color: Yellow (12/11/22 19:20:00) Clarity: Clear (12/11/22 19:20:00) Specific Gravity: >=1.030 (12/11/22 19:20:00) pH: 5.5 (12/11/22 19:20:00) Protein: NEGATIVE (12/11/22 19:20:00) Glucose: NEGATIVE (12/11/22 19:20:00) Ketones: NEGATIVE (12/11/22 19:20:00) Bilirubin: NEGATIVE (12/11/22 19:20:00) Hgb Ur: TRACE. Abnormal (12/11/22 19:20:00) Nitrite: POSITIVE Abnormal (12/11/22 19:20:00) Urobilinogen: NormalUro (12/11/22 19:20:00) Leukocyte Esterase Ur: TRACE. Abnormal (12/11/22 19:20:00) WBC: 11-20 Abnormal (12/11/22 19:20:00) RBC: 3-5 Abnormal (12/11/22 19:20:00) Bacteria: Few Abnormal (12/11/22 19:20:00) Squamous Epithelial: Few (12/11/22 19:20:00) Mucous: PRESENT. (12/11/22 19:20:00) Toxicology: Amphetamine Urine Scn QL: Negative (12/11/22 19:20:00) Methamphetamine Urine Scn QL: Negative (12/11/22 19:20:00) Barbiturates Urine Scn QL: Negative (12/11/22 19:20:00) Benzodiazepines Urine Scn QL: Negative (12/11/22 19:20:00) Cannabinoid Urine Scn QL: Negative (12/11/22 19:20:00) Cocaine Urine Scn QL: Negative (12/11/22 19:20:00) Opiates Urine Scn QL: Negative (12/11/22 19:20:00) PCP Urine Scn QL: Negative (12/11/22 19:20:00) Methadone Urine Scn QL: Negative (12/11/22 19:20:00) Propoxyphene Urine Scn QL: Negative (12/11/22 19:20:00) Oxycodone Urine Scn QL: Negative (12/11/22 19:20:00) Buprenorphine Urine Scn QL: Negative (12/11/22 19:20:00) Tricyclic Antid Urine Scn QL: Negative (12/11/22 19:20:00) Drugs of Abuse Comment: See Comment (12/11/22 19:20:00) Ethanol Pl QN: 94 mg/dL (12/11/22 19:32:00) All Other Labs: COVID 19 Specimen Source: Nasal (12/11/22 17:51:00) Coronavirus SARS-CoV2 Rapid: Detected Abnormal (12/11/22 17:51:00) Micro - Last 7 days Rapid Influenza Method: PCR - Liat (12/11/22 17:51:00) Rapid Influenza A PCR: Not Detected (12/11/22 17:51:00) Rapid Influenza B PCR: Not Detected (12/11/22 17:51:00) Diagnostics Radiology Results - Last 24 hours Across Visits 12/11/2022 19:11 - XR Chest PA or AP IMPRESSION: No acute findings. Thank you for consulting with Radiology. Healthcare providers wishing to discuss this case further can contact the ER Reading Room. Signature Line Electronically Signed on 12/12/22 00:58 EST DO
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Coma scale
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 07.12.2022
- Impfdatum
- 12.10.2022
- Beginn
- 01.12.2022
- Tage bis Beginn
- 50,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
COVID-19
COVID-19 pneumonia
SARS-CoV-2 test positive
Symptomtext
Patient received Moderna COVID vaccine on 2/8/21, 3/8/21, 9/9/21 and Moderna bivalent COVID vaccine on 10/12/22. On 12/1/22, patient admitted to our inpatient facility (med/surg unit) for acute hypoxic respiratory failure due to COVID-19 pneumonia. As of today 12/7/22, patient is still admitted in the med/surg unit.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 6,0
- Labordaten
- COVID status positive 12/1/22.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- SNF resident with history of hypertension, hyperlipidemia, metastatic prostate cancer with dural mets s/p resection on November 2022, peripheral arterial disease, basal cell carcinoma of his forehead, seizure disorder, anemia of chronic disease
- Andere Medikamente
- abiraterone, acetaminophen, albuterol inhaler, aspirin ec 81mg, atorvastatin, bisacodyl supp, lacosamide, Ensure, levetiracetam, melatonin, ondansetron, pantoprazole, potassium chloride, propranolol, Fleet enema, sorbitol 70% soln
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 10.05.2023
- Impfdatum
- 05.10.2022
- Beginn
- 19.04.2023
- Tage bis Beginn
- 196,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Anticoagulant therapy
Computerised tomogram thorax abnormal
Cough
Dyspnoea
Echocardiogram normal
Fibrin D dimer increased
Pulmonary thrombosis
Scan with contrast abnormal
Thrombosis
Ultrasound Doppler abnormal
Symptomtext
I was travelling out of state. A few days before that, I noticed being short of breath and I had some coughing. After around 3 days of that getting worse, I wound up going to the emergency room. The doctor asked all the right questions, and the D-Dimer test came back with some concerns. They did a CT scan with contrast and came back with some indication of blood clots. The next day, the informed me that I did have blood clots that began in my legs and travelled to my lungs. I spent 3 days in the hospital on a Heparin I.V. I was release and was still on oxygen. I was informed that had I not come in, it could have been life threatening. They advised that we travel home very slowly. We only did 3 hours of driving a day and stopped frequently. I am now on Eliquis for the next 6 months.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary thrombosis
- Hospital-Tage
- 3,0
- Labordaten
- 19APR2023 - D-Dimer Test - Indication Of Blood Clots; CT scan With Contrast - Blood Clots Found; Echocardiogram - Nothing Abnormal Found; Ultrasound Of Sound - Confirmed Blood Clots
- Aktuelle Erkrankungen
- Upper Respiratory Infection
- Vorgeschichte
- Rheumatoid Arthritis
- Andere Medikamente
- Amlodipine; Baby Aspirin; Vitamin D3; Coreg; Nexium; Folic Acid; Methotrexate; Multivitamin; Crestor; Diovan
- Allergien
- Ciprofloxacin; Flagyl
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 08.03.2023
- Impfdatum
- 23.01.2021
- Beginn
- 02.03.2021
- Tage bis Beginn
- 38,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Alopecia
Dizziness
Hypotrichosis
Inappropriate schedule of product administration
Injection site pain
Madarosis
Loss of consciousness
Nasopharyngitis
SARS-CoV-2 test negative
Suspected COVID-19
Symptomtext
lost Facial Hair as well; bad cold; some thinning of his hair after the first booster dose; Patient reports adverse Reactions of a sore left injection site arm.; Suspected COVID-19; passed out; felt light headed; first Moderna Covid 19 vaccine primary series on January 23,2021 and second dose on March 2, 2021; This spontaneous case was reported by a pharmacist and describes the occurrence of LOSS OF CONSCIOUSNESS (passed out) in a 56-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 067F21A, 032L20A and 013A21A) for COVID-19 prophylaxis. The occurrence of additional non-serious events is detailed below. No medical history was reported by the reporter. Concomitant products included ATORVASTATIN, TADALAFIL, FISH OIL, VITAMINS NOS (MVI [VITAMINS NOS]), BIOTIN and TADALAFIL (CIALIS) for an unknown indication. On 23-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 02-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 17-Nov-2021, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 02-Mar-2021, the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (first Moderna Covid 19 vaccine primary series on January 23,2021 and second dose on March 2, 2021). On 03-Mar-2021, the patient experienced LOSS OF CONSCIOUSNESS (passed out) (seriousness criterion medically significant) and DIZZINESS (felt light headed). On an unknown date, the patient experienced HYPOTRICHOSIS (lost Facial Hair as well), NASOPHARYNGITIS (bad cold), ALOPECIA (some thinning of his hair after the first booster dose), VACCINATION SITE PAIN (Patient reports adverse Reactions of a sore left injection site arm.) and SUSPECTED COVID-19 (Suspected COVID-19). At the time of the report, LOSS OF CONSCIOUSNESS (passed out), NASOPHARYNGITIS (bad cold), DIZZINESS (felt light headed), VACCINATION SITE PAIN (Patient reports adverse Reactions of a sore left injection site arm.), SUSPECTED COVID-19 (Suspected COVID-19) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (first Moderna Covid 19 vaccine primary series on January 23,2021 and second dose on March 2, 2021) outcome was unknown, HYPOTRICHOSIS (lost Facial Hair as well) had not resolved and ALOPECIA (some thinning of his hair after the first booster dose) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In November 2021, SARS-CoV-2 test: Negative. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Patient also took antioxidant combination for unknown indication. Patient also suspected a possibility of a Covid-19 infection after his first booster dose at the end of November 2021. Patient tested for COVID-19 and it came back negative however patient thought that he may have tested too early and he did not test again as he thought that it was a bad cold. On 14-Oct-2022, the patient received MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5) additional booster dose (Lot number 053D22A) in the left arm. Treatment details was not reported by the reporter. Company comment: This spontaneous case concerns a 56-year-old male patient, with no medical history reported, who experienced the unexpected, serious (medically significant) events of LOSS OF CONSCIOUSNESS on the following day of the second dose of mRNA-1273 vaccine, among other non-serious events. He woke up on the following day of vaccination feeling lightheaded and he passed out. He felt better quickly after resting. No further clinical information was available for medical review. Inappropriate schedule of vaccine administration was also noted, primary vaccination series was administered in a 38-day interval. The benefit-risk relationship of the mRNA-1273 vaccine is not affected by this report. This case was linked to MOD-2023-713956 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- Test Date: 202111; Test Name: Covid-19; Test Result: Negative
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: No medical history was reported by the reporter.
- Andere Medikamente
- ATORVASTATIN; TADALAFIL; FISH OIL; MVI [VITAMINS NOS]; BIOTIN; CIALIS
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 08.03.2023
- Impfdatum
- 23.01.2021
- Beginn
- 02.03.2021
- Tage bis Beginn
- 38,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Alopecia
Dizziness
Hypotrichosis
Inappropriate schedule of product administration
Injection site pain
Madarosis
Loss of consciousness
Nasopharyngitis
SARS-CoV-2 test negative
Suspected COVID-19
Symptomtext
lost Facial Hair as well; bad cold; some thinning of his hair after the first booster dose; Patient reports adverse Reactions of a sore left injection site arm.; Suspected COVID-19; passed out; felt light headed; first Moderna Covid 19 vaccine primary series on January 23,2021 and second dose on March 2, 2021; This spontaneous case was reported by a pharmacist and describes the occurrence of LOSS OF CONSCIOUSNESS (passed out) in a 56-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 067F21A, 032L20A and 013A21A) for COVID-19 prophylaxis. The occurrence of additional non-serious events is detailed below. No medical history was reported by the reporter. Concomitant products included ATORVASTATIN, TADALAFIL, FISH OIL, VITAMINS NOS (MVI [VITAMINS NOS]), BIOTIN and TADALAFIL (CIALIS) for an unknown indication. On 23-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 02-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 17-Nov-2021, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 02-Mar-2021, the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (first Moderna Covid 19 vaccine primary series on January 23,2021 and second dose on March 2, 2021). On 03-Mar-2021, the patient experienced LOSS OF CONSCIOUSNESS (passed out) (seriousness criterion medically significant) and DIZZINESS (felt light headed). On an unknown date, the patient experienced HYPOTRICHOSIS (lost Facial Hair as well), NASOPHARYNGITIS (bad cold), ALOPECIA (some thinning of his hair after the first booster dose), VACCINATION SITE PAIN (Patient reports adverse Reactions of a sore left injection site arm.) and SUSPECTED COVID-19 (Suspected COVID-19). At the time of the report, LOSS OF CONSCIOUSNESS (passed out), NASOPHARYNGITIS (bad cold), DIZZINESS (felt light headed), VACCINATION SITE PAIN (Patient reports adverse Reactions of a sore left injection site arm.), SUSPECTED COVID-19 (Suspected COVID-19) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (first Moderna Covid 19 vaccine primary series on January 23,2021 and second dose on March 2, 2021) outcome was unknown, HYPOTRICHOSIS (lost Facial Hair as well) had not resolved and ALOPECIA (some thinning of his hair after the first booster dose) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In November 2021, SARS-CoV-2 test: Negative. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Patient also took antioxidant combination for unknown indication. Patient also suspected a possibility of a Covid-19 infection after his first booster dose at the end of November 2021. Patient tested for COVID-19 and it came back negative however patient thought that he may have tested too early and he did not test again as he thought that it was a bad cold. On 14-Oct-2022, the patient received MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5) additional booster dose (Lot number 053D22A) in the left arm. Treatment details was not reported by the reporter. Company comment: This spontaneous case concerns a 56-year-old male patient, with no medical history reported, who experienced the unexpected, serious (medically significant) events of LOSS OF CONSCIOUSNESS on the following day of the second dose of mRNA-1273 vaccine, among other non-serious events. He woke up on the following day of vaccination feeling lightheaded and he passed out. He felt better quickly after resting. No further clinical information was available for medical review. Inappropriate schedule of vaccine administration was also noted, primary vaccination series was administered in a 38-day interval. The benefit-risk relationship of the mRNA-1273 vaccine is not affected by this report. This case was linked to MOD-2023-713956 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- Test Date: 202111; Test Name: Covid-19; Test Result: Negative
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: No medical history was reported by the reporter.
- Andere Medikamente
- ATORVASTATIN; TADALAFIL; FISH OIL; MVI [VITAMINS NOS]; BIOTIN; CIALIS
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 17.01.2023
- Impfdatum
- 14.10.2022
- Beginn
- 07.12.2022
- Tage bis Beginn
- 54,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cardiac function test normal
Myocarditis
Nasal congestion
Nasopharyngitis
Oropharyngeal pain
SARS-CoV-2 test positive
Troponin increased
Symptomtext
I received my Covid-19 vaccine on 10/14/2022. On the Morning of 12/07/2022 I woke up and tested positive for Covid-19. I had cold symptoms and nasal congestion with sore throat. Symptoms lasted a few days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocarditis
- Hospital-Tage
- -
- Labordaten
- Troponin level elevated; Covid PCR; Heart protocol test were clear. Diagnosis with Myocarditis.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Arthritis
- Andere Medikamente
- Calcium citrate; zinc; magnesium; glucosamine; vitamin C; omega 369; red yeast rice; vitamin B12; vitamin D3; melatonin; triple action joint health; aspirin
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 01.12.2022
- Impfdatum
- 21.10.2022
- Beginn
- 21.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Anticoagulant therapy
Chest pain
Computerised tomogram thorax abnormal
Embolism
Gene mutation identification test
Painful respiration
Symptomtext
The evening of receiving the vaccine, I began having extreme chest pain on the left side of my chest, significant pain when breathing, and eventually to urgent care and ER from there. They performed a CT scan and discovered three embolisms in my chest. They put me on blood thinners. I was admitted in the hospital for 36 hours before being discharged, and they prescribed me ELIQUIS for the time being for blood thinners and prevent clotting. I have a follow-up with a cardiologist in February to perform another CT scan to ensure the clots have resolved themselves and a genetic testing to see how the clots formed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Embolism
- Hospital-Tage
- 2,0
- Labordaten
- CT scans: 10/23/2022, 11/29/2022
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Daily multivitamin
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 04.11.2022
- Impfdatum
- 20.10.2022
- Beginn
- 20.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Ageusia
Blood pressure decreased
Blood test
Chills
Loss of consciousness
Pain in extremity
Pyrexia
Taste disorder
Symptomtext
It started with the usual pain in the arm that turned into severe chill. I had a really high fever of about 104.0 and everything was tasting different for me for about a week after the vaccine. Foods tasted like other foods, and I felt really lightheaded. I still have that quite often. My blood pressure is reading really low. While having blood work done, my blood pressure dropped extremely low around 90/60 and I passed out. They were not able to get any blood from me. They used ice packs and smelling salts to get me to come back to. I have been working from home since Monday due to this as I do out while having blood work done related to something else. They are afraid to get blood work from me and they are considering stopping the hydrochlorothiazide as they think it could be related to this. I am scheduling an appointment with a cardiologist. There were nights that I thought about going to the ER because the high fever did not break until after 6 days and the taste started to return after 7 or 8 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Blood Pressure; Kidney Stones
- Andere Medikamente
- Hydrochlorothiazide; potassium citrate; ramipril; CRESTOR; fish oil; vitamin D; olive leaf
- Allergien
- Egg yolk; wheat; DEMEROL
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 28.10.2022
- Impfdatum
- 12.10.2022
- Beginn
- 26.10.2022
- Tage bis Beginn
- 14,0
- Dosis
- 4
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal pain upper
Acute coronary syndrome
Alanine aminotransferase normal
Anion gap
Anticoagulant therapy
Aspartate aminotransferase normal
Atrioventricular block first degree
Auscultation
Bacterial test positive
Basophil count decreased
Basophil percentage decreased
Bilirubin urine
Blood albumin normal
Blood alkaline phosphatase normal
Blood bilirubin normal
Blood calcium normal
Blood chloride normal
Blood creatinine normal
Symptomtext
Document Type: ED Physician Progress Note Document Subject: ED Progress Note Performed By: Nurse Practitioner on October 26, 2022 18:52 Verified By: Nurse Practitioner on October 26, 2022 18:52 Encounter Info: Hospital, Emergency, 10/26/22 - 10/26/22 * Final Report * Basic Information Time Seen: Nurse Practitioner / 10/26/2022 15:45 Chief Complaint Chest pain (Complaint of) History of Present Illness Patient presents via private vehicle due to chest pain described as burning and heavy x 2 hours. On arrival he vomited x 1. Denies SOB, fever or cough. Patient is poor historian due to dementia. He was seen by his PCP today for a routine visit and no complaints at that time. Add'l medical hx includes: HTN, HLD, CAD, dementia, GERD, Social hx: non smoker, lives at home with spouse who is caregiver, DNI, comprehensive care Review of Systems Constitutional: Negative, No weakness, No fatigue, No decreased activity. Eye: Negative. Ear/Nose/Mouth/Throat: Negative. Respiratory: Negative. Cardiovascular: chest pain Gastrointestinal: vomiting Hematology/Lymphatics: Negative. Endocrine: Negative. Immunologic: Negative. Musculoskeletal: Negative. Integumentary: Negative. Neurologic: Negative. Psychiatric: No anxiety, No depression. All other systems are negative Physical Exam/Objective Vitals & Measurements last 24 hours VITAL SIGNS Temp C: 36.1 DegC Heart Rate: 53 bpm Resp Rate: 31 br/min BP #1: 127 / 70 mmHg SpO2 (%): 94 % O2 Device: Room air Height CM: 178 cm Weight KG: 84.2 kg Ideal Body Weight: 73.18 kg General: Poor historian, no acute distress Eye: Pupils are equal, round and reactive to light, Normal conjunctiva. HENT: Normocephalic, atraumatic Neck: Non-tender, No jugular venous distention, Cardiovascular: Regular rate, Normal rhythm, S1, S2. No LE edema Respiratory: Lungs are clear to auscultation, Respirations are non-labored. Gastrointestinal: Soft, Non-tender, Non-distended, Normal bowel sounds, Integumentary: Warm, Dry, Intact. Neurologic: Alert, Oriented, Normal sensory, Normal motor function, Psychiatric: Cooperative, Appropriate mood & affect. Medical Decision Making Diff: ACS, HTN emergency, gastritis, pancreatitis, hiatal hernia, esophageal spasm, GERD, Covid 19, costochondritis, pneumonia EKG Time completed: 1543 Rhythm: SB with 1st degree AV block Interp: SB with 1st degree AV block; RBBB, no STEMI; interpreted by doctor rate: 57 QT/QTC: 446/434 Med records reviewed: abnormal stress test in March 2021, cardiac cath completed in March 2021 40 % LAD, no intervention needed. Patient has been maintained on Metoprolol, asa 81 and Statin. Patient also maintained on omeprazole due to frequent complaint of lower chest pain v. epigastric pain that does not appear to be cardiac. Today his EKG is non ischemic, trop negative x 2, BNP unremarkable, ACS or cardiac etiology of current symptoms unlikely. Patient was hypertensive on arrival but BP normalized in department. Patient cannot recall if he has had his BP medication today. CXR suspicious for atypical infection v. pulmonary edema. Covid is negative. Collateral hx from spouse reveals worsening cough x 2-3 days without fever. Will DC to home with antibiotic coverage for atypical pneumonia and encourage medication compliance for GERD. Given patient's unremarkable labs and stable VS admission is not indicated. Condition stable Assessment/Plan 1. Pneumonia 2. HTN (hypertension) 3. GERD (gastroesophageal reflux disease) Orders: doxycycline, 100 mg, = 1 Capsule, Orally, BID, for 10 Days, Acute, Dispense: 20 Capsule, Refills: 0, Total Refills: 1, 10/26/22 17:19:00, 11/05/22 17:19:00 ketoROLAC, 15 mg, IV Push, Injection, ONCE, NOW, 10/26/22 18:51:00, 10/26/22 18:51:00 ondansetron, 4 mg, = 1 Tablet, Orally, Q6H, Maintenance, Dispense: 10 Tablet, Refills: 0, Total Refills: 1, 10/26/22 17:19:00 **Coronavirus SARS-CoV2 Rapid Auto Diff BNP Pl QN Cardiac Monitor CBC w/Differential Comp Metabolic Panel COVID 19 PCR Discharge Patient Electrocardiogram Lipase SerPl QN Peripheral IV Insertion Troponin-I High Sensitivity Troponin-I High Sensitivity UA Microscopic Urinalysis w Culture Rflx Urine CX XR Chest PA or AP Patient Education PNEUMONIA, ADULT Follow Up With When Contact Information doctor Within 3 to 5 days Additional Instructions: Antibiotics as prescribed for atypical pneumonia. Zofran as needed for nausea. Please be sure to continue your omeprazole as prescribed for GERD daily and continue all blood pressure medications as prescribed. If you develop any new or worsening symptoms please return to the ER. Chronic Problem List B12 deficiency Coronary artery disease Dementia DNI (do not intubate) Encounter for long-term current use of medication Erectile dysfunction GERD (gastroesophageal reflux disease) Hyperlipidemia Hypertension Kidney stones Ventral hernia Procedure/Surgical History ?cardiac catheterization (03/19/2021) ?History of kidney stones.. (2015) ?colonoscopy (09/24/2010) ?Appendectomy ?hernia Surgical History Internal 02/08/2022 Foreign Body Retrieval Medications Home Medications (11) Active aspirin 81 mg oral tablet, chewable 81 mg = 1 Tablet, Daily diclofenac sodium 50 mg oral delayed release tablet 50 mg = 1 Tablet, Orally, BID, with food doxycycline monohydrate 100 mg oral capsule 100 mg = 1 Capsule, Orally, BID hydroCHLOROthiazide 12.5 mg oral tablet 12.5 mg = 1 Tablet, Orally, Daily memantine 10 mg oral tablet 10 mg = 1 Tablet, Orally, BID metoPROLOL succinate 25 mg oral tablet, extended release 25 mg = 1 Tablet, Orally, Daily omeprazole 40 mg oral delayed release capsule 40 mg = 1 Capsule, Orally, Daily ProAir HFA 90 mCg/inh inhalation aerosol 2 Puff, PRN, Inhalation, 4 Times Daily rosuvastatin 5 mg oral tablet 5 mg = 1 Tablet, Orally, QHS Vitamin B12 1000 mCg oral tablet 1,000 mCg = 1 Tablet, Orally, Daily, sublingual Zofran ODT 4 mg oral tablet, disintegrating 4 mg = 1 Tablet, Orally, Q6H Medication Administration Given aluminum hydroxide-magnesium hydroxide-simethicone 200 mg-200 mg-20 mg/5 mL oral suspension, 30 mL, Orally aspirin, 324 mg, Orally doxycycline, 100 mg, Orally lidocaine 2% mucous membrane solution, 15 mL, Orally nitroGLYCerin, 0.4 mg, 0.4 mg, 0.4 mg, Sublingually ondansetron, 4 mg, IV Push Allergies Zocor (Unknown) sulfa drugs (Unknown) Social History Alcohol Current, Beer, 3-5 times per week Electronic Cigarette/Vaping E-Cigarette Use Never. Employment/School Home/Environment Tobacco Tobacco Use: Never (less than 100 in lifetime). Family History Heart attack..: Father. Skin cancer..: Grandfather. Lab Results Hemogram-Platelets-WBC Differential FS LATEST RESULTS HISTORICAL RESULTS WBC 10/26/22 16:03 8.5 10/26/22 7.5 RBC 10/26/22 16:03 5.66 High 10/26/22 5.72 High Hgb 10/26/22 16:03 16.5 10/26/22 16.6 Hct 10/26/22 16:03 49.6 10/26/22 50.0 MCV 10/26/22 16:03 88 10/26/22 87 MCH 10/26/22 16:03 29.2 10/26/22 29.0 MCHC 10/26/22 16:03 33.3 10/26/22 33.2 RDW 10/26/22 16:03 13.4 10/26/22 13.3 Platelet 10/26/22 16:03 193 10/26/22 197 MPV 10/26/22 16:03 7.9 10/26/22 8.2 Neutrophils % 10/26/22 16:03 57 10/26/22 60 Lymphocytes % 10/26/22 16:03 33 10/26/22 28 Monocytes % 10/26/22 16:03 9 10/26/22 10 Eosinophils % 10/26/22 16:03 2 10/26/22 2 Basophils % 10/26/22 16:03 0 10/26/22 0 Absolute Neutrophil 10/26/22 16:03 4.8 10/26/22 4.5 Absolute Lymphocyte 10/26/22 16:03 2.8 10/26/22 2.1 Absolute Monocyte 10/26/22 16:03 0.7 10/26/22 0.8 Absolute Eosinophil 10/26/22 16:03 0.1 10/26/22 0.1 Absolute Basophil 10/26/22 16:03 0.0 10/26/22 0.0 Routine Chemistry Tests FS LATEST RESULTS HISTORICAL RESULTS Sodium SerPl QN 10/26/22 16:03 138 10/26/22 142 Potassium SerPl QN 10/26/22 16:03 3.5 10/26/22 4.3 Chloride SerPl QN 10/26/22 16:03 103 10/26/22 101 Carbon Dioxide SerPl QN 10/26/22 16:03 27 10/26/22 31 High Anion Gap 10/26/22 16:03 8 10/26/22 10 BUN SerPl QN 10/26/22 16:03 20 10/26/22 18 Creatinine SerPl QN 10/26/22 16:03 1.08 10/26/22 1.00 Estimated GFR (CKD-EPI, no race) 10/26/22 16:03 69 10/26/22 76 Estimated CRCL (CG) 10/26/22 16:03 59 10/26/22 63 Glucose SerPl QN 10/26/22 16:03 137 High 10/26/22 90 Calcium Total SerPl QN 10/26/22 16:03 9.8 10/26/22 9.8 Alkaline Phos SerPl QN 10/26/22 16:03 55 10/26/22 53 ALT SerPl QN 10/26/22 16:03 15 10/26/22 16 AST SerPl QN 10/26/22 16:03 20 10/26/22 19 Bilirubin Total SerPl QN 10/26/22 16:03 0.4 10/26/22 0.7 Total Protein SerPl QN 10/26/22 16:03 7.0 10/26/22 7.3 Albumin SerPl QN 10/26/22 16:03 4.2 10/26/22 4.1 Lipase SerPl QN 10/26/22 16:03 59 Troponin-I High Sensitivity 10/26/22 17:24 5 BNP Pl QN 10/26/22 16:03 53 Urinalysis FS LATEST RESULTS HISTORICAL RESULTS Color 10/26/22 17:43 Yellow 05/31/21 Yellow Clarity 10/26/22 17:43 Clear 05/31/21 Slightly Cloudy Specific Gravity 10/26/22 17:43 1.025 05/31/21 1.024 pH 10/26/22 17:43 6.0 05/31/21 5.0 Protein 10/26/22 17:43 30 Abnormal 05/31/21 30 Abnormal Glucose 10/26/22 17:43 Negative 05/31/21 Normal Ketones 10/26/22 17:43 Negative 05/31/21 Negative Bilirubin 10/26/22 17:43 See Comment Abnormal 05/31/21 Negative Hgb Ur 10/26/22 17:43 Negative 05/31/21 Large Abnormal Nitrite 10/26/22 17:43 Negative 05/31/21 Negative Urobilinogen 10/26/22 17:43 Normal 05/31/21 Normal Leukocyte Esterase Ur 10/26/22 17:43 Trace Abnormal 05/31/21 Trace Abnormal WBC 10/26/22 17:43 51-100 Abnormal 05/31/21 6-10 Abnormal RBC 10/26/22 17:43 3-5 Abnormal 05/31/21 51-100 Abnormal Bacteria 10/26/22 17:43 Few Abnormal 05/31/21 Trace Squamous Epithelial 10/26/22 17:43 Few 05/31/21 Few Calcium Oxalate Crystals 10/26/22 17:43 Present Molecular Diagnostic Tests LATEST RESULTS HISTORICAL RESULTS COVID 19 Specimen Source 10/26/22 16:03 Nasopharyngeal 02/07/22 Nasopharyngeal Coronavirus SARS-CoV2 Rapid 10/26/22 16:03 Not Detected Diagnostic Results XR Chest PA or AP 10/26/22 16:30:24 IMPRESSION: 1. Perihilar and right basilar interstitial opacities. Differential diagnosis includes atypical infection and pulmonary edema.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary oedema
- Hospital-Tage
- -
- Labordaten
- Serology Tests * 0.26 ng/mL Molecular Diagnostic Tests COVID 19 Specimen Source Nasopharyngeal Coronavirus SARS-CoV2 Rapid * Not Detected Microbiology Studies - Bacterial Urine CX (+) POS In Progress (+) POS In Progress
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 26.10.2022
- Impfdatum
- 09.10.2022
- Beginn
- 10.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Anticoagulant therapy
Aspiration joint
Blood test
Blood uric acid increased
Condition aggravated
Gout
Impaired work ability
Joint injury
Joint swelling
Peripheral swelling
Thrombosis
Ultrasound Doppler abnormal
Weight bearing difficulty
X-ray normal
Symptomtext
The most adverse symptom was that my right leg swelled up and did not go away. I went to my doctor's office and they diagnosed blood clot by doing an ultrasound On Wednesday October 12, 2022. I was prescribed the blood thinner Eloquis, advised to modify my diet and get plenty of rest. I have since got worse and developed a new symptom where I could not put any weight on my leg and my knee swelled. I went to the doctor who sent me to the emergency room. The did several blood test and x-rays and drained the fluid out of my knee. I was diagnosed with Gout. I was prescribed Allopurinol and Colchicine and released after 10 hours. I went to work yesterday but woke up today swollen again and was not able to go to work. I have 2 follow ups at the end of the month. One is for an orthopedic doctor for my ankle as it is also swollen. It was an old injury that flared up pretty bad with everything else.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Thrombosis
- Hospital-Tage
- -
- Labordaten
- Ultrasound-October 12, 2022-blood clots found Blood Panels-October 18, 2022-High Uric acid X-Rays-October 18, 2022-Normal
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Atorvastatin; Lisinopril; Metoprolol
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 22.10.2022
- Impfdatum
- 22.10.2022
- Beginn
- 22.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Feeling abnormal
Head injury
Loss of consciousness
Symptomtext
Client passed out after receiving vaccine. Stated ? I felt weird and than blacked out?. Client hit head on floor when passed out
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- Vitals taken BP- 120/82, 72, 18. 911 notified and came and assessed client. Client left on her own without furry incident. Denies any pain, dizziness, itching, shortness of breath, blurred vision, or difficulty with ROM.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 18.10.2022
- Impfdatum
- 14.10.2022
- Beginn
- 14.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Confusional state
Dizziness
Fatigue
Flushing
Hyperhidrosis
Hypotension
Lethargy
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Confusion-Medium, Systemic: Dizziness / Lightheadness-Medium, Systemic: Exhaustion / Lethargy-Medium, Systemic: Fainting / Unresponsive-Medium, Systemic: Flushed / Sweating-Medium, Systemic: Hypotension-Medium, Additional Details: EMS came to store and took patient to hospital
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 18.10.2022
- Impfdatum
- 14.10.2022
- Beginn
- 14.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Loss of consciousness
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Severe, Additional Details: Patient passed out about 3 minutes afte receiving both vaccines. Informed us he didn't eat in the morning. Once passed out when giving blood.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 17.10.2022
- Impfdatum
- 10.10.2022
- Beginn
- 10.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Seizure
Syncope
Symptomtext
After receiving both vaccines patient felt light-headed then fainted and had convulsions for a few seconds and then came back to consciousness and was coherent and felt fine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 16.10.2022
- Impfdatum
- 10.10.2022
- Beginn
- 10.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Flushing
Headache
Hyperhidrosis
Nausea
Seizure
Vomiting
Symptomtext
Systemic: Flushed / Sweating-Medium, Systemic: Headache-Medium, Systemic: Nausea-Medium, Systemic: Seizure-Mild, Systemic: Vomiting-Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 13.10.2022
- Impfdatum
- 09.10.2022
- Beginn
- 09.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Seizure
Symptomtext
Systemic: Seizure-Medium, Additional Details: Patient has no history of seizures or other neurological disorders. Patient had a seizure lasting approximately 45 seconds within 2-3 minutes after receiving these vaccinations.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 28.11.2023
- Impfdatum
- 24.10.2022
- Beginn
- 04.10.2023
- Tage bis Beginn
- 345,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Angiogram pulmonary normal
Blood creatinine increased
Blood lactic acid normal
COVID-19
Cardiac telemetry abnormal
Chest X-ray normal
Cough
Dehydration
Electrocardiogram abnormal
Glycosylated haemoglobin normal
SARS-CoV-2 test positive
Sepsis
Sinus rhythm
Sinus tachycardia
Tachycardia
Viral infection
White blood cell count normal
Symptomtext
72 y.o. male patient of, MD with history of DM2, CKD, HTN, BPH. Presented to PCP office with COVID-19 and found to have an abnormal tachycardic rhythm and sent to ED for evaluation. He was in sinus tachycardia, and admitted for observation of heart rate and Sepsis criteria met. His vital signs improved after IVF and he was medical stable to go home. Sepsis, resolved COVID-19 infection Cough started 10/3; positive for COVID on 10/04 HR and RR high normal, hemodynamically stable WBC and LA wnl Continued Paxlovid Deferred blood cultures and urine cultures in setting of known viral infection Tachycardia, resolved Likely in the setting of COVID, dehydration EKG in ED with sinus tachycardia (HR 138) CXR, CTPA nonacute S/p IVF Telemetry with sinus tachycardia and NSR Chronic Conditions HTN: Amlodipine, Atorvastatin, Lisinopril, Hydrochlorothiazide DM2: Glyburide, Metformin; 7/2023 A1c 6.9% CKD: Cr 1.47 BPH: finasteride
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dehydration
- Hospital-Tage
- 1,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 01.11.2023
- Impfdatum
- 05.10.2022
- Beginn
- 07.10.2023
- Tage bis Beginn
- 367,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asthenia
Blood potassium abnormal
Blood pressure increased
Blood sodium decreased
COVID-19
Decreased appetite
Dehydration
Diarrhoea
Gastrointestinal disorder
Hypokalaemia
Hyponatraemia
Lethargy
Nausea
SARS-CoV-2 test positive
Symptomtext
Patient is an 80-year-old gentleman who is a patient with a history of chronic hyponatremia, HTN, presents with lethargy and weakness and nausea; noted to have hyponatremia, in the setting of a week of COVID-19 related GI symptoms. He had no respiratory symptoms, saturated well on RA, did not require COVID specific therapy. Sodium slowly improved with IV hydration and holding hydrochlorothiazide. BP has been elevated in the hospital, but patient reports good control at home, and typically has elevated BP at doc appointments. He is medically stable for discharge. Hyponatremia Hypokalemia + Suspect secondary to dehydration and poor oral solute due to COVID - admitted with Na 118, now at 130, with IV hydration; baseline per him is in mid-high 120s - continue to hold hydrochlorothiazide at discharge - nausea due to COVID improved and appetite is improving - K improved to normal Covid infection - Presented with: Nausea, mild diarrhea, anorexia - Symptom onset: 10/1/2023 - Positive COVID-19: 10/3/2023 at home, 10/9 - Vaccination status: Moderna SARS-CoV-2 Vaccination 01/29/2021, 02/26/2021, 10/29/2021, 04/14/2022 - CXR on admission showed Nonacute two-view chest with chronic postsurgical changes. - Oxygen status: Room air - Decadron: Does not qualify without pneumonitis - Remdesivir: Does not qualify without pneumonitis - DVT prophylaxis: Xarelto PAF Sinus node dysfunction PPM in place + Status post dual-chamber Medtronic pacemaker 3/2/2022; follows with OPG electrophysiology - cont Flecainide for rhythm control, Metoprolol for rate control, and Xarelto for AC Insulin-dependent diabetes mellitus + Levemir 10 units nightly, Janumet twice daily, pioglitazone daily -8 units nightly with sliding scale holding p.o. meds - BG well-controlled; resume home regimen at discharge - diabetic diet Essential hypertension - BP elevated but patient states all his home readings are well-controlled; his BP at doctors appointments is typically high due to "white coat HTN" - cont Losartan and Metoprolol; hold hydrochlorothiazide
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dehydration
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 84,0
- Geschlecht
- M
- Eingang
- 17.07.2023
- Impfdatum
- 13.10.2022
- Beginn
- 27.03.2023
- Tage bis Beginn
- 165,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypotension
Ventricular tachycardia
Symptomtext
HYPOTENSION 3/26/2023 VENTRICULAR TACHYCARDIA, UNSPECIFIED TYPE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 14.07.2023
- Impfdatum
- 20.10.2022
- Beginn
- 04.03.2023
- Tage bis Beginn
- 135,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Hypotension
Symptomtext
TRANSIENT HYPOTENSION
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 13.07.2023
- Impfdatum
- 22.10.2022
- Beginn
- 18.03.2023
- Tage bis Beginn
- 147,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Hypotension
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 26.06.2023
- Impfdatum
- 01.12.2022
- Beginn
- 28.04.2023
- Tage bis Beginn
- 148,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypotension
Pemphigoid
Symptomtext
I95.89 CHRONIC HYPOTENSION 5/4/2023 BULLOUS PEMPHIGOID
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 06.06.2023
- Impfdatum
- 08.10.2022
- Beginn
- 14.03.2023
- Tage bis Beginn
- 157,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arthralgia
Condition aggravated
Dermatitis atopic
Inflammation
Pain in extremity
Pyrexia
SARS-CoV-2 test negative
X-ray limb
Symptomtext
On March 14, I suffered a severe flare-up of an old right shoulder injury (originating in 1993) and had to visit urgent care while traveling to obtain treatment for the pain. While I had overworked the shoulder at that time, likely explaining the immediate incident, since that time I have developed a series of inflammatory flare-ups at various sites in my body that persist to this day. Also, in the months surrounding the injury, I have had a serious flare-up of atopic dermatitis. Shortly after the shoulder incident, I had a day of high, unexplained fever (multiple COVID tests were negative). Since then, the inflammation has traveled to my back for a week, to my left knee and leg on and off, and now suffer severe arthritic pain in both hands almost daily. I do not seem to be able to fight off this inflammation, which has now persisted for nearly 3 months. It seems to have come on suddenly, not gradually, and I wonder if having had the original series of COVID vaccines and three boosters has just been "too much." I list my flu vaccine in October above, even though it was not "prior" to the bivalent COVID vaccine, sinply becasue it was close in time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- X-rays of right shoulder and hand on 05/05/2023
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Mild hypertension, obesity
- Andere Medikamente
- 25 mg losartin, 1X daily
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 02.06.2023
- Impfdatum
- 12.10.2022
- Beginn
- 15.11.2022
- Tage bis Beginn
- 34,0
- Dosis
- 5
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Coronary artery disease
Hypotension
Symptomtext
I95.9 HYPOTENSION 11/30/2022 CAD (CORONARY ARTERY DISEASE) WO ANGINA
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 93,0
- Geschlecht
- M
- Eingang
- 23.05.2023
- Impfdatum
- 15.10.2022
- Beginn
- 17.10.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Hypotension
Symptom recurrence
Symptomtext
HYPOTENSION 2/21/2023 -- RECURRENCE OF SAME SYMPTOMS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 26.04.2023
- Impfdatum
- 06.10.2022
- Beginn
- 24.03.2023
- Tage bis Beginn
- 169,0
- Dosis
- 5
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Rhinorrhoea
SARS-CoV-2 test positive
Tachycardia
Symptomtext
I had vaccination 10/06/2022. On 03/24/2023 I had a runny nose frequent cough and tachycardia. I did not have a fever. I had a telehealth appointment and was prescribed Paxlovid. I feel I have completely recovered as of 04/26/2023.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tachycardia
- Hospital-Tage
- -
- Labordaten
- 03/24/2023 test - COVID-19 Positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hyperlipidemia; GERD
- Andere Medikamente
- Atorvastatin; Patrolperson
- Allergien
- Doxycycline; Topiramate; Sulfa Drugs
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 19.04.2023
- Impfdatum
- 15.10.2022
- Beginn
- 04.03.2023
- Tage bis Beginn
- 140,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood glucose increased
COVID-19
Condition aggravated
Cough
Diabetes mellitus
Fatigue
Myalgia
Pain in extremity
Pyrexia
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
At that time of my vaccine, moderate soreness in my arm for two days. I had little bit of fever and was tired. In March 2023, I developed a cough, fever, congestion, muscle aches, exhaustion, some nasal drainage. My symptoms lasted about five days and I was taking Paxlovid on 03/06/2023. I took an at home COVID-19 test on 03/04/2023 which was negative and then I tested positive on 03/06/2023. I then took another COVID-19 test on 03/12/2023 and it was negative. Iam also a type II diabetic and have noticed when I experienced COVID-19 symptoms, my glucose levels are running higher than they used to be.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- 04MAR2023 COVID-19 Test; Negative; 06MAR2023 COVID19-Test- Positive; 12MAR2023 COVID-19 Test- Negative
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Type II Diabetes
- Andere Medikamente
- Elavil; Alfagan; Cozort; Est raise; Glupetrol; Prednisone; Jardiance; Glucophage; Perimetrium; Zocor; Trivatanzine; Chlobec; Acetaminophen, Tylenol; Baby Aspirin; Ibuprofen; Naproxen; Claritin; Acetol Carnitine; Alplalapoloc Acid; Calcium;
- Allergien
- Dust, Cats, Pollen
- Vorherige Impfungen
- 1st COVID-19 vaccine; got menstrual cycle more frequently since then
- Staat
- MS
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 14.04.2023
- Impfdatum
- 13.10.2022
- Beginn
- 26.03.2023
- Tage bis Beginn
- 164,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Chest pain
Cholelithiasis
SARS-CoV-2 test negative
Symptomtext
My adverse event started on 03/26/2023 in the late afternoon. I started feeling pain under my sternum. I was sure it was gallbladder attack. I would rate the pain 8/10. I was in extreme pain. I was in pain from 4-10pm.The next day I called my doctor who told me to go to the ER to make sure I wasn't having Cardia event since the symptoms I describe were similar At the ER they told me that in my gallbladder there was stone which was causing the pain. They recommended to get my gallbladder removed. I am waiting to get my gallbladder removed but I haven't had any pain since the last time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- 14APR2023 COVID-19 Test-Negative
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Pernicious Anemia
- Andere Medikamente
- Vitamin D3; Vitamin C; Vitamin B12 Injection
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 13.04.2023
- Impfdatum
- 08.10.2022
- Beginn
- 01.01.2023
- Tage bis Beginn
- 85,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Cough
Dysphagia
Dyspnoea
Fatigue
Hypertension
Ocular hyperaemia
Oropharyngeal pain
Productive cough
SARS-CoV-2 test positive
Throat irritation
Upper-airway cough syndrome
Symptomtext
I contracted COVID-19 in 01/2023. My eyes became really red. I had a burning sore throat and it was hard to swallow. I was very tired too. The post nasal drip was really bad. I was coughing badly as well. I had trouble breathing and I went to an urgent clinic. They gave me an inhaler which helped quite a bit. In April 2023, I also experienced a really bad sore throat again. I started coughing and my throat tickled a lot. My blood pressure was high as well. I went to the urgent clinic and I took a few tests. They gave me some antibiotics and gave me an inhaler. But I continued to cough and I was dealing with these mucus issues. I went to the ER recently and they gave me a liquid syrup medication to deal with the coughing. They also gave me a z pack.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Jan2023 - COVID-19 Test - Positive; Apr2023 - Pneumonia Test - Negative; Apr2023 - Flu Test - Negative; Apr2023 - COVID-19 Test - Negative
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Elderberry with Zinc
- Allergien
- Dairy products
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 07.04.2023
- Impfdatum
- 05.10.2022
- Beginn
- 01.03.2023
- Tage bis Beginn
- 147,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Choking sensation
Cough
Malaise
Musculoskeletal chest pain
SARS-CoV-2 test positive
Sneezing
Symptomtext
I left for the trip of the 22nd of March. I was on a trip, I tested when I came off the trip. I tested positive on the Thursday after the trip and then the following Sunday I tested Negative. My niece got me medication to take and home remedies. I had a cough and felt like I was going to choke. 36.6 degrees Celsius as a temperature. I had an episode on the 27th on March and I was trying to get my steps in, and I felt that night a cramp in my left rib cage. On the 23rd of March I started to sneeze. I was coughing and wasn?t feeling well.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Musculoskeletal chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Pinched Nerve
- Andere Medikamente
- Mexazolam; Tylenol;
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 03.04.2023
- Impfdatum
- 28.10.2022
- Beginn
- 08.11.2022
- Tage bis Beginn
- 11,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthma
Condition aggravated
Exposure via inhalation
Fatigue
Pain in extremity
Perfume sensitivity
Symptomtext
I had a sore arm and fatigue for about a day after receiving the vaccine. I was exposed to heavy perfume at the end of September which aggravated my asthma. I took a dose of Prednisone to manage my symptoms until I contacted my doctor. After seeing my doctor, I took another dose of Prednisone and Protonic. I have an appointment with a Pulmonologist in about a week.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Asthma; Overweight; Arthritis; GERD
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 31.03.2023
- Impfdatum
- 12.10.2022
- Beginn
- 23.10.2022
- Tage bis Beginn
- 11,0
- Dosis
- 5
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Blood urine present
Computerised tomogram kidney abnormal
Dyspnoea
Laboratory test
Nephrectomy
Renal mass
Renal neoplasm
Urinary tract infection
Symptomtext
On 10/23/2022, I had blood in my urine and went to urgent care assuming it was a UTI. I was given cefalexin and they sent the urine sample off for evaluation. When I followed up with the NP, she recommended that I go see a urologist just to make sure it wasn't cancer. I went to a doctor that I haven't been to before. I went for one visit and he recommended that I get a CT scan. The CT scan showed a large mast on my kidney. He referred me to a choice of two surgeons. A family friend recommended me to the surgeon that I saw. I had surgery the Monday after the holiday and removed the kidney with the tumor. All the margins were clear, lymph nodes were clear. I was started on KEYTRUDA in February as a precautionary thing to self reduce the chance that something may occur and we're monitoring how I am with the medication. I'm waiting on the biopsy for my thyroid nodules as well. Next week I'm getting an echocardiogram and an EKG to see about some recent shortness of breath. They noted that the tumor had been on my kidney for some time because it was so big.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 2,0
- Labordaten
- CT Scan, indicated large mast on Kidney; CAT scans; lab work; other upcoming tests
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Type 2 Diabetes; Thyroid Nodules; Sleep Apnea
- Andere Medikamente
- Atenolol; diclofenac sodium; potassium; vitamin c; omeprazole; METANX; lovastatin; NYSTOP NYSTATIN topical powder; TYLENOL; XANAX; FLEXERIL; multivitamin; TRULICITY
- Allergien
- Seasonal allergies; sulfa drugs
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 14.03.2023
- Impfdatum
- 13.10.2022
- Beginn
- 25.12.2022
- Tage bis Beginn
- 73,0
- Dosis
- 4
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Chest X-ray normal
Chest discomfort
Cough
Dysphonia
Dyspnoea exertional
Fibrin D dimer normal
Headache
Hypoxia
Influenza
Influenza A virus test positive
Oropharyngeal pain
Pain
Pyrexia
SARS-CoV-2 test positive
Symptomtext
On 12/25/2022, patient presented to the emergency department due to shortness of breath with activity, cough, sore throat, headache body aches, hoarse voice, intermittent chest pressure, and fever of 101.3F. Her symptoms started 1-2 days prior (12/23/2022-12/24/2022) to ED visit; She went to a funeral on 12/20/2022 and some of the attendees were sick. In the emergency department on 12/25/2022, patient tested positive for both COVID and influenza A; She has a history of COVID-19 infection in June 2022 which was treated with Paxlovid; She is fully vaccinated, boosted, and up to date on COVID-19 vaccinations. While in the emergency department, patient had hypoxia with oxygen saturation in the 88-89% range on room air, which improved with supplemental nasal cannula oxygen. Her chest x-ray showed no acute findings, and her D-dimer were within normal limits. Patient was treated with Decadron, Tamiflu, and DuoNeb nebulizer, vitamin C, vitamin E, antitussive/mucolytic therapy, and incentive spirometry; Antiviral treatment for COVID-19 was deferred to the inpatient treatment team. Patient was admitted to the hospital for further treatment of COVID-19 and Influenza A. Submitter does not have access to further medical information on this case. If more information is needed, please contact the admitting hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea exertional
- Hospital-Tage
- -
- Labordaten
- 12/25/2022 - positive COVID NAA test; positive Influenza A test; Chest x-ray showed no acute findings; D-dimer within normal limits.
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 15.02.2023
- Impfdatum
- 04.01.2023
- Beginn
- 05.01.2023
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoaesthesia
Paraesthesia
Symptomtext
Arm numbness/tingling down to fingers since day after vaccine, still occuring
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- high cholesterol
- Andere Medikamente
- Atorvastatin
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 09.02.2023
- Impfdatum
- 30.01.2023
- Beginn
- 01.02.2023
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cardiac ablation
Cardiac disorder
Heart rate abnormal
Palpitations
Symptomtext
Two days after having the vaccine I had an issue with heart palpitations. Now I had COVID-19 twice. After having COVID-19 the first time my heart was out of rhythm, and I was having palpations and issues. I had three ablations to correct my A-Fib issues and the last issue I had been resolved by those years prior. After having COVID-19 I had to have an ablation again and it did not work- this post COVID-19 Ablation was the first time that it did not work and get my heart back in rhythm. I then had COVID-19 a second time and this happened again where I had the palpitations and the issues with my heart. I had my most recently vaccine on 01/30/2023 and it was two days later that I was having heart issues and palpations. This was different than with COVID-19 the illness as it was a month to a month and a half before the issue began as to where with the shot, I reacted with a cardiac issue within two days. I am following up with my cardiologist and we do have a plan that if I have an emergency I do to the ER and he will see me the next day or ASAP.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Overweight; Atrial Fibrillation
- Andere Medikamente
- Alopurinol; HCTZ/ spironolactone; telmisartan; ELIQUIS; pantoprazole TR; amlodipine; vitamin B12; vitamin D3; cetirizine; ENTOCORT CT
- Allergien
- Iodine; penicillin
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 03.02.2023
- Impfdatum
- 08.12.2022
- Beginn
- 08.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Palpitations
Symptomtext
Pt reported health palpitations post vaccine around 3:45PM (vax administered at 3:12PM). Pt states HP was present until next morning and resolved on its own.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Mitral Valve Prolapse and Asthma
- Andere Medikamente
- Benadryl and Albuterol
- Allergien
- No known material, food, or drug allergies
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 10.10.2022
- Beginn
- 22.11.2022
- Tage bis Beginn
- 43,0
- Dosis
- 4
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ageusia
Alopecia
Anosmia
COVID-19
Disorientation
Dyspnoea
Dysstasia
Eating disorder
Gastrointestinal disorder
Haemorrhoids
Influenza virus test negative
Oropharyngeal pain
Pain
Pain in extremity
Pyrexia
Respiratory syncytial virus test negative
SARS-CoV-2 test
Somnolence
Symptomtext
I experienced a breakthrough case of COVID-19 with a fever of 100 degrees, pain in my toes, sore throat, disoriented, unable to stand, hair loss, body aches, loss of taste and smell, weight loss, sleepiness, shortness of breath, gastrointestinal issues, hemorrhoids, and I don't want to eat anything crunchy, I also don't have taste so I am not interested in eating any foods.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- COVID-19 test, Strep test, RSV test; negative, Flu test; negative
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 10.01.2023
- Impfdatum
- 08.10.2022
- Beginn
- 09.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Anxiety
Blood test normal
Chest X-ray abnormal
Cough
Dyspnoea
Dyspnoea exertional
Dystonia
Feeling abnormal
Hypersomnia
Hypoaesthesia
Influenza like illness
Middle insomnia
Muscle spasms
Muscle tightness
Muscle twitching
Pain
Panic reaction
Tremor
Symptomtext
Starting 10/09/2022, I got the typical soreness and flu like symptoms. I never felt right after that. I kept feeling like something bad was going to happen. I started sleeping more and waking up numerous times in the night soaking wet. Then, my muscles started twitching and spasming pretty regularly. Around 10/20/2022, it got worse and when I was driving the muscle spasms and tightness got so severe that my head was stuck to the side. I got home and I started panicking because I was concerned. On 10/24/2022, I went out to eat thinking I would feel better. However, I ended up having a full blown dystonia attack that looked like a seizure but I was fully aware. They took me by ambulance to the ER and did routine blood work which came back normal. They told me it was an anxiety attack and I was shaking for 4 hours in the ER. They sent me home and after 4 days of the same symptoms I decided to stop all of my medicines except the pantoprazole. Eventually, the symptoms resolved and I lost 10 pounds. I haven't felt normal since. I still get occasional spasms but not as bad as they were before. Around the beginning of 12/2022, I started noticing that I had trouble breathing and felt short of breath very easily upon exertion. I went to the same ER about 1 week ago due to the trouble breathing. They did a chest x-ray and it was clear. They were unsure what it was but thought it could be a virus. They told me I could take MUCINEX for treatment. The MUCINEX doesn't seem to help. I am still having intermittent dry cough that seems to come out of nowhere. Also I have noticed that some of my skin, more specifically on my back, feels numb. For 15 years, my bloodwork has been abnormal due to my Lupus; however, since receiving the vaccinations my bloodwork is no longer abnormal.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Routine blood work in the ER (10/24/2022): normal; Chest X-ray (01/2023): normal
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Lupus; MCTD; Chronic Severe Migraines; Asthma; Fibromyalgia; Arthritis; Chronic Gastritis and Colitis
- Andere Medikamente
- WELLBUTRIN; pantoprazole; vitamin D; ibuprofen as needed
- Allergien
- Lithium; duloxetine; SUPRAX
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 05.01.2023
- Impfdatum
- 21.10.2022
- Beginn
- 19.12.2022
- Tage bis Beginn
- 59,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Anticoagulant therapy
Asthenia
Atrial fibrillation
Benign prostatic hyperplasia
COVID-19
Chest X-ray
Cough
Dyspnoea
SARS-CoV-2 test positive
Type 2 diabetes mellitus
Symptomtext
Patient is a 79 y.o. male patient of DO with history of hypertension, chronic A. fib on anticoagulation, CAD, dyslipidemia presented to Hospital with generalized weakness, cough and shortness of breath admitted for COVID-19 Clinical Summary Covid-19 Virus Infection Date of onset of symptoms: 2 days PTA Symptoms present on admission: DOE Date of covid positive test: 12/19 Vaccination status: vaccinated Imaging: CXR Oxygen requirements on admission: 2 lit Current oxygen requirements: 2 lit Medical therapy: steroids Consultants following: None Anticipated special isolation end date: 12/29 - Supplemental oxygen requirement resolved Weakness Secondary to COVID PT and OT consult Paroxysmal afib In NSR. On amio and cont on Eliquis HTN Cont on Lisinopril and Toprol Diabetes type-2 Hold Metformin, add SSI BPH Cont on flomax Dyslipidemia Cont on Statin
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 20.12.2022
- Impfdatum
- 04.11.2022
- Beginn
- 13.12.2022
- Tage bis Beginn
- 39,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain lower
Condition aggravated
Impaired work ability
Symptomtext
In the morning it started as a lower quadrant pain that continued to get worse that was not alleviated by ibuprofen and kept me from going to work. I considered going to the emergency room, but the pain started to subside. I called my primary care physician and described what was going on, she ordered a pelvic exam, I am awaiting to get that scheduled. The dull pain did linger for a couple of days and now it gone.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- No
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Anixiety
- Andere Medikamente
- Lyletta IUD; Lexapro
- Allergien
- Kiwi
- Vorherige Impfungen
- 1st COVID-19 vaccine a lot of swelling and itching, reported to vsafe
- Staat
- ME
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 21.11.2022
- Impfdatum
- 18.11.2022
- Beginn
- 19.11.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Oedema peripheral
Pain in extremity
Paraesthesia
Peripheral swelling
Symptomtext
Client had the vaccine on Friday evening at 5pm. She woke up Saturday at approximately 8am with extremely sore left arm, swollen armpit and upper arm, tingling in her left hand worsening into Sunday and Monday. She also has 2 red circles approvimately 2 inches each; one above injection site and one under injection side to the left.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- None at this time. Client has an appointment with her provider at 1 pm today.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None Known
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 17.11.2022
- Impfdatum
- 12.10.2022
- Beginn
- 10.11.2022
- Tage bis Beginn
- 29,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest discomfort
Dyspnoea
Electrocardiogram normal
Symptomtext
I felt a feeling of discomfort across my chest, as if someone was tightening a band on my upper chest. Two episodes occurred, one on 11/10/2022 and the second occurrence on 11/15/2022. It was difficult to breathe in almost to the point of it being painful, but it was more uncomfortable than painful. Both times I had to breathe very slowly and shallowly before I could take a normal breath in. The doctor did an EKG and said that it was perfectly normal. She listened to my heart and lungs, and talked about my asthma. We wondered if it was in relation to the asthma acting up, but we are unsure if it's in relation to the vaccine. We talked about things and she urged me to come back if anything worsened or if it happened again.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 11/16/2022 EKG normal results
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma; High Blood Pressure; Partial Seizure Disorder; Depression; Hay Fever
- Andere Medikamente
- Lisinopril; sertraline; budesonide inhaler; VIMPAT; ZYRTEC; NEXIUM; calcium chews; magnesium; multivitamin; albuterol inhaler
- Allergien
- IV contrast dye
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 16.11.2022
- Impfdatum
- 16.11.2022
- Beginn
- 16.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hypoaesthesia
Tachycardia
Symptomtext
Pt c/o tachycardia and numbness in hand 10 min after vaccination. VS: 120/72 HR76 O2 Sat 100% EMS called VS stable. Declined transport to hospital ED. Encouraged to follow up with PCP. Made it home on own uneventfully.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tachycardia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Iron deficiency
- Vorgeschichte
- Denies
- Andere Medikamente
- Vitamins
- Allergien
- Ceftin Morphine
- Vorherige Impfungen
- Claims had similar reactions following all previous COVID Moderna vaccines but states it did not begin until 12 hours after vacc
- Staat
- GA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 11.11.2022
- Impfdatum
- 06.10.2022
- Beginn
- 22.10.2022
- Tage bis Beginn
- 16,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Condition aggravated
Migraine
Pain
Symptomtext
I have sharp consistent migraines that worsened after the vaccination, a constant shooting pain like someone is drilling in my head.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Blood work
- Aktuelle Erkrankungen
- Sinus infection
- Vorgeschichte
- Diabetic type 2; High Blood pressure that goes between high and low
- Andere Medikamente
- TYLENOL; BC powder
- Allergien
- VIKA tin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 09.11.2022
- Impfdatum
- 10.10.2022
- Beginn
- 17.10.2022
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test normal
Blood urine present
Bronchitis
Chest X-ray normal
Dyspnoea
Epistaxis
Influenza virus test negative
Pharyngeal swelling
Pulmonary congestion
SARS-CoV-2 test negative
Symptomtext
A week later I developed Bronchitis. Then, I started having nose bleeds and I had blood in my urine. I was prescribed an antibiotic, cefdinir. I am still dealing with this at this time. It has gotten so bad. I started having trouble breathing now. It is like my throat is swelling up. I have a lot of congestion in my chest too. They put me on prednisone because I can't seem to get rid of this.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 20OCT2022 chest X-Ray normal; 20OCT2022 Blood panel normal; 20OCT2022 COVID-19 test negative; 20OCT2022 Flu test negative
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Asthma
- Andere Medikamente
- Levothyroxine; estradiol patch; vitamin D; XELPROS
- Allergien
- Benzodiazepines; seasonal allergies
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 31.10.2022
- Impfdatum
- 18.10.2022
- Beginn
- 25.10.2022
- Tage bis Beginn
- 7,0
- Dosis
- 5
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
Blood test normal
COVID-19
Chest X-ray normal
Chest discomfort
Cough
Dyspnoea
Productive cough
Respiratory tract congestion
SARS-CoV-2 test positive
Weight decreased
Symptomtext
I started having symptoms on Tuesday, but I wasn't sure if they were COVID-19 related. On Thursday, the symptoms were not going away and I started coughing. I went to go get a COVID-19 test that was done with saliva. On Friday, I was getting a little pressure in my chest so I went to hospital to get another test and it was positive. I was prescribed Paxlovid for 5 days. Symptoms included congestion, coughing, and producing phlegm. I've had some shortness of breathe and chest pressure. I have been feeling weak and have experienced loss weight. I've lost 7 pounds in 4 days. I have not gotten COVID-19 the entire time during the pandemic, and after the 5th dose, I somehow got it. I've never changed any of my protocol. I've never stopped wearing a mask and I continue to do so.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- COVID-19 Saliva Test 10/27/2022 - Positive; COVID-19 Rapid Test 10/28/2022 - Positive; Chest X-ray 10/28/2022 - Clear, Nothing indicated; Blood work 10/28/2022 - Nothing indicated
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Fibromyalgia; CRPS; Migraines; Asthma; Hypothyroidism; Hypoglycemia
- Andere Medikamente
- Spironolactone; Famotidine; Acyclovir; Calcium; Magnesium; Vitamin D; Zinc; Irish Sea Moss; Apple Cider Vinegar; Vitamin B Complex
- Allergien
- Trees; Sulfa Drugs; Aspirin; Motrin; Morphine; Grasses
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 28.10.2022
- Impfdatum
- 11.10.2022
- Beginn
- 11.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Chest discomfort
Chills
Dyspnoea
Hypopnoea
Rash
Rash macular
Symptomtext
developed a rash all over her body; blotchy black rash all over her torso; shortness of breath; shallow breathing; pressure in her chest; felt weak; In the night she had chills; This spontaneous case was reported by a patient and describes the occurrence of DYSPNOEA (shortness of breath), HYPOPNOEA (shallow breathing), CHEST DISCOMFORT (pressure in her chest), ASTHENIA (felt weak) and CHILLS (In the night she had chills) in a 74-year-old female patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. 053D22A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Auricular fibrillation, Allergy to antibiotic (Ciprofloxacin) and Sulfonamide allergy. Concomitant products included SOTALOL, VITAMIN C [ASCORBIC ACID], TIMOLOL and KETOROLAC for an unknown indication. On 11-Oct-2022, the patient received fifth dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) 1 dosage form. On 11-Oct-2022, the patient experienced DYSPNOEA (shortness of breath), HYPOPNOEA (shallow breathing), CHEST DISCOMFORT (pressure in her chest), ASTHENIA (felt weak) and CHILLS (In the night she had chills). On 12-Oct-2022, the patient experienced RASH (developed a rash all over her body) and RASH MACULAR (blotchy black rash all over her torso). On 14-Oct-2022, RASH (developed a rash all over her body) and RASH MACULAR (blotchy black rash all over her torso) had resolved. At the time of the report, DYSPNOEA (shortness of breath), HYPOPNOEA (shallow breathing), CHEST DISCOMFORT (pressure in her chest), ASTHENIA (felt weak) and CHILLS (In the night she had chills) outcome was unknown. Patient did not have COVID positive test. Patient did not have history of Myocarditis/pericarditis. On 02-APR-2021 patient received First Moderna dose with Lot no.007C21A . On 20-MAY-2021 patient received Second Moderna dose with Lot no.038C21A . On 21-NOV-2021 patient received First Moderna Booster dose with Lot no.034F21A . On an unknown date patient received Second Moderna Booster dose with Lot no.056M21A . No treatment information was reported. This case was linked to MOD-2021-163805, MOD-2021-090452.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Allergy to antibiotic (Ciprofloxacin); Auricular fibrillation; Sulfonamide allergy
- Vorgeschichte
- -
- Andere Medikamente
- SOTALOL; VITAMIN C [ASCORBIC ACID]; TIMOLOL; KETOROLAC
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 27.10.2022
- Impfdatum
- 06.10.2022
- Beginn
- 06.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Joint injury
Paraesthesia
Symptomtext
Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 26.10.2022
- Impfdatum
- 20.10.2022
- Beginn
- 20.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Atrial fibrillation
Condition aggravated
Dyspnoea
Rash erythematous
Rash pruritic
Skin warm
Symptomtext
Hot, itchy, red rash. Went into AFIB a few hours later and had difficulty breathing. Rash has lasted five days now. The AFIB and difficulty breathing lasted the rest of the day. I seem to be slowly recovering.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- T2 diabetes, asthma, AFIB, hypothyroidism, fibromyalgia, hyperlipidemia, GERD, sleep apnea,
- Andere Medikamente
- Pantopraxole, famitidine, colestipol, losartan, basaglat, levethyroxine, vitamin d, annuity ellipta, monyelukast, metroprolol tartrate, digoxin, klor-con, furosemide, atorvastatin, alpraxlam, myrbeyriq, coumadin
- Allergien
- Thimersol, Sulfa, nickel, caffeine
- Vorherige Impfungen
- Moderna covid shot #3 (booster #1); 10/27/2021
- Staat
- WV
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 25.10.2022
- Impfdatum
- 24.10.2022
- Beginn
- 24.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Dyspnoea
Pruritus
Tongue blistering
Symptomtext
Difficulty breathing, itching blisters on t ongue
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Diabetic, HTN
- Andere Medikamente
- Insulin, HTN medication, Valcyclovir, Claritin Prozac
- Allergien
- Monoclonical antibodies
- Vorherige Impfungen
- Itching with first two doses
- Staat
- CA
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 23.10.2022
- Impfdatum
- 17.10.2022
- Beginn
- 17.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Joint injury
Paraesthesia
Symptomtext
Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 21.10.2022
- Impfdatum
- 11.10.2022
- Beginn
- 11.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Joint injury
Pain
Paraesthesia
Symptomtext
Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 47,0
- Geschlecht
- M
- Eingang
- 18.10.2022
- Impfdatum
- 08.10.2022
- Beginn
- 09.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Chest discomfort
Chills
Dyspnoea
Fatigue
Headache
Hyperacusis
Hyperhidrosis
Limb discomfort
Neck pain
Pain
Photophobia
Symptomtext
For 1-3 days after injection, occasional chills/sweats noted and some joint pain, sensitivity to sound/light, severe headache; for 3-5 days after injection, significant pain radiating around to neck/shoulders that was able to be largely controlled with ibuprofen; for just over a week after injection, some shortness of breath and abnormal fatigue noted, particularly late in day; since injection, some tightness/mild pressure in chest and discomfort in left arm continues intermittently and is most noticeable when lying down (no actual pain in chest) but can be eased with ibuprofen Did not seek medical help given mild nature of symptoms but took ibuprofen given similarities to symptoms associated with pericarditis or myocarditis. Symptoms for both this vaccination and prior instance after second vaccine (Pfizer) occurred shortly after vigorous physical activity
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Psyllium fiber, Vitamin D, Vitamin B12
- Allergien
- None
- Vorherige Impfungen
- Tightness in chest, muscle/joint pain/shoulder/neck pain/chills/sweats/extreme fatigue & weakness also occurred after Pfizer cov
- Staat
- -
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 18.10.2022
- Impfdatum
- 07.10.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary mass
Axillary pain
Hypoaesthesia
Limb discomfort
Muscle spasms
Paraesthesia
Symptomtext
muscle cramp that gets worst the higher when raise the arm; Patient did not have full strength in that arm/ experiencing this discomfort since getting the vaccine; numbness in fingers especially pinky fingers of injected arm; tingling in fingers especially pinky fingers of injected arm; Patient experienced pain in underarm of the arm injected, especially when patient extend arm out from side; Under arm was very swollen after the vaccine but the swelling has since went down; This spontaneous case was reported by a patient and describes the occurrence of MUSCLE SPASMS (muscle cramp that gets worst the higher when raise the arm), LIMB DISCOMFORT (Patient did not have full strength in that arm/ experiencing this discomfort since getting the vaccine), HYPOAESTHESIA (numbness in fingers especially pinky fingers of injected arm), PARAESTHESIA (tingling in fingers especially pinky fingers of injected arm) and AXILLARY PAIN (Patient experienced pain in underarm of the arm injected, especially when patient extend arm out from side) in a 60-year-old female patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. 053D22A) for COVID-19 prophylaxis. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 07-Oct-2022, the patient received dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) 1 dosage form. On an unknown date, the patient experienced MUSCLE SPASMS (muscle cramp that gets worst the higher when raise the arm), LIMB DISCOMFORT (Patient did not have full strength in that arm/ experiencing this discomfort since getting the vaccine), HYPOAESTHESIA (numbness in fingers especially pinky fingers of injected arm), PARAESTHESIA (tingling in fingers especially pinky fingers of injected arm), AXILLARY PAIN (Patient experienced pain in underarm of the arm injected, especially when patient extend arm out from side) and AXILLARY MASS (Under arm was very swollen after the vaccine but the swelling has since went down). At the time of the report, MUSCLE SPASMS (muscle cramp that gets worst the higher when raise the arm), LIMB DISCOMFORT (Patient did not have full strength in that arm/ experiencing this discomfort since getting the vaccine) and AXILLARY PAIN (Patient experienced pain in underarm of the arm injected, especially when patient extend arm out from side) had not resolved, HYPOAESTHESIA (numbness in fingers especially pinky fingers of injected arm) and PARAESTHESIA (tingling in fingers especially pinky fingers of injected arm) outcome was unknown and AXILLARY MASS (Under arm was very swollen after the vaccine but the swelling has since went down) had resolved. No concomitant medications were reported. Patient experienced discomfort since getting the vaccine and it had not gotten any better. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 13.10.2022
- Impfdatum
- 10.10.2022
- Beginn
- 11.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- 5
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dehydration
Tongue discolouration
Tongue disorder
Symptomtext
24 hours after booster patient's tongue was coated with a thick, white film that could not be removed by brushing. Decided that dehydration could be the cause. Rehydrated for 48 hours before tongue began to look normal.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dehydration
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- GERD.
- Andere Medikamente
- Centrum Senior Multivitamin, famotidine 40mg.
- Allergien
- Adverse reaction (nausea) to codeine.
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 13.10.2022
- Impfdatum
- 07.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Limb injury
Paraesthesia
Symptomtext
Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 13.10.2022
- Impfdatum
- 09.10.2022
- Beginn
- 09.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
Confusional state
Dizziness
Pallor
Tremor
Symptomtext
Systemic: Confusion-Mild, Systemic: Dizziness / Lightheadness-Mild, Systemic: Shakiness-Mild, Systemic: Weakness-Mild, Additional Details: PATIENT TURNED PALE AND FALLING TO ONE SIDE, SO WE STABILIZED HIM. WHEN THE EMS ARRIVED AFTER 15 MINUTES , HE SEEM LIKE HE WAS RECOVERING AND THEY TOOK AWAY ON A GURNEY. HE NEVER LOST HIS CONSCIOUSNESS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 12.10.2022
- Impfdatum
- 12.10.2022
- Beginn
- 12.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Paraesthesia oral
Symptomtext
Patient stated her tongue felt tingly. She took a dose of 25mg of liquid benadryl. Within a minute, the atient stated it was no longer tingling. She also stated she gets nervous with shots and may just be worked up. She stated she had the initial moderna series and had no problem. The patient waited an additional 15 minutes and stated she felt nothing concerning at that time. She denied any oral swelling or difficulty breathing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia oral
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 12.10.2022
- Impfdatum
- 05.10.2022
- Beginn
- 09.10.2022
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arthralgia
Blood test
Chest X-ray
Chest discomfort
Chest pain
Computerised tomogram thorax abnormal
Dyspnoea
Echocardiogram abnormal
Electrocardiogram
Feeling abnormal
Headache
Pain in extremity
Pain in jaw
Pericardial effusion
Pleural effusion
Red blood cell count abnormal
White blood cell count abnormal
Symptomtext
After vaccine Thursday evening, experienced reaction similar to previous vaccines: sore arm and should, mild headache, follow by out-of-sorts feeling two days later (Saturday). Sunday morning felt fine. Sunday afternoon felt out-of-sorts. By 4-5 pm experienced increasing chest discomfort and pain with shortness of breath and burning sensation in chest while sitting. Also experience jaw discomfort and pain in both shoulders. Had never experienced these symptoms, even prior to surgery, while sitting; only experienced angina on exertion before and never after surgery. Went to hospital ED around 5:30, where tests were perform; kept for observation through Monday afternoon. Discharge Dx: small to moderate pericardial and pleural effusions. Told these should resolve on their own with rest, careful activity, and follow-up with cardiologist
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Multiple EKGs and blood panels. Labs indicated some out-of-range red and white blood cell counts; otherwise normal. Chest x-ray, echocardiogram, and CT scan. Echo showed small effusions. CT scan showed moderate pericardial effusion and small pleural effusion.
- Aktuelle Erkrankungen
- Successfully recovering from open heart triple by-pass surgery on August 8.
- Vorgeschichte
- CAD. some arthritis in spine. mild neuropathy in toes.
- Andere Medikamente
- Levothyroxine, Atorvastatin, Ezetimibe, Metoprolol, Clopidogrel, low-dose aspirin, CoQ10, Vitamin D
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 11.10.2022
- Impfdatum
- 07.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hypoaesthesia
Musculoskeletal stiffness
Pain
Paraesthesia
Symptomtext
Systemic: Body Aches Generalized-Mild, Systemic: Neck stiffness-Mild, Systemic: Numbness (specify: facial area, extremities)-Mild, Systemic: Tingling (specify: facial area, extemities)-Mild, Additional Details: Patient and her husband reported to experience similar symptoms within 10 minutes of receiving Moderna Bivalent Vaccine. The symptoms were reported to be non-focal, generalized, ipsilateral to site of vaccine. At approximatelty 9:35 pm same day patient reported symptoms to have resolved after taking acetaminophen for both her and her husband and that they were no longer concern.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 11.10.2022
- Impfdatum
- 07.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoaesthesia
Paraesthesia
Symptomtext
Systemic: Numbness (specify: facial area, extremities)-Mild, Systemic: Tingling (specify: facial area, extemities)-Mild, Additional Details: Within 10 minutes of vaccination patient c/o numbeness and tingling similar in nature to the sensation that his wife was experiencing after her vaccination occurring a few minutes after him. The patient reported to be experiencing the non-focal generalized ipsilateral numbness and tingling on the left side of his body of which he was vaccinated
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 20.11.2023
- Impfdatum
- 31.10.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 5
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Influenza like illness
Nasal congestion
Pain
Pain in extremity
Post-acute COVID-19 syndrome
Respiratory disorder
Symptomtext
respiratory issues.; Long covid; congestion; cough; sore arm; flu like symptoms; ache/pain; This spontaneous case was reported by a patient and describes the occurrence of RESPIRATORY DISORDER (respiratory issues.), POST-ACUTE COVID-19 SYNDROME (Long covid), NASAL CONGESTION (congestion), COUGH (cough) and PAIN IN EXTREMITY (sore arm) in an 82-year-old female patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. 053D22A) for COVID-19 prophylaxis. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Pneumonia (She had 3 pneumonia vaccine. Since then, she has not had pneumonia.) and Premature atrial contraction (She had double heartbeat PAC (Premature Atrial contraction)). Previously administered products included for COVID-19 prophylaxis: Moderna vaccine (Dose 1 lot number 014M20A) on 12-Feb-2021, Moderna vaccine (Dose 2 lot number 032M20A) on 12-Mar-2021, Moderna vaccine (Dose 3 lot number 034F21A) on 15-Nov-2021 and Moderna vaccine (Dose 4 lot number 004M21A) on 27-May-2022. Past adverse reactions to the above products included No adverse event with Moderna vaccine, Moderna vaccine, Moderna vaccine and Moderna vaccine. Concurrent medical conditions included Allergy (has allergies all her life) and Blood pressure. On 31-Oct-2022, the patient received fifth dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) 1 dosage form. On an unknown date, the patient experienced RESPIRATORY DISORDER (respiratory issues.), POST-ACUTE COVID-19 SYNDROME (Long covid), NASAL CONGESTION (congestion), COUGH (cough), PAIN IN EXTREMITY (sore arm), INFLUENZA LIKE ILLNESS (flu like symptoms) and PAIN (ache/pain). The patient was treated with PREDNISONE at an unspecified dose and frequency. At the time of the report, RESPIRATORY DISORDER (respiratory issues.), POST-ACUTE COVID-19 SYNDROME (Long covid), NASAL CONGESTION (congestion) and COUGH (cough) had not resolved and PAIN IN EXTREMITY (sore arm), INFLUENZA LIKE ILLNESS (flu like symptoms) and PAIN (ache/pain) was resolving. For mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Unknown), the reporter did not provide any causality assessments. She has taken the booster every 6 months since then. She took antibiotic and steroid. All the symptoms of respiratory issues. It would get better and come back. She has not taken a booster since then. Her ENT Doctor rule out long COVID-19. She did not have any other symptoms. Phlegm she has to spit every morning. The steroid help took right after Christmas (Prednisone) she had all the symptoms except fever. On Feb 2020 for 3 weeks she was very sick. She took antibodies and self-medicated which did not help. No sense of smell or taste for a week. She takes blood pressure medication. She was incorrectly diagnosed with asthma and was taking asthma medication for 11 years.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Allergy (has allergies all her life); Blood pressure
- Vorgeschichte
- Medical History/Concurrent Conditions: Pneumonia (She had 3 pneumonia vaccine. Since then, she has not had pneumonia.); Premature atrial contraction (She had double heartbeat PAC (Premature Atrial contraction))
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 03.11.2023
- Impfdatum
- 14.10.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 5
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Pain
Symptomtext
aches; fatigue; This spontaneous case was reported by a patient and describes the occurrence of PAIN (aches) and FATIGUE (fatigue) in a 78-year-old male patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. 053D22A) for COVID-19 prophylaxis. Previously administered products included for Drug use for unknown indication: Metoprolol Tartrate, Mirabegron, Omeprazole and Rosuvastatin; for Post-traumatic stress disorder: Sertraline; for Mood swings: Sertraline. Past adverse reactions to the above products included No adverse event with Metoprolol Tartrate, Mirabegron, Omeprazole, Rosuvastatin, Sertraline and Sertraline. Concurrent medical conditions included Aortic stenosis (since about 5 years ago, pretty stable during that time.), Post-traumatic stress disorder and Mood swings. On 14-Oct-2022, the patient received fifth dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) 1 dosage form. On an unknown date, the patient experienced PAIN (aches) and FATIGUE (fatigue). At the time of the report, PAIN (aches) and FATIGUE (fatigue) outcome was unknown. Concomitant product use was not provided by the reporter. Treatment information was not provided. This case was linked to US-MODERNATX, INC.-MOD-2023-747981, US-MODERNATX, INC.-MOD-2023-747999 (Linked Report). This case was linked to MOD-2023-747981, MOD-2023-747999 (Patient Link).; Sender's Comments: US-MODERNATX, INC.-MOD-2023-747981:Same patient, master case (Spikevax 2023-2024 PFS) US-MODERNATX, INC.-MOD-2023-747999:Same patient monovalet dose
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Aortic stenosis (since about 5 years ago, pretty stable during that time.); Mood swings; Post-traumatic stress disorder
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 03.11.2023
- Impfdatum
- 08.10.2022
- Beginn
- 01.10.2022
- Tage bis Beginn
- -
- Dosis
- 5
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Malaise
Pain in extremity
Symptomtext
she felt soreness in the arm; she felt dizzy and light headedness within about 5 minutes after getting the vaccine; she felt little bit more uncomfortable that with previous doses; This spontaneous case was reported by a consumer and describes the occurrence of MALAISE (she felt little bit more uncomfortable that with previous doses), PAIN IN EXTREMITY (she felt soreness in the arm) and DIZZINESS (she felt dizzy and light headedness within about 5 minutes after getting the vaccine) in a 71-year-old female patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch nos. AS7643E and 053D22A) for COVID-19 prophylaxis. The patient's past medical history included Lip swelling (her lips and tongue swell.) and Swelling of tongue (her lips and tongue swell.). Concurrent medical conditions included Allergy to animal dander (Allergic to cat dander), Latex allergy (oak trees latex), Grass allergy, Ragweed allergy, Allergy to animal dander (horses dander), Allergic to dogs, Environmental allergy, Lactose intolerance (cannot digest lactose), Fruit allergy (bananas), Rubber sensitivity (certain plants related to natural rubber plant), Fruit allergy (avocado), Fruit allergy (kiwi) and Spice allergy (cinnamon). On 08-Oct-2022, the patient received fifth dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) 1 dosage form. On 09-Aug-2023, received sixth dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) dosage was changed to 1 dosage form. In October 2022, the patient experienced MALAISE (she felt little bit more uncomfortable that with previous doses). On 09-Aug-2023, after starting mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)), the patient experienced PAIN IN EXTREMITY (she felt soreness in the arm) and DIZZINESS (she felt dizzy and light headedness within about 5 minutes after getting the vaccine). In October 2022, MALAISE (she felt little bit more uncomfortable that with previous doses) had resolved. On 09-Aug-2023, PAIN IN EXTREMITY (she felt soreness in the arm) and DIZZINESS (she felt dizzy and light headedness within about 5 minutes after getting the vaccine) had resolved. The patient did not receive any other vaccines in the 4 weeks prior to COVID-19 vaccine. After the 1st bivalent dose, the patient felt little bit more uncomfortable that with previous doses, but it was not immediately after the injection, took a nap and next day the patient had no problem. With the last dose it was a bit stronger, the patient felt soreness in the arm, felt dizzy and light headedness within about 5 minutes after getting the vaccine, then went back to the store were the patient was vaccinated, the vaccination provider gave her water to drink, it happened maybe because it was hot outside, the patient sit during 15 or 20 minutes in observation in case she needed further help, but did not need paramedics help and then was able to drive home and took a nap, and was fine. It was not a major concern and she only had mild symptoms in general for each vaccine. This case was linked to MOD-2023-747701 (Patient Link). Reporter did not allow further contact
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Allergic to dogs; Allergy to animal dander (horses dander); Allergy to animal dander (Allergic to cat dander); Environmental allergy; Fruit allergy (kiwi); Fruit allergy (bananas); Fruit allergy (avocado); Grass allergy; Lactose intolerance (cannot digest lactose); Latex allergy (oak trees latex); Ragweed allergy; Rubber sensitivity (certain plants related to natural rubber plant); Spice allergy (cinnamon)
- Vorgeschichte
- Medical History/Concurrent Conditions: Lip swelling (her lips and tongue swell.); Swelling of tongue (her lips and tongue swell.)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 13.10.2023
- Impfdatum
- 08.10.2022
- Beginn
- 01.10.2022
- Tage bis Beginn
- -
- Dosis
- 6
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal discomfort
Arthralgia
Asthenia
Bedridden
Chills
Fatigue
Headache
Illness
Immunisation reaction
Malaise
Myalgia
Nausea
Pain in extremity
Peripheral swelling
Pyrexia
Rash
Sinusitis
Symptomtext
sick; All the side effects possible; sinusitis; she could barely get out of bed for 10 days; didn't feel well for a while; swelling of the arm; digestive upset including nausea; weakness; chills; Joint pain; rash; Headache; digestive upset including nausea; fever; muscle pain; sore arm; fatigue; This spontaneous case was reported by a patient and describes the occurrence of ILLNESS (sick), IMMUNISATION REACTION (All the side effects possible), SINUSITIS (sinusitis), BEDRIDDEN (she could barely get out of bed for 10 days) and MALAISE (didn't feel well for a while) in a 69-year-old female patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. 053D22A) for COVID-19 prophylaxis. The occurrence of additional non-serious events is detailed below. Patient can only wear titanium earring. Patient never diagnosed with COVID-19. The patient's past medical history included Peritonitis (appendicitis with peritonitis), Appendicitis (appendicitis with peritonitis), Small bowel obstruction and Tooth extraction. Previously administered products included for Tooth extraction: lidocaine (slept for 4 days). Past adverse reactions to the above products included Sleep excessive with lidocaine. Concurrent medical conditions included Asthma (severe asthma), Fibromyalgia (fibromyalgia with chronic fatigue), Fatty liver (stomach issues including fatty liver), Irritable bowel syndrome, Gastroparesis, Drug allergy (fentanyl) and Allergy to antibiotic (Patient was allergic to a lot of antibiotics.). On 08-Oct-2022, the patient received sixth dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) 1 dosage form. In October 2022, the patient experienced ILLNESS (sick), IMMUNISATION REACTION (All the side effects possible), SINUSITIS (sinusitis), BEDRIDDEN (she could barely get out of bed for 10 days), MALAISE (didn't feel well for a while), PERIPHERAL SWELLING (swelling of the arm), ABDOMINAL DISCOMFORT (digestive upset including nausea), ASTHENIA (weakness), CHILLS (chills), ARTHRALGIA (Joint pain), RASH (rash), HEADACHE (Headache), NAUSEA (digestive upset including nausea), PYREXIA (fever), MYALGIA (muscle pain), PAIN IN EXTREMITY (sore arm) and FATIGUE (fatigue). The patient was treated with DOXYCYCLINE at a dose of For 10 days; PREDNISONE at a dose of 30 milligram,for 3 days; PREDNISONE at a dose of 20 milligram for 2 day and PREDNISONE at a dose of 10 milligram for 2 day. At the time of the report, ILLNESS (sick), IMMUNISATION REACTION (All the side effects possible), SINUSITIS (sinusitis), BEDRIDDEN (she could barely get out of bed for 10 days), MALAISE (didn't feel well for a while), PERIPHERAL SWELLING (swelling of the arm), ABDOMINAL DISCOMFORT (digestive upset including nausea), ASTHENIA (weakness), CHILLS (chills), ARTHRALGIA (Joint pain), RASH (rash), HEADACHE (Headache), NAUSEA (digestive upset including nausea), PYREXIA (fever), MYALGIA (muscle pain), PAIN IN EXTREMITY (sore arm) and FATIGUE (fatigue) outcome was unknown. Not Provided For mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Unknown), the reporter did not provide any causality assessments. Concomitant product use was not provided by the reporter. Patient's past Moderna-covid 19 vaccine included on First dose on unknown date, second dose on 17-Feb-2021 with batch number 032L20A, third dose on 27-Aug-2021 with batch number 039K20A, fourth dose on an unknown date with lot number 088D4A and fifth dose on 02-May-2022 with batch number 057M21A. Due to the stomach issues, sometimes it was hard for patient to digest food and it gets digested very slowly, including medications. Patient stated that the fatigue was unbearable. Patient had a bad sinus, and she visited the physician. Patient was sick for a long time after this sinus infection, maybe for 6 months even. Physician informed patient that vaccine could not cause sinus infections. Some of these symptoms of the patient lasted for up to 2 weeks or longer. The symptoms usually started 4 hours after getting the vaccine. This case was linked to MOD-2023-745008 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Allergy to antibiotic (Patient was allergic to a lot of antibiotics.); Asthma (severe asthma); Drug allergy (fentanyl); Fibromyalgia (fibromyalgia with chronic fatigue); Gastroparesis; Irritable bowel syndrome
- Vorgeschichte
- Medical History/Concurrent Conditions: Appendicitis (appendicitis with peritonitis); Fatty liver (stomach issues including fatty liver); Peritonitis (appendicitis with peritonitis); Small bowel obstruction; Tooth extraction; Comments: Patient can only wear titanium earring. Patient never diagnosed with COVID-19.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 05.06.2023
- Impfdatum
- 06.10.2022
- Beginn
- 14.03.2023
- Tage bis Beginn
- 159,0
- Dosis
- N/A
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asthenia
COVID-19
Dizziness
SARS-CoV-2 test positive
Symptomtext
The patient has a history of diabetes. He was brought to the ED by EMS on 3/14/23 for evaluation of weakness that began the night prior. He additionally reported lightheadedness . A COVID-19 PCR test performed in the ED resulted positive. Notably, his wife tested positive for COVID four days prior. The patient was admitted 3/14/23 - 3/18/23 with discharge diagnoses of COVID-19 and generalized weakness due to COVID-19. He did not require supplemental O2 during admission and was not on steroids. Paxlovid was started during his admission. Of note, the patient has received the primary COVID vaccine series and three booster doses.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 26.05.2023
- Impfdatum
- 08.10.2022
- Beginn
- 08.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test normal
Erythema
Feeling hot
Induration
Laboratory test abnormal
Pain in extremity
Peripheral swelling
Seasonal allergy
Urticaria
Symptomtext
10/8/22 towards the evening, my arm became very red, hard, hot and swollen, about a 3 inch radius around the point of the vaccine. I sprayed lidocaine on the spot to relieve the pain which did cool it down. In January, I broke out in hives, big red whelps all over my torso. At the end of February, I went to see a Dermatologist. He sent me to an Allergy and Asthma doctor. I was prescribed about five antihistamines to take daily. I still have these whelps.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- (?)May23 Bloodwork, negative for auto immune response; (?)MAY23 Inhalant test, Hay fever
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High Blood Pressure
- Andere Medikamente
- TOPROL XL; hydrochlorothiazide; losartan; hydralazine; clonidine patch; CENTRUM SILVER for women; calcium with vitamin D; coQ10
- Allergien
- Latex; NORVASC
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 15.05.2023
- Impfdatum
- 12.10.2022
- Beginn
- 01.02.2023
- Tage bis Beginn
- 112,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Chills
Pain
Pyrexia
SARS-CoV-2 test positive
Symptomtext
I had chills, fever and body aches for two days after receiving the vaccine. I tested positive for COVID-19 in 02/2023. I contacted my doctor and got a prescription for PAXLOVID. I had no complications taking the medication. As of today, I have no lingering COVID-19 symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- FEB2023 COVID-19 test positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 04.05.2023
- Impfdatum
- 07.10.2022
- Beginn
- 22.02.2023
- Tage bis Beginn
- 138,0
- Dosis
- 5
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Oropharyngeal pain
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
My symptoms began as a sore throat and mild sniffles. I tested positive for COVID-19 on February 24, 2023 and began taking PAXLOVID on the 25th. Within 2 days I was testing negative but wasn't feeling better, but not worse. As of today I have no lingering symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- COVID-19, positive, 02/24/2023
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Pacemaker
- Andere Medikamente
- Atorvastatin; losartan; aspirin; loratadine
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 03.05.2023
- Impfdatum
- 28.10.2022
- Beginn
- 30.10.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site cellulitis
Injection site swelling
Injection site warmth
Symptomtext
Warmth, swelling and cellulitis and pain at the injection site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site cellulitis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Urinary Tract Infection
- Vorgeschichte
- Muscle weakness, Urine Retention, hemorrhoids, post nasal drip, iron deficiency anemia, HX of UTIs
- Andere Medikamente
- Furosemide 20 mg, Acidophilus, Senna 8.5 mg, Vitamin D2 2,000 Oxybutynin CLE 10, Venlafaxine HCL 12.5 mg, Ferrous Sulfate 325 mg, Cranberry Concentrate 500 mg, Levothyroxine 0.112 mg, Hydrocodone Acetamin 5-325 mg and Tylenol 325 mg, Gabape
- Allergien
- Bactrim, Doxycycline, hydralazine, penicillin, zithromax and Zosyn
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 26.04.2023
- Impfdatum
- 07.10.2022
- Beginn
- 04.04.2023
- Tage bis Beginn
- 179,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Fatigue
Headache
Myalgia
Oropharyngeal pain
SARS-CoV-2 test positive
Symptomtext
4/4/2023 in the afternoon I had a sore throat, muscle aches, fatigue, and headache. 4/5 at home COVID-19 test positive. Televisit with doctor who prescribed PAXLOVID. 4/6 I started to feel much better. Fatigue lingered for about 10 days after the beginning of taking PAXLOVID.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 5April2023 at home COVID-19 test positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Parathyroidism; High Blood Pressure; High Cholesterol
- Andere Medikamente
- Carvedilol; lisinopril; allopurinol; famotidine; low dose aspirin; bupropion; amlodipine; atorvastatin; escitalopram; vitamin D3
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 19.04.2023
- Impfdatum
- 04.10.2022
- Beginn
- 20.03.2023
- Tage bis Beginn
- 167,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Fatigue
Oropharyngeal pain
SARS-CoV-2 test positive
Sinus congestion
Symptomtext
First, sore throat, congested sinus up above my head. I tested positive with a rapid home COVID-19 test and it was positive on 03/21/2023. On 03/23/2023 I called my doctor in the morning. The doctor called in a PAXLOVID prescription, if I needed it. I never filled the prescription. That went on for 5 or 6 days. I drank ginger tea, lemon and honey and lots of sleep. I stayed home for 7 days from work then it was Spring break, After the 10 days, I felt normal, I was just tired. I tested and it was still positive after 10 days. I did not test anymore after that.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 21MARCH2023 home COVID-19 test positive; 22MARCH2023 home COVID-19 positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Obesity
- Andere Medikamente
- ONE A DAY women's multivitamin; vitamin D3; LEVOTHROID; vitamin B12; fluoxetine
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 19.04.2023
- Impfdatum
- 16.10.2022
- Beginn
- 27.02.2023
- Tage bis Beginn
- 134,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Headache
Insomnia
Rhinorrhoea
SARS-CoV-2 test positive
Sinus disorder
Symptomtext
I got COVID-19 on 02/27/2023. I tested positive for COVID-19 on 02/28/2023. I went to see doctor on 02/28/2023. I had a headache and runny nose and did not sleep very well for two days. I took PAXLOVID on medication and took one of the pills only and did not take the full course of treatment. I still have some sinus issues today but have well recovered from my symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- 28FEB2023 COVID-19 test positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Turmeric
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 19.04.2023
- Impfdatum
- 18.10.2022
- Beginn
- 17.04.2023
- Tage bis Beginn
- 181,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Cough
Pain
Pyrexia
SARS-CoV-2 test negative
Symptomtext
On Monday I had a high fever, highest has been 102 and chills. The fever continues and I have cough, aches and pains. I've taken TYLENOL, SUDAFED, AFRIN, NYQUIL.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- COVID-19, negative, 04/18/2023
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Migraines; Myotonic Dystrophy
- Andere Medikamente
- N/A
- Allergien
- Mushrooms
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 18.04.2023
- Impfdatum
- 06.10.2022
- Beginn
- 05.12.2022
- Tage bis Beginn
- 60,0
- Dosis
- 5
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Chills
Exposure to SARS-CoV-2
Fatigue
Lethargy
Nasopharyngitis
SARS-CoV-2 test positive
Symptomtext
My wife contracted COVID-19 first, so I got it from her. I had chills for a day. I was just lethargic. I don't remember anything else other than those symptoms. I may have had some cold symptoms but they were mild and I was just tired. I tested positive on 12/05/2022. I did get PAXLOVID and I tested negative on 12/10/2022. I went back to life as normal. I tested positive again on 12/16/2022. I tested negative again on 12/21/2022. I did get a rebound case while my wife did not.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- 05DEC2022 at home COVID-19 test positive; 10DEC2022 at home COVID-19 test, negative; 16DEC2022 at home COVID-19 test, positive; 19DEC2022 at home COVID-19 test, positive; 21DEC2022 at home COVID-19 test, negative
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Lower Back Pain
- Andere Medikamente
- Allopurinol; low dose aspirin; atorvastatin; etodolac; multivitamin
- Allergien
- Lactose; hay fever
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 17.04.2023
- Impfdatum
- 12.10.2022
- Beginn
- 24.02.2023
- Tage bis Beginn
- 135,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Headache
Oropharyngeal pain
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
Started having a headache, sore throat and congestion. Took a home COVID-19 test and was positive. Contacted doctor and told to rest.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- 24FEB02 Home COVID-19 test - Positive.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Bursitis; Torn Rotator Cuffs; Sinus Infections; Heart condition, High blood pressure.
- Andere Medikamente
- Rosuvastatin; Omeprazole; Metoprolol; Loratadine; Irbesartan; Low dose Aspirin; Multivitamin; Potassium; Vitamin E; Niacinamide.
- Allergien
- Lodine; Oxycontin; Penicillin.
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 17.04.2023
- Impfdatum
- 13.10.2022
- Beginn
- 09.04.2023
- Tage bis Beginn
- 178,0
- Dosis
- 5
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
COVID-19
Chills
Cough
Dysphonia
Fatigue
Feeling abnormal
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
I started feeling bad on Sunday, run down, very tired, no fever. My Dad and brother and I were together over the weekend we thought we had a sinus infection because of the weather change. It feels more like a head cold, congestion, runny nose, back pain from coughing, chills. I took a home test on April 8, 2023, it came back negative. On Monday I was feeling worse, I tested again, this time it was positive, I had a telehealth visit and was prescribe PAXLOVID. I have taken the full five take course of medication. I still have congestion, raspy throat. I am not sure if it is my allergies that are bothering me or if I am not completely over COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- 08APR2023 home COVID-19 test negative; 10APR home COVID-19 test positive; 15APR home COVID-19 test positive
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Hypertension; Asthma
- Andere Medikamente
- Enalapril; LIPITOR; baby aspirin; ONE A DAY men's; vitamin C; fish oil; metoprolol; latanoprost; ADVAIR; albuterol inhaler
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 14.04.2023
- Impfdatum
- 13.10.2022
- Beginn
- 01.12.2022
- Tage bis Beginn
- 49,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Diarrhoea
Laboratory test
Medical diet
Symptomtext
I did not have an adverse reaction to the vaccine. I started having diarrhea in 12/2022. I have seen my doctor and I was referred to a gastroenterologist. I have had multiply test but they are unable to determine the cause. I am on a restricted diet and prescribed a prescription and I am to wait for about 3 months. Currently I am trying to stay with the diet to control the diarrhea.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypothyroidism
- Andere Medikamente
- SYNTHROID; ZOLOFT; LIPITOR; PRILOSEC; OCUVITE
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 13.04.2023
- Impfdatum
- 21.10.2022
- Beginn
- 12.02.2023
- Tage bis Beginn
- 114,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Pain in extremity
SARS-CoV-2 test positive
Symptomtext
I had a little arm pain for about two days. I tested positive for COVID-19 on 02/12/2023. I contacted my doctor and got a prescription for PAXLOVID, but I did not take it. I figured I would let it run its course. I am feeling better without any lingering symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- 12FEB2023 COVID-19 test positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Psoriatic Arthritis
- Andere Medikamente
- N/A
- Allergien
- Seasonal allergies
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 13.04.2023
- Impfdatum
- 10.10.2022
- Beginn
- 20.03.2023
- Tage bis Beginn
- 161,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Dizziness
Fatigue
Feeling abnormal
Head discomfort
SARS-CoV-2 test positive
Screaming
Vertigo
Symptomtext
I started feeling a little something. I was just feeling off, but I wanted to take a test because was going to see my grandkids. I got a prescription for PAXLOVID. I took the whole regimen for all 5 days and on the last day I was feeling fine but then I started to notice I was feeling dizzy. I ended up getting diagnosed with vertigo. It was really bad; I woke up screaming because my head felt like it was in a hurricane. I didn't have any other COVID-19 symptoms. I had fatigue after the vertigo. I don't know if it is related to the PAXLOVID or the COVID-19 but the vertigo was the worst part. The vertigo lasted for about 24 hours. It has not returned since then.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- 20MAR2023 COVID-19 test positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Migraines; Leg pain; Back pain
- Andere Medikamente
- Zolmitriptan; ALEVE
- Allergien
- Codeine; tramadol
- Vorherige Impfungen
- -
- Staat
- HI
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 12.04.2023
- Impfdatum
- 16.10.2022
- Beginn
- 27.11.2022
- Tage bis Beginn
- 42,0
- Dosis
- 5
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cold sweat
Fatigue
Headache
Nasal congestion
Pain
Pyrexia
SARS-CoV-2 test positive
Symptomtext
11/27/2022 Symptoms - fatigue, headache, stuffy nose, body aches, low grade fever and cold sweats. I contacted my Physician and was prescribed Paxlovid. I finished the 5-day course. On 12/01/2022 my symptoms returned for another 3 days. I took OTC medications for body aches and fever and antihistamines for nasal congestion.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 27Nov2022 COVID-19 test - Positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Alopurinol; Alprazolam; Descovy prep medication Famotidine; Atorvastatin; Montelukast; Azelastine
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 11.04.2023
- Impfdatum
- 10.10.2022
- Beginn
- 18.02.2023
- Tage bis Beginn
- 131,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Feeling abnormal
Malaise
Rhinorrhoea
Throat irritation
Symptomtext
My symptoms were very mild, I only felt bad for one day. I had a runny nose and scratchy throat. I was able to do normal activities. The first time I had COVID I was sick. This time it was mild. The doctor called in some antibiotics. I think the vaccines are working.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Blood Pressure; Seasonal Allergies
- Andere Medikamente
- High blood pressure medication
- Allergien
- RIFADIN; lisinopril
- Vorherige Impfungen
- COVID vaccines; Body aches
- Staat
- MI
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 07.04.2023
- Impfdatum
- 06.10.2022
- Beginn
- 21.01.2023
- Tage bis Beginn
- 107,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Body temperature increased
Fatigue
Influenza like illness
Myalgia
Oropharyngeal pain
Respiratory tract congestion
SARS-CoV-2 test
Symptomtext
I had a temperature up to 102.0; muscle aches, fatigue, congestion, sore throat and flu like symptoms. The temperature lasted for about 4 days and then on the 5th day my temperature was normal. It wasn't until Monday I reached out and spoke to my doctor and they wanted to give Paxlovid, but I was told I may have a rebound if I took that medicine. I decided to just treat the symptoms and I did just that. The fatigue lasted 4-5 weeks and I was weak and exhausted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 Test
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Rhinotorid Arthritis; Hashimoto
- Andere Medikamente
- Levothyroxine; Folic Acid; Methotrexate; Meloxicam; Multivitamin One a Day; Calcium with Vitamin D; Clairton; Vitamin D; Rosuvastatin Calcium
- Allergien
- Penicillin
- Vorherige Impfungen
- Shingle -Flu like symptoms
- Staat
- MI
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 04.04.2023
- Impfdatum
- 07.10.2022
- Beginn
- 17.02.2023
- Tage bis Beginn
- 133,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Drainage
Oropharyngeal pain
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Sneezing
Symptomtext
I tested positive for COVID-19 on 2/18/23. I noticed that the kit had expired, so I took another test on 2/19/23 and still tested positive. I had congestion, sore throat, coughing, sneezing, fever, and drainage. I contacted my doctor and was prescribed PAXLOVID, but because of my health condition I was only able to take one pill a day instead of two. I recovered and then all the symptoms came back. I contacted my doctor, and they told me that I was probably having a PAXLOVID rebound case. This lasted for about 5 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- 18FEB2023 COVID-19 test positive; 18FEB2023 COVID-19 test positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Blood Pressure; Pacemaker; Prostate Cancer; Diabetic
- Andere Medikamente
- ELIQUIS; hydralazine; lisinopril; LASIX; metformin; tamsulosin; PRESERVISION; multivitamin
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 02.04.2023
- Impfdatum
- 13.12.2022
- Beginn
- 10.01.2023
- Tage bis Beginn
- 28,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Abdominal pain
Asthenia
Bile duct stent insertion
Biopsy liver
Coeliac plexus block
Computerised tomogram abdomen abnormal
Constipation
Endoscopic retrograde cholangiopancreatography
Fatigue
Hallucinations, mixed
Laboratory test
Pain
Pancreatic carcinoma metastatic
Paranoia
Positron emission tomogram
X-ray
Symptomtext
She was diagnosed with metastatic pancreatic cancer at the end of January 2023 and opted for no treatment in follow-up with oncology. 3/7 she saw a pain specialist in the plan clinic and is scheduled for a celiac plexus block 3/27 for pain control. 3/13 she had an ERCP with a covered metal stent placed in the CBD. 3/23 - 3/21 she was admitted to the hospitalist service for pain control. She was started on a fentanyl patch in addition to Norco. CT at that time showed rapidly progressive malignancy. She declined both hospice and home health at that time and opted to discharge home. 3/23 she returns to the emergency room with audio and visual hallucinations, paranoia, weakness, fatigue, severe right abdominal pain, constipation. She discharged 3/27 on hospice.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- 4,0
- Labordaten
- Labs, ERCP 3/13/23 celiac plexus block 3/27/23 xrays, CTs, PET scan 2/10/23 liver biopsy 1/31/23
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma, COPD, prediabetes
- Andere Medikamente
- BUPROPION (WELLBUTRIN SR) 150 MG 12 HR TABLET Take 150 mg by mouth 2 (two) times daily. DIPHENHYDRAMINE (BENADRYL) 25 MG CAPSULE Take 25 mg by mouth every 6 (six) hours as needed for Allergies. KETOROLAC (TORADOL) 10 MG TABLET
- Allergien
- PCN causes hives Erythromycin causes rash Monistat causes rash
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 10.03.2023
- Impfdatum
- 14.10.2022
- Beginn
- 30.12.2022
- Tage bis Beginn
- 77,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Chills
Cough
Fatigue
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Sinusitis
Upper-airway cough syndrome
Symptomtext
I started feeling tired and I had postnasal drip. I started getting more of a runny nose and being tired. Then I developed a fever of around 100 as well as chills. I completed an at home COVID-19 test which was positive. I went to the clinic and was prescribed an anti-virials to shorten the symptoms. I took them for 3 days I felt better. It took about 8 to 9 days to be symptom free. I have another cough now along with another sinus infection. I am not sure whether having COVID-19 is making me more susceptible to sinus infections which I had not had in years prior.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- COVID-19 Home Test-Positive-December 31, 2022.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Acid Reflux
- Andere Medikamente
- Propecia; Pepcid; Vitamin C; Magnesium; Calcium
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 07.02.2023
- Impfdatum
- 04.11.2022
- Beginn
- 28.11.2022
- Tage bis Beginn
- 24,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Fatigue
Influenza virus test negative
Nasopharyngitis
Oropharyngeal pain
Pain
Respiratory tract congestion
SARS-CoV-2 test positive
Throat irritation
Symptomtext
I had a slight cough that Monday and I started to wonder if I was getting sick. It started with a sore throat, and I was tired and achy. I really didn't have much more than that. I contacted the doctor office on Tuesday November 29, 2022, after testing positive using a home COVID-19 test. I was not prescribed any medications and I was advised to remain quarantined. I called the doctor again because I was still testing positive. I was still symptomatic, but I still had a scratchy sore throat. I also had some lingering congestion. I was advised to continue to take over the counter medications for any symptoms I had remaining. It took about 14 days to get better. I got sick again in January with a cold again which lasted for about 2 weeks as well. I went to the doctor, and they tested for COVID-19 and the Flu. Both were negative.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 Home Test- November 29, 2022-Positive
- Aktuelle Erkrankungen
- Cold
- Vorgeschichte
- N/A
- Andere Medikamente
- Low Dose Aspirin; Atorvastatin; Probiotic; Cranberry Supplement
- Allergien
- Sulfa Drugs; Cephalexin; Avocado; Banana
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 25.01.2023
- Impfdatum
- 25.10.2022
- Beginn
- 01.12.2022
- Tage bis Beginn
- 37,0
- Dosis
- 5
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Joint swelling
Muscle spasms
Pain
Ultrasound Doppler
Symptomtext
I started noticing my right ankle was swollen it was big. Then in the night I got charlie horses in my right calf several times at night. I went to see my PCP who wants me to have the veins in my legs scanned. Since I saw him I only now having the pain in the day, it hurts.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Bisoprolol; HTCZ; amlodipine; losartan; senior multivitamin; calcium; vitamin C; E; D3, BAYER aspirin
- Allergien
- Ampicillin; penicillin
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 24.01.2023
- Impfdatum
- 21.10.2022
- Beginn
- 26.12.2022
- Tage bis Beginn
- 66,0
- Dosis
- 5
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Chills
Increased upper airway secretion
Pain
SARS-CoV-2 test positive
Symptomtext
I received my Covid -19 vaccine on 10/21/2022. On 12/26/2022 I started feeling drainage down my throat. I woke up the next day with body aches and chills. I tested positive that day for Covid -19. After contacting my doctor, I took over the counter medications. Symptoms lasted about a week.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Covid-19 PCR test
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Fish oil; Vitamin D
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 20.01.2023
- Impfdatum
- 20.10.2022
- Beginn
- 14.12.2022
- Tage bis Beginn
- 55,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Nasal congestion
Oropharyngeal pain
SARS-CoV-2 test positive
Somnolence
Throat irritation
Symptomtext
I had a scratchy sore throat and stuffy nose. I tested positive for COVID-19 at the clinic. The doctor prescribed me PAXLOVID. I started feeling better the next day other than being sleepy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- COVID-19 test, 12/15/2022, positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Blood Pressure
- Andere Medikamente
- Calcium plus D3
- Allergien
- Hay fever
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 20.01.2023
- Impfdatum
- 17.10.2022
- Beginn
- 26.12.2022
- Tage bis Beginn
- 70,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lip swelling
Mouth swelling
Oral herpes
Pain in extremity
Symptomtext
I only had a sore arm after receiving the vaccine for four days. On 12/26/2022, I developed cold sores around the outside of mouth. A whole line on the bottom lip. Citrus fruit triggers them for me and we had a citrus sauce on something we ate on 12/25/2022. My mouth was very swollen too. I contacted my doctor and was prescribed VALTREX. As of today, the cold sores are gone but I continue to have slightly swollen lips.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Multivitamin
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 19.01.2023
- Impfdatum
- 11.10.2022
- Beginn
- 06.12.2022
- Tage bis Beginn
- 56,0
- Dosis
- 5
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Ear discomfort
Exposure to SARS-CoV-2
Fatigue
Malaise
Oropharyngeal pain
Pain
Respiratory tract congestion
SARS-CoV-2 test positive
Upper respiratory tract congestion
Symptomtext
8 weeks following this vaccination I developed very very mild COVID symptoms, 3 days after my husband developed a severe case of COVID-19 on Dec. 3, 2022. His COVID symptoms occurred 3 days after we flew. I did not test positive for COVID at that time. I did not even think I had COVID. My husband received Paxlovid 24 hours after he developed symptoms (Dec. 3, Dec. 4) and appeared to be sufficiently recovered to fly home on Sat, Dec, 10, 2022, with no symptoms, fever, etc. I still tested negative for COVID Dec. 8 but had a slight cough and was tired. After flying home on Dec. 10, I developed severe COVID symptoms on Sunday, Dec. 11, 2022: heavy congested in my head, a sore throat and aching, plugged up ears, eventually a strong cough and upper respiratory congestion. I tested positive for COVID at this time (home test). My husband also became I?ll that same day with the same symptoms. We did NOT develop fevers. We were very sick for 2 weeks. (Dec. 11-24)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Only home COVID tests.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- -High blood pressure
- Andere Medikamente
- -50 mg Losartan -81 mg aspirin -500 mg Vitamin D -37.5 mg Venlafaxine
- Allergien
- -Gadolinium contrast dye -nickel -ibuprofen -squid, crayfish
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 15.01.2023
- Impfdatum
- 22.08.2022
- Beginn
- 01.08.2022
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- UN / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ear pain
Eye pain
Hyperacusis
Lymph node pain
Lymphadenopathy
Neck pain
Symptomtext
I have pain in the neck , ears, and eye, some sound is painful, and sometime, I do not see clearly. In the neck there some painful swollen glands. This appeared few days after the vaccination, and the pain persists.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ear pain
- Hospital-Tage
- -
- Labordaten
- I was given ibuprofen, cyclobenzaprine, neomycin-polymyxin-hc, (on 12/22/2022) and acetic acid otic solution (on 01/03/2023) but the pain does not go away
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- After the first two doses for (Moderna) vaccine, I felt a little problem about hearing, but after the booster vaccine (Moderna)
- Staat
- MA
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 13.01.2023
- Impfdatum
- 12.10.2022
- Beginn
- 30.12.2022
- Tage bis Beginn
- 79,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Fatigue
Paranasal sinus discomfort
SARS-CoV-2 test positive
Sinus disorder
Symptomtext
I felt very tired after receiving the vaccine for a day. I tested positive for COVID-19 on 12/30/2022. I had sinus pressure and a tickle. I contacted my doctor, and they did not recommend taking Paxlovid. I took Advil for one day to help me with my symptoms. It took thirteen days to test negative for COVID-19, but I finally tested negative on 01/13/2023.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 30DEC2022 COVID-19 Test - Positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypoglycemic
- Andere Medikamente
- Prenatal Vitamin
- Allergien
- Tomatoes; Mangos
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 13.01.2023
- Impfdatum
- 10.10.2022
- Beginn
- 29.10.2022
- Tage bis Beginn
- 19,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Breast pain
Breast swelling
Mammogram normal
Ultrasound scan
Symptomtext
Pain and swelling in left breast. Symptoms gradually subsided and nothing showed on mammogram.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Breast pain
- Hospital-Tage
- -
- Labordaten
- Diagnostic Mammogram & Ultrasound
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High blood pressure; epilepsy; anxiety
- Andere Medikamente
- Losartan; levetiracetam; buspirone; escitalopram; vitamin D; PRESERVISION vitamin supplement; ALLERTEC
- Allergien
- Seasonal allergies
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 13.01.2023
- Impfdatum
- 12.10.2022
- Beginn
- 26.12.2022
- Tage bis Beginn
- 75,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Decreased appetite
Fatigue
Headache
Oropharyngeal pain
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
On 12/26/2022 I tested positive for Covid. Sore throat, coughing, headache, low grade fever, fatigued and severely congested, lack of appetite. All the symptoms are gone except some minor congestion and coughing. First negative test on 1/4, second on 1/6. The low grade fever and headache were gone by 1/1/2023. Still mildly congested from time to time during the day and I cough more when I am trying to lie down. I am getting less fatigued each day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Used rapid test and it was positive.
- Aktuelle Erkrankungen
- Just my normal allergies
- Vorgeschichte
- Overweight, allergies
- Andere Medikamente
- Chlorpheniramine Maleate Extended Release, 12 Mg, Sudafed 12 hour.
- Allergien
- Allergic to Mango, pistachios, cashews. Dust, Mold, Ragweed
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 12.01.2023
- Impfdatum
- 10.10.2022
- Beginn
- 05.01.2023
- Tage bis Beginn
- 87,0
- Dosis
- 5
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
COVID-19
Cough
Diarrhoea
Exposure to SARS-CoV-2
Lacrimation increased
Pain
Rhinorrhoea
SARS-CoV-2 test positive
Sneezing
Symptomtext
A friend had let me know they had tested positive for COVID-19, and I was around them, so I took a COVID-19 home test and it was positive. That night I had a lot of diarrhea, a runny nose, a ton of sneezing, and runny eyes. I did have a cough that now that I think about it may have started the day before because it was different than my normal allergy cough. I called my doctor that same day and they did give me PAXLOVID which I started Friday after adjusting the normal medications I take. I started that on Friday as instructed and I did not really notice if it made a difference or not. I probably about 80% better at this point, I am achy and I do not have a lot of energy but the runny nose, sneezing and coughing are gone.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- COVID-19 home test
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Atrial Fibrillation
- Andere Medikamente
- ELIQUIS; rosuvastatin; metoprolol; TYLENOL; turmeric
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 11.01.2023
- Impfdatum
- 07.10.2022
- Beginn
- 22.12.2022
- Tage bis Beginn
- 76,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Headache
Influenza virus test
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Throat irritation
Upper respiratory tract congestion
Symptomtext
My COVID-19 symptoms started on 12/22/2022 in the evening at 07:00PM. I had fever of 102.08, scratchy throat, runny nose, and chest congestions. It was mostly on my upper respiratory. I went to the urgent care on 12/23/2022 they did COVID-19 test and Flu. I was positive for COVID-19 infection. At the urgent care they prescribe me with PAXLOVID for 5 days. I self tested with a home COVID-19 test on 12/30/2022 which was negative. On 01/03/2023 I had a runny nose and a slight headache. On 01/05/2023 I tested positive for COVID-19 again. I am not taking any medication just trying to stay hydrated. I did not take any COVID-19 tests yet.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- 23DEC2022 COVID-19 test positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Multivitamins CENTRUM SILVER; probiotics; milk capsules; vitamin D3; NAC
- Allergien
- Iodine
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 11.01.2023
- Impfdatum
- 10.10.2022
- Beginn
- 26.12.2022
- Tage bis Beginn
- 77,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Exposure to SARS-CoV-2
Malaise
Oropharyngeal pain
Productive cough
Pulmonary congestion
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
I was not feeling well and had a fever overnight along with a sore throat. I did have a family member who had tested positive for COVID-19, but I had tested negative that same day that I started I not feeling well. The next day I was worse with a sore throat, a cough, runny nose and the fever was still happening. I reached out to my health care provider when my fever was not going away and at that point, I had tested positive. I was offered Paxlovid but declined but was given a medication for the runny nose. I did have my flu shot the same day that I had my COVID-19 vaccine, but I do not have the information for that shot. I am testing negative, but I am still coughing and have a lot of phlegm and lung congestion.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- COVID-19 Home Test
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Flonase; Multivitamin; Vitamin D; Probiotic
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 11.10.2022
- Beginn
- 02.01.2023
- Tage bis Beginn
- 83,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Feeling abnormal
Headache
Oropharyngeal pain
Pyrexia
SARS-CoV-2 test positive
Symptomtext
On Monday I felt pretty terrible. I had a sore throat and a headache. I had a fever of 100.5. I tested negative when I completed a home test. The next day I took another COVID-19 Test and was positive. I called my doctor and he prescribed Paxlovid which I started on Tuesday night. By the next morning I was feeling fine. I was still testing positive, but I immediately felt 100% better. I have felt fine every since like I had a miracle drug.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- COVID-19 Home Test-01/03/2023-Positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Diabetes; High Blood Pressure; High Cholesterol
- Andere Medikamente
- Rosuvastatin; Preservision; Co Q 10; Varilife Multi-Vitamin; Iron; Olmesartan; Hydrochlorothiazide; Metformin Hydrochloride; Tramadol; Allergy Medication as needed
- Allergien
- Augmentin
- Vorherige Impfungen
- Moderna-Dose 2-02/25/2021-inflammation in right arm and vaccine was administered in left arm. It lasted for 15 hours
- Staat
- NY
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 11.10.2022
- Beginn
- 28.12.2022
- Tage bis Beginn
- 78,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest X-ray
Cough
Decreased appetite
Dizziness
Fatigue
Influenza
Positive airway pressure therapy
Pyrexia
Somnolence
Symptomtext
I was very tired, and went to bed. I had a low grade fever and no appetite. I started coughing. The fever went away for a day but then came back and then I went to the urgent care. I had a chest x-ray, and I still had very bad coughing. The doctor put me on CPAP but told to not take it until needed. I took it about 2 days later, and coughing medicine over the counter. I was so tired, all I wanted to do was sleep. I had no appetite. I was diagnosed with influenza type A, which was odd because I had taken the flu shot about 2 weeks after taking the COVID vaccine. I also had lightheadedness, but no aches and pains. 2 weeks later I still have a cough and my fatigue is still lingering. It is not as bad but it is still pretty strong.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- Chest x-ray
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- COPD
- Andere Medikamente
- None
- Allergien
- Latex; penicillin
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 11.10.2022
- Beginn
- 04.01.2023
- Tage bis Beginn
- 85,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Fatigue
Oropharyngeal pain
Productive cough
SARS-CoV-2 test positive
Secretion discharge
Symptomtext
I tested positive for Covid on Wednesday I was prescribed PAXLOVID by my doctor; I was very tired dry cough and I was coughing green mucus and had sore throat for 1 day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Covid-19 positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Diabetes Type 2
- Andere Medikamente
- TRESIBA; metformin; losartan; TRULICITY; iron
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- WV
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 10.01.2023
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 5
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
COVID-19
Chest discomfort
Cough
Dry throat
Fatigue
Headache
Hypersomnia
Nausea
Oropharyngeal pain
Oxygen saturation decreased
SARS-CoV-2 test positive
Throat irritation
Symptomtext
I had my vaccination on 10/08/2022. I started to experience on 11/12/2022 fatigue nausea chest pressure and burning sore and dry throat headache joint pain. I didn't know if the dry mouth was due to Sjogren's. My oxygen level went to 95%. I tested COVID-19 Positive on 11/19/2022. I was prescribed Dipirona Metamizole and Notuss for the cough. I had a lot of joint pain headache and a lot of sleep spells.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- 11/19/2022 COVID-19 Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 10.01.2023
- Impfdatum
- 07.10.2022
- Beginn
- 07.12.2022
- Tage bis Beginn
- 61,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Ageusia
Anosmia
Bacterial infection
Bronchial haemorrhage
COVID-19
Cough
Fatigue
Feeling abnormal
Feeling hot
Headache
Oropharyngeal pain
Productive cough
Rhinorrhoea
SARS-CoV-2 test positive
Secretion discharge
Sinus congestion
Sputum discoloured
Throat irritation
Symptomtext
At the onset there was a scratchy throat, bleeding in left tonsil with a large debris; sore throat persisted the next day. I then became very fatigued and I felt warm but can't say I ever had a high fever. I did not have any muscle aches. Lots of sinus congestion throughout my head. I had a runny nose constant. Severe headache which persisted throughout entire experience. I had a cough. My lungs were clear but my upper respiratory area ad bronchial tubes will filled with phlegm and bloody mucous. It was dark grey/green. I contacted my doctor, he prescribed azithromycin 250mg x 6 tablets 5-day course of antibiotics on 12/15/2022. Event started when my wife and I flew to see family for a vacation before Christmas. Someone in the airport coughed on me and I believe that's where I got sick from. I did not take any action to contact my PCP. I was completely without any medication until I flew back home and went immediately to bed. From that point on, I was isolating myself for the next two to three weeks. I was miserable with these symptoms until the medication kicked in. My sinuses started to clear and my headache started to go away. I had a bacterial and viral infection at the same time. I was pretty much symptom free by about the 4th week. As of today, I still have a little of upper respiratory congestion and spitting up a little bit of phlegm and a cough. My nose finally feels like a nose again since about a week ago with no longer running. I had also lost my sense of taste and smell but gradually has come back.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 13DEC2022 COVID-19 at home test positive; 20DEC2022 COVID-19 at home test inconclusive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Enlarged Prostate
- Andere Medikamente
- Finasteride; tamsulosin; FLOMAX; multivitamin; vitamin D3
- Allergien
- Penicillin; nickel
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 10.01.2023
- Impfdatum
- 07.10.2022
- Beginn
- 27.11.2022
- Tage bis Beginn
- 51,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Dizziness
Ear pain
Feeling abnormal
Headache
Impaired work ability
Nasal congestion
Neck pain
Oropharyngeal pain
Pain
Respiratory tract congestion
SARS-CoV-2 test positive
Throat irritation
Symptomtext
Starting 11/27/2022, I got up and my head was stuffy and my throat was a little sore and I felt achy all over. After eating breakfast, I checked my blood pressure and blood sugar since I still felt poorly and they were normal. My nose felt stuffy and my throat was scratchy so I did an at-home COVID-19 test which was negative. So, I thought I had a cold. The next morning I still felt congested and lightheaded. I took another at-home COVID-19 test (11/28/2022) which was positive. I called my doctor to see what I could do. I was having a headache, body aches all over, some neck pain and no shortness of breath. My doctor sent in a prescription for PAXLOVID that evening. I wouldn't return back to work until 12/11/2022. I started feeling better by about 12/03/2022 and I started testing negative for COVID-19 by 12/09/2022. My right ear was bothering me during this time and, to this day, it is still aching from time to time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- At-home COVID-19 test (11/27/2022): negative; at-home COVID-19 test (11/28/2022): positive; at-home COVID-19 test (12/09/2022): negative
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Diabetes; High Blood Pressure
- Andere Medikamente
- Lisinopril; levothyroxine; atorvastatin; amlodipine; FARXIGA; baby aspirin; TOUJEO; NOVOLOG; multivitamin
- Allergien
- Penicillin; sulfa
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 09.01.2023
- Impfdatum
- 06.10.2022
- Beginn
- 26.12.2022
- Tage bis Beginn
- 81,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Balance disorder
COVID-19
Chills
Dizziness
Ear pain
Headache
Influenza
Insomnia
Oropharyngeal pain
Pain
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Tenderness
Visual impairment
Symptomtext
I took a COVID-19 PCR test on 12/22/2022 and it was negative. Starting around midnight on 12/26/2022, I got a sore throat and a dull pain in my right ear. I went to touch it and I would get a sharp pain. I was unable to sleep due to the ear pain. I went to urgent care the next day and was diagnosed with 2 types of flu: A and B. I was having headaches and, after that, I developed fever and chills. My fever never went higher than 100.5. The PCR test at urgent care came back positive for COVID-19 but the antigen test was negative for COVID-19. I treated myself with TYLENOL and congestion meds. My fever broke on 12/30/2022. After that, I had headaches and congestion still. I had a sore throat during all of this. Also, I had some dizziness and weakened sense of balance over that weekend. On 01/04/2022, I felt my vision fading slightly and I had an event of vision disruption for about 5 min then resolved. I am still having slight congestion to this day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- COVID-19 PCR test (12/22/2022): negative; Influenza tests: positive for A and B; PCR COVID-19 test: positive; antigen test for COVID-19: negative
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Seasonal allergies; CECLOR
- Vorherige Impfungen
- I get somewhat sick 12 hours after each COVID-19 vaccine (including this last one)
- Staat
- MA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 06.01.2023
- Impfdatum
- 06.10.2022
- Beginn
- 20.12.2022
- Tage bis Beginn
- 75,0
- Dosis
- 5
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Chest discomfort
Headache
Oropharyngeal pain
SARS-CoV-2 test positive
Symptomtext
I received the Covid-19 vaccine on 10/06/2022. On the morning of 12/20/2022 my chest was tight, headache and sore throat. By the 23 I went to urgent care and was testing positive for Covid-19. I was prescribed PAXLOVID. I started feeling fine quickly however I got re-infected with Covid 19 again on 01/03/2023. Symptoms came back.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Covid-19 test
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Asthma; Hypertension; Hyperthyroid; Necrotizing autoimmune Myopathy; GERD; Sleep Apnea; Fatty liver; Arthritis; Depression; Pre diabetes; Hyperlipidemia
- Andere Medikamente
- DUPIXENT; REPATHA; levothyroxine; ESTRING; valsartan; montelukast; amitriptyline; cetirizine; vilazodone; trazodone; omeprazole; melatonin; SYMBICORT; ADVIL; calcium; vitamin D; METAMUCIL; probiotic; TRULICITY; vitamin E; immunoglobin; OCTA
- Allergien
- Statin
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 06.01.2023
- Impfdatum
- 03.10.2022
- Beginn
- 26.12.2022
- Tage bis Beginn
- 84,0
- Dosis
- 5
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Fatigue
Injection site pain
Pain
SARS-CoV-2 test positive
Symptomtext
After my Moderna Bivalent 5th vaccine I had the normal soreness at the injection site, some aches and tiredmess all normal. on December 26,2022 I tested positive for Covid-19 by a home test done 2 times, I called my drs. office and was perscribed Paxlovid (Nirmatrelvir & Ritonavir Tablet Therapy Pack) for 5 days . I tested negative on January 1, 2023 and again on January 4, 2023
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Flowflex covid-19 Antigen Home tests
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension, Hypothyroid
- Andere Medikamente
- Lossrtsn tabs, Amlodipine Besylstr Tabs, L-Thyroxine (Synthroid) Tabs
- Allergien
- Lisinopril,
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 04.01.2023
- Impfdatum
- 04.10.2022
- Beginn
- 17.11.2022
- Tage bis Beginn
- 44,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dysgeusia
Headache
SARS-CoV-2 test negative
Sinusitis
Tenderness
Symptomtext
I started having a headache, tenderness in the face, metallic taste in my mouth that I know it's a sinus. I called my doctor and went in for an appointment did a rapid COVID-19 test that came back negative. I was put on an antibiotic for a sinus infection. I am feeling much better more like myself.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Rapid COVID-19 test negative
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- CLARITIN; DYMISTA; minocycline
- Allergien
- Penicillin; codeine; clams
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 22.12.2022
- Impfdatum
- 05.10.2022
- Beginn
- 14.12.2022
- Tage bis Beginn
- 70,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anosmia
COVID-19
Chills
Ear pain
Exposure to SARS-CoV-2
Headache
Influenza virus test negative
Malaise
Pyrexia
SARS-CoV-2 test positive
Taste disorder
Symptomtext
I caught what I thought was a cold and then began to feel not well. I had a low grade fever, chills, a very bad headache, my ears hurt as well. I had another family member test positive for COVID-19 after testing myself I tested positive for COVID-19 as well. This the second time I tested positive for COVID-19 and it is much worse this time with multiple symptoms. Loss of smell or smell and taste disorder as well.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- COVID-19 test positive Influenza test negative.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Seizure disorder; Diabetes
- Andere Medikamente
- Dilantin; Phenobarbital; Carbatrol; Percocet; Ozempic; Novolog; Basilar; Vitamin D; Vitamin B12
- Allergien
- Antibiotics; Dyes; Iodine; Shellfish
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 15.12.2022
- Impfdatum
- 07.12.2022
- Beginn
- 07.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Nausea
Vomiting
Symptomtext
NARRATIVE: Dizziness & Nausea Vomiting. She has been throwing up since receiving the injection @ 8AM. it is now 1456.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 12.12.2022
- Impfdatum
- 02.12.2022
- Beginn
- 28.06.2022
- Tage bis Beginn
- -
- Dosis
- 5
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bacterial test
COVID-19 immunisation
Erythema
Haemorrhage
Interchange of vaccine products
Lip swelling
Mouth ulceration
Oral mucosal eruption
Oropharyngeal pain
SARS-CoV-2 test
Sinusitis
Symptomtext
sinus infection; recurrent RIME; soreness at back of left throat; redness at back of left throat; recurrence of pin point hemorrhages; lip swelling/bumpy texture to lip oral mucosa; small ulcer on the interior oral mucosa of left cheek; Prior vaccinations: 1st Dose: PFIZER BIONTECH COVID-19 VACCINE (07-APR-2021); 2nd Dose: PFIZER BIONTECH COVID-19 VACCINE (28-APR-2021); 3rd Dose: PFIZER BIONTECH COVID-19 VACCINE (18-NOV-2021); Prior vaccinations: 1st Dose: PFIZER BIONTECH COVID-19 VACCINE (07-APR-2021); 2nd Dose: PFIZER BIONTECH COVID-19 VACCINE (28-APR-2021); 3rd Dose: PFIZER BIONTECH COVID-19 VACCINE (18-NOV-2021); This spontaneous case was reported by a physician and describes the occurrence of HAEMORRHAGE (recurrence of pin point hemorrhages) in a 58-year-old female patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. 053D22A) for COVID-19 prophylaxis. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Burning lips (On August 13 I began experiencing a burning lip sensation while traveling), Nasal congestion (On August 13), Sore throat (On August 13), Cough (On August 13), COVID-19 (tested positive with at home COVID 19 antigen test on August 15 (day 1 of COVId 19 infection and tested positive with again on day 10 with final negative test on day 16)), Ulceration, Hemorrhage (pin point hemmorhages, vesicles that spontaneously hemorrhaged involving oral mucosa only), Oral mucosal eruption (mostly effecting lower lip, tongue, and gums diagnosed with reactive infectious mucocutaneous eruption (RIME)) and Sinus infection (Sinus infection on 11/25/2022 treated with 10 day course of Augmentin 825 mg p.o. bid.) on 25-Nov-2022. Previously administered products included for COVID-19 vaccination: PFIZER BIONTECH COVID-19 VACCINE (dose 1 Pfizer lot#ER8729) on 07-Apr-2021, PFIZER BIONTECH COVID-19 VACCINE (dose 3 Pfizer lot # FH80JO) on 18-Nov-2021 and PFIZER BIONTECH COVID-19 VACCINE (dose 2. Pfizer lot # EW0169) until 28-Apr-2021; for COVID-19 prophylaxis: Spikevax (dose 4 Moderna Lot 014B22A) on 28-Jun-2022; for Sinus infection: AUGMENTINE PLUS (10 day course 825 mg p.o. bid.) on 25-Nov-2022 and VALACYCLOVIR MYLAN (500 mg p.o. bid and is still ongoing) on 28-Nov-2022; for Oral infection: TACROLIMUS (topical), PREDNISONE (40 mg prednisone with decreasing taper over two weeks) and CLOBETASOL E (topical). Past adverse reactions to the above products included No adverse event with AUGMENTINE PLUS, CLOBETASOL E, PFIZER BIONTECH COVID-19 VACCINE, PFIZER BIONTECH COVID-19 VACCINE, PFIZER BIONTECH COVID-19 VACCINE, PREDNISONE, Spikevax, TACROLIMUS and VALACYCLOVIR MYLAN. Concomitant products included AMOXICILLIN SODIUM, AMOXICILLIN TRIHYDRATE, CLAVULANATE POTASSIUM (AUGMENTIN SR) for Bacterial infection and Sinus infection, DIPHENHYDRAMINE HYDROCHLORIDE (BENADRYL A) for an unknown indication. On 02-Dec-2022, the patient received fifth dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) 1 dosage form. On 28-Jun-2022, the patient experienced COVID-19 IMMUNISATION (Prior vaccinations: 1st Dose: PFIZER BIONTECH COVID-19 VACCINE (07-APR-2021); 2nd Dose: PFIZER BIONTECH COVID-19 VACCINE (28-APR-2021); 3rd Dose: PFIZER BIONTECH COVID-19 VACCINE (18-NOV-2021)) and INTERCHANGE OF VACCINE PRODUCTS (Prior vaccinations: 1st Dose: PFIZER BIONTECH COVID-19 VACCINE (07-APR-2021); 2nd Dose: PFIZER BIONTECH COVID-19 VACCINE (28-APR-2021); 3rd Dose: PFIZER BIONTECH COVID-19 VACCINE (18-NOV-2021)). On 03-Dec-2022, after starting mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)), the patient experienced HAEMORRHAGE (recurrence of pin point hemorrhages) (seriousness criterion medically significant), LIP SWELLING (lip swelling/bumpy texture to lip oral mucosa) and MOUTH ULCERATION (small ulcer on the interior oral mucosa of left cheek). On 05-Dec-2022, the patient experienced OROPHARYNGEAL PAIN (soreness at back of left throat) and ERYTHEMA (redness at back of left throat). On an unknown date, the patient experienced SINUSITIS (sinus infection) and ORAL MUCOSAL ERUPTION (recurrent RIME). The patient was treated with PREDNISONE ongoing from 06-Dec-2022 at a dose of 40 milligram; TACROLIMUS (topical) ongoing from 03-Dec-2022 at an unspecified dose and frequency and CLOBETASOL (topical) ongoing from 03-Dec-2022 at an unspecified dose and frequency. At the time of the report, HAEMORRHAGE (recurrence of pin point hemorrhages), LIP SWELLING (lip swelling/bumpy texture to lip oral mucosa), MOUTH ULCERATION (small ulcer on the interior oral mucosa of left cheek), OROPHARYNGEAL PAIN (soreness at back of left throat), ERYTHEMA (redness at back of left throat), SINUSITIS (sinus infection), ORAL MUCOSAL ERUPTION (recurrent RIME), COVID-19 IMMUNISATION (Prior vaccinations: 1st Dose: PFIZER BIONTECH COVID-19 VACCINE (07-APR-2021); 2nd Dose: PFIZER BIONTECH COVID-19 VACCINE (28-APR-2021); 3rd Dose: PFIZER BIONTECH COVID-19 VACCINE (18-NOV-2021)) and INTERCHANGE OF VACCINE PRODUCTS (Prior vaccinations: 1st Dose: PFIZER BIONTECH COVID-19 VACCINE (07-APR-2021); 2nd Dose: PFIZER BIONTECH COVID-19 VACCINE (28-APR-2021); 3rd Dose: PFIZER BIONTECH COVID-19 VACCINE (18-NOV-2021)) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Bacterial test: Negative. On an unknown date, SARS-CoV-2 test: (Positive) tested positive with at home COVID 19 antigen test on August 15 day 1 of COVId 19 infection., (Positive) tested positive with again on day 10 and (Negative) final negative test on day 16. For mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Unknown), the reporter did not provide any causality assessments. It was reported that the patient developed recurrent RIME that began 1 day after a fifth dose of COVID-19 vaccine. Initial symptoms on first day after vaccination included lip swelling, recurrence of pin point hemorrhages, bumpy texture to lip oral mucosa and a small ulcer on the interior oral mucosa of left cheek. Began topcial clobetasol and topical tacrolimus day one of vaccination and continuing. On morning of day 3, patient woke up with soreness and redness at back of left throat. Notified both dermatology and Dr. and started 40 mg of prednisone on day 4 after vaccination. Company comment: This spontaneous case concerns a 58-year-old, female patient with medical history of COVID-19 infection, Reactive Infectious Mucocutaneous Eruption and Sinus infection, and past drug history of administration of three doses (doses 1, 2 and 3 in the COVID-19 vaccination series) of the Pfizer/BioNTech COVID-19 mRNA vaccine and a dose (dose 4 in the COVID-19 vaccination series) of the mRNA-1273 original vaccine (revaccination with different COVID-19 vaccine and interchange of vaccine products), who experienced the unexpected, serious (medically significant) event of haemorrhage (recurrence of pinpoint hemorrhages) and the unexpected, non-serious events of lip swelling, mouth ulceration, oropharyngeal pain, erythema, oral mucosal eruption and sinusitis. The events haemorrhage, lip swelling, mouth ulceration, oropharyngeal pain and erythema occurred beginning 1 day and up to 3 days after receiving a dose (dose 5 in the COVID-19 vaccination series) of the mRNA-1273 bivalent BA.4/BA.5 vaccine. The start dates of the other events were not provided, hence, the onset latency could not be assessed. It was reported that on August 13 (year not provided), the patient experienced a burning lip sensation while traveling. Upon returning home, she developed nasal congestion, sore throat and cough, and tested positive with a home COVID-19 Antigen test on August 15 (day 1 of COVID-19 infection). She again tested positive on day 10 with final negative test on day 16. During this time, the patient also developed ulcerations, pinpoint hemorrhages, vesicles that spontaneously hemorrhaged involving the oral mucosa only and mostly affecting the lower lip, tongue and gums. She was then diagnosed with Reactive Infectious Mucocutaneous Eruption (RIME). Treatment included prednisone 40 mg with tapering doses over 2 weeks, as well as topical tacrolimus and topical clobetasol. A swab for bacterial infection was negative. One week prior to vaccination, the patient had a sinus infection and was treated with a 10-day course of Augmentin (amoxicillin/clavulanate) 825 mg twice daily (bid). After 3 days, she was given valacyclovir 500 mg bid in preparation for the fifth dose of COVID-19 vaccine. One day after receiving the fifth dose of the mRNA-1273 bivalent BA.4/BA.5 vaccine, it was reported that the patient developed recurrent RIME. She experienced lip swelling, recurrence of pinpoint hemorrhages, bumpy texture of the lip oral mucosa, and a small ulcer on the interior oral mucosa of the left cheek. The patient used topcial clobetasol and topical tacrolimus. After 2 days, the patient woke up with soreness and redness at the back of left throat. The following day, the patient notified her doctors and she was started on 40 mg of prednisone. The outcomes of the events were unknown at the time of the report. The medical history of RIME remains a confounder for the events haemorrhage, lip swelling, mouth ulceration, oropharyngeal pain, erythema and oral mucosal eruption which are common symptoms of this reactive inflammatory mucositis. Of note, the history of COVID-19 infection may be a contributing factor to the development of RIME since there have been reports of multiple cutaneous manifestations of SARS-CoV-2 infection. The history of Sinus infection remains a confounder for the event sinusitis. The benefit-risk relationship of the mRNA-1273 bivalent BA.4/BA.5 vaccine is not affected by this report.; Sender's Comments: This spontaneous case concerns a 58-year-old, female patient with medical history of COVID-19 infection, Reactive Infectious Mucocutaneous Eruption and Sinus infection, and past drug history of administration of three doses (doses 1, 2 and 3 in the COVID-19 vaccination series) of the Pfizer/BioNTech COVID-19 mRNA vaccine and a dose (dose 4 in the COVID-19 vaccination series) of the mRNA-1273 original vaccine (revaccination with different COVID-19 vaccine and interchange of vaccine products), who experienced the unexpected, serious (medically significant) event of haemorrhage (recurrence of pinpoint hemorrhages) and the unexpected, non-serious events of lip swelling, mouth ulceration, oropharyngeal pain, erythema, oral mucosal eruption and sinusitis. The events haemorrhage, lip swelling, mouth ulceration, oropharyngeal pain and erythema occurred beginning 1 day and up to 3 days after receiving a dose (dose 5 in the COVID-19 vaccination series) of the mRNA-1273 bivalent BA.4/BA.5 vaccine. The start dates of the other events were not provided, hence, the onset latency could not be assessed. It was reported that on August 13 (year not provided), the patient experienced a burning lip sensation while traveling. Upon returning home, she developed nasal congestion, sore throat and cough, and tested positive with a home COVID-19 Antigen test on August 15 (day 1 of COVID-19 infection). She again tested positive on day 10 with final negative test on day 16. During this time, the patient also developed ulcerations, pinpoint hemorrhages, vesicles that spontaneously hemorrhaged involving the oral mucosa only and mostly affecting the lower lip, tongue and gums. She was then diagnosed with Reactive Infectious Mucocutaneous Eruption (RIME). Treatment included prednisone 40 mg with tapering doses over 2 weeks, as well as topical tacrolimus and topical clobetasol. A swab for bacterial infection was negative. One week prior to vaccination, the patient had a sinus infection and was treated with a 10-day course of Augmentin (amoxicillin/clavulanate) 825 mg twice daily (bid). After 3 days, she was given valacyclovir 500 mg bid in preparation for the fifth dose of COVID-19 vaccine. One day after receiving the fifth dose of the mRNA-1273 bivalent BA.4/BA.5 vaccine, it was reported that the patient developed recurrent RIME. She experienced lip swelling, recurrence of pinpoint hemorrhages, bumpy texture of the lip oral mucosa, and a small ulcer on the interior oral mucosa of the left cheek. The patient used topcial clobetasol and topical tacrolimus. After 2 days, the patient woke up with soreness and redness at the back of left throat. The following day, the patient notified her doctors and she was started on 40 mg of prednisone. The outcomes of the events were unknown at the time of the report. The medical history of RIME remains a confounder for the events haemorrhage, lip swelling, mouth ulceration, oropharyngeal pain, erythema and oral mucosal eruption which are common symptoms of this reactive inflammatory mucositis. Of note, the history of COVID-19 infection may be a contributing factor to the development of RIME since there have been reports of multiple cutaneous manifestations of SARS-CoV-2 infection. The history of Sinus infection remains a confounder for the event sinusitis. The benefit-risk relationship of the mRNA-1273 bivalent BA.4/BA.5 vaccine is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- Test Name: swab for bacterial infection; Test Result: Negative ; Test Name: home COVID 19 antigen test; Test Result: Positive ; Result Unstructured Data: tested positive with at home COVID 19 antigen test on August 15 day 1 of COVId 19 infection.; Test Name: home COVID 19 antigen test; Test Result: Positive ; Result Unstructured Data: tested positive with again on day 10; Test Name: home COVID 19 antigen test; Test Result: Negative ; Result Unstructured Data: final negative test on day 16
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Burning lips (On August 13 I began experiencing a burning lip sensation while traveling); Cough (On August 13); COVID-19 (tested positive with at home COVID 19 antigen test on August 15 (day 1 of COVId 19 infection and tested positive with again on day 10 with final negative test on day 16)); Hemorrhage (pin point hemmorhages, vesicles that spontaneously hemorrhaged involving oral mucosa only); Nasal congestion (On August 13); Oral mucosal eruption (mostly effecting lower lip, tongue, and gums diagnosed with reactive infectious mucocutaneous eruption (RIME)); Sinus infection (Sinus infection on 11/25/2022 treated with 10 day course of Augmentin 825 mg p.o. bid.); Sore throat (On August 13); Ulceration
- Andere Medikamente
- AUGMENTIN SR; BENADRYL A
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 09.12.2022
- Impfdatum
- 17.10.2022
- Beginn
- 06.12.2022
- Tage bis Beginn
- 50,0
- Dosis
- 1
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Musculoskeletal stiffness
Neck pain
Pain
Symptomtext
Pt experienced neck stiffness and severe pain - shooting pain going up to her head. Headache and severe pain. Unable to turn head certain directions. Was prescribed a muscle relaxer from PCP but didn't provide relief. Patient experienced this before with original Moderna shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- No.
- Aktuelle Erkrankungen
- NO
- Vorgeschichte
- Cholesterol Hypertension
- Andere Medikamente
- Hydrochlorosciazide 80-12.5MG Rosuzastatin 10MG
- Allergien
- Nickel Sulfate Coal Tar Aspirin
- Vorherige Impfungen
- Same pain as recent. 2/19/2021, 4/23/2021
- Staat
- MD
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 08.12.2022
- Impfdatum
- 09.10.2022
- Beginn
- 10.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Feeling abnormal
Gingival bleeding
Gingival pain
Pain in jaw
X-ray dental abnormal
Symptomtext
I received the vaccine on 10/9. On 10/10, I began having painful, bleeding gums and soreness under my jaw line, which worsened over the next day or two. When I bent my head forward/down, the front of my neck (under my jaw) felt strange. On 10/12, I saw my dentist because I was very concerned about these symptoms. He examined me, took an x-ray, and said he saw no problems except for gum recession (which is not a new problem for me). He denied that the vaccine could be the cause of bleeding gums, saying, "When gums bleed, it's because of gingivitis." However, he also indicated that he saw no evidence of gingivitis! Nonetheless, he recommended a different toothpaste, specially formulated for bleeding gums. However, the pain and bleeding resolved on its own by 10/14 or 10/15.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Gingival pain
- Hospital-Tage
- -
- Labordaten
- Dental x-ray taken on 10/12 showed no problems.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Hypothyroidism, slightly elevated cholesterol
- Andere Medikamente
- Levothyroxine, Metamucil, adult multivitamin
- Allergien
- none known
- Vorherige Impfungen
- Extremely heavy menstrual flow following first or second COVID vaccine, cannot remember which one (Pfizer: 04/2021 and 05/2021).
- Staat
- CA
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 06.12.2022
- Impfdatum
- 21.10.2022
- Beginn
- 26.11.2022
- Tage bis Beginn
- 36,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Headache
Nasal congestion
Oropharyngeal pain
Pain
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
I did not have a reaction to the vaccine. On 11/26/2022, I woke up with a runny and stuffy nose, headache, body aches and sore throat and throughout the day I felt worse. I tested positive for COVID-19 with a home test on 11/26/2022. I contacted my doctor that day and was given the prescription for PAXLOVID. I tested negative for COVID-19 six days later.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- 26NOV2022 COVID-19 test positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Diabetes; High Cholesterol; High Blood Pressure
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- SD
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 02.12.2022
- Impfdatum
- 17.10.2022
- Beginn
- 01.10.2022
- Tage bis Beginn
- -
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Computerised tomogram normal
Fatigue
Magnetic resonance imaging normal
Symptomtext
I initially started to have these symptoms after dose 3 of the vaccine which I was getting better after taking Tylenol. The symptoms returned along with fatigue and a lot of pain in my shoulder. I contacted the doctor who did an MRI and a CT scan in October of 2022. There was no finding, so they referred me to an ENT who gave me anti-allergy medicine which he prescribed. It was not helpful. I plan to readdress the symptoms at that time. There has been no improvement in the symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- MRI-October 2022-no finding CT Scan-October 2022-no finding
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Centrum Vitamins; Sevastian; Prostate Medication-name unknown
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 01.12.2022
- Impfdatum
- 28.11.2022
- Beginn
- 28.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Muscle spasms
Nausea
Pyrexia
Symptomtext
Call from client today. States within 6-12 hours of getting his Moderna Booster at 1:30 on 11/28/22 he developed high fever (he never measured his fever), severe chills to the point of spasms and nausea for 3 days. Symptoms were controlled with Ibuprofen, he called his doctor but was not seen, no hospitalization. He was insistant that a report be filed. I recommended he get tested for flu or covid but he declined. Stated he knew his body and it was a reaction to the vaccine. It was his 5th covid vaccine, only moderate side effects with first dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none listed
- Vorgeschichte
- none listed
- Andere Medikamente
- Unknown
- Allergien
- none listed
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 30.11.2022
- Impfdatum
- 13.10.2022
- Beginn
- 19.11.2022
- Tage bis Beginn
- 37,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Antibody test positive
Blood test
Fatigue
Pain in extremity
Symptomtext
My arm was sore, and I was tired after receiving the vaccine. I went to see my primary care doctor for routine exam and blood work. My doctor referred me to a hematologist for additional testing. I was informed that I have high levels of protein antibodies in my system. On 11/24/2022, I had blood work done again and the levels of decreased.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Blood Pressure; Arthritis
- Andere Medikamente
- N/A
- Allergien
- Amoxicillin
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 29.11.2022
- Impfdatum
- 16.10.2022
- Beginn
- 01.10.2022
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Axillary pain
Breast calcifications
Chills
Dizziness
Feeling abnormal
Groin pain
Mammogram abnormal
Pain
Rhinorrhoea
Sneezing
Symptomtext
I received the bivalent booster on 10/16/22. I have a history of urticaria triggered by cold air or cold surfaces that shows up on my legs. On 10/21/22 I spent several hours outside and it was slightly cool that day. When I came home I started to have a stinging sensation in my nostril followed by sneezing and a runny nose. My body in general felt like I had a cold or allergy. I had chills down my left side (injection side) and no fever. Two COVID home tests were negative and the symptoms completely vanished suddenly after a day or two. This happened again the next week following a walk at night when it was cold out possibly on 10/27/2022 at 9PM. This is a completely new and bizarre experience that happened twice the same way. I took 1/4 Zyrtec and it was gone the next day like nothing happened. I DIDN'T have urticaria but had these other allergy type symptoms. I also had random dizzy spells since receiving the booster. The last one was 11/11/22 in the morning. I also have calcifications in my left breast discovered after mammogram on 10/27/22 and follow up mammogram on 11/09/2022, which is the injection side. I always feel pain in my armpit and in my groin on that side of my body within a few hours post vax.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- I emailed my doctor on 11/14/2022 and spoke to her on the phone on 11/15/2022 for a consult. I did not have an office visit because the symptoms remitted by then. I didn't go to a doctor when the 2 incidents occurred because it didn't occur to me that it might be vaccine related at first.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Dense breasts, premenstrual dysphoric disorder Anxiety, ADHD
- Andere Medikamente
- Vyvanse, Dextroamphetamine, Lorazepam, Prozac D-Chiro Inositol and Myo-Inositol for hormonal imbalance Vitamin B6 and B12 Magnesium glycinate
- Allergien
- Penicillin, sulfa, cipro, bee stings, mold, dust, pollen, cold air sometimes triggers urticaria on legs Some raw fruit skins cause minor itchy throat (apples, peaches)
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 28.11.2022
- Impfdatum
- 10.10.2022
- Beginn
- 11.11.2022
- Tage bis Beginn
- 32,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain
Chills
Computerised tomogram
Haemorrhage
Symptomtext
Started with abdominal pain; irregular bleeding for couple of days and chills I went to the doctor and they put me on pro biotics and antibiotics
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- CT scan
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma; Paroxysmal; Irregular hear beat
- Andere Medikamente
- Atenolol; Montelukast; Estradiol; Medroxyprogesterone; Lisinopril; Atorvastatin; Flecainide; Warfarin; Chlorphenamine; Fish Oil; One a Day Vitamin
- Allergien
- Codeine, Fish
- Vorherige Impfungen
- Fever and chills
- Staat
- MD
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 28.11.2022
- Impfdatum
- 13.10.2022
- Beginn
- 01.11.2022
- Tage bis Beginn
- 19,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Musculoskeletal pain
Pain in extremity
Sciatica
Sitting disability
Symptomtext
I had severe pain from my buttocks down to my foot. There is pain behind my right back and side of my leg. The pain spreads out to the outer side. The pain is absolutely intense. I have never experienced anything like this in my life. It is difficult for me to even sit down. I contacted a doctor, through my insurance, and they contacted me back. I thought it was Bursitis, but when the doctor contacted me, she told me that she believes I have sciatica. I was advised to take one gabapentin at breakfast, one at lunch and two before bedtime. I'm also taking ALEVE to help with the pain. I am unable to see my doctor in person until December 22, 2022. The pain has decreased minimally due to the amount of gabapentin and ALEVE I am currently taking.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Migraines
- Andere Medikamente
- TOPAMAX; gabapentin; furosemide; propranolol; NEXIUM; vitamin D3; vitamin B12; ALEVE; ADVIL.
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 23.11.2022
- Impfdatum
- 26.10.2022
- Beginn
- 10.11.2022
- Tage bis Beginn
- 15,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Aphonia
COVID-19
Dysphonia
Exposure to communicable disease
Oropharyngeal pain
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
Was exposed to grandson on 07/11-11/11 and he was diagnosed with RSV. On 10/11 I became very hoarse, lost my voice, and horrible sore throat. I took cough meds and prednisone for my throat. After I completed the round of prednisone my sore throat returned and I developed congestion. At this time I took a COVID-19 test on 21/11 and tested positive. I called PCP and had telehealth visit and was prescribed PAXLOVID. Began taking PAXLOVID the evening of 11/21. Felt slightly better on the 11/22 and still feeling slightly better today.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- COVID-19 positive
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Lyme Disease
- Andere Medikamente
- Multivitamin; ca; B12; B3; mg
- Allergien
- Sulfa
- Vorherige Impfungen
- COVID vaccines have given me headaches and achiness.
- Staat
- HI
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 23.11.2022
- Impfdatum
- 12.10.2022
- Beginn
- 12.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Symptomtext
Site: Pain at Injection Site-Severe
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 18.11.2022
- Impfdatum
- 06.10.2022
- Beginn
- 15.11.2022
- Tage bis Beginn
- 40,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chills
Dysphonia
Fatigue
Feeling abnormal
Memory impairment
Oropharyngeal pain
Pharyngitis
Productive cough
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Throat clearing
Symptomtext
I started with constantly trying to clear my throat. This started on Monday. By Tuesday November 15, I felt like a cold was starting or it was allergy related or due to a seasonal change. I took CLARITIN. By Tuesday night, my throat felt infected and sore. I took a COVID-19 home test on Tuesday, and it was negative. On Wednesday, I felt like I needed to take a nap by afternoon and the clearing of the throat became a cough with clear mucus. I completed another COVID-19 home on Wednesday, and it was positive. I took another test, and it came back positive as well. I emailed my doctor and asked if he could prescribe the anti-viral treatment due to past issues with cold. I took the first dose on Thursday. My symptoms come and go. This morning I had a raspy voice with lots of mucus that is still clear. I still have the cough and at night I get a slight chill but that has gotten better. Sometimes I am congested and sometimes I have a runny nose. My doctor did not advise me to take any additional test outside of the rapid home test to confirm. I feel a little bit foggier where I forget what I have gone in a room searching for more often than prior to this.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- COVID-19 home test November 16, 2022 positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Atorvastatin calcium; testosterone gel; vitamin B12; vitamin D3; zinc complex; OCUVITE; krill oil
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 15.11.2022
- Impfdatum
- 17.10.2022
- Beginn
- 03.11.2022
- Tage bis Beginn
- 17,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Computerised tomogram abnormal
Inflammation
Oropharyngeal pain
Pain in extremity
Salivary duct obstruction
Sialoadenitis
Swelling
Symptomtext
Very sore arm for one week. on 11/3/2022, swelling of neck with pain in throat. CT determined a salivary infection and inflammation in the area. IV antibiotics for 3 days, released. Taking Amoxicillin for 14 days. Lactobacillus for 12 days. As of 11/15/2022, still some swelling, pain, and blockage of salivary duct.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- 3,0
- Labordaten
- 11/4/2022 CT scan Bloodwork
- Aktuelle Erkrankungen
- cold allergies
- Vorgeschichte
- fibromyalgia sleep apnea diabetes depression tachycardia
- Andere Medikamente
- Aripiprazole aspirin Atenolol bupropion farxiga duloxetine fludrocortisone glimepride hydroxyzine claritin multivitamin omeprazole rosuvastatin ozempic coQ10 flaxseed oil fish oil chromium picolinate zinc stool softener D3 tylenol tramadol
- Allergien
- guaifenesin avelox bactrim keflex petrolatrum
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 13.11.2022
- Impfdatum
- 14.10.2022
- Beginn
- 27.10.2022
- Tage bis Beginn
- 13,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Rash pruritic
Skin warm
Urticaria
Symptomtext
Hot, red, itchy bumps all over my body (Hives). I went to my doctor who prescribed me a steroid, but the hives did not go away. I then saw an allergist who prescribed me Xyzal to take twice a day. I still have hives even with the medication.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash pruritic
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asthma, Acne
- Andere Medikamente
- -
- Allergien
- Morphine, Miralax
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 09.11.2022
- Impfdatum
- 04.11.2022
- Beginn
- 04.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arthralgia
Axillary pain
Injection site bruising
Injection site erythema
Injection site induration
Injection site pain
Injection site swelling
Injection site warmth
Neck pain
Pain
Pain in extremity
Pyrexia
Symptomtext
Friday Night 11/4/2022: extreme body aches - head to toe - different than previous 3 shots - considered emergent urgent care but stayed home. Saturday 11/5/2022: body aches, fevers, arm pain all day noticed red spot developing on arm below injection site and bruising at injection site. Sunday 11/6/2022: body aches, fevers, arm pain continued, and red site continued to grow, swell and became hard and hot and painful. Monday 11/7/2022: tried to go to work and was continuing to have all of the above symptoms including developing shooting pain in my arm (red site was continuing to get larger and was still hot, hard and tender). Was encouraged by employee health (I work at a hospital - where I got the vaccine) to go to urgent care. Urgent care advised continued NSAID and Tylenol use and cold compress on arm and monitoring for signs that would require emergency room visit. Tuesday: symptoms continued; fever worsened otherwise other symptoms were the same. Did not go to work. Was contacted to follow up on my responses and advised to fill out a VAERS form. Wednesday: symptoms seem to be mildly improving. Arm is less red - some areas are bruised, and it is still tender. Body is still painful mostly in shoulders, armpits, and neck. Still feverish. Did not work today.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- Have not taken any tests. Urgent care assessed my arm but did not do any laboratory tests or imaging.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma; Allergies; PCOS; Hypothyroidism; Low Iron
- Andere Medikamente
- Venlafaxine; Metformin; Levothyroxine; Topirimate; Odactra; Cetrezine; Vitamin C; Phentermine Iron.
- Allergien
- Ginger (Nausea and vomiting); Adhesive Tape (Rash/Scabs)
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 09.11.2022
- Impfdatum
- 27.10.2022
- Beginn
- 29.10.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Pain
Symptomtext
Patient reported that two days after receiving the Moderna Omicron Booster he had "excruciating pain" radiating in his right upper back that he attributes to the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- Patient reports he's going to get an MRI to be thorough, but has not done so yet.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 08.11.2022
- Impfdatum
- 07.10.2022
- Beginn
- 02.11.2022
- Tage bis Beginn
- 26,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Discomfort
Nasal congestion
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
I received the Moderna Bivalent booster on 10/7/2022. When I went to bed on the night of 11/2/2022, I had a low-grade fever and nasal congestion. During the night, my nose ran continuously. I then developed a dry cough. I got up at about 5 AM on the morning of 11/3/2022 to see what the symptoms of COVID-19 are. After I found out what they are, I decided to take a home test, which yielded a positive result. I have been self-isolating ever since. Today marks the sixth day of isolation for me. I took another home test this morning and got another positive result. On 11/3/2022, I called my doctor to inform her of the situation. She decided not to prescribe me any medication, such as PAXLOVID, as she feared that there would be a negative interaction with the XARELTO I take. Since I couldn't get any prescription medication for COVID-19, I have been treating my symptoms with OTC DELSYM for the cough and OTC diphenhydramine for the discomfort. I have found them to be helpful.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- 11/3/2022 home COVID-19 test positive result; 11/8/2022 home COVID-19 test positive result.
- Aktuelle Erkrankungen
- Carpal Tunnel Release Surgery on 9/23/2022 (Right Hand).
- Vorgeschichte
- Atrial Fibrillation; Hypercholesterolemia.
- Andere Medikamente
- Vitamin C; vitamin D; multivitamin; ZYRTEC; metoprolol; atorvastatin; XARELTO.
- Allergien
- Latex products.
- Vorherige Impfungen
- Every time I get a shot during the morning, I develop chills and a fever at about 10 PM. The fever usually lasts for a couple of
- Staat
- IN
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 08.11.2022
- Impfdatum
- 21.10.2022
- Beginn
- 02.11.2022
- Tage bis Beginn
- 12,0
- Dosis
- N/A
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Rash
Rash erythematous
Rash macular
Urticaria
Symptomtext
I have not yet determined the cause but since Nov 2 (12 days after I got the booster shot) I've been having rashes/hives that flare up and then go away. The itching is greatly reduced by Zyrtec or Benadryl. The rashes are blotchy and irregular in shape, streaky red lines (especially after itching/rubbing) and sometimes reduce to smaller spots and appear on torso/back/wrists/armpits--frequently after minor contact such as on my wrist after putting my watch on.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- none yet
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Spironolactone 50 mg per day Clindamycin topical lotion for acne Ketaconazole for hair loss Vitamin D 50,000 once per week
- Allergien
- Penicillin No other known allergies
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 04.11.2022
- Impfdatum
- 06.10.2022
- Beginn
- 11.10.2022
- Tage bis Beginn
- 5,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Lymphadenopathy
Rash
Rash erythematous
Rash papular
Scab
Swelling face
Symptomtext
Started on 10/11/2022, the patient had swollen lymph nodes under and in front of the right ear with a rash inside the ear and across the cheekbone. Over the next several days, the lymph nodes continued to swell, the rash became red with papule like structures on the face and in the ear with a yellow/white center. Under the right eye swelled and became red as well. Most of the swelling has since decreased except the lymph node under the right ear. The papule like structures have become raised dark scabs (one in ear and two on the cheekbone- one was quite large the other medium size) at time of interview on October 26th at 2 pm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Just seasonal allergies
- Vorgeschichte
- High Cholesterol, Asthma, Mitral Valve Prolapse, Anxiety, Migraines
- Andere Medikamente
- Singulair, Loratadine, Tagamet, Lipitor, Celexa, Evening Primrose, Vitamin D, Vitamin B Complex, Albuterol as needed, Depo shot, Excedrin Migraine
- Allergien
- Penicillin, Pitocin, Sulfa, Naproxen, Stadol, Pollen, Pet dander
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 03.11.2022
- Impfdatum
- 28.10.2022
- Beginn
- 29.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- N/A
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Chills
Injection site erythema
Injection site pruritus
Injection site swelling
Injection site warmth
Myalgia
Pain
Symptomtext
12 hours post injection intense chills, muscle, full body aches began. 2 hours later joint pain started. No fever was present. Symptoms treated with Tylenol. 24 hours post injection arm where injection occurred became, reddish purple, hot to the touch and slightly swollen. Affected area was from head of the humerus to 4 cm below cubital crease on lateral aspect of the arm. Treated with benadryl without much effect. Chills, body aches and joint pain subsided after 36 hours from onset. Arm of injection site still shows redness, hot to the touch and itchiness in band that is 12 cm wide covering the lower 2/3 of the upper arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- D3, DHEA, Multi-vitamin, L-Carnitine, Krill oil, Fiber
- Allergien
- melons, alcohol
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 02.11.2022
- Impfdatum
- 10.10.2022
- Beginn
- 17.10.2022
- Tage bis Beginn
- 7,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Papule
Pityriasis rosea
Rash
Rash erythematous
Rash pruritic
Skin exfoliation
Skin plaque
Symptomtext
40 y/o female in good health presents with 2 week history of increasing pruritic rash on torso, back/chest/groin/neck. On physical exam, patient is well-appearing. Distributed over her chest, ab, back, flanks, groin, and neck are 0.2 to 3 cm pink discrete papules and plaques, some with collarette scale, consistent with pityriasis rosea. Pt was advised to discontinue anti-fungal cream (clotrimazole 1% cream) and started mometasone 0.1% cream to affected areas bid with partial relief. Patient advised of prolonged course (usually 2 weeks increasing, 2 weeks stable rash, and 2 weeks resolution).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- n/a
- Allergien
- No allergies.
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 01.11.2022
- Impfdatum
- 09.10.2022
- Beginn
- 27.10.2022
- Tage bis Beginn
- 18,0
- Dosis
- 5
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Lethargy
Oropharyngeal pain
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
Started to have congestion and a sore throat; took a Home COVID-19 test and was positive. Then started feeling more lethargic and had a fever. Called Doctor and decided not to take Paxlovid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- Home COVID-19 test - positive
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- Finasteride; Atovastatin.
- Allergien
- Ibuprofen
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 29.10.2022
- Impfdatum
- 19.10.2022
- Beginn
- 19.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Headache
Injection site erythema
Injection site pain
Injection site pruritus
Injection site swelling
Pruritus
Rash
Symptomtext
Site: Itching at Injection Site-Severe, Site: Pain at Injection Site-Severe, Site: Redness at Injection Site-Severe, Site: Swelling at Injection Site-Severe, Systemic: Allergic: Itch Generalized-Medium, Systemic: Allergic: Rash Generalized-Medium, Systemic: Dizziness / Lightheadness-Severe, Systemic: Headache-Severe
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 28.10.2022
- Impfdatum
- 10.10.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 5
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dry skin
Macule
Pruritus
Skin disorder
Skin exfoliation
Skin warm
Symptomtext
skin changes after Moderna Bivalent vaccine; 4-5 cm area of geographic distribution of multiple brown-colored macule and patch in R deltoid area; It was dry; scaly texture; patient feels warm; patient feels itchy/spreading; This spontaneous case was reported by a physician and describes the occurrence of SKIN DISORDER (skin changes after Moderna Bivalent vaccine), MACULE (4-5 cm area of geographic distribution of multiple brown-colored macule and patch in R deltoid area), DRY SKIN (It was dry), SKIN EXFOLIATION (scaly texture) and SKIN WARM (patient feels warm) in a 58-year-old female patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. 053D22A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 10-Oct-2022, the patient received fifth dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced SKIN DISORDER (skin changes after Moderna Bivalent vaccine), MACULE (4-5 cm area of geographic distribution of multiple brown-colored macule and patch in R deltoid area), DRY SKIN (It was dry), SKIN EXFOLIATION (scaly texture), SKIN WARM (patient feels warm) and PRURITUS (patient feels itchy/spreading). The patient was treated with BETAMETHASONE, CLOTRIMAZOLE (CLOTRIMAZOLE AND BETAMETHASONE) at an unspecified dose and frequency. At the time of the report, SKIN DISORDER (skin changes after Moderna Bivalent vaccine), MACULE (4-5 cm area of geographic distribution of multiple brown-colored macule and patch in R deltoid area), DRY SKIN (It was dry), SKIN EXFOLIATION (scaly texture), SKIN WARM (patient feels warm) and PRURITUS (patient feels itchy/spreading) outcome was unknown. For mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Intramuscular), the reporter did not provide any causality assessments. Patient was a healthy with no known allergy or skin issues. HCP stated that he had never seen such reaction before because the vaccine was new. Concomitant medications were not reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 28.10.2022
- Impfdatum
- 12.10.2022
- Beginn
- 16.10.2022
- Tage bis Beginn
- 4,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Fatigue
Feeling drunk
Headache
Influenza like illness
Pain
Pain in extremity
Symptomtext
was given the shot on 10/12/22. Had normal flu-like symptoms (aches, tired, very sore arm, headache) on 10/13. On 10/16/22 I started getting a positional headache when bending over to pick something up and stand up again. Was minor, like a momentary throbbing, or flash and then went away. Happened at least 2-3 times at least. On 10/17/22 I had the positional headache again. That transformed into a slower persistent headache as the day went on, centrally located in the top of my head. Had gotten worse towards bedtime. Eventually crept behind my eyes some too. Also felt a little woozy with the headache today, like I was slightly buzzed, or mildly inebriated. on 10/18, no headache, but the mild dizzy/inebriated feeling on and off all day. 10/19-10/24/22. Mostly felt the intermittent mild dizzy/inebriated feeling, along with occasional positional momentary headache. 10/25/22. I had a repeat of the 10/17 episode, with wooziness, positional headache and growing and spreading dull headache centered on the top of my head. 10/26/22. Mostly felt fine, light intermittent buzzed/inebriated feeling throughout the day. 10/27/22. Woke up and immediately felt positional headache after sitting down to use the bathroom after waking. Felt the buzzed, inebriated feeling and sharper positional headaches on and off throughout the day, with some of the dull top center headache coming on in the afternoon. By evening, headaches mostly backed off on their own, left with the woozy feeling.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- None so far. Would like to get imaging done.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- I've had a degenerative disk in my neck for probably a decade or longer. Caused very specific intense headaches with muscle tightness in rt. shoulder and rt. side of neck with rt. side cervicogenic headaches. Nausea and vomiting would also be associated if bad enough. Had cervical disk arthroplasty on May 16th to replace the disk in my neck. Surgery has been largely successful. Still have nerve issues in Rt shoulder from long term compression. Bulged Lumbar Disc at t12-L1, with facet joint deterioration at that level. Bulged Lumbar Disc at L5-S1, with possible facet joint deterioration at that level and Arthritis around L3-4, L4-5. Torn Meniscus in Rt. knee. IBS. Interstitial Cystitis.
- Andere Medikamente
- Vitamin D 2000 iu across 2 pills. Boswellia 500mg. 1 pill. Ubiquinol. 50mg. 1 pill. Krill Oil 500mg. 1 pill. Omaprazole. 20mg. 1 pill. Methocarbamol 750mg. 1 pill. Taken as needed for muscle spasms.
- Allergien
- Soy sensitivity. Lactose intolerance. I've had bad reactions to a couple anitbiotics (Cipro, and one other I don't recall).
- Vorherige Impfungen
- Covid Shot 1st dose Moderna. 04/28/2021 Lot 016C21A. Had heart fluttering that lingered for weeks after the shot. Also developed
- Staat
- -
- Alter
- -
- Geschlecht
- F
- Eingang
- 26.10.2022
- Impfdatum
- 18.10.2022
- Beginn
- 19.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Myalgia
Pyrexia
Symptomtext
Headache, Myalgia & Fever Narrative:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- yes same reaction to previous doses of Covid
- Staat
- -
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 26.10.2022
- Impfdatum
- 18.10.2022
- Beginn
- 19.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest discomfort
Chills
Cough
Myalgia
Nausea
Pain
Pruritus
Rash
Urticaria
Vomiting
Wheezing
Symptomtext
Myalgia, SkinRash, CoughWheeze, Rash, UrticariaPruritus, NauseaVomiting, chest pressure, cough, chills, body aches, nausea (no vomiting), R arm rash approx 3 inches in diameter Narrative: Most symptoms (chills, aches, nausea) subsided within 48 hours but right arm rash and cough were worse at 48 hours; Antibiotics prescribed
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- Prior adverse reaction to covid vaccinations include chills and aches
- Staat
- -
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 26.10.2022
- Impfdatum
- 18.10.2022
- Beginn
- 18.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Cough
Diarrhoea
Fatigue
Myalgia
Pyrexia
Wheezing
Symptomtext
Myalgia, Fever, CoughWheeze, Diarrhea, Chills, fatigue Narrative:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 26.10.2022
- Impfdatum
- 06.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Axillary pain
Fatigue
Headache
Myalgia
Nasal congestion
Pharyngitis
Pyrexia
Symptomtext
Headache, Myalgia, Fever, fatigue, axillary pain, pharyngitis, nasal congestion Narrative:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- Similar reaction the day after COVID Moderna primary and booster vaccines given: 1/4/21, 2/3/21, 11/2/21, with intensity of symp
- Staat
- IN
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 26.10.2022
- Impfdatum
- 24.10.2022
- Beginn
- 01.10.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature increased
Chills
Injection site pain
Pain in extremity
Sleep disorder
Symptomtext
I'll had terrible after effects. Got these shots at local pharmacy on 10/24 about three o'clock..sore left arm and shoulder expected. Went to sleep about 1:00 am, woke up at 3:00am shivering ( couldn't stop ). watched as my temperature went from 101.5 to 104.3. Thought of the ER. Did that once, temp was 103 ended up the Flu. But this time, I figured it was the shots and would go away. Well it did in the morning ,but it's sort of creeping up again. Should I go to the ER if it goes high ?? I plan on reporting the after effects somewhere. Thank you
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Afib, High blood pressure
- Andere Medikamente
- 1- Losartan/HCT Tab 100-25 Generic for Hyzaar 1 - Metoprolo Succ 100mg TAB (cut in half) 1 - Clonidine-TTS 3-0.3 MG/day (patch) 1- Alprazolam Tab 0.5mg 1- Lansoprazole CAP 15MG DR 1- Nabumetone 750mg- Generic
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 25.10.2022
- Impfdatum
- 07.10.2022
- Beginn
- 08.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Angiogram cerebral
Arteriogram carotid
Nausea
Scan with contrast
Vertigo
Symptomtext
Vertigo/Nausea; Treatment at Emergency room; Treated with Meclizine and ondansetron
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- CT Angio Head Neck w/Contrast;
- Aktuelle Erkrankungen
- UTI
- Vorgeschichte
- Essential hypertension, Prediabetes, Age Related Osteoporosis without current pathological fracture
- Andere Medikamente
- Losartan, Amlodipine, Probiotics, Calcium, Vitamin D, Cranberry, D Manoose, Estradiol
- Allergien
- Lisinopril, Hydrochlorothiazide
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 25.10.2022
- Impfdatum
- 19.10.2022
- Beginn
- 21.10.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Injection site erythema
Injection site pain
Skin warm
Symptomtext
Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Systemic: arm redness, warm to touch-Medium, Additional Details: patient told if worsening symptom to seek emergency room, told to put on cold compresses if no relief contact ER/MD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 25.10.2022
- Impfdatum
- 12.10.2022
- Beginn
- 19.10.2022
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pruritus
Injection site reaction
Pain
Vaccination site pain
Symptomtext
Site: Itching at Injection Site-Mild, Site: Pain at Injection Site-Mild, Site: Redness at Injection Site-Mild, Additional Details: pt states had usual arm soreness at the vaccination site, but she notes that on wednesday, the 19th of october, was more sore, and started itching and throbbing and was red. Pt had attempted to apply cold compresses. advised to apply cold compresses and to take appropriate analgesic and to follow up with pcp. pt stated she was already on an anithistamine. she reports no issues moving arm around, no shoulder pain
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 25.10.2022
- Impfdatum
- 07.10.2022
- Beginn
- 08.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- 5
- 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
Rash pruritic
Symptomtext
Site: Itching at Injection Site-Severe, Site: Redness at Injection Site-Severe, Site: Swelling at Injection Site-Severe, Systemic: Allergic: Itch (specify: facial area, extremeties)-Severe, Systemic: Allergic: Rash (specify: facial area, extremeties)-Severe, Additional Details: patient stated she had "covid arm" following her bivalent booster dose. she did not need any medical intervention and did not see her doctor. she treated with topical hydrocortisone cream only.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 25.10.2022
- Impfdatum
- 06.10.2022
- Beginn
- 13.10.2022
- Tage bis Beginn
- 7,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Rash
Symptomtext
Systemic: Allergic: Itch Generalized-Severe, Systemic: Allergic: Rash (specify: facial area, extremeties)-Severe, Systemic: Allergic: Rash Generalized-Severe
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 24.10.2022
- Impfdatum
- 14.10.2022
- Beginn
- 01.10.2022
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Cellulitis
Inflammation
Injection site erythema
Injection site induration
Injection site pain
Injection site swelling
Pruritus
Symptomtext
Pain at injection site, which turned into swelling, redness, and hardness that wrapped around my entire arm from my shoulder to just past my elbow. First urgent care doctor told me that it was Cellulitis and prescribed antibiotic (cephalexin), while it continued to spread and be painful. The next day at urgent care, doctor told me it was inflammatory response. Redness and swelling continued to expand for about a week, then became itchy. I'm 10 days out and can see some redness still near where I got my shot, but the swelling has gone down and things seem to be back to normal.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- High BP, obesity
- Andere Medikamente
- Levothryoxine, 75 micrograms; Lisinopril 20 mg.
- Allergien
- none known
- Vorherige Impfungen
- Covid arm presented after first Moderna Shot, about a week after my initial shot.
- Staat
- WA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 24.10.2022
- Impfdatum
- 19.10.2022
- Beginn
- 19.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal discomfort
Abdominal pain upper
Diarrhoea
Sleep disorder
Vomiting
Symptomtext
I received both Moderna bivlaent booster and flu shot at the same time in the same arm. 3 hours after receiving the shots I started having intense diarrhea which has lasted for 4 days, on day 5 I'm still having loose stool but it is improving. 37 hours after receiving the two shots I was awoken in the night to a very upset stomach. I violently vomited a dozen times over 12 hours before that symptom started to improve. My stomach continued to be sore and unstable for 2 more days following the vomiting.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Polycystic Kidney Disease, hypertension, persistent PVC's (heart arrhythmia)
- Andere Medikamente
- Amiloride, Lisinopril, Valtrex, CoQ10, calcium supplement, Vit D3, glucosamine
- Allergien
- None known
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 22.10.2022
- Impfdatum
- 14.10.2022
- Beginn
- 15.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Fatigue
Headache
Injection site bruising
Injection site erythema
Injection site pain
Injection site swelling
Lethargy
Nausea
Pain in extremity
Symptomtext
Site: Bruising at Injection Site-Medium, Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Systemic: Chills-Medium, Systemic: Exhaustion / Lethargy-Medium, Systemic: Headache-Medium, Systemic: Nausea-Medium, Additional Details: Pt states site of injection was normal in (L) deltoid &"felt fine and normal, not high in shoulder". Pt states vaccine was given friday & symptoms developed 12 hours after injection HA, Nausea, chills, fatigue, minimal soreness & pain and no swelling at the start. 24-48 hours after injection still fatigue & HA, monday, arm become more sore, still dealing with fatigue and HA, tuesdya pt had soreness & pain, "red and hot, spreading from arm down to elbow" advised to f/u with DR/Urgent care
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 22.10.2022
- Impfdatum
- 12.10.2022
- Beginn
- 14.10.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site bruising
Injection site swelling
Symptomtext
Site: Bruising at Injection Site-Severe, Site: Swelling at Injection Site-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 21.10.2022
- Impfdatum
- 19.10.2022
- Beginn
- 20.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Rash erythematous
Rash macular
Symptomtext
diffuse macular erythematous rash chest, abdominal, back, extending to groin area, no injection site erythema on the RUE. patient received injection approx 12:27pm on 10/19/22 reported having rash approx 10/20/22 22:00pm, was given 50mg po x1 benedryl - seen again on 10/21 as rash has not resolved and is as stated above, now given 50mg po x1 dose now prednisone at 13:30 and RX for 50mg po x 6 days starting 10/22/22. will continue to follow.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- na
- Vorgeschichte
- na
- Andere Medikamente
- Wellbutrin SR, Diclofenac, Gabapentin,
- Allergien
- PCN
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 20.10.2022
- Impfdatum
- 07.10.2022
- Beginn
- 12.10.2022
- Tage bis Beginn
- 5,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Hyperhidrosis
Oropharyngeal pain
Pain
Pyrexia
SARS-CoV-2 test positive
Sinusitis
Sleep disorder
Symptomtext
After I received the vaccine, I had body aches and fever. Twice in the night I woke up with drenched pajamas. I started having symptoms on 10/12/2022 I had a sore throat and it felt like a sinus infection. I tested positive from a home test for COVID-19 on 10/15/2022. I had multiple tests for COVID-19, and it was finally confirmed on 10/19/2022. I got in touch with my doctor and was given a prescription for an inhaler.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- 15OCT2022 COVID-19 test - positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Vitamin C; vitamin B; zinc; CLARIITIN; women's ONE A DAY
- Allergien
- Sulfa; steroids
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 20.10.2022
- Impfdatum
- 12.10.2022
- Beginn
- 14.10.2022
- Tage bis Beginn
- 2,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pain
Injection site pruritus
Injection site swelling
Symptomtext
Site: Itching at Injection Site-Mild, Site: Pain at Injection Site-Mild, Site: Redness at Injection Site-Mild, Site: Swelling at Injection Site-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 19.10.2022
- Impfdatum
- 14.10.2022
- Beginn
- 17.10.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain
Breath sounds abnormal
Chills
Headache
Nausea
Vomiting
Symptomtext
Vomiting, chills and headaches, rattling in chest, nausea and abdominal pain
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 19.10.2022
- Impfdatum
- 17.10.2022
- Beginn
- 17.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Feeling abnormal
Malaise
Symptomtext
I had extreme chills all night. I felt extremely ill and very weird. The symptoms started around 08:00PM. It started improving around 06:00AM the next morning. By about noon, the reaction was almost gone.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Intestinal sickness from expired meat
- Vorgeschichte
- Seizures; High Blood Pressure; High Cholesterol
- Andere Medikamente
- Telmisartan; atorvastatin; KEPPRA; multivitamin; vitamin D; saw palmetto; magnesium
- Allergien
- Pollen; sulfa drugs; dairy
- Vorherige Impfungen
- Both Shingles doses, extreme nausea and vomiting for about a day and a half, Age: 68.
- Staat
- WA
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 18.10.2022
- Impfdatum
- 18.10.2022
- Beginn
- 18.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Confusional state
Dizziness
Feeling drunk
Immediate post-injection reaction
Symptomtext
Pt felt dizzy, confused, "like she was drunk" immediately after vaccination. 911 was called and arrived shortly thereafter. Emergency personnel took vitals and questioned patient, determined no allergic reaction was taking place. Did not give any treatment. Pt refused going to hospital for observation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- Asthma
- Vorgeschichte
- Asthma
- Andere Medikamente
- None
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 17.10.2022
- Impfdatum
- 12.10.2022
- Beginn
- 14.10.2022
- Tage bis Beginn
- 2,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Symptomtext
Onset of unexplained and unusual moderately severe knee pain in left knee approximately 39 hours after vaccination. Pain decreased to moderate the following day, but persisted over the next 48 hours, until disappearing over the course of the next day. The sudden onset of the pain in the knee that is usually not a problem and the rapid rate at which is dissipated relative to its initial severity leads me to believe that it was a side-effect of the vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Knee Osteoarthritis
- Andere Medikamente
- CoQ10, Turmeric, Glucosamine/Chondroitin, low-dose aspirin
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 17.10.2022
- Impfdatum
- 14.10.2022
- Beginn
- 15.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Feeling abnormal
Headache
Neck pain
Somnolence
Symptomtext
Next day, slept extremely late, serious ache in shoulder and neck. Entire body later in day felt extremely creepy and weird. Something like feeling something happening inside, not kidding. Headache. Reporting as this is my 5th Moderna vaccine and I had a mildish reaction w 2nd shot, but none of this with the other vaccines.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- -
- Allergien
- seasonal allergies, ragweed, mold
- Vorherige Impfungen
- Moderna Covid 19 Lot 006B21A
- Staat
- VT
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 17.10.2022
- Impfdatum
- 17.10.2022
- Beginn
- 17.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Nausea
Pallor
Symptomtext
Patient received 2 vaccines this morning at around 10:22 a.m. (covid & flu). After receiving the 2nd injection at 10:24, patient started to feel nauseous and lightheaded. Vaccinator quickly reached out for assistance and patient laid down on the cot with a cool cloth. Vitals obtained at 10:30 HR 64; BP 97/65 (within normal range per patient); SAT 99% RA; skin color = pale Patient was offered fruit bar and water as she stated maybe she hadn't eaten enough at breakfast. She has ever felt this way after attempting to watch a medical procedure on a family member. 10:33 patient sitting up, advised she was feeling better. Repeat B/P 71/43 Patient started to feel lightheaded again and laid back down. Patient was continuously monitored, at 10:46 vitals returned to patients' normal range of B/P 98/64 ; HR 75; SAT 100% RA for 10+ minutes. Patient was up and walking around at the clinic and advised she was feeling back to normal. Patient advised if anything changed to seek medical attention.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Zoloft
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 15.10.2022
- Impfdatum
- 11.10.2022
- Beginn
- 11.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Flushing
Hyperhidrosis
Symptomtext
Systemic: Dizziness / Lightheadness-Mild, Systemic: Flushed / Sweating-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 14.10.2022
- Impfdatum
- 10.10.2022
- Beginn
- 10.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Injection site pain
Symptomtext
Site: Pain at Injection Site-Medium, Additional Details: patient reported having sore shoulder up to neck 5 minutes after getting vaccine. at 15 minutes she stated nothing was worse or better. no signs of allergic reaction.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 11.10.2022
- Impfdatum
- 10.10.2022
- Beginn
- 11.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Injection site pain
Myalgia
Pyrexia
Restlessness
Symptomtext
Low grade fever, restlessness, muscle aches, soreness at injection site, headache. Took 500 mg Tylenol x2 at 4 am and 2 pm on 10/11/22. Limited relief for a couple hours each dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Metoprolol, Eliquis, rosuvastatin, tamsulosin.
- Allergien
- Sulfa
- Vorherige Impfungen
- Similar reactions.
- Staat
- MD
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 11.10.2022
- Impfdatum
- 07.10.2022
- Beginn
- 11.10.2022
- Tage bis Beginn
- 4,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dizziness
Pruritus
Urticaria
Symptomtext
Patient had mild dizziness on Saturday but she said she had similar adverse reaction from her previous moderna (monovalent) shots. Hives and itchness started on Sunday night. It started from her lower extremity but now it is all over her body.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- -
- Andere Medikamente
- No
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 08.10.2022
- Impfdatum
- 08.10.2022
- Beginn
- 08.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Urticaria
Symptomtext
Patient called stating she was experiencing hives on her neck, back, and shoulder.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 08.10.2022
- Impfdatum
- 07.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Flushing
Lip swelling
Pruritus
Rash
Swelling face
Symptomtext
Pre-medicated with 20mg prednisone morning of vaccine and 25mg Benadryl/25mg Phenergan 1hour before due to allergic reactions to previous three Moderna COVID vaccines. Approximately 1 hour and 45 minutes post-vaccination began to experience widespread itching and flushing, along with facial swelling and significant lip swelling. Took 25mg Benadryl and swelling and itching receded, and 20mg prednisone 1.5 hours later. No further allergic symptoms during the remaining 24 hours post-vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- N/A; treated at home with plan from allergist/immunologist as I have for previous three vaccines.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Ehlers-Danlos Syndome, Gastroparesis, Intestinal Dysmotility, Chronic Inducible Urticaria, Idiopathic Anaphylaxis, Postural Orthostatic Tachycardia Syndrome, Small Fiber Neuropathy, Chronic Atypical Migraine, Bipolar II
- Andere Medikamente
- Pepcid, Allegra, Singulair, Dapsone, Phenergan, Prednisone, Motegrity, Mestinon, Midodrine, Florinef, Corlanor, Topomax, Botox for Migraine, Lipitor, Seroquel, Lexapro, Creon
- Allergien
- Latex, Xolair, Non-Steroidal Anti-Inflammatory Drugs, Iodinated IV Contrast, Dilaudid, Vicodin
- Vorherige Impfungen
- Allergic reactions to previous 3 Moderna COVID vaccines
- Staat
- MA
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 13.12.2023
- Impfdatum
- 14.10.2022
- Beginn
- 16.11.2023
- Tage bis Beginn
- 398,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Symptomtext
diagnosed with COVID-19; This spontaneous case was reported by a patient and describes the occurrence of COVID-19 (diagnosed with COVID-19) in a 61-year-old male patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. 053D22A) for COVID-19 prophylaxis. Co-suspect product included non-company product INFLUENZA VACCINE INACT SPLIT 4V (FLUZONE QUADRIVALENT) for an unknown indication. Previously administered products included for COVID-19 prophylaxis: Moderna (Dose:1, Lot number: 037B21A, dose: 0.5 ml, site: Left arm) on 12-Apr-2021, Moderna (Dose:2, Lot number: 022021A, dose: 0.5 ml, site: Left arm) on 11-May-2021, Moderna (Dose:3, Lot number: 069H21A, dose: 0.5 ml and site: Left arm) on 20-Dec-2021. Past adverse reactions to the above products included No adverse event with Moderna, Moderna and Moderna. Concomitant products included OMEPRAZOLE for GERD, ROSUVASTATIN for Hyperlipidemia. On 14-Oct-2022 at 5:15 AM, the patient received fourth dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) .5 milliliter. On an unknown date, the patient received dose of INFLUENZA VACCINE INACT SPLIT 4V (FLUZONE QUADRIVALENT) (unknown route) 1 dosage form. On 16-Nov-2023, after starting mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)), the patient experienced COVID-19 (diagnosed with COVID-19). At the time of the report, COVID-19 (diagnosed with COVID-19) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 16-Nov-2023, SARS-CoV-2 test: Positive. No treatment medications were provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20231116; Test Name: Covid-19 Virus test; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- ROSUVASTATIN; OMEPRAZOLE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 29.09.2023
- Impfdatum
- 12.10.2022
- Beginn
- 22.09.2023
- Tage bis Beginn
- 345,0
- Dosis
- 6
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
hospitalized with covid; vaccinated with 4 boosters
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- positive covid pcr 9/21/23
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- HTN
- Andere Medikamente
- unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 14.09.2023
- Impfdatum
- 14.10.2022
- Beginn
- 13.09.2023
- Tage bis Beginn
- 334,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Breakthrough COVID-19
SARS-CoV-2 test positive
Symptomtext
COVID vaccine breakthrough case. Moderna 2/24/21 023M20A, 3/24/21 030A21A, 12/6/21 060H21A and bivalent Moderna 053D22A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Breakthrough COVID-19
- Hospital-Tage
- -
- Labordaten
- Positive COVID test 09/13/2023
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 04.08.2023
- Impfdatum
- 20.10.2022
- Beginn
- 12.04.2023
- Tage bis Beginn
- 174,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoxia
Symptomtext
R09.02 HYPOXIA 3/25/2023 HX OF ACUTE KIDNEY INJURY
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypoxia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 24.07.2023
- Impfdatum
- 10.10.2022
- Beginn
- 18.04.2023
- Tage bis Beginn
- 190,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Facial paresis
Intracranial mass
Symptomtext
RIGHT FACIAL MUSCLE WEAKNESS 4/18/2023 BRAIN MASS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Facial paresis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 18.07.2023
- Impfdatum
- 12.10.2022
- Beginn
- 19.01.2023
- Tage bis Beginn
- 99,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Angina unstable
Symptom recurrence
Symptomtext
UNSTABLE ANGINA 1/21/2023 -- RECURRENCE OF HOSPITALIZATION WITH SAME SYMPTOMS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Angina unstable
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 17.07.2023
- Impfdatum
- 20.09.2022
- Beginn
- 08.03.2023
- Tage bis Beginn
- 169,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Obstructive sleep apnoea syndrome
Osteoarthritis
Symptomtext
ADULT OBSTRUCTIVE SLEEP APNEA 4/3/2023 OSTEOARTHRITIS OF BILAT SHOULDERS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Obstructive sleep apnoea syndrome
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 17.07.2023
- Impfdatum
- 13.10.2022
- Beginn
- 21.11.2022
- Tage bis Beginn
- 39,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Epilepsy
Symptomtext
EPILEPSY, UNSPECIFIED
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Epilepsy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 14.07.2023
- Impfdatum
- 18.10.2022
- Beginn
- 05.03.2023
- Tage bis Beginn
- 138,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Transient ischaemic attack
Symptomtext
TRANSIENT CEREBRAL ISCHEMIA
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Transient ischaemic attack
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 88,0
- Geschlecht
- F
- Eingang
- 14.07.2023
- Impfdatum
- 08.10.2022
- Beginn
- 01.03.2023
- Tage bis Beginn
- 144,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Aortic valve stenosis
Diverticulitis
Hypersomnia
Sleep apnoea syndrome
Symptomtext
HYPERSOMNIA W SLEEP APNEA 4/21/2023 DIVERTICULITIS HYPERSOMNIA W SLEEP APNEA 4/21/2023 AORTIC VALVE STENOSIS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Aortic valve stenosis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 11.07.2023
- Impfdatum
- 29.10.2022
- Beginn
- 01.01.2023
- Tage bis Beginn
- 64,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Transient ischaemic attack
Symptomtext
TRANSIENT CEREBRAL ISCHEMIA
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Transient ischaemic attack
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 29.06.2023
- Impfdatum
- 03.11.2022
- Beginn
- 09.06.2023
- Tage bis Beginn
- 218,0
- Dosis
- 5
- 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 72-year-old female patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch nos. 042H22A and 053D22A) for COVID-19 prophylaxis. Previously administered products included for COVID-19 prophylaxis: Moderna COVID-19 Vaccine (Dose 1) on 04-Mar-2021, Moderna COVID-19 Vaccine (Dose 2) on 24-Mar-2021, Moderna COVID-19 Vaccine (Dose 3) on 19-Nov-2021 and Moderna COVID-19 Vaccine (Dose 4) on 04-May-2022. Past adverse reactions to the above products included No adverse event with Moderna COVID-19 Vaccine, Moderna COVID-19 Vaccine, Moderna COVID-19 Vaccine and Moderna COVID-19 Vaccine. Concurrent medical conditions included Hypertension. On 03-Nov-2022, the patient received fifth dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) 1 dosage form. On 09-Jun-2023, received sixth dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) dosage was changed to .5 milliliter. On 09-Jun-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 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (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). Patient did not received any other vaccines in the 4 weeks prior to COVID-19 vaccine. Concomitant medication details not reported by the reporter. Treatment details was not reported by the reporter. This case was linked to MOD-2023-730794 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Hypertension
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 28.06.2023
- Impfdatum
- 24.10.2022
- Beginn
- 03.12.2022
- Tage bis Beginn
- 40,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Hypoxia
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypoxia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 93,0
- Geschlecht
- M
- Eingang
- 26.06.2023
- Impfdatum
- 22.10.2022
- Beginn
- 27.03.2023
- Tage bis Beginn
- 156,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoxia
Prostate cancer
Symptomtext
HYPOXIA 3/27/2023 PROSTATE CANCER
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypoxia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 01.06.2023
- Impfdatum
- 15.10.2022
- Beginn
- 13.11.2022
- Tage bis Beginn
- 29,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthma
Atrial fibrillation
Hypoxia
Symptomtext
R09.02 HYPOXEMIA 1/23/2023 ATRIAL FIBRILLATION, UNSPECIFIED R09.02 HYPOXEMIA 1/23/2023 ASTHMA, UNSPECIFIED
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asthma
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 25.05.2023
- Impfdatum
- 10.10.2022
- Beginn
- 02.03.2023
- Tage bis Beginn
- 143,0
- Dosis
- 6
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Fall
Incorrect route of product administration
No adverse event
Symptomtext
No side effects - Had 3rd booster - Administered in the inner fatty part of upper shoulder.; 5th dose (bivalent) - 10-Oct-2022, lot number - 053D22A, 6th dose (bivalent) on 17-May-2023, lot number - AS7172B; No side effects - Had 3rd booster - Administered in the inner fatty part of upper shoulder.; she fell out of bed on 02-Mar-2023; This spontaneous case was reported by a patient and describes the occurrence of FALL (she fell out of bed on 02-Mar-2023), INCORRECT ROUTE OF PRODUCT ADMINISTRATION (No side effects - Had 3rd booster - Administered in the inner fatty part of upper shoulder.), EXTRA DOSE ADMINISTERED (5th dose (bivalent) - 10-Oct-2022, lot number - 053D22A, 6th dose (bivalent) on 17-May-2023, lot number - AS7172B) and NO ADVERSE EVENT (No side effects - Had 3rd booster - Administered in the inner fatty part of upper shoulder.) in a 73-year-old female patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch nos. 053D22A and AS7172B) for COVID-19 prophylaxis. The patient's past medical history included Magnesium deficiency and Whooping cough. Previously administered products included for Product used for unknown indication: TETANUS VACCINE. Past adverse reactions to the above products included No adverse event with TETANUS VACCINE. Concurrent medical conditions included Raynaud's disease (Lupus spectrum), Fibromyalgia, Diabetes, Hypertension, Hypothyroidism (The patient was on Synthroid.) and Gene mutation (The patient has a gene mutation which predisposes her to blood clots (prothrombin II).). Concomitant products included PREDNISOLONE for an unknown indication. On 10-Oct-2022, the patient received fifth dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) 1 dosage form. On 17-May-2023, received sixth dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) dosage was changed to 1 dosage form. On 02-Mar-2023, the patient experienced FALL (she fell out of bed on 02-Mar-2023). On an unknown date, the patient experienced INCORRECT ROUTE OF PRODUCT ADMINISTRATION (No side effects - Had 3rd booster - Administered in the inner fatty part of upper shoulder.), EXTRA DOSE ADMINISTERED (5th dose (bivalent) - 10-Oct-2022, lot number - 053D22A, 6th dose (bivalent) on 17-May-2023, lot number - AS7172B) and NO ADVERSE EVENT (No side effects - Had 3rd booster - Administered in the inner fatty part of upper shoulder.). At the time of the report, FALL (she fell out of bed on 02-Mar-2023) was resolving and INCORRECT ROUTE OF PRODUCT ADMINISTRATION (No side effects - Had 3rd booster - Administered in the inner fatty part of upper shoulder.), EXTRA DOSE ADMINISTERED (5th dose (bivalent) - 10-Oct-2022, lot number - 053D22A, 6th dose (bivalent) on 17-May-2023, lot number - AS7172B) and NO ADVERSE EVENT (No side effects - Had 3rd booster - Administered in the inner fatty part of upper shoulder.) outcome was unknown. For mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Unknown), the reporter considered NO ADVERSE EVENT (No side effects - Had 3rd booster - Administered in the inner fatty part of upper shoulder.) to be not related. No further causality assessments were provided for FALL (she fell out of bed on 02-Mar-2023), INCORRECT ROUTE OF PRODUCT ADMINISTRATION (No side effects - Had 3rd booster - Administered in the inner fatty part of upper shoulder.) and EXTRA DOSE ADMINISTERED (5th dose (bivalent) - 10-Oct-2022, lot number - 053D22A, 6th dose (bivalent) on 17-May-2023, lot number - AS7172B). It was reported that the patient was over 65 years old and has 3 autoimmune diseases (Raynaud's disease, fibromyalgia, and diabetes). The patient received Moderna Monovalent vaccines as Dose 1 on 09-Mar-2021 with lot number - 036A21A, Dose 2 on 06-Apr-2021 with lot number - 036A21A, Dose 3 on 05-May-2021 with lot number 017F21A and Dose 4 on 01-Jun-2022 with lot number - 037A22A. On 02-Mar-2023, the patient fell out of bed. The patient received prednisolone 4 mg for 6 days. It was reported that the patient had her 6th dose (Second bivalent) on 17-May-2023 and it was administered on the inner fatty part of her upper shoulder. Treatment information was not provided. This case was linked to MOD-2023-725295 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 18-May-2023: Live Significant follow-up appended: New event added and narrative updated. On 19-May-2023: Live Significant follow-up appended: Patient details updated, Medical History updated, Suspect product details updated and case narrative updated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Diabetes; Fibromyalgia; Gene mutation (The patient has a gene mutation which predisposes her to blood clots (prothrombin II).); Hypertension; Hypothyroidism (The patient was on Synthroid.); Raynaud's disease (Lupus spectrum)
- Vorgeschichte
- Medical History/Concurrent Conditions: Magnesium deficiency; Whooping cough
- Andere Medikamente
- PREDNISOLONE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 24.05.2023
- Impfdatum
- 06.10.2022
- Beginn
- 16.05.2023
- Tage bis Beginn
- 222,0
- 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 Pfizer 1/14/21 no lot#; Moderna 2/11/21 no lot#; MOderna 4/21/22 Lot# 048L21A; Moderna 10/6/22 lOt# 053D22A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- -
- Geschlecht
- U
- Eingang
- 17.05.2023
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Wrong product administered
Symptomtext
HCP advised that her office administered a vaccine to a patient that is being identified as a pediatric dose; No adverse event; This spontaneous case was reported by an other health care professional and describes the occurrence of WRONG PRODUCT ADMINISTERED (HCP advised that her office administered a vaccine to a patient that is being identified as a pediatric dose) and NO ADVERSE EVENT (No adverse event) in an elderly patient of an unknown gender who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. 053D22A) for COVID-19 prophylaxis. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) 1 dosage form. On an unknown date, the patient experienced WRONG PRODUCT ADMINISTERED (HCP advised that her office administered a vaccine to a patient that is being identified as a pediatric dose) and NO ADVERSE EVENT (No adverse event). At the time of the report, WRONG PRODUCT ADMINISTERED (HCP advised that her office administered a vaccine to a patient that is being identified as a pediatric dose) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for WRONG PRODUCT ADMINISTERED (HCP advised that her office administered a vaccine to a patient that is being identified as a pediatric dose). No concomitant medications were provided. No treatment medication was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 09.05.2023
- Impfdatum
- 06.10.2022
- Beginn
- 12.01.2023
- Tage bis Beginn
- 98,0
- Dosis
- 5
- 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 5 vaccines Moderna 1/29/21 Lot# 026L20A; Moderna 2/26/21 Lot# 001A21A; Moderna 11/3/21 Lot# 071F; Moderna 5/18/22 Lot# 057M21A; Moderna 10/6/22 Lot# 053D22A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 93,0
- Geschlecht
- M
- Eingang
- 02.05.2023
- Impfdatum
- 06.10.2022
- Beginn
- 20.04.2023
- Tage bis Beginn
- 196,0
- 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 1/28/21 Lot# 012L20A; Moderna 2/25/21 Lot# 004M20A; Moderna 4/21/22 Lot# 048L21A; Moderna 10/6/22 Lot# 053D22A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 28.04.2023
- Impfdatum
- 17.10.2022
- Beginn
- 01.04.2023
- Tage bis Beginn
- 166,0
- Dosis
- 5
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a 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 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 17Oct2022 as dose 5 (booster), single (Lot number: 053D22A) at the age of 65 years, in right arm for covid-19 immunisation; BNT162b2 (BNT162B2), on 10May2022 as dose 4 (booster), single (Lot number: FJ4989), in right arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 3 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Mild heart disease" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Apr2023, outcome "recovered" (17Apr2023) and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (17Apr2023) Negative. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: Patient did not received other medication in 2weeks. It was reported that patient was treated with Paxlovid from 11Apr2023 to 15Apr2023. Took the full course of Paxlovid. Tested 2 days after completion and tested negative. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300166762 same reporter/patient, different drug/AE;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20230417; Test Name: Covid-19 test; Test Result: Negative
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Heart disorder
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 19.04.2023
- Impfdatum
- 17.10.2022
- Beginn
- 02.03.2023
- Tage bis Beginn
- 136,0
- Dosis
- 5
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Cough
Nasal congestion
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
I had runny nose, stuffy nose, I did not have fever at all, I had a persistent cough. It was not moist cough. On 03/2/2023 I took a PCR COVID-19 test at an urgent care and the results were positive. I had a telehealth visit with urgent care on 03/3/2023 and was prescribed Paxlovid. I started Paxlovid on 3/3/2023 and continued that for the 5 days. I also received a cough medicine, Benzonatate. I could take it as much as 3 times a day. Within a couple of days, I was significantly better the cough persisted for at least 10 day and it got better and better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- 03MAR2023 - PCR COVID-19 Test - Positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Diabetes 2
- Andere Medikamente
- Losartan; Atorvastatin; Pepcid; Amlodipine; Ozempic
- Allergien
- Erythromycin; Penicillin; Mercury
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 13.04.2023
- Impfdatum
- 09.10.2022
- Beginn
- 10.03.2023
- Tage bis Beginn
- 152,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Vaccine breakthrough infection
Symptomtext
I had a breakthrough case of Covid-19, No symptoms..
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Women's Vitamin Vitamin C, Vitamin D3, Calium
- Allergien
- Cat, Hay Fever
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 13.04.2023
- Impfdatum
- 12.10.2022
- Beginn
- 29.03.2023
- Tage bis Beginn
- 168,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Aphthous ulcer
Dysphagia
SARS-CoV-2 test negative
Sacroiliac joint dysfunction
Streptococcus test positive
Symptomtext
I tested positive for Strep on 3/29/23. I had a slight sore throat and difficulty swallowing. I also had some canker sores on my tongue. I contacted a doctor and was prescribed Penicillin. This lasted for about a week but was prescribed 10 days' worth of medication. I am feeling much better now.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Aphthous ulcer
- Hospital-Tage
- -
- Labordaten
- 29MAR2023 Strep test - Positive; 29MAR2023 COVID-19 Test - Negative
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 12.04.2023
- Impfdatum
- 10.10.2022
- Beginn
- 01.01.2023
- Tage bis Beginn
- 83,0
- Dosis
- 5
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test normal
Scrotal mass
Spermatocele
Tumour marker test
Ultrasound scan abnormal
Symptomtext
In January 2023 I noticed a lump on scrotum that I thought may be a spermatocele. I made an appointment with my primary care physician. He referred me to a urologist who ordered an ultrasound to of the lump on my scrotum to see the viscosity of the tissue, he also ordered bloodwork to check the levels tumor marker checking. The bloodwork came back negative for tumors, the ultrasound did show that I have spermatocele. I will have a follow up visit in three months.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood test normal
- Hospital-Tage
- -
- Labordaten
- 30MAR2023 Ultrasound - positive for the spermatocele; 30MAR2023 Bloodwork - negative for tumors
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Chlorphenamine; Losartan; Lipitor
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- VT
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 12.04.2023
- Impfdatum
- 06.10.2022
- Beginn
- 01.11.2022
- Tage bis Beginn
- 26,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Electrocardiogram
Electrocardiogram ambulatory
Heart rate increased
Lymphadenopathy
Sensory disturbance
Symptomtext
I had swollen glands for a couple weeks and had a sensation across my chest even at rest in Feb of 2023 had an ECG and 72 heart monitor. I had a higher resting heart rate than usual
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Electrocardiogram
- Hospital-Tage
- -
- Labordaten
- EKG, HOLTER,
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma, HSV, Herpes, Depression, Anxiety
- Andere Medikamente
- Tri-estarylla: Albuterol inhaler: equate Multi Vitamin: Vitamin D
- Allergien
- Poppy Seeds:
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 11.04.2023
- Impfdatum
- 07.10.2022
- Beginn
- 13.03.2023
- Tage bis Beginn
- 157,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
C-reactive protein increased
Computerised tomogram head normal
Ear swelling
Erythema
External ear cellulitis
Full blood count normal
Metabolic function test normal
Skin infection
Symptomtext
I had a skin infection diagnosed a cellulitis in my right ear. I had redness and swelling of my right ear. I went to a quick clinic who prescribed Cefalexin & who recommended I go to the emergency room since it was not getting better after the antibiotic. I went to the emergency room, and they gave me a CT scan of my face and put me on an additional antibiotic called Doxycycline for 1 week. My symptoms improved the next day. I have since completely recovered from these symptoms.no fluid in face or jaw or anywhere in the face
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- C-reactive protein increased
- Hospital-Tage
- -
- Labordaten
- CT Scan-no fluid in face or jaw or anywhere in the face-March 15, 2023 CBC-March 15, 2023-normal Metabolic-March 15, 2023-normal C Reactive Protein Level-Levels High-March 15, 2023
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Blood Pressure; Hyperthyroidism
- Andere Medikamente
- Lisinopril; Hydrochlorothiazide; Synthroid; Tylenol
- Allergien
- Benadryl
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 11.04.2023
- Impfdatum
- 06.10.2022
- Beginn
- 08.01.2023
- Tage bis Beginn
- 94,0
- Dosis
- 5
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Exposure to SARS-CoV-2
SARS-CoV-2 test positive
Throat irritation
Symptomtext
I was exposed by my daughter the week before. I took her to the doctor and she was diagnosed 01/05 with the flu and COVID-19 and a sinus infection. I took her home and got her medications. I thought I had already been exposed so I had not put a mask on in the car. That was on a Thursday, so on Sunday 01/08, all of a sudden in the morning, I got a scratchy throat that progressed during the day. I sent a message to my doctor on my online patient portal. I came in the next day so I could test for COVID-19 and flu. I tested negative on both. At that time, I started to have a cough. That's when my doctor gave me the prescription for Bromphen cough syrup. She also gave me a prescription for home COVID-19 kits and I picked those up. She said in two days to test again and see if I was negative or positive. She said I may have come in too soon. She also said if my other family members were sick to contact her as well. Wednesday, I did do one of the COVID-19 tests at home. It wasn't too clear to me at the time but it was positive. I took a picture and let her know I needed to come in to double check. I went and tested again in the office and tested positive again on 01/12. She gave me a prescription for Paxlovid and an antibiotic. I took those and she told me to stay away from my husband for 5 days as well. We wanted to be careful. I called home and told my daughter so he could get his stuff out of the bedroom and move into a different room in the house. He stayed completely away from me and my daughter brought my food to me. I did really well and got up every morning. Once I started taking Paxlovid, my symptoms started getting better. I was also taking Zinc to help with recovery. I sat in my room and did activities to keep my mind occupied. It was hard staying away from my daughter and husband. I would say I had a mild case of COVID-19. When I was done with the medication, I felt great. My last Paxlovid was the morning of the 6th day. I went ahead and stayed in my room all day just in case. I did come out of the room to do some laundry to wash sheets, and I had a mask when I left my room. By 01/19 I was out of quarantine and started eating meals again with my family. We made a lot of changes in the household. Everything is done with precaution. My husband did not move back into the bedroom until 01/20 because he was cautious. Over time he started to feel comfortable being around again.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- 09JAN2023 COVID-19 Test - Negative; 09JAN2023 Flu Test - Negative; 11JAN2023 At Home COVID-19 Test - Positive; 12JAN2023 COVID-19 Test - Positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension; Arthritis; High Cholesterol
- Andere Medikamente
- Amlodipine; Low Dose Aspirin; Buspar; Gabapentin; Pravastatin; Premarin Vaginal Cream; Omeprazole; Loratadine; Tylenol Arthritis; Tylenol Gel Capsule; Vitamin D3; Vitamin E; Folate; Multivitamin; Venlafaxine XR
- Allergien
- Sulfa Drugs; Zyrtec; Penicillin; Seasonal Allergies
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 11.04.2023
- Impfdatum
- 10.10.2022
- Beginn
- 14.11.2022
- Tage bis Beginn
- 35,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Biopsy prostate abnormal
Blood test abnormal
Hormone therapy
Magnetic resonance imaging abnormal
Positron emission tomogram abnormal
Prostate cancer
Prostatic disorder
Prostatic specific antigen increased
Symptomtext
I went for a regularly scheduled physical in November and my Prostate-specific antigen was 8.9. I was prescribed antibiotics to see whether this was due to an infection. I took the medication for 10 days. After the dosage was completed, I returned to my doctor who completed another blood panel which reflected that my PSA was 10.9. I was sent for an MRI which showed Lesions in prostate. A Biopsy was completed, and I received the diagnosis of Prostate Cancer. After the diagnosis I was sent for a Pet Scan on February 23, 2023. to see if it had spread but it had not. I am now completing hormone therapy and will complete radiation I am radiation oncologist and medical oncologist. They are continuing to do blood test and I will be having those regularly. I was advised treatment could last for a couple of years.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Biopsy prostate abnormal
- Hospital-Tage
- -
- Labordaten
- Blood Panel-Prostate-specific antigen at 8.9-November 2022 Blood Panel-PSA 10.9-December 2022 MRI-Lesions in prostate shown- January 18, 2023 Biopsy-February 14, 2023-Diagnosis of Prostate Cancer Pet Scan-Confirmed cancer had not spread and was still in the prostate-February 22, 2023
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Diabetes; High Cholesterol; Acid Reflux; Thyroid Disease; Sleep Apnea
- Andere Medikamente
- Mounjaro Injection; Jardiance; Glipizide; Prilosec; Dasepa, Levothyroxine; Senior Multi-Vitamin; Fexofenadine; 81 mg aspirin; MiraLAX; Vitamin B12; Vitamin D3; Probiotic
- Allergien
- Ace Inhibitors; Ibuprofen; Motrin
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 07.04.2023
- Impfdatum
- 06.04.2023
- Beginn
- 06.04.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Symptomtext
Patient received a Moderna Bivalent on 10/10/2022, and then received a Pfizer Bivalent on 04/06/2023
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None known
- Vorgeschichte
- Diabetes, Hypertension, Diverticulitis, Anxiety, Acquired Hypothyroidism, Sleep Apnea, non cardiac chest pain
- Andere Medikamente
- Glipizide 10mg tab Metformin 500mg tab Trulicity 3mg/0.5mL pen injector Losartan 100mg tab Levothyroxine 112mcg tab Atorvastatin 20mg tab Sertraline 50mg tab Omeprazole 40mg capsule Doxycycline 50mg capsule Aspirin 81mg tab
- Allergien
- NKA other than pollens
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 04.04.2023
- Impfdatum
- 14.10.2022
- Beginn
- 25.11.2022
- Tage bis Beginn
- 42,0
- Dosis
- 4
- Route/Site
- SYR / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Nasal congestion
Pulmonary congestion
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Throat irritation
Symptomtext
I had my vaccination on 10/14/2022. On 11/25/2022 I started to have the sniffles. On 11/26/2022 I woke up with a scratchy throat and a stuffed nose head congestions and lung congestion. I presently feel better on 04/04/2023.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- 11/25/2022 test COVID-19 Positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Citalopram; Trazadone
- Allergien
- Mangos
- Vorherige Impfungen
- All Vaccinations; Frozen Shoulder Syndrome
- Staat
- MI
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 04.04.2023
- Impfdatum
- 07.10.2022
- Beginn
- 27.02.2023
- Tage bis Beginn
- 143,0
- 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 1/12/21 Lot# 037K20A; Moderna 2/9/21 Lot# 037K20a; Moderna 10/15/21 Lot# 017F21A; Moderna 10/7/22 Lot# 053D22A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 24.03.2023
- Impfdatum
- 21.09.2022
- Beginn
- 01.03.2023
- Tage bis Beginn
- 161,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bronchial irritation
Cough
Nasal congestion
Sputum discoloured
Symptomtext
A cough nonproductive, some central bronchial irritation; discolored greenish phlegm, they were continuous for four weeks now. The symptoms remained present but didn't escalate until the last ten days. The symptoms became more prevalent. Not until ten days ago I started treating symptoms, I have developed nasal congestion. Since it progressed on the 18th, I started Erythromycin. Just stopped taking medication by the 21st of the month. There is still cough but better than a week ago. It gets worse in the evening. I do not believe this is COVID-19, I have not tested. I've seen many people with similar profiles, that are negative testing, as a Physician.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bronchial irritation
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Seasonal
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 21.03.2023
- Impfdatum
- 14.02.2023
- Beginn
- 14.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Wrong product administered
Symptomtext
No adverse event; patient was administered with the bivalent vaccine instead of the monovalent for their 1st dose of the primary series; This spontaneous case was reported by an other health care professional and describes the occurrence of WRONG PRODUCT ADMINISTERED (patient was administered with the bivalent vaccine instead of the monovalent for their 1st dose of the primary series) and NO ADVERSE EVENT (No adverse event) in a 40-year-old female patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. 053D22A) for COVID-19 prophylaxis. Patient did not receive any other vaccines in the 4 weeks prior to COVID-19 vaccine. No relevant medical history or conditions, allergy,concomitant diseases and risk factor. On 14-Feb-2023, the patient received first dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) 1 dosage form. On 14-Feb-2023, after starting mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)), the patient experienced WRONG PRODUCT ADMINISTERED (patient was administered with the bivalent vaccine instead of the monovalent for their 1st dose of the primary series). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, WRONG PRODUCT ADMINISTERED (patient was administered with the bivalent vaccine instead of the monovalent for their 1st dose of the primary series) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for WRONG PRODUCT ADMINISTERED (patient was administered with the bivalent vaccine instead of the monovalent for their 1st dose of the primary series). No concomitant medications were reported. An administrator of an urgent care reports that they had an incident in one of their locations where a patient was administered with the bivalent vaccine instead of the monovalent for their 1st dose of the primary series. The patient was in their facility now for the supposed 2nd dose of the primary series. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: Patient did not receive any other vaccines in the 4 weeks prior to COVID-19 vaccine. No relevant medical history or conditions, allergy,concomitant diseases and risk factor.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 06.03.2023
- Impfdatum
- 30.11.2022
- Beginn
- 15.01.2023
- Tage bis Beginn
- 46,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abortion spontaneous
Exposure during pregnancy
Muscle spasms
Preterm premature rupture of membranes
Ultrasound scan
Symptomtext
I started to cramp on the 15th of January, I called the on-call doctor in the middle of all that was going on. My water broke and I had a miscarriage on the 16th of January. They had me come in a day later for an ultrasound to ensure that everything had passed. Due date was July 22, 2023
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abortion spontaneous
- Hospital-Tage
- -
- Labordaten
- Ultrasound
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Prenatal vitamins
- Allergien
- Shellfish
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 20.02.2023
- Impfdatum
- 11.04.2021
- Beginn
- 15.10.2022
- Tage bis Beginn
- 552,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
COVID-19 immunisation
SARS-CoV-2 test
Vaccination failure
Symptomtext
CONFIRMED CLINICAL VACCINATION FAILURE; CONFIRMED COVID-19 INFECTION; REVACCINATION WITH DIFFERENT COVID-19 VACCINE; This spontaneous report received from a patient via other manufacturer (Pfizer) concerned a patient of unspecified age and sex. Initial information was processed along with additional information on 16-FEB-2023. The patient's height, and weight were not reported. The patient's concurrent conditions included: drug allergy (Probably sulfa drugs), and other pre-existing medical conditions included: Patient had no relevant medical history and concurrent conditions. The patient was not taking any other medications/products within 2 weeks of starting COVID-19 treatment. The patient received covid-19 vaccine ad26.cov2.s (dose number in series 1) (suspension for injection, route of admin not reported, batch number: 205A21A expiry: UNKNOWN) dose was not reported, 1 total, administered on 11-APR-2021 in left arm for covid-19 prophylaxis. No concomitant medications were reported. The patient received non-company suspect vaccine included: Moderna covid-19 vaccine (elasomeran) (dose number in series 2) (form of admin, and route of admin was not reported, batch number: 014F21A expiry: UNKNOWN) dose was not reported, administered on 02-NOV-2021 in left arm for covid-19 prophylaxis. It was unknown whether patient had any adverse event following vaccination with Moderna covid-19 vaccine (elasomeran) (dose number in series 2). The patient received non-company suspect vaccine included: Pfizer biontech covid-19 vaccine (tozinameran) (dose number in series 3) (form of admin, and route of admin was not reported, batch number: FM9992 expiry: UNKNOWN), dose, start therapy date were not reported, administered in left arm for covid-19 prophylaxis. It was unknown whether patient had any adverse event following vaccination with Pfizer biontech covid-19 vaccine (tozinameran) (dose number in series 3). The patient additionally received non-company suspect vaccine included: Moderna covid-19 vaccine (elasomeran) (dose number in series 4) (form of admin, and route of admin was not reported, batch number: 053D22A expiry: UNKNOWN) dose was not reported, administered on 15-OCT-2022 in left arm for covid-19 prophylaxis which was revaccination with different covid-19 vaccine (dose number in series 4). On an unspecified date, the patient experienced covid-19 infection (dose number in series 4) for which patient received non-company suspect drug included: Paxlovid (nirmatrelvir/ritonavir) (pill, route of admin was not reported, batch number: 1923797A expiry: UNKNOWN) dose was not reported, 1 time every 0.5 days (5 days-3 pills-2 per day) from 25-JAN-2023 to 30-JAN-2023 for covid-19 treatment. On 01-FEB-2023, patient tested negative or almost negative. Laboratory data included: COVID-19 virus test Negative. On 03-FEB-2023, two days later, the patient tested strongly positive (home tests) and symptoms returned which led to confirmed covid-19 infection (dose number in series 4) and confirmed clinical vaccination failure (dose number in series 1). Laboratory data included: COVID-19 virus test Positive. The action taken with covid-19 vaccine ad26.cov2.s, elasomeran, tozinameran, and elasomeran was not applicable; and action taken with nirmatrelvir/ritonavir was not reported. The patient had not recovered from confirmed covid-19 infection, and the outcome of confirmed clinical vaccination failure and revaccination with different covid-19 vaccine was not reported. This report was serious (Other Medically Important Condition). This report was associated with product quality complaint: 90000271622.; Sender's Comments: V0: 20230236157-Confirmed clinical vaccination failure . The event has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event. Specifically: SPECIAL SITUATIONS. Therefore, this event is considered inconsistent with vaccine administration.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20230201; Test Name: COVID-19 VIRUS TEST; Test Result: Negative ; Test Date: 20230203; Test Name: COVID-19 VIRUS TEST (HOME TEST); Test Result: Positive
- Aktuelle Erkrankungen
- Drug allergy (Probably sulfa drugs)
- Vorgeschichte
- Comments: Patient had no relevant medical history and concurrent conditions. The patient was not taking any other medications/products within 2 weeks of starting COVID-19 treatment.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- F
- Eingang
- 11.02.2023
- Impfdatum
- 06.04.2021
- Beginn
- 19.10.2022
- Tage bis Beginn
- 561,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
COVID-19 immunisation
SARS-CoV-2 test
Vaccination failure
Symptomtext
CONFIRMED CLINICAL VACCINATION FAILURE; CONFIRMED COVID-19 INFECTION; REVACCINATION WITH DIFFERENT COVID-19 VACCINE; This spontaneous report received from a patient via other company (Pfizer Inc.) concerned a female patient of unspecified age, race, ethnicity. Initial information was processed along with the additional information received on 08-FEB-2023. The patient's height, and weight were not reported. The patient's concurrent conditions included: osteoporosis, depression, tinnitus, shellfish allergy, grasses allergy, and dust allergy. The patient received first dose with covid-19 vaccine ad26.cov2.s (Dose number in series 1), (suspension for injection, route of admin not reported, batch number: 201A21A, expiry: UNKNOWN) dose was not reported, single dose 1 total administered on 06-APR-2021 for covid-19 prophylaxis. Concomitant medications included ascorbic acid/calcium/minerals nos/retinol/tocopheryl acetate/vitamin b nos/vitamins nos/zinc, colecalciferol, estradiol, fluoxetine, loratadine, and spironolactone. The patient additionally received 2 doses (second and third dose) with Non-company suspect vaccine Moderna covid-19 vaccine, (elasomeran), (Dose number in series 2), (batch number: 058H21A, expiry: UNKNOWN, form of admin, route of admin were not reported) dose was not reported, administered on 01-DEC-2021, and (batch number: 001M21A, expiry: UNKNOWN, form of admin, route of admin were not reported) dose was not reported, administered on 27-APR-2022 for covid-19 prophylaxis. It was unknown whether patient had any adverse events following vaccination (Dose number in series 2). The patient also received fourth dose with Non-company suspect vaccine Moderna covid-19 vaccine, (elasomeran), (Dose number in series 3), (batch number: 053D22A, expiry: UNKNOWN, form of admin, route of admin were not reported) dose was not reported, administered on 19-OCT-2022 for covid-19 prophylaxis which was associated with revaccination with different covid-19 vaccine (Dose number in series 3). On an unspecified date, the patient experienced confirmed covid-19 infection (Dose number in series 3) and had confirmed clinical vaccination failure (Dose number in series 1). The patient started taking treatment with Non-company suspect drug Paxlovid, (nirmatrelvir/ritonavir) (form of admin, route of admin, batch number and expiry date were not reported) dose and frequency were not reported, (300-100 mg Pack (EUA)) from 14-JAN-2023 to 19-JAN-2023 for treatment of covid-19. On 14-JAN-2023 at 18.00, the patient had bad taste (like bile in throat) everyday during treatment with dizziness, daily Diarrhea 2 times, body aches first 2 days. On 19-JAN-2023, morning, patient took fifth dose of Paxlovid and on 22-JAN-2023, morning, Laboratory data included: COVID-19 virus test Negative. The patient reported that headaches began again on evening of 22-JAN-2023 (Rebound Covid-19) and on 25-JAN-2023, Laboratory data included: COVID-19 virus test Positive. On 28-JAN-2023, Laboratory data included: COVID-19 virus test Positive. The action taken with covid-19 vaccine ad26.cov2.s, elasomeran, elasomeran, and nirmatrelvir/ritonavir was not applicable. The patient was recovering from confirmed covid-19 infection, and the outcome of confirmed clinical vaccination failure and revaccination with different covid-19 vaccine was not reported. This report was serious (Other Medically Important Condition). This report was associated with a product quality complaint: 90000270411.; Sender's Comments: V0: 20230214697-confirmed clinical vaccination failure. The event has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event. Specifically: SPECIAL SITUATIONS. Therefore, this event is considered inconsistent with vaccine administration.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20230122; Test Name: COVID-19 VIRUS TEST; Test Result: Negative ; Test Date: 20230125; Test Name: COVID-19 VIRUS TEST; Test Result: Positive ; Test Date: 20230128; Test Name: COVID-19 VIRUS TEST; Test Result: Positive
- Aktuelle Erkrankungen
- Depression; Dust allergy; Grass allergy; Osteoporosis; Shellfish allergy; Tinnitus
- Vorgeschichte
- -
- Andere Medikamente
- CLARITIN [LORATADINE]; NATURE MADE VITAMIN D3; ESTRADIOL; SPIRONOLACTONE; FLUOXETINE; CENTRUM SILVER [ASCORBIC ACID;CALCIUM;MINERALS NOS;RETINOL;TOCOPHERYL ACETATE;VITAMIN B NOS;VITAMINS; PAXLOVID
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 23.01.2023
- Impfdatum
- 22.10.2022
- Beginn
- 20.12.2022
- Tage bis Beginn
- 59,0
- Dosis
- 5
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
SARS-CoV-2 test positive
Sinus congestion
Sneezing
Symptomtext
I received my covid -19 vaccine on 10/22/2022. On 12/20/2022 I woke up with heavy sinus congestion and frequent sneezing. I tested positive that day. After contacting my provider, I was prescribed Paxlovid. Symptoms were gone within 36 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High blood pressure; high cholesterol
- Andere Medikamente
- Multi vitamin; Multi B vitamins; Mushroom capsules; fish oil; saw palmetto; Probiotic
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 18.01.2023
- Impfdatum
- 11.10.2022
- Beginn
- 11.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Limb injury
Symptomtext
Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Limb injury
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 16.01.2023
- Impfdatum
- 14.10.2022
- Beginn
- 09.11.2022
- Tage bis Beginn
- 26,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypersensitivity
Paranasal sinus discomfort
Tinnitus
Symptomtext
I started to notice a ringing in my ears in early November. The ringing would vary in intensity from barely noticeable up to a 4 to 5 on a 10 scale of intensity. On 12/19 or 20 I sought out my doctor. Doctor advised blood pressure was not the issue and believed it to be related to allergies and sinus pressure. Advised to use SUDAFED and a nose spray. This caused the ringing to subside though it is getting worse again. It is usually the left side but uncommonly both. Occasional peaks at 4-5, but peaks of 3 is typical. Follow up with doctor Jan 30.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypersensitivity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Hypertension; Allergies
- Andere Medikamente
- LOTREL; ZYRTEC; low dose aspirin; sertraline; atorvastatin; calcium with vitamin D; multivitamin; fish oil; NASACORT
- Allergien
- Dust; molds; pollen
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 11.10.2022
- Beginn
- 23.11.2022
- Tage bis Beginn
- 43,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Nodule
Symptomtext
On November 23, 2022, I noticed a small nodule on the right side of my neck. I didn't pay a lot of attention to it at that point. On November 30, 2022, I noticed it again and made an appointment to see my doctor. I was prescribed amoxicillin for five days. I was asked to come back for a follow up visit in three weeks. During the follow up, I was told I needed a CAT scan of my neck. I was referred to an ENT Specialist. The CAT scan is scheduled for Friday. My appointment with the ENT is next week.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nodule
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Arthritis; High Blood Pressure
- Andere Medikamente
- Atenolol; hydrochlorothiazide; baby aspirin; omeprazole; vitamin D; meloxicam
- Allergien
- COMPAZINE; sulfa drugs; DEMEROL; PERCOCET
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 09.01.2023
- Impfdatum
- 02.11.2022
- Beginn
- 05.01.2023
- Tage bis Beginn
- 64,0
- 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 2/1/21 Lot# 031L20A; Moderna 3/11/21 Lot# 044A21A; Moderna 12/10/21 Lot# 060H21A; Moderna 11/2/22 Lot# 053D22A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 07.01.2023
- Impfdatum
- 13.12.2022
- Beginn
- 13.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Product administration error
Symptomtext
Patient did not disclose that she had alredy recieved an dose of the Moderna Bivalent. Patient presented an card that did not have the dose of bivalent Moderna on it. We then entered data into Immunization Registry later and discovered she had already recieved an dose of the Bivalent Booster. Vaccine Adminisration Error.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 05.01.2023
- Impfdatum
- 05.10.2022
- Beginn
- 24.12.2022
- Tage bis Beginn
- 80,0
- Dosis
- 5
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
SARS-CoV-2 test positive
Symptomtext
Felt fine. All good until I tested positive. Dr. prescribed Paxlovid300MG/100MG ten dose meds.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test positive using a home test on 12/24/2022.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Amlodinpine Besylate 10MG tab 1x, Potassium Citrate ER 10MG tab 4x Terazosin 10MG tab 1x
- Allergien
- None known.
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- -
- Geschlecht
- F
- Eingang
- 02.01.2023
- Impfdatum
- 28.12.2022
- Beginn
- 28.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Underdose
Symptomtext
No Adverse Event; bivalent was given in the 0.3 ml instead of the 0.5 ml to a patient; This spontaneous case was reported by an other health care professional and describes the occurrence of UNDERDOSE (bivalent was given in the 0.3 ml instead of the 0.5 ml to a patient) and NO ADVERSE EVENT (No Adverse Event) in an adult female patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. 053D22A) for COVID-19 prophylaxis. No Medical History information was reported. On 28-Dec-2022, the patient received dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Intramuscular) .3 milliliter. On 28-Dec-2022, after starting mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)), the patient experienced UNDERDOSE (bivalent was given in the 0.3 ml instead of the 0.5 ml to a patient). On an unknown date, the patient experienced NO ADVERSE EVENT (No Adverse Event). At the time of the report, UNDERDOSE (bivalent was given in the 0.3 ml instead of the 0.5 ml to a patient) and NO ADVERSE EVENT (No Adverse Event) outcome was unknown. For mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Intramuscular), the reporter considered NO ADVERSE EVENT (No Adverse Event) to be not related. No further causality assessment was provided for UNDERDOSE (bivalent was given in the 0.3 ml instead of the 0.5 ml to a patient). No concomitant drug information was provided. It was unknown if the patient had received any other vaccine 4 weeks prior to COVID-19 vaccine. No treatment drug information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- -
- Geschlecht
- M
- Eingang
- 31.12.2022
- Impfdatum
- 28.12.2022
- Beginn
- 28.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Accidental underdose
No adverse event
Symptomtext
No adverse event; bivalent was given in the 0.3 ml instead of the 0.5 ml to a patient today 28Dec2022; This spontaneous case was reported by an other health care professional and describes the occurrence of ACCIDENTAL UNDERDOSE (bivalent was given in the 0.3 ml instead of the 0.5 ml to a patient today 28Dec2022) and NO ADVERSE EVENT (No adverse event) in an adult male patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. 053D22A) for COVID-19 prophylaxis. No Medical History information was reported. On 28-Dec-2022, the patient received dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) .3 milliliter. On 28-Dec-2022, after starting mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)), the patient experienced ACCIDENTAL UNDERDOSE (bivalent was given in the 0.3 ml instead of the 0.5 ml to a patient today 28Dec2022). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, ACCIDENTAL UNDERDOSE (bivalent was given in the 0.3 ml instead of the 0.5 ml to a patient today 28Dec2022) and NO ADVERSE EVENT (No adverse event) outcome was unknown. The action taken with mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Unknown) was unknown. For mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for ACCIDENTAL UNDERDOSE (bivalent was given in the 0.3 ml instead of the 0.5 ml to a patient today 28Dec2022). No concomitant medications details were reported. It was unknown if patient received any other vaccines in the 4 weeks prior to COVID-19 vaccine. Moderna was not authorized to communicate with the patient's primary healthcare professional regarding this notification. The nurse stated their facility provides Moderna vaccines. The nurse declined to provide further patient information. No treatment medications details were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Accidental underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 47,0
- Geschlecht
- M
- Eingang
- 26.12.2022
- Impfdatum
- 22.12.2022
- Beginn
- 22.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syringe issue
Symptomtext
Error: Leaking from Syringe-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syringe issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 19.12.2022
- Impfdatum
- 14.10.2022
- Beginn
- 14.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Underdose
Symptomtext
No reaction. Patient received 0.25mL of Moderna Bivalent Booster dose. Patient notified.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 09.12.2022
- Impfdatum
- 06.12.2022
- Beginn
- 06.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 6
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
Pt tolerated well, however, dose was the 2nd bivalent dose that the patient got and it should not have been given.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- hypertension, diabetes, BPH, hyperlipidemia
- Andere Medikamente
- Amlodipine, aspirin, atorvastatin, calcium carbonate, clorthalidone, CoQ10, diclofenac gel, fexofenadine, fluticasone, glucosamine/chondroitin, losartan, melatonin, metformin, multivitamin, fish oil, miralax,tamsulosin, tumeric
- Allergien
- Sulfa, ace inhibitors, penicillins
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 26.11.2022
- Impfdatum
- 25.10.2022
- Beginn
- 25.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Wrong product administered
Symptomtext
Error: Wrong Vaccine/Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 17.11.2022
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Underdose
Symptomtext
Error: Wrong Dose of Vaccine - Too Low.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 17.11.2022
- Impfdatum
- 11.11.2022
- Beginn
- 11.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product administered to patient of inappropriate age
Symptomtext
no adverse event; 3 yr old received 0.25 mL Moderna Bivalent vaccine as a booster.; This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (3 yr old received 0.25 mL Moderna Bivalent vaccine as a booster.) and NO ADVERSE EVENT (no adverse event) in a 3-year-old male patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. 053D22A) for COVID-19 prophylaxis. Concomitant products included INFLUENZA VACCINE for an unknown indication. On 11-Nov-2022, the patient received dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Intramuscular) .25 milliliter. On 11-Nov-2022, the patient experienced PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (3 yr old received 0.25 mL Moderna Bivalent vaccine as a booster.). On an unknown date, the patient experienced NO ADVERSE EVENT (no adverse event). At the time of the report, PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (3 yr old received 0.25 mL Moderna Bivalent vaccine as a booster.) and NO ADVERSE EVENT (no adverse event) outcome was unknown. For mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Intramuscular), the reporter considered NO ADVERSE EVENT (no adverse event) to be not related. No further causality assessment was provided for PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (3 yr old received 0.25 mL Moderna Bivalent vaccine as a booster.). No concomitant medications were reported. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 16.11.2022
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Underdose
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 16.11.2022
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Underdose
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 96,0
- Geschlecht
- M
- Eingang
- 16.11.2022
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Underdose
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 16.11.2022
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Underdose
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 16.11.2022
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Underdose
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 16.11.2022
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Underdose
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 16.11.2022
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Underdose
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 16.11.2022
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Symptomtext
Error: Wrong Dose of Vaccine - Too High-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 16.11.2022
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Underdose
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 16.11.2022
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Underdose
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 16.11.2022
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Underdose
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 16.11.2022
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Underdose
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 16.11.2022
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Underdose
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 16.11.2022
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Underdose
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 16.11.2022
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Underdose
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 16.11.2022
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Underdose
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 16.11.2022
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Underdose
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 16.11.2022
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Underdose
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 16.11.2022
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Underdose
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 16.11.2022
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Underdose
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 16.11.2022
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Underdose
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 16.11.2022
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Underdose
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 16.11.2022
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Underdose
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 16.11.2022
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Underdose
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 16.11.2022
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Underdose
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 16.11.2022
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Underdose
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 16.11.2022
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Underdose
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 16.11.2022
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Underdose
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 16.11.2022
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Underdose
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 16.11.2022
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Underdose
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 16.11.2022
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Underdose
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 16.11.2022
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Underdose
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 93,0
- Geschlecht
- F
- Eingang
- 16.11.2022
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Underdose
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 16.11.2022
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Underdose
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 16.11.2022
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Underdose
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 16.11.2022
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Underdose
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 16.11.2022
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Underdose
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 16.11.2022
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Underdose
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 7,0
- Geschlecht
- F
- Eingang
- 15.11.2022
- Impfdatum
- 15.11.2022
- Beginn
- 15.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
No adverse event
Symptomtext
At a public clinic, patient and mother registered and consented to a Moderna Bivalent Vaccine. Prior to vaccination, patient's mother confirmed the child would be receiving Bivalent Moderna dose. After administration, RN asked for patient's vaccine card in order to update and patients mother stated, "This is her first dose". RN immediately informed MD. Patient's mother made aware that the child will need to receive Primary Series. Patient had no adverse reaction.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Flovent PRN
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 15.11.2022
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 11.11.2022
- Impfdatum
- 09.11.2022
- Beginn
- 11.11.2022
- Tage bis Beginn
- 2,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymphadenopathy
Symptomtext
Swollen lymph node in armpit of right arm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymphadenopathy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Diabetic, PCOS
- Andere Medikamente
- Metformin, atorvastatin, prenatal, iron, Lexapro, pantaprazole
- Allergien
- Hydrocodone, pork, some adhesives
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 11.11.2022
- Impfdatum
- 11.11.2022
- Beginn
- 11.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 08.11.2022
- Impfdatum
- 12.10.2022
- Beginn
- 12.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- UN / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 07.11.2022
- Impfdatum
- 28.10.2022
- Beginn
- 28.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 07.11.2022
- Impfdatum
- 03.11.2022
- Beginn
- 03.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Error: Expired Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 02.11.2022
- Impfdatum
- 01.11.2022
- Beginn
- 02.11.2022
- Tage bis Beginn
- 1,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Peripheral swelling
Symptomtext
Patient called into pharmacy to report that after receiving her flu and COVID-19 shot yesterday, her hand and lower arm on the side of the injection began swelling. Patient was advised to contact MD for a prednisone taper or antihistamine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Peripheral swelling
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- arthritis, etc.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 26.10.2022
- Impfdatum
- 21.10.2022
- Beginn
- 21.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
Client presented to vaccine clinic for 1st dose of Moderna (monovalent-primary series). Moderna bivalent given instead of Moderna monovalent. Per CDC, dose repeated with Moderna monovalent.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 26.10.2022
- Impfdatum
- 24.10.2022
- Beginn
- 24.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Accidental underdose
Device connection issue
No adverse event
Symptomtext
No adverse event; During this administration the syringe and the needle became disconnected and the majority of vaccine leaked out; During this administration the syringe and the needle became disconnected and the majority of vaccine leaked out; This spontaneous case was reported by a pharmacist and describes the occurrence of DEVICE CONNECTION ISSUE (During this administration the syringe and the needle became disconnected and the majority of vaccine leaked out), ACCIDENTAL UNDERDOSE (During this administration the syringe and the needle became disconnected and the majority of vaccine leaked out) and NO ADVERSE EVENT (No adverse event) in a 25-year-old male patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. 053D22A) for COVID-19 prophylaxis. No Medical History information was reported. On 24-Oct-2022, the patient received fourth dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Intramuscular) 1 dosage form. On 24-Oct-2022, the patient experienced DEVICE CONNECTION ISSUE (During this administration the syringe and the needle became disconnected and the majority of vaccine leaked out) and ACCIDENTAL UNDERDOSE (During this administration the syringe and the needle became disconnected and the majority of vaccine leaked out). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, DEVICE CONNECTION ISSUE (During this administration the syringe and the needle became disconnected and the majority of vaccine leaked out), ACCIDENTAL UNDERDOSE (During this administration the syringe and the needle became disconnected and the majority of vaccine leaked out) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for DEVICE CONNECTION ISSUE (During this administration the syringe and the needle became disconnected and the majority of vaccine leaked out) and ACCIDENTAL UNDERDOSE (During this administration the syringe and the needle became disconnected and the majority of vaccine leaked out). No concomitant medications was reported. There were no reported symptoms. No additional doses, medications, or treatments had been administered to the patient up to that point.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Accidental underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 23.10.2022
- Impfdatum
- 18.10.2022
- Beginn
- 18.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Wrong product administered
Symptomtext
Error: Wrong Vaccine/Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 22.10.2022
- Impfdatum
- 18.10.2022
- Beginn
- 18.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injury associated with device
Symptomtext
Error: Patient Accidentally Stuck by Needle-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injury associated with device
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 21.10.2022
- Impfdatum
- 17.10.2022
- Beginn
- 17.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Wrong product administered
Symptomtext
Error: Wrong Vaccine/Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 20.10.2022
- Impfdatum
- 16.10.2022
- Beginn
- 16.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Wrong product administered
Symptomtext
Error: Wrong Vaccine/Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WV
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 19.10.2022
- Impfdatum
- 14.10.2022
- Beginn
- 14.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Accidental underdose
No adverse event
Symptomtext
No adverse event; given a 0.25mL dose of the bivalent vaccine; This spontaneous case was reported by a pharmacist and describes the occurrence of ACCIDENTAL UNDERDOSE (given a 0.25mL dose of the bivalent vaccine) and NO ADVERSE EVENT (No adverse event) in a 79-year-old male patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. 053D22A) for COVID-19 prophylaxis. No Medical History information was reported. On 14-Oct-2022, the patient received dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Intramuscular) .25 milliliter. On 14-Oct-2022, the patient experienced ACCIDENTAL UNDERDOSE (given a 0.25mL dose of the bivalent vaccine). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, ACCIDENTAL UNDERDOSE (given a 0.25mL dose of the bivalent vaccine) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for ACCIDENTAL UNDERDOSE (given a 0.25mL dose of the bivalent vaccine). No concomitant medication was reported. On 14-Oct-2022, the four people over the age of 18 were given 0.25 ml dose of the bivalent vaccine. No symptoms were reported. No additional doses, medications or treatment was received.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Accidental underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WV
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 19.10.2022
- Impfdatum
- 14.10.2022
- Beginn
- 14.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Accidental underdose
No adverse event
Symptomtext
given a 0.25mL dose of the bivalent vaccine; given a 0.25mL dose of the bivalent vaccine; This spontaneous case was reported by a pharmacist and describes the occurrence of ACCIDENTAL UNDERDOSE (given a 0.25mL dose of the bivalent vaccine) and NO ADVERSE EVENT (given a 0.25mL dose of the bivalent vaccine) in a 72-year-old female patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. 053D22A) for COVID-19 prophylaxis. No Medical History information was reported. On 14-Oct-2022, the patient received dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Intramuscular) .25 milliliter. On 14-Oct-2022, the patient experienced ACCIDENTAL UNDERDOSE (given a 0.25mL dose of the bivalent vaccine). On an unknown date, the patient experienced NO ADVERSE EVENT (given a 0.25mL dose of the bivalent vaccine). At the time of the report, ACCIDENTAL UNDERDOSE (given a 0.25mL dose of the bivalent vaccine) and NO ADVERSE EVENT (given a 0.25mL dose of the bivalent vaccine) outcome was unknown. For mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Intramuscular), the reporter considered NO ADVERSE EVENT (given a 0.25mL dose of the bivalent vaccine) to be not related. No further causality assessment was provided for ACCIDENTAL UNDERDOSE (given a 0.25mL dose of the bivalent vaccine). The concomitant and treatment medication was not reported. On 14-Oct-2022, the four people over the age of 18 were given 0.25 ml dose of the bivalent vaccine by intramuscular injection. The patient had no reported symptoms, no additional doses, medications and treatments.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Accidental underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WV
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 19.10.2022
- Impfdatum
- 14.10.2022
- Beginn
- 14.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Accidental underdose
No adverse event
Symptomtext
No adverse event; given a 0.25mL dose of the bivalent vaccine; This spontaneous case was reported by a pharmacist and describes the occurrence of ACCIDENTAL UNDERDOSE (given a 0.25mL dose of the bivalent vaccine) and NO ADVERSE EVENT (No adverse event) in a 45-year-old male patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. 053D22A) for COVID-19 prophylaxis. No Medical History information was reported. On 14-Oct-2022, the patient received dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Intramuscular) .25 milliliter. On 14-Oct-2022, the patient experienced ACCIDENTAL UNDERDOSE (given a 0.25mL dose of the bivalent vaccine). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, ACCIDENTAL UNDERDOSE (given a 0.25mL dose of the bivalent vaccine) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for ACCIDENTAL UNDERDOSE (given a 0.25mL dose of the bivalent vaccine). No concomitant medications were reported. No symptoms were reported. No additional doses, medications, or treatments were given.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Accidental underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WV
- Alter
- 83,0
- Geschlecht
- F
- Eingang
- 19.10.2022
- Impfdatum
- 14.10.2022
- Beginn
- 14.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Accidental underdose
No adverse event
Symptomtext
No adverse event; given a 0.25mL dose of the bivalent vaccine; This spontaneous case was reported by a pharmacist and describes the occurrence of ACCIDENTAL UNDERDOSE (given a 0.25mL dose of the bivalent vaccine) and NO ADVERSE EVENT (No adverse event) in an 83-year-old female patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. 053D22A) for COVID-19 prophylaxis. No Medical History information was reported. On 14-Oct-2022, the patient received dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Intramuscular) .25 milliliter. On 14-Oct-2022, the patient experienced ACCIDENTAL UNDERDOSE (given a 0.25mL dose of the bivalent vaccine). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, ACCIDENTAL UNDERDOSE (given a 0.25mL dose of the bivalent vaccine) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for ACCIDENTAL UNDERDOSE (given a 0.25mL dose of the bivalent vaccine). No concomitant medications were reported. No symptoms were reported. No additional doses given were reported. Patient did not receive any treatment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Accidental underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 18.10.2022
- Impfdatum
- 12.10.2022
- Beginn
- 12.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Wrong product administered
Symptomtext
Error: Wrong Vaccine/Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 16.10.2022
- Impfdatum
- 11.10.2022
- Beginn
- 11.10.2022
- 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
Error: Diluent Administered Instead of Vaccine-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 16.10.2022
- Impfdatum
- 13.10.2022
- Beginn
- 13.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Wrong product administered
Symptomtext
Error: Wrong Vaccine/Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 16.10.2022
- Impfdatum
- 11.10.2022
- Beginn
- 11.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Error: Dose in Series Given Too Early-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 15.10.2022
- Impfdatum
- 11.10.2022
- Beginn
- 11.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Wrong product administered
Symptomtext
Error: Wrong Vaccine/Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 13.10.2022
- Impfdatum
- 12.10.2022
- Beginn
- 12.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
patient only received a 0.25 dose instead of 0.5
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 13.10.2022
- Impfdatum
- 12.10.2022
- Beginn
- 12.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
patient only received a 0.25 dose instead of 0.5
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 86,0
- Geschlecht
- M
- Eingang
- 13.10.2022
- Impfdatum
- 12.10.2022
- Beginn
- 12.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
patient only received a 0.25 dose instead of 0.5
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 13.10.2022
- Impfdatum
- 12.10.2022
- Beginn
- 12.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
patient only received a 0.25 dose instead of 0.5
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 85,0
- Geschlecht
- M
- Eingang
- 13.10.2022
- Impfdatum
- 12.10.2022
- Beginn
- 12.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
patient only received a 0.25 dose instead of 0.5
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 13.10.2022
- Impfdatum
- 12.10.2022
- Beginn
- 12.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
Symptomtext
patient only received a 0.25 dose instead of 0.5
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 13.10.2022
- Impfdatum
- 12.10.2022
- Beginn
- 12.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
patient only received a 0.25 dose instead of 0.5
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 13.10.2022
- Impfdatum
- 12.10.2022
- Beginn
- 12.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Underdose
Symptomtext
patient only received a 0.25 dose instead of 0.5
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 13.10.2022
- Impfdatum
- 09.10.2022
- Beginn
- 09.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoaesthesia
Hypoaesthesia oral
Symptomtext
Systemic: Pt reported mild numbness in mouth, described sensation similar to after dental anesthesia and similar senstation in righ arm 30 mins after. pt was monitored for 30 minutes and left without following up with pharmacist.-Mild, Systemic: Numbness (specify: facial area, extremities)-Mild, Additional Details: Pt received 2 vaccinations,moderna bi-valent on L arm and flucelvax on R arm.Pt reported feeling mild numbness around mouth;described sensation similar to after dental anesthesia.Pt was monitored for 30 mins, after initial 15 mins he described similar sensation in R arm but can still feel his arm.Pt denies anaphylaxis,SOB,or light headedness.Pt was alert and oriented.Pt was advised to stay additional 15 mins for monitoring and report numbness to md however pt left without f/u with pharmacist.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypoaesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 13.10.2022
- Impfdatum
- 11.10.2022
- Beginn
- 11.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
No adverse event
Wrong product administered
Symptomtext
No adverse event; Received Bivalent instead of Monovalent 2nd primary dose; Wrongful 2nd primary dose was administered more that 6 months from the first primary dose; This spontaneous case was reported by a pharmacist and describes the occurrence of WRONG PRODUCT ADMINISTERED (Received Bivalent instead of Monovalent 2nd primary dose), INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Wrongful 2nd primary dose was administered more that 6 months from the first primary dose) and NO ADVERSE EVENT (No adverse event) in a 25-year-old male patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. 053D22A) for COVID-19 vaccination. No Medical History information was reported. On 11-Oct-2022, the patient received second dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) 1 dosage form. On 11-Oct-2022, the patient experienced WRONG PRODUCT ADMINISTERED (Received Bivalent instead of Monovalent 2nd primary dose) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Wrongful 2nd primary dose was administered more that 6 months from the first primary dose). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, WRONG PRODUCT ADMINISTERED (Received Bivalent instead of Monovalent 2nd primary dose), INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Wrongful 2nd primary dose was administered more that 6 months from the first primary dose) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for WRONG PRODUCT ADMINISTERED (Received Bivalent instead of Monovalent 2nd primary dose) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Wrongful 2nd primary dose was administered more that 6 months from the first primary dose). No concomitant medications were reported. In 2021, Patient received first dose of Monovalent Moderna COVID-19 vaccine. Lot number and expiry date of vaccine was unknown. No treatment information was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 11.10.2022
- Impfdatum
- 07.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syringe issue
Symptomtext
Error: Leaking from Syringe-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syringe issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 09.10.2022
- Impfdatum
- 06.10.2022
- Beginn
- 06.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Wrong product administered
Symptomtext
Error: Wrong Vaccine/Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 08.10.2022
- Impfdatum
- 04.10.2022
- Beginn
- 04.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
Error: Dose in Series Given Too Early-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 08.10.2022
- Impfdatum
- 04.10.2022
- Beginn
- 04.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
Error: Dose in Series Given Too Early-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -