- Staat
- -
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 26.12.2023
- Impfdatum
- 20.11.2021
- Beginn
- 04.10.2023
- Tage bis Beginn
- 683,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Angiogram pulmonary abnormal
Atypical pneumonia
COVID-19
COVID-19 pneumonia
Chest X-ray abnormal
Device breakage
Dyspnoea
Echocardiogram abnormal
Ejection fraction normal
Hypoxia
Immunodeficiency
Infection reactivation
Interstitial lung disease
Lung disorder
Lung opacity
Pneumonia
Polymerase chain reaction negative
Symptomtext
Patient is a 61 y.o. female with a history of OSA, HTN, Paraneoplastic Syndrome (GAD 65) with COVID 9/4/23 who presented to ED 10/3/23 with persistent fevers, dyspnea found to be septic with hypoxemia. Transferred to Facility for further care. Admitted for acute hypoxic respiratory failure is secondary to COVID-19 reinfection. 1. Acute hypoxic respiratory failure: Required nasal oxymizer, on oxygen through nasal cannula. CTPA 10/5/23 with multifocal opacities consistent with atypical PNA. COVID-19 swab 10/14/23 positive. Sputum culture negative. Chest x-ray on 10/17/23 showed extensive bilateral mixed interstitial and airspace disease compatible with pneumonia . Wean as tolerated to keep sat>90%. On 3 L oxygen on 10/24/23. 2. Recurrent COVID-19 pneumonia, acute COVID: Initially diagnosed 9/4/23, s/p paxlovid with symptom resolution and suspect re-activation given immunodeficient state. Respiratory PCR 10/5/23 negative, COVID PCR 10/14/23 positive. Completed course of decadron on 10/13/23 per pulmonology recs. Started Remdesivir x5-d course (end 10/20 ) per ID recs. Finished 5 day course on 10/20/23. ID followed. No need for IVIG as an outpatient. Off isolation on 10/24/23. 3. Concern for CHF: Patient chest x-ray concerning for pneumonia versus pulmonary edema with cardiomegaly. Lasix . Echo on 10/18/2023 showed EF of 67% with borderline left ventricular hypertrophy. No need for further cardiac work-up. S/p IV lasix. No further diuresis indicated. 4. Autoimmune GAD antibody syndrome: Follows with Dr., neurology. On rituximab q6months. Consulted ID per patient request to discuss long-term goals for ongoing recurrent covid due to immunu- suppression status. 5. Chronic anemia: Baseline 11-12. Stable 6. OSA: Recent noncompliance due to tear in home mask. CPAP at bedtime
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 20,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 95,0
- Geschlecht
- M
- Eingang
- 21.11.2023
- Impfdatum
- 13.11.2021
- Beginn
- 12.01.2022
- Tage bis Beginn
- 60,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute myocardial infarction
Anticoagulant therapy
COVID-19
Condition aggravated
Death
General physical health deterioration
Metabolic encephalopathy
Pneumonia bacterial
Superinfection
Symptomtext
Patient admitted with NSTEMI, covid infection with superimposed bacterial pneumonia. Received IV Rocephin and doxycycline, completed IV Remdesivir, initiated Baricitinib planned x 14 days planned but held at discharge. He was fully anticoagulated with Lovenox for 3 days per Cardiology for NSTEMI and transitioned to lovenox. S/p high dose steroid; planned to taper but will hold at discharge. He had worsening Acute metabolic encephalopathy, on top of alzheimer dementia due to all acute and chronic issues above and continued to decline. Family opted for hospice. Patient was transitioned to inpatient hospice unit. Patient passed away 1.21.22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- 8,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 84,0
- Geschlecht
- M
- Eingang
- 17.08.2023
- Impfdatum
- 18.11.2021
- Beginn
- 08.01.2023
- Tage bis Beginn
- 416,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Breathing-related sleep disorder
Hypoventilation
Hypoxia
Respiratory failure
Symptomtext
SLEEP RELATED HYPOVENTILATION OR HYPOXEMIA ACUTE HYPOXEMIC RESPIRATORY FAILURE ACUTE HYPERCAPNIC RESPIRATORY FAILURE RESPIRATORY FAILURE, UNSPECIFIED ACUITY HYPOXIA
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 15.06.2023
- Impfdatum
- 07.01.2022
- Beginn
- 27.12.2022
- Tage bis Beginn
- 354,0
- Dosis
- 1
- Route/Site
- IM / LA
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
- 66,0
- Geschlecht
- M
- Eingang
- 08.06.2023
- Impfdatum
- 16.12.2021
- Beginn
- 06.11.2022
- Tage bis Beginn
- 325,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Cerebral artery occlusion
Cerebrovascular accident
Ischaemic stroke
Symptomtext
ACUTE STROKE DUE TO OCCLUSION OF LEFT MIDDLE CEREBRAL ARTERY ACUTE STROKE DUE TO ISCHEMIA, UNSPECIFIED TYPE AND ARTERY
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 93,0
- Geschlecht
- F
- Eingang
- 23.05.2023
- Impfdatum
- 12.11.2021
- Beginn
- 26.03.2022
- Tage bis Beginn
- 134,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cerebrovascular accident
Hypercoagulation
Hypertension
Symptomtext
I63.9 ACUTE STROKE, UNSPECIFIED TYPE AND ARTERY 2/23/2022 LATE EFFECT OF STROKE I63.9 ACUTE STROKE, UNSPECIFIED TYPE AND ARTERY 2/23/2022 HTN (HYPERTENSION) I63.9 ACUTE STROKE, UNSPECIFIED TYPE AND ARTERY 2/23/2022 SECONDARY HYPERCOAGULABLE STATE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 12.05.2023
- Impfdatum
- 16.11.2021
- Beginn
- 09.05.2022
- Tage bis Beginn
- 174,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute myocardial infarction
Cardiac failure congestive
Chronic kidney disease
Deep vein thrombosis
Epilepsy
Glomerular filtration rate
Hypokalaemia
Seizure
Status epilepticus
Symptomtext
G40.901 STATUS EPILEPTICUS 10/11/2022 CKD STAGE 3A (GFR 45-59) G40.909 EPILEPSY, UNSPECIFIED 8/16/2022 CKD STAGE 3A (GFR 45-59) I21.4 ACUTE NON ST ELEVATION MI 5/27/2022 CKD STAGE 3A (GFR 45-59) I82.401 ACUTE DVT OF RIGHT LEG, UNSPECIFIED VEIN 5/29/2022 CKD STAGE 3A (GFR 45-59) I82.4Y1 ACUTE DVT OF RIGHT THIGH, UNSPECIFIED VEIN 5/9/2022 CKD STAGE 3A (GFR 45-59) G40.901 STATUS EPILEPTICUS 10/11/2022 CHF (CONGESTIVE HEART FAILURE), UNSPECIFIED G40.909 EPILEPSY, UNSPECIFIED 8/16/2022 CHF (CONGESTIVE HEART FAILURE), UNSPECIFIED I21.4 ACUTE NON ST ELEVATION MI 5/27/2022 CHF (CONGESTIVE HEART FAILURE), UNSPECIFIED I82.401 ACUTE DVT OF RIGHT LEG, UNSPECIFIED VEIN 5/29/2022 CHF (CONGESTIVE HEART FAILURE), UNSPECIFIED I82.4Y1 ACUTE DVT OF RIGHT THIGH, UNSPECIFIED VEIN 5/9/2022 CHF (CONGESTIVE HEART FAILURE), UNSPECIFIED G40.901 STATUS EPILEPTICUS 10/11/2022 SEIZURE, UNSPECIFIED G40.909 EPILEPSY, UNSPECIFIED 8/16/2022 SEIZURE, UNSPECIFIED I21.4 ACUTE NON ST ELEVATION MI 5/27/2022 SEIZURE, UNSPECIFIED I82.401 ACUTE DVT OF RIGHT LEG, UNSPECIFIED VEIN 5/29/2022 SEIZURE, UNSPECIFIED I82.4Y1 ACUTE DVT OF RIGHT THIGH, UNSPECIFIED VEIN 5/9/2022 SEIZURE, UNSPECIFIED G40.901 STATUS EPILEPTICUS 10/11/2022 HYPOKALEMIA G40.909 EPILEPSY, UNSPECIFIED 8/16/2022 HYPOKALEMIA I21.4 ACUTE NON ST ELEVATION MI 5/27/2022 HYPOKALEMIA I82.401 ACUTE DVT OF RIGHT LEG, UNSPECIFIED VEIN 5/29/2022 HYPOKALEMIA I82.4Y1 ACUTE DVT OF RIGHT THIGH, UNSPECIFIED VEIN 5/9/2022 HYPOKALEMIA G40.901 STATUS EPILEPTICUS 10/11/2022 CKD STAGE 3A (GFR 45-59) G40.909 EPILEPSY, UNSPECIFIED 8/16/2022 CKD STAGE 3A (GFR 45-59) I21.4 ACUTE NON ST ELEVATION MI 5/27/2022 CKD STAGE 3A (GFR 45-59) I82.401 ACUTE DVT OF RIGHT LEG, UNSPECIFIED VEIN 5/29/2022 CKD STAGE 3A (GFR 45-59) I82.4Y1 ACUTE DVT OF RIGHT THIGH, UNSPECIFIED VEIN 5/9/2022 CKD STAGE 3A (GFR 45-59) G40.901 STATUS EPILEPTICUS 10/11/2022 ACUTE NON ST ELEVATION MI G40.909 EPILEPSY, UNSPECIFIED 8/16/2022 ACUTE NON ST ELEVATION MI I21.4 ACUTE NON ST ELEVATION MI 5/27/2022 ACUTE NON ST ELEVATION MI I82.401 ACUTE DVT OF RIGHT LEG, UNSPECIFIED VEIN 5/29/2022 ACUTE NON ST ELEVATION MI I82.4Y1 ACUTE DVT OF RIGHT THIGH, UNSPECIFIED VEIN 5/9/2022 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
- 87,0
- Geschlecht
- M
- Eingang
- 12.04.2023
- Impfdatum
- 03.03.2022
- Beginn
- 02.06.2022
- Tage bis Beginn
- 91,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Hypertension
Symptomtext
ACUTE RESPIRATORY FAILURE 6/21/2022 HTN (HYPERTENSION)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 92,0
- Geschlecht
- F
- Eingang
- 22.03.2023
- Impfdatum
- 24.03.2022
- Beginn
- 06.11.2022
- Tage bis Beginn
- 227,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Death
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Patient had a breakthrough infection and passed away.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- 10,0
- Labordaten
- Positive COVID test on 10/20/22.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Dementia CHF CVA
- Andere Medikamente
- Codeine Hydrocodone Penicillin Sulfa
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 92,0
- Geschlecht
- F
- Eingang
- 22.03.2023
- Impfdatum
- 24.03.2022
- Beginn
- 06.11.2022
- Tage bis Beginn
- 227,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Death
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Patient had a breakthrough infection and passed away.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- 10,0
- Labordaten
- Positive COVID test on 10/20/22.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Dementia CHF CVA
- Andere Medikamente
- Codeine Hydrocodone Penicillin Sulfa
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 13.03.2023
- Impfdatum
- 15.11.2021
- Beginn
- 01.11.2022
- Tage bis Beginn
- 351,0
- Dosis
- 1
- Route/Site
- IM / UN
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Brain injury
Cardiac arrest
Cardiomyopathy
Death
Symptomtext
DEATH. Suffered Cardiac arrest, Acute Myocardial, and Anoxic Brain injury. Less than one year after receiving the COVID-19 vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cardiac arrest
- Hospital-Tage
- 5,0
- Labordaten
- Unknown
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 92,0
- Geschlecht
- M
- Eingang
- 21.02.2023
- Impfdatum
- 08.11.2021
- Beginn
- 26.12.2022
- Tage bis Beginn
- 413,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute respiratory failure
Angiogram cerebral abnormal
Angiogram pulmonary normal
Asthenia
Atrial fibrillation
Angiogram cerebral
Angiogram pulmonary
Blood urine
Blood urine present
COVID-19
Carotid artery occlusion
Cerebral small vessel ischaemic disease
Cerebrovascular accident
Cognitive disorder
Computerised tomogram
Computerised tomogram head abnormal
Computerised tomogram thorax normal
Confusional state
Symptomtext
CAROTID ARTERY OCCLUSION; CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE; METABOLIC ENCEPHALOPATHY; THALAMIC INFARCTION; HAEMATURIA; COGNITIVE DISORDER; CONFUSIONAL STATE; MUSCULAR WEAKNESS; ECHOCARDIOGRAM NORMAL; URINE ANALYSIS ABNORMAL; ANGIOGRAM CEREBRAL ABNORMAL; BLOOD URINE PRESENT; COMPUTERISED TOMOGRAM HEAD ABNORMAL; COMPUTERISED TOMOGRAM THORAX NORMAL; SARS-COV-2 TEST POSITIVE; ANGIOGRAM PULMONARY NORMAL; ULTRASOUND DOPPLER NORMAL; ASTHENIA; COUGH; DECREASED APPETITE; COVID-19; CEREBROVASCULAR ACCIDENT; ACUTE RESPIRATORY FAILURE; ATRIAL FIBRILLATION; This spontaneous report received from a health care professional via Regulatory Authority VAERS (Vaccine Adverse Event Reporting System) (VAERS ID: 2572152); concerned a 92 year old male of an unspecified race and ethnicity. The patient's height, and weight were not reported. The patient's concurrent conditions included: prostate cancer, bladder cancer, and hypertension. On 2019, Laboratory data included: Urine analysis not reported. The patient previously received covid-19 vaccine ad26.cov2.s (dose number in series 1, unspecified manufacture) (suspension for injection, route of admin not reported, batch number: unknown, expiry: UNKNOWN) dose was not reported, 1 total, administered on an unspecified date for an unspecified indication. It was unknown whether patient had any adverse event following vaccination with covid-19 vaccine ad26.cov2.s (dose number in series 1, unspecified manufacture). The patient received covid-19 vaccine ad26.cov2.s (dose number in series 2) (suspension for injection, route of admin not reported, batch number: 213D21A, expiry: UNKNOWN) dose was not reported, 1 total, administered on 08-NOV-2021 for an unspecified indication. Age at time of vaccination 92 years old. No concomitant medications were reported. On 2021, Laboratory data included: Computerised tomogram which showed bladder mass. On 26-DEC-2022, the patient experienced weakness (asthenia), cough, poor appetite (decreased appetite) on date of admission and found to have Covid-19, respiratory failure (acute), hypoxia and possible acute CVA (cerebrovascular accident), acute hypoxic respiratory failure (dose number in series 2) and was hospitalized. The patient was hospitalized for 12 days. In setting of COVID-19 Requiring 2L NC, on admission CTPA (Computed tomographic pulmonary angiography) negative for PE (pulmonary embolism) (angiogram pulmonary normal) and No deep vein thrombosis on ultrasound dopplers (normal), Antitussive/mucolytic, prn albuterol, mobilize. On 2-3L NC, wean as tolerated; may need some more time to wean as SNF (sic) pulmonary followed covid-19 virus infection. On 28-DEC-2022, patient had CT of chest (computerised tomogram thorax) which showed no infiltrate (normal) and was tested positive for covid-19 (sars-cov-2 test positive) (dose number in series 2). Oxygen requirements on admission was 2L, Current oxygen requirements was 2L, Medical therapy included remdesivir completed, continued dexamethasone. Consultants following: pulmonary. Anticipated special isolation end date was 06-JAN-2023. On an unspecified date in 2023, patient had confusion (confusional state), slight L (left) arm weakness (muscular weakness), subacute right thalmic stroke (thalamic infarction), likely small vessel disease (cerebral small vessel ischaemic disease). Patient had CTH (computed tomography head) which showed indeterminant infarct R thalamus (abnormal), CTA (Computed Tomography Angiography) (angiogram cerebral abnormal) showed chronic right-ICA (internal carotid artery) occlusion at the level of skull base with distal reconstitution at the cavernous segment, Neurology signed off PT/OT/SLP. Patient had Atrial fibrillation with RVR (rapid ventricular rate), spontaneously converted to NSR (Normal sinus rhythm). Started on low dose Lopressor, had TTE (transthoracic echocardiogram) which was unremarkable. Will need eliquis but had significant hematuria with bladder cancer. Patient had acute metabolic encephalopathy, cognitive (cognitive disorder), decline Aox1 on arrival, family reports suspicion of early dementia not diagnosed, worse confusion in recent days. (dose number in series 2) PTA (Percutaneous transluminal angioplasty) Due to COVID positive, CVA contribution Delirium precautions; Otherwise as above alert to self, Added trazadone for sleep at night, gross hematuria bladder mass. Urine analysis (UA) showed large blood (abnormal) (blood urine present). Patient followed with an outside urologist doctor and had consistently expressed he did not want this treated further. Monitor for gross hematuria with addition of antiplatelet, urology consult if needed. Treatment medications (dates unspecified) included: acetylsalicylic acid, apixaban, trazodone, salbutamol, oxygen, remdesivir, metoprolol tartrate, and dexamethasone. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the acute respiratory failure, angiogram cerebral abnormal, angiogram pulmonary normal, asthenia, atrial fibrillation, blood urine present, covid-19, carotid artery occlusion, cerebral small vessel ischaemic disease, cerebrovascular accident, cognitive disorder, computerised tomogram head abnormal, computerised tomogram thorax normal, confusional state, cough, decreased appetite, echocardiogram normal, haematuria, metabolic encephalopathy, muscular weakness, sars-cov-2 test positive, thalamic infarction, ultrasound doppler normal and urine analysis abnormal was not reported. This report was serious (Hospitalization Caused / Prolonged). This report was associated with a product quality complaint. The suspected product quality complaint has been confirmed to be the reported allegation could not be determined. A manufacturing related root cause could not be identified, based on the PQC evaluation/investigation performed. Additional information was received from Complaint department on 17-FEB-2023. The following information was updated and incorporated into the case narrative: Product quality complaint investigation result.; Sender's Comments: V1: This follow up adds information about Product quality complaint investigation result. This does not alter previous causality assessment of the reported events. 20230228510- Atrial Fibrillation, Carotid Artery Occlusion, Cerebral Small Vessel Ischaemic Disease, Cerebrovascular Accident, Metabolic Encephalopathy, Thalamic Infarction, Haematuria, Cognitive Disorder, Confusional State, Decreased Appetite, Muscular Weakness, Urine Analysis Abnormal, Angiogram Cerebral Abnormal, Blood Urine Present, Computerised Tomogram Head Abnormal, Asthenia. The Event Shows An Incompatible Temporal Relationship. Therefore, This Event Is Considered Inconsistent With Vaccine Administration. 20230228510-Acute Respiratory Failure, Covid-19, Sars-Cov-2 Test Positive, Cough,. The event is deemed to be scientifically implausible, i.e., there is scientific evidence against a drug/event relationship; AND there is no known class effect. Therefore, this event is considered inconsistent with vaccine administration. 20230228510-Echocardiogram Normal, Ultrasound Doppler Normal, Angiogram Pulmonary Normal, Computerised Tomogram Thorax Normal. The event has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event. Therefore, the WHO Causality is considered indeterminate. The company causality is considered unassessable.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 12,0
- Labordaten
- Test Date: 2019; Test Name: URINE ANALYSIS; Result Unstructured Data: not reported; Test Date: 2021; Test Name: COMPUTERISED TOMOGRAM; Result Unstructured Data: bladder mass; Test Date: 20221226; Test Name: ULTRASOUND DOPPLER; Result Unstructured Data: Normal (no DVT (deep vein thrombosis) on dopplers; Test Date: 20221226; Test Name: ANGIOGRAM PULMONARY; Result Unstructured Data: Normal (negative for PE (pulmonary embolism); Test Date: 20221228; Test Name: COMPUTERISED TOMOGRAM THORAX; Result Unstructured Data: Normal (no infiltrate); Test Date: 20221228; Test Name: SARS-COV-2 TEST; Test Result: Positive ; Test Date: 2023; Test Name: ANGIOGRAM CEREBRAL; Result Unstructured Data: Abnormal (chronic right-ICA (internal carotid artery) occlusion at the level of skull base with distal reconstitution at the cavernous segment); Test Date: 2023; Test Name: ECHOCARDIOGRAM; Result Unstructured Data: Normal (unremarkable); Test Date: 2023; Test Name: BLOOD URINE; Result Unstructured Data: Present; Test Date: 2023; Test Name: COMPUTERISED TOMOGRAM HEAD; Result Unstructured Data: Abnormal (indeterminant infarct R thalamus ); Test Date: 2023; Test Name: URINE ANALYSIS; Result Unstructured Data: Abnormal
- Aktuelle Erkrankungen
- Bladder cancer; Hypertension; Prostate cancer
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 14.01.2023
- Impfdatum
- 23.11.2021
- Beginn
- 21.07.2022
- Tage bis Beginn
- 240,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Angiogram cerebral abnormal
Arterial recanalisation procedure
Cerebral artery occlusion
Cerebral artery thrombosis
Cerebrovascular accident
Laboratory test
Thrombectomy
Symptomtext
Stroke, Right distal M1 middle cerebral artery occlusion. Transfermoral cerebral angiography and intra-arterial thrombectomy of right middle cerebral artery clot. Complete recanalization of the primary occlusion.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- 4,0
- Labordaten
- 07/21/2021, numerous tests and labs associated with emergent treatment of stroke
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Myocardial infarction 01/2009
- Andere Medikamente
- Atorvastatin, Clopidigrel, Lisinopril, Spironalactone, Carvedilol, 81mg aspirin
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 10.01.2023
- Impfdatum
- 30.11.2021
- Beginn
- 12.12.2022
- Tage bis Beginn
- 377,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute kidney injury
Acute respiratory failure
Aspiration
Atrial fibrillation
Blood creatinine increased
Confusional state
Electrocardiogram abnormal
Encephalopathy
Endotracheal intubation
Extubation
COVID-19
Cardiac telemetry
Chest X-ray abnormal
Chronic kidney disease
Computerised tomogram abdomen abnormal
Gastrointestinal tube insertion
Gastrointestinal tube removal
Hernia
Symptomtext
Discharge Diagnoses and Associated Hospital Course: Patient is a 78 y.o. male with history of HTN, HLD, DM, prior SBOs managed conservatively (11/2019), L CVA with residual deficit (7/14/22) who presented to hospital as transfer on 12/12/2022 with concern for SBO 2/2 internal hernia & strangulated small bowel. Admitted with these risk variables:Encephalopathy, Acute Kidney Injury, Chronic Kidney Disease, and Acidosis. Please see assessment and plan for further details. CT A/P IV Contrast (12/12): SBO w/ incarceration & strangulation 2/2 internal mesenteric hernia in R abdomen & pelvis. Suspicious for small bowel ischemia. SBO w/ concern for strangulated small bowel Lactic Acidosis, resolved AKI on CKD, resolved Hyperglycemia, resolved COVID Positive - s/p reduction of small bowel volvulus, LOA on 12/13/2022 - kept intubated post-op; extubated 12/13 to HHFNC; now on RA - NGT removed 12/15 - Postoperatively, the patient had slow return of bowel function, his diet and activity were advanced cautiously. He was maintained on DVT prophylaxis throughout his hospitalization. Please refer to daily progress notes for detailed clinical progression. COVID-19 infection tested positive 12/12/2022, unsure symptoms due to encephalopathy however noted hypoxia on presentation with bilateral infiltrates. Decadron started 12/13/22, stopped 12/19/22. Patient on RA as of 12/17/22. Acute respiratory failure with hypoxia CXR with mild opacities in lung base, possibly sec to aspiration vs COVID 19. required O2 prior to surgery. Remained intubated postoperatively 12/13/22 extubated to HHFNC. Required 60L HHFNC with fiO2 50% 12/14/22. Resolved. Acute Metabolic encephalopathy noted on admit. Unclear baseline, suspect sec to above. Management as noted. Remains intermittently confused as of 12/18/22 AKI on CKD stage 3 baseline Cr 1.5-2. On admission 4.39. S/p IVF. Resolved. Monitored. PAF or PSVT EKG in ED showed afib with RVR rate 150's. No history of a fib, +history of SVT, rate back to 110's spontaneously. Repeat EKGs with sinus tachycardia. S/p scheduled IV metoprolol, transitioned to home metoprolol. Continue telemetry monitoring. Recommended outpatient follow-up with cardiology. DM2 hold oral medications, SSI. HTN continue home amlodipine. Held home hydrochlorothiazide, lisinopril for soft BP. Restart as tolerated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 8,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 28.12.2022
- Impfdatum
- 29.11.2021
- Beginn
- 29.11.2022
- Tage bis Beginn
- 365,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute myocardial infarction
Angina unstable
COVID-19
Coronary artery disease
Essential hypertension
Fall
Hyperlipidaemia
Loss of consciousness
Symptomtext
Date of Admission: 11/29/2022 Date of Discharge: 12/1/2022 Active Hospital Problems Diagnosis o NSTEMI (non-ST elevated myocardial infarction) (CMS/HCC) o Fall, initial encounter o COVID-19 o Transient loss of consciousness o Primary hypertension o Coronary artery disease involving native coronary artery of native heart with unstable angina pectoris (CMS/HCC) o 3-vessel CAD o Hyperlipidemia with target low density lipoprotein (LDL) cholesterol less than 70 mg/dL
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 21.11.2022
- Impfdatum
- 19.11.2021
- Beginn
- 19.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Anaphylactic shock
Bronchitis
Condition aggravated
Diarrhoea
Food allergy
Hyperthyroidism
Influenza
Laboratory test
Lethargy
Lymphadenectomy
Lymphadenopathy
Pneumonia
Quarantine
Vomiting
Symptomtext
February 2020; I believe I had COVID-19 before they were able to diagnose it. I was diagnosed with bronchitis, pneumonia, and the flu. The placed me in complete isolation. It took months to recover. After effects from having COVID-19, I became allergic to avocados and I immediately had diarrhea and vomiting. This led me to going into anaphylactic shock and I had to reach out to emergency medical care for treatment. Allergies are continuing to be very deadly and extremely worrisome. For the second vaccination that I had I had extreme lethargy and I was out a day. I also had an extreme growth in my lymph node and it was then removed and it was reported I did not have cancer. Hyperthyroidism had intensified as well and I am unsure of when this began.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anaphylactic shock
- Hospital-Tage
- -
- Labordaten
- JUL2022 Lymph node testing, dead cells.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Blood Pressure; Osteoarthritis
- Andere Medikamente
- Lisinopril; betablocker; FLEXURAL; BENADRYL
- Allergien
- N/A
- Vorherige Impfungen
- Janssen vaccine COVID-19; 06/01/2021; Dose #1: I felt extremely unwell for over 5 days.
- Staat
- SD
- Alter
- 88,0
- Geschlecht
- M
- Eingang
- 09.11.2022
- Impfdatum
- 01.12.2021
- Beginn
- 25.07.2022
- Tage bis Beginn
- 236,0
- Dosis
- 2
- Route/Site
- - / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Atrial fibrillation
COVID-19
Cerebrovascular accident
Death
SARS-CoV-2 test
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
DEATH; ATRIAL FIBRILLATION; ATRIAL FIBRILLATION; COVID-19; CEREBROVASCULAR ACCIDENT; COVID-19; DEATH; SARS-COV-2 TEST POSITIVE; VACCINE BREAKTHROUGH INFECTION; This spontaneous report received from a health care professional by a Regulatory Authority VAERS (Vaccine Adverse Event Reporting System) (VAERS ID) concerned an 88 year old male of an unspecified race and ethnicity. The patient's height, and weight were not reported. The patient's past medical history included: stroke, and concurrent conditions included: hypertension, vascular dementia, chronic kidney disease, kidney carcinoma, combined heart failure, coronary artery disease, obstructive sleep apnea, multiple episodes of pulmonary embolism, and drug allergy (Meperidine Atorvastatin). The patient previously received dose 1 with covid-19 vaccine ad26.cov2.s (Dose number in series 1), (suspension for injection, route of admin not reported, batch number: 1808982, expiry: UNKNOWN, and expiry date: Unknown) dose was not reported, 1 total administered on 13-SEP-2021 for an unspecified indication. It was unknown whether patient had any adverse events following vaccination (Dose number in series 1). The patient received dose 2 with covid-19 vaccine ad26.cov2.s (Dose number in series 2), (suspension for injection, route of admin not reported, batch number: 213D21A expiry: UNKNOWN and expiry date: Unknown) dose was not reported, 1 total administered on 01-DEC-2021 to right arm for an unspecified indication. Age at time of vaccination 88 years old. No concomitant medications were reported. On 25-JUL-2022, the patient had tested positive for sars-cov-2 (severe acute respiratory syndrome coronavirus 2) and experienced covid-19 (vaccine breakthrough infection) (Dose number in series 2), and had complications of cerebrovascular accident and atrial fibrillation (Dose number in series 2). The patient was briefly hospitalized for 1 day and died on 30-JUL-2022 (Dose number in series 2). It was unspecified if an autopsy was performed On 30-JUL-2022, the patient died from atrial fibrillation, covid-19, cerebrovascular accident, death, sars-cov-2 test positive, and vaccine breakthrough infection. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. This report was serious (Death and Hospitalization Caused / Prolonged). This report was associated with a product quality complaint: 90000253952. The suspected product quality complaint has been confirmed to be the reported allegation could not be determined. A manufacturing related root cause could not be identified based on the PQC evaluation/investigation performed. Additional information received from Central Complaint Vigilance department on 07-NOV-2022. The following information was updated and incorporated into the case narrative: Product quality complaint investigation result.; Sender's Comments: V3: This follow up adds information about Product quality complaint investigation result. This does not alter the previous company causality of the reported events. 20220951234-covid-19 vaccine ad26.cov2.s-Death, Atrial fibrillation, Cerebrovascular accident. The event(s) 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(s) than the drug. Specifically: MEDICAL HISTORY(Patient age- 88 years, past medical history of stroke and concurrent conditions of hypertension, chronic kidney disease, kidney carcinoma, combined heart failure, coronary artery disease, multiple episodes of pulmonary embolism are considered as confounding factors). Therefore, this event(s) is considered not related. 20220951234-covid-19 vaccine ad26.cov2.s- Covid-19, Sars-cov-2 test positive, Vaccine breakthrough infection. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s). Therefore, this event(s) is considered unassessable.; Reported Cause(s) of Death: ATRIAL FIBRILLATION; COVID-19; CEREBROVASCULAR ACCIDENT; DEATH; SARS-COV-2 TEST POSITIVE; VACCINE BREAKTHROUGH INFECTION
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- 1,0
- Labordaten
- Test Date: 20220725; Test Name: SARS-COV-2 TEST; Test Result: Positive
- Aktuelle Erkrankungen
- Chronic kidney disease; Congestive heart failure; Coronary artery disease; Drug allergy (Meperidine Atorvastatin); Hypertension; Kidney carcinoma; Obstructive sleep apnea syndrome; Pulmonary embolism; Vascular dementia
- Vorgeschichte
- Medical History/Concurrent Conditions: Stroke
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 14.09.2022
- Impfdatum
- 03.12.2021
- Beginn
- 10.04.2021
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Chest pain
Haemoptysis
Pain in extremity
Pulmonary embolism
Symptomtext
Late February 2022, started having pain in left leg, felt like pulled muscles going up & down my leg. Two months later after jogging I started coughing up blood & having chest pain. 3 weeks later was sent to the E.R. Diagnosed with Pulmonary Embolism
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary embolism
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Seizure Disorder Post Lyme Disease
- Andere Medikamente
- Keppra, Topamax
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- SD
- Alter
- 88,0
- Geschlecht
- M
- Eingang
- 12.09.2022
- Impfdatum
- 01.12.2021
- Beginn
- 25.07.2022
- Tage bis Beginn
- 236,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Atrial fibrillation
COVID-19
Cerebrovascular accident
Death
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
This is an instance of breakthrough COVID-19 after which death occurred. The individual was vaccinated with the Janssen product on 09/13/2021 and 12/01/2021. They tested positive for COVID-19 on 07/25/2022. They experienced complications of Cerebral vascular accident and A-Fib. They were briefly hospitalized and died on 07/30/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- 1,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hypertension, Vascular Dementia, Chronic Kidney Disease, History of Kidney Carcinoma, History of Combined Heart Failure, History of Coronary Artery Disease, History of Obstructive Sleep Apnea, History of multiple episodes of Pulmonary Embolism, Past history of Stroke The individual was a resident of the long term care facility indicated in the Address portion of this form.
- Andere Medikamente
- -
- Allergien
- Meperidine, Atorvastatin
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 89,0
- Geschlecht
- F
- Eingang
- 09.08.2022
- Impfdatum
- 01.02.2022
- Beginn
- 30.05.2022
- Tage bis Beginn
- 118,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cerebrovascular accident
Decreased appetite
Fall
Fluid intake reduced
Food refusal
Gait inability
Hypophagia
Hyporesponsive to stimuli
Magnetic resonance imaging head
Magnetic resonance imaging head abnormal
Mental status changes
Movement disorder
Musculoskeletal disorder
Pyrexia
SARS-CoV-2 test positive
SARS-CoV-2 test
Somnolence
Symptomtext
SARS-COV-2 TEST POSITIVE; SPEECH DISORDER; PYREXIA; SARS-COV-2 TEST POSITIVE; MAGNETIC RESONANCE IMAGING HEAD ABNORMAL; MOVEMENT DISORDER; COVID-19; DECREASED APPETITE; FALL; FLUID INTAKE REDUCED; FOOD REFUSAL; GAIT INABILITY; HYPOPHAGIA; HYPORESPONSIVE TO STIMULI; MOVEMENT DISORDER; SOMNOLENCE; SOMNOLENCE; MENTAL STATUS CHANGES; SPEECH DISORDER; PYREXIA; MUSCULOSKELETAL DISORDER; MAGNETIC RESONANCE IMAGING HEAD ABNORMAL; CEREBROVASCULAR ACCIDENT; MENTAL STATUS CHANGES; MUSCULOSKELETAL DISORDER; This spontaneous report received from a health care professional via Regulatory Authority VAERS (Vaccine Adverse Event Reporting System)(VAERS ID: 2368873) and concerned an 89 year old female. The patient's height, and weight were not reported. The patient's past medical history included: acute cerebrovascular accident, multiple closed fractures of pelvis with stable disruption of pelvic circle, closed head injury, facial laceration, fall, facial contusion initial encounter, and closed fracture of left distal radius, and concurrent conditions included: macular degeneration of left eye, presence of artificial eye, transient ischemic attack, vascular dementia without behavioral disturbance chronic, hyperlipidemia chronic, dementia chronic, scapholunate dissociation of left wrist, failure to thrive in adult, acute cystitis without hematuria, drug allergy (Severity Reactions (Acetaminophen, Atrovent [ipratropium Bromide], Codeine, Darvocet A500 [propoxyphene Nacetaminophen], Motrin [ibuprofen], Norco [hydrocodone-acetaminophen], (Made patient feel crazy), Propoxyphene Napsylate, Simvastatin)), penicillin allergy, influenza virus vaccine allergy (Patient had rash, she went to emergency room (ER)), red dye allergy, hypertension, and bronchial asthma. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: 213D21A expiry: UNKNOWN) dose was not reported, 1 total, administered on 01-FEB-2022 in left arm for an unspecified indication. Age at time of vaccination 89 years old. Concomitant medications included calcium carbonate, colecalciferol and sennosides. On 30-MAY-2022, patient was hospitalized for evaluation of decreased mentation and possible stroke (cerebrovascular accident). Patient was nonverbal (speech disorder) and followed some simple commands. The patient was admitted on 30-MAY-2022 to 01-JUN-2022, for altered mentation (mental status changes). Apparently the patient was being evaluated for seizures, however they opted not to proceed with EEG (electroencephalogram) and MRI (Magnetic resonance imaging). The patient apparently improved after fluids. Hospice was offered to the imaging was admission due to the advanced dementia, however the family refused to sign up for hospice. When patient left the hospital the son reported that patient apparently walked with full assist to about 100 feet and in fact climb a few steps of stairs, was doing fine since the discharge. On 01-JUN-2021, Wednesday, patient started having decreased appetite, refusing to be fed (food refusal) and was chest more somnolent than baseline. The son of patient also noted that the right leg was not moving at all (movement disorder and musculoskeletal disorder) despite different ways to try to encourage to move the right leg. The patient also stopped walking since Wednesday (gait inability). They apparently tried to have patient sit for a meal but patient slid off the chair with right knee going underneath the left leg. They managed to prevent patient from falling to the ground (fall). Patient was hardly responding (hyporesponsive to stimuli) and had not anything to eat or drink at all (fluid intake reduced and hypophagia). They decided to bring patient to the emergency room for further evaluation. Patient was admitted to the neurology floor. The patient was started on aspirin. Patient was considered for a statin but this was deferred due to the dietary limitations and pending hospice status. On 10-JUN-2022, patient underwent MRI (Magnetic resonance imaging) which was consistent with a CVA (cerebrovascular accident). Teleneurology was consulted given poor functional status and poor long-term prognosis family opted for hospice care. The patient had a fever (pyrexia) and tested positive for COVID-19 which delayed hospice transport 10 days waiting period for isolation concerns, recommended diet was a pureed diet. On 14-JUN-2021, Laboratory data included: SARS-CoV-2 test Positive. The patient was non-verbal and interactive with daughter present, limited intake including pocketing food. The patient was discharged to rehab. Patient was hospitalized for 10 days. Treatment medication (dates unspecified) included: acetylsalicylic acid. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from cerebrovascular accident, covid-19, decreased appetite, fall, fluid intake reduced, food refusal, gait inability, hypophagia, hyporesponsive to stimuli, mental status changes, movement disorder, musculoskeletal disorder, somnolence, speech disorder, magnetic resonance imaging head abnormal, sars-cov-2 test positive, and pyrexia. This report was serious (Hospitalization Caused / Prolonged). This report was associated with product quality complaint. The suspected product quality complaint has been confirmed to be the reported allegation could not be determined. A manufacturing related root cause could not be identified based on the evaluation/investigation performed. Additional information received from Central Complaint Vigilance department on 02-AUG-2022. The following information was updated and incorporated into the case narrative: Product quality complaint investigation result.; Sender's Comments: V2: This version updates: Product quality complaint investigation result. The prior causality assessment remains unaltered with this information. 20220747042- COVID-19 VACCINE AD26.COV2.S- cerebrovascular accident, decreased appetite, fall, fluid intake reduced, food refusal, gait inability, hypophagia, hyporesponsive to stimuli, mental status changes, movement disorder, musculoskeletal disorder, somnolence, speech disorder, magnetic resonance imaging head abnormal. The event(s) 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(s) than the drug. Specifically: MEDICAL HISTORY. Therefore, this event(s) is considered not related. 20220747042-COVID-19 VACCINE AD26.COV2.S- COVID-19, pyrexia, SARS-COV-2 test positive. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s). Therefore, this event(s) is considered unassessable.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- 10,0
- Labordaten
- Test Date: 20220610; Test Name: MAGNETIC RESONANCE IMAGING HEAD; Result Unstructured Data: Abnormal (consistent with a CVA (cerebrovascular accident); Test Date: 20220614; Test Name: SARS-COV-2 TEST; Test Result: Positive
- Aktuelle Erkrankungen
- Acute cystitis; Allergy to vaccine (Patient had rash, she went to emergency room (ER)); Bronchial asthma; Dementia; Drug allergy (Severity Reactions (Acetaminophen, Atrovent [ipratropium Bromide], Codeine, Darvocet A500 [propoxyphene Nacetaminophen], Motrin [ibuprofen], Norco [hydrocodone-acetaminophen], (Made patient feel crazy), Propoxyphene Napsylate, Simvastatin)); Eye prosthesis user; Failure to thrive; Food allergy; Hyperlipidemia; Hypertension; Macular degeneration; Penicillin allergy; Scapholunate dissociation; Transient ischemic attack; Vascular dementia
- Vorgeschichte
- Medical History/Concurrent Conditions: Bruising of face; Cerebrovascular accident; Closed fracture; Closed head injury; Fall; Laceration of face; Multiple fractures
- Andere Medikamente
- CALCIUM CARBONATE; VITAMIN D3; SENNOSIDES
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 89,0
- Geschlecht
- F
- Eingang
- 09.08.2022
- Impfdatum
- 01.02.2022
- Beginn
- 30.05.2022
- Tage bis Beginn
- 118,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cerebrovascular accident
Decreased appetite
Fall
Fluid intake reduced
Food refusal
Gait inability
Hypophagia
Hyporesponsive to stimuli
Magnetic resonance imaging head
Magnetic resonance imaging head abnormal
Mental status changes
Movement disorder
Musculoskeletal disorder
Pyrexia
SARS-CoV-2 test positive
SARS-CoV-2 test
Somnolence
Symptomtext
SARS-COV-2 TEST POSITIVE; SPEECH DISORDER; PYREXIA; SARS-COV-2 TEST POSITIVE; MAGNETIC RESONANCE IMAGING HEAD ABNORMAL; MOVEMENT DISORDER; COVID-19; DECREASED APPETITE; FALL; FLUID INTAKE REDUCED; FOOD REFUSAL; GAIT INABILITY; HYPOPHAGIA; HYPORESPONSIVE TO STIMULI; MOVEMENT DISORDER; SOMNOLENCE; SOMNOLENCE; MENTAL STATUS CHANGES; SPEECH DISORDER; PYREXIA; MUSCULOSKELETAL DISORDER; MAGNETIC RESONANCE IMAGING HEAD ABNORMAL; CEREBROVASCULAR ACCIDENT; MENTAL STATUS CHANGES; MUSCULOSKELETAL DISORDER; This spontaneous report received from a health care professional via Regulatory Authority VAERS (Vaccine Adverse Event Reporting System)(VAERS ID: 2368873) and concerned an 89 year old female. The patient's height, and weight were not reported. The patient's past medical history included: acute cerebrovascular accident, multiple closed fractures of pelvis with stable disruption of pelvic circle, closed head injury, facial laceration, fall, facial contusion initial encounter, and closed fracture of left distal radius, and concurrent conditions included: macular degeneration of left eye, presence of artificial eye, transient ischemic attack, vascular dementia without behavioral disturbance chronic, hyperlipidemia chronic, dementia chronic, scapholunate dissociation of left wrist, failure to thrive in adult, acute cystitis without hematuria, drug allergy (Severity Reactions (Acetaminophen, Atrovent [ipratropium Bromide], Codeine, Darvocet A500 [propoxyphene Nacetaminophen], Motrin [ibuprofen], Norco [hydrocodone-acetaminophen], (Made patient feel crazy), Propoxyphene Napsylate, Simvastatin)), penicillin allergy, influenza virus vaccine allergy (Patient had rash, she went to emergency room (ER)), red dye allergy, hypertension, and bronchial asthma. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: 213D21A expiry: UNKNOWN) dose was not reported, 1 total, administered on 01-FEB-2022 in left arm for an unspecified indication. Age at time of vaccination 89 years old. Concomitant medications included calcium carbonate, colecalciferol and sennosides. On 30-MAY-2022, patient was hospitalized for evaluation of decreased mentation and possible stroke (cerebrovascular accident). Patient was nonverbal (speech disorder) and followed some simple commands. The patient was admitted on 30-MAY-2022 to 01-JUN-2022, for altered mentation (mental status changes). Apparently the patient was being evaluated for seizures, however they opted not to proceed with EEG (electroencephalogram) and MRI (Magnetic resonance imaging). The patient apparently improved after fluids. Hospice was offered to the imaging was admission due to the advanced dementia, however the family refused to sign up for hospice. When patient left the hospital the son reported that patient apparently walked with full assist to about 100 feet and in fact climb a few steps of stairs, was doing fine since the discharge. On 01-JUN-2021, Wednesday, patient started having decreased appetite, refusing to be fed (food refusal) and was chest more somnolent than baseline. The son of patient also noted that the right leg was not moving at all (movement disorder and musculoskeletal disorder) despite different ways to try to encourage to move the right leg. The patient also stopped walking since Wednesday (gait inability). They apparently tried to have patient sit for a meal but patient slid off the chair with right knee going underneath the left leg. They managed to prevent patient from falling to the ground (fall). Patient was hardly responding (hyporesponsive to stimuli) and had not anything to eat or drink at all (fluid intake reduced and hypophagia). They decided to bring patient to the emergency room for further evaluation. Patient was admitted to the neurology floor. The patient was started on aspirin. Patient was considered for a statin but this was deferred due to the dietary limitations and pending hospice status. On 10-JUN-2022, patient underwent MRI (Magnetic resonance imaging) which was consistent with a CVA (cerebrovascular accident). Teleneurology was consulted given poor functional status and poor long-term prognosis family opted for hospice care. The patient had a fever (pyrexia) and tested positive for COVID-19 which delayed hospice transport 10 days waiting period for isolation concerns, recommended diet was a pureed diet. On 14-JUN-2021, Laboratory data included: SARS-CoV-2 test Positive. The patient was non-verbal and interactive with daughter present, limited intake including pocketing food. The patient was discharged to rehab. Patient was hospitalized for 10 days. Treatment medication (dates unspecified) included: acetylsalicylic acid. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from cerebrovascular accident, covid-19, decreased appetite, fall, fluid intake reduced, food refusal, gait inability, hypophagia, hyporesponsive to stimuli, mental status changes, movement disorder, musculoskeletal disorder, somnolence, speech disorder, magnetic resonance imaging head abnormal, sars-cov-2 test positive, and pyrexia. This report was serious (Hospitalization Caused / Prolonged). This report was associated with product quality complaint. The suspected product quality complaint has been confirmed to be the reported allegation could not be determined. A manufacturing related root cause could not be identified based on the evaluation/investigation performed. Additional information received from Central Complaint Vigilance department on 02-AUG-2022. The following information was updated and incorporated into the case narrative: Product quality complaint investigation result.; Sender's Comments: V2: This version updates: Product quality complaint investigation result. The prior causality assessment remains unaltered with this information. 20220747042- COVID-19 VACCINE AD26.COV2.S- cerebrovascular accident, decreased appetite, fall, fluid intake reduced, food refusal, gait inability, hypophagia, hyporesponsive to stimuli, mental status changes, movement disorder, musculoskeletal disorder, somnolence, speech disorder, magnetic resonance imaging head abnormal. The event(s) 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(s) than the drug. Specifically: MEDICAL HISTORY. Therefore, this event(s) is considered not related. 20220747042-COVID-19 VACCINE AD26.COV2.S- COVID-19, pyrexia, SARS-COV-2 test positive. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s). Therefore, this event(s) is considered unassessable.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- 10,0
- Labordaten
- Test Date: 20220610; Test Name: MAGNETIC RESONANCE IMAGING HEAD; Result Unstructured Data: Abnormal (consistent with a CVA (cerebrovascular accident); Test Date: 20220614; Test Name: SARS-COV-2 TEST; Test Result: Positive
- Aktuelle Erkrankungen
- Acute cystitis; Allergy to vaccine (Patient had rash, she went to emergency room (ER)); Bronchial asthma; Dementia; Drug allergy (Severity Reactions (Acetaminophen, Atrovent [ipratropium Bromide], Codeine, Darvocet A500 [propoxyphene Nacetaminophen], Motrin [ibuprofen], Norco [hydrocodone-acetaminophen], (Made patient feel crazy), Propoxyphene Napsylate, Simvastatin)); Eye prosthesis user; Failure to thrive; Food allergy; Hyperlipidemia; Hypertension; Macular degeneration; Penicillin allergy; Scapholunate dissociation; Transient ischemic attack; Vascular dementia
- Vorgeschichte
- Medical History/Concurrent Conditions: Bruising of face; Cerebrovascular accident; Closed fracture; Closed head injury; Fall; Laceration of face; Multiple fractures
- Andere Medikamente
- CALCIUM CARBONATE; VITAMIN D3; SENNOSIDES
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 27.07.2022
- Impfdatum
- 13.12.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 19,0
- Dosis
- 1
- Route/Site
- - / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Acute respiratory failure
COVID-19
COVID-19 pneumonia
Cough
Death
Dyspnoea
Endotracheal intubation
General physical health deterioration
Intensive care
Positive airway pressure therapy
Pyrexia
SARS-CoV-2 test positive
Symptomtext
1/5/22 pt initially taken to ED; found to be positive for COVID; increasing sx of cough, fever, SOB; treated with Remdesivir and ABX; 1/9/22 taken to different Hospital for further treatment and care; AHRF due to COVID pneumonia; BiPAP; transferred to ICU and required intubation; pt became DNR; pt's condition worsened and transitioned to comfort care; pt expired in the hospital
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 11,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- DMT2, sleep apnea, schizoaffective disorder, CAD
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 15.07.2022
- Impfdatum
- 09.03.2021
- Beginn
- 04.12.2021
- Tage bis Beginn
- 270,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Death
Symptomtext
Narrative: Patient passed away due to COVID-19. He had received the COVID-19 vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 14.07.2022
- Impfdatum
- 08.11.2021
- Beginn
- 05.02.2022
- Tage bis Beginn
- 89,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Death
Symptomtext
Narrative: Patient passed away due to COVID-19. He was hospitalized and had received a COVID-19 Vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 87,0
- Geschlecht
- M
- Eingang
- 05.07.2022
- Impfdatum
- 13.01.2022
- Beginn
- 25.06.2022
- Tage bis Beginn
- 163,0
- Dosis
- 3
- Route/Site
- - / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Acute respiratory failure
COVID-19
Death
General physical health deterioration
Hypoxia
SARS-CoV-2 test positive
Symptomtext
Pfizer BioNTech and Janssen (J&J) COVID Vaccines: COVID-19 case resulting in Hospitalization / Death. Rec'd Pfizer BioNTech on 1/14/21 and 2/3/21 and Janssen (J&J) on 1/13/22. Presented to the ED for hypoxia. Admitted for acute hypoxemic resp failure 2/2 Covid19. Rec'd dexamethasone, azithromycin, and ceftriaxone. Patient progressively worsened and was transitioned to comfort care. Patient expired 6/28/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 3,0
- Labordaten
- 06/25/21: COVID positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- dementia, sleep apnea, type 2 diabetes, hypertension, hyperlipidemia, tremor, polycythemia vera, paraganglioma, osteoarthrosis, squamous cell carcinoma, macular degeneration
- Andere Medikamente
- amlodipine, aspirin, atorvastatin, calcium carbonate-vit D, cholecalciferol, hydroxyurea, tresiba, lisinopril, metformin, metoprolol, and multivitamin
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 28.03.2022
- Impfdatum
- 14.12.2021
- Beginn
- 25.01.2022
- Tage bis Beginn
- 42,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Acute respiratory failure
COVID-19
COVID-19 pneumonia
Chest pain
Cough
Oxygen saturation decreased
SARS-CoV-2 test positive
Symptomtext
Patient presented to the ED reports he has been coughing a lot. Had chest pain a few days prior but pain is gone by now. His daughter at bedside noted that his O2 waxes and wanes a lot and O2 dropped to 70s today. Pt lives with his wife but with her daughter, but she drove him to ED today. Hospital Course #Acute hypoxic respiratory failure #Severe Covid-19 infection # COVID-19 pneumonia -tested positive 1/18 at hospital -pt presented to ED 1/25 due to hypoxia -completed course of dexamethasone and remdesivir -Baricitinib added and continued until discharge. -He responded to treatment and was weaned off high-flow nasal cannula to RA at the time of discharge -patient was intermittently diuresed Discharge Disposition/Condition Disposition: Home Condition: Stable (s/sx potential problems absent or manageable)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 10,0
- Labordaten
- COVID PCR confirmed positive on 01/25/22
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- He has a past medical history of Personal history of other diseases of the circulatory system and Personal history of other endocrine, nutritional and metabolic disease. Dm Htn OSA ON BIPAP
- Andere Medikamente
- albuterol inhaler aspirin cyanocobalamin famotidine glimepiride lisinopril metformin omeprazole sertraline azithromycin ondansetron
- Allergien
- IV contrast
- Vorherige Impfungen
- -
- Staat
- WV
- Alter
- -
- Geschlecht
- F
- Eingang
- 27.01.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Death
SARS-CoV-2 test
Symptomtext
DEATH; This spontaneous report received from a health care professional concerned a 63-year-old female with an unspecified race and ethnic origin. The patient's height, and weight were not reported. On 30-DEC-2021, the patient was admitted to facility with COVID 19 unvaccinated status for nursing care due to her concurrent conditions which included epilepsy, atrial fibrillation, chronic obstructive pulmonary disease (COPD), iron deficiency anemia, cardiomyopathy, severe protein calorie malnutrition with adult failure to thrive, diabetes mellitus (DM) type II, constipation, contractures to both knees, peripheral vascular disease (PVD) with multiple venous stasis ulcers, neuromuscular bladder, postural kyphosis, hyperlipidemia, hypertension (HTN), gastroesophageal reflux disease (GERD), major depressive disorder, vitamin D Deficiency, history of brain cancer, and vascular dementia. She underwent pacemaker placement, gastrostomy tube (GT) placement for nutritional needs/medication administration and had history of clostridium difficile. On unspecified dates, the outbreak COVID 19 testing were performed which revealed negative tests on patient throughout course of stay. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: 213D21A and expiry: 11-APR-2022) 0.5 ml, 01 in total was administered on 12-JAN-2022 for prophylactic vaccination. No concomitant medications were reported. It was reported that her vital signs remained stable with her being afebrile throughout the process. Following vaccination with covid-19 vaccine ad26.cov2.s, on 13-JAN-2022 at approximately 10:20 hours, certified nursing assistants (CNAs) reported to Licensed practical nurse (LPA) that the patient was unresponsive and upon assessment, she was pronounced dead at 10:20 hours. It was unknown, if an autopsy was performed or not. On 13-JAN-2022 at 10:20 hours, the patient died from unknown cause. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. This report was serious (Death).; Sender's Comments: V0-20220124384-covid-19 vaccine ad26.cov2.s- death. This event(s) is considered unassessable. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s).; Reported Cause(s) of Death: UNKNOWN CAUSE OF DEATH
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID-19 virus test; Result Unstructured Data: negative
- Aktuelle Erkrankungen
- Adult failure to thrive; Atrial fibrillation; Carcinoma brain; Cardiomyopathy; Chronic obstructive pulmonary disease; Constipation; Epilepsy; Gastrooesophageal reflux disease; Hyperlipidemia; Hypertension; Iron deficiency anemia; Joint contracture; Kyphosis (acquired) (postural); Major depressive disorder; Neurogenic bladder; Peripheral vascular disease; Protein-calorie malnutrition; Type II diabetes mellitus; Vascular dementia; Venous stasis ulcer; Vitamin D deficiency
- Vorgeschichte
- Medical History/Concurrent Conditions: Cardiac pacemaker insertion; Clostridium difficile infection; Gastrostomy tube insertion (G-Tube placement for nutritional needs/medication administration); Comments: The patient was admitted to facility with COVID 19 unvaccinated status.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WV
- Alter
- -
- Geschlecht
- M
- Eingang
- 26.01.2022
- Impfdatum
- 15.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Death
Heart rate
SARS-CoV-2 test
Symptomtext
WITHOUT A PULSE NOR HEARTBEAT (DEATH); This spontaneous report received from a health care professional concerned a 78 year old male of an unspecified race and ethnic origin. The patient's height, and weight were not reported. The patient's concurrent conditions included: advanced parkinson's disease, hyperlipidemia, anxiety, vitamin D deficiency, vascular dementia, hypothyroidism, major depressive disorder and aphasia. The patient previously received covid-19 vaccine ad26. cov2.s (suspension for injection, route of administration, batch number were not reported, expiry: unknown) dose was not reported, (dose number in series was 1), 01 in total was administered on 05-MAY-2021 for prophylactic vaccination. The reporter did not report any adverse events following covid-19 vaccine ad26. cov2.s vaccination. The patient was admitted to facility on 14-DEC-2021 for nursing care due to advanced Parkinson's Disease, hyperlipidemia, anxiety, vitamin D deficiency, vascular dementia, hypothyroidism, major depressive disorder and aphasia. On an unspecified date in DEC-2021, outbreak COVID 19 testing revealed negative tests on the resident throughout course of the stay. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: 213D21A, expiry: 11-APR-2022) 0.5 ml, (dose number in series was 2), 01 in total was administered on 15-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. On 17-DEC-2021, following the vaccination with covid-19 vaccine ad26.cov2.s, at approximately 11:44 hours, he was found without a pulse nor heartbeat (death) (dose number in series was 2). It was not reported whether autopsy was performed or not. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of without a pulse nor heartbeat (death) was fatal (dose number in series was 2). This report was serious (Death). This case, from the same reporter is linked to 20220124404 and 20220130332.; Sender's Comments: V0-20220124221-covid-19 vaccine ad26.cov2.s-without a pulse nor heartbeat (death). This event(s) is considered unassessable. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s).; Reported Cause(s) of Death: WITHOUT A PULSE NOR HEARTBEAT (DEATH)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- Test Date: 202112; Test Name: COVID-19 virus test; Result Unstructured Data: Negative; Test Date: 20211217; Test Name: Pulse rate; Result Unstructured Data: pulse absent
- Aktuelle Erkrankungen
- Anxiety; Aphasia; Hyperlipidemia; Hypothyroidism; Major depressive disorder; Parkinson's disease; Vascular dementia; Vitamin D deficiency
- Vorgeschichte
- Comments: Unknown
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WV
- Alter
- -
- Geschlecht
- M
- Eingang
- 25.01.2022
- Impfdatum
- -
- Beginn
- 30.12.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Body temperature
Death
Hyperhidrosis
Hypotension
Pyrexia
SARS-CoV-2 test
Streptococcus test
Unresponsive to stimuli
Symptomtext
DEATH; UNRESPONSIVE; DIAPHORETIC; LOW BLOOD PRESSURE; FEVER; This spontaneous report received from a health care professional concerned a 69-year-old male of an unspecified race and ethnic origin. The patient's height, and weight were not reported. The patient's past medical history included: right femur fracture, and concurrent conditions included: pneumonia, anxiety, hypertension (HTN), constipation, vitamin D deficiency, unspecified intellectual disorder, major depressive disorder, obsessive-compulsive disorder (OCD), parkinsons disease, impaired walking/mobility, seizure disorder, dry eye syndrome, urinary incontinence, benign prostatic hyperplasia (BPH), osteoarthritis, and psychotic disorder. The patient previously received covid-19 vaccine ad26.cov2.s (suspension for injection, route of administration, batch number were not reported, expiry: unknown) dose was not reported, (dose number in series was 1), 01 in total was administered on 26-MAR-2021 for prophylactic vaccination. Batch number not reported: The batch number was not reported and has been requested. No adverse events were reported following vaccination with covid-19 vaccine ad26.cov2.s. (dose number in series 1) On 22-DEC-2021, the patient was admitted to facility for nursing care due to pneumonia, right femur fracture, anxiety, HTN, constipation, vitamin D deficiency, unspecified intellectual disorder, major depressive disorder, OCD, Parkinson's Disease. Impaired walking/mobility, seizure disorder, dry eye syndrome, urinary incontinence, BPH, osteoarthritis, and psychotic disorder. Outbreak COVID 19 testing revealed negative tests throughout course of stay. On 23-DEC-2021, a consent to administer the booster was obtained and signed. The patient additionally received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: 213D21A, expiry: 11-APR-2022) 0.5 ml, (dose number in series was 2), 01 in total was administered on 29-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. Following vaccination with the covid-19 vaccine ad26.cov2.s, the reporter reported that, vital signs remained stable with the patient being afebrile throughout the process. On 30-DEC-2021, at approximately 21:30 hours, licensed practical nurse (LPN) noted that the patient had temperature of 100.7 degree Fahrenheit and medical service was also notified. An order to obtain a rapid strep test was obtained and was found to be negative. At approximately 21:40 hours, LPN noted that he was unresponsive, diaphoretic with fever and low blood pressure. Medical services were notified again and an order was received to send to emergency room (ER) for evaluation. ER reported to facility LPN that resident had passed away while in ER. (dose number in series was 2) On 30-DEC-2021, the patient died from unknown cause. It was not reported whether autopsy was performed or not. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of death was reported as fatal and outcome of unresponsive, diaphoretic, fever, low blood pressure was not reported (dose number in series was 2). This report was serious (Death, and Other Medically Important Condition). This case, from the same reporter is linked to 20220124221 and 20220130332.; Sender's Comments: V0: 20220124404-Covid-19 vaccine ad26.cov2.s-Death and unresponsive. This event(s) is considered unassessable. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s).; Reported Cause(s) of Death: UNKNOWN CAUSE OF DEATH
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- Test Date: 202112; Test Name: COVID-19 virus test; Result Unstructured Data: Negative; Test Date: 20211230; Test Name: Body temperature; Result Unstructured Data: 100.7 degree Fahrenheit; Test Date: 20211230; Test Name: Rapid streptococcal test; Result Unstructured Data: negative
- Aktuelle Erkrankungen
- Anxiety; Benign prostatic hyperplasia; Constipation; Convulsive disorder; Dry eye syndrome; Hypertension; Intellectual development disorder; Major depressive disorder; Obsessive-compulsive disorder; Osteoarthritis; Parkinson's disease; Pneumonia; Psychotic disorder; Urinary incontinence; Vitamin D deficiency; Walking difficulty
- Vorgeschichte
- Medical History/Concurrent Conditions: Femur fracture
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 93,0
- Geschlecht
- F
- Eingang
- 24.01.2022
- Impfdatum
- 19.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cerebrovascular accident
Disorganised speech
Laboratory test
Symptomtext
Patient's son said his moms started talking gibberish. He called the pharmacist to ask questions the pharmacist instructed the patient to seek medical attention if she continues to talk gibberish. The patient's son called an ambulance to go to the hospital. Patient was diagnoses with a stroke.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- 6,0
- Labordaten
- At this time patient is still in the hospital seeking medical attention. She is, according to the patient's relative, doing a lot better. The hospital is doing more test to see if they can release the patient from the hospital. The patient is awaiting to return home.
- Aktuelle Erkrankungen
- No.
- Vorgeschichte
- Type two diabetes, Has a stent
- Andere Medikamente
- Tylenol, Vit b, Clopidogrel 75mg, Isosorbide er 30mg, Ropinirole 0.25mg, Tramadol 50mg. Vit d2 50,000 units, pantoprazole 40mg, amlodipine 2.5mg, Humalog Kwikpen, latanoprost 0.005%, isosorbide er 30mg, metoprolol tartrate 25mg
- Allergien
- penicillin, meperidine
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 92,0
- Geschlecht
- F
- Eingang
- 22.01.2022
- Impfdatum
- 21.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Body temperature increased
Death
Decreased appetite
Dyspnoea
Dysstasia
Fatigue
Hypersomnia
Seizure
Syncope
Symptomtext
Around 10:00 PM on day of booster vax (12/21/21), she became extremely tired, too tired to stand. At 5:00 AM on 12/22/22, I, her daughter, woke up to check on her. Her temp was 102.1. For the next three days she was too weak to stand, slept most of the time and had no appetite. She began to gain her strength back on 12/25/21. Between 12/25 and 12/31, she was more tired than usual, and weaker than usual. On 1/2/22, at approx. 10:15 PM, she collapsed and died, about 20 minutes later. During those minutes, she had difficulty breathing and appeared to have two seizures. Her death took place 12 days after receiving the J&J booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- We did not do an autopsy on her due to her age.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Stage 3 Kidney Disease, AFib, Hypertension
- Andere Medikamente
- 2 blood pressure medications, vitamins C and D, multi-vitamin
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 16.01.2022
- Impfdatum
- 07.12.2021
- Beginn
- 18.12.2021
- Tage bis Beginn
- 11,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Chest discomfort
Chest pain
Myocardial infarction
Symptomtext
Approximately 1 1/2 weeks after I received my booster shot, I started having major chest pressure (evening of 12/18). I rested in hopes it would get better, as pain got worse, we went to emergency room early the next morning. I had a heart attack while in the emergency room.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocardial infarction
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WV
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 13.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Death
Symptomtext
Consent received by family. Resident stable at time of vaccination. Resident administered 0.5 mL of J&J vaccine per order. Resident passed away this date at 10:20 am.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- None at this time
- Aktuelle Erkrankungen
- Epilepsy, paroxysmal atrial fibrillation, COPD, iron deficiency anemia, cardiomyopathy, severe protein calorie malnutrition, abnormal albumin, constipation, DM Type II, contractures of left and right knees, PVD, neuromuscular bladder, postural kyphosis, aphasia, chronic venous hypertension with ulcer to bilateral lower extremities, muscle spasms, muscle weakness, adult failure to thrive, G-Tube, hyperlipidemia, HTN, GERD, MDD, Hx of C-Diff, hx of brain cancer, vascular dementia.
- Vorgeschichte
- same as above
- Andere Medikamente
- Lantus, Vit C, MVI, Prostat, dulcolax, norco, digoxin, baclofen, gabapentin, lactulose, duo-neb, lamotrigine, seroquel, protonix, miralax, midodrine
- Allergien
- Levofloxacin
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 11.01.2022
- Impfdatum
- 09.12.2021
- Beginn
- 10.01.2022
- Tage bis Beginn
- 32,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Activated partial thromboplastin time
Acute myocardial infarction
Anticoagulant therapy
Asymptomatic COVID-19
Chest discomfort
Chest pain
Computerised tomogram normal
Electrocardiogram normal
Rhinorrhoea
SARS-CoV-2 test positive
Sleep disorder
Troponin increased
Symptomtext
The patient is here with complaints of left-sided chest pressure. Patient does have a history of cardiac stents placed in 2017. He is not on any blood thinners at this time. He stated that it woke him up out of his sleep around 4:00 and did get worse with activity at work. He denies any nausea or vomiting or cold sweats. Denies any recent fevers. Does stated that he does have a little bit of nasal drainage but denies any other cough or cold-like symptoms. Denies any shortness of breath. Review of Systems Constitutional: No fevers, chills, sweats, weakness, or fatigue Eye: No recent visual problems ENT: No ear pain, no ear drainage, nasal congestion, or sore throat, small amt of nasal drainage Respiratory: No shortness of breath, no cough, no wheezing Cardiovascular: Left-sided chest pressure, no palpitations, no syncope Gastrointestinal: No nausea, vomiting, diarrhea, abdominal pain, or abdominal distention Musculoskeletal: No back pain, neck pain, joint pain, or muscle pain Integumentary: No rash, pruritus, or abrasions Neurologic: Alert & oriented X 4, no headache, no dizziness, no numbness or tingling Physical Exam General: Alert and oriented, well nourished, no acute distress. Lungs: Clear to auscultation all lung fields, non-labored respiration. Heart: Normal rate, regular rhythm, no murmur, gallop or edema. Abdomen: Soft, non-tender, non-distended, normal bowel sounds, no masses. Musculoskeletal: Normal range of motion and strength, no tenderness or swelling, no deformities or step offs. Skin: Skin is warm, dry and pink, no rashes or lesions. Neurologic: Awake, alert and oriented X4. Psychiatric: Cooperative, appropriate mood and affect. Heart score: 4 Assessment/Plan 1. NSTEMI (non-ST elevated myocardial infarction) I21.4 The patient is not ill-appearing or toxic upon arrival to the emergency room. He stated since laying in the bed he did start having improvement of his chest pain but when he was working and pulling about 25 to 50 pounds worth of steel his chest pain was escalating. He denies taking anything for it. Does have a history of a stent that was placed in 2017. His heart score today is 4 this is a moderate score. His repeat troponin did increase by 11 points. This is concerning for acute injury to the heart and will need to be closely monitored over the next 48 hours. We did contact HCF Dr. who did want the patient to be transferred to their stepdown unit for further investigation of his increasing troponin and most likely need a possible heart cath at that time. He recommend placing him on heparin right away. Unfortunately since the patient did test positive for COVID, they were unable to take him due to lack of beds. I did discuss his case with his cardiologist, recommended putting him in the hospital for at least 48 hours and then sending him home on Plavix and have him follow-up with her for an echo and stress test and most likely a catheterization at that point. Since he tested positive for COVID, he is not a candidate for stent placed seen at this time. We will be placing him on heparin and rechecking his PTT every 6 hours and titrating the heparin per the protocol. He is on the other appropriate medications that include a statin and metoprolol. We did not need to make any changes with that at this time. The patient's chest pain went away completely. His 3-hour troponin did come back elevated again at 44. We will recheck his troponin tomorrow morning unless he starts having chest pain again To make sure that it is trending down. He had no EKG changes. He was given 4 baby aspirin in the emergency room. I discussed the patient with his PCP,, who was agreeable with this plan of c family is also agreeable, they deny any further concerns at this time. I do not suspect a are. DVT or PE that could be causing right sided heart strain, due to negative CT scan. 2. COVID-19 The patient is basically asymptomatic at this time. I do not believe that steroids or remdesivir are needed. I do not suspect pneumonia. We will continue to monitor this. Orders: heparin additive 25,000 unit(s) + premix diluent 250 mL, 250, mL, IV, Routine, Start date 01/10/22 12:23:00 CST, titrate see comments, Total volume (mL): 250, 95.25 kg, 2.08, m2, 01/10/22 12:23:00 CST Consult to Pharmacy, Pharmacy Consult, Misc, N/A, On Call, Routine, Start date 01/10/22 12:23:00 CST, 01/10/22 12:23:00 CST Cardiac Monitoring, 01/10/22 9:25:00 CST, Constant Order Complete Blood Count with Automated Differential, Blood, Routine collect, 01/10/22 12:23:00 CST, Stop date 01/10/22 12:23:00 CST, dc order if already done CT Angio Chest PE w/ Cont, 01/10/22 10:57:00 CST, Routine, 01/10/22 10:57:00 CST, chest pain, elevated troponin, No, Transport Mode: Walk, , No, , No, Rad Type Patient Transfer Order, 01/10/22 9:20:00 CST PT/INR, Blood, Routine collect, 01/10/22 12:23:00 CST, Stop date 01/10/22 12:23:00 CST, dc order if already done PTT, Blood, Routine collect, 01/10/22 12:23:00 CST, q6hr (interval), Lab Collect Pulse Oximetry Check - Nursing, 01/10/22 12:23:00 CST, q4hr (scheduled), to be monitored continuously Telemetry, 01/10/22 12:23:00 CST, q4hr (scheduled) acute profee: medium The patient is to be admitted for at least 48 hours to be placed on a heparin drip and to trend his troponins. The patient is at high risk for worsening cardiac injury. He will be placed on telemetry and we will monitor his chest pain closely. If he has recurrence of his chest pain or his troponin keeps continuing to go up or having changes on his EKG, he will need to be transferred to higher level of care. If discharged to go home or released too early he is at high risk for worsening cardiac injury, arrhythmia, heart failure, death DDx: MI, GERD, chest wall pain, PE, pleurisy, arrhythmia, nerve pain, esophageal spasm, all of the differentials considered and not limited to this list.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hypertension, CAD, Diabetes, Hypercholesteremia, Hypertension
- Andere Medikamente
- allopurinol, aspirin, rosuvastatin, metoprolol, metformin, lisinopril, sildenafil, nitroglycerin, ticagrelor
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 07.01.2022
- Impfdatum
- 14.12.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 17,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Death
Syncope
Symptomtext
Patient's wife reported patient collapsed suddenly and passed away 16 days after vaccine was administered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VT
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 06.01.2022
- Impfdatum
- 22.11.2021
- Beginn
- 22.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Arterial disorder
Arterial occlusive disease
Arterial thrombosis
Cardiac arrest
Cardio-respiratory arrest
Cardioversion
Disorientation
Dizziness
Hyperhidrosis
Laboratory test
Symptomtext
the shot was given 11.22.21. he had cardiac arrest on 12.9.21. there is no history of heart attacks in the family. he had absolutely no warning that anything was wrong until he was having the heart attack. out of the blue he started sweating profusely, feeling disoriented, and dizzy. no chest pain or tightening. he died in the emergency room, but using the paddles several times, they were able to bring him back to life. it was established that the plaque in the wall of the left anterior descending artery burst and platelets went to the site causing a block/clot/full obstruction of the artery. he walked 3-5 miles a day or biked 10 miles. 160 pounds and 6 feet tall. no smoking and drank a beer a day, if anything.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cardiac arrest
- Hospital-Tage
- 8,0
- Labordaten
- full gamut of tests done related to heart attack but none related to the covid vaccine, as that was not contemplated at all.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- excess mucous, mostly due to allergies to dust, mould, mildew
- Andere Medikamente
- none
- Allergien
- dairy, wheat
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 05.01.2022
- Impfdatum
- 18.11.2021
- Beginn
- 25.12.2021
- Tage bis Beginn
- 37,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Acute respiratory failure
Alanine aminotransferase increased
Anion gap
Anticoagulant therapy
Aspartate aminotransferase normal
Atrial fibrillation
Blood albumin decreased
Blood alkaline phosphatase normal
Blood bicarbonate increased
Blood bilirubin normal
Blood calcium normal
Blood chloride decreased
Blood creatinine increased
Blood glucose increased
Blood lactic acid decreased
Blood pH decreased
Blood potassium increased
Blood sodium normal
Symptomtext
Hospitalized (12.25.21 - still admitted currently); COVID-19 positive (12.24.21); fully vaccinated PLUS Booster - J& J H&P: Attestation signed by, MD at 12/25/2021 2:18 PM I have seen and examined patient independently. Discussed with house staff. I agree with the subjective and physical exam findings and assessment and plan. Patient feels much better this am. CPAP will be changed to BiPaP this am. Agree with steroids, lasix,antibiotics and remdesivir for now. - MD, Attending Physician, Im/hospitalist. Expand All Collapse All Hide copied text Hover for details CHIEF COMPLAINT: Acute respiratory failure with hypoxemia Assessment/Plan ASSESSMENT / PLAN: Patient is a 60 y.o. female with a past medical history of morbid obesity, OSA, COPD on 2L continuous and 4L at night, chronic diastolic heart failure, insulin-dependent T2DM, CKD3, Afib/flutter on Eliquis, and hypothyroidism who is admitted for acute respiratory with hypoxia and hypercarbia secondary to likely mixed COPD and diastolic heart failure exacerbations in the setting of COVID-19 infection. Acute respiratory failure with hypoxia and hypercarbia COPD exacerbation Chronic diastolic HF exacerbation COVID-19 infection Patient symptomatic with main symptom of shortness of breath starting 12/20, developed mild viral symptoms, and tested positive in ED 12/24. CXR not consistent with pure COVID-19 pneumonia. Likely COVID-19 triggered COPD and chronic diastolic heart failure exacerbations, as evidenced by fluid overload and expiratory wheezing on examination, as well as edema and pulmonary vascular congestion on CXR. Cannot rule out bacterial superinfection as well given opaque L middle lung finding on CXR, leukocytosis to 15 at OSH, and procalcitonin elevated at 0.98. Last echo in September EF 60-65%, no RWMA. Plan: o COVID-19 infection: ? Solumedrol 40 mg q8h ? Remdesivir ? Home Eliquis for anticoagulation o COPD exacerbation: ? Duonebs q4h scheduled ? Trend VBGs q6h for hypercarbia o Chronic diastolic heart failure exacerbation: ? Given lasix 40 mg IV (prescribed torsemide 20 mg daily outpatient) ? Continue home lisinopril ? Started imdur 10 mg, consider adding hydralazine prn for SBP >180 ? Echo o Bacterial superinfection? ? Sputum cx ? CAP coverage with Azithro/Rocephin ? S pneumo, legionella urine Ag Paroxysmal atrial fibrillation/atrial flutter Currently in sinus rhythm. Plan: - Continue home amiodarone, diltiazem, eliquis Hypothyroidism Plan: - Continue home levothyroxine Type 2 DM, insulin-dependent Last A1c 6.7% two months ago. Home regimen: tresiba 30 units bid + lispro with meals/bedtime. Plan: - Lantus 10, LDC Essentials: Code Status: FULL DVT prophylaxis: Lovenox Diet: NPO Dispo: Continue inpatient care for respiratory failure This assessment and plan was discussed with an attending physician, Dr. For further information see attending attestation. MD PGY-1, Neurology Available on database Subjective HISTORY OF PRESENT ILLNESS: Patient is a 60 y.o. female with a past medical history significant for morbid obesity, OSA, COPD on 2L continuous and 4L at night, insulin-dependent T2DM, CKD3, Afib/flutter, and hypothyroidism who presented to OSH with 4-5 days of shortness of breath, fatigue, body aches, and dry cough. She denied fevers, abdominal pain, nausea, dizziness, lightheadedness, syncope, chest pain, or chest pressure. She endorsed diarrhea for 2 days. OSH workup notable for respiratory acidosis 7.19 with pCO2 81, which corrected after BiPAP to pH 7.31 with pCO2 64, bicarb 29. Cr 1.4 (baseline 1.5), Troponin 0.04->2, BNP 315, Lactic acid 2.3, leukocytosis 15 with left shift, UA without signs of infection. CXR once transferred to facility showed congested pulmonary vasculature and perihilar haziness consistent with CHF or edema, as well as left midlung opacity which could be atelectasis versus pneumonia. VBG on arrival to facility showed pH 7.32, pCO2 68.8. Patient Active Problem List Diagnosis ? Acute respiratory failure ? Acute respiratory failure with hypoxemia OBJECTIVE: BP (!) 182/78 | Pulse 96 | Temp 36.4 ?C (Oral) | Resp 26 | Ht 1.575 m | Wt (!) 140 kg | SpO2 100% | BMI 56.45 kg/m? FIO2 (%): 36 % Physical Exam Constitutional: Appearance: She is obese. She is ill-appearing. She is not diaphoretic. HENT: Head: Atraumatic. Nose: No congestion. Mouth/Throat: Mouth: Mucous membranes are dry. Eyes: Extraocular Movements: Extraocular movements intact. Conjunctiva/sclera: Conjunctivae normal. Pupils: Pupils are equal, round, and reactive to light. Cardiovascular: Rate and Rhythm: Regular rhythm. Tachycardia present. Pulses: Normal pulses. Heart sounds: Normal heart sounds. No murmur heard. Pulmonary: Effort: No respiratory distress. Breath sounds: Wheezing (expiratory) present. Chest: Chest wall: No tenderness. Abdominal: Palpations: Abdomen is soft. Tenderness: There is no abdominal tenderness. Musculoskeletal: Right lower leg: Edema present. Left lower leg: Edema present. Comments: 3+ pitting edema bilaterally, chronic venous stasis changes and scarring to skin of bilateral shins. Skin: General: Skin is dry. Capillary Refill: Capillary refill takes 2 to 3 seconds. Coloration: Skin is not jaundiced. Findings: Rash (redness, odor, and skin breakdown between pannus folds) present. Neurological: Mental Status: She is alert and oriented to person, place, and time. 1/4/22 Progress note: Attestation signed by, MD at 1/4/2022 4:40 PM I have personally interviewed and examined the patient on 1/4/2022. Management was discussed with the resident I agree with the documented findings and plan of care in his note. Brief exam: General- no acute distress Head- Normocephalic and atraumatic Cardiac- regular rate and rhythm, no murmurs Respiratory- clear to auscultation bilaterally Abd- soft and not tender, not distended Skin- no rash Neuro- alert and oriented, no new focal deficits Psych- cooperative, appropriate Brief history and medical decision making: Patient is a 60 yo woman with hx of morbid obesity, OSA, COPD on 2L, Chronic HFpEF, DM2, Afib/flutter on Eliquis presented with acute on chronic hypercarbic and hypoxic resp failure from acute exacerbation of COPD caused by COVID-19 infection and acute on chronic diastolic heart failure. Will d/c home BIPAP. Completed remdesivir and empiric CAP coverage, 5 days. Prednisone taper thru 1/13. Diuresed well. Chronic right heel wound which was seen by Wound Care. PT/OT recommending SAR. Admit Date: 12/25/2021 Chief Complaint Acute respiratory failure with hypoxemia secondary to COVID-19 Assessment/Plan Patient is a 60 y.o. female with a past medical history of morbid obesity, OSA, COPD on 2L continuous and 4L at night, chronic diastolic heart failure, insulin-dependent T2DM, CKD3, Afib/flutter on Eliquis, and hypothyroidism who is admitted for acute respiratory with hypoxia and hypercarbia secondary to COPD and possible diastolic heart failure exacerbations in the setting of COVID-19 infection. Acute on chronic respiratory failure with hypoxia and hypercarbia COPD exacerbation Chronic diastolic HF exacerbation COVID-19 infection Patient symptomatic with main symptom of shortness of breath starting 12/20, developed mild viral symptoms, and tested positive in Allegan ED 12/24. CXR not consistent with pure COVID-19 pneumonia. Likely COVID-19 triggered COPD and chronic diastolic heart failure exacerbations, as evidenced by fluid overload and expiratory wheezing on examination, as well as edema and pulmonary vascular congestion on CXR. Cannot rule out bacterial superinfection as well given opaque L middle lung finding on CXR, leukocytosis to 15 at OSH, and procalcitonin elevated at 0.98. Echo 12/25 EF 60% no rwma Plan: o COVID-19 infection: ? Prednisone 30mg, will taper 10mg every 3 days. Ends 1/13 ? Home Eliquis for anticoagulation o COPD exacerbation: Duonebs q4h scheduled ? BiPAP nightly. Pulm Rehab c/s, will coordinate going home with BiPAP. o Chronic diastolic heart failure exacerbation: ? Lasix 40 once PO daily due to BUN/Cr increasing over the course of hospitalization. ? Continue home lisinopril ? Echo EF 62% Right Heel pressure ulcer Previously known pressure wound on right heel. Was covered with SCDs. Granulation tissue intact with small area of open, weaping wound. Patient complains of pain on wound. Plan: - wound consult, hydrocolloid to be changed every 3 days. Paroxysmal atrial fibrillation/atrial flutter Currently in sinus rhythm. 1 episode Afib RVR 12/26 <1 hour self converted to NSR Plan: - Continue home amiodarone, diltiazem, eliquis, propanolol Hypothyroidism Plan: - Continue home levothyroxine Type 2 DM, insulin-dependent Last A1c 6.7% two months ago. Home regimen: tresiba 30 units bid + lispro with meals/bedtime. Actos on med rec. Hyperglycemia without oral intake due to steroids. Plan: -Goal glycemic control 100-180s -Steroid taper will help -Lantus 30 units daily -HDC Diet: Diabetic DVT Prophylaxis: eliquis Code Status: full Disposition: medically stable for discharge. She is awaiting insurance auth for accepting SAR. This patient was discussed with my attending physician, Dr. Please refer to their attestation for any additional information and changes to the plan outlined above. MD PGY-1 Subjective: No acute events overnight. She states that she is doing well today with no complaints or concerns. States that her breathing is improving today and swelling around the same. States that her heel is not very painful today. Review of Systems Constitutional: Negative for chills and fever. HENT: Negative for congestion. Eyes: Negative for blurred vision. Respiratory: Negative for cough. Cardiovascular: Negative for chest pain and palpitations. Gastrointestinal: Negative for abdominal pain, nausea and vomiting. Genitourinary: Negative for dysuria. Skin: Negative for rash. Neurological: Negative for dizziness. Objective: BP 117/75 | Pulse 64 | Temp 36.9 ?C (Oral) | Resp 20 | Ht 1.575 m | Wt 129.5 kg | SpO2 100% | BMI 52.22 kg/m? Physical Exam Vitals reviewed. Constitutional: General: She is not in acute distress. Appearance: She is obese. She is not diaphoretic. HENT: Head: Normocephalic and atraumatic. Nose: Nose normal. Mouth/Throat: Mouth: Mucous membranes are moist. Pharynx: Oropharynx is clear. No oropharyngeal exudate. Eyes: Conjunctiva/sclera: Conjunctivae normal. Pupils: Pupils are equal, round, and reactive to light. Neck: Vascular: No JVD. Cardiovascular: Rate and Rhythm: Normal rate and regular rhythm. Heart sounds: Normal heart sounds. No murmur heard. No friction rub. No gallop. Pulmonary: Effort: Pulmonary effort is normal. No respiratory distress. Breath sounds: Rales present. No wheezing. Abdominal: General: Bowel sounds are normal. There is no distension. Palpations: Abdomen is soft. Tenderness: There is no abdominal tenderness. Comments: Anasarca present Musculoskeletal: Cervical back: Normal range of motion. Right lower leg: Edema (improving) present. Left lower leg: Edema (improving) present. Skin: General: Skin is warm and dry. Findings: No erythema or rash. Comments: Venous stasis changes lower extremities. Neurological: General: No focal deficit present. Mental Status: She is alert and oriented to person, place, and time. Psychiatric: Mood and Affect: Mood and affect norma
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 11,0
- Labordaten
- Comprehensive Metabolic Panel (CMP) (Abnormal) Collected: 01/05/22 0545 Order Status: Completed Specimen: Blood, Venous Updated: 01/05/22 0621 Sodium Level 138 134 - 146 mmol/L Potassium Level 5.2 High 3.4 - 5.0 mmol/L Chloride 95 Low 98 - 112 mmol/L HCO3 36 High 21 - 29 mmol/L Anion Gap 7 Low 9 - 18 mmol/L Glucose Level 299 High 70 - 99 mg/dL Blood Urea Nitrogen 45 High 8 - 20 mg/dL Creatinine 1.52 High 0.50 - 1.10 mg/dL MDRD eGFR 35 Low >=60 mL/min/1.73 m2 CG eCrCl 31 mL/min/1.73 m2 Calcium Level Total 9.0 8.6 - 10.4 mg/dL Protein Total 6.2 6.0 - 8.0 g/dL Albumin Level 2.5 Low 3.5 - 5.0 g/dL Bilirubin Total 0.5 0.2 - 1.0 mg/dL Alkaline Phosphatase 89 35 - 104 IU/L Alanine Aminotransferase 39 10 - 40 IU/L Aspartate Aminotransferase 20 10 - 40 IU/L Complete Blood Count without Differential (Abnormal) Collected: 01/05/22 0545 Order Status: Completed Specimen: Blood, Venous Updated: 01/05/22 0610 White Blood Cell 17.98 High 4.00 - 10.80 x10*3/uL Red Blood Cell 4.45 4.20 - 5.40 x10*6/uL Hemoglobin 11.1 Low 12.0 - 16.0 g/dL Hematocrit 36.8 Low 37.0 - 47.0 % Mean Cell Volume 82.7 80.0 - 100.0 fL Mean Cell Hemoglobin 24.9 Low 27.0 - 33.0 pg NRBC Absolute Count 0.00 0.00 - 0.01 x10*3/uL NRBC Automated 0.0 0.0 - 0.1 %WBC Mean Cell Hemoglobin Concentration 30.2 Low 32.0 - 37.0 g/dL Red Cell Diameter Width 17.0 High 11.0 - 16.0 % Platelet 257 140 - 400 x10*3/uL Mean Platelet Volume 12.6 High 7.4 - 11 fL USV Arterial Physio ABI With Doppler Lower Extremity Resulted: 01/03/22 2041 Order Status: Completed Updated: 01/03/22 2043 Narrative: Examination: Complete Bilateral Noninvasive Physiologic Studies of the Lower Extremity Arteries, 3 or More Levels. EXAM DATE: 1/3/2022 8:19 PM TECHNIQUE: Ankle-brachial indices and multilevel continuous-wave Doppler assessment of the lower extremity arteries was performed. INDICATION: right heel wound COMPARISON: None. Prior Exam Right ABI: There are no known prior examinations. Prior Exam Left ABI: There are no known prior examinations. ____________________ FINDINGS: The peak systolic pressure in the right and left arm measures 143 mmHg, respectively. _____
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- COPD, chronic pain disorder, oxygen dependent, diabetes type II, hypertension, Hypothyroid, morbid obesity
- Andere Medikamente
- ACTOS 45 MG tablettake 45 mg by mouth Daily. for diabetes ASPIR-TRIN 325 MG TBEC take by mouth. cholestramine (QUESTRAN LIGHT) 4 GM/DOSE powder take 4 g by mouth Daily. 1 packet or scoop with 1st meal of the day. colesevelam (WELCHOL) 6
- Allergien
- bactrim - Trimethoprim - "can't breathe"
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 01.01.2022
- Impfdatum
- 02.12.2021
- Beginn
- 06.12.2021
- Tage bis Beginn
- 4,0
- Dosis
- 1
- Route/Site
- UN / UN
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Autopsy
Death
Dyspnoea
Feeling abnormal
Pulmonary embolism
Symptomtext
Soon after getting J&J Booster, Patient started complaining about shortness of breath that would come and go. On 12/22/2021 he was feeling like "crap" and thought it was COVID and was waiting to get tested. We found him dead in his apartment, and the autopsy revealed pulmonary thrombo embolism.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- autopsy on 12/27/2021
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- the only thing he took was acid reducer over the counter medication.
- Allergien
- Cats, ashtma
- Vorherige Impfungen
- -
- Staat
- WV
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 31.12.2021
- Impfdatum
- 29.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Death
General physical health deterioration
Hyperhidrosis
Hypotension
Inflammation
Pyrexia
Streptococcus test
Tachycardia
Tachypnoea
Throat irritation
Unresponsive to stimuli
Symptomtext
Booster desired by way of consent signed on admission by resident representative. Janssen booster 0.5 mL given as consented to stable resident by LPN on 12/29/21 at approx 11:00am. On 12/30/21, resident status declined with rapid strep being done for fever, throat inflammation. Later resident was found to have low B/P, diaphoretic, unresponsive. Order received to send to local ER for eval. Resident left our facility with tachypnea, tachycardia, febrile and unresponsive and transported to local ER where he later was reported to have passed away in the ER.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- Rapid Strep test (no results are noted at this time)
- Aktuelle Erkrankungen
- right femur fracture, anxiety, HTN, constipation, vit D deficiency, unspecified intelliectual disability, depression, OCD, Parkinsons, seizures, dry eye, urinary incontinence, BPH, osteoarthritis, psychotic disorder,
- Vorgeschichte
- See above
- Andere Medikamente
- Retane Eye Ointment, docusate sodium, miralax, tylenol, ergocalciferol, lacosemide, tamsulosin, senna, lisinopril, keppra, fluoxetine, finasteride, diazepam, sinemet, baby aspirin, oxycodone-acetaminophen, calcium carb-cholecalciferol, onda
- Allergien
- NSAIDS
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 13.12.2021
- Impfdatum
- 11.12.2021
- Beginn
- 13.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Dyspnoea
Hypersensitivity
Respiratory arrest
Throat tightness
Symptomtext
SEVERE ALLERGIC REACTION WITH SEVERE BREATHING DIFFICULTY, THROAT CLOSED FOR ALMOST A MINUTE, COULD NOT BREATH
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Respiratory arrest
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 02.12.2021
- Impfdatum
- 19.11.2021
- Beginn
- 21.11.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Coronary arterial stent insertion
Intracardiac thrombus
Myocardial infarction
Symptomtext
Heart attack. Blood clot in heart. Stent inserted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocardial infarction
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Morphine
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 17.08.2023
- Impfdatum
- 20.11.2021
- Beginn
- 12.01.2023
- Tage bis Beginn
- 418,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Anaphylactic reaction
Symptomtext
ANAPHYLAXIS, INIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anaphylactic reaction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 10.05.2023
- Impfdatum
- 23.11.2021
- Beginn
- 20.10.2022
- Tage bis Beginn
- 331,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Deep vein thrombosis
Hypoxia
Symptom recurrence
Symptomtext
ACUTE DVT OF LEFT PERONEAL VEIN HYPOXIA 10/28/2022 -- RECURRENCE OF SAME SYMPTOMS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Deep vein thrombosis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 05.05.2023
- Impfdatum
- 06.12.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 9,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Guillain-Barre syndrome
Weight decreased
Symptomtext
GUILLAIN-BARRE SYNDROME; This spontaneous report received from a consumer concerned a 66 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included: non-smoker, and non-alcohol user, and other pre-existing medical conditions included: The patient had no known allergies and had no history of drug abuse or illicit drug use. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 213D21A expiry: UNKNOWN) dose was not reported, 1 total was administered on 06-DEC-2021 to left arm for covid-19 prophylaxis. Age at time of vaccination 65 years old. No concomitant medications were reported. On 15-DEC-2021, the patient experienced excruciating back pain which had continued for 2 weeks. On 19-DEC-2021, the paralysis had started with her mouth while patient was at work. The paralysis continued all through the body all the way to her feet. She had been suffering from paralysis since 16 months at the time of reporting. The patient was completely disabled and all her muscles stopped working and she was in the hospital for almost a month from 05-FEB-2022 to 02-MAR-2022. The number of days of hospitalization was 25 days. The patient was unable to speak due to her paralysis, not able to move her lips and she has to take her hands to move her mouth to be able to eat. She had visited lot of doctors and was finally diagnosed with Guillain-Barre Syndrome. The physician stated that the vaccine had caused this syndrome in other patient's as well. The patient was previously working perfectly fine and at the time of reporting she was not able to walk or drive and was completely disabled. The patient was able to take immunoglobulins to get her better health which were recommended by her physician. The patient hands were completely curled up and it was hard time typing on a keyboard but she was able to text on the phone. Her body stopped digesting food and the patient lost 41 pounds in 42 days and was not able to walk even with a walker, could only stand using a walker for a small amount of time. She had been visited rehabilitation for 3 times. The patient had been in the wheelchair whole time and initially she was bed bound when the guillain-barre syndrome first started. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from guillain-barre syndrome. This report was serious (Hospitalization Caused / Prolonged, and Disability Or Permanent Damage).; Sender's Comments: V0: 20230505030- Guillain-Barre syndrome. The event has a compatible/suggestive temporal relationship, and is labeled. There is no information on any other factors potentially associated with the event. Therefore, this event is considered consistent with vaccine administration.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Guillain-Barre syndrome
- Hospital-Tage
- 25,0
- Labordaten
- Test Name: WEIGHT LOSS; Result Unstructured Data: lost 41 pounds in 42 days.
- Aktuelle Erkrankungen
- Abstains from alcohol; Non-smoker
- Vorgeschichte
- Comments: The patient had no known allergies and had no history of drug abuse or illicit drug use.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 21.04.2023
- Impfdatum
- 07.12.2021
- Beginn
- 27.01.2022
- Tage bis Beginn
- 51,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Deep vein thrombosis
Neuropathy peripheral
Symptom recurrence
Symptomtext
PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE NEUROPATHY ACUTE DVT, UNSPECIFIED VEIN 1/31/2022 - RECURRENCE OF SAME SYMPTOMS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Deep vein thrombosis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 21.12.2022
- Impfdatum
- 13.12.2021
- Beginn
- 01.09.2022
- Tage bis Beginn
- 262,0
- Dosis
- 2
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Electric shock sensation
Erythema
Pain
Pain in extremity
Peripheral swelling
X-ray normal
Symptomtext
Starting in September of 2022 I experienced foot pain with a shocking sensation, causing things to swell and get red. Stepping on the foot caused it to be too sore to walk on. This was right foot. Doctor consulted. Doctor X-rayed the foot and referred to podiatrist. Podiatrist examined foot and provided shoe inserts. and asked to review in 6 weeks, which has not happened at time of report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Electric shock sensation
- Hospital-Tage
- -
- Labordaten
- Doctor X-rayed the foot, ruled out bone issue.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Sythroid; Lipitor; Multi Vitamin; Co Qu 10
- Allergien
- Cefalexin
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 17.10.2022
- Impfdatum
- 01.11.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- 30,0
- Dosis
- UNK
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Blood test normal
Deep vein thrombosis
Dyspnoea
Pain in extremity
Peripheral swelling
Pulmonary thrombosis
Symptomtext
A few weeks after the shot my left thigh started hurting. A few months after that the pain travelled down my leg. Over a weekend my left calf increased in size to the point in which I couldn't pull up my pant leg. For a couple weeks leading up to this, I also started having a shortness of breath. My doctor told me to get to the ER. They found two DVTs in my left calf and both of my lungs were covered in blood clots. No doctor could explain what happened because I'm a very active, and not sick, person.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Deep vein thrombosis
- Hospital-Tage
- 3,0
- Labordaten
- My doctor, that I mention on here, is still currently doing blood work. They have done multiple tests and everything has come back fine. No one knows why I got the blood clots, other than me hearing that my J&J shot and booster may be to blame.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- A Men's one-a-day multi vitamin, Colestipol, a daily allergy pill (centrizine), and Dupixent
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- HI
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 16.08.2022
- Impfdatum
- 17.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 4,0
- Dosis
- UNK
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Echocardiogram
Magnetic resonance imaging heart
Pericarditis
Symptomtext
Acute pericarditis.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pericarditis
- Hospital-Tage
- -
- Labordaten
- Transthoracic echocardiogram Jan 2022 Cardiac MRI Aug 2022
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 01.08.2022
- Impfdatum
- 24.03.2021
- Beginn
- 01.05.2021
- Tage bis Beginn
- 38,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Anaemia
Anti-thyroid antibody increased
Blood creatinine decreased
Blood culture negative
Blood thyroid stimulating hormone decreased
Chest X-ray
Computerised tomogram
Computerised tomogram thorax
Diarrhoea
Fibrin D dimer
Hepatic enzyme increased
Illness
Intensive care
International normalised ratio increased
Lymphadenopathy
Monocyte count increased
Neutrophil count increased
Night sweats
Symptomtext
High Fevers (5 illness events leading Up to Hospitalization Starting in 5/2021 Hospitalization 4/8/2022 8 days Cardiac ICU Severely Swollen Glands Night Sweats Diarrhea Weight Loss Thyroiditis Severe Pericarditis (Requiring operative pericardial window) local Medical Center Pneumonia (Requiring Operative Thoracotomy) Left Lung local Medical Center Anemia High Platelets High Monocytes High Neutrophils Negative Blood Culture x 2 Low Creatinine Multiple Cat Scans Chest and Lungs with Contrast and without Multiple Chest X-rays
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Intensive care
- Hospital-Tage
- 8,0
- Labordaten
- High WBC 17-28 High Liver Enzymes High TSH .0005 Low ESR 53 High SARS CoV-2 Covid 19 Not Detected INR 1.2 Anti Thyroid Peroxidase 172 High D Dimer 5.19 High Cat scans x-rays
- Aktuelle Erkrankungen
- Hashimotos' Thyroiditis Controlled
- Vorgeschichte
- None
- Andere Medikamente
- NP Thyroid 180 mg , Vivelle Patch, progesterone 100mg nightly
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 04.07.2022
- Impfdatum
- 30.11.2021
- Beginn
- 27.02.2022
- Tage bis Beginn
- 89,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Gait disturbance
Limb discomfort
Oedema peripheral
Pain
Pain in extremity
Sitting disability
Thrombosis
Ultrasound Doppler abnormal
Symptomtext
I developed discomfort in my right leg while sitting a few weeks after receiving the booster shot. I ignored the discomfort and would stand up and walk around. Over the course of the next couple months I continued to notice discomfort, only when sitting. On February 27th of 2022, I started to limp and felt a burning pain in my right calf. After a week of limping around I couldn't take the pain any more and on Saturday morning the 5th of March I went to urgent care where I was given an ultrasound after the doctor observed a substantial amount of edema in my right leg. After the ultrasound the doctor told me I had a "large blood clot" in my leg and was diagnosed as having DVT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Thrombosis
- Hospital-Tage
- 2,0
- Labordaten
- 03/05/22 Ultrasound administered.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- Alprazolam.
- Allergien
- N/A
- Vorherige Impfungen
- Numbness of the eyelid, eyebrow, forhead. Covid-19 Vaccine Pfyzer. (The reason I tried the Janssen after having the adverse re
- Staat
- -
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 12.05.2022
- Impfdatum
- 12.05.2022
- Beginn
- 12.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Fall
Head injury
Loss of consciousness
Syncope
Symptomtext
Patient fainted, fell and hit head on floor within 2-3 minutes of receiving vaccination. He regained consciousness within seconds. Stated feeling better. EMS was called and care handed off.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 08.04.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Loss of consciousness
Tremor
Symptomtext
Consent form was reviewed with patient. Patient stated that he was receiving his first Janssen vaccine. Patient was seated in the chair. I went over the possible side effects he might experienced and handed a VIS form to the patient. Patient was given the immunization in the left arm. Patient felt lightheaded and lost consciousness for a brief moment (15-30 seconds). I asked him if he had trouble breathing and he shook his head "no". Patient demonstrated tremor, with possible seizure. EMS was called per protocol and emergency kit was available if necessary. I asked the mother regarding prior episodes. She stated that the patient has passed out when blood was drawn. This is possible vasovagal response. EMS arrived to take over the situation. I gave my statement to EMS. I assessed the patient and he stated he was fine. I made him wait for additional 15 minutes to monitor any reaction. I referred them to the nearest hospital if any complications should arise.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- No medical tests were done. Patient was sitting in the chair. Blood pressure machine was available but he needed a moment to breathe. EMS rechecked vitals and assessed blood pressure.
- Aktuelle Erkrankungen
- Not available
- Vorgeschichte
- Asthma per guardian
- Andere Medikamente
- Not Available
- Allergien
- Not Available; specified on the immunization form as yes, but could not elaborate
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 08.03.2022
- Impfdatum
- 20.11.2021
- Beginn
- 20.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood pressure increased
Dizziness
Headache
Heart rate increased
Hypoaesthesia
Palpitations
Paraesthesia
Presyncope
Symptomtext
NUMBNESS AND TINGLING ON RIGHT SIDE OF BODY, NOTED IN RIGHT UPPER AND LOWER EXTREMITIES; DIZZINESS, LIGHTHEADEDNESS, AND NEAR SYNCOPE WITH WORKING OUT OR INCREASED ACTIVITY (NOT PRESENT BEFORE); INCREASE IN RESTING HEART RATE AND BLOOD PRESSURE; INTENSE HEADACHE AND POUNDING HEARTBEAT WITH INCREASED ACTIVITY AND WORKING OUT (NOT PRESENT BEFORE).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- Probiotics
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 95,0
- Geschlecht
- F
- Eingang
- 08.03.2022
- Impfdatum
- -
- Beginn
- 19.11.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Gait disturbance
Headache
Paralysis
Rash
Skin burning sensation
Visual impairment
Symptomtext
MILD HEADACHES; PARALYZED; SKIN FELT LIKE IT WAS ON FIRE; DIZZY; TROUBLE WITH VISION; DIFFICULTY WALKING; RASH ON BACK; This spontaneous report received from a patient concerned a 95 year old African American and non Hispanic or Latino female. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient was previously treated with covid-19 vaccine ad26. cov2. s (Dose number in series 1) (suspension for injection, route of admin not reported, batch number: 201821A and expiry: unknown) dose was not reported, 1 total administered on 28-JUL-2021 for prophylactic vaccination. No adverse events reported following vaccination (Dose number in series 1). The patient received covid-19 vaccine ad26.cov2.s (Dose number in series 2) (suspension for injection, route of admin not reported, batch number: 213D21A, and expiry: 11-APR-2022) dose was not reported, 1 total administered on 19-NOV-2021 in left arm for prophylactic vaccination. No concomitant medications were reported. On 19-NOV-2021, about an hour or hour and a half later, the patient experienced difficulty walking, skin felt like it was on fire, dizzy, felt like to was paralyzed (paralysis), trouble with vision, and rash on back (Dose number in series 2). On an unspecified date, the patient experienced mild headaches (Dose number in series 2). The patient had tried cold water for these side effects and would use aspirin, and rubbing alcohol if the patient needed a pain killer. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from paralyzed, skin felt like it was on fire, dizzy, trouble with vision, difficulty walking, and rash on back, and had not recovered from mild headaches. This report was serious (Other Medically Important Condition).; Sender's Comments: V0- 20220302627-covid-19 vaccine ad26. cov2. s-Paralyzed. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s). Therefore, this event(s) is considered unassessable.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paralysis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 05.02.2022
- Impfdatum
- 17.11.2021
- Beginn
- 19.11.2021
- Tage bis Beginn
- 2,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arthralgia
Chest discomfort
Dizziness
Dyspnoea exertional
Echocardiogram
Electrocardiogram
Gait disturbance
Gait inability
Headache
Heart rate increased
Joint stiffness
Laboratory test
Migraine
Musculoskeletal stiffness
Myalgia
Pericarditis
Tachycardia
Symptomtext
48 hours muscle aches, stiff neck. 84 hours and lasting two weeks large muscle group myalgia, joints (hips, knees, shoulders, metacarpals) pain, Notified PCP on 11/22/21- labs ordered- negative. Preemptive treatment for Lyme disease, eventual Lyme ABY test negative. Joint and muscle stiffness on 11/22/21 severe to prevent ambulation without significant alteration in gait. Slowly improved over the course of two weeks. Remained afebrile. Treated with ibuprofen and doxycycline . Dec 23, 2021- return of muscle aches. Headaches and neck muscle pain 2-3 times per week. Migraine headache frequency notably increased since late November to present about 6-8 per month and ongoing. From Dec 23 symptoms progressed as follows: Development of progressive chest discomfort in supine position and shortness of breath with exertion, intermittent lightheadedness. ECG Jan 5, 2022: sinus rhythm with nonspecific T wave abnormality. Cardiologist examination revealed S4 abnormal heart sound and rapid pulse. Stat ordered echocardiogram completed , negative for effusion. EF normal. Labs completed-told were 'OK'. Diagnosis- Pericarditis and tachycardia. Treated with high dose steroids and anti-inflammatory agents for two weeks. Symptoms returned late January with supine position chest heaviness, treated with another course of steroid and NSAIDS. Headaches , joint pain are ongoing to date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pericarditis
- Hospital-Tage
- -
- Labordaten
- ECG Jan 5, 2022: sinus rhythm with nonspecific T wave abnormality. Cardiologist examination revealed S4 abnormal heart sound and rapid pulse. Stat ordered echocardiogram completed , negative for effusion. EF normal. Labs completed-told were 'OK'. Diagnosis- Pericarditis and tachycardia. Treated with high dose steroids and anti-inflammatory agents for two weeks. Symptoms returned late January with supine position chest heaviness, treated with another course of steroid and NSAIDS. Headaches , joint pain are ongoing to date.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypothyroid Migraine
- Andere Medikamente
- Levothyroxine Ibuprofen as needed Sumatriptan 50mg as needed
- Allergien
- Red dye- severe
- Vorherige Impfungen
- childhood. Unknown
- Staat
- NJ
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 23.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 14,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Blood test
Cerebral thrombosis
Computerised tomogram
Intensive care
Magnetic resonance imaging
Symptomtext
Currently in the icu due to blood clot in my head
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebral thrombosis
- Hospital-Tage
- -
- Labordaten
- Cat Scan, blood work, mri 1/21/22- present
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Lexapro Oral birth control
- Allergien
- Sulfa Mushrooms Mangos Bees
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 21.01.2022
- Impfdatum
- 20.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dyspnoea
Headache
Seizure
Tremor
Symptomtext
patient informed her that during the night he had 2 brief episodes of what he describes as "convulsions". Patient concerned of a possible reaction to the J&J vaccine he received yesterday during his office visit. Patient describes the episodes of convulsions as brief and that he had uncontrollable shaking only from his waist up. Patient also reporting that his breathing felt funny. Patient reporting that he did not lose LOC and was totally aware of what was happening. No loss of bowel or bladder. Mom reports that patient is difficult to get much more details from. Patient reports that he does have a slight headache presently, but otherwise had returned to baseline.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Covid on 12/2/2021
- Vorgeschichte
- ADHD, Autism spectrum
- Andere Medikamente
- Adderall, Zyrtec
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- -
- Geschlecht
- M
- Eingang
- 18.01.2022
- Impfdatum
- -
- Beginn
- 21.12.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Hypoaesthesia
Hypokinesia
Magnetic resonance imaging
Movement disorder
Neck pain
Pain in extremity
Paraesthesia
Paralysis
Symptomtext
NUMBNESS; PINS AND NEEDLES IN ARMS; HANDS FEEL PARALYSIS; NECK PAIN; HANDS NOT WORKING WELL/HARD TO GRIP STUFF/HARD TO MAKE A FIST; CAN NOT MOVE FOREARM AND BICEPS WELL/ARM SEIZED UP; ARM PAIN/HANDS ARM HURTING/SORE FOREARM; This spontaneous report received from a patient concerned a 34 year old male with unspecified race and ethnicity. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: The patient was healthy individual. The patient used to work 12 hours a day, would never experience this arm pain before and never had this experience before. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 213D21A, and expiry: UNKNOWN) dose was not reported, 1 total, administered on 13-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. After eight days of the vaccine (21-DEC-2021) hands and arm of the patient was hurting a lot, patient could not move forearm well and biceps also. Forearm of the patient was super sore right now. It was pretty bad. The patient felt hands paralysis, experienced neck pain, hands not working well, hard to grip stuff, hard to make a fist. On 03-JAN-2022 patient went to primary care physician get a magnetic resonance imaging (result was not reported). On an unspecified date patient experienced numbness, pins and needles in arms and got a professional massage to get pain reduced but that did not help either. On an unspecified date patient visited to emergency room. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the neck pain, hands feel paralysis, arm pain/hands arm hurting/sore forearm, hands not working well/hard to grip stuff/hard to make a fist., can not move forearm and biceps well/arm seized up, numbness and pins and needles in arms was not reported. This report was serious (Other Medically Important Condition).; Sender's Comments: V0: 20220123924-COVID-19 VACCINE AD26.COV2.S-hands feel paralysis. This event(s) is considered unassessable. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paralysis
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220103; Test Name: Magnetic resonance imaging; Result Unstructured Data: Not Reported
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: The patient was healthy individual. The patient used to work 12 hours a day, would never experience this arm pain before and never had this experience before
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 09.01.2022
- Impfdatum
- 08.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Syncope
Symptomtext
Patient fainted shortly after the vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- -
- Allergien
- n/a
- Vorherige Impfungen
- fainted
- Staat
- PA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 07.01.2022
- Impfdatum
- 02.12.2021
- Beginn
- 03.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Balance disorder
Blood pressure increased
Body temperature increased
Chest discomfort
Chest pain
Chills
Discomfort
Electrocardiogram normal
Guillain-Barre syndrome
Head discomfort
Impaired work ability
Muscle spasms
Muscular weakness
Paraesthesia
Pruritus
Symptomtext
Have not been back to work. On 12/29/2021 I went to the PCP and she believed I had Guillain Barre Syndrome, due to my symptoms that started on 12/3/2021. they were chills, back of the head pressure, the left arm and both feet, were tingling. My temperature was extremely high. I had extreme pressure in my lower back. My temperature would stay around the hundreds for weeks. It's still spiking. I had horrible head pressure. And I did have a spell of itching and no rash. I have joint pain. The chest pain elevated blood pressure and muscle cramps and weakness leg and tingling in hands and balance of equilibrium are continuing. I continue to have bouts of high blood pressure. I have tightness and heaviness during chest pain on 12/26/2021. I had been prescribed a steroid treatment. My heart rate was over 100 for three days. My PCP wants me to have a echocardiogram. I do not have insurance, so I have to wait for that procedure. The weakness in my lower legs started 12/5/2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Guillain-Barre syndrome
- Hospital-Tage
- -
- Labordaten
- EKG- 12/29/2021- Normal
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Multivitamin, Omeprazole 20mg
- Allergien
- Morphin , Penicillin
- Vorherige Impfungen
- Flu-vaccine - Extreme high fever and nausea, diarrhea for two months and a cough that lasted about three months.
- Staat
- NJ
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 06.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syncope
Symptomtext
Patient fainted about 10 minutes post vaccine administration. He sat on the bench while his mother held his head upright. He laid on the bench briefly. Patient fully recovered and left the pharmacy without needing medical attention.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None reported
- Vorgeschichte
- None reported
- Andere Medikamente
- Not known
- Allergien
- None reported
- Vorherige Impfungen
- Patient's mother reported patient fainting after vaccination once when he was younger.
- Staat
- VA
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 31.12.2021
- Impfdatum
- 06.11.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 39,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bell's palsy
Facial paralysis
Muscular weakness
Symptomtext
Drooping of left side of face and weakness of leg. Patient doesn?t have a regular doctor. He consulted an online physician and was told it may be Bell?s Palsy. He was prescribed medrol dospak and valcyclovir. Leg seems to be better. But the patient still has drooping face on left side. He plans on seeing another doctor but started to wonder about the cause after reading more about the vaccine. Outcome is still unknown.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bell's palsy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Adhd
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 31.12.2021
- Impfdatum
- -
- Beginn
- 22.11.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Thrombosis
Symptomtext
This spontaneous report received from a patient concerned an 81-year-old female of unspecified ethnicity. The patient's weight was 180 pounds, and height was 66 inches. The patient's concurrent conditions included: seasonal allergies, no alcohol use, and nonsmoker. The patient no medical history. The patient was previously treated with covid-19 vaccine (dose number is series 1) (suspension for injection, route of admin not reported, and batch number: 043A21A, expiry: unknown) dose was not reported, 1 total, administered on 12-APR-2021 for prophylactic vaccination. The reporter did not report any adverse events following vaccination with covid-19 vaccine (dose number in series 1). The patient received covid-19 vaccine (dose number in series 2) (suspension for injection, route of admin not reported, batch number: 213D21A, expiry: UNKNOWN) dose was not reported, 1 total, administered to left arm on 12-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 22-NOV-2021, the patient went to the emergency room and was diagnosed with blood clot (thrombosis in her left leg) (dose number in series 2). The patient was treated in the emergency room at hospital and was discharged on the same day. The patient was treated with blood thinners and the clot had resolved and everything was fine. It took couple weeks to resolve. The action taken with covid-19 vaccine was not applicable. The patient recovered from thrombosis in left leg/blood clot in an unspecified date in DEC-2021.This report was serious (Other Medically Important Condition).; Sender's Comments: V0:20211258312-COVID-19 VACCINE Thrombosis in left leg. This event(s) is considered unassessable. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Thrombosis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Abstains from alcohol; Non-smoker; Seasonal allergy
- Vorgeschichte
- Comments: The patient no medical history.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 29.12.2021
- Impfdatum
- 19.11.2021
- Beginn
- 19.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
Blood thyroid stimulating hormone normal
Chest X-ray normal
Cold sweat
Computerised tomogram normal
Dizziness
Electric shock sensation
Full blood count normal
Heart rate increased
Muscular weakness
Paraesthesia
Scan with contrast
Vitamin D decreased
Symptomtext
about 10 minutes after the injection I was walking around the store and had a very sharp and jolting almost zap in my head. Then my heart rate jumped to about 135bpm from what was around an average of 75bpm prior. I got very dizzy, weak in my whole body and began having cold sweats. My next event was 11-26-2021. I had extreme muscle weakness, tingling in my limbs and felt dizzy. I went to the ER and they ran thyroid blood work, and a CBC. All came back normal. They also performed a CT scan with contrast and to look for clotting. All looked ok. Over the next 3 weeks I went to the ER 2 more times, once in an ambulance. Same symptoms: weakness that one day is on my right side, then to my left, sometimes my entire body. The time I went to the er in an ambulance, was due to sever weakness and very high jump in heart rate while sitting and reading in my home town. I had chest x rays (not sure why) and more blood work...all came back normal. I have NEVER experience anything like this in my 40 years until after I received the JNJ covid 19 shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Electric shock sensation
- Hospital-Tage
- -
- Labordaten
- 11-26-2021: CBC, thyroid TSH and T4 levels, CT scan with contrast: all normal 12-02-2021: CBC, thyroid TSH and chest x rays: all normal 12-10-2021: vitamin D levels and CBC: all normal, vitamin D levels high (105 with high limit in reference range = 100) 02-09-2022: soonest I can see a neurologist
- Aktuelle Erkrankungen
- hashimotos thyroiditis
- Vorgeschichte
- hashimotos thyroiditis
- Andere Medikamente
- levothyroxine, selenium and daily multi-vitamin
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 28.12.2021
- Impfdatum
- 28.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood glucose normal
Heart rate abnormal
Loss of consciousness
Symptomtext
Patient received a Janssen vaccine, dose 1, and about 5 minutes after leaving the pharmacy passed out in the store. She did not hit her head, she was caught by another customer. 911 was called and when she was assessed, most vitals were normal (blood pressure, glucose, pulse ox) but her heart rate was fluctuating up and down ranging from about 180 to 65. She refused to go on the ambulance, but her host father stated he was taking her to the Hospital for evaluation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- Blood Pressure 100/60 Glucose 100 Pulse 65 to 180
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 88,0
- Geschlecht
- F
- Eingang
- 28.12.2021
- Impfdatum
- 08.12.2021
- Beginn
- 14.12.2021
- Tage bis Beginn
- 6,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: ja
ER: unbekannt
Erholt: nein
Angiogram
Computerised tomogram head
Embolic stroke
Magnetic resonance imaging head
Scan with contrast
Symptomtext
Patient had a thromboembolic stroke and admitted to Hospital on 12/14/21
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Embolic stroke
- Hospital-Tage
- 7,0
- Labordaten
- CT Head WO Contrast (12/14/21), MRI Brain W/WO Contrast (12/15/21), CT Angio Head and Neck (12/17/21)
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HTN, A-Fib
- Andere Medikamente
- Diltiazem, Eliquis, Losartan, Furosemide, Tylenol, MultiVit, Vitamin D3
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 27.12.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal pain upper
Blood test
Computerised tomogram
Facial paralysis
Feeling hot
Hypersensitivity
Hypertension
Hypoaesthesia
Tremor
Symptomtext
received booster (jansen) on November 5, 2021, at approx 3:30, While in my car driving, the right side of my face became hot and I felt like it was sagging and felt hot, I drove myself to the fire department while they took my blood pressure (a little high), and other vitals, I waited for about 1/2 hour and did not get worse so I went home, I woke the next morning with more numbness and sagging on left side of my face and extreme pain in my stomach. My right arm began to tremor and clinch in to my side. Soon after my leg did the same. It looked as if I had bells palsy or parkinstons. I called my mother, who took me to emergency room., who after seeing me said I had a severe allergic reaction and treated for such.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Facial paralysis
- Hospital-Tage
- -
- Labordaten
- Blood work, IV Therapy, CT Scan, Pharmacuticals, Cardiac services and treatment.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Vitaman C, D3, Tumeric
- Allergien
- none (reactions but not allergy to morphine (gives me headaches), levaquin (upsets stomach), and estrogen (makes me irritated)
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 18.12.2021
- Impfdatum
- 18.12.2021
- Beginn
- 18.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dyspnoea
Syncope
Symptomtext
At check in, he was alert, conscious, outgoing, nka or medical concerns. He indicated he did not want to watch injection. In waiting area, approximatly 10 minutes into waiting, he suddenly feel to the floor from the chair. At not time did he lose consciousness, but he was lying in a prone postition. Stated he was having difficulty breathing, but RN who observed, noticed no shortness of breath or dyspnea. EMS called. BB 110/68, HR 62 and regular. Diaphoresis and paleness noted. Denied pain. Denied hitting his head. Stated he did not eat or drink anything that morning. EMS arrived and assessed pt and transported to hospital. Patient able to sit up and get himself on stretcher with assistance from EMS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none known
- Vorgeschichte
- none know
- Andere Medikamente
- unknown
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 15.12.2021
- Impfdatum
- 15.12.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syncope
Tremor
Symptomtext
The patient watched the shot being given, saw a tiny drop of blood, then fainted. We laid the patient on the floor and elevated her legs for 5 minutes. Her dad then sat with her and brought her some water. She walked out with him 10 minutes later and seemed fine but a little shaky.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none reported
- Vorgeschichte
- none reported
- Andere Medikamente
- none reported
- Allergien
- none reported
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 15.12.2021
- Impfdatum
- 13.12.2021
- Beginn
- 13.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Loss of consciousness
Symptomtext
Patient passed out after administration of the dose
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 15.12.2021
- Impfdatum
- 27.11.2021
- Beginn
- 28.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Bell's palsy
Facial paralysis
Hypoaesthesia
Paraesthesia
Symptomtext
Patient went to both primary doctor and ER with the outcome of Bell's Palsy. Patient reported tingling/numbness/droping of one side of face following vaccination starting the following day. Patient was put on a treatment of acyclovir and prednisone.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bell's palsy
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Nothing stated by patient
- Andere Medikamente
- N/A
- Allergien
- Nothing stated by patient
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 15.12.2021
- Impfdatum
- 07.12.2021
- Beginn
- 12.12.2021
- Tage bis Beginn
- 5,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Facial paralysis
Facial spasm
Lacrimation increased
Paraesthesia
Symptomtext
Watery Eye on Sunday, then noticed when I spit it was coming out only from one side. Slight tingle/spasm on left side of face. Noticed left side of face wasn't as mobile as right side when smiling, frowning and opening mouth wide.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Facial paralysis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypothyroidism, Hyper tension
- Andere Medikamente
- None
- Allergien
- Minor to eggs, watermelon, dog hair.
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 15.12.2021
- Impfdatum
- 10.12.2021
- Beginn
- 10.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syncope
Symptomtext
Patient fainted >15 minutes after administration.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None listed
- Vorgeschichte
- None listed
- Andere Medikamente
- Unknown
- Allergien
- None listed
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 14.12.2021
- Impfdatum
- 08.12.2021
- Beginn
- 09.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Fatigue
Headache
Pain
Postmenopausal haemorrhage
Pyrexia
Shock
Symptomtext
I had a fever, achy and headache for two days from Thursday am to Saturday am, then a worse headache and very tired all day Saturday. On Sunday, I started spotting as though I was getting my period. I have been post-menopausal for three years, so this was a shock. The spotting is slight but still there today (Tuesday). I also had a very sore armpit on the side that I received my vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Shock
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Thyroid disorder
- Andere Medikamente
- Tirosint, ibuprofen, daily vitamin, omega 3, vitamin D, zinc
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WV
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 14.12.2021
- Impfdatum
- 14.12.2021
- Beginn
- 14.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Anxiety
Fall
Haematoma
Haemorrhage
Head injury
Hyperhidrosis
Seizure like phenomena
Skin laceration
Symptomtext
Patient received vaccination 0.5 ml, then immediately sat down in chair. At approximately 5:08, he fell out of the chair, exhibiting seizure like activity noted by vaccination staff. He fell into the floor, striking the back of his head which resulted in a golf ball size hematoma and laceration. EMT assessed c spine for injury. Reassure applied to active bleeding laceration. emergency was called at 5:06. Vital signs stable. He was diaphoretic. LOC assessed. Able to verbal name and location. Respirations even and unlabored. Neck supported while transferred to gurney and care taken over by emergency responders at 5:15 pm. Patient was alert at departure to hospital by rescue squad. His father was present and stated the patient was apprehensive prior to vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure like phenomena
- Hospital-Tage
- -
- Labordaten
- Unknown
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Denied
- Andere Medikamente
- Denied
- Allergien
- Denied
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 11.12.2021
- Impfdatum
- 11.12.2021
- Beginn
- 11.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Dyspnoea
Loss of consciousness
Symptomtext
Soon after receiving the vaccine client passed out. Denies difficulty breathing, denies swelling of tongue or throat, or chest pain. Just breathing heavy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None per parent andclient
- Vorgeschichte
- None
- Andere Medikamente
- One
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 09.12.2021
- Impfdatum
- 09.12.2021
- Beginn
- 09.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Loss of consciousness
Pallor
Vomiting
Symptomtext
Patient received first dose of her covid vaccine. She was waiting in a chair where I could see her after her vaccine. About 6 minutes later she said she was feeling dizzy. As I was walking to get her water she passed out. I grabbed the emergency kit and ran out to her, she was conscious and I sat her up and she was able to say her name and birthday. She then began throwing up. I tried to then take her blood pressure because she looked very pale, but she began throwing up again. She then wanted to drink something, provided patient with orange juice and stayed with her until EMS arrived.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No.
- Vorgeschichte
- No.
- Andere Medikamente
- N/A
- Allergien
- No.
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 09.12.2021
- Impfdatum
- 07.12.2021
- Beginn
- 07.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dyskinesia
Fall
Head injury
Headache
Loss of consciousness
Migraine
Muscle twitching
Seizure like phenomena
Syncope
Tongue biting
Tongue haemorrhage
Symptomtext
Patient fainted and fell after the vaccine was administered by my tech. Pharmacist observed patient on the floor jerking/twitching like patient was having seizure. 911 was called. Patient came to consciousness in approx 45seconds. Patient bit his tongue during the incident so had bleeding. Pt admitted that he was very nervous, and did not eat any breakfast today. Vitals: BP 105/54 HR 54bpm. Pt was not having anaphylaxis reaction. Pt was breathing fine. Pt was having headache afterwards. Pt declined to go to ER with ambulance, as patient stated he will follow up with his PCP. Followed up with the patient on 12/08 and patient stated patient has migraine and bump on head where he fell but otherwise doing fine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 09.12.2021
- Impfdatum
- 09.12.2021
- Beginn
- 09.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fall
Head injury
Loss of consciousness
Musculoskeletal stiffness
Symptomtext
Before the shot the patient verbally stated and wrote down that he had no history of serious reactions to a vaccine. Administered J&J vaccine and had patient sit on bench for observation for 15 minutes. Within 1 minute of administration he fell over to his right, rolled on the ground, hit his head and was unconscious for 10 seconds. I rushed over and kept him on his side and held his head stable so he wouldn't hit it again as he was stiffening up. After he came to we helped him back up to the bench and gave him water. The color in his face returned shortly after and he insisted he was ok. He then admitted that he had a similar experience to a TB test but denied having a history of seizures. Patient refused us to take his blood pressure or take a glucose tab and persisted that he was ok. He left on his own power after statements were taken by management.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- none listed
- Andere Medikamente
- unknown
- Allergien
- nkda
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 08.12.2021
- Impfdatum
- 07.12.2021
- Beginn
- 07.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site pain
Loss of consciousness
Symptomtext
Patient was in post vaccination monitoring area when she proceeded to pass out. She was unconscious for less then a minute and stated she was fine when she regained consciousness. She stated she has history of syncope with vaccine administration and stated she passed out from the pain of the injection and having a fear of needles. She waited for several more minutes and left on her own accord.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- She states history of occasionally passing out after receiving vaccines in the past
- Staat
- CA
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 06.12.2021
- Impfdatum
- 06.12.2021
- Beginn
- 06.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Amnesia
Fall
Loss of consciousness
Movement disorder
Syncope
Symptomtext
APPROXIMATELY 30 SECONDS AFTER THE VACCINE WAS ADMINISTERED, PT'S HEAD STARTED TO WOBBLE, AND PT PUT HIS ARM ON THE COUNTER AND HIS HEAD ON HIS ARM. PT LOST CONSCIOUSNESS FOR ABOUT 5 SECONDS, BUT WAS BREATHING. NO SEIZURES WERE OBSERVED. PT REGAINED CONSCIOUSNESS QUICKLY AFTER THE 5 SECONDS. PT DID NOT REALIZE HE HAD PASSED OUT. PT HAS NO HISTORY OF SYNCOPE AFTER VACCINES, NO HX OF SEIZURES, NO HX OF MEDICAL CONDITIONS, NO HX OF ANY RX OR OTC MEDICATIONS. PT ASKED FOR WATER, AND WE PROVIDED BOTTLED WATER. PT WAS FULLY CONSCIOUS AND EVERYTHING WAS WITHIN NORMAL LIMITS QUICKLY AFTER PT GAINED CONSCIOUSNESS. PT WAS ABLE TO STAND UP AND WALK TO A CHAIR IN THE WAITING AREA IN FRONT OF THE PHARMACY. PT NEVER FELL OUT OF THE CHAIR DURING THE SYNCOPE EPISODE. AND PT WAS COMFORTABLE WITH SITTING DOWN AFTER REGAINING CONSCIOUSNESS. WE OBSERVED PT FOR 30 MINUTES AND PT WAS OK. WE HAD PT CALL A FRIEND TO COME PICK HIM UP TO TAKE HIM HOME.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NO KNOWN ALLERGIES
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 04.12.2021
- Impfdatum
- 04.12.2021
- Beginn
- 04.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Fall
Head injury
Syncope
Symptomtext
patient fainted couple minutes after vaccination and fell forward from the bench and bumped his forehead but regained consciousness in few seconds and was able to talk and drink water, ambulance took him to the hospital to get his head checked but not sure about the outcome yet
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- unknown but ambulance took him to the hospital to get his head checked but not sure about the outcome yet
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 03.12.2021
- Impfdatum
- 03.12.2021
- Beginn
- 03.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Immediate post-injection reaction
Nausea
Syncope
Vomiting
Symptomtext
Pt fainted immediately after vaccination. He came to but was nauseated and vomited. He declined emergency care from ED. He recovered in about 30 minutes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Not sick today
- Vorgeschichte
- Pt said he always faints and gets sick w/ injections
- Andere Medikamente
- -
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 01.12.2021
- Impfdatum
- 01.12.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Loss of consciousness
Malaise
Unresponsive to stimuli
Symptomtext
PATIENT REPORTED FEELING UNWELL AND THEN BECAME UNRESPONSIVE FOR SEVERAL MINUTES WITH ONLY A COUPLE BREIF RESPONSES TO INDICATE SHE WAS LIGHT HEADED AND DIZZY BUT EVENTUALLY REGAINED CONSCIOUSNESS AND LEFT WITH PARAMEDIC /EMT FEELING OK AND STATING SHE DID NOT WANT TO GO TO THE HOSPITAL
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE REPORTED
- Vorgeschichte
- NONE REPORTED
- Andere Medikamente
- DID NOT ASK
- Allergien
- NONE STATED ON FORM
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 30.11.2021
- Impfdatum
- 26.11.2021
- Beginn
- 26.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Contusion
Fatigue
Headache
Heart rate increased
Myalgia
Pruritus
Syncope
Symptomtext
Pt. states that after receiving the 2nd dose of Jansen J&J Booster 11/26/2021, started experiencing symptoms that evening of Rapid heart beat, headache, chills, muscle aches, fatigue, 11/27/2021 fainted, 11/29/2021 left leg itchiness between the thigh and knee, and 3 slight bruising areas on the left thigh. Symptoms lasted 48hrs. No noted Primary visit/communications.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Antibiotics for Tooth Infection at the time.
- Vorgeschichte
- N/A
- Andere Medikamente
- Clindamycin
- Allergien
- Pennicillin, Macrobid, Cipro
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 26.11.2021
- Impfdatum
- 26.11.2021
- Beginn
- 26.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Confusional state
Crying
Dizziness
Dyspnoea
Feeling abnormal
Panic reaction
Photophobia
Posture abnormal
Respiration abnormal
Screaming
Seizure like phenomena
Unresponsive to stimuli
Symptomtext
Patient received Janssen immunization on 11/26/2021 at 6:20 pm. About a minute or so after receiving the shot, the patient had an adverse reaction to the vaccine. Gave the vaccine, walked out of the immunization booth to print a scan tag, then returned to the booth with the scan tag. Upon entering immunization booth patient appeared slumped in chair with head back and eyes open, but unfocused. Patient was moving erratically around in chair. Called out to patient and patient did not respond. Came up to patient, touched shoulder, and patient still did not respond. Patient screamed out and seemed to be in a panicked state. Touched shoulder again and said patient's name and patient turned to look and her eyes became more focused. Patient seemed to slowly calm down after that. Patient claimed to be dizzy and lightheaded after that. Patient described the event that she could feel the vaccine moving through her body. Patient stated that she felt like she was in her head screaming and then she was seen. Patient seemed confused about what happened after the incident and breathing was labored/erratic. Patient cried and comforted patient for about 10-15 minutes after incident.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure like phenomena
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 24.11.2021
- Impfdatum
- 24.11.2021
- Beginn
- 24.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fall
Loss of consciousness
Syncope
Symptomtext
Vasovagal syncope following COVID vaccine. Patient passed out during the 15 min post-vaccine monitoring period-- Slumped/Fell out of chair in waiting area. Came to in about 10 seconds
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- patient stated that she has a history of fainting after vaccines
- Staat
- FL
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 24.11.2021
- Impfdatum
- 23.11.2021
- Beginn
- 23.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dyskinesia
Fall
Fatigue
Gaze palsy
Laboratory test
Loss of consciousness
Seizure
Symptomtext
Patient was nervous about getting injection but said he wanted it and would be fine. I gave the injection and stood by patient (just in case) after 30 or 40 seconds he told me he felt funny, the next thing I see he slumped in chair, his head dropped back and his eyes rolled to back of his head, he had a mild seizure, body jerking for a few seconds then stopped, he started to come around but then passed back out and had mild seizure again. Patient came to again and stayed awake. He stated that he had a similar reaction when giving blood. EM T came and took care of him, his heart rate was 30 as he was coming to. He was advised to go to hospital but refused. Girlfriend came and picked him up. I called him today and he said he was tired but felt better and even went to the gym.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- Tests were whatever EMT's performed, we did check him with BP monitor and found heart rate to be 30
- Aktuelle Erkrankungen
- None reported
- Vorgeschichte
- None reported
- Andere Medikamente
- N/A
- Allergien
- Biaxin is the only thing reported
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 24.11.2021
- Impfdatum
- 24.11.2021
- Beginn
- 24.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Condition aggravated
Syncope
Symptomtext
Patient fainted about ten minutes after vaccine administration.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- FAINTS AT SIGHT OF NEEDLES
- Vorherige Impfungen
- fainting, feeling dizzy
- Staat
- PA
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 24.11.2021
- Impfdatum
- 22.11.2021
- Beginn
- 23.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Electrocardiogram normal
Head injury
Loss of consciousness
Physical examination
Symptomtext
COMPLAINED HE FELT DIZZY UPON WAKING, THEN LOSS OF CONSCIOUSNESS MORNING AFTER VACCINE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- EXAMINED BY A PROVIDER. SMALL LACERATION TO HIS HEAD. VITAL SIGNS STABLE. EKG WITHIN NORMAL LIMITS. MUCUS MEMBRANES DRY.
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- MODERATE PERSISTANT ASTHMA DEPRESSIVE DISORDER SOCIAL ANXIETY DISORDER HYPERLIPIDEMIA
- Andere Medikamente
- ATORVASTATIN DULOXETINE MIRTAZAPINE VITAMIN D3 XOPENEX MDI
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 24.11.2021
- Impfdatum
- 22.11.2021
- Beginn
- 23.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Nausea
Syncope
Vomiting
Symptomtext
COMPLAINED OF UNWITNESS SYNCOPAL EPISODE WITHOUT INJURY, NAUSEA, AND VOMITING LIQUID EMESISX2.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- VITAL SIGNS STABLE DAY OF REPORTED EVENT
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- MIGRAINES HCV
- Andere Medikamente
- BUPRENORPH/NALOX DOCUSATE SODIUM FLUOXETINE ICY HOT BALM OXYCARBAZEPINE PAIN RELIEVER PLUS TRAZODONE
- Allergien
- BEES CASHEWS PEANUTS NO KNOWN DRUG ALLERGY
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 22.11.2021
- Impfdatum
- 22.11.2021
- Beginn
- 22.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Loss of consciousness
Pallor
Tremor
Symptomtext
Soon after administering the vaccine, patient felt dizzy and sat on the floor. He may have passed out for a couple seconds and upon calling out his name he responded and mentioned that he has this kind of a reaction during blood draws. The patient failed to mention that to me before I gave him the vaccine. He came around and then his arm started to shake as well and he turned very pale at which point we called 911. But within a few seconds he started feeling better and said he was fine and to cancel 911 but they were already on their way.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 19.11.2021
- Impfdatum
- 19.11.2021
- Beginn
- 19.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood glucose normal
Disorientation
Dizziness
Nausea
Syncope
Symptomtext
Pt received 2nd dose J&J vaccine 11/19/21 in right arm, stood to walk towards entrance, got dizzy, and fainted. No witness was able to see if pt hit her head. Pt was disoriented for less than 30 seconds, EMS called. BP was 142/98 laying down at 1615. Pt was A&Ox4, reported nausea, pupils equal and reactive bilaterally. Blood sugar 93 at 1618. EMS arrived at 1623 and assumed care, advised pt and mother I recommend she be evaluated at ER d/t unknown if pt hit her head. Pt refused ER evaluation. Mother and pt educated on warning signs of concussions as well as declining neurological symptoms that warrant immediate medical attention.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- history of syncope with blood draws
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 15.11.2021
- Impfdatum
- 15.11.2021
- Beginn
- 15.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cold sweat
Hyperhidrosis
Loss of consciousness
Pallor
Vomiting
Symptomtext
patient sat down and was very out of it and swaying. pale and clammy very sweaty, passed out put him on the floor and put cold bottle on face his pulse remained steady. finally was coherent did call emergency number the ambulance came and he vomited before he left the building very non coherent at first
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none im aware of
- Vorgeschichte
- none im aware of
- Andere Medikamente
- non im aware of
- Allergien
- none im aware of
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 15.11.2021
- Impfdatum
- 15.11.2021
- Beginn
- 15.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Hypotonia
Paraesthesia
Paraesthesia oral
Syncope
Symptomtext
Post-vaccination, patient was waiting in pharmacy. Husband was standing, and she was sitting. Husband reported that patient slumped head to the side and was demonstrating syncope. Immunizing pharmacist stabilized patient on floor pad, and she took vitals. Patient's blood pressure and temperature were normal, and patient was alert and answering questions. She reported that she had "tingling" in her lips and arms. Local EMS responders arrived and transported patient for medical evaluation at local hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- Unknown
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown medical history
- Andere Medikamente
- ESCITALOPRAM 10MG TAB, BUPROPION XL 150MG TAB
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 15.11.2021
- Impfdatum
- 15.11.2021
- Beginn
- 15.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood glucose decreased
Hyperhidrosis
Nausea
Syncope
Vomiting
Symptomtext
we gave a Janssen Covid imz (1st dose) to the pt. Pharmacy Immunizing tech gave the IMZ. After receiving the IMZ, the pt was seated in the pharmacy area waiting the 15 minutes as instructed. Tech noticed the pt was on the floor and he went out to assist the pt. As tech was helping the pt I went to assist and asked the pt if he needed us to call an ambulance and he said no. We gave him some water and he said he felt like he had low blood sugar so we gave him some candy to eat. After eating the candy and drinking a couple glasses of water he said he felt like nauseated. I brought out a trash can to give to the pt and he threw up a little. I did notice he had some sweat on his forehead and the pt was wearing a winter hat and a jacket so the fainting could have been because he was overheated or a combination of low blood sugar and being over heated. Store management did come around and asked if teh pt needed an ambulance. The pt stayed in the pharmacy area for about 15 minutes and he regained composure. He had called someone to ask for a ride. I went out again to make sure he was allright and he said his ride was here to pick him up and he left.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none that I am aware of
- Vorgeschichte
- none that I am aware of
- Andere Medikamente
- none that I am aware of
- Allergien
- codiene
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 0,6
- Geschlecht
- M
- Eingang
- 14.11.2021
- Impfdatum
- 14.11.2021
- Beginn
- 14.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syncope
Symptomtext
PATIENT FAINTED ABOUT 5 MINUTES AFTER RECIEVING SHOT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 14.11.2021
- Impfdatum
- 06.11.2021
- Beginn
- 06.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Erythema
Pain in extremity
Superficial vein thrombosis
Ultrasound Doppler
Symptomtext
Pt reports onset of R thigh erythema and pain approximately 5 hours after receiving J&J COVID-19 booster dose. Pt was seen in the ER and diagnosed with superficial thrombophlebitis in a small branch of the greater saphenous vein in the right thigh. She was treated with ibuprofen and heat. Of note, she does have a history of superficial thrombophlebitis of her left leg that was diagnosed January 2021. Symptoms at that time were not associated with COVD-19 vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Superficial vein thrombosis
- Hospital-Tage
- -
- Labordaten
- Duplex US of R leg - 11/7/2021
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- Hyperlipidemia Esophageal reflux Esophageal spasm Osteopenia
- Andere Medikamente
- calcium citrate 500mg daily vitamin D daily (unknown dose) vitamin B12 500mcg daily Cartia XT 120mg daily Prilosec 20mg BID prn
- Allergien
- Bactrim - rash, hives Macrobid - rash Ampicillin -rash
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 14.11.2021
- Impfdatum
- 13.11.2021
- Beginn
- 13.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fear of injection
Hypotension
Syncope
Symptomtext
PATIENT FAINTED . PARAMEDICS WERE CALLED. PT HAD LOW BLOOD PRESSURE AT SCENE . BLOOD PRESSURE RETURNED TO NORMAL WITHIN 30 MINUTES. PATIENT DID NOT GO TO ER. PER PATIENT HE IS REALLY AFRAID OF INJECTIONS AND HE ATTRIBUTED THE FAINTING TO HIS FEAR. TWENTY FOUR HOURS AFTER EVENT PATIENT SAYS HE IS FINE WITH NO ADDITIONAL SYMPTOMS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 11.11.2021
- Impfdatum
- 11.11.2021
- Beginn
- 11.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syncope
Symptomtext
5 minutes into the 15-minute observation period patient fainted; after using the ice pack patient slowly felt better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- No.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- No
- Andere Medikamente
- None
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 11.11.2021
- Impfdatum
- 09.11.2021
- Beginn
- 09.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Flushing
Head titubation
Hyperhidrosis
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Fainting / Unresponsive-Mild, Systemic: Flushed / Sweating-Mild, Additional Details: Patient stated "I think I'm gonna pass out" 1 minute after Janssen COVID19 vaccine injection. Pt sitting down, fainted with head drop x 10 seconds. Raised up head and opened eyes after 10 seconds, was fully responsive. Noticed to be diaphoretic and flushed face that lasted for about 5 minutes. Vital signs remained normal throughout. After 5 minutes, diaphoresis and face flushing resolved completely. After 20 mins of observation, pt was able to drive home safely.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 10.11.2021
- Impfdatum
- 10.11.2021
- Beginn
- 10.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pallor
Syncope
Unresponsive to stimuli
Symptomtext
He did fine getting the vaccine then he fainted in chair. I called out for help ,we tried to arouse pt and called code white in store. He stayed in chair we kept trying to get him to respond and he continued to not respond. We were about to prepare epi-pen and when still not responding we had them call 911. We were trying to reach for getting a pulse and trying to rouse him, he was white in face. Then he opened his eyes and started to repsond to our questions. The squad arrived and checked his blood pressure. We gave him cool compress and when he was feeling better he asked for some water. squad said he was fine. He sat a little bit and stood awhile then he left and was okay.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- blood pressure check-fine per squad members
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no, has had fainting before with vaccinations
- Andere Medikamente
- na
- Allergien
- augmentin, cipro
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 10.11.2021
- Impfdatum
- 07.11.2021
- Beginn
- 07.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hypotension
Syncope
Symptomtext
Patient fainted after receiving the immunization
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- patient found to have low blood pressure when evaluated by EMS
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- uknown
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 09.11.2021
- Impfdatum
- 09.11.2021
- Beginn
- 09.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syncope
Symptomtext
patient fainted: ambulance was called-determined patient was ok-patient left with husband
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none known
- Vorgeschichte
- none known
- Andere Medikamente
- unknown
- Allergien
- pcn
- Vorherige Impfungen
- same reaction during blood draw
- Staat
- VA
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 08.11.2021
- Impfdatum
- 08.11.2021
- Beginn
- 08.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Chills
Dizziness
Syncope
Symptomtext
FAINTED, DIZZINESS, CHILLS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 08.11.2021
- Impfdatum
- 08.11.2021
- Beginn
- 08.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Fall
Syncope
Symptomtext
Patient stood up to walk. Fainted and fell. This was about 5-7 minutes post-vaccine. Patient was taken to hospital by ambulance after stabilized and having vitals taken.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 08.11.2021
- Impfdatum
- 08.11.2021
- Beginn
- 08.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syncope
Symptomtext
Pt had syncopal episode 5 minutes after vaccine admin while sitting in chair. Pt reports being nervous prior to vaccine administration. Bp monitored. 911 called per protocol. Pt declined EMS transport. Walking and talking when leaving clinic after being observed by nurses and EMS staff onsite.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Denies any past medical history or illnesses
- Vorgeschichte
- Denies any previous medical history
- Andere Medikamente
- Denies use
- Allergien
- Denies any allergies
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 07.11.2021
- Impfdatum
- 07.11.2021
- Beginn
- 07.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Hyperhidrosis
Syncope
Symptomtext
PATIENT WAS FINE AT THE TIME OF INJECTION. AFTER 5 MINUTES, PATIENT FELL OFF HIS CHAIR. HE WAS WAKE AND ALERT WITH NO BREATHING ISSUE. 911 WAS CALLED. AFTER 5 MINUTES MEDIC CAME AND TOOK HIS VITALS. HIS VITALS WERE ALL NORMAL. PATIENT WAS SWEATING AND WAS ADVISED BY TO SEEK FURTHER EVALUATION AT THE EMERGENCY ROOM. HE AGREED TO SEEK FURTHER EVALUATION AND LEFT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- NO MEDICAL CONDITION
- Vorgeschichte
- NONE
- Andere Medikamente
- N/A
- Allergien
- NO KNOWN ALLERGY
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 07.11.2021
- Impfdatum
- 07.11.2021
- Beginn
- 07.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Blood glucose increased
Feeling cold
Hyperhidrosis
Loss of consciousness
Pallor
Vision blurred
Symptomtext
At 15:10 providers were alerted to situation by wife. Pt. had loss of consciousness. Pt was pale, cool, diaphoretic. He was rousable to stimulation. Pt has HR of 48, O2 of 80, He had respirations of 8 with his head lolling on his shoulder, and his mouth open and deep breaths. A&O was 2 times person and place. With prompting from the paramedic on scene he was able to rouse himself. Upon second assessment at 15:19 he stated he had blurry vision, and was A&O x4. BP was 130/90, O2 90, HR 96. Paramedics were called to scene where they were able to asses BS at 113. Hx from wife Pt diagnosed in 1996 with Diabetes II. He is chronically untreated, and has not seen any MD since 2006. Pt. does not use a BS test kit, and will not check his own sugar. He goes by a "feeling" which he uses to tell him when to eat or not. Per wife pt often appears pale, cool, and diaphoretic. They recommended pt be transported by ambulance to ED to be assessed by physician. Pt. refused and signed out AMA. Paramedics departed scene without pt. 15:40. Paramedics recommended pt stay and be monitored for 15 minutes. Pt.departed scene at 1550. Pt. departed scene AMA. All providers on scene recommended pt. see a specialist for his chronically untreated diabetes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- Blood Glucose 1521: 113
- Aktuelle Erkrankungen
- Diabetes, possible thyroid condition
- Vorgeschichte
- diabetes
- Andere Medikamente
- NA
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 07.11.2021
- Impfdatum
- 07.11.2021
- Beginn
- 07.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Syncope
Symptomtext
patient said he was feeling light-headed and like he was going to pass out, he started sliding out of the chair the pharmacist was able to catch his head so it didnt hit the floor. He was unconscious for about 5 seconds, when he woke back up he wanted to lay there for a few minutes. we got him a water and called 911 immediately
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- no known drug allergies
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 05.11.2021
- Impfdatum
- 04.11.2021
- Beginn
- 04.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Loss of consciousness
Musculoskeletal stiffness
Panic attack
Vomiting
Symptomtext
After administering the 2 vaccines for the patient (covid vaccine and Flu vaccine) the patient stated she feel dizzy and gonna stay in the immunization room till she feels better, then she started to have body stiffness and like black out for 45 seconds , I held her not to fall and injure herself . the pharmacy associates called ambulance and called for code white. customer was still alert , I put her on the floor on her side as instructed by ambulance team .she started vomiting, I cleaned her mouth and made sure she can breath. the ambulance team came, she was alert and communicated with them. they identified the situation as panic attack. the customer stayed in the immunization room with a member of management to take her statement till someone of family members came for her.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- not known
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 04.11.2021
- Impfdatum
- 04.11.2021
- Beginn
- 04.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syncope
Symptomtext
Pt had syncopal episode post administration. Prior to administration, we had discussions with pt. Pt disclose having a history of passing out the past vaccines he had years ago. Upon administering, pt and I was talking and he said he was fine, no symptoms. A few minutes passed and he asked for some water. I went back into the pharmacy being it was a few minutes and he looked and seem fine, upon returning to vaccination booth, pt was found on the floor. Less than 15 seconds was passed. Pt became alert and oriented and was aware he had "passed out". We gave powerade, ice pack, and did some assessments, and patient stated feeling fine. We had him sit for additional 15 mint (30 min total) and he had no episode and he stated feeling fine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- No labs were done, But did verbal assessment on side effects, checked physical and no apparent bruise, cuts, or injury. Checked pupils and they were reactive and intact. No adverse reaction reported
- Aktuelle Erkrankungen
- Pt has Hx of syncope on previous immunizations
- Vorgeschichte
- No known Hx, but pt was aware he had a hx of syncope with vaccines
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 03.11.2021
- Impfdatum
- 03.11.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Loss of consciousness
Symptomtext
Patient lost consciousness for around 30 seconds. Patient remained seated and was not injured.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- Has fainted in the past following immunizations.
- Staat
- TX
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 01.11.2021
- Impfdatum
- 01.11.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Balance disorder
Dizziness
Fall
Haemorrhage
Hyperhidrosis
Loss of consciousness
Nausea
Neck injury
Pallor
Skin abrasion
Syncope
Visual impairment
Symptomtext
Patient fainted during the 15 minute waiting period after vaccination of primary dose of Janssen. Patient stood up from the waiting chair and got dizzy and lost his balance and spun around and fell into the 4 way display. The back of his neck scraped one of the shelves as he fell and the skin was scraped with faint amount of blood appearing. Patient fell to the ground but did not hit his head. Patient's mother was with him and helped him get off the floor. When I arrived to the patient I checked for any injury and verified that he was ok to sit down, then I got him a cold ice pack to apply to his face and neck. Patient had syncope with paleness, sweating, nausea, dizziness, brief loss of consciousness with visual disturbance. I advised patient to lie down on their back and elevate their feet. Patient rested in the waiting area for another 15 minutes and I continued to check on him until he felt better to leave. His parents helped him walk out of the store and said they would drive him home and not let him drive himself.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- avacado
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 31.10.2021
- Impfdatum
- 31.10.2021
- Beginn
- 31.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Loss of consciousness
Syncope
Symptomtext
Patient came in to get booster covid shot. She stated that last time she received the covid vaccination, she passed out for 10 seconds. The EMT was present on site where it was a drive thru clinic. The EMT concluded that her fainting was more of the summer heat vs the vaccination. Based on the information provided, I moved forward with the vaccination. Post shot, I asked her to stay at the vaccination booth and not to stand. Her companion was getting her water and a candy bar. I asked mutilple time was she feeling okay. She replied yes. I stepped away and the technician on duty went over. The technician observed and asked was she feeling okay where the same response was given, yes. The tecnician stepped away and 20 seconds later, a collapse was heard. I ran towards her to find her laid out on the floor unconscious. I tapped on her continuously for 20 seconds and she then responded. ED was called and arrived about 10 minutes later. They asked her a few questions and asked her to slowly stand. She stated she was fine so EMT left. Event Details
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- Patient stated that she faited for 10 seconds during a drive thru clinic when getting her first Covid vaccine.
- Staat
- NY
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 31.10.2021
- Impfdatum
- 31.10.2021
- Beginn
- 31.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Flushing
Syncope
Symptomtext
Patient fainted a few minutes after receiving the vaccine. He was sitting in a chair and did not fall. He felt dizzy and flushed afterward. He was seated for about 10 minutes until he felt better. He had a sip of water after feeling better and left the store. Upon, follow-up, he was sleeping at home but mother reported him to be feeling much better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 30.10.2021
- Impfdatum
- 30.10.2021
- Beginn
- 30.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cold sweat
Dizziness
Immediate post-injection reaction
Loss of consciousness
Musculoskeletal stiffness
Mydriasis
Nausea
Pallor
Panic attack
Respiratory rate increased
Vomiting
Symptomtext
Immediately after receiving the vaccine, the patient showed symptoms of acute panic attack. Pupils were dilated, skin turned pale and clammy, complains of lightheadedness and nauseas. Patient did loose consciousness for less than 1 minute, body went a little stiff during that time. The patient regained consciousness after about 1 min, showing increased respiratory rate and breathing, followed by throwing up for 10-15 minutes. No medication were administered to the patient. After about 30 minutes, the patient was feeling better and was able to leave by himself.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- history of passing out with needles
- Vorherige Impfungen
- unknown to the patient, it was over 10 years ago
- Staat
- NY
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 29.10.2021
- Impfdatum
- 29.10.2021
- Beginn
- 29.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syncope
Symptomtext
Patient fainted after vaccine. He stated it was common for him to faint after vaccines.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- NA
- Allergien
- None
- Vorherige Impfungen
- Fainting, NA
- Staat
- KY
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 28.10.2021
- Impfdatum
- 28.10.2021
- Beginn
- 28.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Syncope
Symptomtext
Patient fainted post vaccination
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- na
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- unknown
- Andere Medikamente
- na
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 28.08.2023
- Impfdatum
- 29.11.2021
- Beginn
- 28.01.2022
- Tage bis Beginn
- 60,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
COVID-19 pneumonia
Dyspnoea
SARS-CoV-2 test positive
Symptomtext
COVID+ 8 days PTA, arrived with worsening SOB. Admit for COVID pna. Recieved O2, steroids, vit-c, vit-d, zinc, IV zithromax, Baricitinib. Progressed to Airvo. Outside of treatment window for remdesivir. DC home on RA.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19 pneumonia
- Hospital-Tage
- 8,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 14.08.2023
- Impfdatum
- 15.11.2021
- Beginn
- 04.08.2023
- Tage bis Beginn
- 627,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Chest discomfort
Dyspnoea
SARS-CoV-2 test positive
Symptomtext
She presented to the emergency department with shortness of breath and chest pressure. Symptoms have been occurring last 2 days. According to the patient she tested positive for COVID-19 -received doxycycline to cover possible superimposed bacterial pneumonia. -received dexamethasone. added pantoprazole 40 mg daily GI prophylaxis while on high-dose steroids
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- hypertension, hyperlipidemia, Pulmonary embolus
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 06.06.2023
- Impfdatum
- 28.03.2021
- Beginn
- 20.06.2022
- Tage bis Beginn
- 449,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood alcohol increased
Blood potassium decreased
COVID-19
Chest X-ray normal
Chest pain
Dyspnoea
Electrocardiogram normal
Fibrin D dimer normal
Pleuritic pain
SARS-CoV-2 test positive
Vaccine breakthrough infection
Viral infection
Symptomtext
BREAKTHROUGH COVID: FULLY VACCINATED COVID POSITIVE WITH BOOSTER. COVID-19 VIRAL SYNDROME WITH PLEURITIC CHEST PAIN AND SOB. NO HYPOXIA, MONITORED CLINICALLY.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Afebrile, VSS. K 3.3. Etoh 231. EKG: no acute STE/STD, d-dimer WNL,CXR without issues
- Aktuelle Erkrankungen
- UNKNONWN
- Vorgeschichte
- ETOH abuse, anxiety and depression
- Andere Medikamente
- UNKNOWN
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 31.05.2023
- Impfdatum
- 27.03.2021
- Beginn
- 08.07.2022
- Tage bis Beginn
- 468,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood potassium normal
Blood sodium normal
COVID-19
Carbon dioxide normal
Cerebral small vessel ischaemic disease
Chest pain
Computerised tomogram head abnormal
Cough
Fibrin D dimer
Haemoglobin normal
Headache
Liver function test normal
Oropharyngeal pain
Pain
Platelet count normal
Troponin
Vaccine breakthrough infection
White blood cell count decreased
Symptomtext
BREAKTHROUGH COVID: FULLY VACCINATED 63 YO WITH ACUTE COVID AND CHEST PAIN. PT history of CAD, cardiac stent in 2015, hypertension, hyperlipidemia who presents to the ER on July 8, 2022 for chest pain. He was diagnosed with COVID 2 days prior at home. He stated that he had chest pain when moving from side to side. He denied shortness of breath but did admit to cough. He admitted to sore throat. He also admitted to headache. He denied lightheadedness or dizziness. No syncope. No vision changes. No numbness. NO COVID MEDICATIONS PRESCRIBED DURING ADMISSION, ASPIRIN AND ALBUTEROL.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- temperature was 98.6? F, heart rate 90. Satting 97% on room air. Blood pressure 154/88. White count 6.1, hemoglobin 15.1, platelets 154. D-dimer 0.4. Sodium 137, potassium 4 potassium 4.2 CO2 23. Liver panel within normal limits. High sensitivity troponin was negative at 7.CT head was performed which showed:1. No mass effect, hemorrhage or large hypodensity to suggest territorial ischemia.2. Age-related involutional changes of the brain and white matter changes of chronic microvascular ischemia.
- Aktuelle Erkrankungen
- UNKNONWN
- Vorgeschichte
- CAD, Hypercholesterolemia with hypertriglyceridemia
- Andere Medikamente
- UNKNOWN
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 04.05.2023
- Impfdatum
- 24.03.2021
- Beginn
- 25.08.2021
- Tage bis Beginn
- 154,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
C-reactive protein increased
Condition aggravated
Impaired gastric emptying
Inflammation
Inflammatory marker increased
Interleukin level increased
Laboratory test abnormal
Rheumatoid arthritis
Symptomtext
New onset of gastroparesis and flare of her RA; Inflammation with high inflammatory markers il-6 and hs-crp
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- 8/25/2021 hs-CRP 4.9, IL-6 is 15, 12/6/2021 Gastric Emptying Study showed delay emptying, 2/22/2022 hs-CRP 6.1, 2/28/2022 IL-6 13.8, 9/14/2022 IL-6 6.4
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Hypothyroidism, Hyperlipidemia, Osteoarthritis Local Primary Hand, Rheumatoid Arthritis, Cervical Disc Degeneration, Actinic Keratosis, Paroxysmal Atrial Fibrillation, Chronic Gastrointestinal Hemorrhage, Liver Enzymes Abnormal, Vitamin Deficiency,
- Andere Medikamente
- Traumeric magnesium Orthomega (fish oil) cyclobenzaprine Phytomulti w/o iron gabapentin DHEA protodophilus Methyl B Complex oxycodone-acetaminophen SPM active CoQ10 Methyl B12 Spectrazyme FOLID ACID tramadol estrocleanse III Zenpep methotre
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 18.02.2023
- Impfdatum
- 23.01.2022
- Beginn
- 14.12.2022
- Tage bis Beginn
- 325,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Angiogram pulmonary
Angiogram pulmonary abnormal
COVID-19
Cerebral artery occlusion
Cerebral small vessel ischaemic disease
Computerised tomogram
Computerised tomogram head
Dysphagia
Encephalopathy
Fall
Hypoxia
Lacunar infarction
Magnetic resonance imaging
Metabolic encephalopathy
Pneumonia
Polymerase chain reaction
SARS-CoV-2 test
SARS-CoV-2 test positive
Symptomtext
CEREBRAL ARTERY OCCLUSION; ENCEPHALOPATHY; CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE; HYPOXIA; ENCEPHALOPATHY; METABOLIC ENCEPHALOPATHY; HYPOXIA; SEPSIS; LACUNAR INFARCTION; COVID-19; METABOLIC ENCEPHALOPATHY; STENOSIS; PNEUMONIA; DYSPHAGIA; SEPSIS; ANGIOGRAM PULMONARY ABNORMAL; COVID-19; CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE; STENOSIS; STAPHYLOCOCCUS TEST NEGATIVE; DYSPHAGIA; LACUNAR INFARCTION; FALL; PNEUMONIA; ANGIOGRAM PULMONARY ABNORMAL; CEREBRAL ARTERY OCCLUSION; SARS-COV-2 TEST POSITIVE; FALL; STAPHYLOCOCCUS TEST NEGATIVE; SARS-COV-2 TEST POSITIVE; This spontaneous report received from a health care professional by a Regulatory Authority VAERS (Vaccine Adverse Event Reporting System) concerned an 85 year old female of an unspecified race and ethnicity. The patient's height, and weight were not reported. The patient's past medical history included: supraventricular tachycardia, chronic diastolic congestive heart failure (history of heart failure with preserved ejection fraction), left displaced femoral neck fracture, sp fixation (spinous process), multiple CVA (Cerebrovascular accident), tobacco abuse, recurrent UTI's (Urinary tract infection), uncontrolled hypertension, and covid-19, and concurrent conditions included: cerebrovascular small vessel disease, essential primary hypertension, bilateral carotid artery stenosis, mild aortic stenosis, peripheral vascular disease unspecified, digestive ileus, rectal prolapse, recurrent clostridium difficile diarrhea, small bowel obstruction, dysphagia (oropharyngeal phase), gastro-esophageal reflux disease (without esophagitis), endocrine hypothyroidism unspecified, psychological severe vascular dementia (without behavioral disturbance, psychotic disturbance, mood disturbance or anxiety unspecified, dementia unspecified, severity without behavioral disturbance psychotic disturbance, mood disturbance and anxiety), respiratory interstitial lung disease, pneumonia unspecified organism, urinary chronic kidney disease stage 3 unspecified, urinary retention, acute kidney injury, dyslipidemia, unintentional weight loss, cigarette nicotine dependence in remission, anemia unspecified, epigastric hernia, vitamin d deficiency, dizziness, constipation, debility, protein-calorie malnutrition, hyponatremia (Frail elderly), muscle weakness generalized, polyosteoarthritis unspecified, cardiac pacemaker, restless legs syndrome, and allergies to statins (HMG-CoA Reductase Inhibitors (Muscle Symptoms)), and other pre-existing medical conditions included: The patient need assistance with personal care. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 213D21A and expiry: Unknown) dose was not reported, 1 total, dose 1 was administered on 23-JAN-2022 for an unspecified indication. Age at time of vaccination 85 years old. No concomitant medications were reported. On 14-DEC-2022, the patient presented with acute encephalopathy and a fall. Encephalopathy was likely multifactorial secondary to COVID (covid-19), hypoxia and baseline dementia (likely at baseline not even able to know her own birthday, dependent for ADLs (activities of daily living)), also experienced metabolic encephalopathy secondary to COVID, hypoxia, sepsis, cerebral artery occlusion, cerebral small vessel ischaemic disease, lacunar infarction, pneumonia (possible aspiration versus superimposed community-acquired), stenosis, dysphagia (failing swallow secondary to dysphagia) and was hospitalized (date unspecified) with covid complications and positive PCR (Polymerase chain reaction). Laboratory data included: Angiogram pulmonary abnormal, SARS-CoV-2 test Positive, Staphylococcus test Negative and PCR Positive (Covid Detected). Laboratory data (dates unspecified) included: Brain CT (Computerised tomogram) no acute process, Computerised tomography (CTA) right internal bulb 70% stenosis multifocal intracranial stenosis P2 segment occlusion on right, MRI (Magnetic resonance imaging) shown old lacunars chronic small vessel ischemia, Methicillin-resistant staphylococcal aureus test Negative. It was reported that the patient was continued with ASA ( acetylsalicylic acid) and as per Neuro recommendations. COVID-19 with hypoxia-resolved at the time of reporting patient was weaned to room air. The patient was hospitalized for 10 days. Treatment medications (dates unspecified) included: vancomycin (vancomycin discontinued as Methicillin-resistant staphylococcal aureus test was negative), acetylsalicylic acid, cefepime for 5 days, remdesivir for 5 days, and dexamethasone for 10 days. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from cerebral artery occlusion, cerebral small vessel ischaemic disease, encephalopathy, hypoxia, lacunar infarction, metabolic encephalopathy, pneumonia, sepsis, covid-19, stenosis, dysphagia, fall, angiogram pulmonary abnormal, sars-cov-2 test positive, and staphylococcus test negative. This report was serious (Hospitalization Caused / Prolonged). This report was associated with a product quality complaint 90000270394. The suspected product quality complaint has been confirmed to be the reported allegation could not be determined. A manufacturing related root cause could not be identified based on the PQC evaluation/investigation performed. Additional information received from Central Complaint department on 16-FEB-2023. The following information was updated and incorporated into the case narrative: Product quality complaint investigation result.; Sender's Comments: V1: This follow up adds information about Product quality complaint investigation result. This does not alter previous causality assessment of the reported events. 20230212621-cerebral artery occlusion, cerebral small vessel ischaemic disease, lacunar infarction, encephalopathy, metabolic encephalopathy, pneumonia, sepsis, stenosis, dysphagia. 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: MEDICAL HISTORY. Therefore, this event is considered inconsistent with vaccine administration. 20230212621-angiogram pulmonary abnormal, fall, staphylococcus test negative. The event has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event. Therefore, the WHO Causality is considered indeterminate. The company causality is considered unassessable. 20230212621-hypoxia, covid-19, sars-cov-2 test positive. The event is deemed to be scientifically implausible, i.e., there is scientific evidence against a drug/event relationship; AND there is no known class effect. Therefore, this event is considered inconsistent with vaccine administration.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pneumonia
- Hospital-Tage
- 10,0
- Labordaten
- Test Date: 20221214; Test Name: ANGIOGRAM PULMONARY; Result Unstructured Data: abnormal; Test Date: 20221214; Test Name: SARS-COV-2 TEST; Test Result: Positive; Test Date: 20221214; Test Name: STAPHYLOCOCCUS TEST; Test Result: Negative; Test Date: 20221214; Test Name: PCR; Test Result: Positive; Comments: Covid Detected; Test Name: CT BRAIN; Result Unstructured Data: no acute process; Test Name: CTA; Result Unstructured Data: right internal bulb 70% stenosis multifocal intracranial stenosis P2 segment occlusion on right; Test Name: MRI; Result Unstructured Data: old lacunars chronic small vessel ischemia; Test Name: MRSA PCR; Test Result: Negative.
- Aktuelle Erkrankungen
- Acute kidney injury; Anemia, unspecified; Aortic stenosis; Artificial cardiac pacemaker user; Carotid artery stenosis; Cerebral small vessel disease; Chronic kidney disease stage 3; Constipation; Debility; Diarrhea, Clostridium difficile; Dizziness; Drug allergy (HMG-CoA Reductase Inhibitors (Muscle Symptoms)); Dyslipidemia; Dysphagia (oropharyngeal phase); Epigastric hernia; Essential hypertension; Gastroesophageal reflux (without esophagitis); Hyponatremia (Frail elderly); Ileus; Interstitial lung disease; Muscle weakness; Nicotine dependence; Osteoarthritis; Peripheral vascular disease; Pneumonia, organism unspecified; Protein-calorie malnutrition; Rectal prolapse; Restless legs syndrome; Small bowel obstruction; Unintentional weight loss; Unspecified hypothyroidism; Urinary retention; Vascular dementia (without behavioral disturbance, psychotic disturbance, mood disturbance or anxiety unspecified, dementia unspecified, severity without behavioral disturbance psychotic disturbance, mood disturbance and anxiety); Vitamin D deficiency
- Vorgeschichte
- Medical History/Concurrent Conditions: Congestive heart failure (History of heart failure with preserved ejection fraction); COVID-19; CVA; Femoral neck fracture; Fracture repair (spinous process fixation); Supraventricular tachycardia; Tobacco abuse; Uncontrolled hypertension; UTI; Comments: The patient need assistance with personal care
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 14.02.2023
- Impfdatum
- 04.02.2022
- Beginn
- 11.02.2022
- Tage bis Beginn
- 7,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Electrocardiogram abnormal
Heart rate increased
Heavy menstrual bleeding
Palpitations
Ultrasound scan vagina normal
Symptomtext
I received the booster on 2/4/22 and one week later I began to have menstrual bleeding like crazy. I had not had this type of bleeding for many months. I went to the doctor and my ultrasound was negative and it was probably a side effect from the vaccine. I also began to have heart palpitations. I wore a heart monitor for two weeks. The palpitations have happened ever since dose 2. My heart rate increased according to my smart watch. The palpitations would happen occasionally one after another, but sometimes they were spread apart. I will have an Ultrasound of the heart next week.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- Vaginal ultrasound, normal, January 2023; EKG, abnormal, December 2022
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Crohn's Disease; Hidradenitis; Reynard's Syndrome; Guillain-Barre Syndrome
- Andere Medikamente
- I carry an EPIPEN for allergic reactions.
- Allergien
- Hair dye; peanuts; shellfish; bee stings; penicillin
- Vorherige Impfungen
- 2009, 43 years old, Flu shot, numbing and partial paralysis is my legs and was diagnosed with Guillain-Barre Syndrome at that ti
- Staat
- MI
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 03.02.2023
- Impfdatum
- 13.11.2021
- Beginn
- 28.01.2023
- Tage bis Beginn
- 441,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Aortic valve incompetence
COVID-19
Dyspnoea
Echocardiogram abnormal
Ejection fraction abnormal
Hypoxia
Lactic acidosis
Mitral valve incompetence
SARS-CoV-2 test positive
Troponin increased
Symptomtext
Admission Date: 1/28/2023 Discharge Date: Jan 30, 2023 PRESENTING PROBLEM: Elevated troponin HOSPITAL COURSE: The patient is a 67 y.o. female with past medical history significant for nonischemic cardiomyopathy, diet controlled DMT2, PVD who present to the ED on 01/27/2023 with shortness of breath. Patient found to have hypoxia from mild CHF, lactic acidosis and was COVID positive. She also had elevated troponin that increased to 120. She improved quickly while still at the hospital but was transferred to another hospital for Cardiology consult and echo. Echo showed worsening EF of 30 along with moderate mitral regurgitation and aortic regurgitation. Cardiology recommended cardiac MRI and right heart catheterization but due to active COVID plan to arrange as outpatient. She was discharged on Lasix 40 mg daily with close cardiology follow-up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Diverticulitis of large intestine with abscess without bleeding Atherosclerosis of artery of right lower extremity Primary osteoarthritis of left knee HLD (hyperlipidemia) DM2 (diabetes mellitus, type 2) Chronic pain Tobacco abuse Cardiomyopathy, nonischemic Mitral valve insufficiency Aortic valve insufficiency Hypertension COVID-19
- Andere Medikamente
- aspirin 81 MG enteric coated tablet carvedilol (COREG) 6.25 MG tablet furosemide (LASIX) 40 MG tablet levothyroxine (SYNTHROID) 50 MCG tablet losartan (COZAAR) 50 MG tablet pravastatin (PRAVACHOL) 20 MG tablet
- Allergien
- AtorvastatinMyalgia, Headache, Other CiprofloxacinGI Upset CodeineItching MetronidazoleGI Upset ShrimpNausea and Vomiting
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 26.01.2023
- Impfdatum
- 23.01.2022
- Beginn
- 14.12.2022
- Tage bis Beginn
- 325,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Angiogram pulmonary abnormal
COVID-19
Cerebral artery occlusion
Cerebral small vessel ischaemic disease
Dysphagia
Encephalopathy
Fall
Hypoxia
Lacunar infarction
Metabolic encephalopathy
Pneumonia
SARS-CoV-2 test positive
Sepsis
Staphylococcus test negative
Stenosis
Symptomtext
"Patient with single J+J vaccine admitted with COVID complications and positive PCR. Provider d/c note: ""Patient is a 85-year-old female with a past medical history of heart failure with preserved ejection fraction who presents with acute encephalopathy and a fall. Encephalopathy is likely multifactorial secondary to COVID, hypoxia and baseline dementia. After discussion with son, she has dementia and is likely at baseline (not even able to know her own birthday, dependent for ADLs). Family's goal is to keep patient happy at home. DC to rehab for acute rehab with hopes on having her return home after. Encephalopathy- likely at baseline Dementia Patient has well known dementia and does not always know her own birthday at baseline. She needs help with even basic care. likely multifactorial metabolic encephalopathy secondary to COVID, hypoxia, sepsis. CT brain no acute process. CTA right internal bulb 70% stenosis, multifocal intracranial stenosis, P2 segment occlusion on right MRI old lacunars, chronic small-vessel ischemia. We will continue ASA per Neuro recommendations. cefepime and Decadron also contributed COVID-19 with hypoxia-resolved Now weaned to room air unable to determine symptoms prior to 12/14 Completed remdesivir x 5 d /Decadron x 10d Pneumonia, possible aspiration versus superimposed community-acquired on top of COVID as above failing swallow secondary to dysphagia, no clear story regarding aspiration MRSA PCR negative discontinue vancomycin -completed 5 day course of IV antibiotics (cefepime)"""
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pneumonia
- Hospital-Tage
- 10,0
- Labordaten
- COVID Detected PCR on 12/14/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Cerebrovascular small vessel disease Essential (primary) hypertension Bilateral carotid artery stenosis Mild aortic stenosis SVT (supraventricular tachycardia) Peripheral vascular disease, unspecified Chronic diastolic (congestive) heart failure Digestive Ileus Rectal prolapse Recurrent Clostridium difficile diarrhea SBO (small bowel obstruction) Dysphagia, oropharyngeal phase Gastro-esophageal reflux disease without esophagitis Endocrine Hypothyroidism, unspecified Psychological Severe vascular dementia without behavioral disturbance, psychotic disturbance, mood disturbance, or anxiety Unspecified dementia, unspecified severity, without behavioral disturbance, psychotic disturbance, mood disturbance, and anxiety Respiratory Interstitial lung disease Pneumonia, unspecified organism Urinary Chronic kidney disease, stage 3 unspecified Urinary retention AKI (acute kidney injury) Other History left displaced femoral neck fracture s/p fixation History of multiple CVA Dyslipidemia History of tobacco abuse History of recurrent UTIs Unintentional weight loss History of uncontrolled hypertension Cigarette nicotine dependence in remission Anemia, unspecified Epigastric hernia Vitamin D deficiency Dizziness Constipation Debility Protein-calorie malnutrition COVID-19 History of COVID-19 Frail elderly Hyponatremia Muscle weakness (generalized) Need for assistance with personal care Polyosteoarthritis, unspecified Presence of cardiac pacemaker Restless legs syndrome
- Andere Medikamente
- -
- Allergien
- Statins-hmg-coa Reductase InhibitorsMuscle Symptoms
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 07.01.2023
- Impfdatum
- 08.12.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Arrhythmia
Cardiac monitoring
Chest pain
Dyspnoea
Electrocardiogram
Symptom recurrence
Symptomtext
chest pains starting a few days after vaccine received, along with shortness of breath. never had chest pain or shortness of breath before. this lasted two months before subsiding in severity, but these symptoms have returned periodically over the past year since I took vaccine. i have arythmia which also started after the vaccine, again never had this before.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arrhythmia
- Hospital-Tage
- -
- Labordaten
- EKG physical and ongoing (monitor)
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 23.12.2022
- Impfdatum
- 09.12.2021
- Beginn
- 13.12.2022
- Tage bis Beginn
- 369,0
- Dosis
- 1
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cardiac failure congestive
Condition aggravated
Symptomtext
Hospitalization for acute CHF exacerbation (also COVID-19 infection) on dates 12/13/22- 12/16/22. Treated with vitamin C 1,000 mg PO daily, vitamin D 25 mcg PO daily, zinc 50 mg PO daily.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- promethazine HCl
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 21.11.2022
- Impfdatum
- 04.06.2021
- Beginn
- 06.11.2022
- Tage bis Beginn
- 520,0
- Dosis
- 2
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Anxiety
COVID-19
Cough
Dyspnoea exertional
Productive cough
SARS-CoV-2 test positive
Wheezing
Symptomtext
Pt to ED 11/6 for cough. Pt COVID+ 11/6, pt denies feeling short of breath, chest pain, or in respiratory distress. 11/7 pt alert and oriented x4 with some anxiousness, on room air. 11/9 Reports productive cough that is worse at night, shortness of breath with exertion, and reports wheeze occasionally. Pt discharged 11/11.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea exertional
- Hospital-Tage
- 6,0
- Labordaten
- see above
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- C. difficile colitis Rectal polyp Acute duodenitis GIB (gastrointestinal bleeding) Rectal bleed GI bleed Fecal impaction Nausea vomiting and diarrhea Diverticulosis of large intestine without hemorrhage Anxiety disorder Mild cognitive impairment Delirium Acute renal failure Vertigo, intermittent Fracture Fracture lumbar vertebra-closed Vertebral fracture Constipation ARF (acute renal failure) Chest pain Unable to ambulate Leg edema Vulvar itching Generalized abdominal pain Abdominal pain Unable to care for self Failure to thrive in adult Rectal pain Rectum pain
- Andere Medikamente
- albuterol (PROVENTIL, VENTOLIN, PROAIR) HFA 108 (90 Base) MCG/ACT INHAL Aero Soln atorvastatin (LIPITOR) 20 MG PO Tab Cholecalciferol (VITAMIN D) 2000 units PO Tab cilostazol (PLETAL) 50 MG PO tablet citalopram (CeleXA) 20 MG PO Tab dilTIAZ
- Allergien
- Latex, codeine, sulfa antibiotics, Nickel
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 13.11.2022
- Impfdatum
- 17.02.2021
- Beginn
- 18.11.2021
- Tage bis Beginn
- 274,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Acoustic stimulation tests
Ear discomfort
Ear pain
Hyperacusis
Muscle spasms
Paraesthesia
Tinnitus
Visual impairment
Symptomtext
Leg cramps, tingling feet Tinnitus, sound sensitivity, pressure in ears, pain in ears, vision changed
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- 1,0
- Labordaten
- Hearing tests, ear and eye doctor and multiple general doctors , hospital Hospital doctors, ENT and general doctor all confirmed these life changing health issues are from the vaccine , was perfectly healthy before had not been sick in years
- Aktuelle Erkrankungen
- None , haven?t been sick in years
- Vorgeschichte
- None
- Andere Medikamente
- Aciphex (acid reflux medicine)
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 04.11.2022
- Impfdatum
- 03.11.2021
- Beginn
- 10.11.2021
- Tage bis Beginn
- 7,0
- Dosis
- 2
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test normal
Chest X-ray normal
Condition aggravated
Muscle spasms
Respiratory tract congestion
Symptomtext
After having vaccine I began having ongoing congestion and it causes the spasms in my throat to get worse. Went to walk in clinic and was prescribed cough syrup which offers varying degrees of relief. The congestion is ongoing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Blood work and chest x-ray both normal.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Meigs
- Andere Medikamente
- KLONOPIN
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 28.10.2022
- Impfdatum
- 02.08.2022
- Beginn
- 02.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood pressure measurement
COVID-19
Hypotension
Off label use
SARS-CoV-2 test
Symptomtext
CONFIRMED COVID-19 INFECTION; BLOOD PRESSURE 80/40; OFF LABEL DOSING FREQUENCY; This spontaneous report received from a patient concerned an 83 year old male. The patient's height, and weight were not reported. The patient's concurrent conditions included: non-hodgkin lymphoma (was immuno- compromised, that overproduces IGM, which is why he can't take any mRNA vaccines, "because they increase IGM), and other pre-existing medical conditions included: The patient was bedridden for different issues. The patient previously received covid-19 vaccine ad26.cov2.s (Dose number in series: 1) (suspension for injection, route of admin not reported, batch number: 1708609 and expiry: UNKNOWN) dose was not reported, 1 total, primary dose administered in right arm on 23-MAR-2021 for covid-19 prophylaxis. On an unspecified date in NOV-2021 following vaccination with primary dose of covid-19 vaccine ad26.cov2.s, the patient had covid-19 with symptoms of coughing with no temperature, no trouble breathing, no pneumonia and tested positive for COVID-19 virus test on 08-NOV-2021 (confirmed covid-19 infection and confirmed clinical vaccination failure) (Dose number in series: 1). It was also reported that patient was home quarantined for 5 days (Date unspecified). On an unspecified date in 2021, the patient experienced COPD (Chronic obstructive pulmonary disease) (Dose number in series 1) and had received treatment with Doxycycline. The patient previously received covid-19 vaccine ad26.cov2.s (Dose number in series: 2) (suspension for injection, route of admin not reported, batch number: 213D21A and expiry: UNKNOWN) dose was not reported, 1 total, first booster administered in right arm on 07-DEC-2021 for covid-19 prophylaxis. On an unspecified date in FEB-2022 following vaccination with covid-19 vaccine ad26.cov2.s (first booster), the patient experienced diarrhea and viral infection with no temperature, no trouble breathing, and tested positive for COVID-19 virus test which was confirmed covid-19 infection and confirmed clinical vaccination failure (Dose number in series: 2). Laboratory data included: COVID-19 virus test Positive. The patient received covid-19 vaccine ad26.cov2.s (Dose number in series 3) (suspension for injection, route of admin not reported, batch number: 213D21A expiry: UNKNOWN) dose was not reported, 1 total, second booster administered at right arm on 02-AUG-2022 for covid-19 prophylaxis which was associated with Off label dosing frequency. Age at time of vaccination 83 years old. Concomitant medications included influenza vaccine for prophylactic vaccination. On 17-AUG-2022, the had the symptoms of diarrhea, temperature, vomiting, went in to the ER where his blood pressure 80/40 and was hospitalised from 17-AUG-2022 to 19-AUG-2022 (Dose number in series 3). The covid-19 virus test was found as positive and had confirmed covid-19 infection (Dose number in series 3). The patient was discharged on 19-AUG-2022 with two days of hospitalization. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the confirmed covid-19 infection, Off label dosing frequency and blood pressure 80/40 was not reported. This report was serious (Hospitalization Caused / Prolonged). This case, involving the same patient is linked to 20221045009 and 20211208454.; Sender's Comments: V0: 20221046895-covid-19 vaccine ad26.cov2.s-confirmed covid-19 infection. The event(s) is deemed to be scientifically implausible, i.e., there is scientific evidence against a drug/event relationship; AND there is no known class effect. Therefore, this event(s) is considered not related. 20221046895-covid-19 vaccine ad26.cov2.s-blood pressure 80/40. The case causality is considered NOT RELATED. Rationale: Concurrent event of covid 19 infection with sign/symptoms of diarrhea and vomiting provide more plausible explanation
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- 2,0
- Labordaten
- Test Date: 20211108; Test Name: COVID-19 TEST; Test Result: Positive ; Test Date: 202202; Test Name: COVID-19 TEST; Test Result: Positive ; Test Date: 20220817; Test Name: BLOOD PRESSURE; Result Unstructured Data: 80/40; Test Date: 20220817; Test Name: COVID-19 TEST; Test Result: Positive
- Aktuelle Erkrankungen
- Non-Hodgkin's lymphoma (was immuno- compromised, that overproduces IGM, which is why he can't take any mRNA vaccines, "because they increase IGM)
- Vorgeschichte
- Comments: The patient was bedridden for different issues.
- Andere Medikamente
- INFLUENZA VACCINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 10.10.2022
- Impfdatum
- 29.11.2021
- Beginn
- 24.09.2022
- Tage bis Beginn
- 299,0
- Dosis
- 2
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dyspnoea
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 7,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 17.09.2022
- Impfdatum
- 02.12.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19 immunisation
Fatigue
Headache
Hypoaesthesia
Paraesthesia
Pyrexia
Scan
Therapeutic response unexpected
Symptomtext
HEADACHE; TIRED; NUMBNESS ON THE BODY; TINGLING ON THE BODY; FEVER (A MILD ONE); UNEXPECTED THERAPEUTIC BENEFIT; REVACCINATION WITH DIFFERENT COVID-19 VACCINE; This spontaneous report received from a patient concerned a 60 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included: asthma (uses puffers), b-thalassemia, osteoporosis, meningioma (tumor had shrunk since the second Janssen booster shot), sulfites allergy (she also had lot of genetic mutations and she gets tested for every medication), non alcohol user, and non smoker, and other pre-existing medical conditions included: The patient had no drug abuse or illicit drug usage. The patient previously received Pfizer Biontech covid-19 vaccine (tozinameran) (dose number in series 1) (form of admin, route of admin not reported, batch number were not reported, expiry: unknown) dose was not reported, administered on 09-FEB-2021 for covid-19 prophylaxis. On 09-FEB-2021, immediately after the vaccination, the patient experienced anaphylactic reaction and had to go to the hospital (dose number in series 1). The outcome of anaphylactic reaction was not reported. The patient received covid-19 vaccine ad26.cov2.s (dose number in series 2) (suspension for injection, route of admin not reported, batch number: 206A21A, expiry: 18-FEB-2022) dose was not reported, 1 total, administered on 08-AUG-2021 in right arm for covid-19 prophylaxis. On an unspecified date in 2021, the patient experienced neurotic (in terms of hysteria around the janssen vaccine), tiny achy, little headache, and tiny fever (dose number in series 2). The patient was recovered from neurotic (in terms of hysteria around the janssen vaccine), tiny achy, little headache, and tiny fever on an unspecified date in 2021. The patient additionally received booster dose of covid-19 vaccine ad26.cov2.s (dose number in series 3) (suspension for injection, route of admin not reported, batch number: 213D21A, expiry: unknown) dose was not reported, 1 total, administered on 02-DEC-2021 in right arm for covid-19 prophylaxis which was coded to revaccinated with different covid-19 vaccine (dose number in series 3). Age at time of vaccination 60 years old. No concomitant medications were reported. On an unspecified date, the patient experienced headache, tired, numbness or tingling on the body and had fever (a mild one) (dose number in series 3). Patient also stated that she was dealing with meningioma and was about to go for a surgery but the scan done after the second booster indicated that the tumor had shrunk and the surgery was currently cancelled (unexpected therapeutic benefit) (dose number in series 3). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the headache, tired, numbness on the body, tingling on the body, fever (a mild one), revaccination with different covid-19 vaccine and unexpected therapeutic benefit was not reported. This report was non-serious. This case, involving the same patient is linked to 20220911774 (dose number in series 1).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- Test Name: SCAN; Result Unstructured Data: tumor had shrunk
- Aktuelle Erkrankungen
- Abstains from alcohol; Asthma (uses puffers); Beta-thalassaemia; Meningioma (tumor had shrunk since the second Janssen booster shot); Non-smoker; Osteoporosis; Sulfonamide allergy (She also had lot of genetic mutations and she gets tested for every medication.)
- Vorgeschichte
- Comments: The patient had no drug abuse or illicit drug usage.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 13.09.2022
- Impfdatum
- 02.12.2021
- Beginn
- 06.09.2022
- Tage bis Beginn
- 278,0
- Dosis
- 2
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Asthenia
Chest pain
Cough
Fatigue
Myalgia
Symptomtext
fatigue, cough, chest pain, myalgias, weakness
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 12.08.2022
- Impfdatum
- 11.11.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest discomfort
Chest pain
Chills
Malaise
Pain
Palpitations
Pyrexia
Symptomtext
Within 7 days of receiving the vaccine; I developed Covid-like symptoms the day after administration, fever (102.5), chills, aches. Shortly thereafter I developed chest pain, tightness, and heart palpitations. I saw my PCP and complained about my symptoms. No treatment was issued. These symptoms mostly resided approximately 21 days after administration, however I have had several bouts of these feelings since the original vaccination. Lasting between 3 and 5 days until the symptoms reside again. This happened in February 2022, and again in May 2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 30.07.2022
- Impfdatum
- 19.11.2021
- Beginn
- 15.07.2022
- Tage bis Beginn
- 238,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Fatigue
Myalgia
Pain
Pain in extremity
Diarrhoea
Hyperhidrosis
Nausea
Paraesthesia
Pyrexia
Symptomtext
BAD DIARRHEA (SCALDING DIARRHEA); SWEATING (SWEAT WAS POURING OFF HER); FEVER; PUKEY; INJECTION SITE WAS A LITTLE TOUCHY WHEN SHE LAID ON IT AT NIGHT, HAD SOME PROBLEMS SLEEPING; This spontaneous report received from a patient concerned an 81 year old female. The patient's weight was 62.6 kilograms, and height was 161 centimeters. The patient's concurrent conditions included: penicillin allergy, and vision problems (She reported that her vision has been going downhill with her age for a long time. Her eyes were going faster than her body. She had to go to the eye doctor and the machines were all germy), and other pre-existing medical conditions included: Patient reported that she used to be 125lbs but has Covid pounds. Patient reported that she was never sick and did not taken any medications. Patient reported that she does not do anything else medically except foods and takes in plenty of Zinc and Vitamin D. Patient did not have any past medical history or illness at time of vaccination with Pfizer covid-19 vaccine. The patient was previously treated with covid-19 vaccine ad26. cov2. s (dose number in series 1) (suspension for injection, route of admin not reported, batch number: 1802068 and expiry: UNKNOWN) dose was not reported, 1 total, administered on 02-APR-2021 for covid-19 prophylaxis. It was unknown if patient experienced any adverse event after covid-19 vaccine ad26. cov2. s (dose number in series 1). The patient received covid-19 vaccine ad26.cov2.s (dose number in series 2) (suspension for injection, route of admin not reported, batch number: 213D21A and expiry: UNKNOWN) dose was not reported, 1 total, administered on 19-NOV-2021 for covid-19 prophylaxis. Age at time of vaccination 80 years old. Concomitant medications included ergocalciferol and zinc for used for unknown indication. It was unknown if patient experienced any adverse event after covid-19 vaccine ad26. cov2. s (dose number in series 2). The patient additionally received non-company suspect vaccine included: Pfizer Biontech Covid-19 vaccine (tozinameran) (dose number in series 3) (form of admin, and route of admin were not reported, batch number: FN2908 and expiry: UNKNOWN) dose was not reported, administered on 15-JUL-2022 in left arm for covid-19 prophylaxis. On 15-JUL-2022 11:11 , the patient had some problems sleeping because the arm she laid on. Patient did not have any pain at the injection site, but reported that it was a little touchy when she laid on it that night (dose number in series 3). On 16-JUL-2022, at around 36-48 hours after the vaccine the patient experienced sweat was pouring off her, she was pukey, sweating, figured she had a fever, so she drank plenty of water (dose number in series 3). On 17-JUL-2022 (12hrs into the sweating), she had bad diarrhea. It was a scalding diarrhea. She had to get A&D ointment. Patient reported that by the end of the third day (18-JUL-2022) it was all over and everything went away (dose number in series 3). The patient did not visit emergency room or physician office for the events. On 15-JUL-2022, the patient experienced injection site was a little touchy when she laid on it at night, had some problems sleeping. On 16-JUL-2022, the patient experienced sweating (sweat was pouring off her), fever, and pukey. On 17-JUL-2022, the patient experienced bad diarrhea (scalding diarrhea). The action taken with covid-19 vaccine ad26.cov2.s, and tozinameran was not applicable. The patient recovered from sweating (sweat was pouring off her), fever, bad diarrhea (scalding diarrhea), and pukey on 18-JUL-2022, and the outcome of injection site was a little touchy when she laid on it at night, had some problems sleeping was not reported. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Penicillin allergy; Visual disturbance (She reported that her vision has been going downhill with her age for a long time. Her eyes were going faster than her body. She had to go to the eye doctor and the machines were all germy.)
- Vorgeschichte
- Comments: Patient reported that she used to be 125lbs but has Covid pounds. Patient reported that she was never sick and did not taken any medications. Patient reported that she does not do anything else medically except foods and takes in plenty of Zinc and Vitamin D. Patient did not have any past medical history with Pfizer covid-19 vaccine.
- Andere Medikamente
- ZINC; VITAMIN D [ERGOCALCIFEROL]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 27.06.2022
- Impfdatum
- 16.12.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood calcium normal
Cardiac stress test normal
Computerised tomogram normal
Echocardiogram normal
Laboratory test normal
Palpitations
Symptomtext
I had heart palpitations several times a day, every day until the end of May 2022 they stopped. I did a bunch of tests and Dr. did not determine anything that was wrong.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- Stress test, echocardiogram, calcium CT score, EKG all normal.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- High blood pressure; Acid Reflux; Borderline diabetic
- Andere Medikamente
- Lisinopril; metformin; omeprazole
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 17.06.2022
- Impfdatum
- 18.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Chest X-ray
Chest pain
Dizziness
Dyspnoea
Electrocardiogram
Headache
Injection site pain
Laboratory test
Pruritus
Rash
Urticaria
Symptomtext
30 y/o male following-up after ED visit at MEDICAL CENTER d/t adverse allergic reaction to J&J Covid- 19 vaccine. States he experienced hives, rash that extended from his forearm to the back of his neck on the side where injection was administered, severe CP, HA, lightheadness, and BPs=220s/100s within 4 hours of vaccine administration. He was transported via ambulance to the ED where labs and some "CXR or EKG" was completed. Per patient, they placed an IV and administered Benadryl. He denies recieving EPI-PEN at the ED. He was monitored and subsequently discharged same-day. Currently, denies rash, CP, HAs, SOB, and lightheadedness. Continues to have some mild pruritis and localized tenderness on injection site. Reports BP has return to his baseline.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- 30 y/o male following-up after ED visit at MEDICAL CENTER d/t adverse allergic reaction to J&J Covid- 19 vaccine. States he experienced hives, rash that extended from his forearm to the back of his neck on the side where injection was administered, severe CP, HA, lightheadness, and BPs=220s/100s within 4 hours of vaccine administration. He was transported via ambulance to the ED where labs and some "CXR or EKG" was completed. Per patient, they placed an IV and administered Benadryl. He denies recieving EPI-PEN at the ED. He was monitored and subsequently discharged same-day. Currently, denies rash, CP, HAs, SOB, and lightheadedness. Continues to have some mild pruritis and localized tenderness on injection site. Reports BP has return to his baseline.
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- ASTHMA
- Andere Medikamente
- ALBUTEROL
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- -
- Geschlecht
- M
- Eingang
- 15.06.2022
- Impfdatum
- 07.12.2021
- Beginn
- 07.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Magnetic resonance imaging
Migraine
Nausea
Sinusitis
Symptomtext
SINUS INFECTION; NAUSEA; SUFFERS FROM MIGRAINES EVERY TWO WEEKS (HEADACHES ON THE FRONT, BACK AND SIDE OF HIS HEAD); This spontaneous report received from a patient concerned a male of unspecified age. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 213D21A expiry: UNKNOWN) dose was not reported, administered on 07-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. On 07-DEC-2021, the patient experienced suffers from migraines every two weeks (headaches on the front, back and side of his head), and nausea. On an unspecified date, the patient experienced sinus infection. Laboratory data (dates unspecified) included: Magnetic resonance imaging sinus infection. Treatment medications (dates unspecified) included: levofloxacin, and acetylsalicylic acid/caffeine/paracetamol/salicylamide. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from nausea, suffers from migraines every two weeks (headaches on the front, back and side of his head), and sinus infection. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- Test Name: MAGNETIC RESONANCE IMAGING (MRI); Result Unstructured Data: sinus infection
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 17.05.2022
- Impfdatum
- 17.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal discomfort
Arthralgia
Blood test
Computerised tomogram abdomen
Diarrhoea
Electrocardiogram
Fatigue
Headache
Immediate post-injection reaction
Immunisation reaction
Laboratory test
Neck pain
Pain
Palpitations
Stool analysis
Urine analysis
Vomiting
X-ray
Symptomtext
Pain in shoulder up my neck immediately. Upset stomach, increased diarrhea, headache, body aches, vomiting, fatigue, heart palpitations started immediately. Contacted doctors office and visited ER. Referred to cardiologist and revisit gastroenteritis. Multiple blood and bowel tests. Doctor refuses to believe its an adverse reaction. Taking Imodium, Ibuprofen changed diet.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- May 12, 2022 Multiple blood test, urine test, xray, CT of abdomen, EKG. The list is very long. I am happy to email them to you. I'm still undergoing testing.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Chronic pancreatitis and diarrhea
- Andere Medikamente
- Bupropion, Creon, Diclofenac, Diphenoxylate-atrop, Gabapenton, Levothyroxine, Morphine, Nortriptyline, Omeprazole, Ondansetron, Tramadol
- Allergien
- Aspirin, Codeine, Valium, Phenergan, Biaxin, EMycin
- Vorherige Impfungen
- 14 years ago to the flu vaccine
- Staat
- WI
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 13.04.2022
- Impfdatum
- 13.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asphyxia
Asthenia
Gait disturbance
Headache
Immediate post-injection reaction
Impaired driving ability
Inflammation
Injection site pain
Palpitations
Symptomtext
Immediately the shot hurt badly when going into the arm, felt like I was suffercating, heart started palpitating, became very weak and needed air and water. Too weak to walk. Sat at pharmacy for over an hour. Couldn?t drive, continued weakness. Headache, full inflammation throughout body.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Lyme Disease Fibromyalgia Hisimotios thyroiditus
- Andere Medikamente
- Thyroid medicine T3/T4 Vitamin D Co-Q10 K-2
- Allergien
- Laytex, gluten, dairy, niacin
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 07.04.2022
- Impfdatum
- 23.11.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- 8,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Dyspnoea
Symptomtext
Coughing bouts early on lasting as long as 10-15 min. On and off for a few hours then a few hours of quiet time then all of a sudden it would start up all over again. When I would lay down for bed my breathing would be fine till a few hours after I get up and the coughing would start all over again.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SD
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 02.04.2022
- Impfdatum
- 01.12.2021
- Beginn
- 31.03.2022
- Tage bis Beginn
- 120,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest discomfort
Chest pain
Computerised tomogram thorax
Fibrin D dimer increased
Scan with contrast
Symptomtext
Lingering chest pain and discomfort for several weeks. Off and on Left side chest pressure. Elevated d-dimer on my physical exam on 03-31-2022 which resulted in very expensive Chest Pulmonary Embolism CT study on 04-01-2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- D-dimer elevated on 03-31-2022 during my physical. Chest Pulmonary Embolism Study CT with contrast on 04-01-2022
- Aktuelle Erkrankungen
- No other illnesses
- Vorgeschichte
- No chronic conditions
- Andere Medikamente
- Aspirin - 81 MG daily NP thyroid - 60 MG daily Alprazolam - 0.5 MG PRN Multivitamin - daily Fish Oil - daily
- Allergien
- Cipro - diarrhea Hydrocodone - bradycardia Prednisone - tachycardia
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 25.03.2022
- Impfdatum
- 05.11.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 42,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Aphasia
Borrelia test
Computerised tomogram head
Dyspnoea
Fatigue
Gait disturbance
Headache
Magnetic resonance imaging head
Magnetic resonance imaging neck
Magnetic resonance imaging spinal
Mobility decreased
Movement disorder
Myelopathy
Ophthalmological examination
Pain
Thirst
Visual impairment
Symptomtext
Patient received the vaccine in November and in December she started experiencing difficulty walking and talking tried to see a doctor unable to see a doctor until January. Went to the emergency room in February with the following symptoms: unable to move legs, difficulty moving arms, trouble breathing, pain all over difficulty with speech, vision problems, headache, excessive thirst, fatigue. CT of head, MRI of head, ophthalmologist exam, MRI cervical and spine. Neurologist reported the following: Examination demonstrates features most consistent with a myelopathy. We will obtain spinal MRI and repulse with steroid. We will also check Lyme tier. A post-vaccination myelitis or Miller Fisher syndrome is a consideration. Cysticercosis is a possibility as well. I will request hospital records as well.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 7,0
- Labordaten
- CT head, MRI head, cervical, spine, Lyme tier, ophthalmologist exam
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 17.03.2022
- Impfdatum
- 01.12.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test normal
Cluster headache
Electromyogram normal
Eye pain
Headache
Hypoaesthesia
Lacrimation increased
Magnetic resonance imaging head normal
Mobility decreased
Nerve conduction studies normal
Neurological examination abnormal
Ocular hyperaemia
Pain of skin
Paraesthesia
Photophobia
Symptomtext
Headache - feeling of slight pain in right side of head, like "just sitting there waiting for something to trigger it", it is ever present. Every 2-3 weeks a full onset headache will occur causing severe throbbing pain in right side of head, starts behind right eye, eyes become read and waters severely, becomes light sensitive, begins to creep along right side of hear to the back of head, feeling like my hair hurts, usually lasts 2-3 hours, only has occurred only in a day, will begin to subside but will come "roaring" back, usually incapable of doing anything during the event. In addition, have tingling and numbness in left arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- EMG/NCS Testing - February 2022, no abnormalizes Brain MRI - February 2022, no abnormalizes Blood work, February 2022, normal Neurology Doctor appointment - diagnosis - Episodic Cluster Headache No previous history of any headaches until after vaccine
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 15.03.2022
- Impfdatum
- 04.12.2021
- Beginn
- 04.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Condition aggravated
Mobility decreased
Myalgia
Pain in extremity
Symptomtext
My left shoulder was still having mobility issues from the first Covid vaccine (by the way, I always get my flu shot in this arm for many years and have never had an issue) and I voiced that to the pharmacist. They thought that I just had my first dose until I told them it ws back in April! They were a bit shocked and surely, didn't believe me. I decided to have them vaccinate me in the same arm because I couldn't afford for both to be compromised. The shot was fine; I had no other effects except that it was still hurting from the first time. On Feb 19th 2022, I went for my Shingles vaccine at store/pharmacy and again voiced that my arm was still giving me pain and certain immobility from the Covid shot. All they ccould tell me was that I could take the Shingles shot in the opposite arm. I told them no because I just had the flu shot from them also, but in the right arm because I never have any challenges from that. I have been taking flu shots for many years but in my left arm. I chose to change up due to having this Covid vaccine reaction. I wanted to monitor what was happening as best as I could. I have not had any noticeable reactions from the Shingles vaccine since taking it on Feb 19. Actually, for a moment, it made my left shoulder feel better but then it quickly resumed the pain in the muscle and possibly the joint. I have not had insurance until recently. On the 25th of this month, I will discuss with the doctor but if my insurance does not cover any referrals he/she may give, I may not know the true cause of my shoulder pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- Covid Vaccine on 4/10/21--info submitted to VAERS, shoulder discomfort/pain/limited mobility
- Staat
- MI
- Alter
- 47,0
- Geschlecht
- M
- Eingang
- 15.03.2022
- Impfdatum
- 17.11.2021
- Beginn
- 21.02.2022
- Tage bis Beginn
- 96,0
- Dosis
- 1
- Route/Site
- UN / OT
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Activated partial thromboplastin time shortened
Alanine aminotransferase increased
Albumin globulin ratio
Anion gap
Arthralgia
Aspartate aminotransferase increased
Atypical pneumonia
Bacterial test negative
Base excess
Basophil count decreased
Bilirubin urine
Blood albumin normal
Blood alkaline phosphatase normal
Blood bicarbonate increased
Blood bilirubin normal
Blood calcium normal
Blood chloride normal
Blood creatinine normal
Symptomtext
Date of Admission: 2/21/2022 Chief Complaint: SOB, Right Shoulder Pain. Source of Information: Patient. History of Present Illness: This is a 47y.o. male with PMH significant for sarcoidosis, cervical radiculopathy and obesity presents to ED with complaints of SOB and right shoulder pain. Pt states his SOB began yesterday and is persistent. He is not on home oxygen and denies history of HF, COPD, or asthma. SOB is worse on exertion. Pt denies fever, chills, chest pain, palpitations, sputum production, abdominal pain, N/V/D constipation or dysuria. Pt also states that he has severe right shoulder pain which he visited the ED for 2 weeks prior. He states he is unable to sleep flat at night due to this pain and that OTC pain medications have not worked. He is scheduled for an orthopedic appointment next month. In the ED, Vitals on arrival of T 97?F, BP 154/84, HR 133, RR 20, SpO2 93% on RA Labs remarkable for CBC BMP unremarkable other than glucose 295. Patient received 1L saline bolus, solumedrol 125mg, ibuprofen, tylenol, and pt was initiated on antibiotic coverage with doxycycline. Past Medical History: Diagnosis Date ? Sarcoidosis History reviewed. No pertinent surgical history. History reviewed. No pertinent family history. Social History Socioeconomic History ? Marital status: Single Tobacco Use ? Smoking status: Never Smoker ? Smokeless tobacco: Never Used Family History No family history on file. Medications: Home Medications Med Sig Last Dose Dt/Time budesonide-formoterol (SYMBICORT) 160-4.5 MCG/ACT INHAL inhaler inhale 2 Puffs into the lungs once daily. 2/20/2022 Unknown time CALCIUM PO take 1 Tablet by mouth once daily. 2/20/2022 Unknown time Mon Feb 21, 2022 2:31 AM) Unknown dose Glucosamine-Chondroitin (OSTEO BI-FLEX REGULAR STRENGTH PO) take 1 Tablet by mouth once daily. 2/20/2022 Unknown time Omega-3 Fatty Acids (FISH OIL PO) take 1 Tablet by mouth once daily. 2/20/2022 Unknown time VITAMIN D PO take 1 Tablet by mouth once daily. 2/20/2022 Unknown time Mon Feb 21, 2022 2:31 AM) Unknown dose Hospital Medications: Current Medications Current Facility-Administered Medications Medication Dose Route Frequency Provider Last Rate Last Admin ? acetaminophen (TYLENOL) tablet 650 mg 650 mg Oral Q 6 H PRN ? albuterol (PROVENTIL, VENTOLIN) (2.5 MG/3ML) 0.083% nebulizer solution 2.5 mg 2.5 mg Inhalation RT-QID ? albuterol (PROVENTIL, VENTOLIN) (2.5 MG/3ML) 0.083% nebulizer solution 2.5 mg 2.5 mg Inhalation Q 2 H PRN ? benzonatate (TESSALON) capsule 200 mg 200 mg Oral Q 8 H PRN ? doxycycline (MONODOX) capsule 100 mg 100 mg Oral Q 12 100 mg at 02/21/22 0220 ? enoxaparin (LOVENOX) injection 40 mg 40 mg Subcutaneous Q 24 H 40 mg at 02/21/22 0818 ? fluticasone-vilanterol (BREO ELLIPTA) 100-25 MCG/INH inhaler 1 Puff 1 Puff Inhalation DAILY ? guaiFENesin (MUCINEX) 12-hour tablet 600 mg 600 mg Oral Q 12 H ? ondansetron (ZOFRAN) injection 4 mg 4 mg Intravenous Q 6 H PRN ? predniSONE (DELTASONE) tablet 40 mg 40 mg Oral DAILY ? senna (SENOKOT) tablet 8.6 mg 1 Tablet Oral BID PRN ? sodium chloride 0.9 % flush injection 3 mL 3 mL Intravenous PRN Current Outpatient Medications Medication Sig Dispense Refill ? budesonide-formoterol (SYMBICORT) 160-4.5 MCG/ACT INHAL inhaler inhale 2 Puffs into the lungs once daily. ? CALCIUM PO take 1 Tablet by mouth once daily. ? Glucosamine-Chondroitin (OSTEO BI-FLEX REGULAR STRENGTH PO) take 1 Tablet by mouth once daily. ? Omega-3 Fatty Acids (FISH OIL PO) take 1 Tablet by mouth once daily. ? VITAMIN D PO take 1 Tablet by mouth once daily. Allergies: Allergen Reactions ? Penicillins Hives ROS: Gen: No fevers, chills, nightsweats, fatigue, weight loss HEENT: No headaches, visual changes, hearing changes, vertigo, congestion, rhinorrhea, sore throat CV: No chest pain, palpitations, diaphoresis, orthopnea, edema RESP: + SOB, +pulomary congestion. Crackles present bilateral bases. Denies wheezing, or cough GI: No nausea, vomiting, constipation, diarrhea, abdominal pain, hematochezia, melena ENDO: No temperature intolerance, sweating, or polyphagia, polyuria, polydipsia GU: No dysuria, hematuria, increased frequency, urgency MSK: + R shoulder pain. 4/5 strength in R shoulder NEURO: No weakness, dizziness, seizures, tremors, lightheadedness HEME: No easy bruising or bleeding PSYCH: No depression, anxiety or memory issues Last Filed Vitals: BP 140/89 | Pulse 95 | Temp 97.6 ?F (36.4 ?C) (Oral) | Resp 22 | Ht 182.9 cm (6') | Wt 129 kg (285 lb) | SpO2 96% | BMI 38.65 kg/m? Body mass index is 38.65 kg/m?. Physical Examination: GEN: A/O x 3. NAD. Well nourished-well developed who appears stated age HENT: Normocephalic. Atraumatic. EOMI. PERRL. No scleral icterus or JVD NECK: Supple. Trachea midline. No JVD, thyromegaly/goiter, carotid bruit. CV: RRR. S1 S2 without S3 or S4. No murmurs, clicks or gallops RESP: Clear to auscultation bilaterally. No wheeze, rhonci, or rales. No accessory muscle use GI: BS x 4. Non-tender, non-distended. Soft. No hepatosplenomegaly EXT: No cyanosis, clubbing or edema NEURO: CN II-XI grossly intact bilaterally. Muscle strength 5/5, sensation intact. No dysdiadokinesis. No focal deficits. No cerebellar signs SKIN: No gross rash, lesion, or breakdown Labs: Recent Results Recent Results (from the past 24 hour(s)) Protime and aPTT Collection Time: 02/21/22 12:56 AM Result Value Ref Range Protime 11.6 9.2 - 13.5 Seconds INR 1.0 APTT 29.3 25.0 - 38.0 Seconds Comprehensive Metabolic Panel (CMP) Collection Time: 02/21/22 12:56 AM Result Value Ref Range Sodium 139 135 - 145 mmol/L Potassium 4.6 3.5 - 5.2 mmol/L Chloride 102 98 - 111 mmol/L Carbon Dioxide (CO2) 24 20 - 29 mmol/L Anion Gap 13 5 - 17 Glucose 151 (H) 60 - 99 mg/dL Blood Urea Nitrogen (BUN) 12 7 - 25 mg/dL Creatinine 1.03 0.60 - 1.30 mg/dL GFR African American 100 >=60 mL/min/1.73m2 Calcium 10.5 8.5 - 10.5 mg/dL Protein Total 8.2 6.4 - 8.3 g/dL Albumin 4.1 3.5 - 5.1 g/dL Globulin 4.1 (H) 2.2 - 4.0 g/dL Albumin/Globulin Ratio 1.0 Alkaline Phosphatase 111 33 - 120 U/L Aspartate Aminotransferase (AST) 37 (H) <35 U/L Alanine Aminotransferase (ALT) 98 (H) 9 - 47 U/L Bilirubin Total 0.7 0.3 - 1.2 mg/dL Troponin I Collection Time: 02/21/22 12:56 AM Result Value Ref Range Troponin I 0.02 <=0.03 ng/mL D-Dimer Collection Time: 02/21/22 12:56 AM Result Value Ref Range D-Dimer 432 0 - 499 ng/mL FEU Covid-19, Flu, RSV by NAA Collection Time: 02/21/22 12:56 AM Specimen: Nasopharyngeal; Swab Result Value Ref Range Influenza A Not Detected Not Detected Influenza B Not Detected Not Detected RSV Not Detected Not Detected SARS-CoV-2 (COVID-19) by NAA, Micro Detected (A) Not Detected Complete Blood Count (CBC) W/Auto Diff Collection Time: 02/21/22 12:56 AM Result Value Ref Range WBC 10.7 (H) 3.5 - 10.1 bil/L RBC 5.10 4.31 - 5.48 tril/L Hemoglobin 14.5 13.5 - 17.0 g/dL Hematocrit 43.8 40.1 - 50.1 % MCV 86 80 - 100 fL MCH 28 28 - 33 pg MCHC 33 32 - 36 g/dL RDW-CV 15 12 - 15 % Platelets 215 150 - 400 bil/L Neutrophils 9.7 (H) 1.6 - 7.2 bil/L Lymphocytes 0.7 (L) 1.1 - 4.0 bil/L Monocytes 0.3 0.0 - 0.9 bil/L Eosinophils 0.0 0.0 - 0.4 bil/L Basophils 0.0 0.0 - 0.1 bil/L Immature Granulocytes 0.11 (H) 0.00 - 0.04 bil/L Immature Granulocyte % 1.0 % Thyroid Stimulating Hormon (TSH) With Reflex to Free Thyroxine (FT4) Collection Time: 02/21/22 1:34 AM Result Value Ref Range Thyroid Stimulating Hormone 0.44 0.40 - 4.50 uIU/mL Blood Gases, Venous (VBG) Collection Time: 02/21/22 1:34 AM Result Value Ref Range Sample Type Blood, venous pH 7.39 7.32 - 7.42 PCO2 51 41 - 51 mmHg Bicarbonate 30 (H) 19 - 27 mmol/L Total CO2 32 (H) 20 - 29 mmol/L Base Excess 4 -5 - 5 mmol/L Oxyhemoglobin 64 55 - 85 % Carboxyhemoglobin 0.8 <1.5 % Methemoglobin 0.7 0.0 - 2.0 % Hemoglobin 14.6 13.5 - 17.0 g/dL Troponin I Collection Time: 02/21/22 2:30 AM Result Value Ref Range Troponin I 0.02 <=0.03 ng/mL Troponin I Collection Time: 02/21/22 4:20 AM Result Value Ref Range Troponin I 0.02 <=0.03 ng/mL Basic Metabolic Panel (BMP) Collection Time: 02/21/22 4:20 AM Result Value Ref Range Sodium 138 135 - 145 mmol/L Potassium 4.2 3.5 - 5.2 mmol/L Chloride 104 98 - 111 mmol/L Carbon Dioxide (CO2) 23 20 - 29 mmol/L Anion Gap 11 5 - 17 Glucose 295 (H) 60 - 99 mg/dL Blood Urea Nitrogen (BUN) 13 7 - 25 mg/dL Creatinine 1.07 0.60 - 1.30 mg/dL GFR African American 95 >=60 mL/min/1.73m2 Calcium 9.6 8.5 - 10.5 mg/dL Complete Blood Count (CBC) Collection Time: 02/21/22 4:20 AM Result Value Ref Range WBC 8.9 3.5 - 10.1 bil/L RBC 4.91 4.31 - 5.48 tril/L Hemoglobin 13.7 13.5 - 17.0 g/dL Hematocrit 42.2 40.1 - 50.1 % MCV 86 80 - 100 fL MCH 28 28 - 33 pg MCHC 33 32 - 36 g/dL RDW-CV 15 12 - 15 % Platelets 208 150 - 400 bil/L Magnesium Level Collection Time: 02/21/22 4:20 AM Result Value Ref Range Magnesium 1.9 1.7 - 2.5 mg/dL Urinalysis, Complete Collection Time: 02/21/22 1:00 PM Result Value Ref Range Color Yellow Clarity Clear Clear Glucose 150 (A) Negative mg/dL Bilirubin Negative Negative Ketones Negative Negative mg/dL Specific Gravity, Urine 1.008 1.005 - 1.030 Blood Negative Negative pH 6.0 5.0 - 8.0 Protein Negative Negative mg/dL Urobilinogen <2.0 <2.0 mg/dL Nitrites Negative Negative Leukocyte Esterase Negative Negative RBC 0-2 (Negative) 0-2 (Negative) /hpf WBC 0-5 (Negative) 0-5 (Negative) /hpf Epithelial, Squamous Negative Negative /lpf Casts, Hyaline 0-2 (Negative) 0-2 (Negative) /lpf Bacteria Negative Negative /hpf Diagnostic Studies: CHEST 2 VIEWS FRONTAL/LATERAL Result Date: 2/21/2022 TWO VIEW CHEST X-RAY INDICATION: Shortness of breath. COMPARISON: Chest radiograph on 2/17/2011. TECHNIQUE: Frontal and lateral views of the chest were obtained. FINDINGS/IMPRESSION: Multifocal patchy airspace disease. No pneumothorax identified. No large effusion. Cardiomediastinal is what is stable. ECG Result Date: 2/21/2022 2:23 AM ECG Date/Time: 2/21/2022 12:22 AM Contemporaneously ECG reviewed by ED Physician in the absence of a cardiologist: yes Interpretation: Interpretation: abnormal Rate: ECG rate: 127 ECG rate assessment: tachycardic Rhythm: Rhythm: sinus tachycardia Assessment and Plan: Active Hospital Problems Diagnosis ? Principal Problem: Atypical pneumonia ? SOB (shortness of breath) ? Tachycardia ? History of sarcoidosis ? Hypoxemia requiring supplemental oxygen ? Pneumonia due to COVID-19 virus Resolved Hospital Problems No resolved problems to display. PLAN Pneumonia - likely 2/2 COVID infection - CXR multifocal patchy airspace disease - Positive COVID 19 - On 2L NC, spO2 96% - Antigen legionella, streptococcus pending - Blood cultures pending - doxycycline 100mg q12 - albuterol 2.5mg q2 prn - fluticasone-vilanterol 100-25 mcg 1 puff daily - decadron 6mg daily - mucinex 600mg q12 R Shoulder Parasthesia/Pain - ER 2 weeks ago for neck pain - CT cervical spine 01/22/2022: multilevel disc degeneration and central canal stenosis. C4-C5 small left central disc herniation - R shoulder radiograph? - acetaminophen 650 prn - Orthopedic consult scheduled next month, pt states he will likely receive steroid shot there HTN - 142/74, HR 108. 154/84 HR 133 on admission - BMI 38.65 - likely 2/2 to pain? -trend, continue acetaminophen Hx Sarcoidosis - whats his home regimen, no steroid/immunosuppresants? Not requiring O2 at present Was wheezing previously, but breathing better after inhaler and steroids. Based on his lack of hypoxia he does not need steroids for Covid, but does for reactive airway ID input- possible candidate for 3 day course of Remedsivir Right shoulder exam consistent with tendonitis- ortho follow up Add norco for breakthrough pain Patient personally seen and examined. The above documentation reflects my own history gathering, physical exam and medical decision making.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Atypical pneumonia
- Hospital-Tage
- 3,0
- Labordaten
- Contains abnormal data Covid-19, Flu, RSV by NAA Status: Final result Next appt: None Specimen Information: Nasopharyngeal; Swab 0 Result Notes Component Ref Range & Units Influenza A Not Detected Not Detected Influenza B Not Detected Not Detected RSV Not Detected Not Detected SARS-CoV-2 (COVID-19) by NAA, Micro Not Detected Detected Abnormal Narrative Methodology: Nucleic Acid Amplification(NAA)/Polymerase Chain Reaction(PCR) Specimen Collected: 02/21/22 12:56 AM Last Resulted: 02/21/22 3:22 AM Order Details View Encounter Lab and Collection Details Routing Result History Result Care Coordination
- Aktuelle Erkrankungen
- Sarcoidosis
- Vorgeschichte
- Sarcoidosis
- Andere Medikamente
- budesonide-formoterol (SYMBICORT) 160-4.5 MCG/ACT INHAL inhaler inhale 2 Puffs into the lungs once daily. 2/20/2022 Unknown time CALCIUM PO take 1 Tablet by mouth once daily. 2/20/2022 Unknown time Mon Feb 21, 2022 2:31 AM) Unknown dose Gl
- Allergien
- Penicillins Hives
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 17.02.2022
- Impfdatum
- 26.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Electromyogram
Fatigue
Headache
Hypoaesthesia
Pain
Pain in extremity
Paraesthesia
Symptomtext
Numbness / tingling, pain, starting in left leg, occasionally left arm, then both legs. Headaches daily Dizziness Severe fatigue Body aches
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- EMG 02/04/2022
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Seizure disorder GERD Allergies Asthma Herpes Zoster, recurrent Herpes, Genital Migraine Headaches Vertigo Concussion ADD
- Andere Medikamente
- Adderall, Valtrex, Azelastine nasal spray
- Allergien
- Phenobarbital, Topamax, Flonase, Nasacort Lactose intolerance Poinsettias, Mums, Trees, snow mold,Seasonal (winter, spring, fall)
- Vorherige Impfungen
- Varicella , age 49, developed Shingles back to back episodes :2 weeks , then 4 weeks after vaccination
- Staat
- CT
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 16.02.2022
- Impfdatum
- 01.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Tinnitus
Symptomtext
This was my booster shot. I noticed a severe increase in tinnitus, before the vaccines i had a very slight ringing in the ears. After the booster it increased significantly.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Vit D2, Losartan, Hydralazine, Metoprolol er succinate
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 16.02.2022
- Impfdatum
- -
- Beginn
- 01.02.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
Chills
Dyspnoea
Insomnia
Lymphadenopathy
Oxygen saturation
Pyrexia
Symptomtext
COULDN'T SLEEP/WOKE UP; SHIVERING; FEVER; TROUBLE BREATHING (FELT LIKE A CAT WAS SITTING ON CHEST BUT NOT TOO MUCH PRESSURE); LYMPH NODE SWELLING UNDER THE ARM WHERE GOT A SHOT; This spontaneous report received from a patient concerned a 21 year old male. The patient's height, and weight were not reported. The patient's concurrent conditions included: non alcohol user, and non smoker, and other pre-existing medical conditions included: The patient had no health conditions and had no known drug allergies. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 213D21A, and batch number: 213D21A expiry: 11-APR-2022) dose was not reported, administered on 09-FEB-2022 18:30 for prophylactic vaccination. No concomitant medications were reported. On FEB-2022, the patient experienced lymph node swelling under the arm where got a shot. Laboratory data included: Oxygen saturation (NR: not provided) 96 %. On 09-FEB-2022, the patient experienced trouble breathing (felt like a cat was sitting on chest but not too much pressure). On 10-FEB-2022, the patient experienced couldn't sleep/woke up, shivering, and fever. Laboratory data included: Body temperature (NR: not provided) 102 F. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient was recovering from fever, had not recovered from lymph node swelling under the arm where got a shot, and the outcome of shivering, couldn't sleep/woke up and trouble breathing (felt like a cat was sitting on chest but not too much pressure) was not reported. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Test Date: 202202; Test Name: Oxygen saturation; Result Unstructured Data: 96 %; Test Date: 20220210; Test Name: Body temperature; Result Unstructured Data: 102 F; Comments: Had fever of 102 F for 2 days
- Aktuelle Erkrankungen
- Abstains from alcohol; Non-smoker
- Vorgeschichte
- Comments: The patient had no health conditions and had no known drug allergies.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 11.02.2022
- Impfdatum
- 02.12.2021
- Beginn
- 13.12.2021
- Tage bis Beginn
- 11,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Breast mass
Breast pain
Chest pain
Inflammation
Mammogram
Pain
Ultrasound scan
Symptomtext
I was vaccinated on December 1 at a medical center and received the J&J Vaccine in my right arm. On December 13th I began experiencing shooting pain across my chest and in my left breast that got progressively worse each day On December 21st I saw my gynecologist for this pain and was sent for an ultrasound of my left breast. January 3rd I got my ultrasound. January 13th I found a lump in my left breast. January 14th I went back to my gynecologist who recommended I see a breast surgeon. January 27th I saw a breast surgeon who said my symptoms are an inflammatory response and possible signs of an auto immune disease. She suggested I may need to see a rheumatologist. She has sent me to go get further testing. I am scheduled for a mammogram and ultrasound on February 18th as well as bloodwork per her request.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Ultrasound, Mammogram, bloodwork
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Synthroid Junel Saxenda
- Allergien
- Amoxicillin, Percocet, Hydrocodone
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 11.02.2022
- Impfdatum
- 10.11.2021
- Beginn
- 12.01.2022
- Tage bis Beginn
- 63,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Deafness
Ear discomfort
Fatigue
Headache
Laboratory test normal
Myalgia
Visual impairment
Symptomtext
Loss of hearing. Muscle pain in lower back and legs. Chest pain. Consistent fatigue. Headache. Eye Pressure with occasional splotchy eyesight
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- On February 7 2022 Doctor Performed a universal swab test in my nose to test for multiple diseases with all negative result. This is my Booster shot of J&J. The First dose was April 12, 2021. Lot # 207 A 21 A
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- immunocompromised
- Andere Medikamente
- Biktarvy Bactrim
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 01.02.2022
- Impfdatum
- 08.04.2021
- Beginn
- 17.01.2022
- Tage bis Beginn
- 284,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ageusia
Anosmia
COVID-19
Chills
Cough
Dyspnoea
Fatigue
Headache
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
Fever, chills, cough, shortness of breath, fatigue, headache, loss of taste and smell, congestion
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- COVID-19 test / positive / January 17, 2022
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 23.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 14,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Oral lichen planus
Symptomtext
Flare up of Lichen Planus on back, scalp, eyelash follicles, and vulva.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- None yet
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Oral Lichen Planus
- Andere Medikamente
- None
- Allergien
- Erythromycin Steri-strips
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 22.01.2022
- Impfdatum
- 20.12.2021
- Beginn
- 20.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Palpitations
Symptomtext
Patient experienced shivering, racing heart and palpitations with HR up to 151 BPM. Symptoms lasted through the 24th of December.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 15.11.2021
- Beginn
- 19.11.2021
- Tage bis Beginn
- 4,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Muscular weakness
Neuropathy peripheral
Paraesthesia
Symptomtext
Pins and needles feeling along with tingling in all 4 limbs, weakness in arms and legs. (Neuropathy)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- MRI of Brain and nerve conduction studies orderd.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 28.11.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 32,0
- Dosis
- 1
- Route/Site
- IM / UN
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
COVID-19 pneumonia
Chest X-ray abnormal
Chills
Diarrhoea
Dyspnoea
Lung infiltration
Nausea
Panic attack
Pneumonia viral
Pyrexia
Respiratory failure
SARS-CoV-2 test positive
Vomiting
Symptomtext
70 Y/O female, visiting her daughter here states was SOB from 12/20 and developed fever, chills, panic attacks, nausea, vomiting and diarrhea. Home Covid test was +. Symptoms improved for a few days and then started getting worse. She came to ER last night due to severe SOB and felt panicky. She was tested + by PCR and was in severe hypoxic resp failure. CXR showed Multifocal Lung infiltrates due to COVID Viral Pneumonia. She also has Hx of chronic colitis. PMHX 1) T2D 2)Chronic Colitis PSHX 1) cholecystectomy 2) BIL THA Soc Hx Divorced, Smokes 3-4 cig/daily ETOH social . Received 1 dose of J&J vaccine end of November. 12/30/2021 tested positive
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19 pneumonia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 17.01.2022
- Impfdatum
- 21.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 8,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Asthenia
Chest pain
Diplopia
Dyspnoea
Electrocardiogram
Fall
Fibrin D dimer increased
Gait inability
Hypoaesthesia
Laboratory test
Magnetic resonance imaging head
Magnetic resonance imaging thoracic
Musculoskeletal disorder
Panic attack
Paraesthesia
Scan with contrast
Vision blurred
Symptomtext
Numbness, parasthesia in extremities starting in feet, working way up legs to upper body, hands fingers. Complete loss of function in left leg resulting in 2 falls, but regained ability to walk. Blurred distance vision left eye, double vision that resolved, chest pain, intermittent panic attacks with SOB- no prior history.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- 2,0
- Labordaten
- Hospitalized 12/30/2021-12/31/2021. MRI of head and chest, CT with and without contrast head and chest, EKG, labs. Elevated D-dimer. Needs f/u with Neuro for further testing, possible MRI spine, lumbar puncture. ER visit on 1/11/2022 for severe exacerbated weakness and paresthesia in all limbs. Referred to outpatient Neurology, to f/u on 1/27/2022 or sooner if can be moved up on the waiting list.
- Aktuelle Erkrankungen
- Covid-19 positive by PCR on 12/04/2021, off quarantine 12/15/2021. Had to receive the vaccine to be able to go back to work as an RN of 20 years.
- Vorgeschichte
- Hx Graves Disease, s/p total thyroidectomy, stable on Levothyroxine.
- Andere Medikamente
- Levothyroxine 112mcg daily ASA 81mg daily
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 13.01.2022
- Impfdatum
- 23.11.2021
- Beginn
- 23.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- UN / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Feeling abnormal
Food craving
Paranoia
Salt craving
Taste disorder
Symptomtext
Mental fog, cravings for sweet/bread, finding meats unappetizing unless they're salty. Paranoia (more than usual)that the vaccine is an immunocastration medication designed to lower my metabolism and cause me to eat less., and I am destined for a life of slavery because I was a bastard child, and by bastard child, I just mean that my father worked a lot, but and was falsely accused of abuse, even though I witnessed my mother instigate a fight by preventing him from sleeping, and threatening him with a knife by jabbing at his face.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Born with one kidney/partial renal dysplasia Being tortured/harassed/threatened/falsely arrested/detained by my parents, police, and mental health professionals because they have been trying to gaslight and convince me that I a sociopath for misspeaking when I was a 7 years old and had a concussion. Most recently intentionally depriving me of sleep, and having the TV so loud that I can clearly hear what they're saying from the garage.
- Vorgeschichte
- Born with one kidney/partial renal dysplasia
- Andere Medikamente
- fish oil/red bull energy drinks/occasional homemade citric acid gel caps I started doing drugs when I was 10 years old because my life was being threatened by police for crimes I didnt commit and I lost hope in having a future. Just tried
- Allergien
- bubble bath when I was a baby, unknown now.
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 91,0
- Geschlecht
- M
- Eingang
- 12.01.2022
- Impfdatum
- 26.11.2021
- Beginn
- 26.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Balance disorder
Burning sensation
Condition aggravated
Dyspnoea exertional
Gait disturbance
Pleural effusion
Symptomtext
Patient reports acute onset of burning in anterior thighs and feet and difficulty with balance and ambulation. He was also subsequently found to have a small pleural effusion adjacent to the right atrium after complaining of dyspnea on exertion which has been ongoing and preceded his booster shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Echocardiogram done for symptoms noted prior to his vaccination, but completed after and showing loculated pleural effusion w/ possibly developing tamponade - pt has been referred to cardiology
- Aktuelle Erkrankungen
- CKD, COPD, asthma, pulmonary hypertension, tachycardia, memory loss, tremor, BPH, hyperlipidemia, hearing loss, hypertension, anemia of chronic disease, protein calorie-malnutrition, cachexia, dyspnea on exertion
- Vorgeschichte
- CKD, COPD, asthma, pulmonary hypertension, tachycardia, memory loss, tremor, BPH, hyperlipidemia, hearing loss, hypertension, anemia of chronic disease, protein calorie-malnutrition, cachexia, first degree AV block, elevated ferritin, history of environmental allergies, history of nicotine dependence, bilateral hearing loss, Dupuytren's contracture
- Andere Medikamente
- Advair 500/50, ferrous gluconate orally, calcium carbonate orally, Flomax 0.4 mg daily, metoprolol ER 50 mg daily, Proventil as needed, Voltaren gel topically.
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 11.01.2022
- Impfdatum
- 18.11.2021
- Beginn
- 19.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dyskinesia
Feeling cold
Feeling hot
Mobility decreased
Symptomtext
Feeling cold, involuntary muscle jerking, unable to move; feeling warm from head to toe Narrative:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 11.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Arthralgia
Blood test normal
Chest X-ray normal
Chest pain
Electrocardiogram normal
Limb discomfort
Muscle discomfort
Symptomtext
Patient received the vaccination in the left arm. A short while after (as noted) experienced chest pain and intermuscular discomfort in the legs accompanied by joint pain. After approximately 24 hrs symptoms did not improve and was admitted into the hospital around 6 pm. An EKG was performed an no abnormalities were overserved. Chest X-Ray and blood work was performed. Doctor did not find any abnormities with the tests performed at the time. Patient followed up with a virtual visit. This doctor is the named contact on this report and for the follow up visit on 1/11/2021 at 3:00PM via video call.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- 1,0
- Labordaten
- 1/8/2021: EKG 1/8/2021: Full Blood workup 1/8/2021: Chest X-Ray
- Aktuelle Erkrankungen
- Covid-19
- Vorgeschichte
- Kidney Stones
- Andere Medikamente
- None.
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 10.01.2022
- Impfdatum
- 17.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 11,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Back pain
Gait inability
Mobility decreased
Tinnitus
Symptomtext
Sore back and hip, unable to walk or lay down, ringing in the ears.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- None.
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 06.01.2022
- Impfdatum
- 01.12.2021
- Beginn
- 07.12.2021
- Tage bis Beginn
- 6,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Agitation
Bipolar disorder
Condition aggravated
Insomnia
Mania
Symptomtext
One week after 2nd Janssen vaccination, patient began having symptoms of mania. He would have increased agitation, stereotypy and severe insomnia. His awake periods would last up to 39 hours, then sleep the next night for about ten hours and then cycle repeated every other day. this pattern began one week after vaccination. This cycle continued for 14 days and did not subside without an increase in his nighttime clonazepam and Lithium dosing. His bipolar disorder had been stable for several years until this occurrence.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hearing Loss Non-verbal Hypogammaglobulinaemia Kyphosis Scoliosis Unbalanced 2/18 Chromosome Translocation Hashimoto's Thyroiditis Bipolar Disorder Autism Spectrum Disorder Anxiety Disorder Dysphagia Chronic Pulmonary Aspiration
- Andere Medikamente
- Melatonin Gabapentin Iron Vitamin D Elderberry Extract Cetirizine Probiotic Clonazepam Lithium Hyosciamine Sulfate
- Allergien
- Sulfa Clindamycin Ciprofloxacin Codeine Valproic Acid
- Vorherige Impfungen
- 03/12/2021 Janssen Lot#1805025, age 30, patient had 12 hours of fever, lethergy, nausea, vomiting, headache
- Staat
- FL
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 06.01.2022
- Impfdatum
- 09.12.2021
- Beginn
- 10.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Agitation
Arthralgia
Chills
Decreased appetite
Fatigue
Headache
Mobility decreased
Myalgia
Nausea
Pyrexia
Symptomtext
The day after the shot 1) 103 degree fever 2) Muscle aches that left me in bed for a day and a half 3) Joint pain that continues to persist (further description at the end) 4) headaches for several days that I needed to take my migraine medication to help 5) Fatigue that has eased up but still currently affecting me 6) Chills that came and went for several days The First week after 1) Left shoulder muscle pain on the opposite side from injection site but in the same location of where I got it (right shoulder) 2) Continued joint pain that mostly persists but with waves of agitation 3) Still some muscle pain that comes and goes 4) Waves of nausea that has affected how much I'm eating in a day (mostly down to getting one small meal in the evenings)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- evaluation underway
- Aktuelle Erkrankungen
- migraines IBS
- Vorgeschichte
- Hyperlipidemia sleep apnea GERD Insomnia Depression hypothyroid
- Andere Medikamente
- Sumatriptan succ 25 mg PRN Diclofenac gel 1% Zolpiden tartrate 10 mg Omeprazole 20 mg Mirtazepine 15 mg Buproprion 150 Levothyroxine 100 mcg Rosuvastaitn 40 mg Dicyclomine 10 mg
- Allergien
- Codeine
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 06.01.2022
- Impfdatum
- 19.11.2021
- Beginn
- 19.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Burning sensation
Ear discomfort
Gait disturbance
Mobility decreased
Muscular weakness
Pain
Pain in extremity
Paraesthesia
Ultrasound Doppler
Urine analysis
Symptomtext
Tingling fingers (both hands), tingling toes (both feet), tingling back & outside of both legs, tingling top of thighs both legs. Also Burning fingers, burning top of both feet Also Wrist weakness. Also Shooting pain in legs. Occasional pressure both ears. Trouble walking and lifting things Severity varies day by day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- (12/21/2021) Ultrasound Vein /Vascular ultrasound (both legs) (12/29/2021) Blood work & urine (11/29/2021) Visit with spine/back doctor and waiting to schedule nerve test and potential MRI
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Thimerosal, Penicillin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 06.01.2022
- Impfdatum
- 28.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest discomfort
Chest pain
Chills
Discomfort
Headache
Heart rate increased
Hyperhidrosis
Pain
Sleep disorder
Symptomtext
12 pm: Time of vaccination. 6 pm - 12 am: Onset and gradually increasing chills. 12 am - 3 am: In addition to continuing chills, heartbeats per second was approximately in the 2.5 to 3 range. Fell asleep shortly after midnight. 3 am: Awakened with sweating and ongoing rapid heartbeat. Burning heart sensation. 3:11 am: Heartbeat began decreasing. 3:41 am: Heartbeats per second in the 2 to 2.5 range. 4 am: Heart issues subsiding, but still uncomfortable. Throbbing pain in head like someone hitting the back of head with lumber. 6:25 am: Heartbeats per second still above 2. Throbbing pain in head continues. Stabbing sensation in heart. 8:12 am: Out of bed. Issues lessening, but throbbing head pain continues. One week later 1/5/2022: Continued soreness/tightness in heart.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 05.01.2022
- Impfdatum
- 14.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 14,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood pressure increased
Chest pain
Dyspnoea
Electrocardiogram
X-ray
Symptomtext
PATIENT CALL 01/05/21 TO LET US KNOW SHE HAS BEEN HAVING CHEST PAIN AND SHORTNESS OF BREATH SINCE SHE HAS RECIEVED THE VACCINE ON 12/14/21. SHE WENT TO EMERGENCY ROOM 12/28/21 HAD X-RAY AND EKG. PATIENT SAYS HAS HAD ELEVATED BLOOD PRESSURE. WENT TO EMERGENCY ROOM AGAIN 01/04/21 FOR SAME REASONS. STAYED FOR 7 HOURS WAS NEVER SEEN. STILL COMPLAININ OF CHEST PAIN. PATIENT TOLD TO FOLLOW UP WITH PCP
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- UNKNOWN
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- UNKNOWN
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 04.01.2022
- Impfdatum
- 21.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Chills
Dyspnoea
Fatigue
Headache
Injection site pain
Insomnia
Myalgia
Pain
Pallor
Pyrexia
Symptomtext
No symptoms for 10 hours. After 10 hours I started to feel tired and some fever. I was pale. After 12 hours high fever (104F) and chills. I started shivering intermittently. With fever my muscles, joints and all areas where I had surgeries (dental implant and appendices) started to hurt (6-7 on a scale from 1-10). Pain was not constant and lasted for about 4 hours. After 14 hours I had difficulty breathing. Eventually I went to bed but could not sleep. I hydrated with water but the taste of it was like cooking oil (strange feeling which I never experienced before). After 16 hours severe headache started to the point where it was hurting turning my head. By morning (24 hours after vaccination) the muscle and general body pain was almost gone but headaches continued for another 12 hours. Fever went down after an afternoon nap. After another night sleep I returned to a functional normal (48 hours after injection). Pain to the injection site lasted for another 5 days but was mild. It is the first injection in my life when I had side effects of this nature. I did not seek medical attention because my heart did not show any abnormal behavior during this time and that was truly my primary concern.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 02.01.2022
- Impfdatum
- 09.12.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 6,0
- Dosis
- 1
- Route/Site
- UN / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Atypical pneumonia
Discomfort
Dyspnoea
Pleurisy
Symptomtext
I felt like I couldn't breathe in deeply for 6 days. It was just very uncomfortable to breathe deeply, I did not feel pain. I initially thought it might be walking pneumonia or pleurisy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Atypical pneumonia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- non
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 30.12.2021
- Impfdatum
- 03.12.2021
- Beginn
- 03.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Cough
Dysphagia
Dyspnoea
Headache
Lip swelling
Nausea
Rash
Swollen tongue
Symptomtext
Within 15 minutes of the injection started having lip and tongue swelling - went ER then started having a rash on neck, nausea, headache, difficulty swallowing, mild SOB and coughing
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- IV Benadryl, Pepcid and steriods
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension Asthma RA
- Andere Medikamente
- Losartan Allegra Ferrous sulfate Vitamin D Symbicort
- Allergien
- Pfizer COVID vaccine
- Vorherige Impfungen
- Pfizer COVID
- Staat
- MI
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 30.12.2021
- Impfdatum
- 18.11.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 42,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Abdominal pain
Pneumonia
Symptomtext
Came to the ED for abdominal pain. Pt also has pneumonia.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pneumonia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 30.12.2021
- Impfdatum
- 30.11.2021
- Beginn
- 30.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Headache
Imaging procedure
Migraine
Symptomtext
Patient claims that she started having headaches the day after she received the vaccine (received on 11/30/21). She claims that she has been having headaches since then and has since been diagnosed with migraine headaches which she says she may have as many as 4/day. She claims that she has had imaging done which showed no evidence of blood clots in her brain and she has been referred to a neurologist.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- imaging - unsure of the date
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 27.12.2021
- Impfdatum
- 16.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bronchitis
Chest X-ray normal
Chest pain
Cough
Diarrhoea
Electrocardiogram normal
Pain
Symptomtext
Went to the doctor on 12/21/2021; Diagnosis: cough and chest pain; Treatment plan: Wanted me to let it pass, but I still feel achy; Did a Teledoc on 12/27/2021. Diagnosis: Bronchitis. Also developed diarrhea No F/u
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Chest X-ray - Normal ECG - Normal
- Aktuelle Erkrankungen
- Asthma, and Lung Scarring
- Vorgeschichte
- Asthma, and lung Scarring
- Andere Medikamente
- Montelukast 10mg 1x at night, Rosuvastatin 5mg 1xday, Amperozide 40 mg 1xday, Terbinafine HCL 250mg 1xday
- Allergien
- Codeine and Amoxicillin
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 14.12.2021
- Beginn
- 14.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Chest X-ray normal
Chest pain
Electrocardiogram T wave abnormal
Feeling hot
Chest X-ray
Electrocardiogram
Feeling of body temperature change
Hypoaesthesia
N-terminal prohormone brain natriuretic peptide
Throat tightness
Troponin
Prohormone brain natriuretic peptide
Symptomtext
THROAT TIGHTNESS; T WAVE ABNORMALITY IN ECG.; PAIN IN ANKLES; SENSATION OF NUMBNESS RADIATED TO PATIENT'S SHOULDER BLADES AND LEFT ARM; FEELING OF FEVER, BUT NO DOCUMENTED FEVER; CHEST PAIN; This spontaneous report received from a health care professional via Regulatory Authority VAERS (Vaccine Adverse Event Reporting System) (VAERS ID: 749438) concerned a 22 year old female. The patient's height, and weight were not reported. The patient's past medical history included: viral pericarditis in 2018. On an unspecified date in 2018, patient underwent lab tests EKG (NR: not provided) Sinus rhythm with moderate T wave abnormality noted in precordial leads. Concurrent conditions included: PSTD (Post-traumatic stress disorder), and dizziness. The patient had no known allergies to medications, food or other products, no illness at the time of vaccination and up to one month prior, no adverse event following any previous vaccine. The patient was not pregnant at the time of vaccination. The patient was previously treated with diphtheria vaccine toxoid/pertussis vaccine acellular/tetanus vaccine toxoid (vaccine given on right arm, intramuscular, batch number:224CG) for unknown indication. The patient received covid-19 vaccine ad26.cov2.s (janssen series 1) (suspension for injection, intramuscular, batch number: 213D21A expiry: unknown) dose was not reported, 1 total administered on left arm on 14-DEC-2021;13:17 for an unknown indication. Concomitant medication included duloxetine for unknown indication. On 14-DEC-2021, patient experienced chest pain and throat tightness 3 hours (16:00) after vaccination. The patient experienced chest pain with a sensation of numbness radiated into patient's shoulder blades and left arm. Patient also endorses pain in ankles and feeling as patient has a fever, but no documented fever present. Patient was admitted, observation for monitoring and was treated with ibuprofen and acetaminophen as needed. Patient was discharged following morning with instruction to continue ibuprofen and/or acetaminophen as needed for vaccine side effects. On an unspecified date, patient experienced throat tightness and T wave abnormality in electrocardiogram. On an unspecified date, the patient was hospitalized. Number of days of hospitalization was 1 day. Laboratory data (dates unspecified) included: Chest X-ray (NR: not provided) negative, EKG (NR: not provided) Sinus rhythm with moderate T wave abnormality noted in precordial leads (similar to previous Electrocardiogram in 2018), NT-proBNP (N-terminal prohormone brain natriuretic peptide) (NR: not provided) 227 and Troponin (NR: not provided) Undetectable. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the chest pain, sensation of numbness radiated to patient's shoulder blades and left arm, pain in ankles, feeling of fever but no documented fever, throat tightness and T wave abnormality in ECG was not reported. This report was serious (Hospitalization Caused / Prolonged).; Sender's Comments: V0-20211242646-Covid-19 vaccine ad26.cov2.s- Chest Pain, Throat tightness, Feeling of fever but no documented fever, T wave abnormality in ECG. This event(s) is considered unassessable. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s). 20211242646-Covid-19 vaccine ad26.cov2.s- Pain in ankles, Sensation of numbness radiated to patient's shoulder blades and left arm. This event(s) is labeled per RSI and is therefore considered potentially related.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- 1,0
- Labordaten
- Test Date: 2018; Test Name: EKG; Result Unstructured Data: Sinus rhythm; Comments: Sinus rhythm with moderate T wave abnormality noted in precordial leads.; Test Name: Chest X-ray; Result Unstructured Data: negative; Test Name: NT-proBNP; Result Unstructured Data: 227; Test Name: EKG; Result Unstructured Data: Sinus rhythm; Comments: Sinus rhythm with moderate T wave abnormality noted in precordial leads (similar to previous Electrocardiogram in 2018).; Test Name: Troponin; Result Unstructured Data: Undetectable
- Aktuelle Erkrankungen
- Dizziness; Post-traumatic stress disorder
- Vorgeschichte
- Medical History/Concurrent Conditions: Viral pericarditis; Comments: Patient had no known allergies to medications, food or other products. No illness at the time of vaccination and up to one month prior. Patient had no adverse event following any previous vaccine.
- Andere Medikamente
- DULOXETINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 14.12.2021
- Beginn
- 14.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Chest X-ray normal
Chest pain
Electrocardiogram T wave abnormal
Feeling hot
Chest X-ray
Electrocardiogram
Feeling of body temperature change
Hypoaesthesia
N-terminal prohormone brain natriuretic peptide
Throat tightness
Troponin
Prohormone brain natriuretic peptide
Symptomtext
THROAT TIGHTNESS; T WAVE ABNORMALITY IN ECG.; PAIN IN ANKLES; SENSATION OF NUMBNESS RADIATED TO PATIENT'S SHOULDER BLADES AND LEFT ARM; FEELING OF FEVER, BUT NO DOCUMENTED FEVER; CHEST PAIN; This spontaneous report received from a health care professional via Regulatory Authority VAERS (Vaccine Adverse Event Reporting System) (VAERS ID: 749438) concerned a 22 year old female. The patient's height, and weight were not reported. The patient's past medical history included: viral pericarditis in 2018. On an unspecified date in 2018, patient underwent lab tests EKG (NR: not provided) Sinus rhythm with moderate T wave abnormality noted in precordial leads. Concurrent conditions included: PSTD (Post-traumatic stress disorder), and dizziness. The patient had no known allergies to medications, food or other products, no illness at the time of vaccination and up to one month prior, no adverse event following any previous vaccine. The patient was not pregnant at the time of vaccination. The patient was previously treated with diphtheria vaccine toxoid/pertussis vaccine acellular/tetanus vaccine toxoid (vaccine given on right arm, intramuscular, batch number:224CG) for unknown indication. The patient received covid-19 vaccine ad26.cov2.s (janssen series 1) (suspension for injection, intramuscular, batch number: 213D21A expiry: unknown) dose was not reported, 1 total administered on left arm on 14-DEC-2021;13:17 for an unknown indication. Concomitant medication included duloxetine for unknown indication. On 14-DEC-2021, patient experienced chest pain and throat tightness 3 hours (16:00) after vaccination. The patient experienced chest pain with a sensation of numbness radiated into patient's shoulder blades and left arm. Patient also endorses pain in ankles and feeling as patient has a fever, but no documented fever present. Patient was admitted, observation for monitoring and was treated with ibuprofen and acetaminophen as needed. Patient was discharged following morning with instruction to continue ibuprofen and/or acetaminophen as needed for vaccine side effects. On an unspecified date, patient experienced throat tightness and T wave abnormality in electrocardiogram. On an unspecified date, the patient was hospitalized. Number of days of hospitalization was 1 day. Laboratory data (dates unspecified) included: Chest X-ray (NR: not provided) negative, EKG (NR: not provided) Sinus rhythm with moderate T wave abnormality noted in precordial leads (similar to previous Electrocardiogram in 2018), NT-proBNP (N-terminal prohormone brain natriuretic peptide) (NR: not provided) 227 and Troponin (NR: not provided) Undetectable. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the chest pain, sensation of numbness radiated to patient's shoulder blades and left arm, pain in ankles, feeling of fever but no documented fever, throat tightness and T wave abnormality in ECG was not reported. This report was serious (Hospitalization Caused / Prolonged).; Sender's Comments: V0-20211242646-Covid-19 vaccine ad26.cov2.s- Chest Pain, Throat tightness, Feeling of fever but no documented fever, T wave abnormality in ECG. This event(s) is considered unassessable. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s). 20211242646-Covid-19 vaccine ad26.cov2.s- Pain in ankles, Sensation of numbness radiated to patient's shoulder blades and left arm. This event(s) is labeled per RSI and is therefore considered potentially related.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- 1,0
- Labordaten
- Test Date: 2018; Test Name: EKG; Result Unstructured Data: Sinus rhythm; Comments: Sinus rhythm with moderate T wave abnormality noted in precordial leads.; Test Name: Chest X-ray; Result Unstructured Data: negative; Test Name: NT-proBNP; Result Unstructured Data: 227; Test Name: EKG; Result Unstructured Data: Sinus rhythm; Comments: Sinus rhythm with moderate T wave abnormality noted in precordial leads (similar to previous Electrocardiogram in 2018).; Test Name: Troponin; Result Unstructured Data: Undetectable
- Aktuelle Erkrankungen
- Dizziness; Post-traumatic stress disorder
- Vorgeschichte
- Medical History/Concurrent Conditions: Viral pericarditis; Comments: Patient had no known allergies to medications, food or other products. No illness at the time of vaccination and up to one month prior. Patient had no adverse event following any previous vaccine.
- Andere Medikamente
- DULOXETINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 22.12.2021
- Impfdatum
- 09.12.2021
- Beginn
- 09.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dizziness
Dyspnoea
Respiration abnormal
Symptomtext
Narrative: Pt went to her car to pick up her thing and went back to the observation. Reported of feeling lightheadedness and dizziness and shortness of breath. noted pt is breathing faster like 25. Sat down and @1505 vs: BP 120/56 HR:90 O2 sat: 96 %. Pt said she hasnt ate lunch yet and she took 2 tablets of loratidine this morning before going to work which makes her sleepy. Offered some snacks, chocolates, verified she doesn't have any food allergies. Drink more fluids and ate some food and pt said she was feeling better. @1520 VS: HR:80 BP 116/73, o2: 98% - looks more comfortable said not feeling lightheaded anymore. At 60min observation checked her VS: HR-83, BP- 119/65, o2- 98%. Pt said she called her son and will picked her up in 30 min. Called transport and wheelchair to go to cafeteria and have waited for her son to pick her up VS are WNL.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 22.12.2021
- Impfdatum
- 06.11.2021
- Beginn
- 06.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Dizziness
Electrocardiogram ambulatory
Fatigue
Headache
Heart rate increased
Interchange of vaccine products
Lymphadenopathy
Petechiae
Pruritus
Urticaria
Symptomtext
hives and itching including eyes, tongue, face; rapid heart rate; additional Benadryl and Pepcid given 2 hours after injection/3 hours after pre-dosing; minor petechiae, fatigue, headache, lymph node swelling on same side as injection site. Dizziness increased began about 7 days after injection and lasted about 6 weeks.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Holter monitor through Cardiology
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Migraines, Environmental Allergies, Anxiety, dizziness that was made significantly worse after Pfizer vaccine that ended after 3 months then mildly began again (have previously had issues with mild dizziness a few years before the Pfizer vaccine)
- Andere Medikamente
- Mucinex, Magnesium Hydroxide, Zyrtec, Claritin, Probiotics, Flonase, Xanax. Benadryl and Pepcid taken per PCP recommendations one hour prior to immunization.
- Allergien
- Ambien, Oxycodone, Reglan, Pfizer Covid-19 immunization (per PCP)
- Vorherige Impfungen
- Pfizer Covid-19
- Staat
- CA
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 20.12.2021
- Impfdatum
- 01.03.2021
- Beginn
- 23.04.2021
- Tage bis Beginn
- 53,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Dysmenorrhoea
Mobility decreased
Pain
Ultrasound pelvis normal
Vomiting
Symptomtext
Relevant history: Had endometrial ablation in 2014, no menstruation, cramping, or anything similar up for >6 years. Got 2nd vax (Pfizer) dose on 3/22/21. Around 4/23-4/24 have some mild cramping, don't realize that it might be menstrual cramps at the time as this is the first time in 6+ years I have had any signs of menstruation. Every month since I have at least some moderate cramping, with about half of the months being incredibly severe and debilitating (vomiting, unable to move from pain). I now have to take narcotics some months to get through. Considering hysterectomy if it doesn't resolve within ~ 1 yr. Made me very hesitant to get booster- if vaccines were less politicized and I could rely on herd health I would not have gotten one but as it were risking death with COVID is probably worse.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- Pelvic ultrasound 8/31/2021- came up essentially normal
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Multivitamin with iron
- Allergien
- Mild allergies to some animals, some foods (hives, itchy eyes or skin, etc. no anaphylaxis)
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 19.12.2021
- Impfdatum
- 20.11.2021
- Beginn
- 19.12.2021
- Tage bis Beginn
- 29,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ophthalmological examination abnormal
Retinal migraine
Vaccine positive rechallenge
Symptomtext
Approx. 1 month after initial vaccine on 03/20/21 and approx. 1 month after booster (11/20/21) I began having retinal migraines. I have had no migraines in my life until these vaccines. I wondered about it after the first vaccine (and reported on vsafe) but now that it has happened again after the booster it seems much more likely related to the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Retinal migraine
- Hospital-Tage
- -
- Labordaten
- Went to the eye dr. after the first vaccine and he said that retinal migraines originate in the brain, not the eyes, and that my eyes looked fine. Thought perhaps it could be hormone related (a few friends and relatives also experienced this during peri-menopause/menopause) so didn't pursue further as they went away.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Estradiol (.075 mg. patch), progesterone (100 mg cap), vitamin D3 (5000 IU), Vitamin B complex, thyroid supplement (A,C,E, Iodine, Selenium, etc.), melatonin/L-tryptophan/B6 supplement , ashwagandha (500 mg.)
- Allergien
- none
- Vorherige Impfungen
- retinal migraines, 52, 03/202/21, J&J COVID
- Staat
- TX
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 17.12.2021
- Impfdatum
- 15.12.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal discomfort
Feeling abnormal
Feeling jittery
Headache
Injection site pain
Pain
Paraesthesia
Symptomtext
Headache throat dryness/scratchiness, parasthesias, skin feels like bubbling all over, jittery, site pain, feels like index finger pressing on left sternum Narrative: 1. First ONE minute - pain at and around site 2. 5 MINUTE parasthesias on injected arm hand/fingers 3. 30 MINUTE dullness, soft headache 4. LESS THAN 3 HOURS vacillating pains, headaches (which moves and varies in intensity) Has had hives previously from an unknown source in the past. "This feels like I am on a drug." stomach upsets jutteriness
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 17.12.2021
- Impfdatum
- 13.12.2021
- Beginn
- 13.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Dysgeusia
Pain in jaw
Swelling
Tooth disorder
Symptomtext
pain in middle of chest, neck swelling, teeth issues, metallic taste, jaw hurt
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- ekg
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 16.12.2021
- Impfdatum
- 30.11.2021
- Beginn
- 04.12.2021
- Tage bis Beginn
- 4,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Balance disorder
Blood test
Chest X-ray
Confusional state
Dyspnoea
Electrocardiogram
Fibrin D dimer increased
Hypoaesthesia
Pain
Ultrasound scan
Symptomtext
By Saturday 3pm Dec 4th. I sought out Emergency room .I had been feeling a numbed sensation in my legs and muscles and or veins throbbed throughout my body, heart was throbbing along with my neck, confusion with thoughts, at times hard to breathe in and out. Not painful just unsteady with walking
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Blood work was drawn, I have had 2 two ultrasounds to rule out blood clots, elevated D-Dimer, chest xray,and an ecg that showed abnormalities dates Are Dec 4th and 6 th and 7th with test my primary ordered and referred me to a cardiologist/thorastic doctor on Dec 22nd . I am unsure what the next steps are for this un coming appointment
- Aktuelle Erkrankungen
- Ibs- d, acid reflux, kidney disease stage 3b, elevated creatine level,
- Vorgeschichte
- history of interstitial lung disease right lung re-sectioned, Raynauds Snydrome ,history of Ulcerative colitis, Fibromyalgia
- Andere Medikamente
- Excedrine migraine,tylenol arthritis 8hr,vitamin d gummy, omgea 3 gummy, woman's multi gummy, lansoprazole 15mg,dicyclomine 20mg
- Allergien
- Sulfa meds,pencillin,penicillin, doesn't react well to ducolax tab or miralax, alot of pain medications result in allergies, ibuprofen
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- -
- Geschlecht
- U
- Eingang
- 16.12.2021
- Impfdatum
- -
- Beginn
- 10.11.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dyspnoea
Oxygen saturation
Oxygen saturation decreased
Symptomtext
get winded much more easily; blood oxygen numbers were below 95; This spontaneous report received from a patient concerned a patient of unspecified age and sex. The patient's height, and weight were not reported. The patient's past medical history included: covid-19, and loss of smell, and other pre-existing medical conditions included: Patient did not have a history of lung issues, allergies, or known comorbidities outlined in the patient or prescriber package inserts. Patient was a healthy and athletic person whose blood oxygen numbers hovered in the 97-100 range prior to received the vaccine. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 213D21A, and expiry: UNKNOWN) dose was not reported, administered on 08-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 10-NOV-2021, the patient experienced blood oxygen numbers were below 95. Laboratory data included: Oxygen saturation (NR: not provided) 94 %, 93 %, 83 %, 75 %. On an unspecified date, the patient experienced get winded much more easily. Laboratory data (dates unspecified) included: Oxygen saturation (NR: not provided) 94 %, 78 %. Treatment medications (dates unspecified) included: salbutamol. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the blood oxygen numbers were below 95 and get winded much more easily was not reported. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Test Date: 20211110; Test Name: Oxygen saturation; Result Unstructured Data: 94 %; Comments: Below 95 (with the home unit).; Test Date: 20211110; Test Name: Oxygen saturation; Result Unstructured Data: 93 %; Comments: Below 95 (with the home unit).; Test Date: 20211110; Test Name: Oxygen saturation; Result Unstructured Data: 83 %; Comments: Below 95 (with the home unit).; Test Date: 20211110; Test Name: Oxygen saturation; Result Unstructured Data: 75 %; Comments: Below 95 (with the home unit).; Test Name: Oxygen saturation; Result Unstructured Data: 94 %, average was 94; Comments: 78 to 100% range.; Test Name: Oxygen saturation; Result Unstructured Data: 78 %, dipped as low as 78; Comments: 78 to 100% range.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19; Loss of smell; Comments: Patient did not have a history of lung issues, allergies, or known comorbidities outlined in the patient or prescriber package inserts. Patient was a healthy and athletic person whose blood oxygen numbers hovered in the 97-100 range prior to received the vaccine.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 13.12.2021
- Impfdatum
- 16.11.2021
- Beginn
- 20.11.2021
- Tage bis Beginn
- 4,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injected limb mobility decreased
Symptomtext
patient unable to move right arm above shoulder line and move backward
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- arthritis
- Vorgeschichte
- unknown
- Andere Medikamente
- sertalin 50mf, valium 5mg
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 13.12.2021
- Impfdatum
- 21.11.2021
- Beginn
- 11.12.2021
- Tage bis Beginn
- 20,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
COVID-19
Chills
Dehydration
Dyspnoea
Electrocardiogram
Fatigue
Orthopnoea
Pyrexia
Respiratory failure
Respiratory symptom
Sleep disorder
Urinary retention
Symptomtext
Patient is a 69-year-old female with a history of a kidney transplant that was performed at Hospital in 2018 presents the emergency department ambulatory complaining of shortness of breath as well as dehydration. Over the last 3 days she has not been able to sleep well. She states that she has been drinking up to a liter to a liter and a half of water every day and has not been able to pee yet. She is also complaining of some shortness of breath. She has been vaccinated for COVID-19 including a booster. She is currently on antirejection medications. Husband states that she has been very short of breath especially when she lays down. Patient denies any chest pain Associated Symptoms: chills, fatigue, fever, orthopnea, shortness of breath, URI symptoms, weakness
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dehydration
- Hospital-Tage
- 3,0
- Labordaten
- Patient was seen immediately on arrival to the emergency department plan of care discussed with the patient and husband at bedside. Patient immediately placed on nasal cannula as she was saturating 65% on room air. We will plan for blood work including BNP, chest x-ray, Covid test and closely monitor patient throughout stay. Case was discussed at length with Dr. on shift change. EKG shows sinus at 85 0927 hours Case DW and accepted for respiratory failure due to covid
- Aktuelle Erkrankungen
- Patient is a 69-year-old female with a history of a kidney transplant that was performed at Hospital in 2018 presents the emergency department ambulatory complaining of shortness of breath as well as dehydration. Over the last 3 days she has not been able to sleep well. She states that she has been drinking up to a liter to a liter and a half of water every day and has not been able to pee yet. She is also complaining of some shortness of breath. She has been vaccinated for COVID-19 including a booster. She is currently on antirejection medications. Husband states that she has been very short of breath especially when she lays down. Patient denies any chest pain Associated Symptoms: chills, fatigue, fever, orthopnea, shortness of breath, URI symptoms, weakness Denies Symptoms: doesn't bruise easily/ no chest pain/ no cough/ no dysphagia/ no eye pain/ no eye redness/ no focal weakness/ no frequency/ no gum bleeding/ no homicidal ideas/ no injury/ no joint pain/ no nausea/ no neck pain/ no palpitations/ no parathesias/ no photophobia/ no rash/ no redness/ no sensory changes/ no skin lesions/ no sore throat/ no substance abuse/ no suicidal ideas/ no UTI symptoms/ no vomiting/ no wheezing Patient was seen immediately on arrival to the emergency department plan of care discussed with the patient and husband at bedside. Patient immediately placed on nasal cannula as she was saturating 65% on room air. We will plan for blood work including BNP, chest x-ray, Covid test and closely monitor patient throughout stay. Case was discussed at length with Dr. on shift change. EKG shows sinus at 85 0927 hours Case DW and accepted for respiratory failure due to covid
- Vorgeschichte
- History of: clinical trial paticipant, acute renal failure, dialysis, HTN, DM, GERD, kidney transplant in 2018. currently on antirejection medications
- Andere Medikamente
- Current Home Medications 1. atorvastatin 20 mg oral tablet : 1 tab(s) orally once a day at bedtime 2. bumetanide 1 mg oral tablet : 1 tab(s) orally every other day 3. folic acid 1 mg oral tablet : 1 tab(s) orally once a day 4. latanoprost o
- Allergien
- Allergy: - Norco; (Drug) Unknown
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 13.12.2021
- Impfdatum
- 26.11.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- 5,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Headache
Hypoaesthesia
Muscle spasms
Palpitations
Paraesthesia
Symptomtext
headache,heart palpitation,chest pain,left side of my face has numbness,muscle cramsp in my legs,tingling in my hands and feet
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 11.12.2021
- Impfdatum
- 04.12.2021
- Beginn
- 04.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Interchange of vaccine products
Tinnitus
Symptomtext
Exaserbated the ringing in my head from the Pfizer vaccine that I received on April 14th. I previously reported this event. The Pfizer number is ER8727. The ringing in my head is persistent and louder.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- I discussed the initial Pfizer triggered event in November with Dr. during my annual physical. He did not recommend treatment.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Trazedone
- Allergien
- None
- Vorherige Impfungen
- Pfizer COVID Vaccine
- Staat
- AZ
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 11.12.2021
- Impfdatum
- 06.12.2021
- Beginn
- 06.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Dizziness
Fatigue
Headache
Immediate post-injection reaction
Injection site bruising
Injection site haemorrhage
Pain
Paraesthesia
Pyrexia
Symptomtext
Bled more than we?ve ever saw from a shot. And left a raised bruise. Almost immediately husband felt tingly in his skin and face. Within an hour he was feeling dizzy and tired. He got chills and a fever. He started to feel aches all over. He slept five hours in the middle of the day. And had a bad headache. This lasted Monday, Tuesday, Wednesday and most of Thursday. By Friday he had just the headache, aches, and tiredness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- Just the COVID shot.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Penicillin and Demerol
- Vorherige Impfungen
- Flu
- Staat
- MD
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 10.12.2021
- Impfdatum
- 02.12.2021
- Beginn
- 07.12.2021
- Tage bis Beginn
- 5,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Back pain
Blood test normal
Fatigue
Headache
Hypertension
Hypoaesthesia
Nasopharyngitis
Paraesthesia
Respiratory tract congestion
Rhinorrhoea
Symptomtext
Tingling/numbness in hands and feet all day and night Back pain High blood pressure (149/90) Fatigue Headache Feeling of head cold Runny nose Congestion
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- 12/7-12/8 Blood test- results normal
- Aktuelle Erkrankungen
- N/a
- Vorgeschichte
- N/A
- Andere Medikamente
- Multivitamin
- Allergien
- Morphine
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 10.12.2021
- Impfdatum
- 18.11.2021
- Beginn
- 19.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal discomfort
Arthralgia
Asthenia
Chills
Diarrhoea
Fear
Feeling abnormal
Feeling hot
Heavy menstrual bleeding
Impaired work ability
Inflammation
Loss of personal independence in daily activities
Mobility decreased
Pain
Peripheral coldness
Polymenorrhoea
Pyrexia
Sleep disorder
Symptomtext
At 2:30 am I was woken up out of my sleep, my feet were frozen cold even though I had on socks and feet were under the cover. My body was shivering and I had extreme aching all over. I got out of bed and started pacing back and forth in the living room because I was frightened at the extreme reaction I was having to the vaccine. I decided to lay down and sleep it off. When I woke up to go to work the following morning, I couldn't move out of the bed. My whole body had severe aching and my hip joints hurt too bad to get out of bed. I layed back down and called out-of-work. I did not leave the bed all day on 11/19/2021. The following morning the pain decreased only a little and I noticed my entire body feeling feverish from my head down to my feet- it felt like fire in my stomached. I got out of bed to use the bathroom and had instant diarrhea, ten episodes of diarrhea that 1 day. I felt awful because I had to sit on the toilet every hour and couldn't leave the house, on top of that I began bleeding vaginally. I thought this was odd because my period just ended a week prior. I put on a maxi-pad and went back to bed after drinking advanced Pedialyte and Ibuprofen 600mg. Third day I was still bleeding vaginally and too sore to leave the house. My family began to wonder what was wrong with me as I didn't leave my room for almost 3 days. I was too weak and still felt extreme INFLAMATION incasing my whole body. It was a VERY scary experience as I have never had symptoms like this before. The diarrhea slowed down on the third day and I was able to have 1 small bowel movement. Nothing I did would make the heat and inflammation go away. The Ibuprofen only relieved the inflammation for 4-6 hours and then it came right back. After 3 days of vaginal bleeding, bright red blood, it stopped. I thought maybe I had an early period but then 3 days after I stopped bleeding, it started again. So now I have been bleeding a total of 3 weeks since receiving the JJ vaccination. I don't know what's going on with my body but its having a severe adverse reaction to the vaccination. I should of development MEMORY cells by now and begun to resolve theses issues. But that's not happening. My body doesn't know what to do with what was introduced to the immune system, its going out of wack!!!! I decided to wait 14 days because the nurse giving the vaccine said I need to watch for severe symptoms for 14 days and "I should be fine" after that timeframe. After 14 days, I still felt the same exact way. I became very worried as this was impacting my life. I was too weak to carry out my regular daily routine and take care of my son as before. I contacted the hospital that administered the vaccine and spoke to my primary care provider NP. She ordered some Benadryl and corticosteroids for window pickup to help with my symptoms. The Nurse Practitioner stated to me," I dont see in your medical record that you received the vaccination." IT WAS NEVER RECORDED!! I have the card, the paper immunization document and they symptoms to prove I got it, but the facility did not document it.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- I have not had any lab testing yet.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- n/a
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- HI
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 08.12.2021
- Impfdatum
- 15.11.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- 16,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Cardiac discomfort
Chest discomfort
Dyspnoea
Symptomtext
Symptoms appeared about two weeks after the shot. Shortness of breath, pressure on my heart, pressure on my lungs, who body feels weak. I have not treatments yet.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 08.12.2021
- Impfdatum
- 06.12.2021
- Beginn
- 08.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Fatigue
Limb discomfort
Muscular weakness
Paraesthesia
Sleep disorder
Symptomtext
Woke up at ~1:34AM with the same chest pains and extremity feelings as previous heart attack. Waited it out, continued until after 8am, slowly receding . Lingering effect include fatigue and extremities (arms) feeling weak and tingly
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- Sinus infection, completed medications 8days prior
- Vorgeschichte
- Heart Conditions
- Andere Medikamente
- cough drops
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 04.12.2021
- Impfdatum
- 01.12.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Chest pain
Dyspnoea
Fatigue
Pyrexia
Vomiting
Symptomtext
At 9:30PM patient started experiencing shortness of breath, chest pain, fever of 102, sharp pain between the shoulder blades, vomiting, and fatigue that has lasted 2 days now.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE KNOWN
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 04.12.2021
- Impfdatum
- 03.12.2021
- Beginn
- 03.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Feeling hot
Nervousness
Paraesthesia
Symptomtext
Patient felt very shaky, lightheaded, hot, and tingly. She felt like she was going to pass out.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none reported
- Allergien
- sulfites
- Vorherige Impfungen
- HAS FELT LIGHTHEADED BEFORE
- Staat
- NY
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 04.12.2021
- Impfdatum
- 29.10.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 7,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Aphthous ulcer
Arthritis allergic
Back pain
Condition aggravated
Dysuria
Epistaxis
Eye pruritus
Fatigue
Fear
Fungal infection
Hair disorder
Headache
Immune system disorder
Mobility decreased
Mucosal infection
Muscle strain
Myalgia
Nasal odour
Symptomtext
My immune system is not protecting me from infections or allergies, see continuation page I have a history of low IGG values. Back in 2020, my Immunoglobulin G was 550 mg/dL. My IG A was 70 mg/dL. Back in 1996 they performed a bone biopsy, to prove this was genetic. After getting the booster of J&J, batch 213D21A on Oct 29.2021, I had no symptoms for one week and then I started to get symptoms which I normally get when I am fighting a cold or a worsening of my Celiac disease. The difference, which wasn't apparent at first, was I'm not clearing them. I will go into detail for each: Two major items are my allergies are not controllable and I'm being attacked by fungus. 1) Fungus infections are not clearing a. On Nov 17 I got Athlete's Foot. In the past I would catch this if I walked in mud in my back yard by the lake. As soon as my feet would start peeling, I would use a tube of Terbinafine cream and a week later they would be better. This time, I did nothing to cause it, and it is not clearing and in fact spreading. It is 2 ? weeks now. b. On Nov 14th I pulled a few hairs from inside my nose, and they got infected, in the past I put Bacitracin on it and expected it would be healed in 2 days, but on Nov 16th it developed into a fungus infection and had an awful smell. I started treating it with Nystatin and Triamcinolone and 2 ? weeks later I still have the infection. It still smells if I touch it. c. Around Nov 10th hairs on my chest, back and crotch were hurting. I tried to shave them off and each hair got red and hurt worse. I have been rubbing Nystatin and Triamcinolone on them twice daily since. Never has this gone on more than two days. 2) Pollen Allergies are the worst I have ever had a. I take Flonase 50 mcg twice daily and was also taking Astelin 131 mcg. I was having problems urinating and was wetting my pants and dripping on the floor. I haven't had these issues since I had prostate surgery 15 years ago. Back then I had an obstruction, and any antihistamine would keep me from urinating, as it is a muscle relaxer. So, about 9 months ago I started to use Astelin to clear a sinus infection and keep on taking it. Well, I stopped it on Nov 22nd and the voiding problem disappeared, but now I am now so sensitive to pollen, it is troubling. My eyes are itching, and I can't run a meeting for work without sucking on a Halls drop, because I'm constantly congested. This is not allergy season and if my wife brings home flowers I start sneezing if I get near them. If it is windy or raining, I get so congested I get headaches. When I blow my nose, I get some blood out, in it. I've been running our home AC fan to filter out her pollen, but it isn't helping. In the 28 years I lived here I have never experienced these problems. 3) Body strain a. When I lay in bed watching TV, or when I wake up in the morning, I can't lean forward, as it really hurts. In fact, if I must sneeze, I scream out and it causes a sharp pain in my lower back. This strain I had for the past three years as our mattress wore out, but I replaced it with a firm, latex mattress back in July. But in the past three weeks the strain is back and stronger. b. Certain muscles to my left arm really hurt for no reason, randomly. I never had that pain before 4) Mouth Infections a. Around Nov 5th, I thought I had a canker sore and treated it with Hydrogen Peroxide 4%, but it didn't clear in the 7 days it normally takes. It may be gone today, but I have another infection on the other side which is still there. I never had anything like this which lasted more than one week. What I'm so concerned about is it appears to me that my immune system is not working, or it is busy. Medicines are not working, and I am getting worse. I'm getting more fatigued, for no reason. I'm fearing this is Antiboby-Dependent Enhancement (ADE). I want to know if this is from the J&J booster and if at some point my immune system will recover, or do I have to be super careful to avoid any infections as they will kill me? I think I should never get another booster for Covid-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Celiac
- Andere Medikamente
- Crestor, Nexium, Flonase, Astelin, Centrim Adult, Topicort, Nystatin & Triamcinolone
- Allergien
- Propylene Glycol, Gluten, Cefzil, Sulfa, Pollen, Orange, Sorghum, Latex, blue cheese, sulfites, jalapenos
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 03.12.2021
- Impfdatum
- 29.11.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pain
Pain in extremity
Paraesthesia
Symptomtext
Patient reported pain and tingling that started 2 days after receiving the Covid vaccine from the feet and calves then went through the body, the symptom resolved the following day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- LUPUS, CKD, HTN, DIVERTICULITIS, SLEEP APNEA
- Andere Medikamente
- -
- Allergien
- OMEPRAZOLE
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 01.12.2021
- Impfdatum
- 02.11.2021
- Beginn
- 15.11.2021
- Tage bis Beginn
- 13,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Dyspnoea
Heart rate increased
Palpitations
Peripheral swelling
Symptomtext
Shortness of breadth, heart palpitations, speedy heart. Swelling of extremities. Dizziness. Lasting 2 weeks, worst of symptoms today.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 01.12.2021
- Impfdatum
- 19.11.2021
- Beginn
- 19.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Anxiety
Dyspnoea
Flushing
Hypersensitivity
Hypoaesthesia
Paraesthesia
Pruritus
Skin oedema
Urticaria
Wheezing
Symptomtext
Pop up Clinic. Patient received Janssen vaccine at 11:59. Immediately began experiencing allergic reaction. Assessed by RN. BP was taken 184/120, pulse 115, states 97%. Patient displayed the following signs and symptoms: Apprehension, Flushing and skin edema, numbness and tingling in extremities, itching, localized urticaria, , wheezing and labored breathing. Emergency was called and patient was given epi-pen in L thigh IM by Employee.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- had an allergic reaction 10-30-21, went to hospital, was not related to medication or drug allergy per patient, but had received epi-pen
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- had an allergic reaction 10-30-21, went to hospital, was not related to medication or drug allergy
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 29.11.2021
- Impfdatum
- 29.11.2021
- Beginn
- 29.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Hypertension
Injection site hypoaesthesia
Injection site paraesthesia
Symptomtext
DIZZINESS, FEELING FAINT, HIGH BLOOD PRESSURE (175/104), TINGLING NUMBNESS AT INJECTION SITE, ALL WITHIN 15 MINUTES OF VACCINE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- HIGH BLOOD PRESSURE
- Vorgeschichte
- HYPERTENSION
- Andere Medikamente
- IBUPROFEN AND ACETAMINOPHEN
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 29.11.2021
- Impfdatum
- 16.11.2021
- Beginn
- 16.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Paraesthesia oral
Symptomtext
Tongue tingling 37 minutes after vaccine administration - was given 50mg diphenhydramine oral solution at pharmacy, mother then picked up patient and went to ED for further evaluation
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia oral
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 28.11.2021
- Impfdatum
- 27.11.2021
- Beginn
- 28.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Fatigue
Feeling hot
Hyperhidrosis
Listless
Pyrexia
Tremor
Symptomtext
Janssen COVID-19 Vaccine EUA Severe chills/fever and shaking lasting about 30 minutes. Afterwards, the opposite, with sweating and overheated for 5 hours. (this felt a more normal reaction) Next day expected side effects: listless, tired, hot/cold, but feel better presently
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- hiv
- Andere Medikamente
- biktarvy valacyclovir terasozin Vit. D; fiber pill;Turmeric w/pepper
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 26.11.2021
- Impfdatum
- 26.11.2021
- Beginn
- 26.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dysphonia
Paraesthesia oral
Sensation of foreign body
Symptomtext
Adminstered vaccine at 6:34. Approximately 6:55 pm patient stated her tongue felt funny and it felt like she had a lump in her throat. She stated it was similar feeling to how she reacts to shellfish which required a steroid to stop the reaction. Patient's voice became more hoarse so I gave the patient 25mg of diphenhydramine around 7 pm (pt refused 50mg). Within 15 minutes the patient started sounding and feeling better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia oral
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- thyroid disorder
- Andere Medikamente
- levothyroxine
- Allergien
- shellfish-hives, penicillin-rash, scopolamine- swelling
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 24.11.2021
- Impfdatum
- 24.11.2021
- Beginn
- 24.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest discomfort
Dizziness
Dyspnoea
Panic attack
Symptomtext
Approximately 10 minutes after immunization with her second dose of Janssen COVID-19 vaccine, patient reporting symptoms including heaviness and tightness in her chest, like "someone is squeezing my heart". She subsequently had difficulty taking a deep, full breath and felt like she was about to faint. I (pharmacist) gave her water and then called 911 as patient was beginning to panic and condition was not improving. Paramedics arrived shortly and took patient on a stretcher for further evaluation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None per patient.
- Vorgeschichte
- None per patient.
- Andere Medikamente
- None per patient.
- Allergien
- None per patient.
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 24.11.2021
- Impfdatum
- 22.11.2021
- Beginn
- 22.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Balance disorder
Gait disturbance
Hypotension
Symptomtext
STATES INABLITY OF NOT BEING ABLE TO MAINTAIN HIS BALANCE OR WALK STEADILY. DOES HAVE H/O L SIDED WEAKNESS POST CVA. HYPOTENSION PER VITAL SIGNS. HEADACHES, LIGHTHEADEDNESS, AND LOW PULSE COMPLAINT PRIOR TO VACCINE. UNSURE SYMPTOMS ARE VACCINE RELATED VS CHRONIC ILLNESSES.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- 3,0
- Labordaten
- VITAL SIGNS. TRANSFERRED TO LOCAL HOSPITAL FOR FURTHER EVALUATION AND WORK UP. LOCAL HOSPITAL TRANSFERRED PATIENT TO DIFFERENT HOSPITAL
- Aktuelle Erkrankungen
- WHEN EVALUATED BY PROVIDER FOR COMPLAINTS, HE ADMITTED TO BEING LIGHTHEADED, DIZZY AND LOW PULSE FOR A WHILE PRIOR TO VACCINE. REPORTS FALLING AND HEADACHES, AS WELL, PRIOR TO VACCINE.
- Vorgeschichte
- ATRIAL FIB HYPERLIPIDEMIA ISCHEMIC CARDIOMYOPATHY HEMIPLEGIA AND HEMIPARESIS FOLLOWING CVA LEFT SIDED WEAKNESS NEUROPATHY PULMONARY EMBOLUS AND THROMBOSIS OF OTHER SPECIFIED DEEP VEIN OF LEFT LOWER EXTREMITY DIABETES II HYPERTENSION
- Andere Medikamente
- ACETAMINOPHEN AMIODARONE AMLODIPINE ATORVASTATIN CLOPIDOGREL DIGOXIN DULOXETINE ELIQUIS GABAPENTIN lamotrigine lisinopril magnesium oxide METFORMIN METOPROLOL NTG SL PRN NOVOLIN 70/30 NOVOLIN R SERTRALINE TAMSULOSIN VITAMIN D3
- Allergien
- SHELLFISH NEOSPORIN AF
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 23.11.2021
- Impfdatum
- 23.11.2021
- Beginn
- 23.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Dizziness
Dyspnoea
Feeling hot
Hyperhidrosis
Symptomtext
Patient stated that he was going to faint, was sweating, felt hot, stated he was having difficulty breathing
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 23.11.2021
- Impfdatum
- 21.11.2021
- Beginn
- 22.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Abdominal discomfort
Back pain
Blood test normal
Chest X-ray normal
Chest pain
Dyspnoea
Electrocardiogram normal
Heart rate irregular
Pain in extremity
Pyrexia
Symptomtext
Sore arm, low grade fever, intestinal discomfort, upper back and chest pain, shortness of breathe, irregular heart rate
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Chest x-ray, ECG, blood work -everything can back negative
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Migraines
- Andere Medikamente
- Migraine medication
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 23.11.2021
- Impfdatum
- 08.11.2021
- Beginn
- 15.11.2021
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Palpitations
Symptomtext
Heart palpitations/heart racing approximately a week after receiving vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- N/a
- Aktuelle Erkrankungen
- N/a
- Vorgeschichte
- Hypothyroidism
- Andere Medikamente
- Levothyroxine
- Allergien
- Sunflower seeds, flax
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 23.11.2021
- Impfdatum
- -
- Beginn
- 17.11.2021
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest discomfort
Dyspnoea
Paraesthesia
Symptomtext
SHORTNESS OF BREATH; CHEST TIGHTNESS AS OF LAST NIGHT AND THIS MORNING; TINGLING; This spontaneous report received from a pharmacist concerned a 45 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included: allergy to peg (poly ethylene glycol). The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 213D21A and expiry: 11-APR-2022) dose was not reported, administered on 17-NOV-2021 17:45 for prophylactic vaccination. No concomitant medications were reported. On 17-NOV-2021, the patient experienced shortness of breath. On 17-NOV-2021, the patient experienced chest tightness as of last night and this morning. On 17-NOV-2021, the patient experienced tingling. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from tingling, chest tightness as of last night and this morning, and shortness of breath. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Polyethylene glycol allergy
- Vorgeschichte
- Comments: Unknown
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 22.11.2021
- Impfdatum
- 09.11.2021
- Beginn
- 09.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Electrocardiogram
Injection site pain
Neck pain
Pain
Palpitations
Tachycardia
Tinnitus
Symptomtext
Heart palpitations, tachycardia, chest pain, ringing/whistling of left ear, pain at injection site with radiating pain down to left elbow and up into left side of neck.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- EKG 11/22/21
- Aktuelle Erkrankungen
- N/a
- Vorgeschichte
- Sarcoidosis, covid long hauler issues
- Andere Medikamente
- N/A
- Allergien
- Erythromycin, codeine, hydrocodone, Belviq, sulfa
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 20.11.2021
- Impfdatum
- 19.11.2021
- Beginn
- 19.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Balance disorder
Dizziness
Fatigue
Limb discomfort
Muscular weakness
Nausea
Oral discomfort
Paraesthesia oral
Pharyngeal paraesthesia
Tongue discomfort
Symptomtext
Patient was given vaccine, and in 5 minutes she walked up to the counter and stated that she felt as if her tongue was tingling. At that time, my technician spoke to her and reported the event to me. She was able to swallow and when I looked at her tongue and throat, there was no swelling present. Patient was given diphenhydramine 50 mg at that time, and I sat her in a chair that had arms on it. I proceeded to put a pulse ox on her. Her O2 sat was 98 percent and heart rate was 73. The pulse ox was left on throughout the entire time that I was with the patient. Patient started saying that she was feeling tired, proceeded by nausea. In about 3 more minutes, the patient stated that she was feeling like she was going to pass out. I asked if she could lie down in the floor so that she would not hit her head if she passed out. While getting the patient from the chair to the floor, patient stated that her legs were heavy. I assisted her to the floor, and her legs were shaky and wobbly. While assisting her to the floor, I had to physically hold the patient up. I had ice packs on her neck, which she stated that were helping her to feel better. She then stated that she felt as if her throat was tingling and that her lips and tongue were feeling worse. At this time, I asked an employee to call 911, as the patient was feeling worse. Medical personnel were here, and within minutes were assessing the patient. The patient was taken via ambulance to Medical Center. At around 3:30 PM, patient called and said the hospital had released her home, and she was told to continue taking diphenhydramine 25 mg TID for 24 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia oral
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Patient did not report any illness to me at the time of vaccination.
- Vorgeschichte
- Patient does not fill at this pharmacy, and no long term health conditions were reported except diabetes.
- Andere Medikamente
- Patient does not fill medication at this pharmacy.
- Allergien
- Patient does not fill at this pharmacy, and did not list allergies. The allergies were given to the emergency personnel.
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 19.11.2021
- Impfdatum
- 12.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Decreased appetite
Eye pain
Fatigue
Insomnia
Migraine
Myalgia
Nausea
Ocular hyperaemia
Pyrexia
Vomiting
Symptomtext
migraines, muscle aches, chills, fever, extreme fatigue to the point can?t sit up for extended period of time, eye pain, loss of apetite, nausea and vomiting, redness in eyes, insomnia
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 19.11.2021
- Impfdatum
- 02.11.2021
- Beginn
- 04.11.2021
- Tage bis Beginn
- 2,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Asthenia
Chills
Fatigue
Headache
Injection site pain
Tremor
Symptomtext
WED 11-3-2021, 0700 AM: Went to work. Overall weakness, soreness in all major joints, including two longest fingers in both hands. No fever. Slight soreness at injection site. WED 11-3-2021, 11:00 AM: Headache started WED 11-3-2021, 12:30 PM: Took four Pain Zapper brand OTC pills WED 11-3-2021, 02:00 PM: Headache gone, fatigue improved, but joint pain remains. WED 11-3-2021, 05:00 PM: Fatigue returns, joint pain remains. Left work early. WED 11-3-2021, 06:00 PM: Chills and bodily shaking begins. No fever. Took 1 gram of Advil. WED 11-3-2021, 07:00 PM: Chills and bodily shaking improved, slept thru the night. THURS 11-4-2021, 07:00 AM: Still somewhat fatigued, joint pain somewhat improved. Went to work. FRI 11-5-2021, 07:00 AM: Most fatigue and joint pain gone. Went to work. SAT 11-6-2021, 08:00 AM: Adverse events gone.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 19.11.2021
- Impfdatum
- -
- Beginn
- 14.11.2021
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
Chest pain
Headache
Pyrexia
Symptomtext
CHEST PAIN; PRETTY BAD HEADACHE; FEVER AS HIGH AS 103 DEGREES; This spontaneous report received from a patient concerned a 25 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included: alcoholic, and non smoker, and other pre-existing medical conditions included: The patient had no medical history. Patient had no known allergies and no known drug abuse or illicit drug usage. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 213D21A, expiry: UNKNOWN) dose was not reported, administered on 14-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 14-NOV-2021, the patient experienced fever as high as 103 degrees. On 15-NOV-2021, the patient experienced pretty bad headache. Laboratory data included: Body temperature (NR: not provided) 103 degrees. On 17-NOV-2021, the patient experienced chest pain. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from fever as high as 103 degrees, and pretty bad headache on NOV-2021, and had not recovered from chest pain. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Test Date: 20211115; Test Name: Body temperature; Result Unstructured Data: 103 degrees F.
- Aktuelle Erkrankungen
- Alcoholic (Social 1-2 times per week); Non-smoker.
- Vorgeschichte
- Comments: The patient had no medical history. Patient had no known allergies and no known drug abuse or illicit drug usage.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 18.11.2021
- Impfdatum
- 14.11.2021
- Beginn
- 17.11.2021
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest X-ray
Chest pain
Computerised tomogram thorax normal
Dyspnoea
Electrocardiogram normal
Fibrin D dimer increased
Laboratory test
Palpitations
Troponin normal
Symptomtext
Patient developed significant sudden onset of chest pain palpitations and shortness of breath.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- EKG, laboratory tests, chest x-ray, CT scan chest. EKG was unremarkable troponin was normal D-dimer was elevated subsequent CT chest was ordered showed no acute pathology or PE. This was all done on date of evaluation 11/17/2021
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 17.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anxiety
Chest pain
Dyspnoea
Fatigue
Fibrin D dimer normal
Full blood count normal
Headache
Nausea
Neck pain
Night sweats
Urticaria
Symptomtext
Shortness of breath Chest Pain Headache Fatigue Hives (face/legs) Severe Neck Pain Nausea Night Sweats Anxiety
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- CBC, (normal) D-Dimer Levels (negative), Physical Exam
- Aktuelle Erkrankungen
- Sinus Infection
- Vorgeschichte
- Asthma Trigeminal Neuralgia
- Andere Medikamente
- Vitamin D3 Montelukast Spironolactone Hydroxyzine
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 17.11.2021
- Impfdatum
- 10.11.2021
- Beginn
- 16.11.2021
- Tage bis Beginn
- 6,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Tongue ulceration
Vaccine positive rechallenge
Symptomtext
Sores on tongue 1 week after vaccine booster, same thing happened on initial vaccine 8/26/21 reported to Vaers as well
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Addison?s, ear tumor, seizures , back injury
- Andere Medikamente
- Gabapentin, zanaflex,Robaxin, lasix, florinef, hydrocortisone
- Allergien
- Vimpat, depakote , morphine
- Vorherige Impfungen
- Sore on tongue and mouth, sores on legs
- Staat
- TN
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 17.11.2021
- Impfdatum
- 08.11.2021
- Beginn
- 09.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Neuralgia
Pain
Flushing
Nausea
Paraesthesia
Symptomtext
Pt. states that after receiving the 1st dose of J&J 11/08/2021, started experiencing symptoms 11/09/2021 of sharp "nerve" pain shooting throughout the body. Primary visit 11/17/2021 recommended Reporting, Blood Work. Still experiencing symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- Blood Work 11/17/2021
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Seroquel, Flonase
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 17.11.2021
- Impfdatum
- 08.11.2021
- Beginn
- 09.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Neuralgia
Pain
Flushing
Nausea
Paraesthesia
Symptomtext
Pt. states that after receiving the 1st dose of J&J 11/08/2021, started experiencing symptoms 11/09/2021 of sharp "nerve" pain shooting throughout the body. Primary visit 11/17/2021 recommended Reporting, Blood Work. Still experiencing symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- Blood Work 11/17/2021
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Seroquel, Flonase
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 16.11.2021
- Impfdatum
- 16.11.2021
- Beginn
- 16.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood pressure increased
Dizziness
Headache
Hypoaesthesia
Nausea
Paraesthesia
Sensation of foreign body
Symptomtext
15 minutes after vaccine patient developed dizziness, left sided cheek numbness and tingling, headache and nausea. Felt as though he was swallowing a ball in his throat. BP elevated after vaccine at 170/102 but decreased to 140/98 15 minutes later. Symptoms did not worsen and patient was taken to health clinic onsight to be seen by NP and monitored. No SOB or chest tightness. Advised patient to contact PCP to discuss further vaccination. Advised on signs and symptoms to monitor for.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- asthma,environmental allergies, high cholesterol
- Andere Medikamente
- Crestor
- Allergien
- Bactrim causes GI upset, asthma med as a child but cannot remember name but is no longer prescribed today.
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 14.11.2021
- Impfdatum
- 14.11.2021
- Beginn
- 14.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dyspnoea
Rhinorrhoea
Sneezing
Throat tightness
Wheezing
Symptomtext
Wheezing, shortness of breath, throat tightness, running nose, sneezing. Symptoms required use of Albuterol rescue inhaler and Benadryl. Symptoms resolved in approximately 2 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma
- Andere Medikamente
- Levothyroxine
- Allergien
- Oats
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 14.11.2021
- Impfdatum
- 07.11.2021
- Beginn
- 07.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Mobility decreased
Pain in extremity
Symptomtext
Patient called today to inform us that she has had a sore arm since she received her vaccine on 11/7/21. It is not getting any better and she can not lift her arm above her head. Her doctor told her to call us. I asked if she had had any reaction to her first dose of the Janssen and she said no. She is concerned since she is not getting any relief. She has taken a pain reliever, used ice and heat with no improvements.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- none reported
- Vorgeschichte
- none reported
- Andere Medikamente
- unknown
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 13.11.2021
- Impfdatum
- 10.11.2021
- Beginn
- 10.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Hypoaesthesia
Migraine
Paraesthesia
Symptomtext
Patient stated she felt a tingling sensation immediately following administration that lasted for ~15 minutes. The next morning around 4am she woke up with a migraine headache that did not begin to fade until ~5pm and did not go away for ~24 hours. On Friday (48 hours after immunization) she began experiencing a tingling sensation in index finger and the tip of her finger would go numb. This would last about 2-3 minutes then go away. She said she is having this intermittently every 20 minutes depending on activity.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Lexapro, Iron, B12
- Allergien
- PCN, Sulfa
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 13.11.2021
- Impfdatum
- -
- Beginn
- 11.11.2021
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
Chills
Dyspnoea exertional
Fatigue
Pain
Pyrexia
Symptomtext
BODY ACHES; SLIGHTLY OUT OF BREATH WHEN CLIMBING THE STAIRS; CHILLS; FEELING RUN DOWN, LIKE PATIENT WAS ABOUT TO COME DOWN WITH FLU; SLIGHTLY FEVERISH (100.0F); This spontaneous report received from a patient concerned a 28 year old male. The patient's height, and weight were not reported. The patient's past medical history included: covid, and positive antibodies, and other pre-existing medical conditions included: he claimed to be in good shape. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 213D21A, and expiry: UNKNOWN) dose was not reported, administered on 10-NOV-2021 17:00 for prophylactic vaccination. No concomitant medications were reported. On 11-NOV-2021, the patient experienced body aches. On 11-NOV-2021, the patient experienced slightly out of breath when climbing the stairs. On 11-NOV-2021, the patient experienced chills. On 11-NOV-2021, the patient experienced feeling run down, like patient was about to come down with flu. On 11-NOV-2021, the patient experienced slightly feverish (100.0f). Laboratory data included: Body temperature (NR: not provided) 100.0 F. Treatment medications (dates unspecified) included: paracetamol. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from chills, body aches, feeling run down, like patient was about to come down with flu, slightly feverish (100.0f), and slightly out of breath when climbing the stairs. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea exertional
- Hospital-Tage
- -
- Labordaten
- Test Date: 20211111; Test Name: Body temperature; Result Unstructured Data: 100.0 F
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Antibody test positive; COVID-19; Comments: he claimed to be in good shape
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 12.11.2021
- Impfdatum
- 12.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest discomfort
Feeling hot
Hyperhidrosis
Throat tightness
Tremor
Wheezing
Symptomtext
About 10 minutes after vaccine shaking, wheezing, tightness in chest/throat, sweating and heat. Called EMS, they assessed patient, she started to recover, patient walked out about 30 minutes later with EMS assistance.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 12.11.2021
- Impfdatum
- 10.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Pain
Symptomtext
Slight chest pain, most prominent after bending over
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma
- Andere Medikamente
- -
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 12.11.2021
- Impfdatum
- 10.11.2021
- Beginn
- 11.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Chills
Headache
Migraine
Myalgia
Nausea
Pyrexia
Symptomtext
Fever, chills, muscle pain & weakness, nausea, headache/migraine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- No prescriptions. OTC: Nervive, Supplements: Multi-mineral, Vit D, Vit B Complex, Vit C, L-lysine, Collagen, Fish Oil, Magnesium, Glucosamine, Fiber powder, Turmeric.
- Allergien
- Food: Corn, Wheat, Dairy, Eggs, Yeast. Other: Molds, Dust, Latex. Medications: Sulfa, Penicillin, Lidocaine, Novocaine, Septicaine, Imitrex, Orphenadrine Citrate, Baclofen, Tizanidine, Methocarbamol, Tdap, Clyndamycin, Erythromycin, Dental numbing agents, Dental tooth polish.
- Vorherige Impfungen
- Tdap in 2017.
- Staat
- TX
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 05.11.2021
- Impfdatum
- 03.11.2021
- Beginn
- 04.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Dyspnoea
Muscle twitching
Pain
Sleep disorder
Symptomtext
Sharp shooting knife-like severe pains and twitching in multiple muscle areas beginning in left lateral chest rib cage area progressing to arms, fingers, legs bilaterally, head and torso, and aggravated by deep breathing(a catch in the breath) following Janssen COVID 19 Booster dose. I was awakened by these pains in the early morning following the injection and the symptoms are continuing. I had a similar but more severe reaction to the initial first dose which lasted over three days in May, but I was unsure if these adverse reactions were related to the vaccine but now after taking the Booster dose I decided to officially report these findings, as they are clearly related. Called doctor's office to report symptoms
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- -
- Allergien
- Ambramycin eye ointment, Ackee
- Vorherige Impfungen
- Sharp shooting knife-like severe pains and twitching over 3 days Age66y 11m 05/02/2021 COVID 19 Janssen
- Staat
- MO
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 05.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Extra dose administered
Hyperhidrosis
Hypotension
Lethargy
Symptomtext
pt started to experience sweating, dizziness, lethargy and low blood pressure approximately 5-8 minutes after receiving his covid booster. i gave him water to drink, took his blood pressure and a cool clothe for his forehead. he remainded upright in a chair and was assisted by his wife. i had my technician call 911, because his blood pressure was very low...approximately 70/55. I also gave him a gatorade to drink.Approximately 20 minutes after he received his vaccine, the paramedics arrived and took his bp and vitals, he was beginning to feel a little better. he refused to go to the ER. the last reading by paramedics of his bp was 100/60 upon standing. he and his wife rested about 15 more minutes and then they took an Uber home at about 8:50pm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- -
- Labordaten
- i took the pts blood pressure with an automatic bp machine at about 8:15pm, it was 70/55; paramedics took his bp at 8;30 and it was 100/60.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 05.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Fall
Tension
Tremor
Symptomtext
Patient slouched to the side after vaccination was administered, arms tensed up, and he began shaking in his seat. He sat back up and opened his eyes after about 10 seconds and was unaware anything had occurred. He claimed he "thought he fell asleep." Paramedics were called and the patient was evaluated but not transported to a hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 04.11.2021
- Impfdatum
- 01.11.2021
- Beginn
- 02.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
Dizziness
Fatigue
Head discomfort
Headache
Mobility decreased
Nausea
Vomiting
Symptomtext
The night of the vaccine, 11/02/2021 @ 2:00 AM I a got really bad headache, nausea, vomiting . The next day, 11/03/2021 was horrible. I had fatigue the headache got worse and I pretty much stayed in bed all day. 11/03/2021- I called my doctor, she wanted me to go to the ER and get evaluated and get fluids for the headache. I went to the ER, they did not do any test or labs; they did not do anything. It was a waste of my time. The ER is not informed and not understanding this type of headache from the booster. They tried to treat it with a cocktail that I was allergic to. I have never had a headache like this before. The headache is incapacitating. I am treating it with Tylenol, which is not helping. These headaches from the vaccine are different from migraines or other headaches. I don't get migraines. I never had a headache like this. I am wearing a hat, because it relieves the pressure a little. I feel if I take off the hat my head is going to explode. If I lay down flat , if I turn my head in any speed, any motion I get dizzy. I get nauseous. It's just a vicious cycle.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- No
- Aktuelle Erkrankungen
- NO
- Vorgeschichte
- 6 auto immune diseases Crone's disease Relapsing Polychondritis Hashimotos Disease Sjogren Lupus positive Anti Coagulant
- Andere Medikamente
- Lisinopril Gabapentin Cymbalta Synthroid Klonopin Baby Aspirin Flax Seed Oil Vitamin D
- Allergien
- I have no allergies listed on the COVID questionnaire Most of them are antibiotics ( I have a long list)
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 02.11.2021
- Impfdatum
- 31.10.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dizziness
Dyspnoea
SARS-CoV-2 test negative
Tachycardia
Symptomtext
Tachycardia began at approximately 9:45 am on 11/01/2021 while patient was sitting upright at a table after finishing breakfast. Tachycardia was accompanied by shortness of breath and dizziness for duration of event. Event lasted approximately 2 and a half hours. Patient went to urgent care to be assessed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Vitals on 11/01/2021 at 11:39 am Ht 62 inches Wt 115 lbs BMI 21.03 Temp 97.9 F BP 130/84 mm Hg RR 24 breaths per minute Pulse sitting 137 Oxygen saturation 100% Covid test was performed on 11/01/2021, results were NOT DETECTED.
- Aktuelle Erkrankungen
- Common cold 3 weeks prior to vaccination.
- Vorgeschichte
- None
- Andere Medikamente
- Tylenol
- Allergien
- Sulfa drugs.
- Vorherige Impfungen
- Flu vaccine in October of 2020. Patient age 31. Patient had hives all over injected arm (left arm)
- Staat
- MO
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 06.04.2023
- Impfdatum
- 20.04.2022
- Beginn
- 31.03.2023
- Tage bis Beginn
- 345,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Cough
Fall
Fatigue
Headache
Myalgia
Oropharyngeal pain
Respiratory tract congestion
Rhinorrhoea
Symptomtext
Symptom onset was 03/28/2023: cough, congestion, fatigue, headache, muscle aches, runny nose and sore throat. Became weak, fell at home and was transported by ambulance to the hospital on 03/31/2023.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- 3,0
- Labordaten
- unknown
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- hypertension, multiple back surgeries
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 31.01.2023
- Impfdatum
- 22.02.2022
- Beginn
- 22.04.2022
- Tage bis Beginn
- 59,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arthralgia
Disability
Gait disturbance
Joint swelling
Pain in extremity
Peripheral swelling
Tenderness
Ultrasound Doppler
Urine uric acid normal
Symptomtext
I had mild gout in the past. Shortly after getting the vax, my foot swelled up and looked like a water balloon. It was very tender and I could not walk. The pain was unbearable. I could hardly walk to the bathroom. The pain was from my knee, down to my foot, although the bad swelling was only from my ankle, throughout my foot. I had to go out on short term disability and I was back and forth to my PCP, Urgent Care and the emergency room. One doctor at the E.R was concerned about blood clots and they gave me an ultra sound (?) to test for them. I also got. A referral to a Rhumatologist and he prescribed steroids, but was never able to come up with a diagnosis. I have had several instances of swelling in different joints, including both feet, ankles, and knees.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- Tested for Gout - No Uris acid in the urine. Ultrasound for blood clots.
- Aktuelle Erkrankungen
- Gout
- Vorgeschichte
- Bronchitis
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 23.01.2023
- Impfdatum
- 23.03.2022
- Beginn
- 24.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- UN / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pain
Injection site swelling
Taste disorder
Tinnitus
Symptomtext
Pain, swelling and redness on arm at vaccine site. Immediately after the vaccine, and for the next 24 hours, my taste was off. The next day, March 24, 2022, I noticed a ringing in my ears. It varies in loudness and has continued daily for the past 10 months. My doctor has said that there is no treatment for tinnitus.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypothyroidism, High Cholesterol, Osteoporosis
- Andere Medikamente
- Levothyroxin, Simvastatin, Alendronate Sodium Tablets
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 14.12.2022
- Impfdatum
- 11.09.2022
- Beginn
- 11.10.2022
- Tage bis Beginn
- 30,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Injection site pain
Scan
Symptomtext
I received my vaccination mild soreness at injection site subsided within 2 days, no other reactions.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- Scan of left leg
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- Kidney failure stage 4 Afib Prosate infection
- Andere Medikamente
- Zyloprim 100mg; vitamin D3 1000mg; multaq 400mg; Toprolxl 25mg; xarelto 20mg
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 28.11.2022
- Impfdatum
- 05.11.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- 26,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abnormal menstrual clots
Back pain
Heavy menstrual bleeding
Symptomtext
Heavy periods with major clots for many days Back pain on right side that was not there before
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 14.11.2022
- Impfdatum
- 03.04.2021
- Beginn
- 20.09.2022
- Tage bis Beginn
- 535,0
- Dosis
- 2
- Route/Site
- - / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Abdominal pain
COVID-19
SARS-CoV-2 test positive
Symptomtext
09/20/22 presents to ED for "abdominal pain". PMHx of alcohol induced pancreatitis with described hemorrhagic pancreatic pseudocyst status post partial gastrectomy, distal pancreatectomy and splenectomy, and left gastric artery pseudoaneurysm status post gelfoam embolization"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- 09/20/22 SARS-CoV-2 (COVID-19) by NAA detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 15.08.2022
- Impfdatum
- 12.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Aphasia
Chills
Deformity
Gait inability
Headache
Symptomtext
Severe headaches chills facial deformities inability to walk or talk etc
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Currently receiving care
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 19.07.2022
- Impfdatum
- 16.12.2021
- Beginn
- 14.07.2022
- Tage bis Beginn
- 210,0
- Dosis
- 2
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Arthralgia
Back pain
Pyrexia
Symptomtext
fever, arthralgias, back pain
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- 5,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 07.07.2022
- Impfdatum
- 01.12.2021
- Beginn
- 15.01.2022
- Tage bis Beginn
- 45,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site reaction
Psoriasis
Symptomtext
He developed plaque psoriasis within weeks of receiving the vaccine. The first area affected was on his right upper arm at the site of the vaccine injection and then additional sites developed on his right arm with the largest patch above his right elbow. To date he now has multiple sites of various sizes all over his body.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site reaction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- CHTN
- Andere Medikamente
- Atorvastatin, lisinopril, sertraline
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 05.07.2022
- Impfdatum
- 03.03.2022
- Beginn
- 04.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood glucose increased
Fatigue
Headache
Malaise
Photophobia
Vitreous floaters
Symptomtext
Onset headaches, eye floaters, light sensitivity, fatigue/malaise, elevated blood glucose levels
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Diabetes T2 HTN
- Andere Medikamente
- Synjardy Lisinopril Lantus
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 04.06.2022
- Impfdatum
- 04.06.2022
- Beginn
- 04.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Symptomtext
Approximately 10 minutes after vaccination, patient began to feel lightheaded. She recognized the symptoms and knew she was going to pass out. Her boyfriend alerted the pharmacist and they had the patient lie down on the floor. Patient got an ice pack and after 5 minutes some orange juice. After another 15 minutes of observation she felt normal.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- dairy, guaifenesin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 04.06.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Feeling hot
Lethargy
Malaise
Symptomtext
LETHARGIC MORE THAN USUAL; FELT HOT LIKE FEVER/FELT WARM IN VEIN; FELT NOT VERY GOOD; TIRED; This spontaneous report received from a patient concerned a 75 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included: diabetic type 2, alcohol use (rarely), non-smoker, and ibuprofen allergy (possibly) and other pre-existing medical conditions included: the patient had no history of drug abuse or illicit drug use. Patient was not pregnant at the time of vaccination. The patient previously received covid-19 vaccine ad26.cov2.s (dose number in series 1) (suspension for injection, route of admin not reported and batch number: 1821286) dose was not reported, 1 total, administered on left arm on 16-MAY-2021 for prophylactic vaccination. On an unspecified date, the patient felt generally not so good, tired, lethargic more than usual, felt heat like fever, felt hot but not like boiling, warm in vein and took it easy for a day or two, patient did not feel well for a day or two so the patient rested and passed following the vaccination with first dose of covid-19 vaccine ad26. cov2. s (dose number in series 1). The patient recovered from lethargic more than usual, felt hot like fever/felt warm in vein, felt not very good, and tired. The patient additionally received first booster of covid-19 vaccine ad26.cov2.s (dose number in series 2) (suspension for injection, route of admin not reported, batch number: 213D21A expiry: UNKNOWN) dose was not reported, 1 total, administered on left arm on 28-NOV-2021 for prophylactic vaccination. Age at time of vaccination 75 years old. No concomitant medications were reported. On an unspecified date after the booster dose, the patient felt generally not so good, tired lethargic more than usual. The patient felt heat like fever, felt hot but not like boiling, warm in vein and took it easy for a day or two. The patient stated that for booster dose she felt more than the primary dose (dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from lethargic more than usual, felt hot like fever/felt warm in vein, felt not very good, and tired. This report was non-serious. This case, involving the same patient is linked to 20220606162 (dose number in series 1).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Alcohol use (rarely); Allergy to NSAIDs; Non-smoker; Type II diabetes mellitus
- Vorgeschichte
- Comments: the patient had no history of drug abuse or illicit drug use. Patient was not pregnant at the time of vaccination.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 02.06.2022
- Impfdatum
- 05.04.2021
- Beginn
- 18.02.2022
- Tage bis Beginn
- 319,0
- Dosis
- 2
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Abdominal pain
Abdominal pain upper
Back pain
COVID-19
Fibrin D dimer increased
Lipase increased
Nausea
SARS-CoV-2 test positive
Symptomtext
Patient initially presented to the ER on 2/18 with epigastric pain, nausea, initial work-up was significant for slightly elevated lipase, elevated D-dimer, positive COVID-19 test on 2/18. 2/20 Pt received A+Ox3 c c/o back/ abdo pain. Prn Iv Fentanyl given as per mar pt tolerated well. Patient seen by infectious disease, patient remained on room air throughout her admission, patient was not qualified for any remdesivir or any antimicrobial treatment, patient initially started on Decadron, this was stopped later as the patient refused. Patient remains A&Ox4 and showing no s/s of distress 2/22. Dishcharged on 2/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- 5,0
- Labordaten
- see above
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Pancreatitis ... Obstructive jaundice Endocrine Pancreatitis Common bile duct (CBD) stricture Obstructive jaundice DM type 2 (diabetes mellitus, type 2) Uncontrolled type 2 diabetes mellitus with hyperglycemia (CMS/HCC) Diabetic polyneuropathy associated with type 2 diabetes mellitus (CMS/HCC) High triglycerides HTN (hypertension) Paresthesia H/O acute pancreatitis Other dyspnea and respiratory abnormality Obesity (BMI 30-39.9) Positive cardiac stress test Syncope Chronic systolic congestive heart failure (CMS/HCC) Use of cannabinoid edibles Coronary artery disease involving native coronary artery COVID-19 virus infection
- Andere Medikamente
- albuterol (2.5 MG/3ML) 0.083% INHAL Nebu Soln ... albuterol (Proventil HFA) HFA 108 (90 Base) MCG/ACT INHAL Aero Soln aspirin 81 MG PO Chew Tab atorvastatin (LIPITOR) 80 MG PO Tab carvedilol (COREG) 12.5 MG PO Tab Dapagliflozin Propanediol
- Allergien
- Morphine and related
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 02.06.2022
- Impfdatum
- 08.11.2021
- Beginn
- 08.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Chills
Fatigue
Injection site pain
Nasal inflammation
Parosmia
Pyrexia
Somnolence
Taste disorder
Symptomtext
Became very tired the evening of 11/8. Slept for 10 hours. Woke up with soreness in back and at injection site. By 8am on 11/9, onset of fever, chills, and exhaustion. Smell and taste became distorted that same day. Little improvement in smell or taste over the next 6 months. Started seeing an ENT in the beginning of May, 2022. Started a cortisone nasal treatment to help heal the inflammation issues in my nose from vaccine. Expected that process will take months to heal correctly, possible even more than a year.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- Examination of throat, nasal, and ear passages 05/03/2022
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Allopurinol
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 24.05.2022
- Impfdatum
- 10.01.2022
- Beginn
- 23.05.2022
- Tage bis Beginn
- 133,0
- Dosis
- 1
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Abdominal pain
COVID-19
Chills
Diarrhoea
Nausea
Rhinorrhoea
SARS-CoV-2 test positive
Vomiting
Symptomtext
Hospitalized with abdominal pain, diarrhea, nausea, vomiting, rhinorrhea, chills. COVID 19 positive
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Type 1 diabetes, Graves disease
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 13.05.2022
- Impfdatum
- 02.12.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Injection site pain
Malaise
Pain
Symptomtext
Patient stated receiving the Janssen vaccine for hist first booster dose at an immunization clinic. Patient stated that the injector "put the needle in really hard." Patient reports shoulder pain since the time of that injection which he currently describes as dull pain with some movements but that does not impact his ability to use his arm or perform daily tasks. Patient stated that the pain did improve with time, but also gets worse at times. Patient also remembered feeling generally sick after the dose of Janssen, about an hour and a half after the administration, but that those symptoms resolved with time. Patient received second booster dose of covid vaccine yesterday in R arm with no complaints.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hypertension, chronic pancreatitis, type 1 diabetes mellitus, hyperlipidemia, microalbuminuria
- Andere Medikamente
- -
- Allergien
- Barium and iodine
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 10.05.2022
- Impfdatum
- 05.11.2021
- Beginn
- 01.03.2022
- Tage bis Beginn
- 116,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood pressure increased
Head discomfort
Headache
Hypertensive crisis
Symptomtext
I have been having bad headaches off and on since I received the second vaccine. It feels like pressure inside my head. My blood pressure has been increasing and at times it has reached Hypertensive Crisis readings. My doctor has started me on medication Metoprolol to help decrease my blood pressure.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- History of Blood Pressure Possible TIA
- Andere Medikamente
- Atorvastatin Clopidogrel HCTZ Vitamin D3 Vitamin B Complex Colace Multivitamin
- Allergien
- Epinephrine Lisinopril Fosinopril Losartan
- Vorherige Impfungen
- Influenza, in the early 1980's, fever.
- Staat
- PA
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 10.05.2022
- Impfdatum
- 07.11.2021
- Beginn
- 10.12.2021
- Tage bis Beginn
- 33,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Dermatitis
Impaired work ability
Pain
Pruritus
Psoriasis
Symptomtext
After the vaccine I had sporadic dermatitis issues that exuberated from a small amount in December to the point in February to April that I was hurting, itching, sore, and burning. This affected my job. I was referred by an Allergist to a Dermatologist who determined that this was Psoriasis. I am now taking Otezla and using Clobetasol Propionate Cream 05%. My symptoms are clearing up, but I do still have flare ups. I have a follow up appointment in July to see what we can do to keep me from having multiple flare ups so often.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 04.05.2022
- Impfdatum
- 06.11.2021
- Beginn
- 07.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Neuralgia
Symptomtext
following a call from Immunization System that informed us that this pt had a Moderna vaccine 3 days prior to his Janssen vaccine I called the patient on 05/04/2022 to verify he had both vaccines, get details and information about adverse reactions. He stated that he has had nerve pain since the 2nd vaccine was administered from his shoulder to his elbow. He stated that he has not sought treatment for this at this time. I advised him to see a doctor regarding this.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- He reports that he has had nerve pain in the shoulder he received the shot in down to his elbow since receiving the Janssen vaccine.
- Andere Medikamente
- He went to the store and received a Moderna vaccine on 11/03/2021, when he found out that he could not get the 2nd shot to become fully vaccinated prior to a concert he had purchased tickets for he sought out a pharmacy that had the single
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 19.04.2022
- Impfdatum
- 01.03.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 34,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Cough
Fatigue
Nasal congestion
Oropharyngeal pain
Pyrexia
SARS-CoV-2 test negative
Tonsillar hypertrophy
Symptomtext
Starting April 4th, I started getting a sore throat and swollen tonsils. I had fever and chills and extreme fatigue. I went to the doctor on 04/07/2022 and they prescribed me antibiotics for tonsillitis. By Saturday, I felt better. However, on 04/12/2022 I developed a sore throat. Then the following day it got worse and then I started the antibiotics. I got tested for COVID on 04/13/2022 which was negative and so I continued the antibiotics and had a stuffy nose and sore throat. By 04/15/20022, the sore throat was gone but I developed a cough. Today, my sore throat and cough are gone but I have a mild stuffy nose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- COVID test (04/13/2022): negative.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Naproxen
- Allergien
- Eggplant; cat; Seasonal
- Vorherige Impfungen
- Extreme fatigue from previous flu shots.
- Staat
- -
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 19.04.2022
- Impfdatum
- 03.11.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Connective tissue disorder
Pain
Symptomtext
Connective tissue discomfort starting approx 3 weeks after COVID vaccine. Pain remains ongoing since 11/2021. Pt referred to rheumatologist and for head CT but refuses.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 19.04.2022
- Impfdatum
- 15.11.2021
- Beginn
- 15.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain upper
Body temperature
Headache
Pyrexia
Symptomtext
STOMACH ACHE; FEVER; HEADACHE; This spontaneous report received from a patient concerned a 72 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included: HTN (hypertension), thyroid, cholesterol, asthma, COPD (chronic obstructive pulmonary disease), seasonal allergies, ex-smoker (The patient stated she smoked for 30 years but quit 18 years ago) and no alcohol use, and other pre-existing medical conditions included: The patient had no history of drug abuse or illicit drug use. The patient had nausea when treated with codeine. The patient previously received covid-19 vaccine ad26.cov2.s (Dose number in series 1) (suspension for injection, route of admin not reported, batch number: 043A21A, expiry: UNKNOWN) dose was not reported, 1 total administered to left arm on 06-APR-2021 for prophylactic vaccination. On 06-APR-2021, the patient experienced fever, chills, headache, stomach hurt (Dose number in series 1). The patient stated that she had initially fever with body temperature 102.4 F and after 5 hours post vaccination fever came down to 99.9 F. The patient recovered from fever, chills, headache, stomach hurt on 06-APR-2021(Dose number in series 1). The patient received covid-19 vaccine ad26.cov2.s (Dose number in series 2) (suspension for injection, route of admin not reported, batch number: 213D21A expiry: UNKNOWN) dose was not reported, 1 total administered on 15-NOV-2021 to left arm for prophylactic vaccination. No concomitant medications were reported. On 15-NOV-2021, the patient experienced fever which reached to 99.9 F, headache, and stomach ache but with less severity than with the initial vaccination (Dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from fever, headache, and stomach ache on 15-NOV-2021 after 10 hours of post vaccination. This report was non-serious. This case, involving the same patient is linked to 20220431821 (Dose number in series 1).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- Test Date: 20211115; Test Name: Body temperature; Result Unstructured Data: 99.9 F
- Aktuelle Erkrankungen
- Abstains from alcohol; Asthma; Cholesterol; COPD; Ex-smoker (smoked for 30 years but quit 18 years ago); Hypertension; Seasonal allergy; Unspecified disorder of thyroid
- Vorgeschichte
- Comments: The patient had no history of drug abuse or illicit drug use.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 13.04.2022
- Impfdatum
- 24.01.2022
- Beginn
- 25.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dermatitis contact
Erythema
Pruritus
Rash
Sensitive skin
Skin discomfort
Skin swelling
Sunscreen sensitivity
Swelling
Symptomtext
The same symptoms as my first and second shot started within 24 to 48 hours of the vaccine. So, it was a skin reaction where at first my skin just got red on my face, neck, ears, chest itchy swollen, it was very itchy. It progressed to the skin around my right eye was red and swollen and impairing my vision. I went to urgent care again and was given a steroid injection and I still had the Benadryl cream I was given previously from the other breakout. I do not feel as though this is resolved, I only got the vaccine because my work required it. My skin is not right, I now have very sensitive skin to everything, for example Items I have always used cause issues for my skin, I can not use the sun screen I have always used. I have to use sun screen that is completely mineral based. Other products that I have used for a while that I never had a reaction to I now have had problems. I need to use very basic products that I put on my skin otherwise I break out and get swollen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- COVID 19 Pfizer vaccine Dose #1 - 04/07/2021 and Dose #2 04/28/2021, age 35 - rash, swollen face, neck, chest, ears, eyes - im
- Staat
- NM
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 10.04.2022
- Impfdatum
- 14.11.2021
- Beginn
- 20.11.2021
- Tage bis Beginn
- 6,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Carpal tunnel syndrome
Hand deformity
Hypoaesthesia
Immobile
Joint swelling
Muscle atrophy
Pain
Symptomtext
SYSTEMIC JOINT SWELLING IN ALL JOINTS, LOSS OF MUSCLE MASS DUE TO IMMOBILITY, THORASIC BURNING PAIN BETWEEN SHOULDERS, NOW HAVE CARPEL TUNNEL IN BOTH WRISTS, CHRONIC PAIN, HANDS ARE NUMB AND CLAWLIKE. GOING ON 6 MONTHS WITH THESE SIDE EFFECTS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 06.04.2022
- Impfdatum
- 07.12.2021
- Beginn
- 12.12.2021
- Tage bis Beginn
- 5,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Aphthous ulcer
Eating disorder
Fatigue
Gingival discomfort
Stomatitis
Throat irritation
Symptomtext
Extremely tired for several days after booster. Within 4-5 days I noticed back of throat, gums & roof of mouth feeling irritated. Few more days & it hurt to eat. I had developed sores in my mouth. Went to my ENT doctor who diagnosed many canker sores in my mouth & stated it was because the booster had over stimulated my immune system. Much better but on last recheck 3 weeks ago I still have a few sores but they are healing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Exam only
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Over active immune system
- Andere Medikamente
- Pepcid 20mg 1x/day
- Allergien
- Soy & anything in the asteraceae family
- Vorherige Impfungen
- Flu vaccine in 2001 resulted in double pneumonia
- Staat
- NY
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 24.03.2022
- Impfdatum
- 14.11.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 32,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Ageusia
Anosmia
COVID-19
Chills
Cough
Illness
Oropharyngeal pain
Pyrexia
SARS-CoV-2 test positive
Symptomtext
I tested Positive for Omicron COVID on 12/16/2021. I had a fever, chills, sore throat, cough and I lost my taste and smell. It very was mild and I was sick for 5 days. I didn't go to the hospital because I was still able to breath. I did stay in for an additional 5 days, to make sure I was better. For as am concern the vaccine worked.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- No
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Premarin 0.625mg, Atorvastatin 10mg, Vitamin D 1000 IU and CoQ 10,
- Allergien
- Codeine; Cephalosporin; Bananas
- Vorherige Impfungen
- Flu Vaccine
- Staat
- NC
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 23.03.2022
- Impfdatum
- 07.04.2021
- Beginn
- 08.04.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Gait disturbance
Joint stiffness
Pain
Pyrexia
Symptomtext
When I got the 1st dose I got a fever 102 and my body was aching, full body sore and barely walk. After that I started to feel pain, sore and stiff wrists .
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- I don?t remember the exact date but I think it was on September 2021 and I haven?t had any health issues, but this one after the vaccine
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Inflammatory symptoms on my wrist
- Andere Medikamente
- None
- Allergien
- None that I know
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 11.03.2022
- Impfdatum
- 08.12.2021
- Beginn
- 08.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Atrial fibrillation
Echocardiogram
Electrocardiogram
Pain in extremity
Symptomtext
My arm has been hurting ever since I got my second dose of the vaccine. I had therapy for it, and it does not seem to be helping. I just started getting atrial fibrillation. I just seen the cardiologist. I had an EKG and TEE done to shock me back in rhythm for 3 times. It does not work. They have put me on blood thinner.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- EKG TEE
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Blood Pressure
- Andere Medikamente
- Procaterol, Locoest, Multivitamin
- Allergien
- Penicillin, EES, Floxacrine, Bananas, Turkey, Morphine, Chlorthalidone, Ciprofloxacin, Eplerenone, Lotrimin, Lyrical, micro bid, Remeron, Tivaze, Vicodin
- Vorherige Impfungen
- TB
- Staat
- VA
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 09.03.2022
- Impfdatum
- 16.12.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 16,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Injection site pain
Vertigo
Symptomtext
2 adverse effects 1. Vertigo beginning in January 2022. Have never experienced it prior 2. Intense, sometimes debilitating pain at injection site beginning towards end of Feb 2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- None yet
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asthma Depression
- Andere Medikamente
- Advair Albuterol Lexapro Zyrtec
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 05.03.2022
- Impfdatum
- -
- Beginn
- 09.12.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Blood test
Symptomtext
JOINT PAIN ALL OVER (KNEE, SHOULDER, ARMS AND ELBOWS); This spontaneous report received from a patient concerned a 45 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included: non-alcohol user, non-smoker, penicillin allergy, and shell fish allergy, and other pre-existing medical conditions included: The patient had no history of drug abuse or illicit drug use. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 213D21A, and expiry: 11-APR-2022) dose was not reported, administered on 06-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. On 09-DEC-2021, the patient experienced joint pain all over (knee, shoulder, arms and elbows). Laboratory data (dates unspecified) included: Blood test (NR: not provided) RA factor more than 250. Treatment medications (dates unspecified) included: celecoxib. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from joint pain all over (knee, shoulder, arms and elbows). This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- Test Name: Blood test; Result Unstructured Data: RA factor more than 250
- Aktuelle Erkrankungen
- Abstains from alcohol; Non-smoker; Penicillin allergy (swelling and itchy throat); Shellfish allergy (swelling and itchy throat)
- Vorgeschichte
- Comments: The patient had no history of drug abuse or illicit drug use.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 04.03.2022
- Impfdatum
- 04.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Hypoaesthesia
Neck pain
Pain
Pain in extremity
Symptomtext
Radiating arm pain and numbness down to fingertips in left arm. Numbness and sever pain in left pointer and middle fingers. Radiating pain in forearm. Radiating pain in left neck and shoulder. Persistent daily since 11/5/21. Stretching and shaking arm helps pain a little. But certain work tasks, such as typing, create great radiating pain in shoulder, neck, bicep, forearm, and fingers.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Adderall, multivitamin, fish oil, turmeric
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 28.02.2022
- Impfdatum
- 26.02.2022
- Beginn
- 26.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain
Diarrhoea
Nausea
Vomiting
Symptomtext
Patient with abdominal pain, diarrhea, and intractable nausea and vomiting beginning about 3 hours after receiving IZ. Seen in clinic today and RXd zofran and scopalamine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- HTN, obesity, GERD, anxiety
- Andere Medikamente
- Chlorthalidone 25mg PO daily
- Allergien
- Shellfish, iodine, Phenergan
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 20.02.2022
- Impfdatum
- 05.11.2021
- Beginn
- 07.11.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Basophil count normal
Basophil percentage increased
C-reactive protein normal
Differential white blood cell count
Eosinophil count normal
Eosinophil percentage increased
Fibrin D dimer increased
Full blood count
Haematocrit normal
Haemoglobin normal
Headache
Immature granulocyte count
International normalised ratio decreased
Lymphocyte percentage
Magnetic resonance imaging head normal
Mean cell haemoglobin concentration decreased
Mean cell haemoglobin increased
Mean cell volume increased
Symptomtext
2 days following the J&J covid vaccine administration, I began to develop mild achy headaches, intermittently, at the lower parietal area of my head. The headaches remain, even today. The intensity and consistency remain unchanged. They occur on a daily basis for short periods of time. I do not take any medications to alleviate the symptoms. I wait for the headaches to dissipate. On 12/16/21, I reported these symptoms to my PCP, and was seen on 12/20/21 by the NP. She ordered a series of labs to rule out any clotting issues, as well as an MRI. All were negative. Today, I still suffer from mild, achy intermittent headaches in the exact location (parietal area). I continue to abstain from any medications to alleviate the symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- 12/20/21: PT 12.6 INR 1.O D-dimer 350 CRP 0.7 ESR 2 MRI brain no acute infarct, mass lesion or hemorrhage CBC w/diff - had to be redrawn 12/28/21 CBC: WBC 7.32 RBC 4.25 HGB 13.6 HCT 43 PLT 237 MCV 101.2 MCH 32 MCHC 31.6 RDW% 13 MPV 11.6 NRBC 0 ABSOLUTE NRBC 0 NEUTS% 59.7 LYMPHS% 28.1 MONOS% 6.3 EOS% 4.2 BASOS % 1.2 GRANULOCYTES, IMMATURE 0.5 ABSOLUTE NEUTS 4.36 ABSOLUTE MONOS 0.46 ABSOLUTE EOS 0.31 ABSOLUTE BASOS 0.09 ABS IMMATURE GRANS 0.04 DIFF METHOD AUTO
- Aktuelle Erkrankungen
- hypothyroidism
- Vorgeschichte
- none
- Andere Medikamente
- -
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 16.02.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Nausea
Pallor
Symptomtext
61-year-old patient was online to sign up. After being vaccinated, the paramedic felt dizzy and was taken to the Tx area. The patient presented nausea, pale skin, and dizziness. Patient was evaluated and placed in anti-shock position. Patient was observed for half an hour. Patient reports feeling fine, she no longer feels nauseous, re-evaluated patient reports that she does not want to go to the hospital, she wants to leave, she is hungry.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- LEVAQUIN
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 16.02.2022
- Impfdatum
- -
- Beginn
- 01.12.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthritis
Fatigue
Rash
Symptomtext
ARTHRITIS WORSENED; WIPED OUT ME OUT; RASH ON BOTH ARMS; This spontaneous report received from a patient concerned a 58 year old white not Hispanic or Latino male. The patient's weight, height, and medical history were not reported. The patient was previously treated with covid-19 vaccine ad26. cov2. s (dose number in series 1) (suspension for injection, route of admin not reported, batch number: unknown, expiry: unknown) dose was not reported, 1 total, administered on 17-MAR-2021 for prophylactic vaccination. The patient did not experienced any issues with the primary vaccination doses of covid-19 vaccine ad26. cov2. s (dose number in series 1). The patient received booster covid-19 vaccine ad26.cov2.s (dose number in series 2) (suspension for injection, route of admin not reported, batch number: 213D21A, and expiry: 11-APR-2022) dose was not reported, 1 total, administered at left arm on 10-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. It was reported that after about two weeks of booster dose (in Dec-2021), the patient had developed a rash (up both arms, especially on the left arm where the shot was administered). The patient went to PCP (primary care provider) for treatment and was prescribed on 08-FEB-2022 tacrolimus Ointment 1% apply topically twice daily, Doxepin 25mg 1 Capsule three times daily. The patient stated that rash was not resolved. The patient stated that dermatologist prescribed these medications. On an unspecified date, the patient experienced arthritis worsened, rash and wiped out me out (all events with dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from rash on both arms, arthritis worsened, and wiped out me out. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 11.02.2022
- Impfdatum
- 18.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Symptomtext
Severe headaches originating from my right eye & thru my head. I have never experienced headaches in my life. I now have them every evening, thru the night, and into the morning. This all started on the day I received this vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Levothyroxine
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 11.02.2022
- Impfdatum
- 18.11.2021
- Beginn
- 25.11.2021
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: unbekannt
Eating disorder
Gait disturbance
Nausea
Parosmia
Taste disorder
Symptomtext
I received my vaccine on 11/18/2021 and 7 days later 11/25/21 was when I began having symptoms walking into a family members house and the smell of the turkey that was cooking making me nauseous. Food was unbearable to eat and when I had a drink of a soda I knew that something was very off. Most food smells and tastes like rotten meat or eggs. Particularly meats whether they are raw, cooking or are ready to be eaten. Other foods taste rotten and smoky at the same time. Coffee and soda also taste like garbage. Certain vegetables smell and taste like they are bad or rotten. Various different things do not smell as they should. Gasoline smells the same as the food I have to eat and drink and if I wasn't able to see I would not be able to tell the difference between food or gasoline. From what I have found all of the symptoms I have are caused by parosmia. Symptoms continue and I haven't seen any improvement thus far.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 11.02.2022
- Impfdatum
- -
- Beginn
- 11.11.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site pain
Symptomtext
PAIN ON THE LEFT ARM WHERE HE GOT THE INJECTION; This spontaneous report received from a patient concerned a 73-year-old male. The patient's height, and weight were not reported. The patient did not have known drug allergies. The patient previously received covid-19 vaccine ad26.cov2.s (dose number in series 1) (suspension for injection, route of admin not reported, batch number: 1805029, and expiry: UNKNOWN) dose was not reported, 1 total, administered on 18-MAR-2021 for prophylactic vaccination at left arm. On 18-MAR-2021, the patient experienced pain on the left arm at site of injection for 2 to 3 hours (dose number in series 1). The patient recovered from pain on the left arm at site of injection. The patient received booster covid-19 vaccine ad26.cov2.s (dose number in series 2) (suspension for injection, route of admin not reported, batch number: 213D21A, and expiry: UNKNOWN) dose was not reported, 1 total, administered on 11-NOV-2021 for prophylactic vaccination at left arm. No concomitant medications were reported. On 11-NOV-2021, the patient experienced pain on the left arm where he got the injection (dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from pain on the left arm where he got the injection on 14-NOV-2021. This report was non-serious. This case, involving the same patient is linked to 20220222828.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: No known drug allergies.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 10.02.2022
- Impfdatum
- 10.02.2022
- Beginn
- 10.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Chest discomfort
Cough
Diarrhoea
Pruritus
Sneezing
Urticaria
Symptomtext
Injection was administered at 1248pm on 2/10/2022. Approximately 10 minutes after the injection, my chest began to itch. I noticed I had hives. I drove to the hospital. Arrived at 1:02pm. Upon arrival, my chest, neck and back were covered in hives and my chest was beginning to feel heavy. I had taken Benadryl and Famotidine by mouth two hours prior to injection as I have had allergic responses to the flu vaccine. I take Zyrtec and Singulair nightly. I was told that I had no choice but to receive the vaccine because of agency rules and that the previous history of adverse reactions and idiopathic urticaria we?re both qualifying medical exemption reasonings. In route to the ER I administered myself my rescue inhaler (Xoepenex) In the ER I was immediately given IV Benadryl, Solu Medrol & Famotidine. I did get relief. I was discharged with a prescription for 20mg prednisone. At 8:00pm this evening, I had to to take 25mg of PO Benadryl and the prednisone. As of 9:18 I am still having break through hives, itching, coughing, sneezing and now some diarrhea.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma Idiopathic urticaria
- Andere Medikamente
- Zyrtec Singular Benadryl Famotidine Xoepenex
- Allergien
- Medical hx of idiopathic urticaria NKDA
- Vorherige Impfungen
- Flu vaccine
- Staat
- NJ
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 10.02.2022
- Impfdatum
- 17.11.2021
- Beginn
- 17.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Diarrhoea
Feeling hot
Flushing
Lymphadenopathy
Pruritus
Rash
Symptomtext
Patient reports: "After receiving J&J covid vaccine I developed a rash all over my back. I also became flushed. I was afebrile. I had diarrhea for 72 hours, I had enlarged lymph nodes and felt like my inner body temperature was extremely high. I was itchy for 3 weeks post shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Zosyn, tetracyclines
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 03.02.2022
- Impfdatum
- 20.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Fatigue
Immediate post-injection reaction
Injection site erythema
Injection site pain
Injection site warmth
Malaise
Mass
Nausea
Pain
Pruritus
Skin irritation
Sleep disorder
Vomiting
Symptomtext
Immediate reactions. A few hours after the vaccine I could not lift my arm from the pain. Injection site red, hot and very sore. Next day light headed, nauseous and vomiting. Body aches. Five days later I could lift my arm but sore and now have hard lumps (3). I am extremely itchy especially on my right side and my scalp near my neck, my neck and shoulder. The itching is sharp pain and irritated skin. The sharp itching pain wakes me two to three times while I'm trying to sleep. I can't sleep well at all. I also have a severe stabbing pain at injection site at random times. I'm very tired and not feeling good at all. I called my primary care Dr office and they were not interested in speaking to me about this since they did not administer the vaccine. They told me to go to the pharmacy where I received the vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- losartan
- Allergien
- none
- Vorherige Impfungen
- Tetnus - very swollen arm as a very young child
- Staat
- -
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 31.01.2022
- Impfdatum
- 23.11.2021
- Beginn
- 26.11.2021
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Joint range of motion decreased
Symptomtext
Patient got vaccination on 11/23/21. Reported to pharmacist that she has had shoulder pain and trouble with moving her should (limited range of motion) since that time. Has seen MD and been prescribed medications and is still experiencing issues with pain and limited range of motion.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 31.01.2022
- Impfdatum
- 04.12.2021
- Beginn
- 05.01.2022
- Tage bis Beginn
- 32,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dyspareunia
Gynaecological examination
Heavy menstrual bleeding
Muscle spasms
Pelvic pain
Ultrasound pelvis
Symptomtext
Pelvic pain during intercourse that started about 6 weeks after receiving vaccine. Heavy menstruation with much more painful cramps than usual even though I have been taking the birth control pill for months. This was is very unusual while on the BC pill, periods are usually light and nearly cramp free. I saw my Gynecologist on 1/19 and she performed an exam and ordered a pelvic ultrasound that showed no significant structural abnormalities. No other explanation for the pain has been found.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pelvic pain
- Hospital-Tage
- -
- Labordaten
- Pelvic Ultrasound 1/22/22
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Birth Control Pill
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 30.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Back pain
Dry throat
Headache
Nasal congestion
Nausea
Rhinorrhoea
SARS-CoV-2 test negative
Throat irritation
Symptomtext
been sick since got the vaccine shot on Friday the 14. very bad headache. back ache. nausea. runny/stuffy nose. dry, irritated throat.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- tested twic for covid. came up negative.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- venlafaxine
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 24.01.2022
- Impfdatum
- 11.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Headache
Pain
Vaginal haemorrhage
Symptomtext
EXTREME body aches, chills, pounding head ache, heavy vaginal bleeding for 3 days and I was 2weeks before the start of mensis, still unkown long term effects
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- COVID19 positive on December 27 2021
- Vorgeschichte
- None
- Andere Medikamente
- VitaminD,C, Zinc, pink stork fertility pill
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 24.01.2022
- Impfdatum
- 22.11.2021
- Beginn
- 21.01.2022
- Tage bis Beginn
- 60,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Chills
Oropharyngeal pain
Pyrexia
SARS-CoV-2 test positive
Streptococcus test negative
Symptomtext
I?m 1/21/22 I developed a sore throat and fever, and chills. I?m 1/23/22 I tested positive for Covid-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Positive for Covid-19, Negative for strep
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 22.01.2022
- Impfdatum
- 14.03.2021
- Beginn
- 19.01.2022
- Tage bis Beginn
- 311,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asthenia
Atelectasis
Back pain
COVID-19
Chest X-ray abnormal
Nausea
Pyrexia
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Covid19 breakthrough. Vaccinated on 03/14/2021. 60 y/o PMH chronic Pancreatitis and biliary obstruction with stent, HTN, Chronic pain opiod dependent, anxiety , CKD stage 4 and recently diagnosed with breast malignancy presents to ED with c/o fever, back pain, weakness and nausea worsening past 3 days. t-103, O2 2L NC, CXR-subsegmental atelectasis lower lobes. Treated with steroids and abx.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- SARS CoV 2 PCR Covid19 -Detected 01/19/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- CKD stage 4, HTN, Hypothyroid, Pancreatitis, Breast BX positive for malignancy
- Andere Medikamente
- -
- Allergien
- ASA, Cipro, contrast dye, codeine, darvocet, Fentanyl, Iodine, Morphine, NSAIDS, Percocet, Vicodin
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 03.12.2021
- Beginn
- 03.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Antinuclear antibody positive
Ear discomfort
Ear pain
Fatigue
Symptomtext
On day 1 significant fatigue; I now have Chronic fatigue going on 7 weeks. On Day 3, I developed ear fullness with stabbing pains (in both ears); I am also reporting this because this has become a chronic issue. I continue to experience ear fullness and pain daily. On December 23, 2021 labs showed a positive ANA. I had a negative ANA prior to vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ear pain
- Hospital-Tage
- -
- Labordaten
- 12/23/2021: ANA labs that are positive 1:40
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Lyme Disease
- Andere Medikamente
- None
- Allergien
- yellow dye, wheat/gluten
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 15.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Frustration tolerance decreased
Malaise
Symptomtext
I began completing and was timed out. If anyone truly cares about my experience you can reach me at phone number or email. This MUST stop! My symptoms were identical to when my husband and I contracted what we believe was the Delta variant. I pray someone cares enough to reach back out and hear our story. God help us!!!!!! We're being manipulated, intimidated, coerced and mandated to do something I believe with have CATASTROPHIC consequences. I beg you to be part of bringing light to this. Please call or email any time for details! I've have several experiences over the course of the last 2 years!!!
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Ulcerative Colitus
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 19.01.2022
- Impfdatum
- 19.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Muscle rigidity
Unresponsive to stimuli
Symptomtext
After injection patient began to slump over in chair, we slowly lowered him flat on his back, he was not responsive as I asked several times if he could breathe, eyes wide open and muscles completely rigid, yelled for fellow coworker to call 911 as I grabbed an EpiPen (didn't have to use it); patient regained consciousness and responded he could breathe; EMS arrived and took his vitals all which were normal. After about 30 minutes patient left with his mother.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- pt stated he has fainted after injections in the past as well as blood draws
- Staat
- CA
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 19.01.2022
- Impfdatum
- 10.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 20,0
- Dosis
- 1
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Haemoptysis
Pyrexia
SARS-CoV-2 test negative
Symptomtext
High fever/chills, followed by coughing up large amounts of dark red blood for 5 days. No other symptoms besides this. Abruptly stopped on 5th day
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- 4 Covid tests day of, during and after event. All negative test results
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- -
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- -
- Beginn
- 12.01.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Headache
Pain
Symptomtext
VERY ACHY AS THE DAY WENT GOT WORSE; CHILLS AS THE DAY WENT GOT WORSE (CURRENTLY COVERED WITH BLANKETS); HEADACHES AS THE DAY WENT GOT WORSE; This spontaneous report received from a patient concerned a female of unspecified age. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 213D21A expiry: UNKNOWN) dose was not reported, administered on 12-JAN-2022 10:00 for prophylactic vaccination. No concomitant medications were reported. On 12-JAN-2022, the patient experienced very achy as the day went got worse, chills as the day went got worse (currently covered with blankets), and headaches as the day went got worse. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from very achy as the day went got worse, chills as the day went got worse (currently covered with blankets), and headaches as the day went got worse. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 15.01.2022
- Impfdatum
- 24.12.2021
- Beginn
- 24.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site pain
SARS-CoV-2 test
SARS-CoV-2 test positive
Symptomtext
COVID-19 TEST POSITIVE; SORENESS AROUND SHOT; This spontaneous report received from a patient concerned a patient of unspecified age and sex. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: The patient had no known allergies. The patient received covid-19 vaccine ad26.cov2.s (dose number in series 1) (suspension for injection, route of admin not reported, batch number: 201A21A , and expiry: UNKNOWN) dose was not reported,1 total, administered on 18-JUN-2021 for prophylactic vaccination. On an unspecified date in late AUG-2021 and early SEP-2021, the patient had 5 or 6 Covid-19 test, all result showed negative. No adverse events reported post vaccination (dose number in series 1). The patient received covid-19 vaccine ad26.cov2.s (dose number in series 2) (suspension for injection, route of admin not reported, batch number: 213D21A, and expiry: UNKNOWN) dose was not reported,1 total, administered on 24-DEC-2021 on left arm for prophylactic vaccination. No concomitant medications were reported. On 24-DEC-2021, the patient experienced soreness around shot. On 03-JAN-2022, the patient was tested positive for Covid-19 through rapid nasal swab, hence covid-19 test positive (dose number in series 2). The patient was enquiring that is it possible to get a positive/false positive result receiving the vaccine. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from soreness around shot on 26-DEC-2021, and the outcome of covid-19 test positive was not reported. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- Test Date: 2021; Test Name: COVID-19 virus test; Result Unstructured Data: Negative; Test Date: 2021; Test Name: COVID-19 virus test; Result Unstructured Data: Negative; Test Date: 2021; Test Name: COVID-19 virus test; Result Unstructured Data: Negative; Test Date: 2021; Test Name: COVID-19 virus test; Result Unstructured Data: Negative; Test Date: 2021; Test Name: COVID-19 virus test; Result Unstructured Data: Negative; Test Date: 2021; Test Name: COVID-19 virus test; Result Unstructured Data: Negative; Test Date: 20220103; Test Name: SARS-CoV-2 rapid diagnostic test; Result Unstructured Data: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: The patient had no known allergies.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 12.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Discomfort
Immediate post-injection reaction
Malaise
Nausea
Pain in extremity
Symptomtext
Pt got Janssen vaccine 1st dose. Did not eat all day. Immediately after the dose was given, she had symptoms of pain in the arm, didn't feel good, nausea, had to put her head down as she was clearly in discomfort. We gave her water, cookies, coldpack on the arm and back of neck. Took blood pressure and it was 122/80. 15 min later, she was feeling better. Called a code white in the store. Manager showed up to file a report and interview pt. Patient was able to leave on her own without medical attention.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 12.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hypersensitivity
Pruritus
Symptomtext
A 64-year-old female presents to the vaccination center for her booster dose. Patient refers that when administering her 2 previous doses of MODERNA'S vaccine, she has presented allergic reactions and that at the vaccination center they had to administer epinephrine. Doctor is consulted, who indicates that the recommendation for the administration of booster doses is to administer Janssen. The Janssen vaccine is administered to the patient, approximately 3 minutes after the administration, the patient reports feeling itching in the area of ??the face, neck and head. Consultation with Doctor is made, who orders 25mg of BENADRYL PO. The patient is reassessed, 15 minutes after the administration of BENADRYL, it refers to having improved the symptoms. Later, the patient leaves the vaccination center under his own feet.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Patient refers not to have any health conditions.
- Andere Medikamente
- Patient refers not to be taking medication
- Allergien
- Patient reports being allergic to aspirin, acetaminophen, and having had adverse reactions to the influenza vaccine and previous doses of Modena's COVID-19 vaccine
- Vorherige Impfungen
- Influenza, Covid 19 Moderna
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 12.01.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Fatigue
Influenza like illness
Myalgia
Symptomtext
Flu like symptoms. Muscle and joint aches, fatigue. Bad the next morning then quickly disappeared about noon. No issues since.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 11.01.2022
- Impfdatum
- 10.12.2021
- Beginn
- 10.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hyperhidrosis
Pruritus
Urticaria
Symptomtext
UrticariaPruritus DIAPHORESIS Narrative: PT SEEN BY EMPLOYEE HEALTH ARNP. V/S STABLE. SHE HAS NEVER HAD A VACCINE BUT HAD TO TAKE A MANDATORY COVID. ITCHING WITH IN 15MINUTES. SHE TOO BENADRYL 25MG PO OF HER OWN MEDS AND REACTION RESOLVED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 11.01.2022
- Impfdatum
- 17.11.2021
- Beginn
- 18.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Fatigue
Symptomtext
chills, fatigue Narrative:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 11.01.2022
- Impfdatum
- 12.11.2021
- Beginn
- 13.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Myalgia
Oropharyngeal pain
Pain in extremity
Symptomtext
Myalgia sore throat, arm pain Narrative:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 11.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 8,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Injection site swelling
Limb discomfort
Symptomtext
Pain at injection site and swelling and discomfort in opposite arm where I received my Influenza injection 6 weeks before.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- Impfdatum
- 02.12.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 29,0
- Dosis
- 1
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
COVID-19
Chills
Cough
Dizziness
SARS-CoV-2 test positive
Symptomtext
chills, cough, dizziness + COVID test
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 10.01.2022
- Impfdatum
- 10.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Fall
Malaise
Symptomtext
Patient was administered the COVID 19 vaccination. Approximately 2 minutes after administration, he alerted pharmacy staff that he wasn't feeling well and stated he felt lightheaded. I went out to the patient in the waiting area at which point he asked for a water. I got him a water and the patient fell off the vaccination seat onto the floor (unsure if he hit his head). Another pharmacy associate called 911 and myself and another customer in the store assisted the gentleman up to his seat. Once seated after taking some sips of water, he began saying that he felt okay. By this point, the ambulance and the patient's father had arrived. Patient told EMTs that he felt okay, but they insisted that they take him outside to get his vitals before his father take him home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- none that we are aware of
- Vorgeschichte
- none that we are aware of
- Andere Medikamente
- unknown
- Allergien
- no allergies per patient informed consent form
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 07.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Chills
Fatigue
Gait disturbance
Headache
Hyperhidrosis
Lymphadenopathy
Pain
Pyrexia
Symptomtext
Symptoms: fatigue, low-grade fever (100.6), body pain (could not walk), extreme chills, severe headache, swollen lymph nodes in both sides of neck,, weakness Time Course: fatigue began at 6 pm on January 5th. On January 6th at 2:30 PM extreme chills began that lasted until morning of January 7th followed by sweating until 1pm. Could not walk until 11:30 am on the 7th. Headache persists Treatment: Tylenol two regular doses (too weak to sit up and take more)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Arthritis
- Andere Medikamente
- junel fe 1.5/30
- Allergien
- Percocet
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 05.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Urticaria
Symptomtext
Patient called about 30 minutes after vaccination to report hives on leg. He remained in pharmacy for 15 minutes (following vaccination) with no issues. He called about 15 minutes after he left to report hives. I questioned him if he was having trouble breathing or felt as if his tongue was swelling. He stated he felt fine except for the hives. Discussed he should take Benadryl and monitor for trouble breathing. If so, report to ER. Discussed severe allergic reaction normally occurs within 15 minutes of vaccination, but he should still be cautious and monitor symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- No allergies
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 05.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Nausea
Oral discomfort
Pruritus
Symptomtext
Dizziness, nausea, lips burning, itching
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 04.01.2022
- Impfdatum
- 15.12.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Hypoacusis
Nausea
Tunnel vision
Symptomtext
Assistance requested at charting. Patient reports lightheadedness nausea and tunnel vision, decreased hearing. Assisted to chair then then wheelchair. no fainting or loss of consciousness. transported to bay 1 medical monitoring pulse oxygen 99%. Pulse 71. Patient went home afterwards.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- daily fluoxetine, adderall, OCP
- Allergien
- peanuts, last epi-pen 5 years ago
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 03.01.2022
- Impfdatum
- 02.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Cold sweat
Feeling abnormal
Illness
Sleep disorder
Symptomtext
Have not been ill in YEARS. Was forced to take vaccine under threat of unemployment and homelessness-for my health. Went to bed early, woke up at 9:30, it felt like I had been thrown off of a building. Took hot epsom salt bath, went back to bed and then violent chills. Got up and ate some hot soup, then back to bed for a round of cold sweats. Intermittent chills and cold sweat all night long. I signed an electronic waiver, but it was done under duress by threat of exile. Plenty of responsible parties involved in forcing this disease on me when I was perfectly healthy. Which one(s) are going to compensate me for the damage to my body?
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 28.12.2021
- Impfdatum
- 01.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 15,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
New daily persistent headache
Pyrexia
Symptomtext
102.2 degree fever 8 hours after injection. Have currently had a headache every single day since the day of the injection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- New daily persistent headache
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Minor cold
- Vorgeschichte
- None
- Andere Medikamente
- Strattera, aurovela FE
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 27.12.2021
- Impfdatum
- 27.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood pressure decreased
Dizziness
Hyperhidrosis
Symptomtext
AFTER ADMINISTRATION OF J&J 1ST DOSE OF VACCINE, @1742, PT'S FELT LIGHTHEADED, SWEATY, HELPED PT'S TO SIT ON THE FLOOR WITH WALL SUPPORT ON HIS BACK, HAD WATER ~@1743. CHECKED PT'S BP DROPPED TO 86/52 MMHG, PULSE 40/MIN ~@1745. Pt's SATRTED FEELING BETTER, CHECKED BP AGAIN ~@1755 BP 120/75 MMHG, PULSE 55/MIN. ~1804 PT'S FELT WAY BETTER AND THOUGHT HE COULD GO HOME, PT'S ASKED TO SATY ATLEAST 30 MINUTES IN OBSERVATION. PT'S LEFT ~1819 PT'S FEELING BETTER LIKE NOTHING HAPPENED. DP 12/27/2021 @1825
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- NO
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 25.12.2021
- Impfdatum
- 02.11.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abnormal faeces
Arthralgia
Back pain
Blood test normal
COVID-19
Chills
Cough
Dry eye
Dry mouth
Influenza like illness
Pain
Pain in extremity
Procedural pain
Productive cough
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Sneezing
Symptomtext
Loss in visual acuity, dry mouth with increased and constant phlegm in throat, dry eyes, increased pain in all previous surgery sites. To include : R-wrist, R-ball of foot, both knees, both hip sockets, C-spine, and L-spine, stool is thinner in diameter. On 22Dec21, extreme flu-like symptoms started, including 102.1F fever, chills, congestion, more body aches, coughing, and sneezing. On 25Dec21 tested positive for COVID.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- On 02Dec21, blood tests revealed no abnormalities.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 24.12.2021
- Impfdatum
- 01.12.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bed rest
COVID-19
Fatigue
Headache
Muscular weakness
Myalgia
Symptomtext
For all intents and purposes the vaccine induced COVID 19 disease. Patient had recovered from previous SARSCoV2 infection in July 2021 (confirmed with positive PCR test at the time). Patient began to experience similar symptoms as experienced the during the previous infection within 30 min of receiving the vaccine. Symptoms included muscle aches and muscle weakness throughout the body, general fatigue, and headache, all as had been experienced in the previous infection. Symptoms were sufficiently severe to warrant bed rest, as in the case of the previous infection. Symptoms persisted for 48 hours, c. 50% of duration / persistence during the previous infection. Of note, lose of sense of smell and taste was not experienced post-vaccine, although had been experienced during the previous infection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None known
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 24.12.2021
- Impfdatum
- 18.12.2021
- Beginn
- 19.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Symptomtext
After receiving vaccination he waited for 15 minutes of observation, later he mentioned he felt fatigue due to working/driving until 2AM and not eating. We gave him water and other snacks. He was under observation for about 30 minutes, he was talking, walking and eating. It was not observed any health related issues or concerns. After that he said he is feeling better and left the vaccination site on his own volition. He was encouraged to report any side effect to V-Safe.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Unknown
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Not that we are aware about
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- VT
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 23.12.2021
- Beginn
- 23.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Axillary pain
Discomfort
Feeling abnormal
Headache
Injection site pain
Myalgia
Pain
Pain in extremity
Sleep disorder
Symptomtext
Around 4PM my arm started to ache - i didn't give it much thought. As the evening went on, the discomfort radiated to my axilla and down the left arm with occasional shooting pain from the injection site down my arm. I woke up during the night with severe muscle pain. I feel like someone has used a club on my entire body. I also have a headache. Tylenol and ibuprofen do nothing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- allergic to all artificial sweeteners; severe reaction to MMR vaccine
- Vorherige Impfungen
- MMR
- Staat
- -
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 20.12.2021
- Impfdatum
- 16.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Rash
Symptomtext
The patient woke the morning after (Friday) her immunization with rash covering majority of her body. took Benadryl and rash resolved by Sunday.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 20.12.2021
- Impfdatum
- 13.12.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Headache
Malaise
Pain
Vision blurred
Vomiting
Symptomtext
PT. HERE WITH HEADACHE, BLURRED VISION AND VOMITING FOR 2 DAYS. PT. STATES HIS WHOLE BODY ACHES AND HE DOES NOT FEEL WELL. PT. HAD JANSSEN BOOSTER ON 12/13. PT. SLEEPING OK. DENIES ANY LEG PAIN OR SHORTNESS OF BREATH. PT. REPORTS BLURRED VISION AND UNABLE TO FOCUS TOO. PT. STATES HE VOMITED TWICE YESTERDAY WHILE GOING FROM WORK TO HIS VEHICLE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 18.12.2021
- Impfdatum
- 12.12.2021
- Beginn
- 12.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Pain
Tinnitus
Symptomtext
BODY ACHES AND BODY PAINS; HEADACHE; RINGING IN THE EARS; This spontaneous report received from a patient concerned a 59 year old white not Hispanic or Latino male. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. On an unspecified date, the patient was previously received covid-19 vaccine ad26. cov2. s (suspension for injection, route of admin and batch number were not reported) dose was not reported (dose number in series 1), 1 total, administered for prophylactic vaccination. No adverse events were reported following vaccination with Covid-19 vaccine ad26.cov2.s. (dose number in series 1). The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 213D21A expiry: 11-APR-2022) dose was not reported (dose number in series 2), administered on 12-DEC-2021 16:30 to Left Arm for prophylactic vaccination. No concomitant medications were reported. On 12-DEC-2021, in the evening, the patient experienced headache, ringing in the ears, body aches and body pains (dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from body aches and body pains, and headache on 14-DEC-2021, and had not recovered from ringing in the ears. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 18.12.2021
- Impfdatum
- 12.12.2021
- Beginn
- 12.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Pain
Tinnitus
Symptomtext
BODY ACHES AND BODY PAINS; HEADACHE; RINGING IN THE EARS; This spontaneous report received from a patient concerned a 59 year old white not Hispanic or Latino male. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. On an unspecified date, the patient was previously received covid-19 vaccine ad26. cov2. s (suspension for injection, route of admin and batch number were not reported) dose was not reported (dose number in series 1), 1 total, administered for prophylactic vaccination. No adverse events were reported following vaccination with Covid-19 vaccine ad26.cov2.s. (dose number in series 1). The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 213D21A expiry: 11-APR-2022) dose was not reported (dose number in series 2), administered on 12-DEC-2021 16:30 to Left Arm for prophylactic vaccination. No concomitant medications were reported. On 12-DEC-2021, in the evening, the patient experienced headache, ringing in the ears, body aches and body pains (dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from body aches and body pains, and headache on 14-DEC-2021, and had not recovered from ringing in the ears. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 17.12.2021
- Impfdatum
- 18.11.2021
- Beginn
- 20.11.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Limb discomfort
Tinnitus
Symptomtext
Developed sores and lesions on the tips of my toes, along with, severve tinnitus and headaches.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 17.12.2021
- Impfdatum
- 19.11.2021
- Beginn
- 20.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Rash
Symptomtext
rash on neck and a headache
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Psoriasis
- Andere Medikamente
- -
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 17.12.2021
- Impfdatum
- 16.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Fatigue
Hallucination
Headache
Myalgia
Nausea
Pyrexia
Symptomtext
Headache Muscle aches Joint pain Fatigue Hallucinations Nausea Fever Over 12 + hours
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Entreaties, nifedipine, furosemide , carvedelol
- Allergien
- Flu vaccine
- Vorherige Impfungen
- Fly vaccine
- Staat
- NY
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 17.12.2021
- Impfdatum
- 05.12.2021
- Beginn
- 07.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Arthralgia
Gait disturbance
Musculoskeletal pain
Pain
Pain in extremity
Symptomtext
Sudden onset, 48 hours after vaccination, of severe and increasing pain in left ankle and foot, radiating up to left buttock. Pain crescendoed for 8 to 12 hours, not relieved by Tylenol, p?rcocet, high dose advil, ice. Severe difficulty walking due to pain in ankle and foot. Gradually eased after 12 hours, but has become chronic and waxing and waning over the past 10 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None so far. I have an upcoming appointment with a Neurologist.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High cholesterol, hypertension in the past.
- Andere Medikamente
- Lipitor, Aspirin, Vitamin C, Zinc, Vitamin D, Vascepa
- Allergien
- None
- Vorherige Impfungen
- Fever, chills, myalgias for 3 weeks after 1st Janssen Covid Vaccine on 4-6-21, age 54.
- Staat
- -
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 16.12.2021
- Impfdatum
- 13.12.2021
- Beginn
- 14.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Headache
Myalgia
Symptomtext
Headache & Myalgia Narrative:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 16.12.2021
- Impfdatum
- 15.12.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Dizziness
Dysphagia
Pruritus
Throat tightness
Symptomtext
Previous Moderna vaccines resulted in the 2nd dose with rash allover body. Recieved the Jansen today 12/6 AT APPROX. 4::05 pm and starting itchiness and scratching after 15-20 min from time of inject . rox. 5:35-5:45 my throat started closing on the left side which made it difficult to swollow. Ended un in emegency for a few hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none, however had rash allover body with the Moderna 2nd shot on april 6, 2021, With Johnson & Johnson Booster, today dec. 16th Itchy originally, but after approx. 1 hr and 1/2 my throat was closing on the left side and had trouble swollowing. calleled 911
- Vorgeschichte
- IBS
- Andere Medikamente
- none
- Allergien
- shellfish, bee stings, zithromax, clindamycin, bactrim, levaquin, zothromax, keflex
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 15.12.2021
- Impfdatum
- 14.12.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Abdominal pain upper
Chills
Dizziness
Feeling hot
Hallucination, auditory
Headache
Hyperhidrosis
Interchange of vaccine products
Nausea
Tinnitus
Visual impairment
Symptomtext
this is my third shot, my first two were pfiezer, and i had covid before i had any vaccine. about 12hrs after taking the shot, i had chills, stomach pain. walked down stairs to get snack and milk, i felt light-headed and had to lay down, close to passing out. vision started to close in. then had hot sweats, and nasuea. i also heard a noise in both ears which sounded like white noise. it was decently loud and lasted about 10s. i then recovered and went back to bed. in the morning, i went downstairs and had the same sequence of symptoms; close to passing out, sweats, nassuea, and heard the noise again. the noise halucination is probably the most concerning symptom. to me. i recovered fine, and have no further symptoms at the moment, other than headache.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- none.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 15.12.2021
- Impfdatum
- 12.12.2021
- Beginn
- 12.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Lymphadenopathy
Pain
Visual impairment
Symptomtext
Pt c/o left axilla swelling/bump that gradually worsened a day after injection. Also c/o visual changes. Had chills, body aches 3 hours after vaccine, but has resolved. Seen in urgent care 3 days after injection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- hypothyroidism , hypertension
- Andere Medikamente
- estrogen patches, flonase, levothyroxine, benazapril/HCTZ, telmesartan,
- Allergien
- anesthesia (unsure what kind), strawberries
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 15.12.2021
- Impfdatum
- 01.12.2021
- Beginn
- 13.12.2021
- Tage bis Beginn
- 12,0
- Dosis
- 2
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Fatigue
Pain
Symptomtext
Fatigue and aches: 48hrs time length. Chills: 5hrs during overnight.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hashimotos.
- Andere Medikamente
- Thyroid.
- Allergien
- Sulfa.
- Vorherige Impfungen
- Covid-19 1st dose, janson, 3/21.
- Staat
- NJ
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 15.12.2021
- Impfdatum
- -
- Beginn
- 08.12.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Symptomtext
ITCHING; This spontaneous report received from a patient concerned a 64 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included: various allergies, chronic migraines, restless leg syndrome, hypothyroidism, asthma, non alcoholic, and non smoker, and other pre-existing medical conditions included: Patient had allergy to steroids increase pressure in the eyes. Patient had no drug abuse or illicit drug usage. The patient experienced drug allergy when treated with tramadol. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 213D21A, expiry: unknown) dose was not reported, administered on 08-DEC-2021 for prophylactic vaccination. Concomitant medications included cetirizine hydrochloride for allergic symptoms, thyroid for hypothyroidism, rimegepant sulfate for migraines, and topiramate for migraines. On 08-DEC-2021, the patient experienced itching. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from itching. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Abstains from alcohol; Allergy; Asthma; Chronic migraine; Hypothyroidism; Non-smoker; Restless leg syndrome.
- Vorgeschichte
- Comments: Patient had allergy to steroids increase pressure in the eyes. Patient had no drug abuse or illicit drug usage.
- Andere Medikamente
- ZYRTEC [CETIRIZINE HYDROCHLORIDE]; ARMOUR THYROID; TOPIRAMATE; NURTEC ODT.
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 12.12.2021
- Impfdatum
- 09.11.2021
- Beginn
- 09.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Immediate post-injection reaction
Incorrect route of product administration
Injection site pain
Pain
Product administered at inappropriate site
Symptomtext
Injection was high on arm and needle hit bone or shoulder joint and was immediately very painful. Within hours the upper arm was sore and continued to be for almost 2 weeks. Now the shoulder area has a burning feel and it's painful in the upper part of the arm when extending the arm forward or upwards. Have not been to see a doctor yet - am hoping with rest and limited use, the shoulder and upper arm will get back to normal.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 12.12.2021
- Impfdatum
- 12.12.2021
- Beginn
- 12.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest discomfort
Dizziness
Throat tightness
Urticaria
Symptomtext
patient presented with dizziness. evaluation was completed and patient was observed. approximately ten minutes after the patient complained of chest tightness and developed urticaria on her neck and chest. she stated that it felt like her throat was closing. one dose of 0.3 mg of Epinephrine was administered to the left anterolateral thigh. immediate relief was noted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Zyrtec
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 11.12.2021
- Impfdatum
- 30.11.2021
- Beginn
- 30.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Pain in extremity
Symptomtext
Lasting pain initially at injection sight spreading with occasional pain shots down the arm. Pain has been on going since injection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- No
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 11.12.2021
- Impfdatum
- 11.12.2021
- Beginn
- 11.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Hyperhidrosis
Peripheral swelling
Symptomtext
ABOUT 3 TO 5 MINUTES AFTER TAKING THE VACCINE, PATIENT STARTING FEELING DIZZING AND SWEETING PROFUSELY AND HAND TIGHTENING. PATIENT ALERT AND BREATHING AT THE TIME
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 11.12.2021
- Impfdatum
- 17.11.2021
- Beginn
- 17.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal pain
Blood test normal
Muscle spasms
Vaginal haemorrhage
Symptomtext
Vaginal bleeding for about 20 days, following the COVID vaccine. I received the vaccine at 10:30 a.m., and started bleeding around 8 p.m. The bleeding last about 10 days, stopped for 2 days, and started again for another 7 days. It was accompanied by cramping and abdominal pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- Hematology ran a number of blood tests. All came back in the normal range.
- Aktuelle Erkrankungen
- Sinus infection in October, 2021
- Vorgeschichte
- No
- Andere Medikamente
- Zyrtek, Allergy Immunotherapy, multivitamins
- Allergien
- No
- Vorherige Impfungen
- Moderna COVID-19 Vaccine. Almost identical issues.
- Staat
- IN
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 11.12.2021
- Impfdatum
- 09.12.2021
- Beginn
- 09.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Balance disorder
Headache
Myalgia
Nausea
Pyrexia
Symptomtext
Fever -6 hours 24 hours other symptoms Headache Muscle aches Extreme weakness Loss of balance Nausea
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Vitamin C
- Allergien
- Vioxx Caffeine Alcohol MSG
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 10.12.2021
- Impfdatum
- 07.11.2021
- Beginn
- 07.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Pain in extremity
Product storage error
Symptomtext
Vaccine was administered outside of proper storage conditions. Vial was at room temp for >2 hours but <6 hours at the time of dose being drawn up. Manufacturer did not have stability information for these storage conditions so it was recommended that this dose be considered invalid and to re-administer. Patient will be coming in to get dose in near future. Patient had no unusual adverse events. He only experienced a sore arm and was tired for a few hours afterwards.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 10.12.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Fatigue
Product storage error
Symptomtext
Patient was given a dose of Janssen vaccine that was stored at room temp longer than 2 hours. (less than 6) Manufacture was contacted and they had no stability data on this vaccine for this window of time at room temperature and suggested we use our clinical expertise. We were advised to revaccinate and consider dose as invalid. Patient was notified of error and stated they did not have any side effects from the vaccine dose that was administered besides feeling a little tired the following day. They are scheduled to come back in to get revaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 10.12.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Fatigue
Product storage error
Symptomtext
Patient was given a dose of Janssen vaccine that was stored at room temp longer than 2 hours. (less than 6) Manufacture was contacted and they had no stability data on this vaccine for this window of time at room temperature and suggested we use our clinical expertise. We were advised to revaccinate and consider dose as invalid. Patient was notified of error and stated they did not have any side effects from the vaccine dose that was administered besides feeling a little tired the following day. They are scheduled to come back in to get revaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 10.12.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Immunisation
Injection site pain
Product storage error
Symptomtext
Patient was given a dose of Janssen vaccine that was stored at room temp longer than 2 hours. (less than 6 hours) Manufacture was contacted and they had no stability data on this vaccine for this window of time at room temperature and suggested we use our clinical expertise. Patient was notified of error. Patient was revaccinated about 1 month later. Patient reported that original vaccine hurt and stung with administration and that they had a sore arm for a few days later but otherwise felt fine. After revaccination with valid dose patient still reported that the vaccine stung with administration . No other side effects.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 10.12.2021
- Impfdatum
- 09.12.2021
- Beginn
- 09.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pyrexia
Rash
Symptomtext
patient recieved a dose of Janssen and later experienced fever and a skin breakout on the face and neck
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 10.12.2021
- Impfdatum
- 06.12.2021
- Beginn
- 08.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Deafness unilateral
Ear pain
Induration
Lymph node pain
Lymphadenopathy
Tinnitus
Symptomtext
Left lymph nodes behind the sternocleidomastoid at the base of the neck swollen to size of pennies, tender, and hard. Tinnitus in the left ear followed by complete hearing loss in the left ear with lots of pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ear pain
- Hospital-Tage
- -
- Labordaten
- Hearing issues self resolved in about 48 hours, still some pain.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Migraines Partial bundle branch block POTS
- Andere Medikamente
- Amitriptyline 20mg 1x daily orally Kyleena IUD
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 10.12.2021
- Impfdatum
- -
- Beginn
- 29.11.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
Chills
Headache
Malaise
Nausea
Pain assessment
Pyrexia
Symptomtext
CHILLS; FEVER; NOT FEELING GOOD; NAUSEA; SEVERE HEADACHE; This spontaneous report received from a consumer concerned a 62 year old male white Not Hispanic/Latino ethnicity. The patient's height, and weight were not reported. The patient's concurrent conditions included: 5 stents in the heart and drug allergy (bactrim). The patient was previously received with covid-19 vaccine ad26. cov2. s (manufacturer not specified) (suspension for injection, route of admin, and batch number were not reported) dose was not reported, administered on unspecified day for prophylactic vaccination (Dose number in series 1). No adverse events were reported for dose series 1. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 213D21A, and expiry: UNKNOWN) dose was not reported, 1 total administered on 29-NOV-2021 on right arm for prophylactic vaccination (Dose number in series 2). No concomitant medications were reported. On 29-NOV-2021, following vaccination with covid-19 vaccine ad26.cov2.s, the patient experienced nausea and severe headache (dose series 2). The reporter stated that in the early morning, the patient was complaining of a major headache (also reported as severe headache) with a pain level of 10/10. The patient took 2 Tylenol (paracetamol) tablets without any relief. Laboratory data included: Pain scale (NR: not provided) 10/10. On 30-NOV-2021, the patient experienced not feeling good, fever, chills, nausea and severe headache (dose series 2). The reporter stated the patient's temperature reached as high as 102.2 and stated he felt freezing and required additional clothing. Laboratory data included: Body temperature (NR: not provided) 102.2 F measured via ear. Treatment medications (dates unspecified) included: paracetamol for headache. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. At the time of this report, the patient had not recovered chills, severe headache, fever, nausea, and not feeling good. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Test Date: 20211129; Test Name: Pain scale; Result Unstructured Data: 10/10; Comments: 10/10; Test Date: 20211130; Test Name: Body temperature; Result Unstructured Data: 102.2 F.
- Aktuelle Erkrankungen
- Coronary stent placement; Drug allergy (drug allergy to bactrim).
- Vorgeschichte
- Comments: Unknown
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 09.12.2021
- Impfdatum
- 09.12.2021
- Beginn
- 09.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cold sweat
Dizziness
Nausea
Pallor
Symptomtext
PATIENT WAS SITTING IN OBSERVATION ROOM. HE GOT LIGHT-HEADED AND PALLOR IN APPEARANCE. HE STATED HE FELT NAUSEA AND THEN FELT LIKE PASSING OUT. WE TOOK HIS VITALS SIGNS, BP WAS 85/60 P-65 AND O2 SAT 98%. SKIN WAS CLAMMY AND COOL. WE APPLIED AN ICE PACK TO HIS NECK AND HAD HIM LAY DOWN ON FLOOR WITH FEET ELEVATED. AT 3:42 PM HE FELT BETTER, BP WAS 98/70, P-87 AND O2 SATS WERE 98%.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE REPORTED
- Vorgeschichte
- NONE REPORTED
- Andere Medikamente
- AMBIEN NIGHTLY PROTONIX DAILY
- Allergien
- NKA
- Vorherige Impfungen
- 4/1/2021
- Staat
- MO
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 09.12.2021
- Impfdatum
- 06.12.2021
- Beginn
- 06.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Pain
Pain in extremity
Symptomtext
Patient reported that when she got home one hour after receiving vaccination and began unloading her groceries she began to feel sharp pain in the back of her right knee. She reports that it has continued for the past three days and is worse upon exertion. She reports that the pain is better at rest but comes back when she walks or moves around. She also notes that the pain has started to spread down her legs and toward her hips. Reports taking tylenol which has helped the pain somewhat. Recommended that patient contact her doctor to explain the situation and receive examination to which the patient agreed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Unavailable
- Andere Medikamente
- Levothyroxine, diazepam, metoprolol tartrate, breo ellipta
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 08.12.2021
- Impfdatum
- 24.11.2021
- Beginn
- 25.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Apathy
Balance disorder
Corrective lens user
Cough
Diplopia
Ocular discomfort
Pyrexia
Symptomtext
fever 100 degrees, coughing, loss of motivation, and sense of imbalance to some degree. But most importantly, my double vision, was substantially worse after this shot. In hindsight, my prescription changed drastically, after first shot. But now, my corrected glasses, do not correct enough, after being increased, after the first shot. my double vision is likely due to muscular damage, and damage to the skeletal cage of the eye, when younger. So my guess is, this has affected the injured muscles. As my eyes, often reflect, whether I am sick. Also during the time with fever, my eyes felt like there was a lot of pressure. My double vision, is not linear. Just below the horizon, my double vision is correctable. But as I raise my eyes, to the horizon, and then above, the problem increases significantly. The eye problem remains after two weeks. I had double vision for years, without really knowing it. I thought it was normal. But as it got worse, I was forced to deal with it, as a problem.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- after the first shot, my double vision was significantly worse, and my last prescription shows this. Now, it appears to be even worse yet, for the prescription I bought to resolve the problem, is no longer sufficient. I expect, when I get my eyes checked next time, I expect my prescription will change, again. I have lived, with double vision for years, and not till the last few year,s did doctors really listen to what I am experiencing. So I live, I am not going to a doctor, until I simply have to. My trust in medicine is lessened, by what I see, being done, on covid.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- multivitamin, adult 50+ eye health, calcium magnesium zinc, bilberry, vitamin d, turmeric curcurmin, lutein, atorvastatin, melatonin, saw palmetto.
- Allergien
- penicillin
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 07.12.2021
- Impfdatum
- 04.12.2021
- Beginn
- 04.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Epistaxis
Headache
Malaise
Pain
Pain of skin
Pyrexia
Symptomtext
11:30am- Vaccine Received. 6:00pm-body aches, fever, headache. 3:00am the following day- fever, body aches, skin hurting, shivering, headache, malaise. 6:00am-bloody nose with giant blood clots that took me 20 to 25 minutes before it would stop. The following 2-3 days still having ongoing fever and headache.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Penicillin, Amoxicillin, Erythromycin, sulfa drugs
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 07.12.2021
- Impfdatum
- 07.12.2021
- Beginn
- 07.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dizziness
Hyperhidrosis
Symptomtext
Dizzy, Lightheaded, Sweaty
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Nortriptline, Provastatin
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 07.12.2021
- Impfdatum
- 26.11.2021
- Beginn
- 26.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Goitre
Headache
Hot flush
Injection site swelling
Oropharyngeal pain
Symptomtext
Injection site of arm swelled to 2xs its size, intense hot flashes at least 3 times an hour for 24 hours, headache for 24 hours, sore throat for 5 days, extreme tiredness (ongoing), and thyroid swelled up for 4 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 06.12.2021
- Impfdatum
- 26.11.2021
- Beginn
- 27.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Asthenia
Pain in extremity
Symptomtext
Patient experienced pain and weakness in the arm, as well as, in the shoulder. The patient continued having this pain almost a week after vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 06.12.2021
- Impfdatum
- 06.12.2021
- Beginn
- 06.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- no
- Allergien
- nka
- Vorherige Impfungen
- Patient said janssen 1st dose and flu vaccination he has taken made him dizzy
- Staat
- OK
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 06.12.2021
- Impfdatum
- 29.11.2021
- Beginn
- 30.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Fatigue
Headache
Pain
Pyrexia
Symptomtext
expeirenced severe head ache, body aches, chills, Fever of 100, extreme fatigue lasting 7 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypothyroidism
- Andere Medikamente
- Thyroid meds, nexplanon
- Allergien
- Allergy to egg whites, beef products, pecan.
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 06.12.2021
- Impfdatum
- 01.12.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Headache
Hypoaesthesia
Pain
Swelling face
Symptomtext
Approx 6 hours after vaccination --numbness and swelling in face bilaterally. Dizziness and HA. HA improved at day 3, Still has numbness in left side of face. Still having dizziness. Body aches
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- None at this time
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Lisinopril 20 mg dymista nasal spray BID
- Allergien
- Azithromycin
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 05.12.2021
- Impfdatum
- 04.12.2021
- Beginn
- 04.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Chills
Headache
Hyperhidrosis
Nausea
Pain
Pyrexia
Symptomtext
Chills, fever, sweats, nausea, headache, body aches, joint pain
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Multi vitamin, magnesium citrate, zinc, vitamin C
- Allergien
- Sulfa drugs
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 05.12.2021
- Impfdatum
- 12.11.2021
- Beginn
- 13.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Fatigue
Pain in extremity
Pyrexia
Symptomtext
Developed a low grade fever about 24 hrs after vaccine administered. Then developed fatigue and severe pain in all joints. Fever and fatigue went away in about 12 hrs but pain in joints persisted. I still have pain in certain joints like knees elbows hands and toes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 04.12.2021
- Impfdatum
- 29.11.2021
- Beginn
- 29.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Hyperhidrosis
Nausea
Symptomtext
4:22 pm-patient reports dizziness, nausea, sweating. Pharmacist applied ice pack and check blood pressure. See blood pressure log below: 4:22 pm 87/52 4:24 pm 83/61 4:28 pm 95/60 4:33 pm 97/76 4:39 pm 113/78 Patient asked for water. Once he drank water and sat for a few minutes, he felt ok to leave. I did call the patient the next day to check on him, but he did not answer. Left a voicemail.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Lithium, Lamotrigine
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 04.12.2021
- Impfdatum
- 01.12.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Asthenia
Joint swelling
Pyrexia
Symptomtext
Patient states she had high fever (102) for 3 days and her joints are swollen , she can't make a fist, her knee joints are sore and don't support her weight when she crouches
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NO
- Vorgeschichte
- NO
- Andere Medikamente
- -
- Allergien
- LATEX ALLERGY
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 35,0
- Geschlecht
- U
- Eingang
- 04.12.2021
- Impfdatum
- -
- Beginn
- 01.12.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Pain
Pyrexia
SARS-CoV-2 test
Symptomtext
BODY ACHES; CHILLS; FEVERING; This spontaneous report received from a patient concerned a 35 year old of unspecified sex. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 213D21A, expiry: UNKNOWN) dose was not reported, administered on 01-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. On SEP-2021, Laboratory data included: COVID-19 virus test (NR: not provided) virus detected. On 01-DEC-2021, the patient experienced body aches. On 01-DEC-2021, the patient experienced chills. On 01-DEC-2021, the patient experienced fevering. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient was recovering from fevering, chills, and body aches. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Test Date: 202109; Test Name: COVID-19 virus test; Result Unstructured Data: virus detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 04.12.2021
- Impfdatum
- -
- Beginn
- 17.11.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Back pain
Fall
Pain
Pain in extremity
Dysgeusia
Symptomtext
BITTER TASTE IN MOUTH; STARTED HURTING ON LEGS, FEET, HEELS AND MUSCLES; STINGING ON LEFT ARM; This spontaneous report received from a patient concerned a 54 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included: sulfonamide allergy, and other pre-existing medical conditions included: No medication. The patient experienced drug allergy when treated with thiamine hydrochloride, and tramadol. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: Unknown) dose was not reported, administered on 17-NOV-2021 for prophylactic vaccination. The batch number was not reported and has been requested. No concomitant medications were reported. On 17-NOV-2021, the patient experienced stinging on left arm. On 18-NOV-2021, the patient experienced bitter taste in mouth. On 18-NOV-2021, the patient experienced started hurting on legs, feet, heels and muscles. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient was recovering from bitter taste in mouth, and had not recovered from stinging on left arm, and started hurting on legs, feet, heels and muscles. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Sulfonamide allergy
- Vorgeschichte
- Comments: No medication
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 03.12.2021
- Impfdatum
- 19.11.2021
- Beginn
- 19.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Rash
Symptomtext
Narrative: Pt is 72 yo with PMH of RLS, arthritis, depressive disorder, insomnia, PTSD, opioid abuse, alcohol dependence, cannabis dependence, GERD, back pain, ADHD. Patient had first dose of Janssen COCIV-19 vaccine 3/10/21. Per provider note 11/23/21 pt had small rash after first dose of COVID-19 vaccine. No documentation in chart that a rash after first vaccine was reported by patient. No other documented ADRs. Rash treated with antihistamine (non-facility hydroxyzine) and OTC hydropcortisone.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- -
- Geschlecht
- M
- Eingang
- 03.12.2021
- Impfdatum
- 29.11.2021
- Beginn
- 30.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
Fatigue
Headache
Pyrexia
Symptomtext
FEVER 101 F; FATIGUE; HEADACHE; This spontaneous report received from a parent concerned a 19 year old male. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: Patient was 19 year old healthy. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 213D21A expiry: UNKNOWN) dose was not reported, administered on 29-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 30-NOV-2021, the patient experienced fever 101 F. On 30-NOV-2021, the patient experienced fatigue. On 30-NOV-2021, the patient experienced headache. Laboratory data included: Body temperature (NR: not provided) 101 F. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from fatigue, and headache on 30-NOV-2021, and had not recovered from fever 101 F. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Test Date: 20211130; Test Name: Body temperature; Result Unstructured Data: 101 F
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: Patient was 19 year old healthy.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 02.12.2021
- Impfdatum
- 01.11.2021
- Beginn
- 02.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Arterial occlusive disease
Hypoaesthesia
Pain in extremity
Peripheral coldness
Ultrasound scan abnormal
Symptomtext
severe arm pain and numb hand emergency arterial occlusion of upper extremity still have numb finger tips and hand gets extremly cold
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- 4,0
- Labordaten
- ultrsound
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 02.12.2021
- Impfdatum
- 30.11.2021
- Beginn
- 30.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Heart rate increased
Urticaria
Symptomtext
Hives within 15 minutes, increased heart rate, dizziness Patient was treated with Benadryl 50 mg
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Naltrexone
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 02.12.2021
- Impfdatum
- 30.11.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Headache
Injection site pain
Pain
Pyrexia
Symptomtext
Fever - 12 hours - Recovered Headache - 24 hours - Recovered Body Aches - 24 hours - Recovered Pain and soreness at Injection Site - 24 hours - Recovered
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- 80 mg Caffeine
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 02.12.2021
- Impfdatum
- 01.12.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal discomfort
Feeling hot
Nausea
Symptomtext
Pt complained of felling hot, and stomach upset. He felt nauseous, and requested an ambulance
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- none,
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- unknown
- Allergien
- none listed
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 02.12.2021
- Impfdatum
- 30.11.2021
- Beginn
- 30.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Chills
Erythema
Hypoaesthesia
Hypoaesthesia oral
Immediate post-injection reaction
Jaw disorder
Nausea
Pyrexia
Rash pruritic
Vomiting
Symptomtext
Within 15 minutes of injection at 11:30 a.m. my face and neck turned bright red. Chills began immediately after and lasted until 2 a.m. Nausea began shortly after chills. Vomiting at 2 a.m. Fever as high as 101.6. Took Tylenol at 5 a.m. and fever came down. Aching in joints. Felt like someone hitting knees with hammer. Wrists too painful to move. Jaws were throbbing. Lower right lip and chin numb until 9 or 10 a.m. the next day. Itchy Rash on fingers, feet and neck. Small raised spots that would remind you of poison ivy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Lifelong Migraine sufferer.
- Andere Medikamente
- Botox injections every 5 months for migraines; Metoprolol ER Succinate; Cambia Powder as needed for migraines.
- Allergien
- Shellfish; Latex.
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 01.12.2021
- Impfdatum
- 06.11.2021
- Beginn
- 29.11.2021
- Tage bis Beginn
- 23,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Blepharospasm
Computerised tomogram normal
Head discomfort
Headache
Magnetic resonance imaging normal
Memory impairment
Scan with contrast normal
Transient ischaemic attack
Symptomtext
Starting with 1st shot Janssen vaccine, I experienced a headache everyday for about 4 weeks. In the following months, forgetfulness. Could not recall simple things. If I saw an everyday object like a cup, or vegetable or fruit I could not bring its name up in my mind. I also could not remember my passwords to different shopping sites which I knew off the top of my head. Had to change them and still had difficulty. Very strange sensation in my head like an explosion, that is the only way I can describe it. This forgetfulness of everyday ordinary things continued until I had my booster on November 6, 2021. After that twitching of my right eye started along with the aforementioned symptoms. On Monday, November 29, 2021 at around 9:22 am I had a TIA in my right eye. Twenty-three days after Janssen vaccine booster shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- 1,0
- Labordaten
- I was taken to the emergency room. I was given a CT with and without contrast and a MRI. Both came back negative. The Neurologist informed that I had had a TIA. I do have high blood pressure and cholestrol.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- High Blood Pressure, Asthma
- Andere Medikamente
- Norvasc 10mg, Lorsartan 25mg, Aspirin 81mg, Vitamin, C, Vitamin D, Multivitamin, B12, Omega.
- Allergien
- Penicillin, sulfa drugs, Codeine, Liptor, Crestor, Wellburtin, Indomethacin, Cefuroxime Axetil. Shellfish.
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 01.12.2021
- Impfdatum
- 30.11.2021
- Beginn
- 30.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Oropharyngeal discomfort
Pruritus
Rash macular
Symptomtext
PATIENT WAS SITTING THROUGH THE WAITING PERIOD. ABOUT 10 MINUTES LATER PATIENT'S HUSBAND NOTIFIES ME (VACCINATING PHARMACIST AND REPORTER OF THIS FORM) THAT THE PATIENT WAS GETTING TIRED, ITCHY, AND RED SPLOTCHES WERE SHOWING UP. I ASKED THE PATIENT HOW SHE WAS FEELING, AND SHE DESCRIBED THE SYMPTOMS ABOVE AS WELL AS HER THROAT "FEELING FUNNY." I ALERTED A FELLOW PHARMACIST WHO THEN MONITORED HER AND CHECKED HER BLOOD PRESSURE. PATIENT TOOK A DOSE OF HER ALBUTEROL HFA INHALER TO SEE IF IT WOULD HELP. AFTER SOME TIME, SHE THEN REQUESTED AN EPIPEN THAT SHE INJECTED HERSELF. A CODE BLUE WAS CALLED AND THE MEDICAL STAFF ASSESSED HER. HER CURRENT STATE DID NOT WARRANT HER TO BE ADMITTED. PATIENT REMAINED IN THE LOBBY FOR STAFF TO MONITOR HER. EVENTUALLY, PATIENT LEFT TO GO TO HER CARDIOLOGIST. I CALLED THE PATIENT TO CHECK UP ON HER THE FOLLOWING DAY, AND PATIENT REPORTS THAT SHE IS DOING WELL.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- BLOOD PRESSURE, OXYGEN LEVELS (11/30/21)
- Aktuelle Erkrankungen
- NONE DISCLOSED
- Vorgeschichte
- HEART DISEASE (ANGINA AND TACHYCARDIA) AND DIABETES
- Andere Medikamente
- PATIENT ONLY DISCLOSED THAT SHE IS PRESCRIBED AN EPIPEN AND WAS STARTED RECENTLY ON OZEMPIC.
- Allergien
- MEDICATIONS (PENICILLIN, ERYTHROMYCIN, ASPIRIN), FOODS (MELONS, BANANAS) IODINE, LATEX, POLLEN
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 01.12.2021
- Impfdatum
- 29.11.2021
- Beginn
- 29.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Fatigue
Hyperhidrosis
Muscle spasms
Myalgia
Pyrexia
Symptomtext
Extreme chills/ convulsions resulting in muscle cramps- 6+ hours Extreme fatigue- ongoing muscle aches- ongoing fever- as high as 104- still ongoing but lower sweating- ongoing
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Vitamin D
- Allergien
- Amoxicillin
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 01.12.2021
- Impfdatum
- -
- Beginn
- 27.11.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Fatigue
Headache
Nausea
Pyrexia
Vomiting
Symptomtext
VOMITING; CHILLS; FEVER; HEADACHE; NAUSEATED; TIREDNESS; This spontaneous report received from a patient concerned a 24 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included: no alcohol use, and non smoker, and other pre-existing medical conditions included: Patient had no medical conditions and no chronic medications. Patient had no known allergies. No drug abuse or illicit drug usage. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 213D21A expiry: 11-APR-2022) dose was not reported, administered on 26-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 27-NOV-2021, the patient experienced tiredness. On 27-NOV-2021, the patient experienced nauseated. On 28-NOV-2021, the patient experienced headache. On 29-NOV-2021, the patient experienced chills. On 29-NOV-2021, the patient experienced fever. On 30-NOV-2021, the patient experienced vomiting. Treatment medications (dates unspecified) included: ibuprofen.The action taken with covid-19 vaccine ad26.cov2.s was not applicable.The patient recovered from tiredness, and headache on 28-NOV-2021, and had not recovered from chills, fever, nauseated, and vomiting. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Abstains from alcohol; Non-smoker.
- Vorgeschichte
- Comments: Patient had no medical conditions and no chronic medications. Patient had no known allergies. No drug abuse or illicit drug usage.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 29.11.2021
- Impfdatum
- 28.11.2021
- Beginn
- 28.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Headache
Oropharyngeal pain
Pharyngeal swelling
Rash pruritic
Swelling face
Urticaria
Symptomtext
Shortly following vaccine administration I experienced the following symptoms: itchy rash/hives on forearms, sore throat with extreme dizziness, a piercing headache, and a mildly swollen face and throat
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- none yet
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Under active thyroid
- Andere Medikamente
- none
- Allergien
- sulfa, pepper/hot spice
- Vorherige Impfungen
- influenza injection, hives, shortness of breath, swollen tongue/lips
- Staat
- GA
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 28.11.2021
- Impfdatum
- 26.11.2021
- Beginn
- 26.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dyspepsia
Fatigue
Injection site pain
Irritability
Myalgia
Nausea
Somnolence
Symptomtext
Injection site pain, Injection site arm sore, feeling very tired, muscle aches, nausea, heartburn, sleeping,irritable
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High blood pressure, overweight
- Andere Medikamente
- Losartan and Valtrex
- Allergien
- Shrimp
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 26.11.2021
- Impfdatum
- 22.11.2021
- Beginn
- 22.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Headache
Influenza like illness
Pyrexia
Symptomtext
Headache, Fever, flu-like symptoms Narrative:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 26.11.2021
- Impfdatum
- 26.11.2021
- Beginn
- 26.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Deafness
Dizziness
Immediate post-injection reaction
Tinnitus
Symptomtext
Immediately after the vaccine was given patient experienced light headedness, and ringing in the ears (said she couldn't hear). We gave her water and monitored and 1 minute later she said she felt fine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 24.11.2021
- Impfdatum
- 13.11.2021
- Beginn
- 14.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain in extremity
Symptomtext
sore arm still 2 weeks later
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Pantoprazole 40mg Aledronate 70mg Crestor 40mg
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 24.11.2021
- Impfdatum
- 11.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Headache
Injection site pain
Pain
Symptomtext
Patient has headache and pain at injection site for 3 days after injection. Those resolved on the 3rd day, but then patient noticed pain in the elbow joint of the right arm (opposite from her injection site). This pain has persevered for 2 weeks. The pain is only when patient extends her arm. It does not occur at rest. The area is not warm to the touch and no redness is apparent at the site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None reported
- Vorgeschichte
- None reported
- Andere Medikamente
- None reported
- Allergien
- Allergy to Elavil
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 24.11.2021
- Impfdatum
- 19.11.2021
- Beginn
- 20.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Fatigue
Injection site pain
Myalgia
Symptomtext
Pain at the injection site (right arm), pain in right pectoral chest muscle, fatigue, joints ache various, both knees and overall body. 12-24 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Blood pressure
- Andere Medikamente
- Norvasc, Micardis, Testosterone, Vitamin D, Atorvastatin (Lipitor)
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 23.11.2021
- Impfdatum
- 23.11.2021
- Beginn
- 23.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Symptomtext
administered patient 1st dose of janssen vaccine. patient stated they have a phobia of needles and immunizations. administered vaccine and had patient wait outside pharmacy for 15 min. went to check on patient a few minutes later and they stated they were feeling light headed but this was normal for them because they get so nervous. had patient move to bench in front of pharmacy to be able to monitor them and went out again a few minutes later to check on patient. they stated they still felt light headed and dizzy so had technician sit with them on bench for remainder of time to be monitored
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- patient stated they felt this way when receiving a previous vaccine elsewhere
- Staat
- -
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 22.11.2021
- Impfdatum
- 15.11.2021
- Beginn
- 15.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dizziness
Symptomtext
8mins post vaccination pt c/o dizziness. Vitals: 137/91, 66, 20 Pt stable and released from vaccination site w/ mother.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- PMH and Medications unknown to this writer
- Andere Medikamente
- PMH and Medications unknown to this writer
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 22.11.2021
- Impfdatum
- 10.11.2021
- Beginn
- 10.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal discomfort
Chills
Diarrhoea
Fatigue
Headache
Pain
Pyrexia
Symptomtext
Gastrointestinal discomfort, diarrhea began approximately 7:00 PM and continued for at least 3 hours (initially attributed by patient to food-induced indigestion) Fatigue, body ache, headache began approximately 8:30 PM and continued for approximately 36 hours Chills, probable low-grade fever (not measured) began approximately 9:30 PM and continued for 12-24 hours
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- seasonal allergies
- Andere Medikamente
- Loratadine, One-a-Day men's multivitamin, elderberry supplement
- Allergien
- amoxicillin, ibuprofen
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 22.11.2021
- Impfdatum
- 21.11.2021
- Beginn
- 22.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Breast pain
Pruritus
Symptomtext
Itchy scalp and pain in left breast area.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Breast pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Insomnia (use 5 mg generic zolpidem tartrate as needed) and Anxiety (use Xanax .5 as needed)
- Andere Medikamente
- Levothyroxine
- Allergien
- Sulfa, Ampicillin, Thyroid USP, Wellbutrin, Yellow Dye for eyes, some hair coloring dyes
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- -
- Geschlecht
- F
- Eingang
- 20.11.2021
- Impfdatum
- -
- Beginn
- 01.11.2021
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site bruising
Injection site pain
Nausea
Symptomtext
NAUSEOUS; ARM SORE AT INJECTION SITE; BRUISING OF ARM/BLUE AND BLACK AROUND INJECTION SITE; This spontaneous report received from a patient concerned a 61 year old female. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 213D21A expiry: UNKNOWN) dose was not reported, administered on 16-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On NOV-2021, the patient experienced bruising of arm/blue and black around injection site. On 16-NOV-2021, the patient experienced arm sore at injection site. On 17-NOV-2021, the patient experienced nauseous. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from nauseous, arm sore at injection site, and bruising of arm/blue and black around injection site. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 19.11.2021
- Impfdatum
- 19.11.2021
- Beginn
- 19.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Hyperhidrosis
Nausea
Pallor
Vomiting
Symptomtext
PATIENT CAME IN FOR J& J VACCINE RECEIVED VACCINE AND WENT TO BE SEATED. UPON SITTING THE PT BECAME PALE AND WAS SWEATING. HE BEGAN TO SEE DARK AND FELT FAINT. I EXPLAINED WHAT WAS HAPPENING AND AND HAD THE PATIENT TRY TO STAY AWAKE AND TALKING. HIS BLOOD PRESSURE WAS 180/154 WITH PULSE OF 99. HE FELT NAUSEOUS AND VOMITED. PT STATED THAT HE DID HAVE THIS REACTION OCCUR ONCE BEFORE WHILE DRAWING BLOOD. HE SAT FOR A FEW MORE MINUTES AND BEGAN TO REGAIN COLOR AND TEMPERATURE WARMED BACK UP AND HE STOPPED SWEATING. I TOOK HIS BLOOD PRESURE AGAIN AND IT WAS IN NORMAL RANGE. HE FELT FINE AND THEN LEFT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- na
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- na
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- -
- Geschlecht
- F
- Eingang
- 19.11.2021
- Impfdatum
- -
- Beginn
- 13.11.2021
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pain
Symptomtext
SORENESS IN ARM WHERE INJECTION WAS RECEIVED/TENDER TOUCH AT INJECTION SITE; REDNESS AT INJECTION SITE 2 INCHES WIDE; This spontaneous report received from a patient concerned a female of unspecified age. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: The patient had no change in lifestyle. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, and batch number: 213D21A expiry: 11-APR-2022) dose was not reported, administered on 12-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 13-NOV-2021, the patient experienced soreness in arm where injection was received/tender touch at injection site. On 13-NOV-2021, the patient experienced redness at injection site 2 inches wide. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from soreness in arm where injection was received/tender touch at injection site, and redness at injection site 2 inches wide. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 18.11.2021
- Impfdatum
- 18.11.2021
- Beginn
- 18.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Vaccine positive rechallenge
Symptomtext
She felt dizzy after receving her 2nd dose of Janssen. She drink cold water and felt better and was monitored for 30minutes. The patient stated she had a similar experience( worst )with her first dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- pencillin
- Vorherige Impfungen
- she stated with her first dose of Janssen, she felt dizzy
- Staat
- MA
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 18.11.2021
- Impfdatum
- 18.11.2021
- Beginn
- 18.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hyperhidrosis
Malaise
Pallor
Symptomtext
Pt's 2nd dose of J&J - Booster. Pt received booster vaccine at 0900. At 0907, the pt called out to the nurse and said he was not feeling well. Pt was pale and diaphoretic. EMS was initiated. Reclined pt back in his seat. Applied col pack and gave water. Vitals taken. BP-138/90, HR-92, 02 sat @ 96%. EMS arrived at 0915. Pt stated he was feeling better. Pt declined being transported to hospital. Pt observed for an additional 20 mins. Pt reassessed and was alert and oriented; skin was warm and dry. Pt verbalized he felt fine. Pt driven by family friend to his home. Total observation time was 35 mins.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Anxiety Depression
- Vorgeschichte
- Anxiety Depression
- Andere Medikamente
- Citalopram 40mg/daily
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 18.11.2021
- Impfdatum
- 17.11.2021
- Beginn
- 18.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Diarrhoea
Musculoskeletal stiffness
Nausea
Pyrexia
Vomiting
Symptomtext
Client called facility today reporting N/V/D, stiff neck and fever through out the night into today.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 17.11.2021
- Impfdatum
- 15.11.2021
- Beginn
- 15.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Dizziness
Fatigue
Feeling abnormal
Hypoaesthesia
Injection site erythema
Injection site pain
Injection site swelling
Muscular weakness
Myalgia
Nausea
Sensation of foreign body
Tinnitus
Symptomtext
I had the JNJ vaccine Monday, November 15. I have had constant ringing in both ears. Pain at injection site with swelling and some redness. Also, numbness in pinky and ring finger on left hand. Weakness in all extremities, especially legs. (felt like jello trying to stand). Dizziness and weakness when rising from sitting position. Feels like there is a lump in my throat when I swallow. Very fatigued, no energy, achy muscles, severe nausea and brain fog.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HTN Palpitations Hypothyroid
- Andere Medikamente
- Flecainide Metoprolol Amitriptyline Atorvastatin Irbesartan Levothyroxine Magnesium Potassium Colace ASA Pantoprazole Vitamin B complex
- Allergien
- Verapamil Minocycline
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 16.11.2021
- Impfdatum
- -
- Beginn
- 11.11.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Off label use
Product administered to patient of inappropriate age
Pyrexia
Symptomtext
15 YEAR OLD MALE PATIENT GOT THE VACCINE; OFF LABEL USE; This spontaneous report received from a pharmacist concerned a 15 year old male. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 213D21A, expiry: 11-APR-2022) dose was not reported, administered on 11-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 11-NOV-2021, the patient experienced 15 year old male patient got the vaccine. On 11-NOV-2021, the patient experienced off label use. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the 15 year old male patient got the vaccine and off label use was not reported. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 16.11.2021
- Impfdatum
- -
- Beginn
- 11.11.2021
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Off label use
Product administered to patient of inappropriate age
Pyrexia
Symptomtext
15 YEAR OLD MALE PATIENT GOT THE VACCINE; OFF LABEL USE; This spontaneous report received from a pharmacist concerned a 15 year old male. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 213D21A, expiry: 11-APR-2022) dose was not reported, administered on 11-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 11-NOV-2021, the patient experienced 15 year old male patient got the vaccine. On 11-NOV-2021, the patient experienced off label use. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the 15 year old male patient got the vaccine and off label use was not reported. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 15.11.2021
- Impfdatum
- 03.11.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Feeling of body temperature change
Nausea
Pyrexia
Somnolence
Symptomtext
Upon receiving the J & J vaccine , I developed a 100.4 for 2 days with chill , nausea & Fever . I now have to sleep 10-14 hours per day & I cannot control my body temperature , I am freezing , then hot etc.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- I have not returned to my medical doctor since injection.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Lorazepam & Lisinopril
- Allergien
- Codeine & Penicillin
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 12.11.2021
- Impfdatum
- 12.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Lip pruritus
Tongue disorder
Symptomtext
Patient observed from 1:22 pm to 1:52 pm. Patient states she feels fine at 1:50 pm. Patient reports tongue feels thick and lips itch at 1:52 pm. RN assessed patient and noted no swelling of tongue or lips. Patient vitals at 1:53 pm= 128/79, 81 heart rate, 14 respirations, 100% on room air. Patient given 25 mg Benadryl tablet at 1:59 pm per MD order. EMS called at 2 pm. CBG= 80 at 2:05 pm. EMS arrives at 2:11 pm. EMT assess patient; pt states her symptoms have not gotten worse and she does not want to go to the hospital. Patient eats cookie at 2:22 pm per NP request. EMS leave at 2:25 pm. Patient observed until 2:45 pm and states she would like to go home. Vital signs at 2:45 pm= 132/77, 76 heart rate, 14 respirations, 100% on room air. Patient discharged home with her husband.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lip pruritus
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None per patient.
- Vorgeschichte
- None per patient.
- Andere Medikamente
- Unknown.
- Allergien
- None per patient. Patient reports previous anaphylactic reaction to Pfizer vaccine in 2021.
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 12.11.2021
- Impfdatum
- -
- Beginn
- 01.11.2021
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anxiety
Fatigue
Feeling abnormal
Joint stiffness
Lethargy
Nausea
Pain
Pyrexia
Symptomtext
STIFF JOINTS; ACHINESS/SORENESS; LETHARGY; FEVER; NAUSEA; TIRED; FELT MESSED UP/BONES GOING TO GET MESSED UP; WORRIED; This spontaneous report received from a consumer concerned a 51 year old female. The patient's weight was 150 pounds, and height was 65 inches. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 213D21A, and expiry: UNKNOWN) dose was not reported, administered on 08-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On NOV-2021, the patient experienced felt messed up/bones going to get messed up. On NOV-2021, the patient experienced worried. On 09-NOV-2021, the patient experienced stiff joints. On 09-NOV-2021, the patient experienced achiness/soreness. On 09-NOV-2021, the patient experienced lethargy. On 09-NOV-2021, the patient experienced fever. On 09-NOV-2021, the patient experienced nausea. On 09-NOV-2021, the patient experienced tired. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the fever, nausea, achiness/soreness, stiff joints, tired, lethargy, felt messed up/bones going to get messed up and worried was not reported. This report was non-serious. This case, from the same reporter is linked to 20211125901.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 11.11.2021
- Impfdatum
- 11.11.2021
- Beginn
- 11.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Injection site pain
Symptomtext
Janssen Covid-19 Vaccine that was stored in the refrigerator was administered 40 minutes after the 6 hour expiration period. Patient was monitored for 30 minutes after administration in which he only experienced soreness at the injection site. Johnson and Johnson was contacted for further guidance. Per manufacturer, they have insufficient data to support stability and was referred to the guidelines Appendix A on the website. Appendix A recommended to repeat the dose immediately however the patient declined at this time and stated he preferred to wait for the usual booster interval.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- -
- Andere Medikamente
- NONE
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 11.11.2021
- Impfdatum
- 09.11.2021
- Beginn
- 11.11.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Eye swelling
Hiccups
Muscle spasms
Pyrexia
Swelling face
Symptomtext
Hiccups every 2 hours for 5 hours long. Eyes and Face swollen after 2 hours vaccine was given. cramps and fever.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- penicillin
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 11.11.2021
- Impfdatum
- 02.11.2021
- Beginn
- 04.11.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypersensitivity
Rash
Rash pruritic
Symptomtext
Patient called me today, 11/11/21, and described an allergic reaction that could be related to her Janssen booster vaccine. She received the vaccine on 11/2/21 and began developing bumps on her hands, elbows, and "multiple other areas" on 11/4/21. She described the bumps as itchy and small. She said they have progressively been spreading every day. She says she is allergic to Benadryl so she has been using OTC Hydrocortisone. She is going to seek medical attention today because it is still not getting better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- She is going to seek medical attention today.
- Aktuelle Erkrankungen
- NONE KNOWN
- Vorgeschichte
- NONE KNOWN
- Andere Medikamente
- ASPIRIN IS THE ONLY ONE THAT I'M AWARE OF
- Allergien
- BENADRYL
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 10.11.2021
- Impfdatum
- 10.11.2021
- Beginn
- 10.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood pressure increased
Dizziness
Symptomtext
Elevated blood pressure, light headedness
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 09.11.2021
- Impfdatum
- 09.11.2021
- Beginn
- 09.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Immediate post-injection reaction
Injection site haemorrhage
Injection site pain
Injection site swelling
Symptomtext
After immunizing technician gave the shot patient immediately started yelling at technician saying they hit a vein and said they could feel it all the way down to their toes and they felt it all over their body; Patient did bleed and swelled at the injection site but did not bleed through the barrier -site bandage; He told technician that it was done incorrectly and was going to report us to the cdc and we were incompetent and it was a terrible experience; He kept saying he was a nurse for 25 years and he had many degrees and we did not know what we were doing; He said he had many degrees and he knew we had hit a vein; Would not allow me to talk to him after that ; he walked away from the pharmacy; He ask to be tested with an antibody test at this time also;'
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site haemorrhage
- Hospital-Tage
- -
- Labordaten
- No test have been done at this time; It has been reported to our dm and clinical pharmacist for this region; At this time he has not called us back or given us any other information;
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- NO
- Andere Medikamente
- He would not allow me to ask any questions about other medication or what he was taking; He was not on a blood thinner at the time of immunization
- Allergien
- Not as far as we no but he would not talk to us after this.
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 09.11.2021
- Impfdatum
- 03.11.2021
- Beginn
- 04.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Hyperhidrosis
Musculoskeletal stiffness
Pain
Pain in extremity
Symptomtext
Next morning I woke up in sweats, headache and mild body aches. Intense Arm stiffness and soreness has persisted the full week following.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- none to date
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Oxycodone 7.5mg 1 time daily, Ambien 10mg nightly, Prilosec 2x daily, Testosterone Cypionate 1x weekly.
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 08.11.2021
- Impfdatum
- 02.11.2021
- Beginn
- 02.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Asthenia
Bedridden
Chest discomfort
Fatigue
Headache
Heart rate increased
Hypoaesthesia
Myalgia
Nausea
Pruritus
Rash
Throat tightness
Vomiting
Symptomtext
Janssen COVID-19 Vaccine EUA Headache within 45 minutes-treated with OTC medications; headaches have continued unresolved, intermittent as recently as today. Accelerated heartrate within 45 minutes-no treatment; symptoms have continued intermittently as recently as today. Weakness and nausea within 1 hour, vomited x1-no treatment; nausea continued for 2 days. Extreme fatigue within 1 hour-confined to bed; symptoms lasted 3 days. Tightness in chest and throat and fine rash to arms and generalized itching within 1.5 hours-2 Benadryl at onset followed by Benadryl twice a day for next 3 days; continued for 3 days. Numbness in both arms within 1.5 hours-no treatment; continued intermittently for 3 days. Muscle and joint soreness/pain within 2 hours-no treatment; continued for 3 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None to date.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None known
- Vorherige Impfungen
- 11 Sep 21 - GlaxoSmithKline influenz vaccine, age 43; muscle and joint pain and soreness, extreme fatigue, and nausea for 24 hou
- Staat
- FL
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 08.11.2021
- Impfdatum
- 31.10.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 3,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Symptomtext
Continous aching in right arm from elbow to shoulder
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- ATRIL FIB
- Andere Medikamente
- ELIQUIS, DILTIAZEM, LISINOPRIL, METOPROLOL TARTRATE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 08.11.2021
- Impfdatum
- 01.11.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Ageusia
Arthralgia
Dizziness
Fatigue
Headache
Injection site pain
Nausea
Peripheral swelling
Symptomtext
Fever (36 hours), swollen hand/arm (2 days), headache (4 days), fatigue (4 days), nausea (3 days), dizziness (3 days), loss of taste (6 days), joint ache (4 days), injection site soreness (7 days)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- atorvastatin (40 mg. daily), Vitamin D3 (5,000 UI daily)
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 05.11.2021
- Impfdatum
- 29.10.2021
- Beginn
- 29.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Myalgia
Pain
Pyrexia
Urticaria
Symptomtext
TPC placed to patient to follow up on email that was sent on 10/31/21 for covid vaccine reaction. Patient reports that he received the J & J Covid vaccine at on 10/29/21. He developed hives within 15 minutes of vaccine administration. He was given benadryl onsite by the pharmacist. Patient c/o 103 fever and body aches. He reports that the hives lasted on/off x 2 days that resolved with benadryl and Pepcid. Today, he c/o muscle pain and low grade fever. Denies chest pain, difficulty swallowing, rash or shortness of breath.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 02.11.2021
- Impfdatum
- 02.11.2021
- Beginn
- 02.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Confusional state
Dizziness
Visual impairment
Symptomtext
patient was given vaccine, shortly after patient experience feeling of passing out, confusion, and unable to see. patient laid on bench was given ice pack and felt better shortly after
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- na
- Vorgeschichte
- none
- Andere Medikamente
- na
- Allergien
- na
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 02.11.2021
- Impfdatum
- 02.11.2021
- Beginn
- 02.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Hyperhidrosis
Immediate post-injection reaction
Nausea
Vomiting
Symptomtext
Patient got extremely light headed, diaphoretic, nauseous, and vomited within 1 minute of shot. After sitting for approximately 10 minutes, patient felt just fine. I encouraged his friend with him that he needed to drive, or patient needed to find ride home. Patient declined any need for help, including drink/snack, ice pack to help cool down.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- None noted
- Vorgeschichte
- None noted
- Andere Medikamente
- Unknown
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 31.10.2021
- Impfdatum
- 31.10.2021
- Beginn
- 31.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Hyperhidrosis
Symptomtext
The patient went from a sitting position to a lying position , sweating, eyes closed, dizzy. The patient was given an ice pack for the back of his neck and emergency services was notified. The paramedics arrived and took vitals. The patients vitals were within range and the patient was asked if he wanted to be transported to the hospital which he refused. The patient was given orange juice to drink due to his reponse to the pharmacist stating he had not eaten yet today. The patient then left the store after stating he felt fine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- no
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 02.08.2023
- Impfdatum
- 02.12.2021
- Beginn
- 17.06.2022
- Tage bis Beginn
- 197,0
- Dosis
- 2
- 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 2 vaccines Janssen 3/28/21 Lot# 1805020; Pfizer 12/2/21 lot# 213D21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 02.08.2023
- Impfdatum
- 23.11.2021
- Beginn
- 08.12.2021
- Tage bis Beginn
- 15,0
- Dosis
- 1
- 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 one Janssen vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 22.06.2023
- Impfdatum
- 27.11.2021
- Beginn
- 02.12.2022
- Tage bis Beginn
- 370,0
- Dosis
- 1
- 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 1 dose Janssen
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 14.06.2023
- Impfdatum
- 18.01.2022
- Beginn
- 23.03.2023
- Tage bis Beginn
- 429,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Aortic aneurysm
Aortic dissection
Aortic surgery
Asthenia
Blood cholesterol normal
Blood glucose normal
Blood test abnormal
Cardiac operation
Computerised tomogram thorax abnormal
Electromyogram abnormal
Muscular weakness
Nerve injury
Obesity
Symptomtext
March 23, 2023 I suffered a near-fatal Thoracic Ascending Aneurysm due to interior surface dissection / damage to the aorta. I required an ambulance. This damage is present in CT scans down to the height of my kidneys. I required emergency open-heart surgery on my Ascending Aorta. The damaged section required it be replaced with rubber tubing, as indicated in the medical report for the surgery. I am currently undergoing periodic monitoring for the damage done to my Lower / Descending Aorta. It is highly expected that I will need a stent (another surgery). Additionally, as a result of the emergency surgery, my right brachial plexus nerve was damage, as shown on an electromyogram, causing significant and likely permanent weakness in my right bicep and chest. All blood samples indicated that I was not obese (BMI >40%), did NOT have high blood sugar, did NOT drink or use drugs, I was NOT under the effects of any prescription, did NOT have high cholesterol and, was of good physical strength and endurance. The only thing I did medically different was take that injection because of "No Jab No Job" mandate, which should be as illegal as any male boss telling a subordinate, "No Head No Bread"!
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Aortic aneurysm
- Hospital-Tage
- 8,0
- Labordaten
- Several CT scans and blood tests on file with Medical Center, March 25, April 17 and June 8th (all 2023).
- Aktuelle Erkrankungen
- None!
- Vorgeschichte
- None!
- Andere Medikamente
- None!
- Allergien
- None!
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 14.06.2023
- Impfdatum
- 13.11.2021
- Beginn
- 25.11.2021
- Tage bis Beginn
- 12,0
- Dosis
- 2
- 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 2 vaccines Janssen 3/16/21 lot# 1802068; Janssen 11/13/21 lot# 213D21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 06.06.2023
- Impfdatum
- 09.02.2022
- Beginn
- 11.07.2022
- Tage bis Beginn
- 152,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Angioedema
Symptomtext
PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ANGIOEDEMA, INIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Angioedema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 01.06.2023
- Impfdatum
- 03.11.2021
- Beginn
- 03.01.2022
- Tage bis Beginn
- 61,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Neuropathy peripheral
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Neuropathy peripheral
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 09.05.2023
- Impfdatum
- 20.11.2021
- Beginn
- 31.08.2022
- Tage bis Beginn
- 284,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Neuropathy peripheral
Sleep apnoea syndrome
Symptom recurrence
Symptomtext
PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE SLEEP APNEA PERIPHERAL NEUROPATHY 1/17/2023 -- RECURRENCE OF SAME SYMPTOMS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Neuropathy peripheral
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 03.05.2023
- Impfdatum
- 07.12.2021
- Beginn
- 19.08.2022
- Tage bis Beginn
- 255,0
- Dosis
- 1
- 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 one dose Janssen
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID+
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 01.05.2023
- Impfdatum
- 30.11.2021
- Beginn
- 24.04.2023
- Tage bis Beginn
- 510,0
- Dosis
- 2
- 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 2 Janssen vaccines Janssen 3/19/21 Lot# 1805020; Janssen 11/30/21 Lot# 213D21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 19.04.2023
- Impfdatum
- 16.12.2021
- Beginn
- 01.04.2023
- Tage bis Beginn
- 471,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dysgeusia
Oral discomfort
Suspected COVID-19
Symptomtext
EXTREME BITTER TASTE; BURNING IN MOUTH; SUSPECTED COVID-19 INFECTION; This spontaneous report received from a patient via other manufacturer (Pfizer) concerned a 67 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included: unspecified drug allergy, and other pre-existing medical conditions included: Patient was not pregnant at the time of vaccination. The patient was previously treated with covid-19 vaccine ad26.cov2.s (Dose number in series 1) (suspension for injection, route of admin not reported, batch number: 202A21A, expiry: UNKNOWN) dose was not reported, 1 total administered on 8-APR-2021 at left arm for covid-19 prophylaxis. It was unknown whether patient had any adverse events following vaccination with first dose of covid-19 vaccine ad26.cov2.s (Dose number in series 1) The patient received second covid-19 vaccine ad26.cov2.s (Dose number in series 2) (suspension for injection, route of admin not reported, batch number: 213D21A, expiry: UNKNOWN) dose was not reported, 1 total administered on 16-DEC-2021 at left arm for covid-19 prophylaxis. Age at time of vaccination 66 years old. Concomitant medications included prednisone, and zolpidem. On unspecified date in APR-2023, the patient experienced suspected covid-19 infection (Dose number in series 2) and received non-company suspect drug Paxlovid (nirmatrelvir/ritonavir) (form of admin, route of admin were not reported, batch number: GG4631 expiry: UNKNOWN) dose and frequency were not reported, administered from 11-APR-2023 to 12-APR-2023 for covid-19 treatment. On 11-APR-2023 at 19:00, the patient experienced extreme bitter taste and burning in mouth (Dose number in series 2), lasts for approximately 10 hours. Patient was taking other medications within 2 weeks of starting COVID-19 treatment. The action taken with covid-19 vaccine ad26.cov2.s was not applicable; and action taken with nirmatrelvir/ritonavir was not reported. The patient was recovering from extreme bitter taste, and burning in mouth, and the outcome of suspected covid-19 infection was not reported. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dysgeusia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Drug allergy
- Vorgeschichte
- Comments: Patient was not pregnant at the time of vaccination
- Andere Medikamente
- ZOLPIDEM; PREDNISONE; PAXLOVID LOT GG4631
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 84,0
- Geschlecht
- M
- Eingang
- 28.03.2023
- Impfdatum
- 02.12.2021
- Beginn
- 01.11.2022
- Tage bis Beginn
- 334,0
- Dosis
- 2
- 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 2 Janssen Janssen 5/12/21 Lot# 206A21A; Janssen 12/2/21 Lot# 213D21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 89,0
- Geschlecht
- M
- Eingang
- 28.03.2023
- Impfdatum
- 13.12.2021
- Beginn
- 04.08.2022
- Tage bis Beginn
- 234,0
- Dosis
- 2
- 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 2 Janssen Janssen 4/8/21 Lot# 042A21A; Janssen 12/13/21 Lot# 213D21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 15.03.2023
- Impfdatum
- 09.04.2021
- Beginn
- 01.03.2023
- Tage bis Beginn
- 691,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 02.03.2023
- Impfdatum
- 18.11.2021
- Beginn
- 09.02.2023
- Tage bis Beginn
- 448,0
- Dosis
- 2
- 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 2 vaccines Janssen 4/6/21 Lot# 042A21A; Janssen 11/18/21 Lot# 213D21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 16.11.2021
- Beginn
- 02.01.2023
- Tage bis Beginn
- 412,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Cough
SARS-CoV-2 test positive
Symptomtext
01/02/23 presents to ED for "cough". PMHx of "asthma, migraines"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- 01/02/23 SARS-CoV-2 (COVID-19) by NAA detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- U
- Eingang
- 31.01.2023
- Impfdatum
- 28.12.2022
- Beginn
- 28.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
RECEIVED EXPIRED VACCINE/PRODUCTS HAD REACHED THEIR LISTED EXPIRATION DATES; This spontaneous report received from a health care professional concerned multiple patients. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 213D21A expiry: 08-SEP-2022) dose was not reported, administered on 28-DEC-2022 for covid-19 prophylaxis. The drug was associated with Drug taken beyond expiry date. No concomitant medications were reported. On 28-DEC-2022, the patient experienced received expired vaccine/products had reached their listed expiration dates. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of received expired vaccine/products had reached their listed expiration dates was not reported. This report was non-serious. This case, from the same reporter is linked to 20230150340, 20230150255, 20230150600, 20230150423, 20230150157, 20230149982, 20230150588 and 20230150716.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- U
- Eingang
- 30.01.2023
- Impfdatum
- 10.11.2022
- Beginn
- 10.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
GIVEN EXPIRED VACCINE/PRODUCTS (HAD REACHED THEIR LISTED EXPIRATION DATES); This spontaneous report received from a health care professional concerned a patient of unspecified age and sex. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 213D21A expiry: 08-SEP-2022) dose was not reported, administered on 10-NOV-2022 for covid-19 prophylaxis. The drug was associated with Drug taken beyond expiry date. No concomitant medications were reported. On 10-NOV-2022, the patient experienced given expired vaccine/products (had reached their listed expiration dates). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of given expired vaccine/products (had reached their listed expiration dates) was not reported. This report was non-serious. This case, from the same reporter is linked to 20230150340, 20230150255, 20230150157, 20230150423, 20230149982, 20230150588, 20230150716 and 20230150777.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- U
- Eingang
- 30.01.2023
- Impfdatum
- 18.11.2022
- Beginn
- 18.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
RECEIVED EXPIRED VACCINE/PRODUCTS HAD REACHED THEIR LISTED EXPIRATION DATES; This spontaneous report received from a health care professional concerned a patient of unspecified age and sex. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 213D21A expiry: 08-SEP-2022) dose was not reported, administered on 18-NOV-2022 for covid-19 prophylaxis. The drug was associated with Drug taken beyond expiry date. No concomitant medications were reported. On 18-NOV-2022, the patient experienced received expired vaccine/products had reached their listed expiration dates. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of received expired vaccine/products had reached their listed expiration dates was not reported. This report was non-serious. This case, from the same reporter is linked to 20230150340, 20230150255, 20230150600, 20230150423, 20230150157, 20230150777, 20230150716 and 20230149982.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- U
- Eingang
- 30.01.2023
- Impfdatum
- 24.10.2022
- Beginn
- 24.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
WAS GIVEN EXPIRED VACCINE/PRODUCTS HAD REACHED THEIR LISTED EXPIRATION DATES; This spontaneous report received from a health care professional concerned a patient of unspecified age and sex. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 213D21A expiry: 08-SEP-2022) dose was not reported, administered on 24-OCT-2022 for covid-19 prophylaxis. The drug was associated with Drug taken beyond expiry date. On 24-OCT-2022, the patient experienced was given expired vaccine/products had reached their listed expiration dates. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of was given expired vaccine/products had reached their listed expiration dates was not reported. This report was non-serious. This case, from the same reporter is linked to 20230149982, 20230150340, 20230150255, 20230150600, 20230150157, 20230150588, 20230150716 and 20230150777.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- U
- Eingang
- 30.01.2023
- Impfdatum
- 06.10.2022
- Beginn
- 06.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
EXPIRED VACCINE USED / PRODUCTS HAD REACHED THEIR LISTED EXPIRATION DATES; This spontaneous report received from a health care professional concerned multiple patients. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 213D21A expiry: 08-SEP-2022) dose was not reported, administered on 06-OCT-2022 for covid-19 prophylaxis. The drug was associated with Drug taken beyond expiry date. No concomitant medications were reported. On 06-OCT-2022, the patient experienced expired vaccine used / products had reached their listed expiration dates. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of expired vaccine used / products had reached their listed expiration dates was not reported. This report was non-serious. This case, from the same reporter is linked to 20230149982, 20230150157, 20230150423, 20230150588, 20230150600, 20230150716, 20230150777 and 20230150255.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- U
- Eingang
- 30.01.2023
- Impfdatum
- 22.09.2022
- Beginn
- 22.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
WAS GIVEN EXPIRED VACCINE/PRODUCTS (HAD REACHED THEIR LISTED EXPIRATION DATES); This spontaneous report received from a health care professional concerned multiple patients. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 213D21A expiry: 08-SEP-2022) dose was not reported, administered on 22-SEP-2022 for covid-19 prophylaxis. The drug was associated with Drug taken beyond expiry date. No concomitant medications were reported. On 22-SEP-2022, the patient experienced was given expired vaccine/products (had reached their listed expiration dates). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of was given expired vaccine/products (had reached their listed expiration dates) was not reported. This report was non-serious. This case, from the same reporter is linked to 20230149982, 20230150157, 20230150423, 20230150600, 20230150588, 20230150716, 20230150777 and 20230150340.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- U
- Eingang
- 30.01.2023
- Impfdatum
- 20.09.2022
- Beginn
- 20.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
RECEIVED EXPIRED VACCINE/PRODUCTS HAD REACHED THEIR LISTED EXPIRATION DATES; This spontaneous report received from a health care professional concerned a patient of unspecified age and sex. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 213D21A expiry: 08-SEP-2022) dose was not reported, administered on 20-SEP-2022 for covid-19 prophylaxis. The drug was associated with Drug taken beyond expiry date. No concomitant medications were reported. On 20-SEP-2022, the patient experienced received expired vaccine/products had reached their listed expiration dates. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of received expired vaccine/products had reached their listed expiration dates was not reported. This report was non-serious. This case, from the same reporter is linked to 20230149982, 20230150340, 20230150255, 20230150600, 20230150423, 20230150716, 20230150777 and 20230150588.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- U
- Eingang
- 30.01.2023
- Impfdatum
- 27.12.2022
- Beginn
- 27.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
EXPIRED VACCINE WAS GIVEN/PRODUCTS HAD REACHED THEIR LISTED EXPIRATION DATES; This spontaneous report received from a health care professional concerned multiple patients. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 213D21A expiry: 08-SEP-2022) dose was not reported, administered on 27-DEC-2022 for covid-19 prophylaxis. The drug was associated with Drug taken beyond expiry date. No concomitant medications were reported. On 27-DEC-2022, the patient experienced expired vaccine was given/products had reached their listed expiration dates. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of expired vaccine was given/products had reached their listed expiration dates was not reported. This report was non-serious. This case, from the same reporter is linked to 20230150340, 20230150255, 20230150600, 20230150423, 20230150157, 20230150777, 20230149982 and 20230150588.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ND
- Alter
- 47,0
- Geschlecht
- M
- Eingang
- 26.01.2023
- Impfdatum
- 02.12.2021
- Beginn
- 01.11.2022
- Tage bis Beginn
- 334,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19 immunisation
Suspected COVID-19
Symptomtext
REVACCINATION WITH DIFFERENT COVID-19 VACCINE; SUSPECTED COVID-19 INFECTION; This spontaneous report received from a patient via other manufacturer (Pfizer) concerned a 48 year old male. The patient's height, and weight were not reported. The patient's concurrent conditions included: oxicodone, trazidone, dextromethorphan hbr allergy, and chronic severe headaches (treated with botox injections, tylenol, and advil). The patient was previously treated with covid-19 vaccine ad26.cov2.s (Dose Number in Series 1) (suspension for injection, route of admin not reported, batch number: 1816022, expiry: UNKNOWN) dose was not reported, 1 total administered at left arm on 12-JUL-2021 for covid-19 prophylaxis. It was unknown whether patient had any adverse events following vaccination with first dose of covid-19 vaccine ad26.cov2.s (Dose Number in Series 1) The patient received additional covid-19 vaccine ad26.cov2.s (Dose number in series 2) (suspension for injection, route of admin not reported, batch number: 213D21A, expiry: UNKNOWN) dose was not reported, 1 total administered at left arm on 02-DEC-2021 for covid-19 prophylaxis. Age at time of vaccination 47 years old. It was unknown whether patient had any adverse events following vaccination with covid-19 vaccine ad26.cov2.s (Dose number in series 2) The patient additionally received non-company suspect drugs included: (Spikevax) Moderna bivalent booster (elasomeran) (Dose number in series 3) (form of admin, route of admin were not reported, batch number: AS7143C, expiry: UNKNOWN) dose was not reported, administered at right arm on 01-NOV-2022 for covid-19 prophylaxis which was revaccination with different covid-19 vaccine (Dose number in series 3). Concomitant medications included botox injections (botulinum toxin type A), Advil (ibuprofen), Tylenol (paracetamol) for chronic severe headaches, Cold Relief (acetylsalicylic acid/chlorphenamine maleate/phenylephrine bitartrate), (guaifenesin), and (pseudoephedrine hydrochloride). On unspecified date in 2022, the patient experienced suspected covid-19 infection (Dose number in series 3) and received non-company suspect drug Paxlovid for treatment of covid-19 (form of admin, route of admin were not reported, batch number: unknown expiry: UNKNOWN) dose was not reported, administered from 05-DEC-2022 to 10-DEC-2022. On 15-DEC-2022, the patient was sick (Dose number in series 3). Although he felt pretty good at the end of the Paxlovid treatment, a few days later he became extremely sick again and that lasted for over a week. He spoke with the physician and was told that this could happen for the next few months. Very slowly he began feeling better, but 2 days ago it started getting worse again. The action taken with covid-19 vaccine ad26.cov2.s, elasomeran was not applicable and with paxlovid was drug discontinued. The patient was recovering from suspected covid-19 infection, and the outcome of revaccination with different covid-19 vaccine was not reported. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19 immunisation
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Chronic headaches (treated with botox injections, tylenol, and advil); Drug allergy
- Vorgeschichte
- -
- Andere Medikamente
- SUDAFED [PSEUDOEPHEDRINE HYDROCHLORIDE]; TYLENOL; ADVIL [IBUPROFEN]; EQUATE COLD RELIEF; MUCINEX; BOTOX
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- -
- Geschlecht
- M
- Eingang
- 23.01.2023
- Impfdatum
- 13.05.2022
- Beginn
- 13.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Off label use
Symptomtext
OFF LABEL DOSING FREQUENCY; This spontaneous report received from a consumer concerned a male of race (other), unspecified age, and ethnic origin. The patient's height, and weight were not reported. The patient was a naturopathic doctor. The patient was previously vaccinated with covid-19 vaccine ad26. cov2. s (Dose number in series 1) (suspension for injection, route of admin not reported, batch number: 204A21A expiry: UNKNOWN) dose was not reported, 01 total administered on 01-MAY-2021 for covid-19 prophylaxis. It was unknown whether the patient experienced any adverse events following vaccination with covid-19 vaccine ad26. cov2. s (Dose number in series 1). The patient received first booster dose of covid-19 vaccine ad26. cov2. s (Dose number in series 2) (suspension for injection, route of admin not reported, batch number: 1855194 expiry: UNKNOWN) dose was not reported, 01 total administered on 05-NOV-2021 for covid-19 prophylaxis. It was unknown whether the patient experienced any adverse events following vaccination with covid-19 vaccine ad26. cov2. s (Dose number in series 2). The patient additionally received second booster dose of covid-19 vaccine ad26.cov2.s (Dose number in series 3) (suspension for injection, route of admin not reported, batch number: 213D21A expiry: UNKNOWN) dose was not reported, 01 total administered on 13-MAY-2022 for covid-19 prophylaxis which was an off label dosing frequency (Off label use) (Dose number in series 3). The consumer reported as they believe that the JANSSEN COVID-19 VACCINE is excellent and the patient has been covid free. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of off label dosing frequency was not reported. This report was non-serious. This case, from the same reporter is linked to 20230138182.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Off label use
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: The patient was a naturopathic doctor.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 09.12.2022
- Impfdatum
- 17.12.2021
- Beginn
- 08.12.2022
- Tage bis Beginn
- 356,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
COVID vaccine breakthrough case J&J 4/6/21 041A21A and 12/17/21 213D21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Positive COVID test on 12/18/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 86,0
- Geschlecht
- F
- Eingang
- 09.12.2022
- Impfdatum
- 07.12.2021
- Beginn
- 28.11.2022
- Tage bis Beginn
- 356,0
- Dosis
- 2
- Route/Site
- SYR / UN
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Respiratory symptom
Symptomtext
Hospitalization for upper respiratory symptoms due to COVID-19 on dates 11/28/2022- 12/4/2022. Treated with Remdesivir.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- cefuroxime, cortisone (hives, rash), codeine (rash), atorvastatin (abnormal movements)
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 04.11.2022
- Impfdatum
- 14.12.2021
- Beginn
- 04.11.2022
- Tage bis Beginn
- 325,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asymptomatic COVID-19
COVID-19
Exposure to SARS-CoV-2
SARS-CoV-2 test positive
Symptomtext
asymptomatic- tested positive on binax rapid antigen test- test performed as follow up to known exposure
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asymptomatic COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- -
- Geschlecht
- U
- Eingang
- 27.10.2022
- Impfdatum
- 24.10.2022
- Beginn
- 24.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
RECEIVED AN EXPIRED VACCINE; This spontaneous report received from a consumer concerned a patient of unspecified age and sex. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 213D21A expiry: AUG-2022) dose was not reported, administered on 24-OCT-2022 for covid-19 prophylaxis. The drug was associated with Medication error. No concomitant medications were reported. On 24-OCT-2022, the patient experienced received an expired vaccine. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of received an expired vaccine was not reported. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 82,0
- Geschlecht
- M
- Eingang
- 25.10.2022
- Impfdatum
- 07.12.2021
- Beginn
- 01.02.2022
- Tage bis Beginn
- 56,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
CONFIRMED CLINICAL VACCINATION FAILURE; CONFIRMED COVID-19 INFECTION; This spontaneous report received from a patient concerned an 82 year old male of an unspecified ethnicity. The patient's height, and weight were not reported. The patient's concurrent conditions included: non-Hodgkin lymphoma (compromised immune system due to a rare blood cancer). The patient received covid-19 vaccine ad26.cov2.s (Dose number in series: 1) (suspension for injection, route of admin not reported, batch number: 1708609 and expiry: UNKNOWN) dose was not reported, 1 total, primary dose administered in right arm on 23-MAR-2021 for covid-19 prophylaxis. On an unspecified date in NOV-2021 following vaccination with primary dose of covid-19 vaccine ad26.cov2.s, the patient had covid-19 with symptoms of coughing and tested positive for COVID-19 virus test on 08-NOV-2021 (confirmed covid-19 infection and confirmed clinical vaccination failure) (Dose number in series: 1). It was also reported that patient was home quarantined for 5 days (Date unspecified). On an unspecified date and month in 2021, the patient experienced COPD (Chronic obstructive pulmonary disease) (Dose number in series: 1) and had received treatment with Doxycycline. The outcome of the confirmed clinical vaccination failure, confirmed covid-19 infection and COPD were not reported. The patient received covid-19 vaccine ad26.cov2.s (Dose number in series: 2) (suspension for injection, route of admin not reported, batch number: 213D21A and expiry: UNKNOWN) dose was not reported, 1 total, first booster administered in right arm on 07-DEC-2021 for covid-19 prophylaxis. Age at time of vaccination 82 years old. No concomitant medications were reported. On an unspecified date in FEB-2022 following vaccination with covid-19 vaccine ad26.cov2.s (first booster), the patient experienced diarrhea and viral infection, and tested positive for COVID-19 virus test which was confirmed covid-19 infection and confirmed clinical vaccination failure (Dose number in series: 2). Laboratory data included: COVID-19 virus test Positive. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the confirmed covid-19 infection and confirmed clinical vaccination failure was not reported. This report was serious (Other Medically Important Condition). This report was associated with a product quality complaint: 90000256360. This case, involving the same patient is linked to 20211208454 (Dose number in series 1) and 20221046895 (Dose number in series 3).; Sender's Comments: V0: 20221045009-covid-19 vaccine ad26.cov2.s- Confirmed Clinical Vaccination failure. The event(s) 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(s) than the drug. Specifically: SPECIAL SITUATIONS. Therefore, this event(s) is considered not related.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20211108; Test Name: COVID-19 VIRUS TEST; Test Result: Positive ; Test Date: 202202; Test Name: COVID-19 VIRUS TEST; Test Result: Positive
- Aktuelle Erkrankungen
- Non-Hodgkin's lymphoma (compromised immune system due to a rare blood cancer)
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 24.10.2022
- Impfdatum
- 14.12.2021
- Beginn
- 23.10.2022
- Tage bis Beginn
- 313,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
has had primary Janssen plus Janssen booster developed sx cough, runny nose, congestion, temp 100.7F tested positive for covid on abbott id now molecular
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- hx CVA, vascular dementia , CKD3, HTN, hypothyroidism, prev hx covid 3/29/21
- Andere Medikamente
- -
- Allergien
- Penicillin, Latex, VICODIN
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 05.10.2022
- Impfdatum
- 02.12.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product administered to patient of inappropriate age
Symptomtext
After vaccine was entered in system, it stated vaccine "NOT VALID" due to age. Patient was 17 years old when she received JJ vaccine which is only for 18 yrs. old and up. It is unknown if patient had any symptoms or adverse events due to this, but I was told to file a report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 07.09.2022
- Impfdatum
- 08.04.2021
- Beginn
- 31.08.2022
- Tage bis Beginn
- 510,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asymptomatic COVID-19
SARS-CoV-2 test positive
Suicidal ideation
Symptomtext
Pt here for suicidal ideation. Pt needed inpatient psychiatric care, but had to be tested for COVID before placement and was positive. Pt asymptomatic.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asymptomatic COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 23.08.2022
- Impfdatum
- 13.11.2021
- Beginn
- 14.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Eye swelling
Symptomtext
My eyes swelled shut, this was the booster. When I got the first JOHNSON and JOHNSHON in March of 2021 I was extremely nervous because I have the lupus anticoagulant and a week later it was taken off the shelves for blood clots.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Eye swelling
- Hospital-Tage
- -
- Labordaten
- Family history, mom and both aunts got deep vein thrombosis.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Lupus anticoagulant, scoliosis, anxiety, depression
- Andere Medikamente
- -
- Allergien
- Amoxicillin
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 19.08.2022
- Impfdatum
- 02.12.2021
- Beginn
- 07.08.2022
- Tage bis Beginn
- 248,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Pt tested positive for COVID on 08/07/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 19.08.2022
- Impfdatum
- 03.11.2021
- Beginn
- 04.05.2022
- Tage bis Beginn
- 182,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Chest X-ray normal
Computerised tomogram head normal
Confusional state
Electrocardiogram normal
Mental status changes
Transient global amnesia
Symptomtext
61-year-old female with no significant past medical history presenting for evaluation of altered mental status. Patient arrives via EMS. Brought from urgent care due to increased confusion. Patient's son took her to Urgent Care per EMS. Urgent Care was concerned as patient had repetitive questioning in the increased. No known past medical history. No psychiatric history. Denies SI/HI. Denies any hallucinations at this time. Denies any recent illness. Review of Systems Review of Systems Constitutional: Negative for chills and fever. Respiratory: Negative for shortness of breath. Cardiovascular: Negative for chest pain. Gastrointestinal: Negative for abdominal pain, nausea and vomiting. Psychiatric/Behavioral: Positive for confusion. All other systems reviewed and are negative.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest X-ray normal
- Hospital-Tage
- 1,0
- Labordaten
- EKG Interpretation: Normal sinus rhythm at 99 beats per minute. Intervals within normal limits. No evidence of acute ischemia or ST elevation. Normal axis. No ectopy. CT HEAD WO IV CONTRAST--FINDINGS: The ventricles and sulci are normal in size and configuration for age. No acute hemorrhage or extra-axial collection. No evident acute mass effect. Basilar cisterns are patent. No conclusive CT findings of acute transcortical infarct. Note that MRI is more sensitive for detecting acute ischemia. No calvarial fractures are identified. The visualized paranasal sinuses are clear. The visualized mastoid air cells are clear. AMS. PROCEDURE: Single AP view of the chest Lungs and Pleura: Clear lungs. No pleural effusion. No pneumothorax. Cardiovascular and Mediastinum: The cardiac silhouette is within limits of normal. Mediastinal contour is within limits of normal Impression: 1) Altered mental status, unspecified altered mental status type 2) TGA (transient global amnesia)
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- Zic/Quercetin
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 02.08.2022
- Impfdatum
- 02.12.2021
- Beginn
- 28.07.2022
- Tage bis Beginn
- 238,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after two Janssen vaccines Janssen 4/8/21 Lot# 042a21A; Janssen 12/2/21 Lot# 213D21A;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 02.08.2022
- Impfdatum
- 15.12.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
CONFIRMED CLINICAL VACCINATION FAILURE; CONFIRMED COVID-19 INFECTION; This spontaneous report received from a patient via other manufacturer (Pfizer) concerned a 52 year old male. Initial information was processed along with additional information received on 28-JUL-2022. The patient's height, and weight were not reported. The patient's concurrent conditions included: high cholesterol/triglycerides, and drug allergy. The patient was previously treated with two doses of Pfizer covid-19 vaccine (tozinameran) (dose number in series 1). The patient received first dose (form of admin and route of admin were not reported and batch number: EN6207 expiry: UNKNOWN) dose was not reported, administered on 16-MAR-2021 for covid-19 prophylaxis. The patient received second dose (form of admin, route of admin was not reported and batch number: ER8729 expiry: UNKNOWN) dose was not reported, administered on 13-APR-2021 for covid-19 prophylaxis. It was unknown whether patient had any adverse events following vaccination with two doses of Pfizer covid-19 vaccine (tozinameran) (dose number in series 1). The patient received covid-19 vaccine ad26.cov2.s (dose number in series 2) (suspension for injection, route of admin not reported, batch number: 213D21A expiry: UNKNOWN) dose was not reported, 1 total, administered on 15-DEC-2021 for covid-19 prophylaxis. Age at time of vaccination 51 years old. Concomitant medications included acetylsalicylic acid, brompheniramine, cetirizine hydrochloride, ergocalciferol, ezetimibe, fluticasone propionate, ibuprofen, rosuvastatin, and zinc were used for unknown indication. On an unspecified date in 2022, the patient experienced covid-19 infection (confirmed clinical vaccination failure, and confirmed covid-19 infection) (dose number in series 2). The patient received non company suspect Paxlovid (form of admin, route of admin, and batch number were not reported) dose was not reported, administered from 12-JUL-2022 to 16-JUL-2022 for covid-19 treatment. The patient reported that symptoms were started again four days after last dose of Paxlovid treatment. Symptoms were mild and included runny nose, sore throat and diarrhoea (dose number in series 2). On 18-JUL-2022, Laboratory data included: COVID-19 rapid antigen test result was fain compared to the control. On 20-JUL-2022, Laboratory data included: COVID-19 rapid antigen test result was as strong as the control (dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable and with paxlovid was drug discontinued. The patient had not recovered from confirmed covid-19 infection, and the outcome of confirmed clinical vaccination failure was not reported. This report was serious (Other Medically Important Condition). This report was associated with product quality complaint.; Sender's Comments: V0: 20220754628- Covid-19 vaccine ad26.cov2.s -CONFIRMED CLINICAL VACCINATION FAILURE. The event(s) 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(s) than the drug. Specifically: SPECIAL SITUATIONS. Therefore, this event(s) is considered not related.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220718; Test Name: COVID-19 RAPID ANTIGEN TEST; Result Unstructured Data: result was fain compared to the control; Test Date: 20220720; Test Name: COVID-19 RAPID ANTIGEN TEST; Result Unstructured Data: result was as strong as the control
- Aktuelle Erkrankungen
- Drug allergy; High cholesterol
- Vorgeschichte
- -
- Andere Medikamente
- EZETIMIBE; ROSUVASTATIN; CETRIZINE; IBUPROFEN; FLUTICASONE PROPIONATE; BROMPHEN; ZINC; VITAMIN D2; ECOTRIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 27.07.2022
- Impfdatum
- 01.12.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 31,0
- Dosis
- 1
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anosmia
Symptomtext
Loss of nearly all smell (95% loss) about a month after receiving the J&J COVID vaccine. Smell has not returned.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anosmia
- Hospital-Tage
- -
- Labordaten
- No testing directly related to my adverse event.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 23.07.2022
- Impfdatum
- 27.11.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 34,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
CONFIRMED CLINICAL VACCINATION FAILURE; CONFIRMED COVID-19 INFECTION; This spontaneous report received from a patient concerned a 63 year old male. The patient's weight, height, and medical history were not reported. The patient was previously received covid-19 vaccine ad26.cov2.s (dose number in series 1) (suspension for injection, route of admin not reported, batch number: 042A21A expiry: UNKNOWN) dose was not reported, 1 total, administered on 31-MAR-2021 in left arm for covid-19 prophylaxis. On an unspecified date in 2021, patient experienced upper left shoulder pain (minimal) that lasted one day (dose number in series 1). The patient additionally received covid-19 vaccine ad26.cov2.s (dose number in series 2) (suspension for injection, route of admin not reported, batch number: 213D21A expiry: UNKNOWN) dose was not reported, 1 total, administered on 27-NOV-2021 in left arm for covid-19 prophylaxis. Age at time of vaccination 63 years old. No concomitant medications were reported. On 31-DEC-2021, patient developed symptomatic covid (confirmed covid-19 infection) and he tested positive 2 days later with a rapid test (got the result within the hour) which resulted to confirmed clinical vaccination failure (dose number in series 2). Patient had quite the fever (lasted 4 days before it broke), had no thermometer, didn't know temperature. He felt his head was full, but there was no congestion. About a week later, he developed a cough and it lasted a month. He took 5 days off of work. He didn't see a doctor when he got covid, so his doctor was not aware. On 02-JAN-2022, Laboratory data included: COVID-19 rapid POC test Positive. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the confirmed clinical vaccination failure and confirmed covid-19 infection was not reported. This report was serious (Other Medically Important Condition). This report was associated with product quality complaint (PQC): 90000242713 and 90000242714. This case, involving the same patient is linked to 20220737591 (dose number in series 1).; Sender's Comments: V0-20220735184-covid-19 vaccine ad26.cov2.s-Confirmed Clinical vaccination failure. The event(s) 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(s) than the drug. Specifically: SPECIAL SITUATIONS. Therefore, this event(s) is considered not related.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220102; Test Name: COVID-19 RAPID POC TEST; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 16.07.2022
- Impfdatum
- 13.07.2022
- Beginn
- 13.07.2022
- 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
Patient received a third dose (second booster) of Janssen which is not recommended or approved by the CDC.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 16.07.2022
- Impfdatum
- 13.07.2022
- Beginn
- 13.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
Patient received a third dose (second booster) of Janssen which is not recommended or approved by the CDC.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 08.07.2022
- Impfdatum
- 08.07.2022
- Beginn
- 08.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Interchange of vaccine products
Symptomtext
The adverse event was that she was given 0.3 ml of J &J vaccine and will not have as much immunity coverage if she had received 0.5 ml of J&J. She came into receive 4th dose of Pfizer (2nd booster), erroneously given J& J vaccine, Because I thought I had picked up the Pfizer vaccine vial, 0.3 ml was given. Patient notified.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- No daily medications. The adverse event was that she was given 0.3 ml of J &J vaccine. She came into receive 2nd booster of Pfizer, erroneously given J& J instead. Patient notified.
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 27.06.2022
- Impfdatum
- 08.11.2021
- Beginn
- 08.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Eczema
Skin lesion
Skin test
Symptomtext
In December I started having issues with red lesion's on my left thigh then to my right thigh. The doctor took a skin sample and they found that I have Sirius/eczema. It has now spread to my back and my forearms and the back of my triceps. The doctor prescribed some creams were a low dose cortisone. My eye doctor told me I should discontinue it because I have a eye condition. Tacrolimus is the name of the cream I was given. I think the creams are helping and then out of nowhere I will have a weird reaction somewhere else on my body. Calcipotriene cream is another ointment that I have been instructed to use as well. The medicine the doctor wants me to stop taking triamcinolone.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Eczema
- Hospital-Tage
- -
- Labordaten
- Skin test
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Asthma; sinus issues; low thyroid
- Andere Medikamente
- AIMOVIG; albuterol; alprazolam; ANDROGEL; azelastine; esomeprazole; eszopiclone; famotidine; levothyroxine; PERCOCET; pramipexole; rizatriptan; valacyclovir
- Allergien
- LEVAQUIN
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 27.06.2022
- Impfdatum
- 27.05.2021
- Beginn
- 25.06.2022
- Tage bis Beginn
- 394,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Fall
Mental status changes
SARS-CoV-2 test positive
Symptomtext
Pt presented from a nursing home with increasing falls and altered mental status. He was found to be COVID positive.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 24.06.2022
- Impfdatum
- 03.11.2021
- Beginn
- 09.06.2022
- Tage bis Beginn
- 218,0
- Dosis
- 2
- 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 two Janssen vaccines Janssen 3/11/21 Lot# 180525; Janssen 11/3/21 Lot# 213D21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- -
- Geschlecht
- M
- Eingang
- 16.06.2022
- Impfdatum
- 14.06.2022
- Beginn
- 14.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Poor quality product administered
Product storage error
Symptomtext
This spontaneous report received from a health care professional concerned a male of unspecified age. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received Covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin, and batch number were not reported) dose was not reported, administered on 14-JUN-2022 for prophylactic vaccination. The drug was associated with Medication error. The batch number was not reported and has been requested. No concomitant medications were reported. On 14-JUN-2022, the patient experienced vaccine administered from a vial that was left at room temperature for 2 hours 30 minutes, and incorrect product storage. The action taken with Covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the vaccine administered from a vial that was left at room temperature for 2 hours 30 minutes and incorrect product storage was not reported. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 03.06.2022
- Impfdatum
- 02.12.2021
- Beginn
- 01.06.2022
- Tage bis Beginn
- 181,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
I got covid on March 31st, 2022, tested positive on June 1st.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- June 1st home test
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hand inflammation
- Andere Medikamente
- Women's multivitamin
- Allergien
- Xithromax, gluten
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 26.05.2022
- Impfdatum
- 25.05.2022
- Beginn
- 25.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Janssen COVID-19 Vaccine EUA Vaccine was inadvertently given to unauthorized age group (ages 12-17). Patient Guardian was notified of error once realized. No ADR at time of Vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 26.05.2022
- Impfdatum
- 25.05.2022
- Beginn
- 25.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Janssen COVID-19 Vaccine EUA Vaccine was inadvertently given to unauthorized age group (ages 12-17). Patient Guardian was notified of error once realized. No ADR at time of Vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- -
- Geschlecht
- M
- Eingang
- 25.05.2022
- Impfdatum
- -
- Beginn
- 09.05.2022
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Eye discharge
Hypersensitivity
Symptomtext
GREEN OUT OF MY EYES; ALLERGY; This spontaneous report received from a patient concerned a 50 year old male. The patient's height, and weight were not reported. The patient's concurrent conditions included: blurry eyes, and pollen allergy. The patient previously received with covid-19 vaccine ad26.cov2.s (dose number in series 1) (suspension for injection, route of admin not reported, batch number: 04A21A, expiry: UNKNOWN) dose was not reported, 1 in total, administered on 02-APR-2021 for prophylactic vaccination. It was unknown whether patient had any adverse events following vaccination with first dose of covid-19 vaccine ad26.cov2.s (dose number in series 1). The patient received additional dose of covid-19 vaccine ad26.cov2.s (dose number in series 2) (suspension for injection, route of admin not reported, batch number: 213D21A, and expiry: UNKNOWN) dose was not reported, 1 in total, administered on 02-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. On 09-MAY-2022, following vaccination with covid-19 vaccine ad26.cov2.s, the patient experienced allergy (dose number in series 2) which lasted for one day but would still follow up with his doctor to make sure it was an actual allergy. On an unspecified date, the patient experienced green out of his eyes (dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from allergy on 10-MAY-2022, and the outcome of green out of my eyes was not reported. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Eye discharge
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Blurring of eyes; Pollen allergy
- Vorgeschichte
- Comments: Unknown
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- -
- Geschlecht
- M
- Eingang
- 19.05.2022
- Impfdatum
- -
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acoustic stimulation tests
Tinnitus
Symptomtext
TINNITUS OR EAR RINGING; This spontaneous report received from a patient concerned a male of unspecified age. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: the patient never had hearing problems. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, and batch number: 213D21A expiry: UNKNOWN) dose was not reported, administered on NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On JAN-2022, the patient experienced tinnitus or ear ringing. Laboratory data (dates unspecified) included: Hearing test (NR: not provided) hearing was fine, and Hearing test (NR: not provided) hearing was fine. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from tinnitus or ear ringing. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acoustic stimulation tests
- Hospital-Tage
- -
- Labordaten
- Test Name: Hearing test; Result Unstructured Data: hearing was fine; Test Name: Hearing test; Result Unstructured Data: hearing was fine
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: the patient never had hearing problems.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- -
- Geschlecht
- M
- Eingang
- 19.05.2022
- Impfdatum
- -
- Beginn
- 26.04.2022
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Body temperature
Suspected COVID-19
Vaccination failure
Symptomtext
This spontaneous report received from a patient via a company representative via other company (Pfizer, Inc) concerned a 32 year old male of an unspecified race and ethnicity. Initial information was processed along with the additional information received on 16-MAY-2022. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: The patient had no medical conditions. On an unspecified date, the patient previously received Covid-19 vaccine ad26.cov2.s (unspecified manufacturer) (suspension for injection, route of admin, and batch number and expiry date were not reported) dose was not reported, (Dose number in series 1), 1 total administered for prophylactic vaccination. It was unknown whether patient had any adverse events following vaccination (Dose number in series 1). The patient received Covid-19 vaccine ad26.cov2.s (Dose number in series 2), (suspension for injection, route of admin, batch number: 213D21A and expiry date was not reported) dose, start therapy date were not reported, 1 total administered for prophylactic vaccination. No concomitant medications were reported. On 26-APR-2022, the patient experienced suspected Covid-19 infection (suspected clinical vaccination failure), (Dose number in series 2), and had a fever of 102 degree F. constant with symptoms progressing to the chest area and throat. He was prescribed with Paxlovid 3 days later and the next day on 30-APR-2022, the symptoms seemingly dissolved within 24 hours after taking the Paxlovid. Laboratory data included: Body temperature (NR: not provided) 102 F. The action taken with Covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from suspected Covid-19 infection on 30-APR-2022, and the outcome of suspected clinical vaccination failure was not reported. This report was serious (Other Medically Important Condition). This report was associated with a product quality complaint: 90000230988. Sender's Comments: V0-20220526805-Covid-19 vaccine ad26.CoV-2.s-Suspected clinical vaccination failure. The event(s) has an unknown/unclear temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: SPECIAL SITUATIONS. Therefore, this event(s) is considered not related.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Body temperature
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220426; Test Name: Body temperature; Result Unstructured Data: 102 F, constant.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: The patient had no medical conditions.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 10.05.2022
- Impfdatum
- 01.04.2022
- Beginn
- 02.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Feeling of body temperature change
Tenderness
Symptomtext
Narrative: "I have a intense burning sensation from my elbow to just before my underarm daily, also there is feeling of a cold and hot drip under my skin. This are is very tender and feels raw. Symptoms started one or two days after injection."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Burning sensation
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 87,0
- Geschlecht
- F
- Eingang
- 10.05.2022
- Impfdatum
- 15.12.2021
- Beginn
- 10.05.2022
- Tage bis Beginn
- 146,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Symptomtext
COVID-19 hospitalization; requiring increase in baseline O2
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 04.05.2022
- Impfdatum
- 02.05.2022
- Beginn
- 02.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product administered to patient of inappropriate age
Symptomtext
Jannsen vaccine was requested by mother for her daughter age 15. Pharmacy student did not verify patient age and administered vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 03.05.2022
- Impfdatum
- -
- Beginn
- 31.01.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Off label use
Product use issue
Symptomtext
ADMINISTERED TO A 14 YEARS OLD; OFF LABEL USE; This spontaneous report received from a health care professional concerned a 14 year old male. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: The patient had no known drug allergies. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 213D21A, and expiry: UNKNOWN) dose was not reported, administered on 31-JAN-2022 for prophylactic vaccination. Age at time of vaccination 14 years old. No concomitant medications were reported. On 31-JAN-2022, the patient experienced administered to a 14 years old, and off label use. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the administered to a 14 years old and off label use was not reported. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Off label use
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: The patient had no known drug allergies.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 02.05.2022
- Impfdatum
- 31.01.2022
- Beginn
- 31.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
Vaccine given on 01/31/22. Appointment made through agency who provided translation assistance at that vaccine clinic. Called agency on 04/29/2022 at 11:52a. Agency reports that he was a walk-in that day requesting J&J. Stated that they didn?t have a DOB on file for him. He is not a regular client of agency, and they were not familiar with this client. Stated that they would call the patient for translation assistance and to determine his age. Agency called and visited the residence on 4/29/22 and was told that he was not living at that address. On 4/30, Agency continued to try to call and text the client. On 5/01/2022, Agency was able to reach the patient by phone, who stated he did not know that he could not get J&J under 18 years old. He stated that he felt fine after the receiving the vaccine and that he has felt fine since then. Discussed with RN that provided the vaccine on 01/31/2022 and states that she cannot recall this incident or this patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- None - patient states he felt fine after receiving the vaccine and has felt fine since then.
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- None noted
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- -
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Sensory loss
Symptomtext
LOOSES FEELING IN RIGHT ARM FROM ELBOW TO WRIST; This spontaneous report received from a patient concerned a 44 year old male. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, and batch number: 213D21A expiry: 08-SEP-2022) dose was not reported, administered on 29-DEC-2021 for prophylactic vaccination. Age at time of vaccination 44 years old. No concomitant medications were reported. On JAN-2022, the patient experienced looses feeling in right arm from elbow to wrist. Treatment medications (dates unspecified) included: paracetamol. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from looses feeling in right arm from elbow to wrist. This report was non-serious.; Sender's Comments: Medical assessment comments not required as per standard procedure as the case is considered non serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Sensory loss
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 16.04.2022
- Impfdatum
- -
- Beginn
- 28.12.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Poor quality product administered
Product storage error
Symptomtext
VACCINE WAS NOT STORED PROPERLY; POOR QUALITY VACCINE ADMINISTERED; This spontaneous report received from a physician concerned a patient of unspecified age and sex. Initial information was processed along with the additional information received on 12-APR-2022. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 213D21A, expiry: unknown) dose was not reported, administered on 28-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. On 28-DEC-2021, the patient experienced poor quality vaccine administered. On an unspecified date, the patient experienced vaccine was not stored properly. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the vaccine was not stored properly and poor quality vaccine administered was not reported. This report was non-serious. This report was associated with product quality complaint: 90000225546. The suspected product quality complaint has been confirmed to be voided. Product was stored frozen until 19-NOV-2021 (when product was received) and then was not properly stored after that. On 07-APR-2022, the shelf life for the vaccine has been extended from 9 months to 11 months refrigerated (stored at 2-8 degree C). It is not clear how the product was stored after it was received. There is no product quality issue described in the information reported as the product was not within Janssen custody during this potential temperature excursion. Based on the evaluation/investigation performed. This case, from the same reporter is linked to 20220421157.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Poor quality product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 16.04.2022
- Impfdatum
- -
- Beginn
- 04.12.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Poor quality product administered
Product storage error
Symptomtext
PRODUCT STORAGE ERROR; THE VACCINE WAS STORE FROZEN UNTIL RECEIVED SINCE 19-NOV-2021; This spontaneous report received from a physician concerned multiple patients. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 213D21A expiry: UNKNOWN) dose was not reported, administered on 04-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. On 04-DEC-2021, the patient experienced the vaccine was store frozen until received since 19-nov-2021. On an unspecified date, the patient experienced product storage error. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the product storage error and the vaccine was store frozen until received since 19-nov-2021 was not reported. This report was non-serious. This case, from the same reporter is linked to 20220421741. This report was associated with product quality complaint: 90000225540.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Poor quality product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 30.03.2022
- Impfdatum
- 26.11.2021
- Beginn
- 26.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Patient received the Janssen COVID vaccination at age 17 years, 11 months. Patient should not have received the vaccination until he was 18 years of age. He reported no adverse reaction to the Janssen COVID vaccination. VAERS report has been completed because the patient was not yet 18 years of age when he received the vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- None required
- Aktuelle Erkrankungen
- Patient reports no adverse reaction to the Janssen COVID vaccination. VAERS report was completed as patient was under the age of 18 when he received the Janssen COVID vaccination.
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- M
- Eingang
- 29.03.2022
- Impfdatum
- 29.11.2021
- Beginn
- 29.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Acoustic stimulation tests
Foetal exposure during pregnancy
Pyloric stenosis
Symptomtext
This solicited pregnancy report received from a consumer concerned a male neonate of unspecified age, race and ethnic origin. The patient's mother was enrolled in a non-company sponsored study C-VIPER: COVID 19 Vaccines International Pregnancy Exposure Registry number: "PRIVATE"). The patient's weight was 3.44 kilograms, and height was 54 centimeters. No birth defects, genetic or inherited disorders have been diagnosed since birth. The mother had no relevant medical history. Concomitant medications included prenatal vitamins, levothyroxine, vitamin D and Select-OB Plus DHA Prenatal Supplement Plus DHA. Maternal obstetrical history included one previous pregnancy, resulting in a miscarriage. The mother had no history of tobacco or recreational drug use, however reported alcohol use during the first three months of current pregnancy. Maternal first day of the last menstrual period (LMP) was calculated to be 23-Apr-2021. The estimated delivery date (EDD) was reported to be 28-Jan-2022. Type of pregnancy was reported as singleton. The patient's mother previously received two doses of Comirnaty (Pfizer BioNTech Covid-19 vaccine) (dose number in series 1) (form of admin, route of admin, and batch number: ER8737 and ER8735, expiry: unknown) dose was not reported, 1 total administered on 03-APR-2021 and 24-APR-2021 for Covid-19 immunisation. At gestational age 31 weeks and three days, The patient's mother received Covid-19 vaccine ad26.cov2.s (dose number in series 2) (suspension for injection, route of admin not reported, batch number: 213D21A, expiry: unknown) dose was not reported, 1 total administered on 29-NOV-2021 for Covid-19 immunization. Maternal concomitant medications included calcium carbonate/colecalciferol for drug used for unknown indication, fish oil for drug used for unknown indication, levothyroxine sodium for drug used for unknown indication, and minerals NOS/vitamins NOS for drug used for unknown indication. On 29-NOV-2021, the patient experienced fetal exposure during pregnancy. On FEB-2022, Laboratory data included: Hearing test (NR: not provided) Not reported. at gestational age 41 weeks and one day, the mother delivered vaginally a live, full-term, male neonate. The mother spent two days in the hospital for the delivery. The neonate's birth weight was 3440 grams, body length 54 cm. On an unspecified date, the patient experienced pyloric stenosis (dose number in series 2). On 05-Mar-2022, the baby was hospitalized due to pyloric stenosis. On 06-Mar-2022, the baby underwent surgery for pyloric stenosis. At the time of the initial report on 14-Mar-2022, baby's weight was 4200 grams, body length 58 cm. The action taken with Covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from fetal exposure during pregnancy on 05-FEB-2022, and the outcome of pyloric stenosis was not reported. The reporter considered the causality between Covid-19 vaccine ad26.cov2.s, and pyloric stenosis as unassessable. The reporter did not provide a causality assessment between Covid-19 vaccine ad26.cov2.s, and fetal exposure during pregnancy. Company causality between Covid-19 vaccine ad26.cov2.s, and pyloric stenosis was related, and between Covid-19 vaccine ad26.cov2.s, and fetal exposure during pregnancy was not related. This report was serious (Hospitalization Caused / Prolonged, Congenital Anomaly/Birth Defect, and Other Medically Important Condition). This parent/child case is linked to 20220118594. Sender's Comments: V0: 20220350441-Covid-19 vaccine ad26.cov2.s-Pyloric stenosis. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s). Therefore, this event(s) is considered related. 20220350441-Covid-19 vaccine ad26.cov2.s-fetal exposure during pregnancy. The event(s) 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(s) than the drug. Specifically: SPECIAL SITUATIONS. Therefore, this event(s) is considered not related.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acoustic stimulation tests
- Hospital-Tage
- -
- Labordaten
- Test Date: 202202; Test Name: Hearing test; Result Unstructured Data: Not reported.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: No birth defects, genetic or inherited disorders had been diagnosed since birth.
- Andere Medikamente
- Vitamin D 2000; DHA For Pregnancy & Breastfeeding; Levothyroxine Sodium
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- -
- Geschlecht
- U
- Eingang
- 25.03.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Poor quality product administered
Product storage error
Symptomtext
OUT OF SPECIFICATION PRODUCT USE; 10 VIALS UNDERWENT A SHORT TEMPERATURE EXCURSION LASTING FOR 3 MINUTES EXCEEDING IN 0.74 F THE MANUFACTURER'S UPPER RECOMMENDED LIMIT; This spontaneous report received from a pharmacist concerned a patient of unspecified age and sex. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 213D21A expiry: 10-JUL-2022) dose, start therapy date were not reported for prophylactic vaccination. No concomitant medications were reported. On an unspecified date, the patient experienced out of specification product use, and 10 vials underwent a short temperature excursion lasting for 3 minutes exceeding in 0.74 f the manufacturer's upper recommended limit. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the out of specification product use and 10 vials underwent a short temperature excursion lasting for 3 minutes exceeding in 0.74 f the manufacturer's upper recommended limit was not reported. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Poor quality product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 23.03.2022
- Impfdatum
- 25.02.2022
- Beginn
- 23.03.2022
- Tage bis Beginn
- 26,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Interchange of vaccine products
Retching
Symptomtext
Patient came in to receive 2nd Moderna vaccine. Was given Janssen 0.5ml instead. Patient says he has been having dry heaves.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Not known
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 18.03.2022
- Impfdatum
- 08.12.2021
- Beginn
- 08.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product administered to patient of inappropriate age
Symptomtext
GIVEN TO SOMEONE UNDER 18
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 85,0
- Geschlecht
- M
- Eingang
- 17.03.2022
- Impfdatum
- 09.03.2021
- Beginn
- 02.03.2022
- Tage bis Beginn
- 358,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Hyponatraemia
Symptomtext
Hospitalization for hyponatremia, COVID. Treated with dexamethasone, vitamin C 1,000 mg PO daily, vitamin D 25 mcg PO daily, zinc 50 mg PO daily.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 16.03.2022
- Impfdatum
- 06.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 5,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anion gap
Blister
Blood calcium normal
Blood chloride normal
Blood creatinine normal
Blood glucose normal
Blood potassium normal
Blood sodium decreased
Blood urea normal
Carbon dioxide normal
Full blood count
Glomerular filtration rate normal
Haematocrit decreased
Haemoglobin decreased
Mean cell haemoglobin concentration normal
Mean cell haemoglobin normal
Mean cell volume normal
Metabolic function test
Symptomtext
foot blister which developed within the week of getting booster. Coming into ER after clinic visit, needing admission and antibiotics
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anion gap
- Hospital-Tage
- -
- Labordaten
- Test Results From Your Hospital Stay Results for orders placed or performed during the hospital encounter of 03/16/22 Foot XR, G/E 3 views, left Impression IMPRESSION: Lateral forefoot soft tissue ulceration. There is no radiographic evidence of adjacent osteomyelitis with attention to the fifth MTP region. No acute fracture. CBC with platelets Result Value Ref Range WBC Count 15.4 (H) 4.0 - 11.0 10e3/uL RBC Count 3.91 3.80 - 5.20 10e6/uL Hemoglobin 11.5 (L) 11.7 - 15.7 g/dL Hematocrit 33.6 (L) 35.0 - 47.0 % MCV 86 78 - 100 fL MCH 29.4 26.5 - 33.0 pg MCHC 34.2 31.5 - 36.5 g/dL RDW 12.5 10.0 - 15.0 % Platelet Count 253 150 - 450 10e3/uL Basic metabolic panel Result Value Ref Range Sodium 134 (L) 136 - 145 mmol/L Potassium 4.0 3.5 - 5.0 mmol/L Chloride 102 98 - 107 mmol/L Carbon Dioxide (CO2) 24 22 - 31 mmol/L Anion Gap 8 5 - 18 mmol/L Urea Nitrogen 12 8 - 22 mg/dL Creatinine 0.71 0.60 - 1.10 mg/dL Calcium 9.5 8.5 - 10.5 mg/dL Glucose 176 (H) 70 - 125 mg/dL GFR Estimate >90 >60 mL/min/1.73m2
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- DM
- Andere Medikamente
- blood-glucose meter Add as: unknown Dispense meter, test strips, lancets covered by pt ins. NIDDM type II, uncontrolled - Test 1 time/day 7/30/2021 7/30/2021 flash glucose sensor (FreeStyle Libre 14 Day Sensor) kit
- Allergien
- Allergies Bees Not Specified 6/15/2012 Cephalexin Other (See Comments) Not Specified Side Effect 2/22/2008 bloody nose and sever pressure in head left side Tolerated cefuroxime 5/16 Corn-related Products
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 13.03.2022
- Impfdatum
- 19.11.2021
- Beginn
- 19.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Symptomtext
Patient came in on 11/19/2021 new to the pharmacy. He gave 6/28/2002 as his DOB, and asked for the Janssen COVID-19 vaccine. On his patient questionnaire, he also wrote 6/28/2002 as his DOB, making him 19 years old. Right before vaccination patient verified DOB. He was vaccinated. 5 days later, he called and asked to change his DOB to 6/28/2005 (making him 16 years old). Janssen is not indicated for a 16-year-old. I called him, but he hasn't returned my messages.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- DE
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 10.03.2022
- Impfdatum
- 20.12.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 12,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Amenorrhoea
Symptomtext
Have not had a menstral cycle since getting the vaccine and prior to vaccine I have always been regular.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Amenorrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/a
- Vorgeschichte
- N/a
- Andere Medikamente
- N/a
- Allergien
- N/a
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 09.03.2022
- Impfdatum
- 09.03.2022
- Beginn
- 09.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Interchange of vaccine products
Symptomtext
PATIENT CAME TO PHARMACY STATING THEY NEEDED THEIR FIRST DOSE OF COVID VACCINE AND WANTED TO RECEIVE JANSSEN VACCINE. PATIENT WAS GIVEN THIS VACCINE, BUT LATER IT WAS REALIZED WHEN INSURANCE WAS CONTACTED FOR A BILLING ISSUE THAT THE PATIENT HAD ALREADY RECEIVED A MODERNA VACCINE ON 2/14/22. THIS INFORMATION WAS NOT RECORDED IN THE IMMUNIZATION INFORMATION SYSTEM. PATIENT WAS THEN CONTACTED TO VERIFU\Y THAT THE PATIENT DID RECEIVE THIS VACCINE. THE PATIENT CONFIRMED RECEIPT OF THIS VACCINE AND STATED THAT SHE WAS TRAVELLING AND WAS INFORMED BY A TRAVEL AGENT THAT IN ORDER TO BE FULLY VACCINATED IN TIME FOR TRAVEL THAT SHE SHOULD RECEIVE THE JANSSEN VACCINE SO SHE DID NOT INFORM THE PHARMACY THAT SHE ALREADY RECEIVED A DOSE OF VACCINE. I CALLED THE PHARMACY WHERE SHE RECEIVED THE VACCINE TO INFORM THEM THAT THE RECORD WAS NOT SHOWING IN THE IMMUNIZATION INFORMATION SYSTEM.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 04.03.2022
- Impfdatum
- 30.11.2021
- Beginn
- 30.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product administered to patient of inappropriate age
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- -
- Geschlecht
- F
- Eingang
- 26.02.2022
- Impfdatum
- -
- Beginn
- 16.01.2022
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood test
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
CONFIRMED CLINICAL VACCINATION FAILURE; CONFIRMED COVID-19 INFECTION; This spontaneous report received from a patient concerned a 61 year old of unknown race female. The patient's height, and weight were not reported. The patient's concurrent conditions included: immunocompromised. The patient was previously treated with covid-19 vaccine (dose number in series 1) (suspension for injection, route of admin not reported, batch number: 1805022, and expiry: 23-AUG-2021) dose was not reported, 1 total administered at right arm on 11-MAR-2021 for prophylactic vaccination. It was unknown if patient experienced any adverse events following vaccination with covid-19 vaccine (dose number in series 1). It was reported that be on an unspecified date between her dose number in series 1 and dose number in series 2, the patient's doctor drew her blood and it was normal. The patient received covid-19 vaccine (dose number in series 2)(suspension for injection, route of admin not reported, batch number: 213D21A, and expiry: 11-APR-2022) dose was not reported, 1 total, administered at right arm on 29-NOV-2021 for prophylactic vaccination. Concomitant medications included tofacitinib citrate (Xeljanz 5mg twice). On 16-JAN-2022, the patient reported that after receiving booster dose she developed covid which was confirmed by rapid and PCR (polymerase chain reaction) test. On 16-JAN-2022, the patient tested positive by rapid test at home (confirmed covid-19 infection). On 19-JAN-2022, the patient tested positive by PCR test (confirmed clinical vaccination failure) (all events with dose number in series 2). On 22-JAN-2022, Laboratory data included: COVID-19 virus test (NR: not provided) Positive. On 26-JAN-2022, Laboratory data included: COVID-19 virus test (NR: not provided) Negative. The action taken with covid-19 vaccine was not applicable. The patient recovered from confirmed covid-19 infection, and the outcome of confirmed clinical vaccination failure was not reported. This report was serious (Other Medically Important Condition). This report was associated with product quality complaint.; Sender's Comments: V0:20220250779-COVID-19 VACCINE -confirmed clinical vaccination failure. The event(s) 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(s) than the drug. Specifically: SPECIAL SITUATIONS. Therefore, this event(s) is considered not related.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood test
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220116; Test Name: COVID-19 virus test; Result Unstructured Data: Positive; Test Date: 20220119; Test Name: COVID-19 PCR test; Result Unstructured Data: Positive; Test Date: 20220122; Test Name: COVID-19 virus test; Result Unstructured Data: Positive; Test Date: 20220126; Test Name: COVID-19 virus test; Result Unstructured Data: Negative; Test Name: Blood test; Result Unstructured Data: Normal
- Aktuelle Erkrankungen
- Immunocompromised
- Vorgeschichte
- Comments: Unknown
- Andere Medikamente
- XELJANZ
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 18.02.2022
- Impfdatum
- -
- Beginn
- 10.02.2022
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
CONFIRMED CLINICAL VACCINATION FAILURE; CONFIRMED COVID-19 INFECTION; This spontaneous report received from a patient concerned a 60 year old female of unspecified race and ethnic origin. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient was previously treated with MRNA 1273 (Dose Number in Series 1) (Moderna vaccine, route of administration, dose, batch number 039B21A,expiry 02-OCT-2021 (first shot) and received the second dose on 12-MAY-2021 (batch number 022C21A, expiry 23-DEC-2021 (second shot). The patient had a reaction to both the shots.(dose number in series 1). The patient received covid-19 vaccine ad26.cov2.s (Dose number in series 2)(suspension for injection, intramuscular, batch number:213D21A, expiry: UNKNOWN) dose not reported, 1 total administered on 15-DEC-2021 to the left arm for prophylactic vaccination. No concomitant medications were reported. On 10-FEB-2022, the patient experienced confirmed clinical vaccination failure, and confirmed covid-19 infection. (Dose number in series 2). The patient did two rapid tests at home, one was negative and one was positive. As per the advice of her doctor she got tested again at the county testing site on 10-FEB-2022 for a Covid test, and they contacted her back with a positive test result. They had done a rapid test and a PCR (polymerase chain reaction) test. The patient did not specify any symptoms but reported that she does not have a fever. The patient also enquired if there was a problem with asthma and the Janssen booster. Laboratory data included: On 10-FEB-2022, COVID-19 PCR (polymerase chain reaction) test (NR: not provided) positive, and COVID-19 rapid POC test (NR: not provided) positive. Laboratory data (dates unspecified) included: COVID-19 rapid POC test (NR: not provided) positive, negative. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the confirmed clinical vaccination failure and confirmed covid-19 infection was not reported. This report was serious (Other Medically Important Condition). This report is associated with a product quality complaint number 90000217187.; Sender's Comments: V0:20220230227-COVID-19 VACCINE AD26.COV2.S-Confirmed clinical vaccination failure. The event(s) 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(s) than the drug. Specifically: SPECIAL SITUATIONS. Therefore, this event(s) is considered not related.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220210; Test Name: COVID-19 rapid POC test; Result Unstructured Data: positive; Test Date: 20220210; Test Name: COVID-19 PCR test; Result Unstructured Data: positive; Test Name: COVID-19 rapid POC test; Result Unstructured Data: positive; Test Name: COVID-19 rapid POC test; Result Unstructured Data: negative
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 14.02.2022
- Impfdatum
- 04.02.2022
- Beginn
- 10.02.2022
- Tage bis Beginn
- 6,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Vision blurred
Symptomtext
Symptoms of blurred vision at longer distances. I wear no prescription glasses. I have never had eye issues all through my life. I have been recorded to have 20/20 vision all through my life. Starting on the date documented. I began having slightly blurred vision at far distances. This has not been a usual occurrence for me all my life. This symptom has started approximately 1 week after a vaccine injection. I have yet to receive medical attention. It is not life threatening at the moment. However it is quite alarming and brought on suddenly.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vision blurred
- Hospital-Tage
- -
- Labordaten
- None as of yet.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 12.02.2022
- Impfdatum
- 30.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
ADULT DOSE WAS GIVEN TO PATIENT UNDER 18 YEARS OLD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- N/A
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 11.02.2022
- Impfdatum
- 10.11.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anxiety
Blood folate decreased
Blood test abnormal
Vitamin B12 deficiency
Vitamin D deficiency
Symptomtext
I started feeling more anxious and having anxiety attacks. I don't believe this was related to the vaccine. I have had various health issues starting in February 2021 and I believe it just all caught up with me. The anxiety started and the worsening anxiety attacks started towards the middle of November and got progressively worse from there.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anxiety
- Hospital-Tage
- -
- Labordaten
- Doctor appointment on 12/27/21 and started medication. Follow-up on 2/7/22 with blood work to check b-12, vit d, and folate. Results showed deficiency in all 3 vitamins. Will follow-up in 3 months.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Esophageal spasm, high blood pressure, PCOS, allergies
- Andere Medikamente
- Lisinopril, Zyrtec, birth control, Bentyl, Singular, Nexium
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 09.02.2022
- Impfdatum
- 09.02.2022
- Beginn
- 09.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
Outside age range without any side effects
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 09.02.2022
- Impfdatum
- 29.04.2021
- Beginn
- 22.01.2022
- Tage bis Beginn
- 268,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Event occurred after 2nd vaccine; hospitalized with COVID
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- 1/22/22 COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 09.02.2022
- Impfdatum
- 07.12.2021
- Beginn
- 07.02.2022
- Tage bis Beginn
- 62,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Event occurred after full vaccination. Patient was diagnosed with COVID Remdesivir, Tylenol In-patient
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 2,0
- Labordaten
- Covid test positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Depression, Chronic UTI, AKI
- Andere Medikamente
- -
- Allergien
- Penicillin, Pollen
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- -
- Geschlecht
- M
- Eingang
- 09.02.2022
- Impfdatum
- -
- Beginn
- 20.01.2022
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
SARS-CoV-2 test
SARS-CoV-2 test positive
Symptomtext
COVID-19 TEST POSITIVE; This spontaneous report received from a patient concerned a male, unspecified age and ethnicity. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient previously received covid-19 vaccine ad26.cov2.s (dose number in series 1) (suspension for injection, route of admin not reported, batch number: 1808609, expiry: unknown) dose was not reported, 1 total administered on an 25-MAR-2021 to left arm for prophylactic vaccination. It was unknown if the patient experienced any adverse event after vaccination with covid-19 vaccine ad26.cov2.s (dose number in series 1). The patient received booster covid-19 vaccine ad26.cov2.s (dose number in series 2) (suspension for injection, route of admin not reported, batch number: 213D21A, expiry: unknown) dose was not reported, 1 total administered on 11-NOV-2021 to left arm for prophylactic vaccination. No concomitant medications were reported. On 20-JAN-2022, the patient took rapid PCR (polymerase chain reaction) test and tested positive. On 22-JAN-2022, the patient took regular PCR (polymerase chain reaction) test and tested positive. (Dose number in series 2) The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of covid-19 test positive was not reported. This report was non-serious This report was associated with product quality complaint: 90000215646, 90000215655, 90000215657. The suspected product quality complaint has been confirmed to be voided (did not meet criteria) based on the RA evaluation/investigation performed. This case is a duplicate of 20220204336 and 20220203694.; Sender's Comments: V0: Medical assessment comment not required as per standard procedure since case was assessed as non-serious
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- SARS-CoV-2 test
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220120; Test Name: COVID-19 rapid POC test; Result Unstructured Data: Positive; Test Date: 20220122; Test Name: SARS-CoV-2 PCR test; Result Unstructured Data: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 02.02.2022
- Impfdatum
- 02.02.2022
- Beginn
- 02.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
No adverse event
Symptomtext
Patient came in for a scheduled COVID booster appointment. Upon arrival, he presented his COVID card which showed only one dose on Janssen given 5/29/21. He was then given the vaccine and he left shortly after. Upon running the claim through insurance, it was discovered that the patient has gotten multiple vaccines from different facilities (Pfizer 5/13/21 and 1/11/22; Moderna 10/30/21). The patient was immediately contacted and he confirmed that this was true. He stated that he wanted to get the multiple vaccine based on "research" he found that showed changing the vaccine would be more effect against fight COVID. He was then counseled that the protocol for the vaccine does not allow for multiple vaccines to be given as he had done.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- N/A. Patient had no side effects
- Aktuelle Erkrankungen
- None known at this time.
- Vorgeschichte
- None known at this time.
- Andere Medikamente
- None known at this time.
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 02.02.2022
- Impfdatum
- 08.03.2021
- Beginn
- 03.12.2021
- Tage bis Beginn
- 270,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asthenia
COVID-19
SARS-CoV-2 test positive
Symptomtext
Weakness resulting in hospitalization after testing positive for COVID-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asthenia
- Hospital-Tage
- 5,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Benign essential hypertension Breast cancer Chronic acquired lymphedema Chronic osteoarthritis Colostomy in place Diverticulosis History of malignant neoplasm of right breast Hypertension Hyperuricemia Hypokalemia Lymphedema of both lower extremities Morbid obesity with BMI of 45.0-49.9, adult Pacemaker Peripheral neuropathy Sleep apnea Vitamin D deficiency
- Andere Medikamente
- Vitamin B12, allopurinol
- Allergien
- Codeine, Cipro, Lisinopril
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 02.02.2022
- Impfdatum
- 17.12.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 14,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Alcohol poisoning
Chest X-ray abnormal
Computerised tomogram head abnormal
Computerised tomogram spine
Fall
Mucosal hypertrophy
Sinusitis
Symptomtext
Patient presents to the ED on 12/31/2021 with a Chief Complaint of Alcohol intoxication and Fall after receiving one dose of vaccine on Dec 17. Per guidelines, all hospitalizations are reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Alcohol poisoning
- Hospital-Tage
- 5,0
- Labordaten
- CT CERVICAL SPINE WO CONTRAST Radiologist Impression IMPRESSION: Mucosal thickening and air-fluid levels in the paranasal sinuses, which appear worse compared to the prior CT head dated 8/24/2020. Correlate for sinusitis.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 28.01.2022
- Impfdatum
- 27.01.2022
- Beginn
- 27.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product storage error
Symptomtext
Pt received a dose that was beyond use date of the vial. Vial was stored in the refrigerator and was administered past the expiration. Pt had no adverse event and was recommended to be given another dose without interval based on CDC guidelines.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 27.01.2022
- Impfdatum
- 26.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Photophobia
Vertigo
Symptomtext
patient mentioned she is been going though vertigo effect and light sensitivity
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Photophobia
- Hospital-Tage
- -
- Labordaten
- follow up appt with pcp and physiotherapist
- Aktuelle Erkrankungen
- LYME DISEASE
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 26.01.2022
- Impfdatum
- 30.11.2021
- Beginn
- 12.01.2022
- Tage bis Beginn
- 43,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Exposure to SARS-CoV-2
SARS-CoV-2 test positive
Symptomtext
Covid positive through household contact
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 26.01.2022
- Impfdatum
- 20.11.2021
- Beginn
- 12.01.2022
- Tage bis Beginn
- 53,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Covid positive contact unknown
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 25.01.2022
- Impfdatum
- 25.01.2022
- Beginn
- 25.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Medication error
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Medication ERROR: PT is 16 YO male and was inadvertently given Janssen as a first dose instead of Pfizer. No adverse event was reported. PT will follow up to receive second primary dose of Pfizer/BioNtech COVID-19 vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Medication error
- Hospital-Tage
- -
- Labordaten
- None required
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 24.01.2022
- Impfdatum
- 24.11.2021
- Beginn
- 24.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Menstruation delayed
Symptomtext
Delayed menstrual period, 2 months post vaccination without a menstrual cycle since (normally a 21 day cycle)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Menstruation delayed
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Losartan Atenolol
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 24.01.2022
- Impfdatum
- 30.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Wrong product administered
Symptomtext
Client requested Moderna booster dose but received Janssen 0.25 ml dose in error.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 24.01.2022
- Impfdatum
- 30.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Wrong product administered
Symptomtext
Client requested Moderna booster dose but received Janssen 0.25 ml dose in error.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 24.01.2022
- Impfdatum
- 30.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Interchange of vaccine products
Symptomtext
Client requested Moderna booster dose but received Janssen 0.25 ml dose in error.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 24.01.2022
- Impfdatum
- 30.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Interchange of vaccine products
Symptomtext
Client requested Moderna booster dose but received Janssen 0.25 ml dose in error.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 24.01.2022
- Impfdatum
- 30.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Wrong product administered
Symptomtext
Client requested Moderna booster dose but received Janssen 0.25 ml dose in error.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 24.01.2022
- Impfdatum
- 30.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Wrong product administered
Symptomtext
Client requested Moderna booster but received Janssen 0.25 ml dose in error.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 24.01.2022
- Impfdatum
- 30.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Wrong product administered
Symptomtext
Client requested Moderna booster dose but received Janssen 0.25 ml dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 24.01.2022
- Impfdatum
- 02.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 10,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Computerised tomogram normal
Oedema
Peripheral swelling
X-ray normal
Symptomtext
left leg and foot swelling and edema for several days, still persisting, never happened before. presumed blood clot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Computerised tomogram normal
- Hospital-Tage
- 1,0
- Labordaten
- x-ray shows no fractures, clot not found on ct
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 47,0
- Geschlecht
- M
- Eingang
- 19.01.2022
- Impfdatum
- 06.12.2021
- Beginn
- 06.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Musculoskeletal discomfort
Symptomtext
Patient states that he has had shoulder problems ever since his vaccine was injected in December.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Musculoskeletal discomfort
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- -
- Beginn
- 09.01.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Poor quality product administered
Product storage error
Symptomtext
ADMINISTRATION OF VACCINE WHICH WAS STORED OUTSIDE OF THE ACCEPTABLE LIMITS; ADMINISTRATION ERROR/INCORRECTLY STORED VACCINE ADMINISTERED; This spontaneous report received from a physician concerned a 57 year old female. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 213D21A, and expiry: 11-APR-2022) dose was not reported, administered on 09-JAN-2022 14:09 for prophylactic vaccination. No concomitant medications were reported. On 09-JAN-2022, the patient experienced administration error/incorrectly stored vaccine administered. On an unspecified date, the patient experienced administration of vaccine which was stored outside of the acceptable limits. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the administration error/incorrectly stored vaccine administered and administration of vaccine which was stored outside of the acceptable limits was not reported. This report was non-serious. This case, from the same reporter is linked to 20220123990 and 20220124443.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- -
- Beginn
- 09.01.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Poor quality product administered
Product storage error
Symptomtext
ADMINISTRATION OF VACCINE WHICH WAS STORED OUTSIDE OF THE ACCEPTABLE LIMITS; ADMINISTRATION ERROR/INCORRECTLY STORED VACCINE ADMINISTERED; This spontaneous report received from a physician concerned a 57 year old female. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 213D21A, and expiry: 11-APR-2022) dose was not reported, administered on 09-JAN-2022 14:09 for prophylactic vaccination. No concomitant medications were reported. On 09-JAN-2022, the patient experienced administration error/incorrectly stored vaccine administered. On an unspecified date, the patient experienced administration of vaccine which was stored outside of the acceptable limits. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the administration error/incorrectly stored vaccine administered and administration of vaccine which was stored outside of the acceptable limits was not reported. This report was non-serious. This case, from the same reporter is linked to 20220123990 and 20220124443.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -