- Staat
- -
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 18.08.2023
- Impfdatum
- 05.11.2021
- Beginn
- 19.01.2023
- Tage bis Beginn
- 440,0
- 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
- 60,0
- Geschlecht
- F
- Eingang
- 18.08.2023
- Impfdatum
- 12.11.2021
- Beginn
- 16.11.2021
- Tage bis Beginn
- 4,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Symptomtext
ACUTE RESPIRATORY FAILURE ACUTE HYPOXEMIC RESPIRATORY FAILURE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 17.08.2023
- Impfdatum
- 18.11.2021
- Beginn
- 03.04.2022
- Tage bis Beginn
- 136,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute myocardial infarction
Symptom recurrence
Symptomtext
ACUTE NON ST ELEVATION MI 2/1/2023 -- RECURRENCE OF HOSPITALIZATION WITH SAME SYMPTOMS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 21.02.2023
- Impfdatum
- 11.01.2021
- Beginn
- 01.07.2022
- Tage bis Beginn
- 536,0
- Dosis
- 1
- Route/Site
- - / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Acute kidney injury
COVID-19
Chest pain
Death
Dyspnoea
General physical health deterioration
Intensive care
SARS-CoV-2 test positive
Symptomtext
pt admitted to hospital with CP and SOB on 7/31/22; found to be positive for COVID; AKI; pt's demand for O2 increased and on 8/16/22 he was transferred to ICU; pt's condition continued to decline and the family transitioned him to comfort focused care; he passed away in the hospital
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- 36,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- CKD, CHF, CAD, DM HLD, HTN
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 08.06.2022
- Impfdatum
- 26.11.2021
- Beginn
- 03.01.2022
- Tage bis Beginn
- 38,0
- Dosis
- 1
- Route/Site
- SYR / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Acute respiratory failure
COVID-19 pneumonia
Cardio-respiratory arrest
Death
Unresponsive to stimuli
Symptomtext
Patient arrived to ER via EMS d/t being found unresponsive. Patient admitted to hospital for comfort measures. Diagnosed with cardiopulmonary arrest, Covid-19 PNA, acute hypoxic respiratory failure. Patient expired on 01/13/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 03.04.2022
- Impfdatum
- 04.12.2021
- Beginn
- 15.02.2022
- Tage bis Beginn
- 73,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Anticoagulant therapy
Asthenia
Chest pain
Computerised tomogram thorax abnormal
Deep vein thrombosis
Dizziness
Dyspnoea
Nasal congestion
Palpitations
Paraesthesia
Pulmonary embolism
Right ventricular dysfunction
Tachycardia
Ultrasound Doppler abnormal
Symptomtext
Narrative: 68-year-old male with PMH of Bilateral knee pain, Sensory hearing loss, Gastroesophageal reflux disease, History of gastrointestinal bleed, and Elevated blood-pressure reading without diagnosis of hypertension who presented to ED for chest pain. Approximately 1 hour prior to arrival, patient was walking down the stairs when he began feeling lightheadedness with a racing heart beat and palpitations. Palpitations were associated with moderate left-sided chest pain that did not radiate as well as difficulty taking a full inspiration. In addition, he described feeling generalized weakness with tingling of his right hand. These symptoms lasted approximately 5-10 minutes at their worst and subsequently started to improve. He does state that he has had nasal congestion over the past 4 days however denies fever or cough and states he has been in his normal health up until today. No history of anticoagulation, DVT, PE. When EMS arrived, patient was mildly tachycardic however able to ambulate and communicate in full. He is not hypotensive or hypoxic. Diagnosed with extensive PE and right RLE DVT. Treated with IV heparin, transitioned to oral apixaban.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary embolism
- Hospital-Tage
- -
- Labordaten
- 2/15/22: CT thorax Extensive pulmonary embolism to all lung lobes. Findings suggestive of right heart strain. No pulmonary infarcts. 2/16/22: Duplex extremities Right femoral vein near occlusive DVT. No findings of DVT in the left lower extremity.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 21.03.2022
- Impfdatum
- 20.11.2021
- Beginn
- 02.01.2022
- Tage bis Beginn
- 43,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Angioplasty
Anticoagulant therapy
Aortic thrombosis
Deep vein thrombosis
Fibrin D dimer decreased
Fibrin D dimer increased
Heparin-induced thrombocytopenia test
Heparin-induced thrombocytopenia test positive
Iliac artery stenosis
Immunoglobulin therapy
Pain in extremity
Peripheral artery occlusion
Platelet count decreased
Pulmonary embolism
Renal infarct
Thrombectomy
Thrombocytopenia
Thrombosis
Symptomtext
Narrative: 61 y/o male presented to ER on 1/2/22. Received the COVID-19 (JANSSEN), VECTOR-NR, RS* vaccine on 11/30/21 and presented to the ED on 1/2/22 with worsening LLE pain. CTA revealed pulmonary emboli, extensive aortic thrombus, L renal infarct, common iliac stenosis, CFA/SFA/profunda occlusion on the left. LE duplex 1/4 with multiple b/l DVTs. Patient also had a new thrombocytopenia with PLTs of 61 and D-dimer of 13.62. Hem/Onc was consulted and patient was transitioned from a heparin drip to an argatroban drip and received 2 doses of IVIG for possible Thrombosis with Thrombocytopenia Syndrome (TTS) related to the COVID-19 vaccine. He underwent thrombectomy of left iliac, CFA, SFA, profunda and patch angioplasty on 1/14/22 HIT panel has resulted and is positive and patient appears to meet the 5 criteria for definitive diagnosis of TTS. Definitive Diagnosis (must meet all five criteria) per Hematology: - COVID vaccine 4 to 42 days prior to symptom onset - Any venous or arterial thrombosis (often cerebral or abdominal) - Thrombocytopenia (platelet count < 150 x 109/L) - Positive PF4 "HIT" (heparin- induced thrombocytopenia) ELISA - Markedly elevated D-dimer (> 4 times upper limit of normal) Discharged on 1/19/22 on apixaban. PMH includes HTN, GERD, depression, RLS, and lung nodules
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary embolism
- Hospital-Tage
- -
- Labordaten
- Platelets: 1/2/22 61 1/3/22 58 1/4/22 59 1/5/22 90 1/6/22 154 1/7/22 207 1/8/22 232 1/9/22 266
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 04.03.2022
- Impfdatum
- 29.11.2021
- Beginn
- 02.02.2022
- Tage bis Beginn
- 65,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: ja
ER: unbekannt
Erholt: nein
Blood creatine phosphokinase increased
Brain oedema
Cerebral artery thrombosis
Cerebral infarction
Decompressive craniectomy
Cerebrovascular accident
Impaired work ability
Intensive care
Laboratory test
Loss of consciousness
Microcytic anaemia
Packed red blood cell transfusion
Malaise
Symptomtext
She got her vaccine shew as fine. On 2/2/22 she got sick, she didn't go to work and the sent the police to her apartment and found out that she had passed out and was transported to the hospital where they determined that she had a stroke. She still continues to be in the hospital in ICU. She is improving little by little.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- 30,0
- Labordaten
- Multiple while in the hospital.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- None.
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- -
- Geschlecht
- M
- Eingang
- 14.02.2022
- Impfdatum
- -
- Beginn
- 30.12.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anticoagulant therapy
Chest pain
Computerised tomogram thorax abnormal
Dyspnoea
Fibrin D dimer
Computerised tomogram
Cyanosis
Dizziness
Oxygen saturation
Paraesthesia
Pulmonary embolism
Skin exfoliation
Thrombosis
Ultrasound scan
Pulmonary thrombosis
Symptomtext
FEELING LIKE GOING TO PASS OUT; DIZZINESS; TINGLING; SKIN STARTED COMING OFF; HANDS AND FEET BLUISH; PULMONARY EMBOLISM; BLOOD CLOTS IN LEFT KNEE AND LEFT LEG; This spontaneous report received from a patient concerned a 50 year old male of unspecified ethnicity. 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: 211D21A, expiry: UNKNOWN) dose was not reported, administered 1 in total to the left arm on 27-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. On 30-DEC-2021, the patient experienced chest pain. On 06-JAN-2022, patient experienced his hands and feet become bluish and skin started coming off. On 17-JAN-2022, patient visited his primary doctor and found out he has high D-dimer and later found out patient has blood clots in lower left lung (pulmonary embolism). CT scans, sonogram and ultrasound in legs and arms showed blood clots in knee and left leg. On an unspecified date, patient experienced dizziness and when patient has dizziness his oxygen level falls below 90-92 and pulse goes up as the patient monitors and measures them himself. patient also experience of tingling and feeling like he will pass out. Treatment medications included: acetylsalicylic acid for chest pain. On JAN-2022, treatment medications included: apixaban for pulmonary embolism and blood clots in knee and left leg. On 17-JAN-2022, Laboratory data included: CT scan (NR: not provided) blood clots, Diagnostic ultrasound (NR: not provided) blood clots, Fibrin D dimer (NR: not provided) high, and Sonogram (NR: not provided) blood clots. On FEB-2022, treatment medications included: apixaban. Laboratory data (dates unspecified) included: Oxygen saturation (NR: not provided) below 90-92. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from pulmonary embolism, and blood clots in left knee and left leg, and the outcome of tingling, skin started coming off, feeling like going to pass out, hands and feet bluish and dizziness was not reported. This report was serious (Other Medically Important Condition).; Sender's Comments: V0: 20220221100- covid-19 vaccine ad26.cov2.s-Pulmonary embolism, Blood clots in left knee and left leg. 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
- Pulmonary embolism
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220117; Test Name: Fibrin D dimer; Result Unstructured Data: high; Test Date: 20220117; Test Name: CT scan; Result Unstructured Data: blood clots; Test Date: 20220117; Test Name: Sonogram; Result Unstructured Data: blood clots; Test Date: 20220117; Test Name: Diagnostic ultrasound; Result Unstructured Data: blood clots; Test Name: Oxygen saturation; Result Unstructured Data: below 90-92
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- -
- Geschlecht
- M
- Eingang
- 14.02.2022
- Impfdatum
- -
- Beginn
- 30.12.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anticoagulant therapy
Chest pain
Computerised tomogram thorax abnormal
Dyspnoea
Fibrin D dimer
Computerised tomogram
Cyanosis
Dizziness
Oxygen saturation
Paraesthesia
Pulmonary embolism
Skin exfoliation
Thrombosis
Ultrasound scan
Pulmonary thrombosis
Symptomtext
FEELING LIKE GOING TO PASS OUT; DIZZINESS; TINGLING; SKIN STARTED COMING OFF; HANDS AND FEET BLUISH; PULMONARY EMBOLISM; BLOOD CLOTS IN LEFT KNEE AND LEFT LEG; This spontaneous report received from a patient concerned a 50 year old male of unspecified ethnicity. 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: 211D21A, expiry: UNKNOWN) dose was not reported, administered 1 in total to the left arm on 27-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. On 30-DEC-2021, the patient experienced chest pain. On 06-JAN-2022, patient experienced his hands and feet become bluish and skin started coming off. On 17-JAN-2022, patient visited his primary doctor and found out he has high D-dimer and later found out patient has blood clots in lower left lung (pulmonary embolism). CT scans, sonogram and ultrasound in legs and arms showed blood clots in knee and left leg. On an unspecified date, patient experienced dizziness and when patient has dizziness his oxygen level falls below 90-92 and pulse goes up as the patient monitors and measures them himself. patient also experience of tingling and feeling like he will pass out. Treatment medications included: acetylsalicylic acid for chest pain. On JAN-2022, treatment medications included: apixaban for pulmonary embolism and blood clots in knee and left leg. On 17-JAN-2022, Laboratory data included: CT scan (NR: not provided) blood clots, Diagnostic ultrasound (NR: not provided) blood clots, Fibrin D dimer (NR: not provided) high, and Sonogram (NR: not provided) blood clots. On FEB-2022, treatment medications included: apixaban. Laboratory data (dates unspecified) included: Oxygen saturation (NR: not provided) below 90-92. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from pulmonary embolism, and blood clots in left knee and left leg, and the outcome of tingling, skin started coming off, feeling like going to pass out, hands and feet bluish and dizziness was not reported. This report was serious (Other Medically Important Condition).; Sender's Comments: V0: 20220221100- covid-19 vaccine ad26.cov2.s-Pulmonary embolism, Blood clots in left knee and left leg. 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
- Pulmonary embolism
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220117; Test Name: Fibrin D dimer; Result Unstructured Data: high; Test Date: 20220117; Test Name: CT scan; Result Unstructured Data: blood clots; Test Date: 20220117; Test Name: Sonogram; Result Unstructured Data: blood clots; Test Date: 20220117; Test Name: Diagnostic ultrasound; Result Unstructured Data: blood clots; Test Name: Oxygen saturation; Result Unstructured Data: below 90-92
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 93,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 13.12.2021
- Beginn
- 14.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Cerebrovascular accident
Computerised tomogram abnormal
Dysphagia
Speech disorder
Symptomtext
Narrative: The patient was noted to have impaired speech and difficulty swallowing on the morning of 12/14/21. She was at baseline when she went to bed the evening prior. She was transported to Hospital. A CT scan showed a CVA. The patient was then transported to Medical Center for a higher level of care.
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
- 18.01.2022
- Impfdatum
- 13.12.2021
- Beginn
- 14.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Cerebrovascular accident
Computerised tomogram head abnormal
Drooling
Dysphagia
Fluid intake reduced
Incoherent
Intensive care
Neurological symptom
Symptomtext
Narrative: Patient developed stroke like symptoms 1 day s/p Janssen vaccine 2nd dose administration including incoherent speech, drooling, inability to drink fluids. She was transported to local ER, CT + for stroke and airlifted to trauma level 1 hospital. She currently remains in neuro ICU there.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 16.12.2021
- Impfdatum
- 20.11.2021
- Beginn
- 05.12.2021
- Tage bis Beginn
- 15,0
- Dosis
- 2
- Route/Site
- IM / UN
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Death
Symptomtext
Diagnosed, hospitalized and expired with COVID while fully vaccinated
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- 7,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 17.11.2021
- Impfdatum
- 12.11.2021
- Beginn
- 16.11.2021
- Tage bis Beginn
- 4,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cardiac arrest
Death
Hyperhidrosis
Hypoxia
Influenza A virus test negative
Influenza B virus test
Respiratory arrest
Respiratory distress
Respiratory syncytial virus test negative
Resuscitation
SARS-CoV-2 test negative
Tachycardia
Troponin I increased
Ventricular fibrillation
Symptomtext
Report made to agency 11/16/2021 @ 17:45: Severe respiratory distress, profuse diaphoresis, hypoxia, tachycardia 11/16/2021 @ 18:06: Respiratory arrest 11/16/2021 @ 18:10: Ventricular fibrillation, cardiac arrest. Unsuccessful resuscitation. Time of death 18:52 on 11/16/2021
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cardiac arrest
- Hospital-Tage
- -
- Labordaten
- Troponin I: 0.20 (H) Cepheid GeneXpert PCR: (post-mortem) SARS-Co-V-2: negative Influenza A: negative Influenza B: negative RSV: negative
- Aktuelle Erkrankungen
- Obesity
- Vorgeschichte
- Obesity
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 10.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- UN / UN
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Death
Malaise
Symptomtext
Not feeling well. Decedent found deceased 2 days after vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- 09/29/2021 was diagnosed COVID positive. 10/26/2021 complaints of chest pain post COVID-19 11/03/2021 notified by PCP office of a decreased sodium level (126) and elevated potassium levels (5.4).
- Vorgeschichte
- Addison's disease, Hodgkin's lymphoma, acute on chronic kidney disease, erectile dysfunction.
- Andere Medikamente
- Numerous supplements, Benzonatate, Valacyclovir, Tadalafil, Fludrocortisone
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 24.11.2022
- Impfdatum
- 10.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal pain upper
Angina pectoris
Axillary pain
Back pain
Blood test normal
Colitis ulcerative
Echocardiogram normal
Electrocardiogram normal
Electromyogram abnormal
Endoscopy normal
Gait disturbance
Haematochezia
Musculoskeletal chest pain
Neuropathy peripheral
Pain in extremity
Paraesthesia
Parosmia
Presyncope
Symptomtext
Next day after shot I had chest pains (Heart area). Went to the ER maybe a week later and had blood drawn and an EKG. Everything checked out ok. I was still having chest pains and almost passed out about a week after that. Went to ER by way of rescue squad. Had blood taken and an EKG. Again everything seemed to be ok. I was referred to a cardiologist and had an Echo Cardiagram. I was told everything was ok. Not long after that I started getting underarm and rib pain. I was concerned about my lymph nodes so I went to see a rheumatologist. I had an extensive blood panel done and everything seemed to check out. I then started to smell burning cigarettes every day. I researched this and I made an appointment to see an ENT. He put a scope up my nose and he said everything looked good. That smell lasted for more than a month. While still experiencing underarm and rib pain I started to have pain in my chest, stomach, and back also. I started to see blood in my stool. I made an appointment with a gastroenterologist. I scheduled a colonoscopy and an eddoscopy. I was diagnosed with ulcerative colitis. I also started experiencing tingling hands and feet. I scheduled an appointment with a neurologist. I had an EMG and was diagnosed with neuropathy. I had none of this before the shot. I still experience pain in my ribs, back, chest and stomach on a daily basis. I have tingling in my hands and feet. The bottoms of my feet hurt when I walk.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None before the covid shot.
- Andere Medikamente
- Multi-vitamin, fish oil
- Allergien
- None
- Vorherige Impfungen
- None, I do not get vaccines. I did not want this
- Staat
- MI
- Alter
- -
- Geschlecht
- F
- Eingang
- 19.10.2022
- Impfdatum
- 29.12.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood test
Cardiac failure
Enzyme level test
Loss of consciousness
Vomiting
Symptomtext
HEART FAILURE; VOMITING; PASSED OUT; This spontaneous report received from a patient concerned female unspecified age. The patient's height, and weight were not reported. The patient's concurrent conditions included: HPA secondary hypothalamic- pituitary adrenal insufficiency (since she was a kid). On an unspecified date, The patient received covid-19 vaccine ad26.cov2.s (Dose number in series 1) (suspension for injection, route of admin not reported, batch number: 063A21A expiry: UNKNOWN) dose was not reported, 1 total for covid-19 prophylaxis. The patient experienced pain in arm when treated with 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: 211D21A expiry: UNKNOWN) dose was not reported, 1 total administered to left arm on 29-DEC-2021 for covid-19 prophylaxis. No concomitant medications were reported. On DEC-2021, since she received the booster, she passed out, 3 times in total (Dose number in series 2). On an unspecified date, the patient experienced vomiting for 3 months since 4AM-5AM in the morning until 2PM-3PM in the afternoon about 2-3 times a day, every hours. She also mentioned having trouble breathing, she saw her doctor and they did a blood work and find out that she had a heart problem, early stage of heart failure. Heart failure was worst around March and April 2022. Her doctor explained to her that her enzymes were really low and they were causing her heartbeat to be slower (Dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from vomiting, and the outcome of heart failure and passed out was not reported. This report was serious (Other Medically Important Condition). This case, involving the same patient is linked to 20221024078.; Sender's Comments: V0: 20221022922-COVID-19 VACCINE AD26.COV2.S- Heart 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: MEDICAL HISTORY- HPA secondary hypothalamic- pituitary adrenal insufficiency. Therefore, this event(s) is considered not related. V0: 20221022922-COVID-19 VACCINE AD26.COV2.S- Passed Out. 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
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- Test Name: ENZYME COUNT; Result Unstructured Data: Very low and were causing her heartbeat to be slower.; Test Name: BLOOD WORK; Result Unstructured Data: heart problem
- Aktuelle Erkrankungen
- Hypothalamo-pituitary disorder (since she was a kid)
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 23.06.2022
- Impfdatum
- 23.06.2022
- Beginn
- 23.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Fall
Loss of consciousness
Symptomtext
pt was administered a janssen vaccine. he was asked to sit for 15 minutes and wait. 5 minutes later he passed out and fell to the floor. he came to quickly said he felt ok and wanted water. we took his blood pressure and got him cool towels and ice packs since he was sweating while waiting for EMTs to arrive. EMT's encouraged him to go the er since he had hit his head so he agreed
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- not unknown
- Vorgeschichte
- not known
- Andere Medikamente
- not known
- Allergien
- pt checked no allergies on questionnaire
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 87,0
- Geschlecht
- F
- Eingang
- 23.06.2022
- Impfdatum
- 21.06.2022
- Beginn
- 22.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Blood pressure immeasurable
Computerised tomogram head
Drooling
Facial paralysis
Hypopnoea
Mydriasis
Respiratory rate increased
Staring
Syncope
Unresponsive to stimuli
Symptomtext
At 1155AM resident was in dinging room in wheelchair. The resident "slumped over" in her wheelchair with "blank stare and pupils dilated, right side of mouth dropped open and drooling," resident did not respond to verbal or painful stimuli, respirations rapid and shallow, VS: temp97.3 forehead scan, pulse with machine 94 respiration 30, 02 Sat 90% room air, machine will not give BP reading, attempted manual BP and unable to hear any beats, res taken to ER via W/C with 2 staff assist ER Course: Evaluated in ER-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Facial paralysis
- Hospital-Tage
- -
- Labordaten
- 6/22/22 Head CT
- Aktuelle Erkrankungen
- Herpes Zoster
- Vorgeschichte
- History of femur fracture COPD HTN Atherosclerosis
- Andere Medikamente
- Acidophilus 1 capsule daily Docusate Sodium 100mg 1 tab twice daily Levothyroxine 100mcg 1 tab daily Magnesium Oxide 400mg 1 tab daily Multivitamin 1 tab daily Potassium Chloride ER 10mEq 1 capsule three times daily Valcyclovir 1000mg eve
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 06.05.2022
- Impfdatum
- 27.03.2021
- Beginn
- 01.04.2021
- Tage bis Beginn
- 5,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Anaemia
Condition aggravated
Laboratory test
Thrombosis with thrombocytopenia syndrome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Thrombosis with thrombocytopenia syndrome
- Hospital-Tage
- -
- Labordaten
- Yes, labs were taken as routine for general healthcare.
- Aktuelle Erkrankungen
- PTSD
- Vorgeschichte
- Spine disc degenerative. Fused l5s1, multiple neck disc degenerative issues. I was told by the doctor yesterday that I have TTS. I bleed from my nose constantly, doctor says I am anemic, my blood platelets are large, and I'm not making enough blood. My throat/sinuses stick together and block my air intake and I'm afraid to sleep for fear of suffocating. These conditions are exacerbating my already severe PTSD. I'm a mess.
- Andere Medikamente
- Valtrex, sertraline
- Allergien
- Tomatoes, peanuts, grass trees medical tape
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 01.05.2022
- Impfdatum
- 10.11.2021
- Beginn
- 30.01.2022
- Tage bis Beginn
- 81,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
COVID-19
Chills
Laboratory test
Muscle twitching
Pyrexia
Seizure
Seizure like phenomena
Symptomtext
After being vaccinated I suffered from chills and twitching which I was told would subside. After a couple days the symptoms did subside, however on 1/30/2022 I suffered my first seizure. Since then I have been having minor seizure activity. On 4/30/2022 I was diagnosed with covid 19 after again suffering from chills and high fever. Subsequently my seizure activity has stopped while suffering from COVID. The vaccine caused me to have seizures.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- Results were inconclusive. Drs could neither confirm nor deny the correlation due to the lack of research, which is malpractice.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 21.04.2022
- Impfdatum
- 21.04.2022
- Beginn
- 21.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Loss of consciousness
Syncope
Symptomtext
After vaccine administration, the patient lost consciousness/fainted for about 10 seconds. Pharmacy staff elevated patient's legs and applied cold compress to patient's neck and face and he regained consciousness. He was in a chair with armrests and didn't fall from chair or injure himself. Pharmacy team provided water and monitored patient for a further 15 minutes and allowed him to go home with caregiver at that time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- None reported
- Aktuelle Erkrankungen
- None reported
- Vorgeschichte
- Asthma
- Andere Medikamente
- None reported
- Allergien
- None reported
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 09.04.2022
- Impfdatum
- 18.11.2021
- Beginn
- 06.03.2022
- Tage bis Beginn
- 108,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Facial paralysis
Lacrimation increased
Pruritus
Symptomtext
DEVELOPED A RIGHT SIDED VIITH CN PALSY (FACIAL PARALYSIS); MILD FACIAL (LEFT) ITCHING; LEFT EYE TEARING; This spontaneous report received from a patient patient (also a healthcare professional) concerned a 73 year old, male. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: The patient had no recent significant medical history. The patient was a physician. The patient previously received covid-19 vaccine ad26. cov2.s (Dose number in series 1) (suspension for injection, route of admin, and batch number, expiry were not reported) dose was not reported, 1 total administered on unspecified date in MAY-2021 for prophylactic vaccination. It was unknown if patient experienced any adverse reactions following administration of covid-19 vaccine ad26.cov2.s vaccine (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: 211D21A expiry: Unknown) dose was not reported, 1 total administered to left arm on 18-NOV-2021 for prophylactic vaccination. The product was stored in appropriate temperature conditions and it was properly stored from receipt to administration. No concomitant medications were reported. On 06-MAR-2022, the patient experienced left eye tearing. On 30-MAR-2022, (Reported as 28 weeks after vaccination) the patient developed a right sided VII th cranial nerve (CN) palsy (facial paralysis) and also experienced prodromal symptoms included left side mild facial itching (Dose number in series 2). On 05-APR-2022, patient started treatment with prednisone (taped dossing 30 mg/qd x 5). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered with sequelae from left eye tearing, and the outcome of developed a right sided vii th CN palsy (facial paralysis) and mild facial (left) itching was not reported. This report was serious (Other Medically Important Condition).; Sender's Comments: V0:20220410169-COVID-19 VACCINE AD26.COV2.S- Developed a right sided VIIth CN palsy (facial paralysis), Left eye tearing, Mild facial (left) itching. 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
- Facial paralysis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: The patient had no recent significant medical history. The patient was a healthcare professional.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 09.04.2022
- Impfdatum
- 18.11.2021
- Beginn
- 06.03.2022
- Tage bis Beginn
- 108,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Facial paralysis
Lacrimation increased
Pruritus
Symptomtext
DEVELOPED A RIGHT SIDED VIITH CN PALSY (FACIAL PARALYSIS); MILD FACIAL (LEFT) ITCHING; LEFT EYE TEARING; This spontaneous report received from a patient patient (also a healthcare professional) concerned a 73 year old, male. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: The patient had no recent significant medical history. The patient was a physician. The patient previously received covid-19 vaccine ad26. cov2.s (Dose number in series 1) (suspension for injection, route of admin, and batch number, expiry were not reported) dose was not reported, 1 total administered on unspecified date in MAY-2021 for prophylactic vaccination. It was unknown if patient experienced any adverse reactions following administration of covid-19 vaccine ad26.cov2.s vaccine (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: 211D21A expiry: Unknown) dose was not reported, 1 total administered to left arm on 18-NOV-2021 for prophylactic vaccination. The product was stored in appropriate temperature conditions and it was properly stored from receipt to administration. No concomitant medications were reported. On 06-MAR-2022, the patient experienced left eye tearing. On 30-MAR-2022, (Reported as 28 weeks after vaccination) the patient developed a right sided VII th cranial nerve (CN) palsy (facial paralysis) and also experienced prodromal symptoms included left side mild facial itching (Dose number in series 2). On 05-APR-2022, patient started treatment with prednisone (taped dossing 30 mg/qd x 5). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered with sequelae from left eye tearing, and the outcome of developed a right sided vii th CN palsy (facial paralysis) and mild facial (left) itching was not reported. This report was serious (Other Medically Important Condition).; Sender's Comments: V0:20220410169-COVID-19 VACCINE AD26.COV2.S- Developed a right sided VIIth CN palsy (facial paralysis), Left eye tearing, Mild facial (left) itching. 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
- Facial paralysis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: The patient had no recent significant medical history. The patient was a healthcare professional.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 05.04.2022
- Impfdatum
- 03.01.2022
- Beginn
- 13.02.2022
- Tage bis Beginn
- 41,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Alcohol use
Alcohol withdrawal syndrome
Anticoagulant therapy
Epistaxis
Fall
Haemorrhage
Hypotension
Injury
Shock
Symptomtext
Patient admitted after fall and trauma, EtoH involved, apparently had shock from blood loss with epistaxis and anticoagulation, was persistently hypotensive in hospital, treated for Etoh withdrawal. Discharged with holding PTA BP/diuretics medications and Xarelto. ED visit and hospital admission within 6 weeks of receiving the COVID vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Shock
- Hospital-Tage
- 6,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 19.03.2022
- Impfdatum
- 08.02.2022
- Beginn
- 10.02.2022
- Tage bis Beginn
- 2,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest pain
Electrocardiogram normal
Full blood count normal
Myocarditis
Pericarditis
Platelet count normal
Troponin normal
Symptomtext
Stabbing chest pain while lying on back, and chest pain while breathing deeply during moderate exercise. Suspected myocarditis or pericarditis. Treated with ibuprofen 200 mg daily for 5 days. Severity of chest pain gradually reduced over time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocarditis
- Hospital-Tage
- -
- Labordaten
- Troponin levels and ECG results normal. CBC results normal, including normal platelet levels.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Below-the-knee amputation of left leg.
- Andere Medikamente
- Vitamin D - 1000 IU daily
- Allergien
- Shellfish, Penicillin (suspected)
- Vorherige Impfungen
- Chills, headache, extreme fatigue following Janssen vaccination on 05/15/2021. Age 27. Lot number 205A21A.
- Staat
- OK
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 18.03.2022
- Impfdatum
- 18.03.2022
- Beginn
- 18.03.2022
- 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
Cyanosis
Dizziness
Electrocardiogram
Grunting
Loss of consciousness
Pallor
Symptomtext
Pt came in to receive a Janssen vaccine (1st dose). The presented calm and nothing of concern was noted on pt intake form, including no history of reaction to vaccines. After the injection the pt began to get pale and asked for a cup of water. He then passed out for ~10-15 seconds. After he woke up he appeared pale and was dizzy. No swelling was noted or redness at injection site. Pt was not having any signs of breathing distress. ~3-5 min later he passed out again and started snorting and lips were tinged blue. An epipen was then administered and 911 was called. He came back to after ~15 seconds. Pt still appeared pale and dizzy. EMS arrived shortly after and monitored the pt for ~15 min afterward he was released. Pt wife stated (after she arrived after EMS) that pt had a history of passing out during blood donations. Reaction suspected due to pt's apprehension to getting the vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- EMS performed heart rate/02/ECG/etc.
- Aktuelle Erkrankungen
- NONE REPORTED
- Vorgeschichte
- NONE REPORTED
- Andere Medikamente
- NONE REPORTED
- Allergien
- NONE REPORTED
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 11.03.2022
- Impfdatum
- 15.06.2021
- Beginn
- 10.03.2022
- Tage bis Beginn
- 268,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Hypoaesthesia
Pain in extremity
Peripheral swelling
SARS-CoV-2 test positive
Thrombosis
Symptomtext
No covid symptoms were reported by this case. Case experienced severe pain, swelling and numbness in his leg. He drove himself to the hospital and once there tested positive for COVID. Case is now being treated for blood clots in his leg.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Thrombosis
- Hospital-Tage
- -
- Labordaten
- for pain and swelling in his leg.
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 01.03.2022
- Impfdatum
- 05.02.2022
- Beginn
- 05.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Anaphylactic reaction
Dyspnoea
Pharyngeal swelling
Symptomtext
Anaphylaxis, swelling of the throat, unable to breathe within 15 minutes of injection Epinephrine injected into the upper arm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anaphylactic reaction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma, Allergies, Elliptocytosis
- Andere Medikamente
- None
- Allergien
- Polyethylene glycol, polysorbate 80
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 24.02.2022
- Impfdatum
- 24.02.2022
- Beginn
- 24.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Loss of consciousness
Syncope
Symptomtext
Pt. passed out for about 10 seconds. Paramedics arrived within 5 minutes. Pt. basically fainted from shot. Breathing was and vitals were all normal. Paramedics released under his own will.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 22.02.2022
- Impfdatum
- -
- Beginn
- 19.01.2022
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
Blood magnesium decreased
Blood potassium
Blood potassium decreased
Blood test
Chest X-ray
Computerised tomogram head
Echocardiogram
Electroencephalogram
Electrolyte imbalance
Eye pain
Facial pain
Fall
Head injury
Heart rate
Hypoaesthesia
Lethargy
Loss of consciousness
Symptomtext
PASSED OUT/ UNCONSCIOUS; HAND STUCK OPEN; LOW POTASSIUM; ELECTROLYTES WERE OFF; INAPPROPRIATE TACHYCARDIA; URINATED ON HERSELF; FELL; HITTING THE HEAD ON WALL; EYE WAS TENDER; LEFT SIDE OF FACE WAS TENDER; LOW MAGNESIUM; HAND AND ARM NUMBNESS; WEAKNESS; FELT LETHARGIC; This spontaneous report received from a patient concerned a 34 year old female of unspecified ethnicity. 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: 205A21A, expiry: 21-SEP-2021) dose was not reported, 1 total, administered to left arm on 19-AUG-2021 for prophylactic vaccination. It was unknown whether patient had any adverse events following vaccination 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: 211D21A, expiry: 11-APR-2022) dose was not reported, 1 total administered to right gluteus medius on 19-JAN-2022 around 13:00 for prophylactic vaccination. No concomitant medications were reported. On 19-JAN-2022, around 19:00 following vaccination with covid-19 vaccine ad26.cov2.s, the patient felt lethargic. The patient also experienced crazy/wild dreams and weakness. On 20-JAN-2022, the patient woke up around 04:00 with hand and arm numbness. The sensation slowly returned after running water on them. Her hand was stuck open and she had to work to close it. It took repeated attempts approximately 10 minutes to get the strength back and to close hand. The patient was lightheaded and had tachycardia/ heart was racing. The patient laid down and when she sat up she passed out hitting her head on wall in bedroom. The left side of face and eye was tender. The patient fell, was unconscious and urinated on herself. The patient was taken to the emergency department and had her blood work done which showed low magnesium level. It was replenished and patient was released. The patient felt lightheaded again with palpitations and was taken back to the Emergency room again. They said that her potassium was low and that her electrolytes were off. The patient was admitted to the hospital on 20-JAN-2022 and was discharged on 21-JAN-2022. The duration of hospitalization was 1 day. On JAN-2022, Laboratory data included: Brain CT (Computed tomogram) (NR: not provided) normal, Chest X-ray (NR: not provided) normal, EEG (electroencephalogram) (NR: not provided) normal, Echocardiogram (NR: not provided) normal. 4 days later the patient's resting heart rate went from 80 to 85 to be elevated to approximately 150. The physician put the patient on Metoprolol succinate 25mg daily and said it looked like a reaction to the vaccine. On 10-FEB-2022, the patient had an episode again with the elevated heart rate. The Metoprolol Succinate 25mg was increased to twice a day with breakfast and dinner. The patient reported that she had experienced serious adverse events with the company booster vaccine. The physicians weren't sure on what was happening. It was reported that the patient was going to visit the Rheumatologist. (Dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from hand stuck open, felt lethargic, and low magnesium on 20-JAN-2022, and electrolytes were off, and weakness on 27-JAN-2022, was recovering from hand and arm numbness, had not recovered from inappropriate tachycardia, and the outcome of passed out/ unconscious, hitting the head on wall, eye was tender, left side of face was tender, fell, urinated on herself and low potassium was not reported. This report was serious (Hospitalization Caused / Prolonged).; Sender's Comments: V0:20220230270-Covid-19 vaccine ad26.cov2.s- passed out/ unconscious,hand stuck open, electrolytes were off,low magnesium ,inappropriate tachycardia,felt lethargic, hitting the head on wall, eye was tender, left side of face was tender, fell, urinated on herself ,low potassium .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. 20220230270-Covid-19 vaccine ad26.cov2.s-weakness,hand and arm numbness- This event(s) is labeled per Agency and is therefore considered potentially related
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- 1,0
- Labordaten
- Test Date: 202201; Test Name: Brain CT; Result Unstructured Data: normal; Test Date: 202201; Test Name: Heart rate; Result Unstructured Data: approximately 150; Test Date: 202201; Test Name: Heart rate; Result Unstructured Data: 85; Test Date: 202201; Test Name: Echocardiogram; Result Unstructured Data: normal; Test Date: 202201; Test Name: EEG; Result Unstructured Data: normal; Test Date: 202201; Test Name: Chest X-ray; Result Unstructured Data: normal; Test Date: 202201; Test Name: Heart rate; Result Unstructured Data: 80; Test Date: 20220120; Test Name: Potassium; Result Unstructured Data: low; Test Date: 20220120; Test Name: Blood test; Result Unstructured Data: low magnesium; Test Date: 20220210; Test Name: Heart rate; Result Unstructured Data: elevated
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 17.02.2022
- Impfdatum
- 17.02.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Loss of consciousness
Pain in extremity
Seizure like phenomena
Urinary incontinence
Symptomtext
Customer received vaccination. Initially, said she was fine receiving vaccinations in the past with only one incidence where she fainted/needed medical attention. After consulting the patient, she felt confident she can still receive her vaccine based on her history. Within seconds after receiving the vaccine, the patient stated she felt like fainting. I responded by holding her upright as she began to fall an then she began to have seizure-like symptoms followed by being guided to the floor (as she was falling off the edge of the chair) and then subsequently urinating. Within seconds, the patient regained consciousness and was checked for alertness and orientation (by verifying name, location, and what was happening). They were asked if they would like for an ambulance/emergency services to be called to which she declined. They were further counseled to assess for other signs/symptoms but only reported a pain in her foot as she put pressure on it while being guided off the chair to the floor. This pain resolved in minutes. She was subsequently picked up by her significant other and then proceeded to wait for the recommended 30 minutes after receiving a vaccine. During this time she was continually monitored by me for changes in cognitive function and further signs and symptoms. Patient was ambulatory at end of incidence and showed no further signs and symptoms of cognitive impairment, seizures, or any other conditions that may have required medical attention.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 17.02.2022
- Impfdatum
- 17.02.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anaphylactic reaction
Cough
Dizziness
Dysphonia
Dyspnoea
Flushing
Headache
Hyperhidrosis
Pruritus
Symptomtext
Anaphylactic Reaction Standing Order Worksheet Nursing Assessment Patient presents at 10:05 am with the following symptoms: pruritus, flushing, dizziness, diaphoresis, headache, dyspnea/SOB, hoarseness and cough Patient's weight 99.8kg per patient reports Medical History Patient has hypersensitivity/allergy to: medication Codeine High Anaphylaxis Cyclinex [tetracycline] High Breathing Difficulty Meloxicam High Edema,generalized Sulfa Antibiotics High Cardiovascular arrest Nurse Actions: 911 called: no, provider at chairside Clinician informed: yes, Clinicians Name: Suspected trigger removed: No Epinephrine Epipen Adult IM held. Benadryl 50mg PO 1012 Positioned patient Lying supine Vitals obtained and documented 1006-1035 (enter in vitals section) Narrative Code charting 1006 Patient coughing continuously, unable to say more than a word or two at a time. Dr. assessed patient. SAO2 99% (RA), P 90, RR 30, B/P 127/82 1010 Continues to cough continuously SAO2 100% (RA), P 110, RR 30 1012 Benadryl 50mg PO 1017 Coughing less, flushed face resolved. Dr. assessed patient. SAO2 98% (RA), P 107, RR 30 1020 Able to talk in full sentences, coughing less, RR 24 1025 Talking, drinking, very rare cough. Dr. assessed patient. SAO2 100% (RA), P 85, RR 20 1030 Sitting up, RR 20 1035 Moved to chair, Dr. discussed d/c plan and left room. RR 20 1040 RN left room. 1052 Patient discharged Oxygen Oxygen: Patient >94% O2 saturation at initial assessment (enter in vitals section) Glucagon Held. IV initiated per standing order no Additional intervention for bronchospasms/wheezing. Not applicable. Response Respiratory rate decreased, coughing lessened. Patient able to talk Disposition/Outcome Disposition: discharged from clinic with husband driving, Patient was given the following prior to leaving the clinic Patient Education take benadryl the next few days and Personal belongings with: Patient RN 2/17/2022, 10:58 AM
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anaphylactic reaction
- Hospital-Tage
- -
- Labordaten
- Not applicable
- Aktuelle Erkrankungen
- Irregular periods N92.6 Menorrhagia with irregular cycle N92.1
- Vorgeschichte
- Obesity (BMI 30-39.9) (HRC)
- Andere Medikamente
- Progesterone (PROMETRIUM) 200 MG capsule Take 1 Capsule by mouth daily., Disp-10 Capsule, R-3, DAILY Starting Fri 9/10/2021, Oral, E-Prescribing, Last Dose: Taking
- Allergien
- Codeine Codeine Anaphylaxis High Allergy 1/6/2016 Cyclinex [Tetracycline] Cyclinex [Tetracycline] Breathing Difficulty High Allergy 1/6/2016 Meloxicam Meloxicam Edema,generalized High 9/10/2021 Sulfa Antibiotics Sulfa Antibiotics Cardiovascular arrest High Allergy 1/6/2016
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 14.02.2022
- Impfdatum
- 14.02.2022
- Beginn
- 14.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Flushing
Hyperhidrosis
Loss of consciousness
Symptomtext
patient was given covid vaccine and 3 minutes after shot was given patient passed out in waiting room. patient came to and was diaphortic cool rag applied and fan applied and flushed. VS 02 sat 97% HR 82 BP 125/84 R 22 After 15minutes additional patient stated felt fine and was able to drive home denied dizzyness and was not going to pass out. patient has had passing out episodes after flu shot as well and forgot to tell us. patient was going to eat lunch now due to has not eaten yet.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- depression, pancreatitis
- Andere Medikamente
- none
- Allergien
- Azithromycin
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 14.02.2022
- 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: ja
ER: ja
Erholt: nein
Back pain
Blindness
Blood test
Burning sensation
Deafness
Dysstasia
Gait inability
Guillain-Barre syndrome
Influenza like illness
Infusion
Paralysis
Red blood cell count
SARS-CoV-2 antibody test negative
Spinal X-ray
Spinal pain
T-lymphocyte count
Tremor
Visual impairment
Symptomtext
Flu like symptoms, followed by sunburn feeling on 11/9/2021, followed by severe back pain from spine on 11/18/2021, emergency room visits on 11/18/2021 and 11/19/2021. Was given pain medication and sent home. 11/20/2021 paralyzed from the chest down. aw PCP on 11/22/2021 who did nothing but refer me to a physiologist, neurologist and to get MRI's of my brain and spine. physiologist did not help and sent me home. Did not get MRI due to paralysis and pain. went to an alternative medical center where I was diagnosed with Guillin Barr syndrome on 12/13/2021. I started ultraviolet blood infusion therapy on 12/21/2021 I. I had an antibodies blood draw on 21/20/2021 to check for COVID antibodies, none were found. Since starting treatment I am managing my pain better, I can move to a standing position but cannot stand alone, I am still unable to walk but making progress. Tremors through my body are still present. Loss of vision and hearing, but has since returned since starting treatment. Vision is not where it was pre-vaccine but is improving. The list of symptoms from this "vaccine" is far too large to name everything in this small space.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Guillain-Barre syndrome
- Hospital-Tage
- -
- Labordaten
- COVID antibodies test Blood test for T-Cell count Blood test for white and red blood cell count X-ray of back blood test for infection
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Autoimmune and pulmonary
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 10.02.2022
- Impfdatum
- 09.02.2022
- Beginn
- 09.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Chest discomfort
Cyanosis
Dizziness
Dyspnoea
Heart rate decreased
Heart rate increased
Hypoaesthesia
Oral discomfort
Palpitations
Presyncope
Pruritus
Respiratory distress
Sensory loss
Skin discolouration
Swelling face
Throat tightness
Urticaria
Symptomtext
Within 30 seconds after the injection, I could feel lightheadedness. Within 5 minutes there was an increase in heart rate and palpitations. 7-10 minutes I could feel itchiness along my face, neck, and chest. Reported to Pharmacist. At 10 minutes I began to feel throat tightness and fuzziness inside of my mouth. At 12-15 minutes I had difficulty breathing, rapid heart rate 120bpm (my normal resting is 46-54bpm), blue finger tips with no capillary refill. Pharmacist assisted in breathing coaching without success. Pharmacist asked team for an epipen and 911 assistance. Overall body color changes. Pharmacist reached for radial pulse and could not feel one. Pharmacist reached for carotid pulse and could not feel one due to weak grade. I felt near syncopal and pharmacist assisted me from chair to floor. I could not feel sensation in bilateral hands up to my elbows. Pharmacist injected epipen to right thigh. Relief of respiratory distress was felt within 2 minutes. I still could not feel my hands. Paramedics arrived on scene and began a cardiac monitor and O2 monitoring. Heart rate was still rapid but O2 sats improved. Paramedics assisted me from floor to chair and injected unknown dose of Benadryl to right arm. Hives were still visible at this point and some facial swelling around the mouth. I was transported to Hospital for observation. After discharge I am still experiencing rapid heart rate 120-130s bpm and experience slight chest pressure and discomfort.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Obesity, MTFHR gene mutation
- Andere Medikamente
- Ibuprofen PRN , Klonopin PRN (not within the last 30 days)
- Allergien
- Latex, Dilaudid, Doxycline, kiwi fruit, mango, banana, avocado.
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 03.02.2022
- Impfdatum
- 05.11.2021
- Beginn
- 14.11.2021
- Tage bis Beginn
- 9,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Anal haemorrhage
Anticoagulant therapy
Blood fibrinogen abnormal
Blood test abnormal
Blood urine present
Computerised tomogram
Dyspnoea exertional
Dysuria
Epistaxis
Fatigue
Feeling abnormal
Fibrin D dimer increased
Haemorrhoids
Immunoglobulin therapy
Paraesthesia
Platelet disorder
Thrombosis with thrombocytopenia syndrome
Tremor
Symptomtext
7:00 am - Onset of event was bleeding while urinating. Following this, extreme pain while urinating. Within a few hours, bleeding vaginally. Later that day, a huge hemmorhoid appeared with bleeding from anus and Bleeding from nose. Extreme pain trying to urinate, but minimal amount would pass. 5:00 a.m. following day - Went to hospital, was admitted through Emergency. Transferred to larger hospital. Was put on IVIG, and admitted to hospital, High Acute Unit. Was in hospital 6 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Thrombosis with thrombocytopenia syndrome
- Hospital-Tage
- 6,0
- Labordaten
- I do not have my records from hospital. Bloodwork was done every few hours through the first 3 days in hospital. Platelet levels, d-dimer, fibrinogen were beyond acceptable range. CT Scan was performed. Tests were sent to a healthcare facility confirming VITT. IVIG was continued while in hospital, then switched to Xarelto Riveroxaban blood thinner while at home for 3 months. When released, while recovering, I have tremors in my left hand, extreme fatigue, foggy brain. tingling in my fingers, shortness of breath when going for walks.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Supplements: Omega 3, Vitamin D, Zinc, Vitamin C
- Allergien
- Morphine
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 03.02.2022
- 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
Fall
Loss of consciousness
Presyncope
Syncope
Symptomtext
While waiting post-vaccination, patient had a syncopal event and temporarily lost consciousness. No injuries sustained during his fall. Patient was taken to the ER for further evaluation (which the main basis for my VAERS submission), but was ultimately discharged without further issue. Most likely a vasovagal episode.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- 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
Anaphylactic reaction
Laboratory test
Symptomtext
PATIENT RECEIVED DOSE AND WITHIN 5 MINS NOTICED SYMPTOMS OF ONSET OF ANAPHYLASIS - PATIENT EXPERIENCED THESE SYMPTOMS BEFORE WITH A PNEUMONIA IMMUNIZATION. PATIENT HAD PRE-MEDICATED WITH 25 MG OF DIPHENHYDRAMINE AND HAD BROUGHT THE LIQUID FORM WITH HER. WE ADVISED A SECOND DOSE AND TO SIT DOWN IN FRONT OF THE PHARMACY, staff member STAYED WITH THE PATIENT AND WHEN SHE FELT SHE NEEDED TO ADMINISTER A DOSE OF EPINEPHRINE staff member CALLED 911. PARAMEDICS ARRIVE WITHIN 5 MINS APPROX 1:35PM AND ESTABLISHED AN IV PORT. PATIENT TOOK ONE MORE DOSE OF DIPHENHYDRAMINE WITH THE PARAMEDICS AN WAS TAKEN TO HOSPITAL. IN A FOLLOW UP CALL TO THE PATIENT SHE STATED SHE WAS WELL. SHE BELIEVED SHE RECEIVED ONE MORE DOSE OF EPINEPHRINE AND A DOSE OF STEROID BEFORE DISCHARGE HOME.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anaphylactic reaction
- Hospital-Tage
- -
- Labordaten
- DONE AT HOSPITAL- NO ACCESS TO RECORDS
- Aktuelle Erkrankungen
- NONE KNOWN
- Vorgeschichte
- ASTHMA, CHOLESTEROL
- Andere Medikamente
- DIPHENHYDRAMINE 25MG, VIT D3, MAGNESIUM
- Allergien
- PESTICIDES, PEG, POLYSORBATE
- Vorherige Impfungen
- PNEUMONIA
- Staat
- PA
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- -
- Beginn
- 04.01.2022
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Fall
Lip discolouration
Loss of consciousness
Migraine
Pain
Pyrexia
Skin discolouration
Symptomtext
SHE PASSED OUT; FACE TURNED WHITE; LIPS TURNED PURPLE; MASSIVE MIGRAINES; BED WITH ACHES AND PAIN; FELL IN CHAIR; CHILLS; FEVER; This spontaneous report received from a consumer concerned a 44 year female. The patient's height, and weight were not reported. The patient's concurrent conditions included: lot of allergies to things. The patient was previously vaccinated with Pfizer (BNT 162) (form of admin, route of admin, batch number and expiry was not reported) dose was not reported (dose number in series was 1), administered for prophylactic vaccination. On an unspecified date, following vaccination with Pfizer (BNT 162), the patient was sick for one day (dose number in series 1). The patient received additionally covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number:211D21A and expiry:11-APR-2022) dose was not reported (dose number in series 2), 01 total administered on 04-JAN-2022 at left deltoid for prophylactic vaccination. No concomitant medications were reported. On 04-JAN-2021, following administration of covid-19 vaccine ad26.cov2.s, her face turned white, lips turned purple and just passed out. She sat down and fell in chair. Pharmacist gave her lollipop to suck but did not gave anything to drink, 30 minutes later when they went home, she had massive migraines, chills and fever, she had bed with aches and pains (dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from face turned white, lips turned purple, massive migraines, chills, fever, and bed with aches and pains, and the outcome of she passed out and fell in chair was not reported. This report was serious (Other Medically Important Condition). This case, from the same reporter is linked to 20220112619 and 20220112632.; Sender's Comments: V0- 20220112654-covid-19 vaccine ad26.cov2.s-She passed out. 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
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Multiple allergies
- Vorgeschichte
- Comments: Unknown
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 15.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fall
Loss of consciousness
Symptomtext
21-year-old female received her initial Janssen COVID-19 vaccine and left the immunization room to sit in the waiting area. We monitor the patients for 15 minutes after vaccination. Patient didn't mention she felt dizzy, but after about 10 minutes we found her passed-out. She slipped forward out of the chair and on to the floor. Patient came back to herself fairly quickly. She was helped back into the chair, drank water and ate an energy bar. No injuries observed. A friend came to drive her home. As she was leaving, she stated she felt so much better. Her blood pressure was checked. It was normal.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 18.01.2022
- Impfdatum
- 18.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Head injury
Lip haemorrhage
Syncope
Symptomtext
Patient fainted after receiving vaccine after a minute of receiving vaccine. He hit his head and had a lip bleeding. Patient rejected the paramedics advise to go to hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- nkda
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 18.01.2022
- Impfdatum
- 14.12.2021
- Beginn
- 02.01.2022
- Tage bis Beginn
- 19,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Anticoagulant therapy
Benign prostatic hyperplasia
Bundle branch block left
COVID-19
Deep vein thrombosis
Hypertension
Hypothyroidism
Suicidal ideation
Symptomtext
01/02/22 presents to ED for "suicidal ideation". PMHx of "HFrEF, CAD s/p DES, AAA, atrial flutter s/p ablation, atrial fib s/p cardioversion 12/15/21 on Eliquis, LBBB, HTN, DVT, hypothyroidism, BPH, COVID 12/15/21"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Deep vein thrombosis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 14.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Chills
Syncope
Symptomtext
pt was fainting around 5 mins after the shot; but woke up right away & we're watching him for 30min. checked bp: was 150/84, was ok after 15min, did not have to give any meds. Followed up with him today; pt just had some chills no pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 14.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arthralgia
Fall
Head injury
Headache
Loss of consciousness
Magnetic resonance imaging
Muscle spasms
Neck pain
Symptomtext
Approximately 5 minutes after injection while patient was in waiting area for monitoring, he lost consciousness and fell and hit his head. A few moments later he recovered but complained of head pain most like due to the impact after falling. He then said his shoulders and neck were hurting. Later in the day after MRI showed everything was ok, he still complained of neck spasms. It seems like he is ok but it is unknown at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 18,0
- Geschlecht
- M
- 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: ja
Erholt: nein
Blood glucose normal
Blood pressure immeasurable
Condition aggravated
Loss of consciousness
Syncope
Symptomtext
1 minute post-vaccination the patient experienced syncope and fainted. The patient was transfered to from the chair to the floor and his feet positioned slightly elevated. He regained conciousness while in the laying position. Blood pressure was checked several times. Called 911 and EMS evaluated him on site. He was removed from the premisis via gurney after roughly 20 minutes. He was transported to ER due to inability to maintain BP at sitting and standing positions.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- BP <85/<55 mmHg (1/12/22) Blood glucose 106 (1/12/22) Pulse < 50 bpm (1/12/22)
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- The patient reported a syncopal episode in response to a vaccination once before.
- Staat
- -
- 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 / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fall
Nervousness
Syncope
Symptomtext
Within 10 minutes after receiving vaccine, while patient seated for observation, he passed out and fell on floor. Regained conscious in less than a minute. Patient stated he was just a little nervous and was ok after he regained consciousness but we called paramedics to ensure there ensure he was ok and if any injury. He refused the paramedics to go in for checkup to ED and stated that he was ok.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none reportedf=
- Vorgeschichte
- none reported
- Andere Medikamente
- -
- Allergien
- no known drug allergies
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 08.01.2022
- Impfdatum
- -
- Beginn
- 01.12.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Back pain
Feeling abnormal
Injection site pain
Presyncope
Tachycardia
Symptomtext
WEAKNESS/NO ENERGY; BACK PAIN; ARM PAIN AT INJECTION SITE; WEIRD FEELING LIKE AGONY; FEELING LIKE FAINTING; TACHYCARDIA; This spontaneous report received from a patient concerned a 35 year old female. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: None as per patient. The patient was previously treated with covid-19 vaccine ad26. cov2. s for prophylactic vaccination. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211D21A, and expiry: UNKNOWN) dose was not reported, administered on 03-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. On DEC-2021, the patient experienced tachycardia, weird feeling like agony, and feeling like fainting. On 03-DEC-2021, the patient experienced arm pain at injection site. On 04-DEC-2021, the patient experienced back pain. On 28-DEC-2021, the patient experienced weakness/no energy. Treatment medications (dates unspecified) included: meloxicam. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from back pain on 07-DEC-2021, had not recovered from tachycardia, weakness/no energy, and weird feeling like agony, and the outcome of arm pain at injection site and feeling like fainting was not reported. This report was non-serious.; Sender's Comments: V0: Medical assessment comment not required as per standard operating procedure as the case assessed as non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: None as per patient
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 30,0
- 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
Fall
Syncope
Symptomtext
Patient said he fell and fainted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- N/A.
- Aktuelle Erkrankungen
- Anxiety
- Vorgeschichte
- Anxiety
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 30,0
- Geschlecht
- F
- 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: unbekannt
Blood glucose normal
Blood pressure decreased
Feeling hot
Hyperhidrosis
Loss of consciousness
Unresponsive to stimuli
Symptomtext
Patient Passed out multiple times became sweaty hot and unresponsive. Lasted for 4-5 minutes before patient recovered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- EMS was called they checked BP/Pulse BP I saw on maching was ~90/60 BG was checked and was 118mcg/dl at around 11:30 am 1/6/21
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- HX Thyroid Cancer
- Andere Medikamente
- Levothyroxine, liothyronine
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 02.01.2022
- Impfdatum
- 02.01.2022
- Beginn
- 02.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Presyncope
Symptomtext
Patient experienced light-headedness and almost fainted
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 02.01.2022
- Impfdatum
- 02.01.2022
- Beginn
- 02.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Fall
Syncope
Symptomtext
The patient received his first dose of the Janssen Covid 19 vaccine and was instructed to stay sitting in the same chair for observation by the pharmacist for 15 minutes. After approximately 1 to 2 minutes they patient fainted and fell off of the chair to the ground. The pharmacist got to the patient and checked that they were breathing and had a pulse. Another person nearby was instructed by the pharmacist to call 911. The patient was now alert and sitting up. EMS arrived approximately 10 minutes later and transported the patient to a local hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 29.12.2021
- Impfdatum
- 29.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Condition aggravated
Fear of injection
Syncope
Symptomtext
PT FAINTED AFTER RECEIVING VACCINE. SHE DOES HAVE A HISTORY OF FAINTING AFTER SHOTS DUE TO FEAR OF NEEDLES SO THIS WAS NO SURPRISE TO HER OR MOM
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- FAINTING
- Staat
- RI
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 29.12.2021
- 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
Syncope
Vomiting
Symptomtext
A few minutes after administering the vaccine, patient slumped off of bench to floor then vomited a few minutes later. It appeared that she fainted but did not fully lose consciousness, she caught herself on hands and knees, and did not hit her head. She confirmed she did not eat before coming to the pharmacy for vaccine. She was monitored for 15-20 minutes after until all symptoms resolved. Recommended she report fainting history and eat before any future vaccines.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 29.12.2021
- Impfdatum
- 29.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syncope
Symptomtext
PATIENT HAD A VASOVAGAL SYNCOPE REACTION AFTER VACCINATION
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- -
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 29.12.2021
- Impfdatum
- 08.12.2021
- Beginn
- 10.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: ja
ER: unbekannt
Erholt: nein
Arthralgia
Blood test
Chest X-ray
Chills
Dizziness
Electrocardiogram
Fatigue
Headache
Neuralgia
Pruritus
Guillain-Barre syndrome
Hyperaesthesia
Hypoaesthesia
Magnetic resonance imaging abnormal
Muscular weakness
Myelitis transverse
Spinal cord disorder
Urinary retention
Symptomtext
Patient developed bilateral leg weakness, foot numbness, urinary retention, and abdominal hyperesthesia. MRI showed findings consistent with Guillan Barre Syndrome / transverse myelitis. He is currently being admitted to the hospital for further work up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Guillain-Barre syndrome
- Hospital-Tage
- -
- Labordaten
- Today: Subtle cord signal abnormality in the midthoracic spine with diffuse enhancement around the cauda equina. Given the rest of the history, findings are suggestive of postvaccinal transverse myelitis and Gillian Barre syndrome.
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- SITUS INVERSUS ALLERGIC RHINITIS
- Andere Medikamente
- SINGULAIR CLARITIN ALLERGY SHOTS
- Allergien
- METHYLPREDNISOLONE SULFA
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 29.12.2021
- Impfdatum
- 08.12.2021
- Beginn
- 10.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: ja
ER: unbekannt
Erholt: nein
Arthralgia
Blood test
Chest X-ray
Chills
Dizziness
Electrocardiogram
Fatigue
Headache
Neuralgia
Pruritus
Guillain-Barre syndrome
Hyperaesthesia
Hypoaesthesia
Magnetic resonance imaging abnormal
Muscular weakness
Myelitis transverse
Spinal cord disorder
Urinary retention
Symptomtext
Patient developed bilateral leg weakness, foot numbness, urinary retention, and abdominal hyperesthesia. MRI showed findings consistent with Guillan Barre Syndrome / transverse myelitis. He is currently being admitted to the hospital for further work up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Guillain-Barre syndrome
- Hospital-Tage
- -
- Labordaten
- Today: Subtle cord signal abnormality in the midthoracic spine with diffuse enhancement around the cauda equina. Given the rest of the history, findings are suggestive of postvaccinal transverse myelitis and Gillian Barre syndrome.
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- SITUS INVERSUS ALLERGIC RHINITIS
- Andere Medikamente
- SINGULAIR CLARITIN ALLERGY SHOTS
- Allergien
- METHYLPREDNISOLONE SULFA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 23.12.2021
- Impfdatum
- 23.12.2021
- Beginn
- 23.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dizziness
Head injury
Loss of consciousness
Syncope
Symptomtext
Pt was given booster dose of Janssen vaccine and seasonal flu vaccine. Pt began to feel lightheaded and dizzy approximately 5 mintues after administration. When I went to check on patient, he fainted in the pharmacy's immunization booth. Patient briefly lost consciousness and denied any itching, swelling, difficulty breathing. Sat patient up and gave him water. Patient states began to feel a little better with water, but was still lightheaded and dizzy. Did not administer Benadryl or epinephrine due to patient denying anaphylactic symptoms. Patient hit forehead when he fainted, and EMS arrived approx 10 minutes after event started to evaulate patient. Patient was with significant other who denied any prior reaction to any vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- EMS evaluation 12/23/21 due to possible head injury. Result/status unknown
- Aktuelle Erkrankungen
- None known
- Vorgeschichte
- None known
- Andere Medikamente
- None known or reported
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 23.12.2021
- Impfdatum
- 22.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Fatigue
Syncope
Symptomtext
Patient fainted and regained consciousness in 45 seconds, did feel weak and fatigued. Patient left with a family member after feeling better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 22.12.2021
- Impfdatum
- 22.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syncope
Symptomtext
Patient fainted after vaccination
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- unknown
- Allergien
- none
- Vorherige Impfungen
- fainting
- Staat
- KY
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 21.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hyperhidrosis
Loss of consciousness
Retching
Syncope
Symptomtext
Pt had syncopal episode about 5 minutes after receiving vaccine. Pt was sweating and dry heaving for a couple of minutes before briefly losing consciousness. Pt recovered and was fine within about 10 minutes. Pt stated the same thing happens when he gives blood.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- BP taken. result was 113/89.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 20.12.2021
- Impfdatum
- 20.12.2021
- Beginn
- 20.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Anaphylactic reaction
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anaphylactic reaction
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 20.12.2021
- Impfdatum
- 20.12.2021
- Beginn
- 20.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Syncope
Symptomtext
Patient fainted after vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 17.12.2021
- Impfdatum
- 17.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dizziness
Syncope
Unresponsive to stimuli
Symptomtext
Patient stated he has fainted before with vaccines & blood draws prior to him receiving the J&J vaccine. After I gave him the vaccine, he asked me if he could lay down on the ground because he was feeling lightheaded. I kept the pharmacy door open so we can monitor him while he was on the ground. He was doing fine until he decided to get back up after about 5 minutes to have a seat outside our waiting room. Less than a minute after he sat down on the chair, patient fainted on the chair. I ran outside to try to wake him up & told my technicians to call EMT. Patient wasn't responsive for about 1-2 minutes, EMT arrived about 5-10 minutes later. Patient refused to go to hospital and had a family member / friend drive him home. Patient was advise by EMT to call them if anything else happens after getting home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- no known allergies
- Vorherige Impfungen
- patient stated he has fainted with prior vaccinations (example he gave me was the flu shot a few years ago).
- Staat
- CO
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 17.12.2021
- Impfdatum
- 17.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Altered state of consciousness
Asthenia
Condition aggravated
Hyperhidrosis
Hypotonia
Pallor
Respiration abnormal
Seizure
Syncope
Unresponsive to stimuli
Symptomtext
Immediately (within five seconds or less) after intramuscular injection in the left deltoid the patient experienced syncope and then rapidly fell into whole body convulsions. Patient was unresponsive to my voice or touch for about twenty seconds during which I held his wrist to be ready to lower him to the floor gently if necessary as the convulsions slowly subsided. He was then briefly able to rouse himself to track my face with his eyes, then lapsed back into syncope with lack of muscle tone and a heavy deep breathing. The patient was steady in his chair, though in a slightly awkward position, so I allowed him perhaps thirty seconds or a minute for him to recover. After a time I snapped my fingers at him and he immediately roused enough to sense his situation, but was not fully conscious. He held his finger up indicating that he needed a moment. After another minute or so I addressed him and he was able to open his eyes and reply. He appeared pale, sweaty, and weak but present. I confirmed he did not feel he was in immediate danger and he told me that incidents like this were common for him, and that he would be fine. I found him some orange juice and a bag of frozen peas nearby, and allowed him ten or fifteen minutes alone in the shot room to recover, checking on him every few minutes. After a time he put his sweater back on and seemed steady. He confirmed that he was experiencing no symptoms of hives or swelling in the throat. He remained in the store for five minutes or so then left.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- Patient reported that the reaction was common after prior injections.
- Staat
- CA
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 14.12.2021
- Impfdatum
- 14.12.2021
- Beginn
- 14.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Face injury
Rhinalgia
Skin abrasion
Syncope
Symptomtext
The patient has a history of anxiety and passing out with vaccinations. The patient did not tell us she had this type of reaction to vaccinations in the past. The technician, administered the Janssen COVID-19 vaccination to the patient. The patient sat down in the observation area. 5 minutes later, she notified the pharmacy staff that she may have fainted in her seat. She has a couple of abrasions on her face and felt soreness in her nose. She was given water and orange juice and rested in the observation area for another 30 minutes. She said she felt fine and went home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- The patient has a history of passing out with vaccinations.
- Staat
- OR
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 12.12.2021
- Impfdatum
- 12.12.2021
- Beginn
- 12.12.2021
- 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
Hypophagia
Pallor
Presyncope
Skin warm
Symptomtext
Patient states that he felt light headed and near syncopal. Onset immediately after having received vaccination to LT deltoid. Vital signs were assessed by medics on site standby. Patient appeared diaphoretic, pale and warm . Patient states he does not have medical HX, NKA, last oral intake was yesterday, unknown time. Patient denies use of paraphernalia, no medication taken prior to vaccination. Vital signs Pulse 56, SPO2 97%, BP 86/palp. No interventions performed. Fire/rescue was called to site to further assess patient. After approximately 10 minutes, patient states he started to feel better and refused assistance/transportation by EMS. Last set of vital signs BP 110/78, P 58, SPO2 100%. Patient regained normal color, skin warm and dry. Patient was kept an additional 15 minutes for observation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- NA/
- Allergien
- NA
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 26,0
- Geschlecht
- F
- 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: unbekannt
Syncope
Symptomtext
patient fainted about 1 minute after administration, came around a minute or 2 later, and left feeling fine about 15 minutes after that
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 29,0
- 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: ja
Erholt: nein
Loss of consciousness
Syncope
Tremor
Symptomtext
patient fainted twice and lost consciousness twice for about 15 seconds. upon 2nd fainting episode, started having full body shakes/possible seizure
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- unknown
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- patient stated no known allergies
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 52,0
- 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: ja
Erholt: nein
Loss of consciousness
Symptomtext
after 10 minutes patient had loss of consciousness with spontaneous recovery evaluated by telehealth physician and sent to ED at hospital in stable condition for further monitoring and testing as needed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- to be done
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 21,0
- Geschlecht
- F
- 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
Depressed level of consciousness
Disorientation
Dizziness
Hypoacusis
Syncope
Vision blurred
Symptomtext
Patient sat down after receiving a booster dose of Janssen. She began feeling dizzy and light headed with blurry vision and muffled hearing. Patient stood up to ask for water and fainted. She became alert and oriented a few seconds later. Vital signs were stable, and she was able to stand up and walk to the treatment area. She laid down on the cot for approx. 15 minutes and was given water and juice. She recovered and left the clinic. Of note, the patient had not eaten anything since 9:00PM the previous night.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Methylphenidate daily, Rizatriptan as needed
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 08.12.2021
- Impfdatum
- 05.11.2021
- Beginn
- 30.11.2021
- Tage bis Beginn
- 25,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bell's palsy
Facial paralysis
Symptomtext
Bell's Palsy occurred 4 weeks after J&J vaccine. Nonfunctioning left side of mouth PREDNISONE 60 mg q d x 7 days
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bell's palsy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Type 2 diabetes mellitus - Onset: 03/21/2019 Mixed hyperlipidemia - Onset: 01/05/2020 Obesity - Onset: 07/26/2021 Obstructive sleep apnea syndrome - Onset: 01/01/2020 Paroxysmal atrial fibrillation - Onset: 01/16/2020 Chronic systolic heart failure - Onset: 01/01/2020 History of myocardial infarction - Onset: 01/16/2020 Stented coronary artery - Onset: 01/16/2020 - x3
- Andere Medikamente
- Xarelto 20 mg tablet metoprolol tartrate 25 mg tablet metFORMIN ER 500 mg tablet,extended release 24 hr atorvastatin 40 mg tablet aspirin 81 mg tablet,delayed release
- Allergien
- No Known Drug Allergies venom-wasp allergy (facial swelling, moderate)
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 06.12.2021
- Impfdatum
- 21.11.2021
- Beginn
- 21.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Seizure
Symptomtext
Patient presented for administration of his first Janssen and Janssen vaccine. After receiving his vaccine, he was sitting in his wheelchair in the waiting area when he started seizing. It is not clear how long after vaccine administration he started seizing. The patient?s mother, informed me that he has chronic recurrent seizures. She reported that he usually experiences about 10 seizures per day. She reported that he had been seizing for more than 4 minutes when she called me to provide help. I attempted to take his blood pressure without success due to seizure activity. I noticed that he was receiving oxygen though a nasal cannula, so I noted his oxygen saturation, which was 100% at the time of seizure. I called for the rapid response team, who transferred him to the ER for evaluation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Per medical record review: central sleep apnea syndrome, history of left localization-related focal partial epilepsy, neuromuscular disease, impaired cognitive ability, mood disorder, dysphagia, history of essential hypertension in the past, prior diagnosis of autism, incomplete bladder emptying, constipation, cerebral, anoxia at birth, spastic, cataplexy, dysfunctional voiding of urine, oxygen dependent, wheelchair bound, neurogenic bladder.
- Andere Medikamente
- -
- Allergien
- Per medical record: "antieleptics: severe depression" Divalproex: mental status changes Lamotrigine: rash Oxcarbazepine: Mental status changes
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 05.12.2021
- Impfdatum
- 05.12.2021
- Beginn
- 05.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Loss of consciousness
Symptomtext
Patient was nervous prior to receiving the vaccination. Patient sat down in a chair to wait 15 minutes and about 2 minutes later he passed out cold in the chair.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 01.12.2021
- Impfdatum
- 01.12.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood pressure increased
Condition aggravated
Gaze palsy
Musculoskeletal stiffness
Posture abnormal
Seizure
Syncope
Tremor
Vomiting
Symptomtext
The patient was waiting in the waiting room for her 15 minute reaction time. Her father gave her a bottled water to drink and she drank a few sips of water, then she bent over to start vomiting. I ran to her with a garbage can. Then, she started to faint with her eyes rolled back and all of her limbs became stiff. We immediately called 911. We gently placed her on the ground from her chair and raised her legs. Her body began to have tremors like a seizure and her neck bent backwards, then we offered an epi pen injection, but her father refused. She started talking again and we took her blood pressure. It was elevated. Then, the paramedics arrived and they started to treat her and monitor her vitals. After their assessment and cleared her to go home, they offered to take her to the ER, but she refused to go to the hospital. Her father told me that she fainted with her first dose of Janssen back in April at a different pharmacy and along with other vaccines; however, the patient lied on the pre-screening questions about reactions to vaccines and did not inform the immunizer. She only stated that she is afraid of needles. The patient decided to go home and the paramedics released her as their patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- The paramedics provided treatment for the patient. They checked and monitored her vitals until she was stable.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 30.11.2021
- 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: unbekannt
Erholt: nein
Loss of consciousness
Nausea
Symptomtext
Patient was given the vaccine and shortly after passed out, she was passed out for approximately 5-10 seconds before waking up and being responsive. Emergency was notified as soon as possible and EMS was sent to the pharmacy. While waiting to EMS, Patient was responsive stating she was nauseous and was given a plastic bag and a water from the store. As time went on she was more responsive and talking a bit more. Store pharmacist and store manager stood with patient and boyfriend waiting for EMS. EMS showed up approximately 10 minutes after phone call and assessed patients vital signs and did their eval. She was taken by EMS out to the ambulance for further evaluation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 30.11.2021
- 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
Feeling hot
Presyncope
Symptomtext
After receiving vaccination, patient had vaso-vagal episode. Continued to feel dizzy, nauseous, and hot afterwards. Was able to tell staff where she was and what her name was.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Seasonal cold within last week
- Vorgeschichte
- NO
- Andere Medikamente
- Oral Birth Control
- Allergien
- Amoxicillin, seasonal allergies
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 29.11.2021
- Impfdatum
- 01.11.2021
- Beginn
- 29.11.2021
- Tage bis Beginn
- 28,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Adverse reaction
Dyskinesia
Eye movement disorder
Flushing
Foaming at mouth
Hyperhidrosis
Seizure
Syncope
Symptomtext
At 3:20pm, the patient received his Janssen Covid shot and sat in the post vaccination area afterwards. At 3:23pm, another patient witnessed the patient moving strangely and noticed something was wrong with the patient, so she called out for assistance. Pharmacy technician heard the other patient and responded by asking a Pharmacist to assist a patient who is having an adverse reaction. I was the Pharmacist that responded to the incident. I grabbed the immunization caddy that contained the epi=pen and ran over to the patient. I witnessed the patient eyes rolling back, his body jerking, and the patient was foaming in the month. I asked the technician to call 911 and the other Pharmacist on duty to call code white. As I was talking to the Pharmacist and Technician, the patient began jerking violently and the other patient tried to help the patient down on the floor because she thought he patient was having a seizure. Once the patient was on the floor, I immediately tried to assess whether he was having a true allergic reaction but his symptoms seem similar to fainting therefore, a epi pen was not necessary. A few moments later the patient came to it and sat up. He was sweating and flushed but he was responsive. We gave the patient water and an ice pack, and waited for the ambulance to arrive. The ambulance arrived 30 mins later and checked the patient's vitals. All vitals were normal and that patient refused to be taken to the hospital. The Paramedic thought the patient had Vago down symptoms which is similar to fainting but can present like a seizure. The patient left shortly after he was checked by the paramedics. The patient does not have any medical conditions or a history of allergies to medications. The patient needed the covid shot for work. The patient was nervous about receiving his Covid shot which may have resulted in the adverse reaction he had to the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- No
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OH
- 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 / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Epilepsy
Fall
Malaise
Seizure
Syncope
Tremor
Symptomtext
Patient received his first dose of JANSSEN COVID19 vaccine at approx. 10:10 am this morning. He was seated in the pharmacy waiting area per post-vaccination protocol. Within about 5 minutes of receiving his dose, the patient fainted from the seated position, fell to the floor and within about a minute of fainting, started convulsing on the floor in what appeared to be an epileptic episode. The seizing lasted <2 minutes and the patient came to thereafter but was feeling ill, shaky, chills for at least 30 minutes port-episode. The squad was called and evaluated the patient but he did not allow them to take him to the ED to be evaluated further.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 27.11.2021
- Impfdatum
- 24.11.2021
- Beginn
- 24.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Anaphylactic reaction
Symptomtext
Patient has told me prior to be vaccinated by her situation. She has stated that she has had an allergic reaction when taking the pfizer vaccine so her doctor recommended that she should take Janssen for her next shot. I've let my PA, know about her condition and to observe her while she was receiving the vaccine. Once injected, she had already started to develop anaphylaxis which the PA got the epi pen and injected her with it. The patient asked to be sent to the Emergency Room to be treated. Since our clinic was inside the hospital, I called in the hospital staff and they took her to the ER for further evaluation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anaphylactic reaction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Yes, she has had a severe allergic reaction towards the pfizer vaccine. Her doctor recommended to try with the Janssen vaccine instead which is why she came to our clinic.
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 30,0
- Geschlecht
- M
- 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
Cyanosis
Dizziness
Skin discolouration
Syncope
Symptomtext
dizziness, fainting, bluish discoloration of skin
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 23.11.2021
- 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
Dizziness
Fatigue
Nausea
Syncope
Tinnitus
Symptomtext
Patient felt nauseous and then fainted for a few seconds. She woke up with dizziness and ringing in her ears. I kept monitoring her. I asked her if she had any trouble breathing. Patient said she just felt tired, dizzy and had ringing in her ears. Her symptoms started to resolve after 5 minutes. She finally felt 100% better after about 20 minutes. She left home with her mom. She declined for us to call 911 because she said this happens most of the time when she gets shots.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 19,0
- 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
Disorientation
Fall
Nausea
Pallor
Syncope
Symptomtext
Patient received vaccine at 09:45 am, at 9:50 am he fainted and fell out of chair that he was seated in. Within seconds he recovered. He appeared pale, nauseous, disoriented briefly. His blood pressure at 10 am was 88/45. He drank some orange juice and put his head between legs. By 10:10 am his blood pressure was 117/74.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- "A shot a few years ago" Patient did not remember details
- Staat
- TX
- Alter
- 22,0
- Geschlecht
- F
- 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
Syncope
Symptomtext
Patient fainted briefly after getting the vaccine. The pharmacy called the paramedics. She became conscious a few minutes after and was fine. She did not go with the paramedics. I called her later in the day to check on her. She was fine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 22,0
- 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
Loss of consciousness
Syncope
Symptomtext
Pt received Janssen vaccine at 1404, pt felt lightheaded, sweating, and had syncope episode. 2 LVNS and 1 RN assisted pt until pt regained consciousness. Assisted pt to lie down in recumbent position. Ice pack, water and apple juice given. V/S done and WNL. Pt back to baseline with no complaints. Pt left at 1440.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- -
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 22.11.2021
- 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
Immediate post-injection reaction
Syncope
Unresponsive to stimuli
Symptomtext
PT FAINT IMMEDIATELY FOLLOWING ADMINISTRATION OF JANSSEN VACCINE. PT REPORTS FAINTING AFTER BLOOD DRAWS BUT NEVER WITH VACCINATIONS. CALLED 911, PT DID NOT WANT TO GO TO HOSPITAL FOR OBSERVATION. ONCE RESPONSIVE, HAD SIPS OF ORANGE JUICE AND WATER. STATED SHE WAS FEELING BETTER.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- PENICILLIN
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 22.11.2021
- Impfdatum
- 17.11.2021
- Beginn
- 17.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test normal
Computerised tomogram normal
Echocardiogram normal
Electrocardiogram normal
Gaze palsy
Hyperhidrosis
Scan with contrast normal
Seizure
Symptomtext
Recieved vaccine at 4pm At 408 pm Bystanders witnessed while seated in recovery room chair my arms fall to my side, head went back against the wall, eyes rolled back in my head but remained open, they said it looked like I hade a seizure. I was instantly profusely sweating from head to toe and had no real sense of where I was for 5-10 min. I was taken to the ER. And received a full cardiovascular checkup while I was held over night for observation. I was released from the hospital woth a clean bill of health cardiovascular wise with no answers on why I had a seizure at pharmacy. I contacted pharmacy a d they were uncooperative in completing this form or providing anything in writing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- 1,0
- Labordaten
- Ekg Ct Scan with contrast on heart Echo cardio Blood test
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Cheflex antibiotic Fish oil Cholest off Multivitamin one a day Focus factor
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 19.11.2021
- Impfdatum
- 12.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Hyperhidrosis
Nausea
Syncope
Symptomtext
PATIENT FELT LIGHT HEADED AND FAINTED AFTER GETTING THE SHOT AND WAS WALKING OUT OF THE EMS ROOM. PATEINT WAS SWEAT AND FELT NAUSEATED. PATIENT LAID DOWNAND USED COLD PACKS AND GAVE PATIENT A SNACK AND WATER. PATIENT FELT WELL AFTER A FEW MINUTES.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 17.11.2021
- 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: unbekannt
Erholt: unbekannt
Hyperhidrosis
Seizure
Syncope
Tremor
Symptomtext
patient had an episode of syncope (more like seizure), sweaty and shaky.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 17.11.2021
- Impfdatum
- 16.11.2021
- Beginn
- 17.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Loss of consciousness
Muscle twitching
Syncope
Symptomtext
after giving patient the vaccine, he sat at the waiting for a few minutes. then he starts to faint. and he was experiencing a little twitching of his extremities and lost conscience for a minute and regain it back. He was laying on the floor. rolled on to his side and then remained in the position and until the 911 crews came in.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- unaware.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 17.11.2021
- 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: ja
Erholt: ja
Hypotonia
Immediate post-injection reaction
Seizure
Symptomtext
Patient slumped immediately after injection then went into a seizure. He revived and EMS responded.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- Patient was taken to local hospital by EMS
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- -
- Geschlecht
- F
- Eingang
- 17.11.2021
- Impfdatum
- -
- Beginn
- 02.11.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anaphylactic reaction
Injection site pain
Injection site swelling
Symptomtext
ANAPHYLACTIC REACTION; PAIN ON LEFT ARM AT SITE OF INJECTION; MINOR SWELLING OF LEFT ARM AT SITE OF INJECTION; This spontaneous report received from a patient concerned a 68 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included allergic reactions to Penicillin and erythromycin, tetracycline, Streptomycin, sulfa, salmon, eggs, sensitivity to nuts, orange juice, anaphylaxis, non smoker, and non alcohol user and asthma other pre-existing medical conditions included: The Patient did not had history of drug abuse/illicit drug use. Patient not on any other medication at the time the adverse event started. Patient did not had illness at the time of vaccination and adverse event after any previous vaccination. Patient did not had pre-existing acute illness 30 days prior to vaccination, history of hospitalization in last 30 days, with cause. Patient did not had family history of any disease (relevant to vaccination) and allergy. Patient was not pregnant at time of vaccination and currently was not breastfeeding. The patient experienced achiness and tired when they received covid-19 vaccine ad26.cov2.s (Series 1) for prophylactic vaccination. The patient received covid-19 vaccine ad26.cov2.s (Series 2 Booster dose) (suspension for injection, route of admin not reported, batch number: 211D21A and expiry: UNKNOWN) dose was not reported, frequency one total, administered at left arm, on 02-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 02-NOV-2021 within 5 minutes of received the booster, the patient experienced anaphylactic reaction and pain on left arm site of injection and minor swelling on left arm site of injection .The patient experienced coughing non stop, it was more a reaction and not exposure to something therefore the patient took a dose of rescue inhaler pro air and did not tell the pharmacy staff as the patient did not want to give epi-pen or the ambulance to be called. The patient waited in the pharmacy for 15 minutes then went to a store and realized that face felt hot, as prone to allergic reactions and anaphylaxis so went home and took liquid Benadryl (4 doses). The patient experienced swollen face red and hot and had a post nasal type drip type reaction (difficulty breathing). The patient was much better and it was about an hour and 10 minutes. The patient only had a little achiness and felt tired after the original dose, patient received (Series 1) on 11-MAR-2021, lot number was 1802072 and it was also administered on left arm. Treatment medications included: salbutamol sulfate. The action taken with covid-19 vaccine ad26.cov2.s was not applicable The patient recovered from anaphylactic reaction ,Pain on left arm at site of injection, and minor swelling of left arm at site of injection. This report was serious (Other Medically Important Condition). This case, involving the same patient is linked to 20211122735.; Sender's Comments: V0: 20211106318-covid-19 vaccine ad26.cov2.s-anaphylactic reaction. This event(s) is labeled per regulatory authority and is therefore considered potentially related.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anaphylactic reaction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Abstains from alcohol; Allergic reaction; Anaphylaxis; Asthma; Non-smoker
- Vorgeschichte
- Medical History/Concurrent Conditions: Food allergy (salmon, eggs, sensitivity to nuts, orange juice); Comments: The Patient did not had history of drug abuse/illicit drug use. Patient did not had history of drug abuse/illicit drug use. Patient not on any other medication at the time the adverse event started. Patient did not had illness at the time of vaccination and adverse event after any previous vaccination. Patient did not had pre-existing acute illness 30 days prior to vaccination, history of hospitalization in last 30 days, with cause. Patient did not had family history of any disease (relevant to vaccination) and allergy. Patient was not pregnant at time of vaccination and currently was not breastfeeding.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 40,0
- 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: ja
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Bradykinesia
Dizziness
Dyspnoea
Eye movement disorder
Fall
Feeling hot
Hypotonia
Increased bronchial secretion
Loss of consciousness
Moaning
Pallor
Unresponsive to stimuli
Symptomtext
APPROXIMATELY 5 MINUTES AFTER RECEIVING JANSSEN VACCINE, PATIENT REPORTED FEELING FAINT AND ASKED TO HAVE A SEAT IN THE OBERSERVATION AREA. PATIENT WAS MOVED TO OBSERVATION AREA, WAS INITIALLY SEATED, THEN WAS LAID ON THE FLOOR WITH FEET ELEVATED. PHARMACIST REMAINED TALKING TO PATIENT FOR APPROXIAMTELY 5 ADDITIONAL MINUTES. PATIENT DRANK A SPRITE WHILE TRYING TO RECOVER FROM FEELING FAINT. PATIENT THEN SAT UP TO TALK TO HIS WIFE AND FELL BACK LOSING CONSCIOUSNESS. WITHIN SECONDS AFTER LOSING CONSCIOUSNESS, PATIENT BEGAN GROANING/MAKING GARGLING SOUNDS AND GASPING FOR AIR AND SLOWLY MOVING APPENDAGES. 911 WAS CALLED. AFTER 5-10 SECONDS PATIENT WENT COMPLETELY LIMP AND UNRESPONSIVE. PATIENT LOST ALL COLOR AND EYES WERE OPEN BUT ROLLED BACK INTO THE HEAD. PHARMACIST ADMINISTERED EPIPEN. WITHIN 15 SECONDS OR SO, PATIENT REGAINED CONSCIOUSNESS AND TRIED TO SIT UP ASKING WHAT HAPPENED. PATIENT REPORTED FEELING HOT AND LIGHT HEADED. FIRE TRUCK ARRIVED LESS THAN FIVE MINUTES LATER. PATIENT WAS MOVED TO A SITTING POSITION AND RECOVERED AFTER APPROXIMATELY 10 TO 15 MINUTES AND LEFT THE PHARMACY STATING HE FELT BETTER.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 12.11.2021
- Impfdatum
- 12.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pruritus
Syncope
Symptomtext
Passed out from vasovagal syncope after 15 minutes with itching on arm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Panic attack disorder
- Andere Medikamente
- Zoloft, Ativan
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 10.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Condition aggravated
Confusional state
Fall
Fear of injection
Heart rate decreased
Hyperhidrosis
Mydriasis
Syncope
Symptomtext
PATIENT HAD A FAINTING SPELL SECONDS AFTER THE SHOT GIVEN. HE FELL OUT OF THE CHAIR, APPEARED CONFUSED, DIAPHORESIS, MYDRIASIS, LOW PULSE RATE 30 SECONDS PER MINUTE, THAT LASTED MAYBE A MINUTE OR 2 MINUTES AT MOST. AFTER THE PATIENT CAME THROUGH FROM THE SPELL, HE CONTINUED TO TELL ME THAT THIS HAPPENS WHENEVER HE GIVES BLOOD OR OTHER VACCINES. PRIOR TO THE SHOT, ALL HE SAID IS THAT HE IS AFRAID OF NEEDLES. DUE TO THE CONFUSION AND THE BRIEF MOMENTS WHERE HE WAS NOT WITH IT, I HAD MY TECHNICIAN CALL 911 OUT OF ABUNDANCE OF CAUTION. WHEN EMS ARRIVED, HE WAS COMPLETELY FINE AND DRINKING WATER AND CONVERSING FULLY.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- NA
- Allergien
- NA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 08.11.2021
- Impfdatum
- 08.11.2021
- Beginn
- 08.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cold sweat
Dizziness
Flushing
Hyperhidrosis
Immediate post-injection reaction
Loss of consciousness
Nausea
Pallor
Syncope
Thirst
Symptomtext
IMMEDIATELY AFTER VACCINATION, PT SEEMED TO ALMOST LOSE CONSCIOUSNESS OR FAINT. VASOVAGAL SYNCOPE / DIZZINESS, FLUSHED/PALE, CLAMMY SKIN, NAUSEA, PROFUSE SWEATING, THIRST, NEEDED TO LAY DOWN ON GROUND. THIS LAST FOR AROUND 15 TO 20 MINUTES, PT THEN LEFT STORE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- UNKNOWN
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 06.11.2021
- Impfdatum
- 06.11.2021
- Beginn
- 06.11.2021
- 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 30-60 seconds after administration of the vaccine. Did not fall, was lowered to the floor and came to quickly. Sat on the floor for a few minutes, then moved to a chair. Left 15 minutes later with his spouse stating he was fine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 05.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Fall
Head injury
Skin laceration
Syncope
Symptomtext
The patient fainted approximately 1-2 mins after administration of the vaccine, fell out of the chair he was sitting in and hit his head on the floor causing a laceration that needed medical attention.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- none
- Andere Medikamente
- unknown
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 26,0
- 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
Blood glucose
Blood pressure measurement
Fall
Fatigue
Hyperhidrosis
Loss of consciousness
Syncope
Symptomtext
Patient fell out of chair while waiting 15 minutes for monitoring after vaccination. He was unconscious for less than a minute. I checked for pulse which was present along with breathe sounds. He proceeded to gain consciousness and sat in a chair. He was coherent but tired and started sweating. We called EMS who checked him out and stated he had vasovagal syncope. The patient left on his accord after EMS left.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- Blood Pressure and glucose test by EMS
- Aktuelle Erkrankungen
- Headache and upset stomach
- Vorgeschichte
- None
- Andere Medikamente
- N/A
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 02.11.2021
- Impfdatum
- 02.11.2021
- Beginn
- 02.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Loss of consciousness
Symptomtext
I passed out about 30 seconds (according to physician) after the injection. 911 was called and arrived on site to take my vitals and check to see if I needed to be taken to the hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Starbucks Creamer (sold in stores)
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 01.11.2021
- Impfdatum
- 01.11.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Lethargy
Presyncope
Symptomtext
Patient experience lethargy, weakness, and vasovagal episode following booster vaccine (Janssen) at 10:20 AM. Vital signs initiated, legs elevated, PO fluids given, ice pack provided. Patient was observed for 40 additional minutes, minimal change in mental status, patient followed commands with spouse present. Patient verbalized feeling better at 11:00 AM than initial assessment. EMS activated for further assessment. Patient left via EMS ambulatory and accompanied by spouse at 11:22AM. Patient transferred to hospital per spouse request.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 29.10.2021
- Impfdatum
- 29.10.2021
- Beginn
- 29.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Nausea
Seizure
Vomiting
Symptomtext
Seizure, followed by nausea, vomiting
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 29.12.2023
- Impfdatum
- 10.11.2021
- Beginn
- 22.11.2023
- Tage bis Beginn
- 742,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Back pain
Blood thyroid stimulating hormone increased
COVID-19
Chest X-ray normal
Chronic obstructive pulmonary disease
Chronic respiratory failure
Condition aggravated
Cough
Dyspnoea
Hypertension
Hypothyroidism
Limb injury
Pain
Pain in extremity
SARS-CoV-2 test positive
Tobacco user
Symptomtext
Patient is a 68 y.o. female patient of No primary care provider on file. with a history of shortness of breath Discharge Diagnoses: 1. Covid-19 Virus Infection Date of onset of symptoms: 11/20/23 Symptoms present on admission: cough, SOB, leg pain, back pain Date of covid positive test: 11/22/23 Vaccination status: vaccinated once with J&J Imaging: 11/22/23: CXR: nothing acute Oxygen requirements on admission: 2 L NC Current oxygen requirements: 2 L NC per home regimen Medical therapy: steroids started 11/23/23 Consultants following: not at this tiime Anticipated special isolation end date: 11/30/23 2. COPD exac 3. Chr resp failure; wears 2 L NC at home 4. Current smoker For the above - duoneb tx q 6 hrs - goal o2 sat is 88-92 % - routine VS with pulse ox checks - encourage smoking cessation 5. Hypothyroid - July TSH 5.16 - will cont synthroid 75 mcg daily while here 6. Chr pain syndrome - will cont home Lyrica and Mobic while here 7. HTN - will cont home Norvasc while here - July 2023 normal STT 8. Multiple wounds left hand - left thumb, index, and middle fingers all with various wounds. Do not appear infected. Keep dressed with gauze. Patient presented to hospital with shortness of breath on November 22. As she has known COPD and is supposed to wear 2 L of oxygen at home although she reports that she does not even use it at night. She was found to be COVID-positive. Has previously been vaccinated. Was initiated on dexamethasone. Patient currently is doing well on 2 L here. Does states she is uncertain of the oxygen she has set up home will consult care management to make sure that patient can get her 2 L continuous and discussed the importance of using this. Patient feels back to her baseline and is requesting discharge. Is to follow-up closely outpatient with primary care.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- 6,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 05.05.2023
- Impfdatum
- 07.02.2022
- Beginn
- 23.03.2023
- Tage bis Beginn
- 409,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Bacterial disease carrier
Bacterial infection
Bronchial secretion retention
Bronchoscopy abnormal
COVID-19
COVID-19 pneumonia
Condition aggravated
Cystic fibrosis
Enterovirus infection
Fatigue
Infection
Laboratory test abnormal
Night sweats
Pneumonia
Rhinovirus infection
SARS-CoV-2 test positive
Sputum culture positive
Stenotrophomonas test positive
Symptomtext
Discharge Provider: MD Primary Care Provider: MD Admission Date: 3/23/2023 Discharge Date: 3/28/23 PRESENTING PROBLEM: Cystic fibrosis [E84.9] Status post lung transplantation [Z94.2] COVID [U07.1] Pneumonia due to COVID-19 virus [U07.1, J12.82] HOSPITAL COURSE: 47 yo s/p double bilateral lung transplant 1/11/1993, ESRD post renal transplant 1998, PTLD, right bronchial stenosis, bronchiectasis, recurrent pneumonia (stenotrophomonas, pseudomonas, and MSSA) , recent rhino-enterovirus pneumonia Jan 2023, presented to ER with one week of worsening wheezing, fatigue, and night sweats. Did not have increased cough, sputum production, or hypoxemia. ER workup found RLL PNA and film array + COVID 19. He was admitted for treatment. Pt given a 5 day course of remdisivir. He was also treated for suspected secondary bacterial infection, initially with Doxycycline to cover his hx of MSSA then extended to minocycline that is sensitive to the stenotrophomonas he is colonized with (and grew on sputum). He developed worsening secretion retention once admitted therefore bronchoscopy was completed morning of discharge, moderate mucus plugging identified and BAL cultures pending . He overall was feeling well and discharged 3/28/23 with instructions to follow up with local pulmonary clinic and transplant clinic.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19 pneumonia
- Hospital-Tage
- 5,0
- Labordaten
- -
- Aktuelle Erkrankungen
- 1/22/2022 - 1/29/2022 (7 days) Hospital PRESENTING PROBLEM: Pneumonia [J18.9]
- Vorgeschichte
- Cystic fibrosis Kidney replaced by transplant Lung transplant status, bilateral Other osteoporosis without current pathological fracture Chronic sinusitis Essential hypertension History of renal cell cancer PTLD (post-transplant lymphoproliferative disorder) Immunocompromised Small cell B-cell lymphoma Diabetes mellitus related to CF (cystic fibrosis) Mittendorf dot Myopia of both eyes Stage 3b chronic kidney disease Abnormal CT scan of lung Bronchial stenosis Pancreatic insufficiency due to cystic fibrosis Hyperparathyroidism due to renal insufficiency Status post kidney transplant Recurrent pneumonia Dry eyes, bilateral H/O nocardiosis Rash of groin Bronchiectasis without complication CAP (community acquired pneumonia) due to Chlamydia species Dyspnea COVID Infection due to multidrug-resistant Stenotrophomonas maltophilia
- Andere Medikamente
- acetaminophen (TYLENOL) 500 MG tablet albuterol (PROVENTIL) (2.5 MG/3ML) 0.083% nebulization albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler Alcohol Swabs (ALCOHOL PREP) PADS azithromycin (ZITHROMAX)
- Allergien
- Avelox [Moxifloxacin Hcl In Nacl]Dizziness Contrast Dye [Ivp Dye, Iodine Containing]Hives Flagyl [Metronidazole]Nausea and Vomiting, Headache LevaquinNausea Only, Dizziness AmlodipineDizziness CiprofloxacinEdema Keflex [Cephalosporins]Edema Miacalcin [Calcitonin]Itching
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 09.03.2023
- Impfdatum
- 17.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain
Paraesthesia
Paraesthesia oral
Swollen tongue
Symptomtext
1 HR AFTER RECEIVING THE J&J COVID-19 VACCINE PATIENT STARTED FEELING TINGLING IN LIPS. IT PROGRESSED THROUGH THE DAT TO TINGLING DOWN THE ARMS, LIP AND TONGUE SWELLING AND ABDOMINAL PAIN. PATIENT CALLED TO REPORT THE ADVERSE EVENT AT 10AM ON 18/18/2021 AND INDICATED HE DID NOT TAKE ANYHTING AND REMAINED AT HOMW, HE INDICATED HE THOUGHT THE SWELLING WAS GOING DOWN BUT COULD STILL FEEL HE WAS NOT BACK TO NORMAL. PATIENT WAS INSTRUCTED TO NOTIFY HIS PCP, TAKE BENADRYL AND CALL EMS IF EMERGENT SYMPTOMS PRESENTED (SOB, CHEST PAIN, SEVERE SWELLING). PATIENT WAS ALSO INSTRUCTED TO GO TO URGENT CARE IF SYMPTOMS DO NOT GET BETTER OR THEY GET WORSE BY THE AFTERNOON.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- ZYRTEC, TOPIRAMATE
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 01.03.2023
- Impfdatum
- 29.11.2021
- Beginn
- 09.02.2023
- Tage bis Beginn
- 437,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute kidney injury
COVID-19
Chest X-ray normal
Fatigue
Hypophagia
Hypotension
Malaise
Metabolic acidosis
SARS-CoV-2 test positive
Symptomtext
Patient admitted for fatigue and AKI thought to be due to COVID infection and poor oral intake. She was started on IVF hydration with resolution of AKI. Patient remains on room air without resp symptoms of COVID. She is stable for discharge home an encouraged to increase oral intake and ensure hydration. Clinical Summary Assessment and Plan Patient is a 66 y.o. female patient of DO with history of mitral regurgitation status post mitral valve replacement, valvular atrial fibrillation, hyperlipidemia, anxiety, hypothyroidism, hypertension, GERD, and CKD stage III. She is admitted as a transfer from freestanding for AKI and fatigue in the setting of recent COVID diagnosis. AKI-resolved Metabolic acidosis-resolved Suspect most likely prerenal in the setting of COVID-19 and decreased intake. Continue IV fluids-change to bicarb infusion Avoid nephrotoxins Held home hydrochlorothiazide and lisinopril S/P IVF Covid-19 Virus Infection Date of onset of symptoms: 2/5/2023 Symptoms present on admission: Malaise Date of covid positive test: 2/6/2023 Vaccination status: Only received Johnson & Johnson vaccine Imaging: Chest x-ray 2/9/2023 unremarkable Oxygen requirements on admission: None Current oxygen requirements: None Medical therapy: Not indicated Anticipated special isolation end date: 2/14/2023 Hypertension Held home lisinopril and hydrochlorothiazide in the setting of AKI Held home diltiazem in the setting of soft BPs on admission and poor intake Continue home metoprolol Restart BP meds when able DC back on home meds Mitral valve insufficiency status post replacement Valvular atrial fibrillation Continue home Coumadin (takes 3 mg daily) INR goal 2.5-3.5, pharmacy to dose Continue home metoprolol and holding home diltiazem as above GERD Continue PPI Hypothyroidism Continue home Synthroid
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Back pain
Blood urine present
Heavy menstrual bleeding
Hyperhidrosis
Mobility decreased
Pain
Pain in extremity
Pyrexia
Tinnitus
Symptomtext
Started having the same problems I had after the 1st and 2nd dose, this time the reactions were a little milder; Within hours after vaccine started getting arm pain, sweating; started feely achy and began urinating blood; For the next 2 days I stayed in bed and had a fever, chills and lower back pain where my kidneys are; Also started to have a ringing in my ears; After first day in bed I started having severe joint pain, it got progressively worse with time; I couldn't close my hand all the way, not able to hold onto anything; The joint pain slowly got a little better; Returned to work, though ringing in my ears never subsided; The next month I got a really heavy period for 2 weeks.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- ZOLOFT; multivitamin
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 05.01.2023
- Impfdatum
- 07.02.2022
- Beginn
- 10.02.2022
- Tage bis Beginn
- 3,0
- Dosis
- 2
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Aphasia
Arthralgia
Blood follicle stimulating hormone normal
Blood iron decreased
Blood luteinising hormone normal
Blood test
Blood testosterone decreased
Cognitive disorder
Condition aggravated
Decreased appetite
Epstein-Barr virus antibody positive
Glycated albumin increased
Head discomfort
Headache
Iron binding capacity total decreased
Joint noise
Low density lipoprotein increased
Malaise
Symptomtext
Problems (report below is from what I've said to a doctor and some blood tests). The only thing missing is Parasthesias that I had for 3 months after the vax. Elevated EBV antibody titer R76.0 (796.4): Onset Date: 07/26/2022 Elevated LDL cholesterol level E78.00 (272.0):Onset Date: 07/26/2022, with elevated Glyca A Low iron E61.1 (280.9):Onset Date: 07/26/2022 Low testosterone in male R79.89 (790.99): Onset Date: 07/26/2022, normal LH & FSH Low TIBC Heart palpitations R00.2 (785.1):Chronic, Poorly Controlled, Onset Date: 03/01/2022, sensation increased in frequency over past month. Observed HR 80-90s during events Occured when active and on an airplane Sitting or walking slower helps Vision changes H53.9 (368.9): Acute, Unstable, Onset Date: 03/08/2022, Initally right eye, then left eye. Blurry vision, occurs intermittantly Opthalitrist review in past 4 months w/ no changes to prescription of prescribed corrective lenses BMI 27.0-27.9,adult Z68.27: H/O sleep disturbance Z87.898 (V13.89): Acute, Well Controlled, Onset Date: 02/11/2022, emerged s/p 2nd J&J vaccine has subsided since beginning low-inflammation diet Informs sleeps 5 hr / night Muscle weakness (generalized) M62.81 (728.87):Acute, Unchanged, Onset Date: 02/11/2022, emerged s/p 2nd J&J vaccine Decreased appetite R63.0 (783.0): Acute, Unchanged, Onset Date: 02/11/2022, emerged s/p 2nd J&J vaccine Neck pain on right side M54.2 (723.1): Acute, Poorly Controlled, Onset Date: 02/11/2022, informs pops/cracks, is causing nerve pain Frequent headaches R51.9 (784.0): Onset Date: 02/11/2022, Described a head pressure. non-intrurrputive to life at this time. Pattern first in lifetime emerged s/p J&J CV19 vaccine Tinnitus H93.13 (388.30): Acute, Poorly Controlled, Onset Date: 02/11/2022, Observed throughout life but was not concerning or interruptive until 2nd dose of J&J CV19 vaccine Joint pain after vaccination M25.50 (719.40): Onset Date: 02/11/2022 Malaise R53.81 (780.79):Onset Date: 02/11/2022, Not concerning or interupting ADLS / work / daily demands & responsibilities. Cognitive changes R41.89 (799.59): Onset Date: 02/11/2022, slight delay in word recall Not concerning or interupting ADLS / work / daily demands & responsibilities. COVID-19 vaccine series completed Z92.29 (V87.49): Onset Date: 02/07/2022, 1st dose J&J - no health changes noted. 2nd dose of J&J taken 2/7/22 w/ emergence of new health changes in 4 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- I have lab results from blood tests taken in March 2022, July 2022 and October 2022 of this year. They are comprehensive and would be happy to submit if requested.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Allegra
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 15.12.2022
- Impfdatum
- 08.11.2021
- Beginn
- 06.10.2022
- Tage bis Beginn
- 332,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain
Bronchial wall thickening
COVID-19
Chest X-ray normal
Computerised tomogram abdomen abnormal
Chest X-ray
Computerised tomogram abdomen
Computerised tomogram thorax
Computerised tomogram thorax abnormal
Condition aggravated
Cough
Cytomegalovirus test
Echocardiogram normal
Echocardiogram
Epstein-Barr virus test
Laboratory test
Lung opacity
Myeloproliferative neoplasm
Symptomtext
MYELOPROLIFERATIVE NEOPLASM; CYTOMEGALOVIRUS TEST; SPLENIC INFARCTION; SARS-COV-2 TEST POSITIVE; ABDOMINAL PAIN; MYELOPROLIFERATIVE NEOPLASM; BRONCHIAL WALL THICKENING; SPLENIC INFARCTION; COVID-19; ABDOMINAL PAIN; CONDITION AGGRAVATED; COUGH; COUGH; LUNG OPACITY; LUNG OPACITY; COMPUTERISED TOMOGRAM THORAX ABNORMAL; RHINORRHOEA; EPSTEIN-BARR VIRUS TEST; SPLENOMEGALY; ULTRASOUND DOPPLER ABNORMAL; CHEST X-RAY NORMAL; BRONCHIAL WALL THICKENING; COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL; COVID-19; COMPUTERISED TOMOGRAM THORAX ABNORMAL; CONDITION AGGRAVATED; CYTOMEGALOVIRUS TEST; RHINORRHOEA; ECHOCARDIOGRAM NORMAL; SPLENOMEGALY; EPSTEIN-BARR VIRUS TEST; CHEST X-RAY NORMAL; LABORATORY TEST; COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL; SARS-COV-2 TEST POSITIVE; LABORATORY TEST; ULTRASOUND DOPPLER ABNORMAL; PYREXIA; PYREXIA; ECHOCARDIOGRAM NORMAL; This spontaneous report received from a health care professional via Regulatory Authority VAERS (Vaccine Adverse Event Reporting System) (VAERS ID: 2486178) concerned a 73 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: myalgia, pes planus, cough secondary to angiotensin converting enzyme inhibitor (ACE-i), pain due to total left knee replacement, abdominal pain, and edema, and concurrent conditions included: osteoarthritis, trochanteric bursitis, multiple lung nodules, hypertension, renal cyst, obesity, asthma (Mild persistent asthma with mild exacerbation on rescue inhaler), hyperlipidemia, prediabetes, colovesical fistula, HCC (hepatocellular carcinoma), lyme disease, von willebrand disease, infarction of spleen (splenic infarct), drug allergy (Advair Diskus, Duloxetine, Fluticasone, Gabapentin), onion allergy, former smoker (history of smoking), abnormal left thigh lump, and chronic arthritis. The patient experienced joint pain when treated with ciprofloxacin hydrochloride, and myalgia when treated with sertraline, and GI (gastrointestinal) upset and joint pain when treated with doxycycline, and throat swelling when treated with duloxetine hydrochloride, and cough when treated with lisinopril, swelling when treated with metronidazole, and amlodipine besilate. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211D21A, expiry: unknown) dose was not reported, 1 total, administered on 08-NOV-2021 for an unspecified indication. Age at time of vaccination 73 years old. Concomitant medications included allopurinol, aspirin, alprazolam, benzonatate, biotin, calcium carbonate, and celecoxib. On 06-OCT-2022, the patient presented to emergency department with several months of cough, runny nose (rhinorrhea), fevers, abdominal pain and found to have splenic infarct (D73 5), also covid-19 positive and condition aggravated. Abdominal CT (Computerised tomogram) was done and showed a splenic infarct with splenomegaly. Splenic infarct was thought to be 2/2 recent covid infection. The patient was seen by Hematology who felt in the absence of associated vessel thrombus, itself did not require anticoagulation. Data had shown no benefit with anticoagulation over aspirin for organ infarct. Patient was already on ASA (acetyl salicylic acid) 81 mg daily long term, doctor recommended a short course of increased dose to 325 mg daily per 1 month, empirically in the setting of COVID positive and associated hypercoagulability with this she conceded to two baby ASA tablets (equals to 162 mg) daily. Echocardiogram was negative for cardio-embolic sources (echocardiogram normal). Hematology checked for other viral illnesses that can cause splenomegaly (EBV (epstein-barr virus), CMV (cytomegalovirus) and appropriate to screen for some hematologic conditions like myeloproliferative condition with Jak2/MPN (Janus kinase 2/myeloproliferative neoplasm) and BCR-ABL FISH (Fluorescence In Situ Hybridization) and PNH (Paroxysmal nocturnal hemoglobinuria). Most of these labs (laboratory test) were pending at the time of discharge and will be followed up by hematology who plan to see patient in their clinic outpatient. Chest x-ray did not show any evidence of lung infection. The patient had been on room air with oxygen saturation above 97%. During the hospitalization, patient had a CT chest (computerised tomogram thorax) which showed stable, several a small 1-2 mm solid pulmonary nodule likely benign in etiology. New 3 mm groundglass nodule within the left upper lobe most likely due to infection and inflammation (lung opacity). Mild bronchial wall thickening due to infection or inflammation. No bronchiectasis. No focal airspace consolidation. The patient was placed on a short course of prednisone due to her underlying asthma by Pulmonology. A left UE soft tissue ultrasound (ultrasound doppler abnormal) showed an ill-defined focus of increased echogenicity within the subcutaneous fat of the anterior thigh correlates with the patient's palpable lump. Differential considerations would include a focus of fat inflammation versus a ill-defined hyperechoic mass. MRI LLE (Magnetic resonance imaging left lower extremities) was recommended however, the patient opted to have it done outpatient with her PCP (primary care physician). The patient was discharged in stable condition on 09-OCT-2022. Patient was hospitalized for 3 days. Treatment medications (dates unspecified) included: prednisone, and acetylsalicylic acid. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from myeloproliferative neoplasm, splenic infarction, abdominal pain, bronchial wall thickening, covid-19, condition aggravated, cough, lung opacity, rhinorrhoea, splenomegaly, chest x-ray normal, computerised tomogram abdomen abnormal, computerised tomogram thorax abnormal, cytomegalovirus test, echocardiogram normal, epstein-barr virus test, laboratory test, sars-cov-2 test positive, ultrasound doppler abnormal, and pyrexia. This report was serious (Hospitalization Caused / Prolonged). This report was associated with product quality complaint: 90000258347. 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 department on 13-DEC-2022. The following information was updated and incorporated into the case narrative: Product quality complaint investigation result.; Sender's Comments: V1:The additional information in this version is Product quality complaint investigation result. This doesnot alter causality of previously reported events. 20221113313- myeloproliferative neoplasm, splenic infarction, abdominal pain, bronchial wall thickening, covid-19, condition aggravated, cough, lung opacity, rhinorrhea, splenomegaly, chest x-ray normal, computerised tomogram abdomen abnormal, computerised tomogram thorax abnormal, cytomegalovirus test, echocardiogram normal, epstein-barr virus test, laboratory test, sars-cov-2 test positive, ultrasound doppler abnormal, pyrexia. The event shows an incompatible temporal relationship (considering latency of 332 days, vaccination date:08-Nov-2021 and onset: 06-Oct-2022). Therefore, this event is considered inconsistent with vaccine administration.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- 3,0
- Labordaten
- Test Date: 20221006; Test Name: CHEST X-RAY; Result Unstructured Data: Normal (did not show evidence of lung infection); Test Date: 20221006; Test Name: COMPUTERISED TOMOGRAM ABDOMEN; Result Unstructured Data: Abnormal (showed a splenic infarct with splenomegaly Splenic infarct was thought to be 2/2 recent covid infection); Test Date: 20221006; Test Name: COMPUTERISED TOMOGRAM THORAX; Result Unstructured Data: Abnormal (showed Stable several a small 1-2 mm solid pulmonary nodule likely benign in etiology. New 3 mm groundglass nodule within the left upper lobe most likely due to infection and inflammation. Mild bronchial wall thickening due to infection or inflammation. No bronchiectasis. No focal airspace consolidation); Test Date: 20221006; Test Name: CYTOMEGALOVIRUS TEST; Result Unstructured Data: Not reported; Test Date: 20221006; Test Name: ULTRASOUND DOPPLER; Result Unstructured Data: Abnormal (showed an Ill-defined focus of increased echogenicity within the subcutaneous fat of the anterior thigh correlates with the patient's palpable lump. Differential considerations would include a focus of fat inflammation versus a ill-defined hyperechoic mass.); Test Date: 20221006; Test Name: EPSTEIN-BARR VIRUS TEST; Result Unstructured Data: not reported; Test Date: 20221006; Test Name: LABORATORY TEST; Result Unstructured Data: Not reported; Test Date: 20221006; Test Name: SARS-COV-2 TEST; Test Result: Positive ; Test Date: 20221006; Test Name: ECHOCARDIOGRAM; Result Unstructured Data: Normal (negative for cardio-embolic sources)
- Aktuelle Erkrankungen
- Arthritis; Asthma (Mild persistent asthma with mild exacerbation on rescue inhaler); Carcinoma hepatocellular; Colovesical fistula; Drug allergy (Advair Diskus, Duloxetine, Fluticasone, Gabapentin); Ex-smoker; Food allergy; Hyperlipidemia; Hypertension; Lower extremity mass; Lung nodule; Lyme disease; Obesity; Osteoarthritis; Prediabetes; Renal cyst; Splenic infarction; Trochanteric bursitis; Von Willebrand's disease
- Vorgeschichte
- Medical History/Concurrent Conditions: Abdominal pain; Cough; Edema; Myalgia; Pes planus; Postoperative pain
- Andere Medikamente
- ZYLOPRIM; XANAX; TESSALON; BIOTIN; CALCIUM CARBONATE; CELEBREX
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 22.11.2022
- Impfdatum
- 17.11.2021
- Beginn
- 15.08.2022
- Tage bis Beginn
- 271,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test normal
Cardiac dysfunction
Dyspnoea
Echocardiogram
Heart rate increased
Symptomtext
I went to primary doctor for an unrelated issue, he listens to my heart, he said that my heart was elevated and that I needed to go to the hospital; I went to the ER unit, and I was there for 5 days; now I am in a care of a Cardiologist and Pulmonary. My only symptom was a short of breath but since I have asthma, I thought that it was due to the asthma condition. My heart is now working at 30% of its capacity.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Aug2022 blood test normal; Aug2022 Heart Ultrasound abnormal
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Diabetes; Asthma; Hyper Blood Pressure
- Andere Medikamente
- AREDS 2; citalopram HBR; furosemide; lisinopril; LIPITOR; potassium chloride; FARXIGA; AMARYL
- Allergien
- Erythromycin; sulfa; minocycline
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 06.09.2022
- Impfdatum
- 07.12.2021
- Beginn
- 24.08.2022
- Tage bis Beginn
- 260,0
- Dosis
- 2
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Chest discomfort
Dyspnoea
Symptomtext
dyspnea, chest discomfort
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 9,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 27.08.2022
- Impfdatum
- 09.06.2021
- Beginn
- 10.04.2022
- Tage bis Beginn
- 305,0
- Dosis
- 1
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Acute kidney injury
COVID-19
Chest pain
Diarrhoea
Pancreatitis
SARS-CoV-2 test positive
Symptomtext
Narrative: Patient received two doses of Pfizer COVI 19 Vaccine in Jun and Dec 2021. The patient tested positive for COVID 19 on 30 March 2022. The patient presented to the ED on 10 April 2022 with chest pain and diarrhea. The patient was admitted with COVDI 19, acute kidney injury, and pancreatitis. The patient was discharged on 15 April 2022 in stable condition. Reported per EUA.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 16.07.2022
- Impfdatum
- 13.07.2022
- Beginn
- 15.07.2022
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Paraesthesia
Peripheral swelling
Tenderness
Symptomtext
Per pt upper arm is swollen, armpit is swollen and front of pec muscle is swollen. Patient also has some tenderness in neck and tingling down pinky finger. Pt will monitor and contact MD.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Meperidine, Sulfa
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 06.07.2022
- Impfdatum
- 06.11.2021
- Beginn
- 16.02.2022
- Tage bis Beginn
- 102,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Arthralgia
Blood magnesium
Blood thyroid stimulating hormone
COVID-19
Cardiac stress test normal
Cervical spinal stenosis
Computerised tomogram normal
Ejection fraction
Electrocardiogram
Electrocardiogram ambulatory abnormal
Headache
Hypoaesthesia
Injection site pain
Intervertebral disc degeneration
Intervertebral disc protrusion
Lumbar puncture
Magnetic resonance imaging spinal abnormal
Malaise
Symptomtext
Pseudotumor cerebri Log Feb 16,2022 s/s: neck pain 6/10, left shoulder, left arm pain 6/10, numbness/tingle to fingertips 2,3,4. TX: Bio freeze to neck, ibuprofen 2 tabs, appoint scheduled with Dr. Feb 23, 2022 Dr. - X-ray C-spine C-5 stenosis. Ordered Physical Therapy March 5, 2022 PT @11:30 March 10,2022 PT@12:30 March 17,2022 ***PT@8:30-first time with mechanical machine traction on cervical neck Massage ***March 18,2022***ER visit @0430 woke up with left facial tingle and numbness in addition to left sided numbness Worked for 11 hours?increased blurred vision, headache, left sided increased numbness, severe neck pain and shoulder pain, tinnitus. ER March 24, 2022- Lumbar Puncture opening pressures 24cm /H2O 30cc removed 11cm/H2O. All symptoms subsided. Medications: Diamox 750mg BID PO Foricet PRN ***March 30-31,2022***ER visit CT negative EKG 49 VBGH-Lumbar Puncture opening pressures 19 cm/H2O 30 cc removed 6 cm/H2O April 5,2022 PCP appointment- Sleep study appointment, cardiology appointment April 6, 2022 Mammogram- negative April 14, 2022 Dr.- Changed Diamox to Topamax d/t side effects of Diamox April 15,2022 Cortisol 10.2 April 22,2022 Dr.- Order rotational CT scan for possible Craniocervical instability and EMG May 2, 2022 Cervical Spinal flex/ext: moderate C5/6 degenerative disc disease. Slight subluxation at some levels during flex/ext, without sign instability. Ext: slight retrolisthesis at c3/4 (2mm) C4/5 (1.5 mm) and C5/6 (1.5 mm) May 3, 2022 Dr.- pulmonologist/sleep study May 13, 2022 MRI-mild straightening of cervical lordotic curature. No large disc herniation, cord compression or cord signal adnormality. C5-6 degeneratie disc disease w/mild diffuse disc bulging. C6-7 mild central disc bulge No significant facet arthropathy, foraminal stenosis or nerve root compression. May 25, 2022 Nuclear stress test: Normal study, low risk, LVEF 69% May 26, 2022 Woke up this morning feeling almost normal, slight headache to left but energy uplifted. HR check 65 compared to 45 as before. Only difference was the cardiolite medication given yesterday for the nuclear stress test to raise my HR. LABS: TSH, T4, T3, Mag Stopped Topamax. Only on Diamox June 1, 2022 DR. (cardiac)- Echo rescheduled due to wearing Zio Holter monitor for 14 days. (SR 43-168 HR with x1 episode SVT) June 7, 2022 DR. (Neurosurgeon)- Improved symptoms so no shunt at this time. June DR.-reorder Diamox medication. Annual training waiver June 29, 2022 Covid symptoms July 3, 2022 Tested positive for covid July 12, 2022 Future fitting
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- 4,0
- Labordaten
- ***March 22,2022***ER visit No papillary edema. Blurred vision remained but no vision change. increased symptoms of left sided numbness and headache, expressive
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Vit D, Ca+2, Allegra
- Allergien
- Shrimp
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 21.06.2022
- Impfdatum
- 28.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Dyspnoea
Ejection fraction
Ejection fraction abnormal
Magnetic resonance imaging heart
Troponin
Symptomtext
EJECTION FRACTION LOW NORMAL RANGE; CHEST PAIN; SHORTNESS OF BREATH; This spontaneous report received from a physician concerned a 36 year old male. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: No significant past medical history and no medications. 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 28-DEC-2021 for prophylactic vaccination. The batch number was not reported and has been requested. Age at time of vaccination 36 years old. No concomitant medications were reported. On 28-DEC-2021, the patient experienced chest pain, and shortness of breath. On an unspecified date, the patient experienced ejection fraction low normal range. Laboratory data (dates unspecified) included: Cardiac MRI does not show evidence of pericarditis or myocarditis, Ejection fraction low normal range, and Troponin normal, no evidence of pulmonary embolism. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from chest pain, and shortness of breath, and the outcome of ejection fraction low normal range was not reported. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Test Name: TROPONIN; Result Unstructured Data: normal, no evidence of pulmonary embolism; Test Name: EJECTION FRACTION; Result Unstructured Data: low normal range; Test Name: CARDIAC MRI; Result Unstructured Data: does not show evidence of pericarditis or myocarditis
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: No significant past medical history and no medications
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 16.06.2022
- Impfdatum
- 16.01.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 16,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Neuralgia
Paraesthesia
Small fibre neuropathy
Symptomtext
I started having burning and tingling all over my body that was nerve pain. I called my PCP because I had a similar reaction to my flu shot last year. She advised me to start taking the gabapentin that I took last year after my flu reaction. Then I was referred to a Neurologist, and it was determined that I have Small Fiber Neuropathy. I was put on the 2 medications, that made me too sleepy. The medications are amitriptyline and duloxetine I have a follow up appointment today.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Respiratory Infection on antibiotics.
- Vorgeschichte
- Asthma
- Andere Medikamente
- Levothyroxine; TRULICITY; albuterol sulfate inhaler; ADVAIR; SINGULAIR; ZYRTEC.
- Allergien
- Aspirin; corn; tomatoes; peanuts; grasses; tree's; more
- Vorherige Impfungen
- I had a similar reaction to my flu shot last year. She advised me to start taking the gabapentin.
- Staat
- OK
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 01.06.2022
- Impfdatum
- 29.12.2021
- Beginn
- 30.05.2022
- Tage bis Beginn
- 152,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chest pain
Cough
Respiratory tract congestion
SARS-CoV-2 test positive
Streptococcus test
Throat clearing
Throat irritation
Vaccine breakthrough infection
Symptomtext
Breakthrough covid case. Patient tested positive with an covid test at the Hospital. Presented to ER with c/o itchy throat, sore chest from forced cough and clearing throat, chest congestion. Prescribed Paxlovid. Discharged home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Abbott ID Now covid test Strep test
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Headache disorder
- Andere Medikamente
- carboxymethylcellulose NA Cyclobenzaprine diclofenace NA 1% top gel duloxetine ergocalciferol folic acid lamotrigine meloxicam ondansetron sumatriptan succinate topiramate curcumin multivitamin omega 3 zinc
- Allergien
- Bactrim methotrexate Plaquenil sulfate Septra
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 23.05.2022
- Impfdatum
- 22.05.2022
- Beginn
- 22.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood glucose
Dizziness
Pallor
Tremor
Unresponsive to stimuli
Symptomtext
Patient became pale and dizzy, gave him water. He then became unresponsive and started to shake slightly for a few seconds. He did not lose consciousness and began to respond again quickly. Called EMS who responded and checked on patient. He did not go to hospital. Left after symptoms resolved in about 20 minutes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- EMS checked BP and blood sugar. They did not provide us with results.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Diabetes Type 1
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- History of fainting
- Staat
- MD
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 19.05.2022
- Impfdatum
- 15.11.2021
- Beginn
- 10.01.2022
- Tage bis Beginn
- 56,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Hypoaesthesia
Injected limb mobility decreased
Muscle spasms
Pain in extremity
Sleep disorder
Symptomtext
Pain in left arm that runs from forearm to fingers, loss of strength in left arm, inability to lift more than 3 lbs with left arm, sporadic pain and cramping in left hand and difficulty straightening hand and fingers, inability to sleep on my stomach without left arm going completely numb
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- none at this time
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 19.05.2022
- Impfdatum
- 18.11.2021
- Beginn
- 05.05.2022
- Tage bis Beginn
- 168,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Dyspnoea
Haemoptysis
Palpitations
Productive cough
Sputum discoloured
Symptomtext
Patient presented with SOB, cough w/ yellow sputum production with blood streaks, palpitations, weakness. Started on supp. O2, albuterol, robitussin-DM, apap, decadron, remdesivir.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- afib, bipolar, fibromyalgia, OAB, constipation, osteoarthritis, HTN
- Andere Medikamente
- asa, baclofen, coreg, cetirizine, vit d3, cyanocobalamin, voltaren, eliquis, fentanyl, ferosul, trelegy, lasix, novolog, atrovent, acidohilus, linzess, imodium, ativan, remeron, singulair, nitrostat, mycostatin, zofran, protonix, klor-con
- Allergien
- Acetaminophen Adenosine Azithromycin Bupropion Hcl Daliresp [roflumilast] Dilaudid [hydromorphone] Duloxetine Gabapentin Ibuprofen Isosorbide Mononitrate Lexiscan [regadenoson] Morphine Mushroom Nalbuphine Naproxen Toradol [ketorolac] Tramadol
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 17.05.2022
- Impfdatum
- 10.11.2021
- Beginn
- 11.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Angina pectoris
Asthenia
Dizziness
Fatigue
Hangover
Laboratory test
Malaise
Mobility decreased
Pain
Paraesthesia
Symptomtext
Initially I just felt sick similar to a hangover, weakness, fatigue, dissyness. The following morning I started experiencing heart pains. Similar to pins and needles piecing my heart. I thought it would get better over time and it hasn't. More recently it started getting worse to the point where turning my body certain ways amplifies the pain impeding my daily mobility.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- Many test taken on 5-11-2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 17.05.2022
- Impfdatum
- 16.05.2022
- Beginn
- 16.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest pain
Headache
Nervousness
Throat tightness
Symptomtext
Patient stated headache and shaky feeling shortly after receiving vaccine around 3pm, symptoms worsening to throat tightness and chest pain, Epi 0.3mg given at 3:10pm in left thigh, VS slightly elevated at that time: B/P 156/92, HR 109, Temp 98.1, O2 sat 99%, RR 32. EMS called at time of Epi given, symptoms not improving at 3:18pm another Epi 0.3mg given in right thigh. Patient stated she received 1st dose of Janseen on 12/18/21 but symptoms were not this bad. Also stated had adverse reaction to Moderna on 4/13/21. Patient transported to nearest hospital and report given to EMS upon arrival at 3:20.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Patient stated no illnesses
- Vorgeschichte
- None
- Andere Medikamente
- Unknown
- Allergien
- Peanuts, Penicillin
- Vorherige Impfungen
- Moderna on 4/13/21 patient stated went to hospital after anaphylaxis via ambulance. Age 52.
- Staat
- TN
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 04.05.2022
- Impfdatum
- 28.04.2022
- Beginn
- 29.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Fatigue
Headache
Malaise
Migraine
Symptomtext
Migraine/headache for 3 days. Dull, mild headache has continued - on day 6 chills, exhaustion, overall sick feeling 2 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Vitamin C, Fish Oil
- Allergien
- Alpha-gal allergy
- Vorherige Impfungen
- Sore arm for 6 months after yellow fever vaccine in 2007.
- Staat
- GA
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 03.05.2022
- Impfdatum
- 27.04.2022
- Beginn
- 03.05.2022
- Tage bis Beginn
- 6,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Feeling abnormal
Muscle twitching
Palpitations
Vertigo
Visual impairment
Symptomtext
Patient called 05/03 (6 days after vaccination) stating he woke up with arm twitching down his right arm, head spinning, heart racing, and head feels foggy and cant see straight. Asked if it could be due to vaccine. Patient was instructed to go to emergency room for assessment and observation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- none at this time
- Aktuelle Erkrankungen
- 6 weeks prior he had seizure that led to a medical induced coma for 6 days. Reports history of chain reaction seizures. Nurse called MD for clearance before giving vaccine.
- Vorgeschichte
- seizures
- Andere Medikamente
- antiseizure medication but not consistent
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 02.05.2022
- Impfdatum
- 31.12.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injected limb mobility decreased
Insomnia
Neck pain
Pain
Pain in extremity
Spinal X-ray
Symptomtext
Starting the day after the vaccine on Jan 1st 2022 my right arm was very sore. I was unable to reach fully, the by day 3 the pain went to my neck and then to my left arm. I am unable to sleep because of the pain. I have had a neck Exray I have been to my chiropractor several times and my doctor set me up with physical therapy, and I have gone 6 times so far and have tried Message therapy that helps for a short time. I have had chronic pain since Jan 1st 2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- Xray of my neck
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Daily multi vitamins
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 26.04.2022
- Impfdatum
- 03.08.2021
- Beginn
- 01.09.2021
- Tage bis Beginn
- 29,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Electromyogram normal
Hypoaesthesia
Nerve conduction studies normal
Paraesthesia
Sensory loss
Symptomtext
Numbing and tingling sensation decreased feeling or sensitivity that is still ongoing. Did EMG Nerve conductionNOV 5th 2021 and it turned out negative. was told its paresthesia . When I did have Covid19 in Janary 2022 the paresthesia worsened and still having issues with it. I reached out to Jassen and Jassen about the risk of paresthesia and was sent information on it my inquiry number is 03090238 and under the risks is listed the paresthesia and the issues I'm experiening. My pcp is listed that its a common side effect and scanned in the information I was given from Jassen and Jassen. I can provide notes if need be. Still monitoring with pcp
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- EMG nerve condution test November 5th 2021 test was normal
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 21.04.2022
- Impfdatum
- 28.01.2022
- Beginn
- 06.02.2022
- Tage bis Beginn
- 9,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Anxiety
Depression
Fatigue
Feeling abnormal
Hallucination
Influenza like illness
Malaise
Migraine
Restlessness
Suicidal ideation
Symptomtext
I started feeling different and hearing voices and was feeling quite unusual where I was tired yet restless, almost zombie-like. Because of this I was dealing with anxiety and depression and thinking suicidal thoughts. Tried some physical working out to kind of sweat it out. Did not help too much. 4 days after the booster, I had started feeling genuinely sick with flu-like symptoms and migraines. I don't normally get migraines, so at that time I went to urgent care and was referred to a neurologist. This required preapproval and only just recently did get approval but have yet to see him.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- No test or labs as of yet.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Ibuprofen (sensitivity, nausea)
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 16.04.2022
- Impfdatum
- 21.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Exercise tolerance decreased
Injected limb mobility decreased
Injection site pain
Symptomtext
Pt came to local Pharmacy on Saturday April 16th, 2022 for her first booster dose. Upon arrival, the patient presented her vaccination card and asked a question about existing pain on her left shoulder/arm. When asked about the pain, the patient stated she noticed it when she resumed exercising. Date when she first noticed the pain is unknown, and how long after the vaccine is unknown. Since the vaccine,her ability to lift are not what they once were due to the pain. She states she experiences pain when lifting the weights on her left arm, and cannot raise her arm as high as she was previously able to do, nor is she able to lift the same amount of weights she was use to. The pain continues to this day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None reported
- Vorgeschichte
- none reported
- Andere Medikamente
- None reported
- Allergien
- None reported
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 12.04.2022
- Impfdatum
- 04.11.2021
- Beginn
- 31.01.2022
- Tage bis Beginn
- 88,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Drug hypersensitivity
Dyspnoea
Memory impairment
Symptomtext
I noticed that I was getting short of breath so when I was at church. I started singing & I couldn't hold the note which I was always able to hold a note but I was very short winded & also I am forgetting things. I was told I was allergic to one of my meds that I had been taking for over 6 yrs so they took me off Lisinopril & put me on another med.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Bloodwork
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- Diabetes, Heart condition
- Andere Medikamente
- Lisinopril, Furosemide, Atenolol, Insulin
- Allergien
- Lisinopril, Adhesive tapes
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 12.04.2022
- Impfdatum
- 08.12.2021
- Beginn
- 10.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Alopecia
Blood urine present
Condition aggravated
Culture
Laboratory test
Pruritus
Ultrasound scan
Urine analysis
Symptomtext
Within a day of two getting the booster I had blood when I went to the restroom. I called my doctor and they sent me to get checked. This was unusual for me since I no longer have this happen. The original thought was that it may be a UTI but that was not the case. I was sent for testing to try and figure out what was happening. I had my normal 3 year physical and I had told them I had this itch on my head. They began looking at my head and noticed that there was hair loss which was new. I had not noticed this because my hair is very thick but this led to us testing for an autoimmune disorder. I was put on an antibiotic and will be on it until June of 2022 so six months of this antibiotic. After talking with my doctors the time line leads me to think the vaccine is the only thing that could have led to this occurring.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Lab work, urine sample, culture of the bladder, ultrasound.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Mushrooms; Latex
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 11.04.2022
- Impfdatum
- 06.04.2022
- Beginn
- 07.04.2022
- 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
Migraine
Vaccine positive rechallenge
Symptomtext
Severe Migraine 12 hours later. It has been on and off since booster (I had the same issues with the first dose) This has been going on for 6 days. Standard Migraine symptoms. Unusual as I have had these under control with only 2 - 3 one day events until I got the injection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- chronic migraine (since 5 years old) Arthritis
- Andere Medikamente
- standard multi vitamins taken for over 55 years. Soma for back pain Aimovig for severe miagraine (once a month)
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 01.04.2022
- Impfdatum
- 01.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dyspnoea
Paraesthesia
Symptomtext
Patient started experiencing facial tingling and shortness of breath within 10 minutes of vaccine administration. Patient had a history of anaphylaxis reaction and carried their own epipen and benadryl in case of emergencies. Patient immediately administered the Epipen and then administered 25mg of oral benadryl prior to EMS arriving . EMS arrived within 5 minutes of patient administering Epipen and benadryl. Patient's full recovery was monitored by EMS and patient departed the pharmacy with spouse.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 26.03.2022
- Impfdatum
- 28.02.2022
- Beginn
- 28.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Dizziness
Dyspnoea
Headache
Injection site erythema
Myalgia
Pyrexia
Tinnitus
Symptomtext
Airway restriction, shortness of breath resolved after several hours . Headache,ringing in the ears,muscle aches, dizziness and weakness for several days. Fever around 10 hours after injection. Redness at injection site
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- No
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- -
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 14.03.2022
- Impfdatum
- 15.02.2022
- Beginn
- 15.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Computerised tomogram
Migraine
Symptomtext
Migraine, beginning the night of vaccine and continuing for one month so far. Ongoing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- Visit with PCP and neurologist. CT scan with contrast 2/23/22, blood work 2/24/22.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- SVT Sciatic nerve pain
- Andere Medikamente
- Metoprolol Gabapentin Multivitamin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 05.03.2022
- Impfdatum
- 06.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood pressure measurement
Blood test
Chest pain
Chills
Computerised tomogram
Fibrin D dimer
Fibrin D dimer increased
Hypertension
Influenza like illness
Nervousness
Pain in extremity
Pyrexia
Ultrasound scan
Symptomtext
CHEST PAIN; HIGH BLOOD PRESSURE; FIBRIN D DIMER HIGH; NERVOUS; LEG PAIN; LOW GRADE FEVER; FLU LIKE SYMPTOMS; CHILLS; This spontaneous report received from a patient concerned a 44 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included: alcohol use, and non-smoker, 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: 211D21A expiry: UNKNOWN) dose was not reported, administered on 06-JAN-2022 for prophylactic vaccination. No concomitant medications were reported. On 11-JAN-2021, Laboratory data included: CT scan (NR: not provided) unknown. On 06-JAN-2022, the patient experienced flu like symptoms, chills, and low grade fever. On 11-JAN-2022, the patient experienced chest pain, high blood pressure, fibrin d dimer high, nervous, and leg pain. Laboratory data included: Blood pressure (NR: not provided) High, Blood test (NR: not provided) Unknown, Diagnostic ultrasound (NR: not provided) unknown, and Fibrin D dimer (NR: not provided) High. On FEB-2022, Laboratory data included: Blood test (NR: not provided) Unknown, and Fibrin D dimer (NR: not provided) D Dimer was going back up. Laboratory data (dates unspecified) included: Blood test (NR: not provided) unknown, and Fibrin D dimer (NR: not provided) Increased to 1000. Treatment medications (dates unspecified) included: apixaban. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from flu like symptoms, chills, and low grade fever, had not recovered from leg pain, and fibrin d dimer high, and the outcome of chest pain, high blood pressure and nervous was not reported. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Test Date: 20210111; Test Name: CT scan; Result Unstructured Data: unknown; Test Date: 20220111; Test Name: Diagnostic ultrasound; Result Unstructured Data: unknown; Test Date: 20220111; Test Name: Blood test; Result Unstructured Data: Unknown; Test Date: 20220111; Test Name: Blood pressure; Result Unstructured Data: High; Test Date: 20220111; Test Name: Fibrin D dimer; Result Unstructured Data: High; Test Date: 202202; Test Name: Blood test; Result Unstructured Data: Unknown; Test Date: 202202; Test Name: Fibrin D dimer; Result Unstructured Data: D Dimer was going back up; Test Name: Fibrin D dimer; Result Unstructured Data: Increased to 1000; Test Name: Blood test; Result Unstructured Data: unknown
- Aktuelle Erkrankungen
- Alcohol use (social but not since the Janssen COVID-19 vaccine due to adverse reactions she was experiencing.); 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
- WI
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 04.03.2022
- Impfdatum
- 01.03.2022
- Beginn
- 02.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Body temperature increased
Dizziness postural
Feeling cold
Headache
Hyperhidrosis
Myalgia
Nausea
Suppressed lactation
Tremor
Symptomtext
Janssen COVID-19 Vaccine EUA Starting at 1am, I became very cold. Within about 30 minutes, I was shaking uncontrollably. This went on for about 2 hours. Upon taking my temperature orally, it was 103.1 degrees F. I was sweating and cold. I then got a headache and muscle aches. When I stood up, I was very dizzy and was only able to crawl to the bathroom as I felt nauseous (I did not vomit). I am also breastfeeding a 1month old (delivered via c-section 1/31/22) and my milk supply dropped significantly. I went from being able to pump 2oz out of one breast to barely 1oz. As of 3/4/22, this has not recovered yet.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Prenatal vitamin daily, Magnesium Oxide 500mg daily
- Allergien
- Penicillins, Sulfa, Metronidazole (flagyl)
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 28.02.2022
- Impfdatum
- 29.01.2022
- Beginn
- 12.02.2022
- Tage bis Beginn
- 14,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest X-ray
Chest discomfort
Chest pain
Dyspnoea
Headache
Laboratory test
Painful respiration
Symptomtext
About 2 weeks of the vaccine, I started getting tightness in my chest for 2 days and I got more symptoms, day 3 I had tightness in chest and pain in my chest day 4 same thing. day 5 same but shortness of breathing. I had to use my inhaler it didn't work so I had to go to the emergency they gave me a breathing treatment it worked but not a lot. I got my doctor's appointment, and she gave me medication not sure it worked but I still have it. Day after ER I still have the same symptoms. I had a headache for 2 days along with other symptoms. short of breath, pain with breathing my inhaler didn't work so I took hot shower it helped a little. Still now I have same symptoms. its' getting better but very slowly.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Chest X-ray Lab test
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Multivitamin, Zyrtec
- Allergien
- Seasonal Allergies
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 47,0
- Geschlecht
- M
- Eingang
- 22.02.2022
- Impfdatum
- 10.02.2022
- Beginn
- 10.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arthralgia
Chest pain
Computerised tomogram head
Electrocardiogram
Headache
Musculoskeletal stiffness
Nausea
Neck pain
Pain in extremity
Pyrexia
Vision blurred
Visual acuity tests
Symptomtext
Headache lasted 12 days and still have it. Blurry vision lasted 3+ days. Neck pain lasted 12 days still have it. Arm and shoulder pain lasted 10 days. Chest pain came and went for 3+ days. Blood pressure went up to 181/109 went to hospital ER in an ambulance. Nausea for 3 days. Low grade fever for 3 days. Medicine was given in ambulance. IV medication in ER and prescriptions. Nabumetone for headache, Tizanidine for neck pain/ stiffness. Ibuprofen for headache. Several follow up visits to hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Blood pressure check and vision check 02/10/2022, and 2/16/2022, Two EKG's 2/10/2022. CT of brain 2/19/2022.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Sleep Apnea
- Andere Medikamente
- No, multi vitamin
- Allergien
- Naproxen- upsets stomach
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 86,0
- Geschlecht
- F
- Eingang
- 17.02.2022
- Impfdatum
- 25.01.2022
- Beginn
- 25.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Mobility decreased
Pain in extremity
Symptomtext
patient states her arm still hurts, unable to lift above head.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- heart disease, asthma
- Andere Medikamente
- Lorazepam, ventolin hfa, metoprolol ER, flonase, diltiazem, lutein, Vitamin C, Multivitamin
- Allergien
- NO
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 15.02.2022
- Impfdatum
- 10.02.2022
- Beginn
- 10.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest discomfort
Dyspnoea
Paraesthesia oral
Urticaria
Symptomtext
Chest tightness; shortness of breath; tingling of the lips and tongue; hives on face, neck, upper body. Symptoms lasted around 12hrs "overnight". Benadryl X2 doses. Followup with PCP.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- acute cough
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 13.02.2022
- Impfdatum
- 08.12.2021
- Beginn
- 11.12.2021
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Aphasia
COVID-19
Chills
Cognitive disorder
Pneumonia
Pyrexia
Respiratory failure
SARS-CoV-2 test positive
Symptomtext
Fever and chills
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pneumonia
- Hospital-Tage
- 8,0
- Labordaten
- At home Covid test on 12/12/2021 was positive for Covid. Went to ER on 12/16/2021 with Fever, Chills, Cognitive dysfunction and trouble speaking. Pneumonia in both lugs, Covid 19, Hypoxic Respiratory failure,
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Omeprazole Dr. Caps 40 mg.
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 10.02.2022
- Impfdatum
- 09.12.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cardiac flutter
Electrocardiogram normal
Headache
Muscle spasms
Palpitations
Symptomtext
On 01/27/2022 at approximately 06:45pm, patient called the pharmacy to report a side effect she believes is a result from the Janssen J&J Vaccine that was administered in her left deltoid on 12/09/2021. She stated about 10 days after receiving the vaccination she noticed a "butterfly feeling" in the right side of her chest. She reports it feels like a flutter/muscle spasm. She does not have a history of any heart condition (e.g. hypertension, heart murmur, or heart palpitations). She contacted her PCP on 01/26/2022 who scheduled an EKG for her on 02/04/2022 and told her to report the symptoms to the pharmacy. Patient also reports a headache occurring after the vaccination and the day after the vaccine was administered. *** Update 02/10/2022 09:48am *** I spoke with staff at PCP's office regarding the EKG from 02/04/2022. Staff stated the patient is okay, she only had some palpitations and will be monitored by the office.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- EKG 02/04/2022
- Aktuelle Erkrankungen
- Asthma
- Vorgeschichte
- Asthma
- Andere Medikamente
- None known
- Allergien
- Sulfa, penicillin, latex
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 09.02.2022
- Impfdatum
- 17.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Condition aggravated
Dizziness
Dyskinesia
Dyspnoea
Exercise tolerance decreased
Eye movement disorder
Fatigue
Feeling abnormal
Feeling hot
Headache
Illness
Impaired work ability
Loss of personal independence in daily activities
Malaise
Migraine
Mobility decreased
Muscular weakness
Symptomtext
The evening after I received the shot, I had extreme fatigue and a severe headache. The headache was very different and more severe than any headache or migraine that I have ever had. I also had weakness in my extremities. I laid down to rest for the evening and while trying to sleep, the headache continued to get worse and I also became very warm and had a fever. While laying down and trying to sleep I felt as if I was paralyzed and had difficulty opening my eyes and controlling muscle movements. I also was incontinent and urinated the bed that night which I have never in my adult life ever done. The headache, weakness and fatigue continued for approximately 3 days and then slightly improved. During that time my arm was sore but was a minor concern given my other symptoms. I continued to have a headache which then triggered a severe migraine about a week after the shot. During this entire time, I was unable to work or perform my normal duties as I normally would. It impacted my daily activities significantly. About a week and a half after the shot, I did not have the severe headache and migraine but still had lingering headaches and was fatigued. Then approximately 3 weeks after the shot I contracted COVID and was extremely ill for about 1 month and went to Urgent Care since I was still not feeling well from side effects from the shot and now felt worse with COVID exacerbating the side effects. Finally, now, almost 2 months after the shot and one month after COVID, I finally am feeling somewhat back to normal, although I still have general fatigue and weakness and am unable to perform my normal fitness and exercise routine without becoming short of breath and lightheaded (I generally am very active prior to this, a runner, and workout regularly).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- N/A - I am a healthcare provider and am not generally inclined to seek medical tests/treatments even when I am very ill. I was extremely concerned during the initial reaction to the shot in the first day or two and considered calling an ambulance but decided to stay home and have my husband take care of me who is also a healthcare provider. The only time I went to the urgent care was after having both the side effects and then severe COVID symptoms at the same time. I went to the urgent care on 1/10/2022 and tested positive for COVID that say as well as tested positive on a home test also.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Migraine headaches
- Andere Medikamente
- Norethindrone
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 06.02.2022
- Impfdatum
- 27.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Headache
Migraine
Pain
Vomiting
Symptomtext
Massive migraine, massive body aches, vomiting. The worst of it lasted 2 days and gradually eased up. Took nausea meds and drank lots of fluids. Still waking up with a headache every morning. Hasn?t gotten as bad as it was. I?m taking a lot of ibuprofen on a daily basis.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- I did not seek medical attention
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hsv2
- Andere Medikamente
- Omeprazole, ocella
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 05.02.2022
- Impfdatum
- -
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood pressure measurement
Contusion
Eye pain
Heart rate irregular
Hypertension
Influenza like illness
Laboratory test
Lacrimation increased
Neck pain
Peripheral swelling
Throat tightness
Vascular pain
Vein discolouration
Symptomtext
This spontaneous report received from a patient concerned a 58 year old female. The patient's height and weight were not reported. The patient's past medical history included: blood clot. Patient had blood clot previously. The patient received Covid-19 vaccine ad26.cov2.s (Dose number in series 1) (suspension for injection, route of admin not reported, batch number: 1808609 and expiry: 07-SEP-2021) dose was not reported, 1 total, administered on 04-APR-2021 for prophylactic vaccination. The patient didn't have any problem with the primary vaccine. She woke up at 4 AM with night sweats when treated with Covid-19 vaccine ad26.cov2.s (Dose number in series was 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: 211D21A and expiry: 11-APR-2022) dose was not reported, 1 total, administered on 29-JAN-2022 on left arm for prophylactic vaccination. No concomitant medications were reported. On 29-JAN-2022, the patient had her blood pressure elevated and had flu like symptoms (felt nauseated, bone aches, shaking, incontrollable freezing then body felt hot and headache). Her heart rate was unstable, her body felt like it did when she had a blood clot previously. The patient felt like throat was starting to close, the back of her neck hurt and eye felt like they were going to burst from eye pain and were red and watery. Her fingers since were swollen and having a hard time moving them. On 30-JAN-2022, the patient went to emergency room (urgent care) and did tests at the urgent care. In JAN-2022, the patient had bruising, veins looked budging green and painful. The patient went to urgent care (Dose number in series was 2). The action taken with Covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from elevated blood pressure on JAN-2022, was recovering from heart rate was unstable, felt like throat was starting to close, and back of neck hurt, had not recovered from watery eye, swollen fingers, bruising, veins looking budging green, eye feels like they were going to burst from eye pain and were red, and painful veins, and the outcome of flu like symptoms was not reported. This report was non-serious. This case, involving the same patient is linked to 20220208604 (Dose number in series 1 case).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220129; Test Name: Blood pressure measurement; Result Unstructured Data: elevated; Test Date: 20220130; Test Name: Laboratory test; Result Unstructured Data: not reported.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Clot blood
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 04.02.2022
- Impfdatum
- 30.11.2021
- Beginn
- 07.12.2021
- Tage bis Beginn
- 7,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Alanine aminotransferase
Aspartate aminotransferase
COVID-19
Cough
Dyspnoea
Feeling abnormal
Hepatitis acute
Hypertransaminasaemia
Pain
Pyrexia
SARS-CoV-2 test positive
Vomiting
Symptomtext
Narrative: Patient is 75 y/o male who presented to the ER on 12/7/21 with cough, fever, body aches, and shortness of breath for the 5 days. Emesis after coughing. Diagnosed with COVID-19 3 days ago at an outside facility and presented to the ER on 12/5/21 feeling worse. Oxygen saturations at home and ER were less than 90% on room air. Transaminitis/acute hepatitis suspected to be secondary to COVID infection. Admitted and treated with dexamethasone (12/7-12/17) and remdesivir (12/7-12/12). Discharged 12/25/21. Vaccinated with Janssen one dose vaccine on 3/30/21 at a facility. Second "booster dose" on 11/30/21 through the health care facility. PMH: OSA, CAD, and emphysema.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- COVID Positive (12/7/21) AST (12/7-12/12) and ALT (12/7-12/25) above ULN
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 04.02.2022
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Feeling cold
Hypoaesthesia
Tremor
Symptomtext
Shaky and cold. Stable vitals 120/80. Numbness in her hands and shivering. Ambulance called at 11:35 am for evaluation. Vitals taken by emergency team. Patient released in her own private vehicle with husband as the driver.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- Pulse rate; BP taken.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Pfizer (12+) vaccine 1st dose
- Vorherige Impfungen
- Pfizer; 4/1/2021; patient advised by physician to get Janssen for 2nd dose.
- Staat
- OR
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 04.02.2022
- Impfdatum
- 31.01.2022
- Beginn
- 31.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dyspnoea
Eye pain
Headache
Hypersomnia
Hypoaesthesia
Nausea
Photophobia
Retching
Tinnitus
Visual impairment
Vomiting
Symptomtext
Since the 31st I have had Ringing in my ears (Constant) Severe Headache (Constant) Fingers go numb (On Occasion), left arm, goes numb (On Occasion) Severe Breathing problems (cant even walk up the stairs) (Constant) The top of my head is numb (Constantly), hard to see out of my left eye. Dry Heaves all night (Constant), Heavy Sleep patterns (13 to 20 hours a day) continued Nauseating to the point of throwing up at night cant keep food in my system because I feel like throwing up. It hurts to look at Lights.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Dr refused to allow me time to perform them. I will never go back to that doctor EVER. I am looking for a new doctor now.
- Aktuelle Erkrankungen
- Thyroid
- Vorgeschichte
- Thyroid
- Andere Medikamente
- None
- Allergien
- Several, Most all medications including Tyonal advil, Several different types of food including All fish including, Shrimp Crabs several unknown substances. Symptoms include Hallucinations all the way to Anaphylaxis
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 04.02.2022
- Impfdatum
- 02.02.2022
- Beginn
- 02.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Headache
Heart rate increased
Myalgia
Pyrexia
Symptomtext
Chest Pain, Muscle Aches, Headaches, Fever, Increased heart rate.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 02.02.2022
- Impfdatum
- 16.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest discomfort
Chest pain
Dizziness
Injection site pain
Tremor
Symptomtext
Experienced pain and soreness at injection site for 3 days after injection. The day after injection I was feeling light headed and began to experience several bouts of uncontrollable tremors across my whole body. I have also experienced general chest discomfort and pain since the injection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 01.02.2022
- Impfdatum
- 27.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Diarrhoea
Mobility decreased
Pain in extremity
Peripheral swelling
Pyrexia
SARS-CoV-2 test negative
Symptomtext
. Patient received Janssen booster shot on 12/27/2021 and stated she had a swollen and achy arm the same day. Two weeks later patient stated she had diarrhea for four days then it went away and then occurred again one week later. She also stated she had a fever 2 days after receiving the vaccine. Throughout the course of events patient said her swollen arm continued and worsened and has difficulty maintaining full range of motion. She met with physician who advised the pharmacy to report side effects.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- Patient stated she was negative for COVID when side effects occurred.
- Aktuelle Erkrankungen
- None reported
- Vorgeschichte
- None reported
- Andere Medikamente
- None reported
- Allergien
- None reported
- Vorherige Impfungen
- Did not state but mentioned she has gone through this process before.
- Staat
- MN
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 01.02.2022
- Impfdatum
- 12.11.2021
- Beginn
- 22.01.2022
- Tage bis Beginn
- 71,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
COVID-19 pneumonia
SARS-CoV-2 test positive
Symptomtext
Received Janssen vaccine on 3/4, 11/12/21 COVID-19 positive by PCR on 1/22/22 admitted to hospital on 1/30/22 for COVID pneumonia underlying Type 1 DM
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19 pneumonia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 01.02.2022
- Impfdatum
- 21.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cardiac discomfort
Chest pain
Eye swelling
Feeling cold
Swollen tongue
Tremor
Symptomtext
Initially my right eye and tongue swelled. Fortunately, I did not go into full anaphylaxis. At 10:00 that night I had incredibly severe chest pain. This insane chest pain persisted for 32 hours. My heart still does not feel "normal" or "precovid vaccine". Along with the chest pain, around 1:00 a.m. I began shaking uncontrollably and could not get warm. The shaking and cold persisted for 12 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- asthmatic
- Andere Medikamente
- asthma medications
- Allergien
- no founded ones - history of unknown anaphylaxis
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 27.01.2022
- Impfdatum
- 26.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Eye pruritus
Feeling abnormal
Oropharyngeal pain
Paraesthesia oral
Pruritus
Rash
Tachycardia
Throat irritation
Symptomtext
Itching head and eyes, rash on neck and arms, tingling of tongue, sore throat, and tachycardia, heart rate 100. did not feel right at all.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia oral
- Hospital-Tage
- -
- Labordaten
- 1/27/21 Still has scratchy throat and mild itching.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Hashimotos thryoiditis, and ADD.
- Andere Medikamente
- None.
- Allergien
- Gluten, msg. preservatives in food.
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 26.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 7,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test normal
Computerised tomogram head normal
Electrocardiogram normal
Gait disturbance
Loss of personal independence in daily activities
Muscular weakness
Tremor
Weight decreased
Symptomtext
On January 20, 2022 (1 week after his booster shot), he woke up and his arms and legs were shaking severely. His legs were weak and he had difficulty walking. He was taken to Hospital ER. He had a blood work up, EKG, CT of the head and nothing was found. He used to get up and work on things around the house. Now he just sits in the chair and his arms and legs continue to shake. According to his wife, he shakes so badly that it is very hard for him to eat or drink. She reports he has lost 20 pounds in a week. He saw his PCP today and was given lorazepam. He has an appointment with a neurologist on February 2nd.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- January 20, 2022 at the Hospital - Blood work up, EKG, CT of the head, Wife reports that nothing was found.
- Aktuelle Erkrankungen
- He had a colonoscopy earlier in the month and was congested after that. He was given a prescription for Metronidazole. He was to take 4 daily, but he took 2 daily and only took them for 4 days.
- Vorgeschichte
- Afibrillation x 12 years, Glaucoma
- Andere Medikamente
- Eliquis, Furosemide, Carvedilol, Losartan, Eye drops: Dorzolamide, Latanoprost , Occasional Centrum Silver
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 26.01.2022
- Impfdatum
- 21.11.2021
- Beginn
- 21.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Biopsy skin
Cautery to nose
Epistaxis
Hypertension
Inflammation
Biopsy
Blister
Eczema
Pemphigoid
Rash
Pustule
Post procedural infection
Rash erythematous
Rash macular
Rash pruritic
Skin warm
Symptomtext
This report is being submitted to list details missing from previous submission. From patient, began to have problems 24-48 hours after vaccination. Rash all over, blisters 1 inch long and 1/2 inch high,along with eczema. Pt stated physician diagnosed bullous pemphigoid. Pt said these are covering all over body and have improved with treatment but he still has them. He is post treatment with penicillin and continues to take prednisone and see dermatologist.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- Biopsy,
- Aktuelle Erkrankungen
- not known, pt previously had a case of covid-19 8 or 9 months prior to vaccination
- Vorgeschichte
- High cholesterol High blood pressure
- Andere Medikamente
- verapamil, atorvastatin
- Allergien
- no known allergies
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 26.01.2022
- Impfdatum
- 21.11.2021
- Beginn
- 21.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Biopsy skin
Cautery to nose
Epistaxis
Hypertension
Inflammation
Biopsy
Blister
Eczema
Pemphigoid
Rash
Pustule
Post procedural infection
Rash erythematous
Rash macular
Rash pruritic
Skin warm
Symptomtext
This report is being submitted to list details missing from previous submission. From patient, began to have problems 24-48 hours after vaccination. Rash all over, blisters 1 inch long and 1/2 inch high,along with eczema. Pt stated physician diagnosed bullous pemphigoid. Pt said these are covering all over body and have improved with treatment but he still has them. He is post treatment with penicillin and continues to take prednisone and see dermatologist.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- Biopsy,
- Aktuelle Erkrankungen
- not known, pt previously had a case of covid-19 8 or 9 months prior to vaccination
- Vorgeschichte
- High cholesterol High blood pressure
- Andere Medikamente
- verapamil, atorvastatin
- Allergien
- no known allergies
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 25.01.2022
- Impfdatum
- -
- Beginn
- 21.01.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest pain
Dyspnoea exertional
Gait disturbance
Headache
Symptomtext
SHORTNESS OF BREATH WHEN WALKING FROM ONE ROOM TO ANOTHER; CHEST PAIN; DIFFICULTY WALKING/WANTING TO JUST LAY DOWN; HEADACHE; This spontaneous report received from a consumer concerned a 19 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: 211D21A, and expiry: 11-APR-2022) dose was not reported, administered on 21-JAN-2022 for prophylactic vaccination. No concomitant medications were reported. On JAN-2022, treatment medications included: paracetamol. On 21-JAN-2022, the patient experienced shortness of breath when walking from one room to another, chest pain, difficulty walking/wanting to just lay down, and headache. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from shortness of breath when walking from one room to another, headache, chest pain, and difficulty walking/wanting to just lay down. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 22.01.2022
- Impfdatum
- -
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Cough
Fatigue
Injection site discomfort
Musculoskeletal pain
Pain
Symptomtext
ARM DISCOMFORT AT INJECTION SITE; PAIN WENT UP TO LEFT UPPER CHEST; PAIN WENT UP TO COLLARBONE NEAR ARMPIT / INCREASED PAIN; COUGHING; EXCRUCIATING PAIN IN SHOULDER BLADE; TIRED A LITTLE BIT; This spontaneous report received from a patient concerned a 43 year old male. The patient's weight was 245 pounds, and height was 77 inches. The patient's concurrent conditions included: allergy to nuts, fish allergy, wheat allergy, and environmental allergy. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211D21A and expiry: 11-APR-2022) dose was not reported, administered on 12-JAN-2022 for prophylactic vaccination. No concomitant medications were reported. On JAN-2022, the patient experienced tired a little bit. Treatment medications included: ibuprofen. On 14-JAN-2022, the patient experienced arm discomfort at injection site, pain went up to left upper chest, pain went up to collarbone near armpit / increased pain, coughing, and excruciating pain in shoulder blade. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient was recovering from arm discomfort at injection site, pain went up to left upper chest, excruciating pain in shoulder blade, tired a little bit, pain went up to collarbone near armpit / increased pain, and coughing. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Allergy to nuts; Environmental allergy; Fish allergy; Food allergy
- Vorgeschichte
- Comments: Unknown
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 83,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- -
- Beginn
- 13.01.2022
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Dyspnoea
Eye pruritus
Headache
Injection site rash
Pain in extremity
Rash erythematous
Symptomtext
ITCHY EYES; BREATHING ISSUE; RED SPOTS; SORE ARM; BUMP BELOW INJECTION SITE; NOT ENERGETIC; SLIGHT HEADACHE ON AND OFF; This spontaneous report received from a patient concerned an 83-year-old female. The patient's height, and weight were not reported. The patient's past medical history included: spinal surgery in 2013, and carotid artery surgery in 2010, and concurrent conditions included: asthma, chronic obstructive pulmonary disease (COPD), heart condition, pacemaker, and penicillin allergy, and other pre-existing medical conditions included the patient had allergy with unspecified pain medications and multiple other medications. The patient previously received covid-19 vaccine ad26. cov2. s (suspension for injection, route of admin not reported, batch number: unknown and expiry: unknown) 1 total, dose was not reported, administered on unspecified date for prophylactic vaccination (Dose number in series 1). The patient experienced no adverse events 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: 211D21A and expiry: unknown) 1 total, dose was not reported, administered at left arm on 13-JAN-2022 for prophylactic vaccination (Dose number in series 2). The patient' s concomitant medications included blood thinners, the patient stated she bruises easily with blood thinners. On 13-JAN-2022, the patient stated after receiving booster shot she had reaction, sore arm (like if someone punched in the arm), bump below the injection site, red spots, feel not energetic, slight headache on and off, itchy eyes, breathing issue (the patient stated that it might be due to her asthma) (Dose number in series 2). She took 2 Tylenol and then the headache felt better. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from slight headache on and off, had not recovered from bump below injection site, sore arm, not energetic, itchy eyes, and red spots, and the outcome of breathing issue was not reported. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Asthma; Cardiac pacemaker insertion; COPD; Heart disorder; Penicillin allergy
- Vorgeschichte
- Medical History/Concurrent Conditions: Arterial therapeutic procedure; Bruise; Spinal operation; Comments: the patient had allergy with unspecified pain medications and multiple other medications.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 19.01.2022
- 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: unbekannt
Erholt: nein
Chills
Fatigue
Flushing
Headache
Hypoaesthesia
Lethargy
Paraesthesia
Peripheral coldness
Peripheral swelling
Pyrexia
Swelling face
Symptomtext
Fingers/Toes are numb/cold/prickly. Also experienced throbbing Headache, Fever (102.5), Chills, Fatigue, Lethargy since 5 last afternoon. Flushed, swollen face and limbs.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Known reported
- Vorgeschichte
- None
- Andere Medikamente
- Multivitamin, Zinc, Vitamin D
- Allergien
- None known
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Fatigue
Headache
Hyperhidrosis
Injection site bruising
Myalgia
Pain
Pain in extremity
Pyrexia
Rash
Rash erythematous
Tremor
Symptomtext
I received the vaccination around 5pm on Friday, as soon injection went in a felt a stinging down my arm. At 1230am I woke up from sleeping with horrible body aches, I had a fever, and I was shaking (like a tremor in both of my hands). I took 1000mg of Tylenol and took a warm shower but the shaking did not stop for 1-1.5 hours. I then woke up with muscle pain and sweating. The muscle pain, fatigue, and headache. I have bruising to my right arm near the injection site and pain in my arm. On Sunday I woke up with a red, blanching rash on my trunk and arms and continued have muscle pain and a headache. Monday continued having a headache and fatigue and keep getting a sharp pain in my left chest. Tuesday I have an intermittent sharp pain in the left side of my chest.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- none.
- Vorgeschichte
- none.
- Andere Medikamente
- Clomid, excedrin, multi-vitamin
- Allergien
- none known.
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 18.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Back pain
Blindness unilateral
Chest pain
Chills
Cognitive disorder
Confusional state
Cough
Delusion
Eye pain
Headache
Hyperhidrosis
Lymphadenopathy
Malaise
Nausea
Neck pain
Photophobia
Pyrexia
Symptomtext
Acute Covid Symptoms. Headache, eye pain, neck pain, back pain, chest pain, vertigo, nausea, energy loss, throat irritation, cough. 102 fever for 8 hours, with chills, sweats, and delusional visions. Elevated temperature 99.8 for 48hours with continued cough, eye pain, chest pain. Continued swollen lymph nodes under arms, confused/ cloudy cognitive function, chest pain, energy loss, light sensitivity and measurable vision loss in right eye.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Doctor stated that these adverse reactions are common and not in need of testing.
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 17.01.2022
- Impfdatum
- 27.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Injected limb mobility decreased
Injection site pain
Symptomtext
Woke up the next morning with pain in my left shoulder. Pain continued and increased since then. Unable to raise arm, or move shoulder area without severe pain, and mobility is limited.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- 1/17/2022 - office visit to the clinic - doctor indicated it was a reaction from receiving the shot. Prescribed anti inflammatory medication to see if that gives some relieft.
- Aktuelle Erkrankungen
- Psoriasis (which is what the Methotrexate and Folic Acid are for)
- Vorgeschichte
- Psoriasis
- Andere Medikamente
- Methotrexate Folic Acid Citalopram Imitrex (as needed - haven't taken in about 4 months) Lorazepam (as needed)
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 26.12.2021
- Beginn
- 13.01.2022
- Tage bis Beginn
- 18,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Body temperature increased
COVID-19
Chest X-ray abnormal
Cough
Dyspnoea
Malaise
Oxygen saturation decreased
Pneumonia
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Covid19 breakthrough. Vaccinated on 12/26/2021. 58 y/o PMH HTN presents to ED with Covid19 symptoms that started 6 days ago when tested + for Covid. Pt c/o worsening cough, SOB and low O2 sats recorded at home. Denies fever, chills, N/V, HA or dizziness. CXR- multifocal PNA. T-102.5 , requires O2 at 2L NC-94%. Started on IV ABX/IV steroids and Remdesivir.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Positive Covid test 1/8/2022-no records available
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HTN
- Andere Medikamente
- -
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 14.01.2022
- 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
Chest discomfort
Depression
Fatigue
Headache
Heart rate increased
Heart rate irregular
Hypertension
Insomnia
Myalgia
Pyrexia
Symptomtext
Within 6 hours I had a fever, muscle/headaches, increased heart rate and chest tightness. Persisting symptoms are increased heart beat rate, chest tightness, increased resting heart rate, high blood pressure, irregular heart beat, fatigue, trouble sleeping and depression.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- Blood pressure of 165/90 increased from baseline of 120/60.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Acid reflux
- Andere Medikamente
- Finasteride, Omeprazole
- Allergien
- Eggs
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 11.01.2022
- Impfdatum
- 12.11.2021
- Beginn
- 12.01.2022
- Tage bis Beginn
- 61,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Burning sensation
Derealisation
Feeling abnormal
Lymphadenopathy
Neck pain
Paraesthesia
Symptomtext
Tingling and burning sensations for a week in hand and feet and persistent Brain Fog, Derealization, Swollen left armpit lymph node Neck and Back Pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Multi Vitamin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 11.01.2022
- Impfdatum
- 08.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Arthralgia
Back pain
Chest pain
Pain
Symptomtext
Patient has a history of cancer and DVT, received first dose Janssen on saturday 1/8/22. She calls the pharmacy complaining that she is experiencing chest pain radiating to her back/ shoulder. She describes it as constant and has been ongoing for an hour today (1/11/22). I informed patient that she would need to go to the ER/ call emergency as this can be an emergency.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 10.01.2022
- Impfdatum
- 10.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Nausea
Paraesthesia
Piloerection
Vomiting
Symptomtext
Patient said he was feeling tingling in his arms and hands both sides. Then he started feeling nauseous, vomited on site for about 1 minute. Went to the restroom to clean up. Came back shivering with goose bumps. Sat down in an observation chair for about 10 more minutes waiting for a parent to come and drive him home. Felt better and went home
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- -
- Andere Medikamente
- Abilify 2mg Bupropion SR 150mg
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 10.01.2022
- Impfdatum
- 02.12.2021
- Beginn
- 26.12.2021
- Tage bis Beginn
- 24,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dyspnoea
Influenza A virus test
Influenza B virus test
Nucleic acid test
SARS-CoV-2 test
Symptomtext
Worsening SOB
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- SARS-CoV-2 (COVID-19) and Influenza AB by Nucleic Acid Amplification, POC
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HTN, CHF, COPD, DM, Macular Degeneration, Pacemaker,
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 09.01.2022
- Impfdatum
- 29.11.2021
- Beginn
- 03.12.2021
- Tage bis Beginn
- 4,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Headache
Nightmare
Pain
Pyrexia
Tremor
Symptomtext
Severe headache, fever of 102, tremors, body aches, nightmares. Fever lasted for 36 hours, but was kept <100 with Tylenol.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- -
- Allergien
- Penicillin- rash
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 08.01.2022
- Impfdatum
- 23.11.2021
- Beginn
- 23.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain
Diarrhoea
Dyspnoea
Lip swelling
Nausea
Pruritus
Rash
Swelling face
Urticaria
Symptomtext
elevate heart rate (120-125). facial swelling, 30 minutes post injection - lasting approximately 12 hours. Hives, itching, approximately 45 minutes post injection lasting 24 hours. Rash 30 minutes post injection lasting 3 days. Swollen lips approximately 45 minutes post injection lasting approximately 12 hours., Breathing problems approximately 45 minutes post injection lasting 12 hours. Abdominal cramping with nausea and diarrhea 2 hours post injection lasting approximately 2 days. Physician instructed patient to take Benadryl and ibuprofen approximately 45 minutes after injection and continue until resolved. Patient used inhaler to assist with breathing issues.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- hemochromatosis, hypoglycemia,
- Andere Medikamente
- None
- Allergien
- Latex, codeine, penicillin, sulfur, strawberries, kiwi, banana, avocado, water chestnuts
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 08.01.2022
- Impfdatum
- 03.12.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Tachycardia
Symptomtext
ITCHING SENSATION ON LEFT FOOT VEIN (FEELING AS A PRICK); TACHYCARDIA; This spontaneous report received from a consumer 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 (Dose number in series 1) (suspension for injection, route of admin not reported, batch number: 1805031 and expiry: UNKNOWN) dose was not reported, 1 total, administered on 13-Mar-2021 on left arm for prophylactic vaccination. The patient experienced phlebitis when treated with first dose of covid-19 vaccine ad26.cov2.s. The patient received covid-19 vaccine ad26.cov2.s (Dose number in series 2) (suspension for injection, route of admin not reported, batch number: 211D21A and expiry: UNKNOWN) dose was not reported, 1 total, administered on 03-DEC-2021 on left arm for prophylactic vaccination. No concomitant medications were reported. On an unspecified date in DEC-2021, the patient experienced itching sensation on left foot vein where she got phlebitis after first dose (feeling as a prick) and tachycardia (Dose number in series was 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the itching sensation on left foot vein/ feeling as a prick and tachycardia was not reported. This report was non-serious. This case, involving the same patient is linked to 20211260960 (Dose number in series 1).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tachycardia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 08.01.2022
- Impfdatum
- -
- Beginn
- 16.11.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Blood glucose
Dyspnoea
Ear pruritus
Pruritus
Urticaria
Cough
Swelling of eyelid
Swollen tongue
Symptomtext
ITCHING ALL OVER THE BODY; DIFFICULTY BREATHING; HIVES; ITCHING IN EARS; This spontaneous report received from a patient concerned a 57 year old female. The patient's height and weight were not reported. The patient's past medical history included: hives and concurrent conditions include: asthma, hypothyroidism, diabetes mellitus type 2, sulpha allergy, non-alcohol user, and non-smoker, and the patient was allergic to grape leaves. The patient did not have any drug abuse or illicit drug use. The patient was previously received with covid-19 vaccine ad26. cov2. s (Unspecified manufacturer) (suspension for injection, route of admin not reported, batch number: unknown, and expiry: unknown) dose was not reported, 1 total administered on an unspecified date for prophylactic vaccination (dose number in series 1). The patient did not have side effects with the initial vaccine dose (dose number in series 1). The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211D21A, and expiry: 11-APR-2022) dose was not reported, 1 total, administered on 15-NOV-2021 for prophylactic vaccination on the left arm (dose number in series 2). No concomitant medications were reported. On 16-NOV-2021 (the day after the booster dose), the patient experienced itching in ears. On 17-NOV-2021, the patient experienced hives, itching all over body, and difficulty breathing (dose number in series 2). The patient went to the emergency room on the same day but was not admitted. She was treated and released with prednisone, and given pills to take for a few days upon discharge that day. On 19-NOV-2021, Laboratory data included: Blood glucose (not provided) Increased. The patient stated that due to increased blood glucose level she did not take the last prednisone. On 24-NOV-2021, Laboratory data included: Blood glucose (not provided) unknown. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from itching in ears on 17-NOV-2021, itching all over the body, and difficulty breathing on 19-NOV-2021, and hives on 18-NOV-2021. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Test Date: 20211119; Test Name: Blood glucose; Result Unstructured Data: Increased; Test Date: 20211124; Test Name: Blood glucose; Result Unstructured Data: unknown
- Aktuelle Erkrankungen
- Abstains from alcohol; Asthma; Hypothyroidism; Non-smoker; Sulfonamide allergy; Type II diabetes mellitus
- Vorgeschichte
- Medical History/Concurrent Conditions: Hives; Comments: Patient was allergic to grape leaves. Patient did not have any drug abuse or illicit drug use.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 08.01.2022
- Impfdatum
- -
- Beginn
- 16.11.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Blood glucose
Dyspnoea
Ear pruritus
Pruritus
Urticaria
Cough
Swelling of eyelid
Swollen tongue
Symptomtext
ITCHING ALL OVER THE BODY; DIFFICULTY BREATHING; HIVES; ITCHING IN EARS; This spontaneous report received from a patient concerned a 57 year old female. The patient's height and weight were not reported. The patient's past medical history included: hives and concurrent conditions include: asthma, hypothyroidism, diabetes mellitus type 2, sulpha allergy, non-alcohol user, and non-smoker, and the patient was allergic to grape leaves. The patient did not have any drug abuse or illicit drug use. The patient was previously received with covid-19 vaccine ad26. cov2. s (Unspecified manufacturer) (suspension for injection, route of admin not reported, batch number: unknown, and expiry: unknown) dose was not reported, 1 total administered on an unspecified date for prophylactic vaccination (dose number in series 1). The patient did not have side effects with the initial vaccine dose (dose number in series 1). The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211D21A, and expiry: 11-APR-2022) dose was not reported, 1 total, administered on 15-NOV-2021 for prophylactic vaccination on the left arm (dose number in series 2). No concomitant medications were reported. On 16-NOV-2021 (the day after the booster dose), the patient experienced itching in ears. On 17-NOV-2021, the patient experienced hives, itching all over body, and difficulty breathing (dose number in series 2). The patient went to the emergency room on the same day but was not admitted. She was treated and released with prednisone, and given pills to take for a few days upon discharge that day. On 19-NOV-2021, Laboratory data included: Blood glucose (not provided) Increased. The patient stated that due to increased blood glucose level she did not take the last prednisone. On 24-NOV-2021, Laboratory data included: Blood glucose (not provided) unknown. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from itching in ears on 17-NOV-2021, itching all over the body, and difficulty breathing on 19-NOV-2021, and hives on 18-NOV-2021. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Test Date: 20211119; Test Name: Blood glucose; Result Unstructured Data: Increased; Test Date: 20211124; Test Name: Blood glucose; Result Unstructured Data: unknown
- Aktuelle Erkrankungen
- Abstains from alcohol; Asthma; Hypothyroidism; Non-smoker; Sulfonamide allergy; Type II diabetes mellitus
- Vorgeschichte
- Medical History/Concurrent Conditions: Hives; Comments: Patient was allergic to grape leaves. Patient did not have any drug abuse or illicit drug use.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 05.01.2022
- 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
Fatigue
Muscular weakness
Pyrexia
Tremor
Vomiting projectile
Symptomtext
Fever 102+, projectile vomiting, tremors, muscle weakness, fatigue lasting 30 hours
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Atorvistatin 40mg
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 05.01.2022
- Impfdatum
- 04.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Chest pain
Neck pain
Paraesthesia
Symptomtext
Dose #1 - headaches, loss of taste / smell, fatigue, diarrhea, fever Dose #2 - Tingling in fingers / hands, tingling in toes / feet, left neck side pain, upper back pain, chest pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- going to doctor 1/7/22
- Aktuelle Erkrankungen
- IBS, Fibromyalgia, HBP, Afib, Diabetes
- Vorgeschichte
- Chronic Cough, Chronic Inflammation, Chronic Migraine, Chronic Blood Clots
- Andere Medikamente
- none
- Allergien
- latex, penicillin
- Vorherige Impfungen
- Janssen Covid 19 Vaccine
- Staat
- MN
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 03.01.2022
- Impfdatum
- 09.04.2021
- Beginn
- 12.04.2021
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Acoustic stimulation tests
Dizziness
Laboratory test
Magnetic resonance imaging
Vertigo
Vestibular migraine
Symptomtext
After first JANSSEN vaccine had ongoing vertigo and dizziness for 5 five months. Was not able to drive, etc. Received the JANSSEN booster shot on 11/11/2021 and 3 days later had a debilitating migraine that lasted for two weeks. Multiple visits to my primary physician as well as an ENT, emergency care visit resulted in a diagnosis of vestibular migraines. No history of migraines previously or health issues. Still having chronic migraines and vestibular issues.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vestibular migraine
- Hospital-Tage
- -
- Labordaten
- Lab panels, hearing and vision testing, MRI 11/24/2021.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Womens multi vitamin
- Allergien
- Dairy
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 03.01.2022
- Impfdatum
- 09.12.2021
- Beginn
- 10.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Computerised tomogram
Diarrhoea
Dizziness
Dyspnoea
Fibrin D dimer
Mass
Nausea
Urine analysis
Symptomtext
Pt developed SOB, nausea, diarrhea, lightheadedness, and lumps in arms and legs
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- D-Dimer, CT lungs, US of lower extremities
- Aktuelle Erkrankungen
- DM, HTN, A. Fib, Edema, Anxiety, hypothyroidism, gout, diverticulosis, asthma, h/o DVT, MDD, esophageal dysmotility, stress-induced cardiomyopathy, IBS, arthritis, LVH, peripheral neuropathy, vertigo, anemia, osteoporosis, gastroparesis, iron deficiency, Takotsubo syndrome, pacemaker, heart block, constipation, fibromyalgia.
- Vorgeschichte
- See above.
- Andere Medikamente
- Prolia, Synthroid, Pantoprazole, Dicyclomine, Albuterol.
- Allergien
- Iodine, Meperidine, Peanut Butter, Metformin, Tradjenta, Codeine.
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 31.12.2021
- Impfdatum
- -
- Beginn
- 01.12.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Burning sensation
Fatigue
Influenza
Musculoskeletal chest pain
Pain
Pain in extremity
SARS-CoV-2 test
Sensory disturbance
Symptomtext
LEFT ARM FELT LIKE IT WAS JUST VACCINATED FOR ONE DAY ONLY; BOTH ARMS HURT; FLU/CHILLS SYMPTOMS; BACK ACHE/ BACK DISCOMFORT/PAINS ARE BETWEEN SHOULDER BLADES; RIBCAGE ACHE/ RIB DISCOMFORT; FEELING TIRED; NO FEVER BUT FELT LIKE IT WAS BURNING UP INSIDE; LITTLE ACHINESS; This spontaneous report received from a patient concerned a 54 year old female. The patient's weight was 120 pounds, and height was 63 inches. The patient's concurrent conditions included: bronchitis, allergenic asthma, environmental allergies, and seasonal allergies. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211D21A, and expiry: 11-APR-2022) dose was not reported, administered on 11-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. On DEC-2021, the patient experienced little achiness. Laboratory data included: COVID-19 virus test (NR: not provided) negative, negative. On 11-DEC-2021, the patient experienced no fever but felt like it was burning up inside, and feeling tired. On 12-DEC-2021, the patient experienced flu/chills symptoms, back ache/ back discomfort/pains are between shoulder blades, ribcage ache/ rib discomfort, and both arms hurt. On 22-DEC-2021, the patient experienced left arm felt like it was just vaccinated for one day only. Treatment medications (dates unspecified) included: paracetamol, and ibuprofen. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from no fever but felt like it was burning up inside, flu/chills symptoms, and both arms hurt, and left arm felt like it was just vaccinated for one day only on 23-DEC-2021, had not recovered from back ache/ back discomfort/pains are between shoulder blades, ribcage ache/ rib discomfort, and little achiness, and the outcome of feeling tired was not reported. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Musculoskeletal chest pain
- Hospital-Tage
- -
- Labordaten
- Test Date: 202112; Test Name: COVID-19 virus test; Result Unstructured Data: negative; Test Date: 202112; Test Name: COVID-19 virus test; Result Unstructured Data: negative
- Aktuelle Erkrankungen
- Allergic asthma; Bronchitis; Environmental allergy; Seasonal allergy
- Vorgeschichte
- Comments: Unknown
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 29.12.2021
- Impfdatum
- 29.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Tremor
Unresponsive to stimuli
Symptomtext
Patient received janssen booster vaccine at around 1:40pm on 12/29/2021. Shortly after at around 1:50 pm patient was observed having his head tilted back and shaking repeatedly. At that moment patient was not alert and oriented, was not responsive to verbal commands. VS signs taken promptly BP: 156/128 , HR 131, RR: 24, T:97.9, oxygen level 96%. 911 called immediately. While waiting for EMS patient had the same cycle of being in and out and not responding to verbal commands. EMS arrived shortly and took patient to nearest hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Patient reported PMH of hypertension. Patient had brain surgery in the past and also reported history of having a seizure.
- Andere Medikamente
- Patient reported not being on prescription medications or taking OTC, supplements etc.
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 29.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Headache
Pyrexia
SARS-CoV-2 test negative
Tachycardia
Symptomtext
Patient complained of feeling feverish and mild headache after receiving the Janssen vaccine. He was seen by a medical provider on 12/22/21, and his vitals were within normal limits except mild tachycardia (100-113 bpm). He received Ibuprofen for symptomatic treatment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tachycardia
- Hospital-Tage
- -
- Labordaten
- 12/11/21 and 12/22/21 SARS-Cov-2, NAA were both negative.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 27.12.2021
- Impfdatum
- 26.12.2021
- Beginn
- 26.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Palpitations
Pyrexia
Symptomtext
Severe headache, racing heart, fever 104 degrees F Healthy athlete who previously had Covid 19 in Fall of 2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 20.11.2021
- Beginn
- 21.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Cardiac discomfort
Cardiac monitoring
Chest X-ray
Chest discomfort
Chest pain
Dizziness
Echocardiogram
Electrocardiogram
Inflammation
Symptomtext
I have tried to right this down no 4 times and every time the document times out and makes me start over. At this point, call me, I would love to explain for an hour about everything I have been going through with significant chest pain since vaccination, and feeling of having mini heart attacks. Started 14hours after vaccine with significant chest pain and squeezing, and has not gone away with constant daily chest pressure. Almost collapsed in a grocery store from what felt like a heart attack 12/15 which I ended up in the ER and was told to seek Cardiologist care.... CALL ME FOR MORE INFORMATION
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- 11/22: EKG, Blood Work 12/15: EKG, Blood work, Chest Xray 12/22: Echocardiogram, Heart Monitor, inflammation blood work on order
- Aktuelle Erkrankungen
- Absolutely None
- Vorgeschichte
- Absolutely None
- Andere Medikamente
- None
- Allergien
- Penicillin, Vicodin, Egg Whites
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 22.12.2021
- Beginn
- 23.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site swelling
Paraesthesia
Symptomtext
swelling at site of injection and tingling in toes day after
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- not known
- Vorgeschichte
- not known
- Andere Medikamente
- not known
- Allergien
- no known
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 15.12.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anxiety
Blood pressure increased
Blood pressure measurement
Feeling hot
Flushing
Tremor
Symptomtext
FEEL WARM FROM MY HEAD TO MY NECK /WARMTH SENSATION ALL OVER/ LIGHT WARM SENSATION IN CHEST AREA; ANXIETY; ELEVATED BLOOD PRESSURE; FLUSHED FACE/GOT RED IN THE FACE; SHAKY LEGS; This spontaneous report received from a patient concerned a 79-year-old elderly female. The patient's weight was 180 kilograms, and height was 67 centimeters. The patient's past medical history included: constipation (the patient stated that Cholestyramine 4g gave her horrendous Constipation), and concurrent conditions included: hernias, Crohn's symptoms, and irritable bowel symptoms (IBS), and other pre-existing medical conditions included: The patient had no known allergies. The Patient added that her stomach started going bad when COVID hit, and that currently she was in remission from Crohn's/IBS and was currently undergoing GI diagnostic testing for her recent reappearance of GI (gastro intestinal) symptoms. The patient previously received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: Unknown and expiry: unknown) 1 total, dose not reported, administered on 18-MAR-2021 for prophylactic vaccination (dose number in series 1), and reported no side effects at all. The patient received booster covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211D21A and expiry: 11-APR-2022) 1 total, dose was not reported, administered at right arm on 15-DEC-2021 at 10:30 for prophylactic vaccination (dose number in series 2). Concomitant medications included Cholestyramine Oral powder 4g (colestyramine) for Chron's symptoms (For stomach issues, not for Cholesterol). The patient skipped the medication as per her HCP (Health care provider) at the day of reporting. On 15-Dec-2021, the patient reported that she started getting warm, started in feet, went to neck too, all over, like getting IV dye, but not internal, more like in the skin- she got red in the face, flushed, became anxious after the 10-minute observation period was over and they had kept her there for another 45 minutes and then she got really anxious. The patient stated that there was 4 separate episodes of this, they started about 5'' after, occurring every 5-10''. The patient added that her blood pressure was elevated, no temperature was taken, and she had "shaking legs". The patient stated that vaccine facility suggested her to go to Emergency room but the episodes subsided, nothing else happened, so she went home. The patient was reporting that she was still having light warm sensation in chest area (dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from elevated blood pressure, flushed face/got red in the face, and shaky legs on 15-DEC-2021, was recovering from anxiety, and had not recovered from feel warm from my head to my neck /warmth sensation all over/ light warm sensation in chest area. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- Test Date: 20211215; Test Name: Blood pressure; Result Unstructured Data: Elevated
- Aktuelle Erkrankungen
- Crohn's disease (The doctors are debating if it Chrons' "leaky gut" or IBS- X40 years. currently she is in remission from Chrons/IBS); Hernia; Irritable bowel (IBS- X40 years)
- Vorgeschichte
- Medical History/Concurrent Conditions: Constipation; Comments: The patient had no known allergies.
- Andere Medikamente
- CHOLESTYRAMINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 22.12.2021
- Impfdatum
- 08.12.2021
- Beginn
- 09.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal pain upper
Chest pain
Constipation
Decreased appetite
Diarrhoea
Gastrooesophageal reflux disease
Nausea
SARS-CoV-2 test negative
Ultrasound abdomen
Vomiting
Symptomtext
The day following the vaccine I had little to no hunger, every bite I would feel full. My stomach would cramp after eating. I would attempt to use the restroom and each time the nausea would get worse. I had acid reflux, which I have never had before. The acid reflux was bad to the point where I vomited and yellow mucus came out but only a small amount. I also had diarrhea, followed by constipation. Even with my chronic conditions, I have never vomited, had acid reflux, or had diarrhea. I also had some sharp chest pain in my upper chest both on the left and then the right side. My chronic condition had improved and I had no symptoms from around August until my vaccine, and then they came back.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Ultrasound of the abdomen 12/21/21, Covid test 12/20/21. Ultrasound showed SMA was there, covid test was negative.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- IBS, Gastroparesis, SMA (Superior Mesenteric Artery) Syndrome.
- Andere Medikamente
- Erythromycin, Omeprazole, Elavil, Probiotics, Milk of Magnesia
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 22.12.2021
- Impfdatum
- 16.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Paraesthesia
Symptomtext
PT WAS BURNING UP, HOT TINGLING SENSATION IN ARMS AND FEET
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- PATIENT DID NOT TAKE ANTHING
- Allergien
- NONE THAT THE PATIENT WAS AWARE OF
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 21.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Anxiety
Dizziness
Dyspnoea
Symptomtext
A few minutes after patient received Janssen vaccine he informed me that he was feeling dizzy and for a few seconds he felt like he was having trouble breathing. He stated that vaccines cause him a lot of anxiety and that he has gotten nauseous in the past. I continued to observe him at the pharmacy for another 20 minutes to make sure he was not developing an anaphylactic reaction. I told him to call pharmacy if anything changes or go to ER. After 20 minutes he said that he felt alright and thinks it was just anxiety that was making him dizzy and very briefly short of breath.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WY
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 21.12.2021
- Impfdatum
- 15.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Rash
Swelling face
Tremor
Symptomtext
Rash to face, chest, back and upper extremities, facial swelling x 5 days, lightheadedness and shakiness persists.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Bactrim
- Vorherige Impfungen
- -
- Staat
- SD
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 19.12.2021
- Impfdatum
- 23.11.2021
- Beginn
- 06.12.2021
- Tage bis Beginn
- 13,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Cardiac monitoring
Chest discomfort
Chest pain
Chills
Dizziness
Dyspnoea
Groin pain
Heart rate increased
Hypertension
Impaired work ability
Loss of personal independence in daily activities
Night sweats
Pain in extremity
Tachycardia
Ultrasound scan
Symptomtext
Stabbing chest pain, dizziness Shortness of breath, tachycardia, right arm pain along with chest tightness, Right leg/groin pain. Chills, night sweats, high blood pressure and heart rate. I was admitted to the ER 3 times in the 2 weeks since my first dose. I havent worked due to the severity of my symptoms. I'm prescribed beta blockers to treat the tachycardia but nothing helps the chest pain. The high heart rate episodes occur multiple times daily and have interfered with every aspect of my daily life.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Blood test, ultra sound, 48 hour of heart monitor, doctor appointment for referral to cardiologist appointment.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 18.12.2021
- Impfdatum
- 04.11.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 43,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Palpitations
Symptomtext
Heart palpitations occur randomly throughout day. Severe headaches while commuting to work.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- HI
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 17.12.2021
- Impfdatum
- 15.12.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test normal
Hypoaesthesia
Magnetic resonance imaging head normal
Magnetic resonance imaging normal
Paraesthesia
Symptomtext
Numbness in left arm right after receiving the booster lasting all day and through the night. The next morning numbness and tingling in right hand and lower arm and occasionally right and left leg lasting all day the second day after reciting the booster. Third day after, slight tingling in right hand.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- 12/16/21: Bloodwork, MRI of brain and neck, everything came back normal.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- 3/22/21, Janssen, chills body aches, fever
- Staat
- TX
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 16.12.2021
- Impfdatum
- 15.12.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Paraesthesia
Swelling
Symptomtext
Tingling of arms and feet, joint pain and swelling
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Prenatal vitamin
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 16.12.2021
- Impfdatum
- 16.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dyspnoea
Erythema
Face oedema
Heart rate increased
Swelling face
Symptomtext
A 35-year-old female patient reports having an allergy to the Janssen booster dose. Swelling on the left side of the face and redness. By administering the second dose of modern the next day, he created facial edema on the left side of his face and he felt SOB. He is considered alert, does not present edema in the respiratory tract, strong peripheral pulses and presents facial edema.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Anxiety; Depression; Epilepsy; Alopecia folliculitis
- Andere Medikamente
- Kepra 500mg, Clonopin 1mg, Prosac 60mg, Ambien 10mg and Melatonin (2 tablets of 10mg
- Allergien
- NO
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 16.12.2021
- Impfdatum
- 06.11.2021
- Beginn
- 07.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Burning sensation
Chest X-ray
Chest pain
Erythema
Headache
Hypoaesthesia
Injection site erythema
Migraine
Pyrexia
Rash
Urticaria
Vision blurred
Symptomtext
Received the vaccine at approximately 4:00PM on 11/6/2021 and developed hives/rash on my chest with burning and redness approximately 12 hours later which spread to my stomach and the injection site, lasting approximately 6 hours. Developed a fever of 101.7 18 hours after receiving injection along with a bad headache, mild chest pains, and some numbness feeling in the legs. Took advil and the fever subsided within 6 hours. Headache and mild chest pains persisted on, from 11/7 through 11/10. On 11/10 around 7pm the headache intensified to the point that i had some blurry vision, intense pressure and felt like a migrain. I went to the emergency room and was treated and released (administered fluids and migrain medicine via iv). Migraine subsided but recurred for at least 24 hours. I have had daily headaches on and off since then. 12/15 migraine came back and lasted 4 hours, took Advil and migraine subsided. 12/16 migrain returned - took advil and migraine subsided. I've never experienced migraines prior to taking the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- 11/10 emergency room visit blood work, xrays (for chest), medication for migraine treatment. Tested for stroke - negative
- Aktuelle Erkrankungen
- Gastritis
- Vorgeschichte
- None
- Andere Medikamente
- Omeprazole
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 15.12.2021
- 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: nein
Chest pain
Cluster headache
Contusion
Dysphagia
Hypoaesthesia
Infection
Neck pain
Injected limb mobility decreased
Muscular weakness
Musculoskeletal stiffness
Paraesthesia
Petechiae
Swelling
Vision blurred
White blood cell count increased
Symptomtext
Severe pain/pressure developed along my left sternocleidomastoid within 2 hours of getting vaccine, followed by severe cluster headaches that were intermittent in nature for the following days. 3 days after, along with continued previous symptoms, I developed numbness and tingling across my face and some blurred vision. This resolved by day 5 post vaccine but on day 7, I had sudden lower leg weakness (along with continued headaches, pain and stiffness/swelling to left shoulder/ collarbone, neck region. I went to a Urgent Care 11/10/2021 and was referred to a Emergency Room. I went to a ER the following evening and was told my blood work was normal and was ?outside the window? for a serious event from the vaccine but had notable swelling on left side and was recommended ?massage? and rest. Swelling / pain and headaches continued along with lessening mobility to left arm due to pain. I called a teledoc 11/16/2021 to ask for steroids to help with swelling while I reached out to my doctor. Two days later, I started with a petechial rash on my abdomen and sporadic bruising throughout my legs. One week later- 11/19/2021, I returned to the ER due to worsening headaches, pain and difficulty swallowing. CT was negative, WBC was elevated and was told I had a soft tissue infection from the vaccine. I was started on Bactrim and continue Prednisone, along with RX Norco for pain and to follow up with my PCP. I saw my PCP 11/24/2021 and dx with toxic reaction from the vaccine, with continued antibiotics/ steroids and pain management and follow up labs in two weeks. Labs were done last week, results reported today 12/15/2021 and appear benign. However, being off antibiotics and steroids for almost a week- the severe pain has returned to my neck along with cluster headaches. I am awaiting my doctor to return my call for further orders. I have not been able to work for this period.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- 11/12/2021- swelling noted at ER 11/19/2021 - elevated WBC
- Aktuelle Erkrankungen
- Cold/ URI 10/30/2021
- Vorgeschichte
- Hypertension, Seasonal Asthma, Irregular Menstrual Cycles, Fibromyalgia Obesity
- Andere Medikamente
- Metoprolol, Spironolactone, Metformin, Omeprazole, Montelukast, Flovent, Tramadol, b12
- Allergien
- doxycycline
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 12.12.2021
- Impfdatum
- 30.11.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Chest pain
Ear discomfort
Fatigue
Gastrooesophageal reflux disease
Hypotension
Myalgia
Sinus congestion
Symptomtext
Had extreme fatigue, muscle (mostly back) pain, sinus congestion/clogged ears, shooting chest pain (not in the center of chest), symptoms of acid reflux, possible low blood pressure. Fatigue and low blood pressure symptoms subsided after a couple of days, but the other symptoms still persist. I have had extensive tests on my heart in the past and heart issues have been ruled out prior to this shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- None yet
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Ulcerative Colitis CPTSD
- Andere Medikamente
- Xeljanz 5mg 2x/day Silodosin 8mg 1x/day Omeprazole 40mg 2x/day GNC Mega Men Sport Multi Vitamin Barleans 25mg CBD 1x/day
- Allergien
- 6 MP
- Vorherige Impfungen
- Fatigue, 51 years old, 03/14/2021, Pfizer Covid Vaccine
- Staat
- PA
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 10.12.2021
- Impfdatum
- 08.12.2021
- Beginn
- 08.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Amnesia
Chest pain
Fall
Head injury
Joint injury
Symptomtext
The patient and her spouse report that the vaccination went fine and they left the pharmacy after the 15 minute waiting period and drove home. Somewhere between about 45 to 60 minutes after the vaccine, the patient reports that she fell at home. She reports hitting her head and her chest and hurting her knee during the fall. Her spouse reports patient then went to lay in bed "for a while". Patient does not remember putting herself to bed. She has not sought treatment and says she is improving as far as her chest and knee injuries go.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 10.12.2021
- 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: ja
Erholt: nein
Chest pain
Dizziness
Headache
Heart rate increased
Hypertension
Nausea
Palpitations
Symptomtext
Chest pain, dizziness, high heart rate, headache, high blood pressure, light headed, nausea, palpitations.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 09.12.2021
- 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: nein
Chills
Headache
Hypoaesthesia
Pain
Paraesthesia
Pyrexia
Symptomtext
12/8 - 9:30 pm: chills start but no fever 12/8- 11:00 pm: slight fever of 99-100 12/9 - 1:30 am: woken up because legs and arms and tingling and numb. Adjusted sleeping position but no relief. 12/9 - 5:00 am : leg tingling and numbness gone but wrist numbness had gotten worse. Felt like someone was squeezing my wrists. 12/9 - 9:00 am to 7:00 pm: numbness and tingling gone in limbs. Headache and body aches for remainder of day
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypothyroidism
- Andere Medikamente
- Ocella and synthroid (88mcg)
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 09.12.2021
- 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: nein
Chills
Heart rate irregular
Impaired work ability
Loss of personal independence in daily activities
Pain
Spinal pain
Tachycardia
Symptomtext
Tachycardia, irregular heart, chills, body aches, spine pain, neck pain, unable to go to work or perform normal activity due to s/s.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tachycardia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 08.12.2021
- Impfdatum
- 08.12.2021
- Beginn
- 08.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Immediate post-injection reaction
Muscle spasms
Paraesthesia
Symptomtext
47 y/o female patient presents with cramping and paresthesia in her left upper extremity, immediately after vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- V/S P:79, B/P: 130/60, R: 17 O%: 97
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 08.12.2021
- 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: unbekannt
Erholt: nein
Arthralgia
Chest pain
Epistaxis
Symptomtext
Chest pains starting the day after getting the shot. Chest pains coming and going for 2 weeks and still occurring. Left should has remained sore for 3 weeks after getting the shot. I've felt like I was on the cusp of a heart attack while playing hockey and have never had this feeling in my life having played hockey regularly for the last 30 years. I've had nose bleeds the last couple of weeks as well.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- NA
- Allergien
- NA
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 07.12.2021
- Impfdatum
- -
- Beginn
- 18.11.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal discomfort
Body temperature
Chills
Condition aggravated
Dry throat
Euphoric mood
Feeling jittery
Hypoaesthesia
Injection site pain
Migraine
Nervous system disorder
Neuralgia
Pain
Paraesthesia
Pyrexia
Sleep disorder
Somnolence
Therapeutic response unexpected
Symptomtext
MILD GASTROINTESTINAL (GI) UPSET; JITTERY; SLEEPY; MIGRAINE/HEADACHE; MINIMAL SLEEP; CHILLS; TINGLING TO FEET; NUMBNESS TO FEET; INJECTION SITE SORENESS; HIGH FEVER; NERVOUS SYSTEM DISORDER; FLARE UP; LIGHTS GOT BRIGHT/EUPHORIA/FELT LIKE SHE TOOK AMPHETIMINES; VISION GOT SHARPER MOMENTARILY, SPEEDED UP AND WAS THINKING SHARPER; BODY ACHES; PARCHED DRY THROAT; NEUROPATHIC PAIN; This spontaneous report received from a patient concerned a 72-year-old female. Initial information received on 18-NOV-2021 was processed with additional information received on 22-NOV-2021. This case was reassessed as serious based upon new information received from the patient on 22-NOV-2021. The patient's height, and weight were not reported. The patient's concurrent conditions included: spinal stenosis, migraines, neuro inflammatory, penicillin allergy, topical sulpha drugs allergy, nonsmoker, and non-alcohol user. The patient had no history of drug abuse or illicit drug usage. The patient experienced drug allergy when treated with acetylsalicylic acid, proton pump inhibitors (PPIs) and macrogol. On an unspecified date, the patient previously received initial covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin, and batch number were not reported), 1 in total, dose was not reported (dose number in series was 1), for prophylactic vaccination. On an unspecified date, following vaccination with covid-19 vaccine ad26.cov2.s, the patient experienced citrus taste and throat burning (Captured : 20211159138). The patient received a booster dose of covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211D21A, expiry: 11-APR-2022) dose was not reported (dose number in series was 2), 1 total administered on 18-NOV-2021 to left arm for prophylactic vaccination. No concomitant medications were reported. On 18-NOV-2021, evening of injection, the patient experienced sleepy as if she took a tranquilizer, slight chills and achy and by 23:00 the patient experienced fever of 99.3 F (high of fever), body aches, parched dry throat, injection site soreness and minimal sleep. On 18-NOV-2021, the patient also experienced "lights got bright/euphoria," neuropathic pain, tingling to feet, numbness to feet, headache, vision got sharper momentarily, "speeded up" and was "thinking sharper" (therapeutic response unexpected) and felt like she took amphetimines. The patient also experienced neuro inflammatory "flare up" (coded as nervous system disorder, and flare up). Laboratory data included: Body temperature ( not provided) 99.3 F, 100.1 F. On 20-NOV-2021, the patient experienced migraine and the next day (21-NOV-2021) she experienced mild gastrointestinal (GI) upset and jittery. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from nervous system disorder, flare up, lights got bright/euphoria/felt like she took amphetimines, body aches, tingling to feet, and numbness to feet on 18-NOV-2021, vision got sharper momentarily, speeded up and was thinking sharper, parched dry throat, sleepy, migraine/headache, minimal sleep, and chills on 20-NOV-2021, mild gastrointestinal (GI) upset, jittery, and high fever on 21-NOV-2021, and injection site soreness on 22-NOV-2021, and had not recovered from neuropathic pain. This report was serious (Other Medically Important Condition). This case, involving the same patient is linked to 20211159138.; Sender's Comments: V0: 20211143069-covid-19 vaccine ad26.cov2.s- nervous system disorder, flare up. 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
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Test Date: 20211118; Test Name: Body temperature; Result Unstructured Data: 100.1 F; Test Date: 20211118; Test Name: Body temperature; Result Unstructured Data: 99.3 F
- Aktuelle Erkrankungen
- Abstains from alcohol; Autoimmune disorder; Drug allergy (The patient experienced drug allergy when treated with Proton pump inhibitors (PPIs)); Non-smoker; Penicillin allergy; Spinal stenosis; Sulfonamide allergy
- Vorgeschichte
- Medical History/Concurrent Conditions: Migraine; Comments: The patient had no history of drug abuse or illicit drug usage.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 06.12.2021
- Impfdatum
- 02.12.2021
- Beginn
- 04.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hypertension
Migraine
Symptomtext
MIGRAINES AND HIGH BLOOD PREASSURE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 01.12.2021
- Impfdatum
- 04.11.2021
- Beginn
- 04.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Blood test
Bronchitis
Cough
Crying
Dry throat
Dyspnoea
Fatigue
Feeling hot
Headache
Hyperhidrosis
Injection site discolouration
Injection site erythema
Insomnia
Lacrimation increased
Lethargy
Malaise
Mouth breathing
Symptomtext
6-7 minutes after injection, thumping on neck main vein (left-side) rapid like Morse code; watery eyes like crying, sweating profusely, very hot needed aire; notified the pharmacy immediately, water was given and waiting 1/2 hour after injection; first day headache and tired; next 2-4 days, lethargic, sick, throwing up, sleepy, location of the injection red/pink color grow from a quarter size to larger than .50 cent piece, gone after day 5, no sore right arm never had soreness, later that day and evening difficult sleeping ache joints, muscle from head to toe took Advil PM to get sleep; day 6 (Nov 9th, 2021) scratchy throat, like throat closing, body aches, throat sore and difficult to talk; day 7 very sore throat talking difficulty and becoming congestion in sinsus symptoms, was not able to breathe thru nose, breathing from mouth very cold hear, sinsus congestion for 2-3 days; called sever sinsus infection spitting up yellowish grey from sinus and difficulty breathing brochicitus, having other adverse reactions after injection, family and coworkers were worried, thru November 29, 2021 fatigued and now having chronic cough dry throat due the Johnson Johnson vaccinations. A total of 25 days for recovery or feeling back to normal.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Before the Johnson vaccinations taken ....Antibodies testing COVID and SARsCO2 - Negative test results on October 1, 2021 I telework from home 1 year and 7 months and practice social distancing never gone sick and proof from medical blood work stated above.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High Blood Pressure Thyroid Marfans - aorta aneurysm - discovery April 2021 - Family history.
- Andere Medikamente
- High Blood Pressure Thyroid (Hypo) Vitamin D and C
- Allergien
- Niacin
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 26.11.2021
- Impfdatum
- 23.11.2021
- Beginn
- 25.11.2021
- Tage bis Beginn
- 2,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Angiogram
Anxiety
Cough
Dyspnoea
Electrocardiogram
Full blood count
Metabolic function test
Pain
Pulmonary pain
Symptomtext
Shortness of breath, anxiety, body aches, cough, lung pain
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- cbc, cmp, ct chest angio, ekg,
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 26.11.2021
- Impfdatum
- 24.11.2021
- Beginn
- 25.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Dehydration
Headache
Insomnia
Myalgia
Pyrexia
Tremor
Symptomtext
Fever, dehydration, severe tremours, shiver/chills, headache, muscle aches, interrupted sleep
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dehydration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 26.11.2021
- Impfdatum
- 22.11.2021
- Beginn
- 22.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Hypoaesthesia
Paraesthesia
Symptomtext
Numbness in both legs, moderate pain in hip joints, tingling is both feet.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- No e
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Prilosec, Flonase
- Allergien
- Morphine, iodine
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 25.11.2021
- Impfdatum
- 15.11.2021
- Beginn
- 16.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Cough
Fatigue
Injection site pain
Insomnia
Migraine
Pyrexia
Wheezing
Symptomtext
At injection site, normal administration pain and sensation of burning in arm. Within 24 hours of administration patient reached 101 fever and fatigue. Within 36 hours of administration, patient reached 103 fever and fell asleep. Upon waking the next day, patient had developed significant coughing and wheezing. On the second night, patient developed difficulty sleeping with continuous coughing and migraines hypothesized as aggravating factors. It is now ten 10 days after the vaccine administration and the patient still has significant coughing and a light fever which has been continuous since the 15th.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 24.11.2021
- Impfdatum
- 17.11.2021
- Beginn
- 20.11.2021
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cellulitis
Mobility decreased
Rash
Swelling
Symptomtext
rash, inability to raise arm over shoulder, swelling. Nurse advised to go to Urgent Care, who prescribed Bactrim for Cellulitis.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Spironolactone - 50mg
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 24.11.2021
- Impfdatum
- 23.11.2021
- Beginn
- 24.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Headache
Heart rate increased
Pain
Paraesthesia
Symptomtext
Tingling all over body, headache, increased heart rate, dizzy, pain all over body
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Major Depression General Anxiety Tinnitus
- Andere Medikamente
- Duloxetine 90mg daily Guanfacine 2mg daily
- Allergien
- Amoxicillin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 23.11.2021
- Impfdatum
- 18.11.2021
- Beginn
- 19.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Headache
Malaise
Muscle spasms
Pain
Paraesthesia
Tremor
Symptomtext
Severe headache for hours, Tylenol did not help Dizziness Body shaking Tingling sensations in legs Feeling sick Muscle cramps, was painful to move
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Vitamin B12, Vitamin D
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 22.11.2021
- Impfdatum
- 22.11.2021
- Beginn
- 22.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Disorientation
Dizziness
Extra dose administered
Paraesthesia
Symptomtext
Client stated, "I was sitting in my chair for 2 minutes and then I began to feel a rush to my head. It felt like a wave of tingling all over my body and I started to feel disoriented for like 10 seconds. I then felt fine but I said to myself I need to get up and let the nurse know." Secondary RN helped transfer client into anti-gravity chair at 12:05 PM. First set of vitals were then taken at that time by Observation RN prior to Co Lead PHN responding to observation room: BP 115/75, pulse 60, O2 SAT 100%, 16 respirations per minute. At 12:08 PM Co Lead PHN advised client to take face mask off and for client to take deep breaths. Client was offered water and snacks but client declined snacks and already had a water bottle. Client stated, "I am not surprised I felt like this after the shot because back when I received my first Janssen shot the next day I felt slight chest tightness while driving. It only lasted for 15 seconds then I felt fine. I am not sure if it was due to the covid-19 vaccine so I didn't feel the need to let my doctor know." Co Lead PHN clarified whether she was short of breath during that experience while driving to which client said "no." Client stated, "I felt like I was gasping for air and not so much choking. It only lasted for 15 seconds while I was driving and I then felt fine." Client then disclosed to Co Lead PHN, "I've had similar experiences with blood draws where I feel like I'm going to faint." Client does not have any medical conditions nor is taking any medications. Client has no history of allergies. Client did state, "I am sensitive to soaps, lotions, and I always take half the dose of any medication." Co Lead PHN observed client to be A&Ox4 throughout entire conversation. Co lead PHN recommended for client to follow up with PCP regarding post vaccination symptoms and to enroll in V-SAFE. Client stated, "I have an appointment with my PCP on Tuesday, I will let them know." At 12:16 PM secondary RN educated the client on when to call 911 or go to urgent care for adverse symptoms of covid-19 vaccination. Client verbalized understanding. Co Lead PHN recommended for client to call a family member to assist the client in driving home to which client declined because she only lives 1 mile away from vaccination site. Co Lead PHN recommended for one last set of vitals after another 10 minutes of monitoring. at 12:27 PM Secondary RN took last set of vitals: BP LA 115/70, pulse 64, O2 SAT 100%. Client expressed she was ready to go home. At 12:31 PM Co Lead PHN walked with client as standby assist towards the exit of vaccination site. Client walked with steady gait and thanked us for assisting her.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 22.11.2021
- 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: nein
Chest pain
Pain in extremity
Spinal pain
Testicular pain
Symptomtext
Persistent pain in spine, arms, legs, testicles. Intermittent chest pain. Level of pain gradually reducing since injection, but still noticeable as of 11/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 20.11.2021
- 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: ja
ER: ja
Erholt: ja
Breath sounds abnormal
Chest X-ray abnormal
Cough
Dyspnoea
Fatigue
Increased upper airway secretion
Pneumonia
Wheezing
Symptomtext
Approx. 15 hrs. after vaccine, i woke up with severe fatigue, coughing and difficulty breathing. since the shot, I'm still coughing severely and still have difficulty breathing .
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Chest x-ray was done 48 hrs. after shot and - pneumonia was found, MD listened to lungs and heard fluid and wheezing in left lobe, gave albuterol treatment in Emergency room and sent home with an inhaler that I now use on a regular basis. I wake up during the night with a gurgling in my throat and severe coughing attack chronically. Since the ED visit I've been to an Urgent Care where they prescribed Predenone and 600mg of Advil. still without relief. I am an active Firefighter and was seen in medical facility where they have advised me to seek my own medical treatment, I have reached out to a Lung and Heart Specialist and will seek treatments and testing to find out what is going on. since the shot, difficulty breathing and coughing, both are chronic with mild relief with albuterol pump.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- HI
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 20.11.2021
- Impfdatum
- -
- Beginn
- 17.11.2021
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Asthenia
Body temperature
Chills
Dizziness
Dyspnoea
Headache
Palpitations
Pyrexia
Vision blurred
Symptomtext
FEVER; WEAK LIKE GOING TO PASS OUT; DIZZY/CANT TURN HEAD; PALPITATIONS; SLIGHT BLURRED VISION; SLIGHT DIFFICULTY BREATHING; EXTREME JOINT PAIN; UNCONTROLLABLE CHILLS; HEADACHE; This spontaneous report received from a patient concerned a 44 year old male. The patient's height, and weight were not reported. The patient's past medical history included: brain tumor, and concurrent conditions included: migraine. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211D21A, expiry: 11-APR-2022) dose was not reported, administered on 17-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 17-NOV-2021, the patient experienced dizzy/cant turn head. On 17-NOV-2021, the patient experienced palpitations. On 17-NOV-2021, the patient experienced slight blurred vision. On 17-NOV-2021, the patient experienced slight difficulty breathing. On 17-NOV-2021, the patient experienced extreme joint pain. On 17-NOV-2021, the patient experienced uncontrollable chills. On 17-NOV-2021, the patient experienced headache. On 17-NOV-2021, the patient experienced weak like going to pass out. On 18-NOV-2021, the patient experienced fever. Laboratory data included: Body temperature (NR: not provided) 102 C. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from uncontrollable chills on 18-NOV-2021, was recovering from extreme joint pain, and had not recovered from dizzy/cant turn head, slight difficulty breathing, headache, slight blurred vision, fever, weak like going to pass out, and palpitations. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Test Date: 20211118; Test Name: Body temperature; Result Unstructured Data: 102 C
- Aktuelle Erkrankungen
- Migraine
- Vorgeschichte
- Medical History/Concurrent Conditions: Brain tumor
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 19.11.2021
- Impfdatum
- 19.11.2021
- Beginn
- 19.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dyspnoea
Fatigue
Interchange of vaccine products
Swelling face
Symptomtext
Client presented to the vaccination site on 11/19/2021. The client notified PHN that she received a single dose of Moderna COVID vaccine on 3/18/2021. Patient reported that 12 hours after receiving dose 1 of Moderna COVID vaccine, she experienced swelling on her chin to her neck, difficulty breathing, extreme fatigue. The side effects resolved within 4 days post injection. The patient reported no allergies. Medical conditions include hypertension and hypotention. Medications include losartan, amlodipine, aspirin, and a statin drug. PHN submitted a medical consult via message to Vaccine Operations Leads, requesting to proceed with the COVID vaccine Janssen. Approval to proceed with COVID vaccine Janssen was obtained from medical consult team via message from another PHN, Vaccine Operations Lead. Client received COVID vaccine Janssen Lot 211D21A on 11/19/2021. The client did not report any symptoms during the 30 minute observation period. RN educated client on possible adverse reactions and when to seek medical care. The client left the vaccination site at 1530 walking with steady gait.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- moderna
- Staat
- OH
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 17.11.2021
- Impfdatum
- 16.11.2021
- Beginn
- 17.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest discomfort
Palpitations
Tinnitus
Symptomtext
Chest discomfort, tinnitus, heart palpitations, pulse of 140, blood pressure - 155/102.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- None.
- Andere Medikamente
- None.
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 17.11.2021
- Impfdatum
- -
- Beginn
- 01.11.2021
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Tinnitus
Symptomtext
TINNITUS HAS INCREASED IN AMPLITUDE BY 3-4 TIMES, UNBEARABLE; POSSIBLY WORSENED DISC DISEASE AND BONE SPURS CONDITION SINCE VACCINATION; This spontaneous report received from a patient concerned a 57 year old male. The patient's weight was 260 pounds, and height was 77 inches. The patient's concurrent conditions included: mild tinnitus, bone spurs, medically controlled hypertension, mid range hearing loss, and neck/back pain with disc disease, and other pre-existing medical conditions included: Patient did not had any known allergies. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211D21A, expiry: 11-APR-2022) dose was not reported, administered on 05-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On NOV-2021, the patient experienced possibly worsened disc disease and bone spurs condition since vaccination. On 05-NOV-2021, the patient experienced tinnitus has increased in amplitude by 3-4 times, unbearable. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from tinnitus has increased in amplitude by 3-4 times, unbearable, and the outcome of possibly worsened disc disease and bone spurs condition since vaccination was not reported. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Bone spur; Controlled hypertension; Hearing loss; Intervertebral disc disorder; Tinnitus
- Vorgeschichte
- Comments: Patient did not had any known allergies.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 16.11.2021
- Impfdatum
- 16.11.2021
- Beginn
- 16.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Feeling hot
Headache
Hyperhidrosis
Hypoaesthesia
Paraesthesia
Vision blurred
Vitreous floaters
Symptomtext
Client received vaccine. Client states she has a history of fainting. Client was moved to anti-gravity chair before vaccine. After vaccine, about five minutes after 1243 Client reported feeling ?sweating? and ?hot?. Client stated this was a normal whenever she gets a shot Client was offered a cool pack,. Client was AAOx3 and client stated she was feeling numbness and tingling, Headache, and dizzy. Vitals signs at 1243 BP 132/86 HR 86 02 99%. Client states she did eat before vaccine and had water. Client had no shortness of breath, no difficulty breathing, no itchiness in any part of her body, no redness on face, neck or arms observed by RN. Water was given and client was able to drink water. Vitals at 1252 BP 124/79 HR 82 RR 14 02 97%. Client stated she could see like ?floaties? in her eyes, ?blurry vison? and legs tingling. At 1255 Client stated ?tingling is going away?. 1258 BP 120/72 HR 79 RR 14 02 99%. 1258 Client stated tingling was slightly better. At 1307 Client stated blurriness is less and there?s only tingling waist down. At 1308 Client sat up in chair and placed feet on ground. At 1309 snack was given, which client ate. At 1311 RN checked pupils, they were equal and reactive bilaterally. Vitals 1311 BP 150/89 HR 86 RR 14 02 99%. At 1313 Client stated ?sitting down helped, it?s going away? 1316 Vitals BP 124/82 HR 83 02 99% RR 16. At 1317 client stated, ?blurriness is gone?. Client was offered EMS for further assessment client declined. Client was recommended to follow up with her PCP in 24 hrs by RN , also recommended ER precautions if symptoms worsen or in case of any life-threatening symptom. Vsafe website was provided for client. Client was accompanied by her ex-husband and was going to drive her home. At 1320 Client left vaccination site in a steady gait
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none reported
- Vorgeschichte
- none reported
- Andere Medikamente
- none reported
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 16.11.2021
- Impfdatum
- 09.11.2021
- Beginn
- 10.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Eye disorder
Migraine
Muscle discomfort
Myalgia
Neck pain
Pain in extremity
Peripheral swelling
Vitreous floaters
Symptomtext
My right arm swelled initially the next morning and then my muscles began locking up. My left arm, shoulder, trapezoid, neck were all locked up and in pain for 4 days. I suffered a sever migraine for 3 days. I have noticed that since the shot I see "floatees" in my right eye and other issues with my eyes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- none, I don't normally go to the doctor for such things.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 16.11.2021
- Impfdatum
- -
- Beginn
- 08.11.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Diarrhoea
Headache
Hypoacusis
Injection site pain
Injection site swelling
Joint range of motion decreased
Pain in extremity
Muscle rigidity
Paraesthesia
Tinnitus
Peripheral swelling
Symptomtext
SWOLLEN INJECTION SITE; MUFFLED HEARING; TINGLING BELOW THE INJECTION SITE TO THE WRIST OF LEFT ARM; TINNITUS TO THE RIGHT EAR THAT BECOMING UNBEARABLE; DIARRHEA; BARELY ABLE TO RAISE LEFT ARM; INJECTION SITE PAIN; HEADACHE; This spontaneous report received from a patient concerned a 48 year old female. 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 was prescribed a steroid pack. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211D21A expiry: 11-APR-2022) dose was not reported, administered on 08-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 08-NOV-2021, the patient experienced injection site pain. On 08-NOV-2021, the patient experienced headache. On 09-NOV-2021, the patient experienced barely able to raise left arm. On 09-NOV-2021, the patient experienced tinnitus to the right ear that becoming unbearable. On 09-NOV-2021, the patient experienced diarrhea. On 10-NOV-2021, the patient experienced tingling below the injection site to the wrist of left arm. On 11-NOV-2021, the patient experienced muffled hearing. On 12-NOV-2021, the patient experienced swollen injection site. Treatment medications (dates unspecified) included: ibuprofen. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from injection site pain, barely able to raise left arm, headache, tingling below the injection site to the wrist of left arm, tinnitus to the right ear that becoming unbearable, muffled hearing, diarrhea, and swollen injection site. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: The patient had no known allergies. The patient was prescribed a steroid pack.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 16.11.2021
- Impfdatum
- -
- Beginn
- 08.11.2021
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Diarrhoea
Headache
Hypoacusis
Injection site pain
Injection site swelling
Joint range of motion decreased
Pain in extremity
Muscle rigidity
Paraesthesia
Tinnitus
Peripheral swelling
Symptomtext
SWOLLEN INJECTION SITE; MUFFLED HEARING; TINGLING BELOW THE INJECTION SITE TO THE WRIST OF LEFT ARM; TINNITUS TO THE RIGHT EAR THAT BECOMING UNBEARABLE; DIARRHEA; BARELY ABLE TO RAISE LEFT ARM; INJECTION SITE PAIN; HEADACHE; This spontaneous report received from a patient concerned a 48 year old female. 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 was prescribed a steroid pack. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211D21A expiry: 11-APR-2022) dose was not reported, administered on 08-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 08-NOV-2021, the patient experienced injection site pain. On 08-NOV-2021, the patient experienced headache. On 09-NOV-2021, the patient experienced barely able to raise left arm. On 09-NOV-2021, the patient experienced tinnitus to the right ear that becoming unbearable. On 09-NOV-2021, the patient experienced diarrhea. On 10-NOV-2021, the patient experienced tingling below the injection site to the wrist of left arm. On 11-NOV-2021, the patient experienced muffled hearing. On 12-NOV-2021, the patient experienced swollen injection site. Treatment medications (dates unspecified) included: ibuprofen. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from injection site pain, barely able to raise left arm, headache, tingling below the injection site to the wrist of left arm, tinnitus to the right ear that becoming unbearable, muffled hearing, diarrhea, and swollen injection site. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: The patient had no known allergies. The patient was prescribed a steroid pack.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 15.11.2021
- Impfdatum
- 15.11.2021
- Beginn
- 15.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Anxiety
Dizziness
Hypotension
Immediate post-injection reaction
Nausea
Symptomtext
patient received Janssen booster vaccine and immediately felt lightheaded, feeling of wanting to throw up, dizzy. pharmacist measured blood pressure reading and it was low, paramedics evaluated patient told us it was most likely due to anxiety
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- na
- Vorgeschichte
- na
- Andere Medikamente
- na
- Allergien
- na
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 14.11.2021
- Impfdatum
- 08.11.2021
- Beginn
- 10.11.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Angiogram
Blood test
Computerised tomogram head
Computerised tomogram thorax
Headache
Hypertension
Nausea
Vision blurred
Vomiting
Symptomtext
Extremely high blood pressure, severe headache, nausea, vomiting, blurred vision.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- 3,0
- Labordaten
- CT Scan chest area, CT Brain , Angiogram and bloodwork.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Low back pain
- Andere Medikamente
- Tramadol, zinc, Vitamin D3 Krill Oil, Bountiful Beats, organic Superfoods
- Allergien
- Keflex
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 11.11.2021
- Impfdatum
- 06.11.2021
- Beginn
- 06.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Decreased appetite
Fatigue
Headache
Mobility decreased
Pain
Pain in extremity
Pyrexia
Vomiting
Symptomtext
Headache, aches, chills, feverish, no appetite, fatigue. Vomited three times during the first night & once next morning. Had to remain in bed entire next day. No appetite. Sore arm got worse after 2 days. Symptoms subsided on fourth day, except still have sore arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- arthritis
- Andere Medikamente
- calcium supplements
- Allergien
- penicillin, formaldehyde, lactose & gluten-intolerances
- Vorherige Impfungen
- Severe rash from flu vaccine in 2018.
- Staat
- OH
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 09.11.2021
- 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: ja
Erholt: nein
Condition aggravated
Dyspepsia
Swelling
Symptomtext
Patient reported having increased heartburn 2 hours after receiving the vaccine to the point of needing to double up on her omeprazole. She reports being completely swollen from "head to toe," and she can make an indent in her leg with her finger.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 04.11.2021
- Impfdatum
- 04.11.2021
- Beginn
- 04.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Dyspnoea
Euphoric mood
Vomiting
Symptomtext
Pharmacy technician administered to patient vaccine. Patient was given vaccine and told to wait 15 minutes post vaccination in observation area. Initially, he felt ok, with no signs of adverse effects. After 5 minutes, patient stated he felt dizzy, shortness of breath, and had a feeling of "feeling high." Technician asked pharmacist to examine patient after hearing this. Pharmacist asked patient how he was feeling, if his shortness of breath and feeling dizzy was getting worse or stabilizing. Patient stated to pharmacist he feels only dizzy at the moment. Pharmacist recommended patient to take a sip of water and patient complied. Shortly after this (about 3 minutes), patient vomited. After patient vomited, he stated he felt better. Pharmacist and technician asked patient to continue sitting for observation for another 20 minutes. After 20 minutes, patient stated he felt normal again with no previous adverse effects. We advised patient to be careful and should he feel anything else at home to contact medical services.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE NOTED
- Andere Medikamente
- NONE NOTED
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 04.11.2021
- Impfdatum
- 03.11.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Chest discomfort
Condition aggravated
Cough
Dizziness
Gastrooesophageal reflux disease
Injection site pain
Joint swelling
Oropharyngeal discomfort
Oropharyngeal pain
Palpitations
Paraesthesia
Peripheral swelling
Somnolence
Throat irritation
Throat tightness
Symptomtext
Had shot at 15:10 15:15 had slight swelling in right wrist and hand 15:20 began to feel very sleepy 15:30 released by pharmacy 15:35 face began to tingle and throat was tight (not tight enough to wheeze or I would have gone to ER) 16:10 began to feel dizzy 16:25 heart rate was racing 16:30 still dizzy and noticed that if I tried to take a deep breath to counteract my tight throat, that it would make me cough due to throat irritation. Noticed tightness in chest now too. 16:46 still very sleepy even with other symptoms throat and chest stayed tight through about 20:00 when I noticed chest lessening throat still not right when went to bed at 21:00 21:35 woke with mouth full of stomach acid which aggravated my already irritated throat --- 11/4/2021 08:00 still very sleepy but throat tightness seems to have waned. Throat is sore thought. Right arm sore around injection site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- allergies including sinus drainage within 1 month
- Vorgeschichte
- lower back pain depression allergies
- Andere Medikamente
- 800mg ibuprofen xTID 20mg baclofen xTID 900mg gabapentin xTID 27mg methylphenidate xonce 150 mg oxcarbazepine xBID 5 mg buspirone HCl xBID fish oil vitamin D B complex took 8mg chlorpheniramine before shot
- Allergien
- Rocephin sulfa aloe paba surgical super glue bandaid adhesive plants in daisy family some grasses creosote bush molds bee stings reacted to flu shots before
- Vorherige Impfungen
- flu shots, years before so don't remember, arm very swollen and hot to touch, could not exercise with arm for about 3 days each
- Staat
- MN
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 02.11.2021
- Impfdatum
- 30.10.2021
- Beginn
- 30.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Chest pain
Chills
Feeling abnormal
Headache
Inflammation
Laboratory test
Nausea
Pyrexia
SARS-CoV-2 test
Symptomtext
Chills, then fever, splitting headache, nausea, brain fog. Next morning most symptoms had abated but brain fog remained and chest pain had started. Visited doctor, then continued resting. Tests showed general inflammation. Will follow up for further blood clotting tests. Chest pain and brain fog have slowly reduced.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- 10/31/2021 Multiple tests and covid test ordered at Health doctor. Blood clotting and covid test negative. General inflammation slightly higher than normal.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 32,0
- 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: ja
Erholt: nein
Dyspnoea
Speech disorder
Symptomtext
Patient received his 1st dose of Janssen COVID-19 in his left arm and about 1 minute after receiving the patient slumped in the chair. When the patient was able to speak to the pharmacist he stated that he felt like he could not breathe. The patient was given 1 dose of epipen 0.3 mg and emergency services was called. A police officer and the EMT's arrived on the scene and took over the patient's care.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none noted
- Andere Medikamente
- unknown
- Allergien
- no known allergies
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 13.12.2022
- Impfdatum
- 01.12.2021
- Beginn
- 15.11.2022
- Tage bis Beginn
- 349,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Diarrhoea
Malaise
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Throat irritation
Symptomtext
Several people were noticeable ill in my place of employment. I started out with scratchy throat, cough, fever, diarrhea, I took a home COVID-19 test that came back positive quickly. I called my doctor and was advised to quarantine from the family and to COVID-19 protocol. It took me until day 13 to finally get over the symptoms, I do have a lingering cough and some congestion.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- Home COVID-19 test positive
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Multivitamin; omeprazole
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 30.10.2022
- Impfdatum
- 24.11.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 21,0
- Dosis
- 2
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Arthralgia
Blood test abnormal
Gait disturbance
Impaired work ability
Inflammatory marker increased
Joint swelling
Peripheral swelling
Rheumatoid arthritis
Rheumatoid factor negative
Symptomtext
2-3 weeks after the booster shot my hands swelled up and then my knees after some days and then my feet and ankles. All my joints (wrists, fingers, elbows, shoulders, jaw, knees and ankles and feet became very painful. By the end of the year (2021) the pain was so much that I started taking Advil to cope. That helped. The joint condition did not a bare and in February I had a video interview with Dr. He diagnosed me with Rheumatoid Arthritis. I have had no such problems before. He had me take a blood test and a week or two later when the results came in, he said the inflammation markers were very high, but the rheumatoid factor was normal. One subsequent blood test (a month or two later) confirmed the above. Dr. prescribed Prednisone at 40mg per day. I started that and it alleviated the pain and visible swelling. Problem is - 8 months later I have been unable to wean off the Prednisone. I have tried twice and whenever I get to the level of 10mg per day the pain in my joints comes back full force. I have tried Prednisone substitutes to no avail. The Prednisone causes side effects which I cannot tolerate (mainly problems breathing which disappear at the lower dosages ie 15 mg per day which I am now taking) At 15 mg the joint pain is high but somewhat tolerable, though I have difficulty walking and have reduced my work hours so as to get more sleep. 8-9 hours per day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- Blood tests in March 2022 and later inJune 2022.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Daily multi-vitamin
- Allergien
- None
- Vorherige Impfungen
- Same vaccination from Jansen some months earlier. Very light cold effects for an hour.
- Staat
- FL
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 23.10.2022
- Impfdatum
- 27.10.2021
- Beginn
- 28.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: ja
Asthenia
Echocardiogram
Fatigue
Ultrasound scan
Symptomtext
Severe fatigue, weakness for 7 months
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Ecocardiogram 11/2021 Ultrasound 11/2021 Doctor visit 11/2021 Physical therapy 1/2022
- Aktuelle Erkrankungen
- None known
- Vorgeschichte
- I'm tired easily, my endurance is still building back up, and I had alot of muscle atrophy.
- Andere Medikamente
- Caffeine, greens supplement, ZMA, protein, fish oil Omega 3
- Allergien
- She'll fish sometimes
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- -
- Geschlecht
- F
- Eingang
- 30.08.2022
- Impfdatum
- 15.11.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pain in extremity
Symptomtext
This spontaneous report received from a patient concerned an 80 year old female. The patient's height, and weight were not reported. The patient's past medical history included: lost part of the thyroid (taking thyroid medication a little over weight), and concurrent conditions included: hay fever, shellfish allergy, alcohol use (very rarely), and non-smoker. The patient previously received with covid-19 vaccine ad26.cov2.s (Dose number in series 1) (suspension for injection, route of admin not reported and batch number: 041A21A, expiry: UNKNOWN) dose was not reported, 1 total, administered on 07-APR-2021 for covid-19 prophylaxis. The patient did not experienced any negative effects with the first shot and handled the Janssen vaccine well. No fever no tiredness (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: 211D21A expiry: UNKNOWN) dose was not reported, administered on 15-NOV-2021 for covid-19 prophylaxis. No concomitant medications were reported. On an unspecified date, the patient experienced slightly sore arm that lasted for 24 hours. There was no other symptoms with both vaccination. No fever no tiredness (Dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from slightly sore arm. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Alcohol use (very rarely); Hay fever; Non-smoker; Shellfish allergy
- Vorgeschichte
- Medical History/Concurrent Conditions: Thyroidectomy (taking thyroid medication a little over weight)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 29.08.2022
- Impfdatum
- 29.11.2021
- Beginn
- 22.08.2022
- Tage bis Beginn
- 266,0
- Dosis
- 2
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Pyrexia
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 12.08.2022
- Impfdatum
- 12.08.2022
- Beginn
- 12.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ageusia
Amnesia
Headache
Parosmia
Selective eating disorder
Taste disorder
Symptomtext
Patient states she had an extreme headache the day following vaccination. She is now stating on a phone call on 8/12/2022 nearly 8 months after vaccination that she has an enhanced sense of smell, a loss of taste, short term memory loss and she is complaining she now hates many foods that she used to love. Specifically, she stated eggs as a food she used to love but now she can taste the albumin in them and disgusted by said food.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- none that we have been made aware. She was advised to self report and seek further medical advice regarding these issues
- Aktuelle Erkrankungen
- previous meningitis infection per patient however unknown timing in accordance with vaccination. patient attested on vaccination sheet she was not sick at the time of vaccination
- Vorgeschichte
- chronic headaches per patient. carpal tunnel syndrome, joint disorder, multiple cervical disc displacements, impingement of right shoulder, hip and thoracic/lumbar sprain, chronic pain syndrome, long term opiate use
- Andere Medikamente
- xtampza er 36 mg, gabapentin 300 mg, oxycodone 15 mg, fioricet, sumatriptan, baclofen
- Allergien
- cephalosporins, patient states she is allergic to everything including hay weed and other allergens not related to medications.
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 02.08.2022
- Impfdatum
- 29.10.2021
- Beginn
- 31.07.2022
- Tage bis Beginn
- 275,0
- Dosis
- 2
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Asthenia
Chest discomfort
Fatigue
Symptomtext
generalized weakness, fatigue, chest discomfort
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- F
- Eingang
- 29.07.2022
- Impfdatum
- 17.11.2021
- Beginn
- 07.12.2021
- Tage bis Beginn
- 20,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Sinusitis
Vomiting
Symptomtext
SEVERE SINUS INFECTION; VOMITING/THROWING UP; This spontaneous report received from a patient concerned a female of an unspecified age, race and ethnicity. The patient's height, and weight were not reported. The patient's past medical history included: covid (in MAR-2021). The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211D21A expiry: UNKNOWN) dose was not reported, dose 1, 1 total was administered on 17-NOV-2021 on right arm for covid-19 prophylaxis. No concomitant medications were reported. Around 07-DEC-2021, the patient experienced severe sinus infection, a high fever and for vomiting/throwing up and was hospitalized (date unspecified). Number of days of hospitalization was not reported. It was unknown if patient was discharged. She think it was a case of meningitis but it was not confirmed by the doctor. She was prescribed antibiotic, steroid and she needed to be on bed rest. She did not received the booster. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from severe sinus infection, and vomiting/throwing up. This report was serious (Hospitalization Caused / Prolonged).; Sender's Comments: V0: 20220749810-covid-19 vaccine ad26.cov2.s- Severe sinus 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. 20220749810-covid-19 vaccine ad26.cov2.s- Vomiting/throwing up. This event(s) is labeled per RA and is therefore considered potentially related.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vomiting
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 14.07.2022
- Impfdatum
- 12.07.2022
- Beginn
- 13.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Epistaxis
Headache
Symptomtext
Patient called this afternoon and wanted to speak to the nurse regarding questions about the Covid vaccine. Patient conveyed that he has had a headache with an onset of 1100am today and 2 episodes of nose bleeds today as well. He reported epistaxis x2 different episodes and stated "just a trickle of blood and I wiped it off and it was done." Patient reports he took some over the counter aleve a short time ago and his headache has "eased up." Denies any other s/sx. Educated patient to follow up with ER for evaluation or PCP at minimum, reviewed ASE and ITP from patient fact sheet with patient over the phone. Encouraged patient to take Janssen fact sheet to MD/ER with him as well as vaccine card. Spoke to patient second occasion about 45 minutes after 1st call and patient was on the way to be seen at his PCP. He conveyed he called them and they were going to try to work him in to see the NP at 1500. Reiterated need to follow up with urgent care or PCP if unable to be seen at PCP. -----------------------------------7/14/21 TC to patient he stated all of his symptoms have resolved, he thinks it may have been just a fluke. He has not seen his PCP at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 01.07.2022
- Impfdatum
- 01.07.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Abdominal discomfort
Dysphonia
Headache
Throat clearing
Symptomtext
patient had anaphylaxis to dose #2 of Pfizer Covid Vaccine so opted to receive J&J as booster. approximately 33 minutes after administration, patient started to have hoarse voice and felt the need to clear throat; when questioned further stated she also had a slight headache and upset stomach; patient's care was transferred to Urgent Care department in same facility as vaccine administered where she was administered an EpiPen, diphenhydramine 50mg IM, dexamethasone 10mg IM; she was monitored for one hour with no return of symptoms, sent home with prednisone 40mg po x 5 days and instructed to take another dose of Benadryl in the evening; patient also has EpiPen prescription due to previous anaphylaxis
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- allergic rhinitis Urticaria
- Andere Medikamente
- Mirapex Lasix phentermine metronidazole cetirizine
- Allergien
- clindamycin penicillin sulfa COVID-19 MRNA vaccine HCTZ Macrobid
- Vorherige Impfungen
- 2/2/21 Pfizer COVID vaccine dose #2, anaphylaxis 45 years of age
- Staat
- NM
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 27.06.2022
- Impfdatum
- 12.07.2021
- Beginn
- 30.11.2021
- Tage bis Beginn
- 141,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: ja
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal pain
Biopsy
Contusion
Rash
T-cell lymphoma
Symptomtext
Rashes and unexplained bruises because apparent Nov 30, 2021. COVID booster was given on 12/20/2021. Started having abdominal pain January 2022. March 2, 2022 diagnosed with rare Anaplastic T Cell Non Hodgkins Lymphoma ALK type negative
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- biopsy performed 2/14/2022
- Aktuelle Erkrankungen
- N/A- Completely healthy
- Vorgeschichte
- Patient diagnosed with rare anaplastic T-cell Non-Hodgkins lymphoma ALK type negative in March 2022 after vaccination/booster
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 13.06.2022
- Impfdatum
- 17.03.2021
- Beginn
- 17.02.2022
- Tage bis Beginn
- 337,0
- Dosis
- 2
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Chest X-ray abnormal
Chest discomfort
Chronic obstructive pulmonary disease
Cough
Pain
Pulmonary congestion
Pulmonary fibrosis
SARS-CoV-2 test positive
Symptomtext
Pt to ED 2/17 c/o cough, chest congestion, chest tightness for the past 2 days. COVID positive upon admission, rx remdesivir for 3 d only on 2/17, not on oxygen. 2/18 reported no acute issues overnight. CXR showed COPD, right basilar scarring. Denied chest pain, c/o shortness of breath, no abd pain, no fever or chills. 2/19 pt has aches and pain, but not on O2, and tolerating activy. Pt is A&Ox4, cooperative and pleasant. Pt discharged 2/21.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- 5,0
- Labordaten
- see above
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Gastroesophageal reflux disease without esophagitis Gastroesophageal reflux disease without esophagitis SVT (supraventricular tachycardia) (CMS/HCC) Dizziness Mixed hyperlipidemia Syncope Atrial fibrillation (CMS/HCC) Status post cardiac catheterization Chest pain Mitral regurgitation S/P MVR (mitral valve replacement) Hematoma of groin Former smoker Presence of cardiac pacemaker Pulmonary embolism (CMS/HCC) Acute deep vein thrombosis (DVT) of tibial vein of left lower extremity (CMS/HCC) Orthostatic hypotension Chronic systolic heart failure (CMS/HCC) Stage 3 chronic kidney disease (CMS/HCC) CHF (congestive heart failure) (CMS/HCC) NSTEMI (non-ST elevated myocardial infarction) (CMS/HCC) Acute chest pain COVID-19
- Andere Medikamente
- albuterol (PROVENTIL, VENTOLIN, PROAIR) HFA 108 (90 Base) MCG/ACT INHAL Aero Soln apixaban (ELIQUIS) 5 MG PO Tab aspirin 81 MG PO Chew Tab atorvastatin (LIPITOR) 10 MG PO Tab atorvastatin (LIPITOR) 10 MG PO Tab bumetanide (BUMEX) 1 MG PO Ta
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 09.06.2022
- Impfdatum
- 24.05.2022
- Beginn
- 24.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Interchange of vaccine products
Pain
Symptomtext
Pt was to receive 2nd booster of Pfizer, but Tech did not follow safety protocol, pulled a Janssen & Placed at Pfizer station, drew up 0.3 ml and labelled sheet as Pfizer, documented Pfizer lot number and expiration. Gave sheet and drawn up syringe to pharmacist, who knew a Moderna and Pfizer were at the stations already. Pharmacist pulled the Moderna and saw a Pfizer at the station. Pharmacist gave IM shot to patient, Patient stated it stung . Pharmacist noted that. 30 minutes later when the tech went to draw the Pfizer doses for the next group. She realized she had pulled out a Janssen and had set it at the Pfizer station and drew it as a Pfizer. (at end of the day pharmacist drew out of Pfizer what was left. Based on our shots that day it was one shot over. Drew out contents of Janssen and sure enough , some vaccine was missing in spite of no Janssen shots scheduled. Confirmed pt got a substandard dose of Janssen instead of mRNA Pfizer shot).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none stated
- Andere Medikamente
- n/a
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 27.05.2022
- Impfdatum
- 27.05.2022
- Beginn
- 27.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Eye movement disorder
Fall
Nausea
Symptomtext
8 minutes after administration of the vaccine, the patient began to experience nausea. She rolled her eyes and the individual accompanying her noticed that she was about to fall to the ground, so he helped her in order to prevent head trauma. The patient reports that she does not remember falling. Her legs were elevated, and she was given water. The patient recovered and returned to a seating position. After 5 minutes, her nausea resolved and the patient's symptoms improved. She was alert and oriented. The patient was examined by Dr., who recommended that she be examined at the urgent care clinic nextdoor. A staff member from the clinic walked the patient to the urgent care. The patient had no issues walking, did not expereince dizziness, and arrived at the care clinic in a stable condition.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Chronic migraines
- Andere Medikamente
- Vitamin E, Omega 3, Magnesium, CQ10, multivitamin, emgalty
- Allergien
- Topamax
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 25.05.2022
- Impfdatum
- 22.11.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Loss of personal independence in daily activities
Musculoskeletal stiffness
Poor quality sleep
Symptomtext
low back pain, followed by muscle stiffness in upper front legs, worsening to the point I couldn't do daily activities or sleep well
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None that I recall
- Vorgeschichte
- Multiple Chemical Sensitivities Asthma Seasonal allergies (primarily maple and oak pollen at the present time) Rheumatoid arthritis
- Andere Medikamente
- Multivitamin, EFAs, L-lysine, Iron, boswellia, lithium, magnesium, digestive enzymes
- Allergien
- I have adverse reactions to petrochemicals, such as solvents, pesticides, artificial fragrances, paints, adhesives, and more. I have to avoid gluten, corn, soy, wheat, rye, rice that is high in arsenic, and citrus that is not certified organice
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 25.05.2022
- Impfdatum
- 29.11.2021
- Beginn
- 12.03.2022
- Tage bis Beginn
- 103,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Herpes zoster
Pain of skin
Skin lesion
Symptomtext
Developed symptoms of shingles 03/12/2022. Had painful sores on left peck area, left side below armpit and left back in deltoid area. Sores and pain increased over weekend. Sought medical diagnosis and treatment 03/14/2022. Doctor immediately diagnosed shingles. Prescribed Valacyclovir 1gr, Gabapentin 600 mg and Lidocaine patches 5%. Sores increased in size and intensity of pain over next 7 days approximately. Pain and sores continued for approx 3 weeks. Sores and pain began to subside but took another 3 weeks to be mostly gone.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain of skin
- Hospital-Tage
- -
- Labordaten
- None. Only doctor diagnosis of shingles and being informed that I had taken the vaccine only 4 months prior.
- Aktuelle Erkrankungen
- Covid, 01/15/2022-02/18/2022
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 23.05.2022
- Impfdatum
- 01.03.2021
- Beginn
- 01.03.2021
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pain
Symptomtext
(1st dose) Pfizer on 3/1/2021 Made Peripheral Neuropathy worse then (2nd dose) Pfizer on 3/22/21 led to Severe pain for at least 4 months. Pt. was advised from CDC to only receive J&J COVID-19 vaccine due to severe reactions from previous doses CDC approval also to give 2nd booster J&J
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- UNKNOWN
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- NKDA, BUT PFIZER ADDED TO ALLERGY LIST AFTER REACTIONS WITH 2ND DOSE ON 3/22/21 &
- Vorherige Impfungen
- 3/01/2021 PFIZER EN6198 -INCREASED PERIPHERAL NEUROPATHY 3/22/2021 PFIZER EN6204 CAUSED SEVERE PAIN
- Staat
- CA
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 23.05.2022
- Impfdatum
- 20.11.2021
- Beginn
- 20.12.2021
- Tage bis Beginn
- 30,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Sensation of foreign body
Symptomtext
A month after the vaccine I developed a rash on my chest arms and hands. I went to my doctor which referred me to dermatology and they prescribed 3 different steroid creams. The creams help some but the rash didn't completely go away. I also developed a lump in the left side of my throat I have an appointment for an ultrasound on Wednesday. The lump has been here for the past two months.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- No; Chronic eczema
- Andere Medikamente
- Zinc; Zyrtec; magnesium; D3; quercetin; vitamin C; elderberry; fish oil
- Allergien
- Flagel
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 12.05.2022
- Impfdatum
- 12.05.2022
- Beginn
- 12.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Decreased gait velocity
Fall
Feeling abnormal
Gait disturbance
Hyperhidrosis
Nausea
Pallor
Posture abnormal
Rash macular
Unresponsive to stimuli
Symptomtext
RE: Patient DOB 08/24/1994 12:45p Received first dose Janseen vaccine, instructed to wait 15 minutes. 12:55p Self-reported while waiting he became nauseous ?a few minutes? after administration of vaccine, walked to bathroom, began feeling ?worse? and returned to Health Department office. Upon entering the HD office, observed client to be pale, three small reddish blotches on left cheek, no verbal response, leaning and stumbling to left, holding onto furniture. Client took two steps and began falling forward toward floor. Landed on floor, slightly on left side, head did not impact floor, eyes closed, no verbal response. 911 called. Smelling Salt effective and began responding to questions, remained lying on left side. 1:00 Paramedics arrived, client sitting upright on floor, drinking water, responding appropriately. VS within normal range. Able to stand up on own, unassisted gait slow and steady. Color natural, red blotches fading, skin remains diaphoretic. States he is ?feeling better?. Declined transport to hospital. 1:10p Remained in office drinking water, talking. Encouraged to follow up with physician. Left building without further incident.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- None at time of event.
- Aktuelle Erkrankungen
- none listed
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- none listed
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 04.05.2022
- Impfdatum
- 09.02.2022
- Beginn
- 10.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Asthenia
Blood test normal
Computerised tomogram head normal
Computerised tomogram spine
Electrocardiogram normal
Headache
Hypoaesthesia
Lumbar puncture normal
Magnetic resonance imaging head normal
Movement disorder
Vision blurred
Symptomtext
Weakness with numbness to both hands and legs. Severe headache the next morning after the vaccine. 1st visit 2/10/2022, bloodwork; EKG; CT head done. Given solumedrol, Zofran, Pepcid, and Demerol for the severe headache. Next day, continued severe headache with progressive numbness to left arm hand, leg, and foot. 2/12/2022 2nd visit. Symptoms: Complete immobility of the left arm and left leg. Numbness to the left-side of the face. Continued severe headache. Blurred vision. Bloodwork, EKG, CT head and spine obtained. Lumbar puncture attempted. No significant finding. Informed to follow-up with PCP Monday. By Monday continued immobility with numbness to left-side of the body.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- CT head, EKG, bloodwork, CT spine and MRI brain.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypothyroidism, GERD, seasonal sinus allergies
- Andere Medikamente
- Synthroid, Nexium, Zyrtec, Multivitamin
- Allergien
- Medrol Dosepak, tape
- Vorherige Impfungen
- Flu vaccine: hives and itching.
- Staat
- WV
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 05.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Feeding disorder
Pyrexia
Stomatitis
Symptomtext
FEVER, SORES IN MOUTH, UNABLE TO EAT FOR A WEEK
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 23.04.2022
- Impfdatum
- 23.04.2022
- Beginn
- 23.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Hyperhidrosis
Nausea
Vomiting
Symptomtext
Patient was given a dose of vaccine and had symptoms while waiting. About 5 minutes after vaccination, he experienced weakness, nausea, sweatting, and vomiting. His blood pressure was 105/65 with pulse 60. He was evaluated by paramedics and released.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NA
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 18.04.2022
- Impfdatum
- 27.01.2022
- Beginn
- 15.02.2022
- Tage bis Beginn
- 19,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abnormal clotting factor
Clostridium difficile infection
Colitis
Enteritis
Laboratory test
Pyrexia
Red blood cell count decreased
Sepsis
White blood cell count increased
Symptomtext
I began running a fever daily for over a month, my doctor ordered lab work. Elevated WBC along with elevated clotting factors causing my blood to be too thick. Put on antibiotics for 5 days. Symptoms seemed to clear and then came back a week later. Repeat labs done but when the doctor did not get the results fast enough she sent me to the ER and I was admitted with Sepsis, C-Diff, Colitis and Enteritis on 3/25/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- 3,0
- Labordaten
- I can send copy of lab work. Elevated WBC and low RBC along with many others.
- Aktuelle Erkrankungen
- Gastritis
- Vorgeschichte
- Gastritis
- Andere Medikamente
- Clonazepan
- Allergien
- Penicillin, Morphine, Bactrim and Sulfa based medications and Morphine
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 18.04.2022
- Impfdatum
- 02.03.2022
- Beginn
- 07.03.2022
- Tage bis Beginn
- 5,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Hair disorder
Headache
Joint stiffness
Muscular weakness
Nausea
Onychoclasis
Pain
Sensitive skin
Symptomtext
From 3-8-22 and continuing; fatigue gradually increased, body aches gradually increased, joint stiffness gradually increased, weak muscles gradually weakened, hair feels oddly different, brittle nails, occasional nausea, transient headaches, skin pressure sensitivity
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Magnesium 400 mg, Vitamin D 5000 IU
- Allergien
- Thimerosal, Cobalt, metal alloys, Methylchloroisothiazolonone, Thimerosal, Cobalt, metal alloys, various preservatives, Annatto, Bell Peppers,
- Vorherige Impfungen
- Toxic reaction, Rubella-severe body aches age 32, HepB - stomach cramps for 2 days each dose age 40, Tetanus - severe body ache
- Staat
- KS
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 06.04.2022
- Impfdatum
- -
- Beginn
- 02.04.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain lower
Dry throat
Feeling abnormal
Feeling hot
Symptomtext
LOWER RIGHT QUADRANT PAIN WHEN BREATHING IN; DRY THROAT; FELT AS IF HE IS ABOUT TO BE SICK; FELT WARM; This spontaneous report received from a patient concerned a 29 year old male. The patient's weight was 240 pounds, and height was 69 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: 211D21A expiry: 10-JUL-2022) dose was not reported, administered on 02-APR-2022 for prophylactic vaccination. No concomitant medications were reported. On 02-APR-2022, the patient experienced lower right quadrant pain when breathing in, dry throat, felt as if he is about to be sick, and felt warm. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from dry throat on 02-APR-2022, and had not recovered from lower right quadrant pain when breathing in, felt as if he is about to be sick, and felt warm. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain lower
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 04.04.2022
- Impfdatum
- 22.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Headache
Inflammation
Pain
Pyrexia
Symptomtext
headache Feet inflamed Fever Pain in body Loss stamina
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- -
- Geschlecht
- F
- Eingang
- 29.03.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Heart rate
Pain in extremity
Vaccination failure
Vaccine breakthrough infection
Symptomtext
TWO BREAKTHROUGH COVID-19 INFECTIONS; SUSPECTED CLINICAL VACCINATION FAILURE; PAIN RADIATED DOWN THE ARM; This spontaneous report received from a patient concerned a 42 year old female of unspecified race. The patient's height, and weight were not reported. Patient was not pregnant or breastfeeding. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211D21A, expiry: 10-JUL-2022) dose was not reported, 1 total, administered on 16-DEC-2021 at left arm for prophylactic vaccination. Concomitant medications included cyanocobalamin (Vitamin B12) and salbutamol (blue inhaler). On an unspecified date, the patient experienced chest pains, pain radiated down her arm, heart palpitation, shortness of breath, rapid heart rate and had two breakthrough COVID-19 infections ever since she received the JNJ vaccine and had suspected clinical vaccination failure. Patient went to her PCP who advised her to go home and relax. Laboratory data included: Heart rate (NR: not provided) 117 beats/min even when she stood still. Patient stated that she monitored her heart rate and said that it went even higher when she moved around. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from breakthrough covid-19 infections, had not recovered from pain radiated down the arm, 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: 90000222820.; Sender's Comments: V0: 20220342279-Covid-19 vaccine ad26.cov2.s-Suspected clinical vaccination failure . The event(s) has a 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. 20220342279-Covid-19 vaccine ad26.cov2.s- Two breakthrough covid-19 infections. The event(s) has a unknown/unclear 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
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- Test Name: Heart rate; Result Unstructured Data: 117 {beats}/min; Comments: Heart rate gone even higher when patient was moving around.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: Patient was not pregnant or breastfeeding
- Andere Medikamente
- SALBUTAMOL; B12-VITAMIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 28.03.2022
- Impfdatum
- 26.03.2022
- Beginn
- 26.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Muscle spasms
Pain
Pain in extremity
Pyrexia
Symptomtext
Fever, muscle spasm, left arm pain, clavicle pain and sharp pain in right arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 24.03.2022
- Impfdatum
- 09.03.2022
- Beginn
- 14.03.2022
- Tage bis Beginn
- 5,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Erythema
Urticaria
Symptomtext
Red raised hives all over body that would creep and move around my legs neck arms and torso.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 23.03.2022
- Impfdatum
- -
- Beginn
- 20.03.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
Cough
Oropharyngeal pain
Pyrexia
Rhinorrhoea
SARS-CoV-2 test
Symptomtext
FEVER 101F; RUNNY NOSE, THICK DISCHARGE FROM NOSE; SORE THROAT; COUGH; This spontaneous report received from a patient concerned a 39 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: 211D21A, and expiry: 10-JUL-2022) dose was not reported, administered on 06-JAN-2022 for prophylactic vaccination. No concomitant medications were reported. On 20-MAR-2022, the patient experienced runny nose, thick discharge from nose, sore throat, and cough. On 21-MAR-2022, the patient experienced fever 101f. Laboratory data included: Body temperature (NR: not provided) 101 F, and COVID-19 virus test (NR: not provided) Negative. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from runny nose, thick discharge from nose, sore throat, cough, and fever 101f. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220321; Test Name: Body temperature; Result Unstructured Data: 101 F; Test Date: 20220321; Test Name: COVID-19 virus test; Result Unstructured Data: Negative
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 22.03.2022
- Impfdatum
- 17.02.2022
- Beginn
- 18.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Blood test
Fatigue
Myalgia
Pyrexia
Therapy change
Symptomtext
I had a fever, muscle pain, joint pain and serve fatigue that been going on since my vaccine. I spoke with my doctor. He did blood work and increased my thyroid medicine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- Bloodwork
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hosmo thyroidism
- Andere Medikamente
- Levothyroxine, Liothyronine, Vitamin d
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 14.03.2022
- Impfdatum
- -
- Beginn
- 17.12.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Administration site pain
Asthenia
Muscle atrophy
Pain
Symptomtext
WHOLE BODY ACHINESS (UPPER AND LOWER BODY, WORSE ON THE RIGHT LEG AND WHOLE UPPER BODY); LOSS OF MUSCLE; LOSS OF STRENGTH (RIGHT SIDE IS DETERIORATED AND HIS STRENGTH IS GOING DOWN); FEELING ACHINESS IN RIGHT ARM AT ADMINISTRATION SITE; This spontaneous report received from a patient concerned a 70 year old white male. 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: 201A21A, and expiry: UNKNOWN) dose was not reported, 1 total, administered on 04-MAY-2021 for prophylactic vaccination. No concomitant medications were reported. On JUN-2021, the patient felt (body and joint soreness and achiness) soreness throughout his body and joints when started to get active and went outside. The patient stated it was a continuous aching and had made working and activities difficult for him. The patient stated whenever he walked or did something it was painful he described the event was not debilitating but something was not right. The patient stated the achiness went on all summer long and subsided in OCT-2021. At first he thought it might be lyme disease but never got tested for lyme disease. (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: 211D21A and expiry: UNKNOWN) dose was not reported, 1 total, administered on 15-DEC-2021 at right arm for prophylactic vaccination. No concomitant medications were reported. On 17-DEC-2021 two days after taking booster, the patient experienced feeling achiness in right arm at administration site which lasted for more than a month. Patient stated that the achiness traveled throughout whole body, upper and lower body and he feel it daily. He stated that he has some good days and sometime it hurts to move. Patient described that it was worse on the right leg and whole upper body. His shoulder, elbows and arms were achy and felt like workout soreness. Patient noticed loss of muscle and strength as if his right side was deteriorated and his strength was going down (dose number in series 2). Patient has not discussed his symptoms with his doctor yet. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from feeling achiness in right arm at administration site, and had not recovered from loss of muscle, loss of strength (right side is deteriorated and his strength is going down), and whole body achiness (upper and lower body, worse on the right leg and whole upper body). This report was non-serious. This case, involving the same patient is linked to 20220306407 (Dose number in series 1).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Administration site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 10.03.2022
- Impfdatum
- 04.03.2022
- Beginn
- 04.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anxiety
Nightmare
Rash
Rash vesicular
Vomiting
Symptomtext
Pt reports that the night that she was vaccinated, she developed a full body rash with blistering. Also experienced "nightmare anxiety." Reported vomiting.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- COVID positive on 1/17/2022.
- Vorgeschichte
- Overweight, Reynaud's, Migraine headaches.
- Andere Medikamente
- Imitrex; Ortho Tricycline; Phentermine.
- Allergien
- NKDA.
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- -
- Geschlecht
- M
- Eingang
- 09.03.2022
- Impfdatum
- -
- Beginn
- 23.02.2022
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain upper
SARS-CoV-2 test
Suspected COVID-19
Vaccination failure
Symptomtext
SUSPECTED CLINICAL VACCINATION FAILURE; SUSPECTED COVID-19 INFECTION; STOMACH ACHE; This spontaneous report received from a consumer 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 previously received covid-19 vaccine ad26. cov2.s (unspecified manufacturer) (suspension for injection, route of administration not reported, batch number: unknown expiry: unknown) dose was not reported, (Dose number in series 01), 01 in total was administered on an unspecified date for prophylactic vaccination. No adverse events were reported following vaccination covid-19 vaccine ad26. cov2.s (Dose number in series 01). The patient additionally received covid-19 vaccine ad26.cov2.s (suspension for injection, route of administration not reported, batch number: 211D21A, and expiry: 11-APR-2022) dose was not reported, (Dose number in series 02) 01 in total was administered on 14-JAN-2022 for prophylactic vaccination. No concomitant medications were reported. On 23-FEB-2022, following vaccination with covid-19 vaccine ad26.cov2.s, the patient started to experience fever, head and chest congestion, coughing which resulted in suspected COVID-19 (Coronavirus disease-19) infection. On the same day, the patient experienced stomach ache (Dose number in series 02). On 26-FEB-2022, the patient tested positive for COVID-19 virus test (NR: not provided) (using the iHealth rapid take home antigen provided by the federal government) which resulted in suspected clinical vaccination failure (Dose number in series 02). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the suspected clinical vaccination failure, suspected COVID-19 infection and stomach ache was not reported. This report was serious (Other Medically Important Condition). The case was associated with product quality complaint (RA): 90000219343.; Sender's Comments: V0: 20220260810-COVID-19 VACCINE AD26.COV2.S-Suspected Clinical Vaccination Failure. The event has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event than the drug. Specifically: SPECIAL SITUATIONS. Therefore, this event is considered not related.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220226; Test Name: COVID-19 virus test; Result Unstructured Data: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 07.03.2022
- Impfdatum
- 07.03.2022
- Beginn
- 07.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Inappropriate schedule of product administration
Interchange of vaccine products
Symptomtext
Patient CALLED AND ASKED IF WE HAD J&J VACCINE IN STOCK. WE SAID YES AND SHE CAME BY TO GET THE SHOT. SHE FILLED OUT THE PAPERWORK. WE ASKED IF THIS WAS HER FIRST SHOT AND SHE SAID YES "IT WAS GOING TO BE HER FIRST J&J SHOT". WE CHECKED Database AND IT DIDNT SHOW THAT SHE HAD RECIEVED ANY COVID VACCINES. WE GAVE HER THE SHOT AND VACCINE CARD. AFTER SHE RECEIVED HER VACCINE CARD SHE CONFESSED THAT SHE HAD GONE TO another facility FOR A J&J SHOT THAT MORNING BUT THEY GAVE HER PFIZER INSTEAD. SHE WAS TOLD TO COME BACK IN 21 DAYS AND SHE SAID SHE COULD NOT BECAUSE SHE NEEDED TO BE FULLY VACINATED. SO SHE CAME TO OUR STORE TO GET THE J&J VACCINE. WE CALLED AND CHECKED ON HER LATER THAT AFTERNOON AND SHE SAID SHE HAD A HEADACHE. WE RECOMMENDED TYLENOL AND THAT SHE TAKE IT EASY FOR THE NEXT DAY OR SO AND TO NOTIFY US OR HER DOCTOR IF SHE HAD ANY OTHER SYMPTOMS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE KNOWN
- Vorgeschichte
- NONE KNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 06.03.2022
- Impfdatum
- 28.01.2022
- Beginn
- 19.02.2022
- Tage bis Beginn
- 22,0
- Dosis
- 1
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Disturbance in attention
Dizziness
Dysphonia
Eye pain
Infectious mononucleosis
Mononucleosis heterophile test positive
Neck pain
Oropharyngeal pain
Pain
Pyrexia
Rash
Respiratory tract congestion
Tonsillar erythema
Tonsillar hypertrophy
Tonsillar inflammation
Tonsillitis
Symptomtext
Dizziness, lack of ability to concentrate, eye pain, neck pain onset 2/19/22. Sore throat on 2/27/22. Tonsillitis on exam on 3/1/22 with antibiotic Cefdinir ordered on 3/1/22. (Grossly inflamed, red, swollen, painful, white-patched tonsils. Muffled voice. Low grade fevers. Congestion.) Worsening condition on 3/3/22 that prompted laboratory testing for mononucleosis. Confirmed mononucleosis on 3/4/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- Blood test for Mononucleosis on 3/3/22, confirmed positive on 3/4/22.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Amoxil
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 01.03.2022
- Impfdatum
- 13.11.2021
- Beginn
- 13.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Diarrhoea
Dizziness
Hyperhidrosis
Nausea
Vision blurred
Symptomtext
Within 10 minutes of receiving vaccine, patient reported excessive sweating, blurred vision, light headedness while seated in observation area. Patient then walked to bathroom. She came back stating she remained sitting for about 20 minutes with nausea and chills. Patient states she experienced diarrhea as well. Patient returned to observation area for another 10 minutes for observation before feeling better and well enough to leave. Patient was advised to state hydrated and take acetaminophen if she experiences fevers and body aches later in the day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- -
- Geschlecht
- M
- Eingang
- 26.02.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Headache
Muscular weakness
Pain
Symptomtext
WHOLE BODY ACHE; JOINT PAIN; WHOLE BODY WEAKNESS/ RIGHT LOWER LEG WEAKNESS; SEVERE HEADACHE; This spontaneous report received from a patient via a company representative concerned a 73 year old male. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: patient had four stents and was on unspecified blood thinners. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of administration not reported, batch number: 201A21A, expiry: unknown) dose was not reported, dose number in series 1, 01 total, administered on 04-MAY-2021 for prophylactic vaccination. On an unspecified date, following vaccination with covid-19 vaccine ad26.cov2.s, the patient experienced muscles aches for two months (dose number in series 1). The patient recovered from muscles aches for two months. The patient additionally received covid-19 vaccine ad26.cov2.s (suspension for injection, route of administration not reported, batch number: 211D21A, expiry: 11-APR-2022) dose was not reported, dose number in series 2, 01 total, administered at right arm on 01-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. On an unspecified date, the patient had joint pain, whole body weakness/ right lower leg weakness, severe headache, and whole body ache (dose number in series 2). At the time of report, the patient's ache and weakness spread into the whole body. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from whole body weakness/ right lower leg weakness, and whole body ache, and the outcome of joint pain and severe headache was not reported. This report was non-serious. This case, involving the same patient is linked to 20220241253.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: Patient had four stents and was on unspecified blood thinners.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 21.02.2022
- Impfdatum
- 13.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Blood test
Computerised tomogram thorax
Fibrin D dimer increased
Injection site erythema
Injection site induration
Injection site nodule
Injection site pruritus
Injection site swelling
Injection site warmth
Symptomtext
High racing heart rate began at 6 pm after shot was peaked at highest at 530 am with 155 bpm at rest went to er d diner elevated ct of chest taken was clear sent home. Continued to have little spikes of high hr for about 7 days. Also site was swollen and rock hard about size of orange red and itchy . Red and itchy for seven days and warm to touch. Hard knot that took 1 month to completely go away
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- Ct Jan 14 of chest neg Blood test Jan 14 d dimer slightly elevated
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Nifedipine fish oil mag ox aspirin calcium zinc vitamin c vitamin d prenatal colace folic acid aspirin 81
- Allergien
- None known
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 21.02.2022
- Impfdatum
- 18.02.2022
- Beginn
- 18.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Angina pectoris
Arthralgia
Dizziness
Headache
Hyperhidrosis
Immediate post-injection reaction
Nausea
Pain
Pain in extremity
Symptomtext
Immediately after vaccination - profuse sweating, dizziness, and nausea. Resolved in 15 minutes with water Day after vaccination - headache 2 days after - intense body aches and pain through shoulders. Heart pain. Soreness in legs
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 18.02.2022
- Impfdatum
- 18.02.2022
- Beginn
- 18.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Pruritus
Symptomtext
Patient presented to the community vaccine clinic for a Janssen Vaccine for COVID-19 at 2:18 pm. Prepped patient's arm with an alcohol pad and gave the injection in the right arm deltoid muscle. Due to patient' previous response to the Pfizer vaccine, staff was monitoring patient closely for signs/symptoms of a reaction. Within 10 minutes of receiving the vaccine patient complained of itching all over. AT ~2:32pm HR:100 and oxygen saturations:99%, % were obtained. Writer called the emergency response team and then gave an injection of an epi-pen 0.3 mg dose at 2:32 pm. At ~2:38 pm, the patient was transported to the emergency department of this facility, for further monitoring and treatment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- unknown
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- Multiple severe allergic reactions to other vaccines, other unknown.
- Andere Medikamente
- Unknown
- Allergien
- Augmentin, Sulfa, Covid - 19 Pfizer vaccine, MMR
- Vorherige Impfungen
- anaphylaxis to Pfizer and MMR
- Staat
- LA
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 17.02.2022
- Impfdatum
- 17.02.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Immediate post-injection reaction
Symptomtext
Felt dizzy and lightheaded immediately after vaccine. Verbalized had not eaten today. Provided water snd crackers. Denied any additional sx Vitals: 98% 66 110/60 repeat 90/66. Had pt lay down in seat of car. Feet up. Drink water. Eat crackers. Repeat BP 110/66 Pt reported feeling better. Thinks it was anxiety
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- M
- Eingang
- 16.02.2022
- Impfdatum
- -
- Beginn
- 08.11.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site rash
Injection site reaction
Symptomtext
ROUGH PATCH, RED DOTS, ITCHY AND SCRATCHING AT INJECTION SITE; RASH AT INJECTION SITE; This spontaneous report received from a patient concerned a 33 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: 211D21A, expiry: 11-APR-2022) dose was not reported, administered on 07-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 08-NOV-2021, the patient experienced rough patch, red dots, itchy and scratching at injection site, and rash at injection site. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from rash at injection site, and rough patch, red dots, itchy and scratching at injection site. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- HI
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 15.02.2022
- Impfdatum
- 07.02.2022
- Beginn
- 07.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoaesthesia
Myalgia
Symptomtext
THE PATIENT RECEIVED A JOHNSON AND JOHNSON COVID-19 BOOSTER SHOT ON 1/7/2022. PER PT, SHE HAS BEEN HAVING NUMBNESS ON HER LEFT ARM EVER SINCE SHE GOT THE SHOT. SHE SAID SHE WAS TOTALLY FINE WITH HER FIRST JOHNSON AND JOHNSON COVID-19 VACCINE, WHICH SHE RECEIVED ON 9/1/2021 AT OUR PHARMACY. SHE REPORTED THAT SHE HAD MUSCLE ACHE ON HER NECK AND SHOULDER FOR THE FIRST 3 DAYS. NOW SHE STILL HAS NUMBNESS ON HER LEFT ARM THAT HAS BEEN GETTING BETTER LITTLE BY LITTLE. PER PT, HER DOCTOR TOLD HER TO WAIT FOR HER SYMPTOMS GO AWAY ON 2/15/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- NO, AS OF 2/15/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- -
- Geschlecht
- F
- Eingang
- 12.02.2022
- Impfdatum
- -
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Gait inability
Middle insomnia
Pain in extremity
Shoulder arthroplasty
Symptomtext
SHOULDER REPLACEMENT; WOKE UP IN MIDDLE OF THE NIGHT; CANNOT WALK; RIGHT HIP PAIN; RIGHT LEG PAIN; This spontaneous report received from a patient concerned a 67 year old female. The patient's height, and weight were not reported. The patient's past medical history included: covid-19 infection for 9 days. However, still feels sick after that. The patient previously received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: unknown, expiry: unknown) dose was not reported, dose number in series was 1, 01 in total administered on 09-APR-2021 for prophylactic vaccination. Following administration of covid-19 vaccine ad26.cov2.s, the patient woke up in the middle of the night with right leg pain that disappeared and came back with the first vaccine (dose number in series was 1). The patient thought she had a blood clot but it was never confirmed by a doctor. The outcome of woke up in middle of the night and right leg pain was not reported (dose number in series was 1). The patient additionally received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211D21A, expiry: unknown) dose was not reported, dose number in series was 2, 01 in total, administered on 06-JAN-2022 to left arm for prophylactic vaccination. No concomitant medications were reported. On an unspecified date in JAN-2022, the patient again woke up with same issues, which she had after first dose. The patient had a shoulder replacement and was feeling good initially but afterwards, she was unable to walk due to right leg and hip pain (dose number in series was 2). As per patient's doctor, did not correlate covid-19 vaccine with her decrease in walking. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from right hip pain, cannot walk, and right leg pain, and the outcome of woke up in middle of the night and shoulder replacement was not reported (dose number in series was 2). This report was serious (Other Medically Important Condition). This case is associated with a product quality complaint number: 90000214807 This case, involving the same patient is linked to 20220213452.; Sender's Comments: V0: 20220200404-COVID-19 VACCINE AD26.COV2.S-shoulder replacement. 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
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Feeling sick
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19 (For 9 days)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 47,0
- Geschlecht
- M
- Eingang
- 11.02.2022
- Impfdatum
- 01.12.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Eye pruritus
Fatigue
Hot flush
Pruritus
Symptomtext
Day 1: Hot flashes in head. Day 2: Mild itchiness around left arm. Day 3-5: Itchiness more frequent around upper body. Day 6-14: Constant itchiness throughout body/eyes. Day 14 to present: Minor fatigue. Doctor visit 12/9/2021. I was prescribed loratadine and prednisone.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Eye pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Vitamin D
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 05.02.2022
- Impfdatum
- 26.01.2022
- Beginn
- 29.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Chest discomfort
Cough
Eye pruritus
Eye swelling
Fatigue
Feeling cold
Headache
Heart rate increased
Myalgia
Ocular hyperaemia
Pain in extremity
Tinnitus
Symptomtext
Symptoms after 12 hrs included headache, freezing cold, leg pain, tight chest, high heart rate, cough , lasted 5 - 8 hrs. Next day bad head ache and exhausted. Then on 01/29/2022 3 days later I developed what I know no to be tinnitus of the ear. I also still have a head ache, red itchy swollen eyes, and different muscle aches daily. Treatments are Tylenol, Motrin, and Lipo Flavonoid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Eye pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- co vid 01/07/2022
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 02.02.2022
- Impfdatum
- 27.01.2022
- Beginn
- 27.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest discomfort
Depressed level of consciousness
Fatigue
Headache
Hypoaesthesia
Inner ear disorder
Musculoskeletal stiffness
Nasal congestion
Respiratory tract congestion
Swelling
Vomiting
Symptomtext
E.R. Almost Loosing consciousness. Bad headache, swelling and numbness in extremities and L face. Severe fatigue, vomiting. Swelling then continued to crawl up and broaden over face and other side. Body swelling , stiffness, congestion, swelling of inner ears, nasal congestion, chest congestion, severe fatigue
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- hospital records
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Escitalopram 20 mg, multivitamin, bcomplex, D3, Claritin redi-tab, Zyrtec.
- Allergien
- Cherries, carrots, bees
- Vorherige Impfungen
- Moderna
- Staat
- VT
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 01.02.2022
- Impfdatum
- 01.02.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood glucose decreased
Dizziness
Hypoglycaemia
Symptomtext
At time of shot, blood glucose level was at 160. I drank a 20oz soda which was 60 grams of sugar and carbs. To cover the soda I took 3 units of insulin instead of the full 6 units I would normally take. At this time which was 12:45PM I did not have any active insulin in my system. At 2:45PM I had 2 slices of bread with peanut butter and no insulin. At 3:15PM I felt light headed and dizzy so I checked my blood glucose levels and it was 46. I ate an entire bowl of cereal and drank 2 tbsp of maple syrup. After the hypoglycemia incident, I tested my blood sugar at 3:30 and it was 94.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Type 1 Diabetes Mellitus
- Andere Medikamente
- Novolog insulin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 31.01.2022
- Impfdatum
- 27.11.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 30,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Symptomtext
Severely dizzy and lightheaded.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 27.01.2022
- Impfdatum
- 02.12.2021
- Beginn
- 04.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Dizziness
Haemorrhoids
Symptomtext
Suffered from hemorrhoids for two weeks. Never before had suffered from the condition. Chills and dizziness for three days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 26.01.2022
- Impfdatum
- 21.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Chills
Dizziness
Fatigue
Nausea
Pain
Pyrexia
Symptomtext
Chills, nausea, dizziness, weak, fatigue, body aches, fever
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- COVID (1/7/22 was first symptom day)
- Vorgeschichte
- none
- Andere Medikamente
- Turmeric, glucosamine chondroitin, magnesium sulfate, zinc picolinate
- Allergien
- Latex
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 23.01.2022
- Impfdatum
- 21.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Nasopharyngitis
Pruritus
Symptomtext
Systemic itching, headache and feels like I have a cold.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- N/A.
- Aktuelle Erkrankungen
- COVID-19 12/21/2021
- Vorgeschichte
- Allergies
- Andere Medikamente
- None
- Allergien
- PCN, IVP dye, Statins, metals, Keflex, Premarin, dogs, cats and grass
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 21.01.2022
- Impfdatum
- 20.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Vomiting
Symptomtext
Resident was in observation area. Noted to by lying across husband's lap. Resident was taken to EMS room & threw up. Given ice pack, snack & water. Afterwards voicing relief. Vitals BP 122/78, HR73, 99% RA, RR 18. At 1830 denied being lightheaded or dizzy, refused wheelchair & walked out with husband was asymptomatic
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vomiting
- Hospital-Tage
- -
- Labordaten
- unknown
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 21.01.2022
- Impfdatum
- -
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Heart rate
Heart rate increased
Injection site pain
Insomnia
Oxygen saturation
Oxygen saturation decreased
Vision blurred
Symptomtext
BLURRY VISION (ALARMED HIM); VERY BAD INSOMNIA; INJECTION SITE ARM PAIN; OXYGEN SATURATION AT 88; HEART RATE OF 105; This spontaneous report received from a patient concerned a 25 year old male. The patient's height, and weight were not reported. The patient's concurrent conditions included: penicillin allergy, and allergic to sulfa and other pre-existing medical conditions included: The patient had known medical conditions and no previous medication usage. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211D21A, expiry: unknown) dose was not reported, 1 total, administered on 14-JAN-2022 to left arm for prophylactic vaccination. No concomitant medications were reported. On 14-JAN-2022, post receiving vaccine the patient experienced arm pain in the injection site arm. On 16-JAN-2022, patient blurry vision which alarmed the patient. Patient was not sure whether to contact a physician or go to work. On 16-JAN-2022, patient experienced the very bad insomnia and was not slept at all. In JAN-2022, the patient checked the oxygen saturation and heart rate. Oxygen saturation was at 88 and heart rate was 105. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the injection site arm pain, blurry vision (alarmed him), very bad insomnia, heart rate of 105 and oxygen saturation at 88 was not reported. This report was serious (Other Medically Important Condition).; Sender's Comments: V0: 20220128712-COVID-19 VACCINE AD26.COV2.S- oxygen saturation at 88. 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
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- Test Date: 202201; Test Name: Oxygen saturation; Result Unstructured Data: 88; Test Date: 202201; Test Name: Heart rate; Result Unstructured Data: 105
- Aktuelle Erkrankungen
- Penicillin allergy; Sulfonamide allergy
- Vorgeschichte
- Comments: The patient had known medical conditions and no previous medication usage.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GU
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 21.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dizziness
Erythema
Eye swelling
Feeling hot
Respiratory tract congestion
Throat clearing
Throat irritation
Vaccination complication
Symptomtext
PT had an adverse reaction to first dose of Pfizer and was advised to switch to Janssen by PCP. No reaction to first dose of Janssen. This is her booster shot. At 1125 PT developed redness on chest, felt heat radiating from shoulders to neck, itchy throat, felt faint and swelling of eyes 9 minutes post vaccination. Vitals at 1125 BP:195/118, SPO2: 100%, HR: 100. At 1128 PT complained of feeling congested and feeling the need to clear throat, 1 tablet of 25mg PO of Benadryl was given to PT at 1128. EMS was contacted and PT was transported at 1151. Last vitals at BP: 182/93, SPO2:100%, HR:100.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Percocet, penicillin
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Headache
Pain
Pyrexia
Symptomtext
Fever, Chills, Whole body aches, Headache
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Synthroid, Vitamin D3, C, B12
- Allergien
- Minocyclin (anything in the tetracyclin family of antibiotics) Ceftin
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 17.01.2022
- Impfdatum
- 15.11.2021
- Beginn
- 06.01.2022
- Tage bis Beginn
- 52,0
- Dosis
- 2
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Arthralgia
Cough
Myalgia
SARS-CoV-2 test positive
Symptomtext
Cough, arthralgias, myalgias.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- Positive COVID test.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- M
- Eingang
- 14.01.2022
- Impfdatum
- -
- Beginn
- 11.01.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Fatigue
Feeling abnormal
Headache
Hypersomnia
Hypokinesia
Myalgia
Somnolence
Symptomtext
DROWSINESS; SLEPT THE WHOLE DAY; FELT SLOW; COULD NOT REALLY MOVE; JOINT ACHES IN LEGS; TIREDNESS; HEADACHES; MUSCLE ACHES; 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 concurrent conditions included: alcohol user (2 beers a week), and non smoker, and other pre-existing medical conditions included: The patient had no known allergies. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211D21A expiry: UNKNOWN) dose was not reported, administered on 10-JAN-2022 for prophylactic vaccination. No concomitant medications were reported. On 11-JAN-2022, the patient experienced drowsiness, slept the whole day, felt slow, could not really move, joint aches in legs, tiredness, headaches, and muscle aches. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from joint aches in legs, and muscle aches on 12-JAN-2022, was recovering from tiredness, and drowsiness, had not recovered from headaches, and the outcome of could not really move, slept the whole day and felt slow was not reported. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Alcohol use (2 beers a week); Non-smoker.
- Vorgeschichte
- Comments: The patient had no known allergies.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- -
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Pain in extremity
Tenderness
Symptomtext
SORE ARM; ACHES AND PAINS IN JOINTS; TENDER; This spontaneous report received from a consumer concerned a 67 year old female. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient was previously vaccinated with covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: unknown and expiry: unknown) (dose number in series 1), 01 in total was administered, dose was not reported for prophylactic vaccination. On an unspecified date, following vaccination with covid-19 vaccine ad26.cov2.s, she had sore arm and just tender (dose number in series 1). The patient additionally received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211D21A and expiry: 11-APR-2022) dose was not reported, dose number in series 2, 01 in total was administered on 04-JAN-2022 at left deltoid for prophylactic vaccination. No concomitant medications were reported. On JAN-2022, the patient experienced tender. On 04-JAN-2022, she had side effects of sore arm, and aches and pains in joints (dose number in series 2), and also stated that her arms still hurt. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from sore arm, and aches and pains in joints, and the outcome of tender was not reported (dose number in series 2). This report was non-serious. This case, involving the same patient is linked to 20220112619. This case, from the same reporter is linked to 20220112654 and 20220112293.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- -
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Pain in extremity
Tenderness
Symptomtext
This spontaneous report received from a patient concerned a 66 year old white 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 previously received Covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: unknown, expiry: Unknown) dose was not reported, dose number in series 1, 01 in total, administered on an unspecified date in MAR-2021 for prophylactic vaccination. On an unspecified date, following administration of Covid-19 vaccine ad26.cov2.s, the patient experienced blotchiness on the skin, sore arm and tender when treated with Covid-19 vaccine ad26.cov2.s (dose number in series 1). The patient additionally received Covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211D21A, expiry: 11-APR-2022) dose was not reported, dose number in series 2, 01 in total, administered on 04-JAN-2022 at left deltoid for prophylactic vaccination. No concomitant medications were reported. On an unspecified date in JAN-2022, following administration of Covid-19 vaccine ad26.cov2.s, the patient experienced tender arm (dose number in series 2). On 04-JAN-2022, the patient experienced aches and pains in joints, and sore arm (dose number in series 2). The action taken with Covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from aches and pains in joints, sore arm/ arm still hurt, and tender arm (dose number in series 2). This report was non-serious. This case, involving the same patient is linked to 20210424792. This case, from the same reporter is linked to 20220112619.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 13.01.2022
- 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: nein
Chills
Pain
Pyrexia
Vertigo
Symptomtext
Patient stated the evening of vaccination she went to sleep and woke up later experiencing vertigo. She then began to have fever, chill, and body aches exactly like she had when she was experiencing COVID-19 infection. The patient is continuing to have symptoms 27 hours post vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- COVID-19, three months prior
- Vorgeschichte
- History of traumatic brain injury
- Andere Medikamente
- Gabapentin, clonazepam, and lamotrigine
- Allergien
- Morphine
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 12.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cold sweat
Dizziness
Symptomtext
Patient reported feeling light headed, dizzy, and clammy after immunization. Remained in the pharmacy for 20-30 min after. Given some water, granola bar, cool compress. Reported feeling better and left the pharmacy without further issues.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 12.01.2022
- Impfdatum
- -
- Beginn
- 29.12.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal pain upper
Diarrhoea
Haematochezia
Nausea
Pain in extremity
Symptomtext
STOMACH IS HURTING; NAUSEA; DIARRHEA; BLOOD IN STOOL/BLEEDING WITH DEFECATION/POOPING BLOOD FOR THE PAST FEW DAYS; ARM IS HURTING; This spontaneous report received from a patient concerned a 35 year old male. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: The patient had no medical history. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211D21A, and expiry: UNKNOWN) 1 total, dose was not reported, administered on 29-DEC-2021 for prophylactic vaccination (Dose number in series 1). No concomitant medications were reported. The patient claimed that his arm hurt after taking the vaccine (29-Dec-2021). Patient experienced some nausea and diarrhea afterwards. On 09-JAN-2022, the patient experienced blood in stool/bleeding with defecation/ pooping blood for the past few days. This prompted him to go to the emergency room. The patient was in perfect health before the vaccine. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from blood in stool/bleeding with defecation/pooping blood for the past few days, and the outcome of nausea, diarrhea, stomach is hurting and arm is hurting was not reported. This report was serious (Other Medically Important Condition).; Sender's Comments: V0 20220113776-COVID-19 VACCINE AD26.COV2.S-blood in stool/bleeding with defecation/pooping blood for the past few days. 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
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: The patient had no medical history.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 11.01.2022
- Impfdatum
- 01.11.2021
- Beginn
- 17.11.2021
- Tage bis Beginn
- 16,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood pressure increased
Chills
Dizziness
Fatigue
Heart rate increased
Hypoacusis
Loss of personal independence in daily activities
Pain
Pyrexia
Tinnitus
Symptomtext
3 days of : Fever over 102, aches, chills, elevated blood pressure and heart rate. Decrease in hearing . Tinnitus, fatigue are some dizziness started within 5-7 days It has been almost 2 months since shot and tinnitus is still significant, disrupting daily life.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Scheduling appointment regarding tinnitus, dizziness and fatigue.
- Aktuelle Erkrankungen
- None Recovered from Covid November 2020 - still had detectable antibodies week before vaccine
- Vorgeschichte
- None
- Andere Medikamente
- Multi vitamin, probiotic
- Allergien
- Allergic to Sulfa Adverse reaction to Ketek Adverse reaction Heb B vaccine (did not complete series)
- Vorherige Impfungen
- Hep B, in the early 2000s Back pain, head ache, arm/hand weakness/numbness
- Staat
- MN
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 11.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Pruritus
Urticaria
Symptomtext
No reaction at time or day of injection. Patient called the pharmacy on 1/7 to discuss that starting on 1/5 he was breaking out in hives. So significant that he did present to Urgent Care for it. Started on one shoulder, then spread to the other, then trunk of body, down the legs. Hives and itching were his chief complaints. Denies other systemic involvement. As of 1/7 afternoon when I talked to him there had NOT been improvement yet with his systems but denied worsening. He was advised by urgent card MD to take OTC benadryl to help with the reaction. He was advised to follow-up with primary care MD and allergist or to return if worsening occurs. On 1/7 when I talked with the patient he as taking the benadryl only about once daily - mainly because of the drowsiness potential was making him nervous. We discussed using OTC once daily antihistamines that aren't as sedating . Could also use benadryl at bedtime if itching was bothersome. Advised he could use cold compress or washcloth on areas that are bothering him as a comfort measure. I did discuss that taking hot showers or baths could make the skin look more red or the hives look worse. Also discussed about what to do if worsening, if new symptoms started and then the importance of following up with MD/allergist.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- I don't know if any were done in urgent care. Patient didn't think so.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- None
- Allergien
- alupent
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 11.01.2022
- Impfdatum
- 08.12.2021
- Beginn
- 08.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site hypoaesthesia
Muscle spasms
Symptomtext
Patient began to feel numbness and cramps in left arm after inoculation. Doctor gives a doctor's order to administer acetaminophen PO, the patient refuses the FX since, according to what, he does not take medication. It is left under observation for 30 min and PO water is administered by medical prescription
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site hypoaesthesia
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 09.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Erythema
Headache
Injection site erythema
Muscle spasms
Pain in extremity
Symptomtext
pt states severe headache, redness and red spots at injection site, soreness and muscle spasms in arm and down right side of back, pt called pharmacy 01/08/22 pm and asked if anyone else had reported such symptoms said she had headache with first dose but not this severe, i recommended she call her physician and meantime hydrocortisone at injection sight along with ice and continue tylenol or ibuprofen
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- none
- Vorherige Impfungen
- janssen covid 19 vac 4/7/2021 headache
- Staat
- WA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 08.01.2022
- Impfdatum
- -
- Beginn
- 31.12.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dry mouth
Pruritus
Rash
Symptomtext
NON-RAISED RASH ABOVE LEFT KNEE; ITCHING ON ARMS AND LEGS; DRY MOUTH; This spontaneous report received from a patient concerned a 64 year old white not hispanic or latino female. The patient's height, and weight were not reported. The patient's past medical history included: bursitis, and concurrent conditions included: allergy to antibiotics, environmental allergies, and drug allergy with lidocaine. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of administration not reported, batch number: 202A21A, expiry: Unknown) dose was not reported (dose number in series 1), 01 in total, administered on 07-APR-2021 at 13:00 hours on left deltoid for prophylactic vaccination. On 07-APR-2021, within 15 minutes of vaccination, the patient had redness of face, and fever (dose number in series 1). It subsided within the next 15 minutes. On 08-APR-2021, in the evening, 24 hours after vaccination, the patient had bursitis type irritation (dose number in series 1) which didn't last very long. The patient also had headache in the back of the head on the right side on the base of the skull and felt like pulsating pain (dose number in series 1). The headache subsided within next 20 minutes. As per patient, she had Bursitis in the past and the vaccine seemed to trigger it, hence she contacted doctor's office at that time. The patient recovered from bursitis type irritation on an unspecified date, redness of face and fever on 07-APR-2021, and headache in the back of the head on the right side on the base of the skull and felt like pulsating pain on 08-APR-2021 (dose number in series 1). The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of administration not reported, batch number: 211D21A, expiry: Unknown) dose was not reported (dose number in series 2), 01 in total, administered on 30-DEC-2021 at right deltoid for prophylactic vaccination. Concomitant medications included cetirizine hydrochloride for environmental allergy. On 31-DEC-2021, the patient experienced itching on arms and legs (dose number in series 2) in the middle of the night and it had continued till the morning of reporting, without a rash. On 01-JAN-2022 (in the morning), the patient had some pink dots/ non-raised rash above her knee on the left side (dose number in series 2). According to the patient, it might had happened due to itching. The patient reported that she did not have dry mouth in past. At the time of reporting patient's mouth was dry and she felt thirsty (dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from itching on arms and legs, and dry mouth, and the outcome of non-raised rash above left knee was not reported (dose number in series 2). This report was non-serious. This case, involving the same patient is linked to 20220100909 (Dose number in series 1).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Allergy to antibiotic; Drug allergy (Lidocaine); Environmental allergy
- Vorgeschichte
- Medical History/Concurrent Conditions: Bursitis
- Andere Medikamente
- ZYRTEC [CETIRIZINE HYDROCHLORIDE]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 08.01.2022
- Impfdatum
- -
- Beginn
- 29.12.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
Influenza like illness
Injection site pain
SARS-CoV-2 test
Suspected COVID-19
Symptomtext
COVID-19 SYMPTOMS; FLU-LIKE SYMPTOMS; INJECTION SITE PAIN; This spontaneous report received from a patient concerned a 57-year-old male. The patient's weight was 181 pounds, and height was 71 inches. The patient's past medical history included: covid-19 (SEP-2020), patient had COVID-19 virus test which was positive, and concurrent conditions included: hypertension (well controlled) and drug allergy (allergic to most opioids). The patient previously received covid-19 vaccine ad26. cov2. s (suspension for injection, route of admin not reported, batch number: 1805018, and expiry: 23-AUG-2021) dose was not reported, frequency 1 total, administered at right arm on 10-APR-2021 for prophylactic vaccination (dose number in series 1). On 10-APR-2021, in the evening, the patient experienced headache, so he stayed in bed for a few days, felt "flu- like" with general body aches, injection site pain (all events with dose number series 1). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had recovered from headache, flu like symptoms and injection site pain. The patient received booster dose covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211D21A, and expiry: 11-APR-2022) dose was not reported, frequency 1 total, administered at right arm on 28-DEC-2021 for prophylactic vaccination (Dose number in series 2). Concomitant medications included influenza vaccine (received on 28-DEC-2021). The patient stated that after receiving vaccine he felt ok until this morning of 29-DEC-2021, and also checked his temperature with oral digital thermometer, which was at 99.8F. The patient stated that he was experiencing the same symptoms (flu like symptoms, headache, slight fever, injection site pain), most notable was the headache (Dose number in series 2). The patient added that he also "got a flu shot" at same time as covid-19 booster and was unsure if the symptoms he was feeling were from that, the covid booster, or if he actually had covid, as he stated that his symptoms "felt just like when he did have covid back in 2020." (Dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s, and influenza vaccine was not applicable. The patient had not recovered from flu-like symptoms, injection site pain, and covid-19 symptoms. This report was non-serious. This case, involving the same patient is linked to 20220100850.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- Test Date: 202009; Test Name: COVID-19 virus test; Result Unstructured Data: positive; Test Date: 20211229; Test Name: Body temperature; Result Unstructured Data: 99.8 F
- Aktuelle Erkrankungen
- Drug allergy (Allergic to most opioid); Hypertension (WELL CONTROLLED)
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19
- Andere Medikamente
- INFLUENZA VACCINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- -
- Geschlecht
- F
- Eingang
- 08.01.2022
- Impfdatum
- 27.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Chills
Dysmenorrhoea
Headache
Injection site pain
Injection site swelling
Menstruation irregular
Nausea
Vaginal haemorrhage
Symptomtext
IRREGULAR VAGINAL BLEEDING; MENSTRUAL CRAMPING; HORRIBLE LOW BACK PAIN LIKE BACK LABOR; CHILLS; SWELLING AT INJECTION SITE/ARM; PAIN AT INJECTION SITE/ARM; HEADACHE; NAUSEA; SPONTANEOUSLY BEGAN BLEEDING/ GOT PERIOD; This spontaneous report received from a patient concerned an adult female, age, race and ethnicity unknown. The patient's height, and weight were not reported. The patient's concurrent conditions included: perimenopausal for several years. The patient was not pregnant at the time of reporting. The patient previously received bnt 162 (Pfizer vaccine) (Dose number in series 1) on 24-MAR-2021 for prophylactic vaccination, and experienced severe reaction (dose number in series 1) and did not completed the series. The outcome of severe reaction was not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211D21A and expiry: Unknown) dose was not reported, frequency 1 total, administered on 27-DEC-2021 at 11:00 for prophylactic vaccination (Dose number in series 2). No concomitant medications were reported. On 27-DEC-2021, after receiving the vaccine the patient spontaneously began to bleed and got her period, she stated it was a weird cycle not normal. On 28-DEC-2021, the patient had reactions of headache, nausea, swollen and painful injection site/arm and chills. The patient added that she was also experiencing irregular vaginal bleeding during perimenopause, along with horrible low back pain like back labor, and reports that by 14:00 on 28-DEC-2021 she had vaginal spotting which then turned into a very heavy flow, no clots, bright red, with menstrual-like cramps. On 29-DEC-2021, the patient reported that she still had the heavy flow and the same symptoms, improving slightly except for the vaginal bleeding and injection site/arm pain which she states were the same (dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient was recovering from headache, nausea, chills, horrible low back pain like back labor, and menstrual cramping, and had not recovered from irregular vaginal bleeding, swelling at injection site/arm, pain at injection site/arm, and spontaneously began bleeding/ got period. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Perimenopause
- Vorgeschichte
- Comments: Unknown
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 08.01.2022
- Impfdatum
- -
- Beginn
- 27.12.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Drug delivery system malfunction
Feeling cold
Headache
Incorrect dose administered
Hypoaesthesia
Needle issue
Pain in extremity
Underdose
Injection site hypoaesthesia
Injection site pain
Pain
Symptomtext
BODY ACHES; CHILLS; FEELING COLD; HEADACHE; SORENESS AT INJECTION SITE; NUMBNESS AT INJECTION SITE/NUMBNESS FROM ELBOW TO HAND ON INJECTED ARM; POSSIBLE ADMINISTRATION OF MORE THAN RECOMMENDED DOSE; NEEDLE ASSEMBLY DETACHED; ADMINISTERED SLIGHTLY LESS THAN THE ACTUAL DOSE/ONLY 0.1ML HAD BEEN ADMINISTERED; This spontaneous report received from a parent concerned a 22 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included: asthma, seasonal allergy and pet allergy. The patient previously received with covid-19 vaccine ad26. cov2. s (suspension for injection, route of admin not reported, batch number: 1805025 and expiry: unknown) dose was not reported, 1 total, administered on 17-MAR-2021 for prophylactic vaccination (dose number in series 1). It was unknown whether patient had any adverse event following vaccination with covid-19 vaccine ad26.cov2.s. The patient received booster of covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211D21A and expiry: unknown) dose was not reported,1 total, administered at right arm on 27-DEC-2021 for prophylactic vaccination (dose number in series 2). No concomitant medications were reported. On 27-DEC-2021 at the time of vaccination, the patient felt water running down arm as the needle detached from the syringe (needle assembly detached) and according to nurse's clinical judgement, only 0.1ml had been administered (dose number in series 2). The patient was administered another dose of the same vaccine (unknown whether it was the same vial/LOT) into the same arm. On 27-DEC-2021, the patient experienced soreness and numbness at injection site starting at moment of administration. The patient's mother asked the details about incident and pharmacist said that, they had administered slightly less than the actual dose. Pharmacy team insisted that, it was not their fault and that needles were very cheap quality. The patient's mother was concerned, that her daughter could have received more than the recommended dose (coded as inappropriate dose of drug administered). Patient complained of numbness without mobility loss from elbow to hand on the same arm that started the same day. No swelling or hot to touch.(dose number in series 2) On 28-DEC-2021 04:45 hours, patient complained of chills, body aches, very bad headache but no fever as per reporter but the patient stated that, she felt really cold. (dose number in series 2) The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from chills, body aches, headache, feeling cold, soreness at injection site, and numbness at injection site/numbness from elbow to hand on injected arm, and the outcome of possible administration of more than recommended dose, needle assembly detached and administered slightly less than the actual dose/only 0.1ml had been administered was not reported. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Allergy to animals; Asthma; Seasonal allergy
- Vorgeschichte
- Comments: Unknown
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 08.01.2022
- Impfdatum
- -
- Beginn
- 27.12.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Drug delivery system malfunction
Feeling cold
Headache
Incorrect dose administered
Hypoaesthesia
Needle issue
Pain in extremity
Underdose
Injection site hypoaesthesia
Injection site pain
Pain
Symptomtext
BODY ACHES; CHILLS; FEELING COLD; HEADACHE; SORENESS AT INJECTION SITE; NUMBNESS AT INJECTION SITE/NUMBNESS FROM ELBOW TO HAND ON INJECTED ARM; POSSIBLE ADMINISTRATION OF MORE THAN RECOMMENDED DOSE; NEEDLE ASSEMBLY DETACHED; ADMINISTERED SLIGHTLY LESS THAN THE ACTUAL DOSE/ONLY 0.1ML HAD BEEN ADMINISTERED; This spontaneous report received from a parent concerned a 22 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included: asthma, seasonal allergy and pet allergy. The patient previously received with covid-19 vaccine ad26. cov2. s (suspension for injection, route of admin not reported, batch number: 1805025 and expiry: unknown) dose was not reported, 1 total, administered on 17-MAR-2021 for prophylactic vaccination (dose number in series 1). It was unknown whether patient had any adverse event following vaccination with covid-19 vaccine ad26.cov2.s. The patient received booster of covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211D21A and expiry: unknown) dose was not reported,1 total, administered at right arm on 27-DEC-2021 for prophylactic vaccination (dose number in series 2). No concomitant medications were reported. On 27-DEC-2021 at the time of vaccination, the patient felt water running down arm as the needle detached from the syringe (needle assembly detached) and according to nurse's clinical judgement, only 0.1ml had been administered (dose number in series 2). The patient was administered another dose of the same vaccine (unknown whether it was the same vial/LOT) into the same arm. On 27-DEC-2021, the patient experienced soreness and numbness at injection site starting at moment of administration. The patient's mother asked the details about incident and pharmacist said that, they had administered slightly less than the actual dose. Pharmacy team insisted that, it was not their fault and that needles were very cheap quality. The patient's mother was concerned, that her daughter could have received more than the recommended dose (coded as inappropriate dose of drug administered). Patient complained of numbness without mobility loss from elbow to hand on the same arm that started the same day. No swelling or hot to touch.(dose number in series 2) On 28-DEC-2021 04:45 hours, patient complained of chills, body aches, very bad headache but no fever as per reporter but the patient stated that, she felt really cold. (dose number in series 2) The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from chills, body aches, headache, feeling cold, soreness at injection site, and numbness at injection site/numbness from elbow to hand on injected arm, and the outcome of possible administration of more than recommended dose, needle assembly detached and administered slightly less than the actual dose/only 0.1ml had been administered was not reported. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Allergy to animals; Asthma; Seasonal allergy
- Vorgeschichte
- Comments: Unknown
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 34,0
- 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: ja
Dizziness
Hyperhidrosis
Pallor
Symptomtext
Patient got extremely light-headed, pale and sweaty, blood pressure was 100/78 initially and did normalize to 110/68 5 minutes later. Patient drank water and had some orange juice and remained in the pharmacy for approx 30 mins until he felt better. He did have a companion with him and did not leave alone
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- no
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- nono
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 04.01.2022
- Impfdatum
- 02.12.2021
- Beginn
- 04.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal discomfort
Arthralgia
Blood test
Computerised tomogram
Influenza like illness
Joint swelling
Pain
Pain in extremity
Peripheral swelling
Ultrasound scan
Symptomtext
Flu like symptoms, upset stomach, joint pain, hip, knee, shoulder and elbow pain. Swelling in right calf and knee. Shooting pain down right and left leg starting at the hip and moving down.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- CT scans, ultrasounds, blood tests
- Aktuelle Erkrankungen
- Inflamed disc.
- Vorgeschichte
- none.
- Andere Medikamente
- Prednisone
- Allergien
- none.
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- -
- Geschlecht
- M
- Eingang
- 04.01.2022
- Impfdatum
- -
- Beginn
- 31.12.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Body temperature
Dizziness
Nausea
Pyrexia
Symptomtext
LIGHTHEADED/DIZZY; WEAK; NAUSEOUS; 102.7 FEVER; This spontaneous report received from a patient concerned a 37 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: 211D21A, expiry: UNKNOWN) dose was not reported, administered on 30-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. On 31-DEC-2021, the patient experienced lightheaded/dizzy, weak, nauseous, and 102.7 fever. Laboratory data included: Body temperature (NR: not provided) 102.7 F. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from 102.7 fever, lightheaded/dizzy, weak, and nauseous. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- Test Date: 20211231; Test Name: Body temperature; Result Unstructured Data: 102.7 F; Comments: 102.7 F fever
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 31.12.2021
- Impfdatum
- -
- Beginn
- 21.11.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Anxiety
Axillary pain
Injection site pain
Injection site swelling
Lymphadenopathy
Pain
Peripheral swelling
Ultrasound scan
Urticaria
Vision blurred
Symptomtext
BODY ACHES; EXTREME ANXIETY; BLURRED VISION; REACTIVE LYMPH NODE; LEFT AND RIGHT SORE ARMPIT; LEFT ARM SWELLED UP; INJECTION SITE SWELLED UP (RIGHT ARM); TENDERNESS AT THE INJECTION SITE; HIVES (LOOKED LIKE MOSQUITO BITES IN THE LEFT ARM AND UPPER ARM)/ITCHY/SCABBED OVER; This spontaneous report received from a patient concerned a 75 year old female. Initial information was processed along with additional information received on 24-DEC-2021. The patient's height, and weight were not reported. The patient's past medical history included: covid-19, and concurrent conditions included: prothrombin issue, non alcohol user, non smoker, body aches antibiotics allergy (body aches, malaise, fatigue, flulike symptoms, and other pre-existing medical conditions included: The patient had no drug abuse or illicit drug usage. The patient sister had history of breast cancer and her daughter has factor V issue. The patient previously received covid-19 vaccine ad26. cov2. s (Janssen, Dose number in series 1) (suspension for injection, route of admin not reported, batch number were not reported) dose was not reported, 1 total, administered on 07-APR-2021 for prophylactic vaccination. No adverse events where reported. (Dose number in series 1) The patient received covid-19 vaccine ad26.cov2.s (Janssen, Dose number in series 2) (suspension for injection, route of admin not reported, batch number: 211D21A, expiry: 11-APR-2022) dose was not reported, 1 total, administered on 17-NOV-2021 to Right Arm for prophylactic vaccination. No concomitant medications were reported. On 21-NOV-2021, Post booster dose about 4 to 5 days the patient developed hives which looked like mosquito bites in the left arm and upper arm (4-5 bites) that were very itchy and then scabbed over. she also mentioned she lived in Florida and that could had been possible that it was by mosquito bites and then her right arm (where injection was done) swelled up and the left arm also swelled up 2-3 days after around 22-NOV-2021 and also the location of the injection is still tender and she felt the shot as it went in. On 24-NOV-2021, around the patient went to urgent care, as patient was worried about blood clot (she has prothrombin issue. The patient did ultrasound and told her that there was no blood clot. After ultrasound was done it was found that patient had a reactive lymph node on the left side, her left armpit has been sore and now the right one is sore a bit. Patient is also suffering from blurred vision which thinks is because of the video games she plays on her phone. The patient had body aches when she wakes up but says she had them before vaccination as well. The patient is quite worried and says that she had anxiety in the past about blood clot and has taken alprazolam for it. The Patient also mentioned she suffers from extreme anxiety and it is possible for her to experience all of the symptoms associated with blood clots if she is extremely anxious. The patient stated that her doctor informed her that the reactive lymph node detected by ultrasound on her left arm was a sign her he had them before vaccination as well. (Dose number in series 2) The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from left arm swelled up, hives (looked like mosquito bites in the left arm and upper arm)/itchy/scabbed over, and injection site swelled up (right arm), had not recovered from tenderness at the injection site, reactive lymph node, and left and right sore armpit, and the outcome of body aches, extreme anxiety and blurred vision was not reported. This report was non-serious. This case, from the same reporter is linked to 20211255466.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- Test Date: 20211124; Test Name: Diagnostic ultrasound; Result Unstructured Data: No blood clot detected.; Test Name: Diagnostic ultrasound; Result Unstructured Data: reactive lymph node detected; Comments: reactive lymph node detected which reflects immune system was working after booster dose.
- Aktuelle Erkrankungen
- Abstains from alcohol; Allergy to antibiotic (She had allergy to (all antibiotics) made her sick (body aches, malaise, fatigue, flulike symptoms)); Generalised aching; Non-smoker; Prothrombin abnormal
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19; Comments: The patient had no drug abuse or illicit drug usage. The patient sister had history of breast cancer and her daughter has factor V issue. The patient was quite worried and had anxiety in the past about blood clot and has taken alprazolam for it.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 31.12.2021
- Impfdatum
- -
- Beginn
- 10.12.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain in extremity
Poor quality product administered
Product storage error
Symptomtext
VIAL FIRST PUNCTURED THE DAY BEFORE(NOT A SPECIFIC AMOUNT OF TIME BUT GREATER THAN 6 HOURS AFTER PUNCTURE; SORE ARM; 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 previously received covid-19 vaccine ad26.cov2.s (dose number in series 1, unspecified manufacturer) (suspension for injection, route of admin not reported, batch number and expiry not reported) dose was not reported, 1 total, administered on an unspecified date for prophylactic vaccination. No adverse event reported post primary 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: 211D21A, and expiry: 11-APR-2022) dose was not reported, 1 total, administered on 10-DEC-2021 on left deltoid for prophylactic vaccination. No concomitant medications were reported. On 10-DEC-2021, the patient received booster shot that came from a vial first punctured the day before, not a specific amount of time but greater than 6 hours after puncture (out of specification product use). The only side effect he experienced was sore arm (dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the vial first punctured the day before (not a specific amount of time but greater than 6 hours after puncture) and sore arm was not reported. This report was non-serious. This case, from the same reporter is linked to 20211248642.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 31.12.2021
- Impfdatum
- -
- Beginn
- 10.12.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain in extremity
Poor quality product administered
Product storage error
Symptomtext
VIAL FIRST PUNCTURED THE DAY BEFORE(NOT A SPECIFIC AMOUNT OF TIME BUT GREATER THAN 6 HOURS AFTER PUNCTURE; SORE ARM; 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 previously received covid-19 vaccine ad26.cov2.s (dose number in series 1, unspecified manufacturer) (suspension for injection, route of admin not reported, batch number and expiry not reported) dose was not reported, 1 total, administered on an unspecified date for prophylactic vaccination. No adverse event reported post primary 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: 211D21A, and expiry: 11-APR-2022) dose was not reported, 1 total, administered on 10-DEC-2021 on left deltoid for prophylactic vaccination. No concomitant medications were reported. On 10-DEC-2021, the patient received booster shot that came from a vial first punctured the day before, not a specific amount of time but greater than 6 hours after puncture (out of specification product use). The only side effect he experienced was sore arm (dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the vial first punctured the day before (not a specific amount of time but greater than 6 hours after puncture) and sore arm was not reported. This report was non-serious. This case, from the same reporter is linked to 20211248642.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 29.12.2021
- Impfdatum
- 29.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Feeling hot
Symptomtext
AFTER VACCNATION, PATIENT BECAME EXTREMELY LIGHTHEADED AND DIZZY. HE DESCRIBED THE SENSATION AS "A RUSH ALL OVER HIS BODY". PATIENT WAS AFRAID HE MAY PASS OUT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 29.12.2021
- Impfdatum
- 15.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 7,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymph node pain
Symptomtext
Pain in lymph nodes left arm pit/breast area
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymph node pain
- Hospital-Tage
- -
- Labordaten
- none but I just had a mammogram and the tech told me it was most likely from the covid vaccine
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- high blood pressure, anxiety
- Andere Medikamente
- Levothyroxin 75mcg Tab, Ropinirole 4mg Tab, Cartia Xt 120/24hr Cap, Duloxetine 30mg Cap
- Allergien
- adhesive, morphine, codeine
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 29.12.2021
- Impfdatum
- -
- Beginn
- 02.12.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Diarrhoea
Headache
Symptomtext
CHRONIC DIARRHEA; EPISODES OF HEADACHE; This spontaneous report received from a patient concerned a 53 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included: bioidentical hormone therapy, pollen allergy, alcohol user, non smoker, and menopause, and other pre-existing medical conditions included: The patient does not have history of 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: 211021A, and expiry: 04-11-2022) dose was not reported, administered on 26-NOV-2021 for prophylactic vaccination. Concomitant medications included testosterone for drug used for unknown indication, estradiol/estriol for menopause, and progesterone for menopause. On 02-DEC-2021, the patient experienced chronic diarrhea. On 02-DEC-2021, the patient experienced episodes of headache. Treatment medications (dates unspecified) included: acetylsalicylic acid/caffeine/paracetamol/salicylamide, bismuth subsalicylate, and acetylsalicylic acid. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from chronic diarrhea, and episodes of headache. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Alcohol use (occasionally (very very rarely)); Hormone therapy; Menopause; Pollen allergy (hay fever)
- Vorgeschichte
- Medical History/Concurrent Conditions: Non-smoker; Comments: The patient does not have history of drug abuse or illicit drug usage.
- Andere Medikamente
- PROGESTERONE; ESTRADIOL;ESTRIOL; TESTOSTERONE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 29.12.2021
- 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
Abdominal discomfort
Aphasia
Balance disorder
Cholecystectomy
Coordination abnormal
Diplopia
Eye pain
Feeding disorder
Gallbladder disorder
Memory impairment
Neuralgia
Neuropathy peripheral
Pityriasis rosea
Speech disorder
Symptomtext
Neuralgia shooting down right arm amd leg (not resolved); neuropathy in right hand (not resolved); loss of balance and coordination (resolved); anomic aphasia and word finding difficulties (partially resolved); diplopia (resolved); left sided ophthalmalgia (resolved); difficulty with short term memory (not resolved); severe GI distress (resolved); breakout of pityriasis rosea (resolved); near constant gallbladder attacks that left me unable to eat anything but bread and pretzels and required a cholecystectomy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Eye pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Cholelithiasis without cholecystitis
- Andere Medikamente
- None
- Allergien
- Flu vaccine
- Vorherige Impfungen
- Flu vaccine. Extensive rash and mild angioedema. At approximately 28 years age.
- Staat
- CA
- Alter
- -
- Geschlecht
- F
- Eingang
- 28.12.2021
- Impfdatum
- -
- Beginn
- 10.12.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain in extremity
Poor quality product administered
Symptomtext
VIAL FIRST PUNCTURED THE DAY BEFORE NOT A SPECIFIC AMOUNT OF TIME BUT GREATER THAN 6 HOURS AFTER PUNCTURE; SORE ARM; This spontaneous report received from a consumer concerned a female of unspecified age, race and ethnic origin. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received vaccination with covid-19 vaccine ad26.cov2.s (unspecified manufacturer) (suspension for injection, route of admin not reported, batch number: Unknown and expiry; Unknown) dose was not reported, 1 total, administered on an unspecified date for prophylactic vaccination (Dose number in series 1). It was unknown whether patient had any adverse events following primary 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: 211D21A, and expiry: 11-APR-2022) dose was not reported,1 total, administered on 10-DEC-2021 for prophylactic vaccination (dose number in series 2). No concomitant medications were reported. On 10-DEC-2021, after receiving the booster shot the patient came to know that the product given came from a vial first punctured the day before, not a specific amount of time but greater than 6 hours after puncture (Out of specification product use) (also reported as expired dose give (after 6 hours post puncture)) (dose number in series 2). The only side effect she experienced was sore arm (dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the vial first punctured the day before not a specific amount of time but greater than 6 hours after puncture and sore arm was unknown. This report was non-serious. This case, from the same reporter is linked to 20211247381.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 23.12.2021
- Impfdatum
- 26.11.2021
- Beginn
- 28.11.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Gait disturbance
Muscle spasms
Symptomtext
DEVELOPED INTENSE LOWER BACK PAIN/MUSCLE SPASMS THAT HAVE LASTED SINCE 11/28/2021. HE COMPLAINS OF IT BEING DIFFICULT TO WALK DUE TO THE PAIN.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 63,0
- Geschlecht
- M
- 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: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Decreased appetite
Diarrhoea
Dizziness
Fatigue
Headache
Loss of personal independence in daily activities
Nausea
Symptomtext
The night after the shot I felt dizzy, tired, and in two days nauseous, diarrhea, headaches, I was unable to function any daily routine. I had no appetite and still don?t have much of one 9 days later,
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 22.12.2021
- Impfdatum
- 22.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Symptomtext
Patient c/o dizziness and wanted to pass out. Patient felt nervous when it comes to needle and report that happened in the past. Vital was taken BP: 129/82, HR: 60, Oxygen: 98. Nurse attended and gave patient 2 ice packs. Patient was observed longer and cleared by nurse.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 22.12.2021
- Impfdatum
- 17.11.2021
- Beginn
- 19.11.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Blood pressure increased
Headache
Heart rate increased
Platelet count normal
Symptomtext
Began experiencing severe headaches along with heart rate increase from normal (44) to over 100 on or around November 20th 2021. Also my blood pressure increased to 160/100 for weeks until I was seen by the cardiologist and prescribed Norvasc (Amlodipine) to reduce high blood pressure.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- I was seen by local Cardiology 12/15/21 and my blood pressure was taken multiple times at or around 160/100. My normal blood pressure before the vaccine had never reached that high at rest. I also had a blood panel done at a local urgent care to check platelet levels which came back normal. The local cardiology prescribed Norvasc (Amlodipine) to reduce high blood pressure.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Erythromycin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- M
- Eingang
- 22.12.2021
- Impfdatum
- -
- Beginn
- 01.12.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Myalgia
Nonspecific reaction
Poor quality product administered
Product storage error
Symptomtext
MUSCLE ACHES; STORED OUTSIDE OF THE RECOMMENDED TEMPERATURE RANGE; OUT OF SPECIFICATION PRODUCT USE; MINOR REACTIONS; This spontaneous report received from a pharmacist concerned a male of unspecified age, race and ethnicity. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received with covid-19 vaccine ad26. cov2. S (dose number in series: 1), (suspension for injection, route of admin not reported, batch number: unknown, and expiry: unknown) dose was not reported, 1 total, administered on 21-MAY-2021 for prophylactic vaccination. On an unspecified date, following administration of covid-19 vaccine ad26.cov2.s, the patient experienced muscle ache (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: 211D21A, and expiry: unknown) dose was not reported, 1 total, administered on 10-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. On 10-DEC-2021, vial was stored outside of the recommended temperature range which is incorrect product storage (dose number in series 2), 2 doses were drawn from vial and placed back in the fridge then the next day another 2 doses were drawn from that and 1 of the dose was given to the patient which is out of specification product use (dose number in series: 2). In DEC-2021 (unspecified date), following administration of covid-19 vaccine ad26.cov2.s the patient experienced minor reactions and muscle aches (both events dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the stored outside of the recommended temperature range, muscle aches, minor reactions and out of specification product use was not reported. This report was non-serious. This case, involving the same patient is linked to 20211233937. This case, from the same reporter is linked to 20211233321 and 20211233061.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- F
- Eingang
- 22.12.2021
- Impfdatum
- -
- Beginn
- 01.12.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Myalgia
Poor quality product administered
Product storage error
Symptomtext
STORAGE OF VACCINE VIAL OUTSIDE OF THE RECOMMENDED TEMPERATURE RANGE; POOR QUALITY VACCINE ADMINISTERED; MUSCLE ACHE; This spontaneous report received from a pharmacist concerned a female of unspecified age, race and ethnicity. 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: unknown and expiry: UNKNOWN) dose was not reported, 1 total administered on MAY-2021 for prophylactic vaccination (Dose number in series 1). Later, (date not specified) the patient experienced muscle ache (Dose number in series 1). The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211D21A and expiry: UNKNOWN) dose was not reported, 1 total administered on 10-DEC-2021 for prophylactic vaccination (Dose number in series 2) from a vial that was stored outside of the recommended temperature range (incorrect product storage). 2 doses were drawn from the vial and placed back in the fridge, then the next day another 2 doses were drawn and were given to the patient (poor quality vaccine administered). No concomitant medications were reported. In DEC-2021, the patient experienced muscle aches (Dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the storage of vaccine vial outside of the recommended temperature range, muscle ache and poor quality vaccine administered was not reported. This report was non-serious. This case, from the same reporter is linked to 20211233061, 20211233514 and 20211233937.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 20.12.2021
- Impfdatum
- 13.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 4,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site nodule
Injection site pain
Symptomtext
Knot in upper right arm where shot was given. It also burned a little bit a week later.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site nodule
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Iron deficiency, anemia (B12)
- Andere Medikamente
- None
- Allergien
- Penicillin, Lactose, shellfish
- Vorherige Impfungen
- Penicillin.
- Staat
- OR
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 19.12.2021
- Impfdatum
- 08.12.2021
- Beginn
- 18.12.2021
- Tage bis Beginn
- 10,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dysmenorrhoea
Fatigue
Haemorrhage
Heavy menstrual bleeding
Symptomtext
Very heavy period following 2nd shot. Similar to my period after the first shot but much worse. Intense cramping, fatigue and bleeding.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Skin sensitivities to some perfumes and dyes
- Vorherige Impfungen
- First J&J vaccine.
- Staat
- IL
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 18.12.2021
- Impfdatum
- 14.12.2021
- Beginn
- 14.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fear
Pruritus
Skin irritation
Symptomtext
Patient states after receiving the vaccination he experienced (and now has experienced since then about 4 days in total) an itchiness within his chest and additionally near the nipple on his left side. He states it is constant and irritating and is in fear of a potential blood clot versus a local allergic reaction. We discussed since he is working a night shift tonight, to try 2 25mg benadryl tablets upon arriving home before he sleeps to see if he gets any relief from an antihistamine. Either way, I recommended following up with his PCP who he has recently seen for his physical (which was normal). I explained if he gets relief from the benadryl it is possible it is just an allergic reaction however it is important to inform his PCP either way. I informed him I would report the incident to VAERS for him and he agreed. We will follow up with him Monday.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- -
- Geschlecht
- M
- Eingang
- 17.12.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Symptomtext
BURNS MORE AT INJECTION SITE; This spontaneous report received from a patient via a company representative 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, and batch number were not reported) dose, start therapy date were not reported for prophylactic vaccination (manufacturer unspecified - dose series 1). The batch number was not reported and has been requested. No concomitant medications were reported. On an unspecified date the patient experienced injection burnt a bit (injection site burning). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome for the event of injection burnt a bit was not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin, and batch number were not reported) dose, start therapy date were not reported for prophylactic vaccination (dose series 2). The batch number was not reported and has been requested. On an unspecified date the patient experienced burns more at injection site (injection site burning) compared to the initial dose. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of injection site burning was not reported. This report was non-serious. This case, involving the same patient is linked to 20211214174.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 16.12.2021
- Impfdatum
- 16.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Headache
Muscular weakness
Neurological symptom
Symptomtext
Pt was very anxious before getting the vaccine. Rph went over the questions & per pt's consent administered the vaccine. After 5 min pt complained weakness in arm, legs, headache dizziness. & said felt like stroke like symptoms- 911 was called immediately. pt stated she was starting to feel better. 911 came & paramedics did a check up in ambulance & per pts statement of feeling ok pt went home after being checked by paramedics.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- N/A
- Andere Medikamente
- Amovig 140mg
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 97,0
- Geschlecht
- F
- Eingang
- 16.12.2021
- Impfdatum
- 02.09.2021
- Beginn
- 14.12.2021
- Tage bis Beginn
- 103,0
- Dosis
- 2
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest X-ray
Cough
Fatigue
SARS-CoV-2 test
Symptomtext
Cough, fatigue
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Chest x-ray COVID test 12/14/2021
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Chronic renal failure Acute renal failure (ARF) Obesity (BMI 30-39.9) Paroxysmal atrial fibrillation Gout Additional information for Item 12:
- Andere Medikamente
- acetaminophen (TYLENOL) 325 MG PO Tab Additional information for Item 9: allopurinol (ZYLOPRIM) 100 MG PO Tab ammonium lactate (Lac-Hydrin) 12 % EXTERNAL Cream furosemide (LASIX) 40 MG PO Tab gabapentin (NEURONTIN) 100 MG PO Cap guaiF
- Allergien
- Aspirin Unable to specify Additional information for Item 10: Aspirin Unable to specify Pt unable to specify o Ciprofloxacin Unable to specify Pt unable to specify o Codeine Unable to specify Pt unable to specify o Dyazide [Hydrochlorothiazide W-Triamterene] Unable to specify Pt unable to specify o Erythromycin Unable to specify Pt unable to specify o Fentanyl Unable to specify Pt unable to specify o Hydrochlorothiazide Unable to specify Pt unable to specify o Penicillins Unable to specify Pt unable to specify o Prednisone Unable to specify Pt unable to specify o Sulfa Antibiotics Unable to specify Pt unable to specify o Tetanus Toxoids Unable to specify Pt unable to specify o Triamterene Unable to specify Pt unable to specify o Valacyclovir Unable to specify Pt unable to specify o Versed [Midazolam] Unable to specify Pt unable to specify
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 16.12.2021
- Impfdatum
- -
- Beginn
- 05.12.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain in extremity
Tenderness
Unevaluable event
Symptomtext
TATTOO ON INJECTION SITE DISAPPEARED; SORE ARM; TENDERNESS; This spontaneous report received from a patient concerned a 54-year-old adult female. The patient's height, and weight were not reported. The patient's concurrent conditions included: the patient was hypersensitive, drug allergy (narcotics), and other pre-existing medical conditions included the patient had Chest pain and was sick with Narcotics. The patient was previously received with covid-19 vaccine ad26. cov2. s (unspecified manufacturer) (suspension for injection, route of admin, and batch number: unknown, Expiry: unknown) dose not reported, frequency 1 total, start therapy date were not reported for prophylactic vaccination (Dose number in series 1). It was unknown whether patient had any adverse event following vaccination with covid-19 vaccine ad26.cov2.s. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211D21A, and expiry: Unknown) dose was not reported, 1 total, administered at right arm on 03-DEC-2021 for prophylactic vaccination (Dose number in series 2). No concomitant medications were reported. On 05-DEC-2021, the patient experienced tenderness. On 06-DEC-2021, the patient experienced sore arm and tattoo on injection site disappeared. It was reported that, the patient had tattoo of about 2 by 2 inches and noticed tattoo was dissolving. Treatment medications (dates unspecified) included Motrin (Naproxen) for the sore arm and tenderness.(Dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient was recovering from tattoo on injection site disappeared, sore arm, and tenderness. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Drug allergy (Narcotics makes her sick and gives her chest pain); Hypersensitivity.
- Vorgeschichte
- Comments: Unknown
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 15.12.2021
- Impfdatum
- 19.11.2021
- Beginn
- 07.12.2021
- Tage bis Beginn
- 18,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood pressure increased
Feeling cold
Headache
Hot flush
Nausea
Vomiting
Symptomtext
Elevted blood pressure, headaches, nausea, vomiting and hot flashes leading to cold flashes. . INcrease blood pressure meds to keep blood pressure at a normal range. 12/14/21 md office visit to comfirm blood pressures out of range with take prescribed meds.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- hypertension
- Andere Medikamente
- None
- Allergien
- Latex,
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 14.12.2021
- Impfdatum
- 31.10.2021
- Beginn
- 02.11.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Feeling hot
Hypoaesthesia
Injection site pain
Pain
Rotator cuff syndrome
Swelling
Symptomtext
Received the J & J vaccine 10/31/21 in left deltoid, increased pain, noted into shoulder x 3 weeks and radiating into elbow with occasional numbness extending into ring and pinky finger. Redness, heat, and swelling noted in upper arm. 11/22/21 initial visit in the occupational health department, Keflex 500 mg QID x 5 days prescribed. A referral is given to Orthopaedics. 11/30/21, occupational health department follow-up, continues with swelling, discomfort, and heat, Keflex 500 mg TID prescribed. 12/3/21, occupational health visit follow-up. 12/7/21 Orthopaedic, Dr. consult, determined rotator cuff inflammation recommended exercises. 12/10/21 occupational health follow-up, D/C from service. Continues with aching in the upper arm. Prior Hx of Covid-19 infection 12/20, + antibody test 04/21.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Ehlers-Danlos Syndrome
- Andere Medikamente
- Topamax 50 mg BID
- Allergien
- NDA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 14.12.2021
- Impfdatum
- 22.11.2021
- Beginn
- 28.11.2021
- Tage bis Beginn
- 6,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Rash
Symptomtext
On 11/22/21, came in for a J&J JANSSEN COVID-19 VACCINE. Patient answered all 14 questions of the consent form and they were all answered as No. Patient had no other medical conditions or allergies. Gave the patient full consultation prior to administration of vaccine and observed patient for a full 15 minutes and no patient had no issues. The next day patient came in with his wife to accompany her while she was receiving a vaccine as well. I did ask if he had any reaction from the vaccine, and he stated none whatsoever. On 12/13/21, patient came in and stated that he had noticed a rash mainly on his back and hand 6 days post injection. I recommended that he be seen by his doctor to further evaluate the rash. I will document this case in VAERS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 13.12.2021
- 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: ja
Dizziness
Tinnitus
Symptomtext
A 29-year-old male patient reported feeling dizzy and tinnitus 7 minutes after receiving his first dose of Janssen. Patient remained standing, walking and oriented x3 at the time of the incident.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- Vital Signs B / P -100/60, Breaths 20, Pulse 63 and 98% saturation
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 13.12.2021
- Impfdatum
- 28.11.2021
- Beginn
- 29.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Tinnitus
Symptomtext
I have had a headache since the day after I received the vaccine. Also my ears are now ringing since receiving the vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Multi vitamins
- Allergien
- Shellfish and contrast dye
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 99,0
- Geschlecht
- F
- Eingang
- 11.12.2021
- Impfdatum
- 10.12.2021
- Beginn
- 10.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Symptomtext
Patient complained of feeling light headed and dizzy at 10:05 am. I turned the fan on and took vitals which were stable. Stayed with patient until she was feeling completely fine, total time 45 min.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 11.12.2021
- 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
Asthenia
Back pain
Chest discomfort
Discomfort
Herpes zoster
Muscle spasms
Pain
Pain in extremity
Somnolence
Symptomtext
Same day I experienced a sore arm (to be expected). Within 24 hours I still had a sore arm and body aches. Within 3 days I still had a sore arm and back pain in my mid back (never had any back pain before). Day 4-5 developed a tightening feeling on my chest. Back pain worsened on my left side and became more of a spasm/jabbing feeling. Day 6 developed shingles all on the left side of my torso from the front of my chest (on left breast), around the under side of my left breast all the way to the middle of my back. The back pain is still there on the left side, like someone is putting an annoying pressure around where just under my shoulder blade is. Today is day 9 after the vaccine and is the worst day so far in terms of pressure on my back, itchiness/soreness/pain of having shingles. The past 9 days I have been sleeping 10-12 hours (usually at 8 hours) and taking 1.5-3 hour naps in the afternoon. Energy level continues to be low.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- I take Vitamins D3, C and B12 daily
- Allergien
- Allergy to Sulpha and Dairy
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 11.12.2021
- Impfdatum
- 09.12.2021
- Beginn
- 09.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Headache
Nausea
Pain
Symptomtext
Severe fatigue and headache; body aches and sensitivity; mild nausea; possible light fever Events started 6 hours after administration, began clearing overnight after full day of symptoms Generic brand NyQuil was taken both nights of symptoms due to acetaminaphin content. Ibuprofin pills were taken to ease headache before it was understood to be a vaccine reaction. The ibuprofin did not seem to have an effect.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Allergies
- Andere Medikamente
- Multivitamin, over-the-counter allergy medication (loratidine)
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 10.12.2021
- Impfdatum
- 10.12.2021
- Beginn
- 10.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Vomiting
Symptomtext
* patient started vomiting about 7-10 minutes after vaccination; he recovered without incidence in about 10-15 minutes
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vomiting
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- * patient was anxious about vaccination *
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 10.12.2021
- 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: ja
Dizziness
Malaise
Vomiting
Symptomtext
Patient said that she started to feel sick and somewhat dizzy approximately 5 minutes after receiving the vaccination. She vomited; after about 5-10 minutes later the vomiting/dizziness subsided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- * Patient was very anxious prior to vaccination *
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 10.12.2021
- Impfdatum
- 09.12.2021
- Beginn
- 10.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Headache
Myalgia
Pain in extremity
Pyrexia
Symptomtext
Sore arm, muscle ache all over body, fever, headache. Chills,
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Lymphocytic colitis
- Andere Medikamente
- None
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 09.12.2021
- Impfdatum
- 09.12.2021
- Beginn
- 09.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain
Asthenia
Dizziness
Nausea
Pelvic pain
Vomiting
Symptomtext
21-year-old female received her first dose of Janssen at 2:33 pm and it begins with symptoms of emesis, nausea, dizziness and weakness. She was taken to the incident observation area to evaluate her and her vital signs were: 71 for Pulse, 36 for Temperature, 100/60 B/P, 19 Resp, and 98 Dextro. Nurse communicates with Dr. and refers to placing the patient in the Trendelenburg position and giving her a GATORADE and then keeping her under observation for 30 minutes. After re-evaluating her, the patient continues with the same vital signs, but the patient refers to having severe abdominal pelvic pain and Dr. is notified again and refers to transfer her to the Hospital by the Medical Ambulance and was treated by the EMT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Synthroid
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- ND
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 09.12.2021
- Impfdatum
- 02.12.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Angioedema
Diarrhoea
Dysphagia
Enlarged uvula
Lymphadenopathy
Peripheral swelling
Pharyngeal swelling
Swelling face
Swollen tongue
Symptomtext
First 4-9minutes after shot; Swollen uvula, tongue, throat, difficulty swallowing. Benadryl and EpiPen. After discharge medications: prednisone 50mg x 4days, Benadryl every 6hrs. Other symptoms; swollen underarms both sides, pubic area, recurrent angioedema, still taking zyrtec Am, benadryl Pm day #7. Day #6 diarrhea, after 72hrs left side face arm, leg swollen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Shell fish allergies(clam, crab, lobster, shrimp), penicillin, Others(trees, grasses, mold)
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 09.12.2021
- Impfdatum
- 03.12.2021
- Beginn
- 04.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal distension
Abdominal pain
Abdominal pain upper
Arthralgia
Back pain
Chest discomfort
Cough
Diarrhoea
Fatigue
Fibrin D dimer
Full blood count
Nausea
Pain
Platelet count
Pyrexia
Vomiting
Symptomtext
Saturday when I woke up I had tightness in my chest. I went to work, came home, and I ended up that night from chest pain to abdominal pain. Sunday I had a tight cramping in stomach but still went to work. I had mild cough, mild fever, but no body aches until Monday when I woke up. I was fatigued with abdominal pain, nausea, diarrhea, and vomiting. Tuesday and Wednesday was the same thing and I still have mild abdominal pain but my stomach is bloated and everything is turning to liquid in my gut with diarrhea. I'm taking Zofran, Tylenol, and Pepcid to try and help bring me back. I have lower back pain, joint pain, and not as much abdominal pain but I still have it. It's moving up and all the way down.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- Blood work, CBC, Dimers, Platelet counts.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Sinuses; Lower back injury
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 09.12.2021
- Impfdatum
- 23.11.2021
- Beginn
- 25.11.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Symptomtext
Started having low level headache 2 days after injection. Headache has lasted up until the present day. Headache is almost none-existent when I wake up in the morning. Then over the course of the day the pain increases from about a 2 or 3 to about a 7. That was early in the headache. Now it increases to about a 4 or 5. Pain is located on left side of my head behind the left eye. No history of headaches lasting more than 2 days. Pain/pressure increases if I cough, sneeze or strain in any way or when bending over. Pain can also increase after looking at computer or phone screens or when wearing glasses for an extended period of time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Polymyositis in remission
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 86,0
- Geschlecht
- M
- Eingang
- 08.12.2021
- Impfdatum
- -
- Beginn
- 17.11.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Headache
Symptomtext
VERY BAD HEADACHE; This spontaneous report received from a consumer concerned an 86 year old male of unknown race and ethnicity. The patient's height, and weight were not reported. The patient's past medical history was not reported. Concurrent conditions are non-alcohol user, quit smoking (patient quit smoking in 1980's) and glaucoma. The patient was previously treated with covid-19 vaccine ad26. cov2. s. (manufacturer not specified) (suspension for injection, route of admin not reported, batch number: UNKNOWN) dose was not reported, 1 in total, for prophylactic vaccination (dose series 1). The patient received additional covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211D21A, expiry: UNKNOWN) dose was not reported, 1 in total, on right arm administered on 16-NOV-2021 for prophylactic vaccination. (dose series 2). Concomitant medications included brimonidine tartrate/brinzolamide and latanoprost for glaucoma; and famotidine, losartan, metformin, metoprolol succinate, and pravastatin for unknown indications. On 17-NOV-2021, the patient experienced very bad headache after he woke up (dose series 2). The headache lasted all day. Tylenol (Paracetamol) did not help to reduce the headache. Patient did not experience the headache on the night of 17-NOV-2021, and it went away during sleep. Headache was gone on 18-NOV-2021. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from very bad headache on 18-NOV-2021. This report was non-serious. This case, from the same reporter is linked to 20211142267.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Abstains from alcohol; Ex-smoker (quit smoking in the 1980s); Glaucoma
- Vorgeschichte
- Comments: Unknown
- Andere Medikamente
- PRAVASTATIN; FAMOTIDINE; LOSARTAN; METFORMIN; LATANOPROST; TOPROL XL; SIMBRINZA
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 08.12.2021
- Impfdatum
- -
- Beginn
- 17.11.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Headache
Symptomtext
HEADACHE; This spontaneous report received from a patient concerned a 74 year old female. The patient's height, and weight were not reported. The patient's past medical history included: fibromyalgia, and concurrent conditions included: non-alcohol user, non-smoker, and blood pressure. The patient was previously treated with covid-19 vaccine ad26.cov2.s for prophylactic vaccination (unspecified manufacturer) (Dose Number In Series 1) and experienced drug allergy when treated with hydrocodone (for fibromyalgia), duloxetine hydrochloride, fluconazole, diltiazem, doxycycline (received only for 7 days), famotidine, fluticasone, irbesartan, gabapentin, carisoprodol, budesonide/formoterol fumarate and topiramate. The patient received booster dose of covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211D21A expiry: UNKNOWN) dose was not reported, administered on 16-NOV-2021 for prophylactic vaccination (Dose Number In Series 2). No concomitant medications were reported. On 17-NOV-2021, the patient experienced headache. Treatment medications (dates unspecified) included: hydrocodone, and paracetamol. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from headache on 18-NOV-2021. This report was non-serious. This case, from the same reporter is linked to 20211142554.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Abstains from alcohol; Blood pressure; Non-smoker (quit smoking in the 1980s).
- Vorgeschichte
- Medical History/Concurrent Conditions: Fibromyalgia.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 06.12.2021
- Impfdatum
- 30.11.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Headache
Insomnia
Muscle spasms
Symptomtext
Lower back spasms, leg spasms, back pain. Unable to sleep, headache. Going on 5 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Short gut syndrome, low IgA, low IgG.
- Vorgeschichte
- Short gut syndrome, seizure disorder
- Andere Medikamente
- Keppra, Multivitamins
- Allergien
- NSAIDS, Watermelon
- Vorherige Impfungen
- Flu shot
- Staat
- LA
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 06.12.2021
- Impfdatum
- 01.12.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain upper
Chills
Dizziness
Fatigue
Headache
Injection site erythema
Injection site pain
Injection site swelling
Nausea
Pyrexia
Symptomtext
Janssen COVID-19 Vaccine EUA 100.5 fever for 6+ hours followed by fever of 99 for next 18 or so hours. Chills for 2-4 hours. Stomach cramping and nausea for 3 days. Very tired and had dissyness for first couple of day. Severe headache for 2 days followed by mild headache for 3 days. Arm soreness at injection site. Swelling and redness at injection site on day 2, swelling has expanded each day following. Treated fever with dayquil, or nitequil every 6 hours or so for 2 days. Took extra strength tylenol on days following when I was not taking the dayquil. Took pepto bismol and imodium for stomach issues. Only took one dose of either per day, not together.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Sertraline (100mg), Multivitamin Women
- Allergien
- Milk
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 06.12.2021
- 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: nein
Back pain
Sciatica
Symptomtext
Severe back pain, sciatica pain
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- this is the weekend I will find a neurologist or pain doctor this week
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Polycystic Ovarian Syndrome
- Andere Medikamente
- mugwort, metformin, Lexapro
- Allergien
- white chocolate, Lortab, Prilosec
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 04.12.2021
- Impfdatum
- 18.11.2021
- Beginn
- 04.12.2021
- Tage bis Beginn
- 16,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Erythema
Peripheral swelling
Rash macular
Symptomtext
My legs are very swollen, I got back pain and red spots on my skin
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- I have not gone to the doctor yet. I don't know what to do
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 03.12.2021
- Impfdatum
- 28.11.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- 3,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal pain upper
Chills
Culture urine
Differential white blood cell count
Fatigue
Full blood count
Hot flush
Lipase
Metabolic function test
Pain
Pregnancy test urine
Urine analysis
Vomiting
Symptomtext
Received booster on 11/28/2021: Felt fatigue, chills, hot flashes, body ache on day two and three after the vaccine was administered. On Wednesday 12/1/2021 around 0800 I started to vomit continuously for two straight hours, had excruciating stomach pain on the lift side. Family transported my to urgent care where the ED doctor did the following tests: CBC with Differential Comprehensive metabolic panel Lipase Pregnancy screen, urine Urinalysis, Microscopic Urinalysis, culture if indicated Treatment: IV of sodium chloride, ondansetron (PF) (ZOFRAN), ketorolac (TORADOL)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- : CBC with Differential Comprehensive metabolic panel Lipase Pregnancy screen, urine Urinalysis, Microscopic Urinalysis, culture if indicated
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- migraines
- Andere Medikamente
- Nurtec, Topiramate, Primella
- Allergien
- chlorohexidine
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 03.12.2021
- Impfdatum
- 30.11.2021
- Beginn
- 30.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site rash
Symptomtext
Rash Developed around injection site (right arm) and then spread to left arm. Resolved when patient took additional diphenhydramine but did reappear after 1st dose of diphenhydramine wore off (~4hours after vaccination).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site rash
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Diabetes
- Andere Medikamente
- Diphenhydramine 25mg taken prior to vaccine.
- Allergien
- Penicillin, Guaifenesin
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 02.12.2021
- Impfdatum
- 24.11.2021
- Beginn
- 24.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dysgeusia
Fatigue
Headache
Joint stiffness
Myalgia
Pyrexia
Symptomtext
Fevers after 10 hours of getting shot and lasting up to 27 hours after getting shot with them getting up to 102.3 and 102.8. Joint stiffness and severe muscle aches. Headache for 2 days. Metal taste when eating for 1 full day after getting shot. Severe fatigue for 3 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 28.11.2021
- 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
Body temperature increased
Chills
Eye pain
Feeling cold
Headache
Nausea
Symptomtext
Baseline temperature before injection was 97.5 degreees. Temperature spiked up to 102 degrees by 9:45pm and intense chills. Extremeties extremely cold. Intense headache began at same time and became almost intolerable by midnight with the feeling of stabbing behind the eyes. Nausea began the next morning and fever/chills continued throughout following day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- VIT C, D, B-12, probiotics, Quercitin, Rhodiola
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 24.11.2021
- Impfdatum
- 09.11.2021
- Beginn
- 10.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site bruising
Injection site pain
Symptomtext
patient came to the pharmacy on 11/24/21 to report bruising and mild pain at the site of injection. The first Janssen injection was given on 11/9/21.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- ?
- Vorgeschichte
- ?
- Andere Medikamente
- rx for ivermectin 3mg #6 tabs11/3/21
- Allergien
- sulfa, tetanus, latex
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 24.11.2021
- Impfdatum
- 12.11.2021
- Beginn
- 19.11.2021
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Lip swelling
Periorbital swelling
Peripheral swelling
Swelling face
Throat tightness
Symptomtext
Throat closing, face swollen, lips enlarged, puffy eyes, dizzy, arms and hands swollen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 24.11.2021
- Impfdatum
- 24.11.2021
- Beginn
- 24.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Fall
Nausea
Symptomtext
PATIENT RECEIVED HIS FLU SHOT AND JANSSEN SHOT BOTH IN RIGHT ARM AND A FEW MINUTES LATER HE FELT DIZZY AND FELL TO THE GROUND BUT WAS STIL CONSCIOUS. WE RAISED HIS LEGS ON THE CHAIR TO HELP HIS BLOOD PRESSURE STABILIZE AND HE FELT BETTER.HE ALSO SAIDHE FELT NASUOUS, WE GAVE HIM WATER AND HE FELT BETTER. HE SAT DOWN FOR 15 MINUTES AND FELT BETTER AFTER.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- n/a
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 31,0
- Geschlecht
- M
- 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: unbekannt
Erholt: nein
Adverse reaction
Amnesia
Dizziness
Eye movement disorder
Feeling hot
Mental status changes
Symptomtext
After administering the vaccine to the customer, he was advised to wait 15-20 minutes in the waiting area, which he did. I returned to the pharmacy and after a few minutes, another customer in the waiting area said the source individual was having a bad reaction. I immediately rushed over and say the patient reclined more than normal in his chair. There was a rack holding canes behind his chair which he had knocked over, presumably with his head. I approached the patient and his eyes were rolling all over (back and forth, left and right) for approximately ten seconds, during which time he was totally unaware of his surroundings. After approximately ten seconds, he mentally returned "to normal", for the first time noticed that I was standing there and asked "what happened?" I explained to him he was having an adverse reaction to the COVID shot. He said he felt lightheaded and extremely warm, so I advised him that we should take his sweatshirt off, which he did. We also gave him an ice pack to place on his forehead and a bottle of cold water to drink. He was completely coherent by this point and said he had no other symptoms. 911 was called upon my immediate entrance to the scene by the front end manager. I stayed with the patient until first responders came. Soon after, EMS arrived to evaluate the patient. I returned to the pharmacy at this point. After a few minutes, I returned to the waiting area and the patient along with EMS were gone. It is unknown if the patient received any medical treatment or if he was taken by EMS to the hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- Unknown.
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- None
- Andere Medikamente
- Unknown
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 24.11.2021
- Impfdatum
- 22.11.2021
- Beginn
- 22.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Symptomtext
Due to h/o anaphylaxis was observed for 30 minutes post COVID vaccine. Received both COVID and flu vaccines. 10 minutes into observation reported generalized itching (arms, legs, back). Skin assessed. NO visible rash/hives/edema noted. Throat inspected. No edema noted. No complaints from pt. Benadryl 25mg self-administered after 20 minutes. VS obtained and stable. released at 30 minutes post.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- migraine headaches, complex regional pain syndrome, OSA, DVT, morbid obesity, hyperlipidemia, Factor V Leiden, Roux En Y status post, TBI, Insomnia, Generalized anxiety D.O., Depression,
- Andere Medikamente
- -
- Allergien
- animal dander (RUNNY NOSE), quinoa-kale-hemp, tree and shrub pollen, grass pollen, clindamycin, erythromycin (RASH/HIVES), povidone-iodine (BURN), fish, seafood, colored dyes, iodine contrast media, penicillins (ANAPHYLAXIS)
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 24.11.2021
- 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
Feeling abnormal
Pallor
Vomiting
Symptomtext
Patient reported feeling "fuzzy". Pallor in appearance. She vomitted once. This lasted 30 minutes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vomiting
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None reported
- Vorgeschichte
- None reported
- Andere Medikamente
- Reports no medications.
- Allergien
- Reports no allergies
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 23.11.2021
- Impfdatum
- 18.11.2021
- Beginn
- 18.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cold sweat
Dizziness
Hyperhidrosis
Pallor
Skin warm
Vision blurred
Symptomtext
Patient received his vaccine and sat down for his 15 minute observation period. After approx 5 min of sitting, staff noticed patient was sweating profusely. patient skin pale and clammy, very sweaty. Patient stated he felt dizzy and his vision was blurry and he felt like he was going to pass out. staff used an ammonia inhalant under patient's nose. Cool papertowels applied to head. Patient's mask and jacket were removed. Patient given cold beverage. Patient declined to lie on the floor. BP 110/82, pulse 76 and regular. Breathing normal, non labored. staff sat next to patient for 15 minutes until patient stated he no longer felt he had to pass out. Patient sat for an additional 15 minutes. After 40 minutes of sitting, patient's color of face was no longer pale, skin warm to touch, no longer clammy and sweaty. staff stood next to patient as he stood from sitting position. patient stated he felt fine, no dizziness. Patient stated he was fine to drive himself home and he was going to go home and rest.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 23.11.2021
- 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
Flushing
Nausea
Refusal of treatment by patient
Symptomtext
The patient felt nauseated and wanted to throw up fifteen minutes after the vaccination. The patient did not eat breakfast or lunch and she could not throw up anything, but felt like she needed to throw up and got flushed in the face. We offered her ice cold bottled water, a cool paper towel for her forehead, and a trash can to use just in case she needed to vomit. We offered to call 911 and she and her husband refused us to call 911. We offered an epi-pen injection and she refused to be injected. She waited another fifteen minutes and got up from her chair and said that she felt much better and not nauseated anymore. She wanted to go home. Her husband drove her home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Asthma
- Andere Medikamente
- Celexa, Abilify, Adderall
- Allergien
- Macrobid
- Vorherige Impfungen
- MMR, as a child she was sick for 4 days and as an adult she got a meassle like rash from the vaccine.
- Staat
- NH
- Alter
- 41,0
- Geschlecht
- F
- 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: nein
Cold sweat
Dizziness
Feeling hot
Malaise
Pallor
Unresponsive to stimuli
Symptomtext
Patient received the Janssen vaccine in the left arm in the immunization room. She then got up and walked over to chair to stay for observation. Within 5 minutes she walked to pharmacy counter and stated she did not feel well. Immediately myself and one technician ran over to help. She stated she felt hot and like passing out. We elevated her feet initially, she did become unresponsive for 1-2 minutes. Other technician called 911 at this time. We then put her flat on the floor and monitored her blood pressure, heart rate and O2. She did begin to talk. A nurse was in the store and offered her assistance. Patient never stopped breathing but was hot, clammy and slight gray in color. Ambulance arrived within 10 minutes from call.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown. Patient did not indicate anything on the Vaccine Informed Consent form.
- Andere Medikamente
- Unknown
- Allergien
- Patient checked off NO to any allergies or allergic reactions on the Vaccine Informed Consent form
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 88,0
- Geschlecht
- F
- Eingang
- 23.11.2021
- Impfdatum
- -
- Beginn
- 16.11.2021
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Injection site erythema
Injection site swelling
Symptomtext
SWELLING AT INJECTION SITE; REDNESS AT INJECTION SITE; HEADACHE; This spontaneous report received from a patient concerned an 88 year old female. The patient's height, and weight were not reported. The patient's past medical history included: right hip replacement, and concurrent conditions included: hypertension, osteoarthritis, calcium channel blockers allergy, cholesterol medication allergy, dust allergy, mold allergy, pacemaker, and watchman. The patient experienced drug allergy when treated with hydromorphone hydrochloride, and morphine. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211D21A, and expiry: 11-APR-2022) dose was not reported, administered on 15-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 16-NOV-2021, the patient experienced swelling at injection site. On 16-NOV-2021, the patient experienced redness at injection site. On 16-NOV-2021, the patient experienced headache. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from headache on 16-NOV-2021, and had not recovered from redness at injection site, and swelling at injection site. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Allergy to molds; Artificial cardiac pacemaker user; Drug allergy; Dust allergy; Hypertension; Osteoarthritis
- Vorgeschichte
- Medical History/Concurrent Conditions: Hip replacement; Medical device implantation
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 22.11.2021
- Impfdatum
- 22.11.2021
- Beginn
- 22.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Immediate post-injection reaction
Injection site swelling
Symptomtext
Patient experienced immediate swelling at the injection site. It was treated with a cold compress for 15 minutes and 50 mg of diphenhydramine. The swelling was resolved when I followed up 5 hours later. The vaccine was administered with a safety needle and monoject syringe.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site swelling
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- hypertension
- Andere Medikamente
- telmisartan
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 22.11.2021
- Impfdatum
- 15.11.2021
- Beginn
- 16.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Arthralgia
Cardiac function test
Chest X-ray
Computerised tomogram head
Dizziness
Electrocardiogram
Metabolic function test
Myalgia
Pyrexia
Retching
Urine analysis
Vertigo
Symptomtext
11/16/21-11/17/21 Fever up to 102; myalgia, arthralgia, dizziness 11/18/21-11/19/21 Asymptomatic 11/20/21 Experienced acute severe vertigo with retching; husband called EMS due to my inability to stand or walk without staggering. Went to ER where had CT of head, 12-lead EKG, labs and chest xray. Had IV Zofran and PO meclizine with slight improvement. D/C'd home with presumed diagnosis of vertigo. Vertigo continued despite Meclizine until 6pm 11/22/21
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- Cardiac and metabolic labs including urine, chest xray, CT of head, 12-lead EKG
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- DM Type 2 (controlled. A1c 6.1% on 10/25/21) HTN (controlled) HLD (controlled) Hypothyroidism (controlled) S/P roux n Y bariatric surgery (12/2019)
- Andere Medikamente
- Bariatric Advantage Solo without iron vitamin daily Vitamin D 1000 IU daily Humalog insulin via insulin pump 1.25units/hour HCTZ 25mg daily ASA 81mg daily Atenolol 25mg daily Synthroid 0.150mcg daily Lovastatin 40mg daily Biotin 5000mcg dai
- Allergien
- Invokana (had blood clots in urine)
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 22.11.2021
- Impfdatum
- 16.11.2021
- Beginn
- 18.11.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash erythematous
Rash papular
Tenderness
Symptomtext
Pt started to experience erythematous papular eruption that is tender to touch around the lips and chin and diffuse papular eruption with surrounding erythema tender rash on the right lower forearm Treatment: Continue loratidine, pt does not like to take benadry Prednisone taper prescribed
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash erythematous
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- ADHA Seasonal Allergies Herpes Labialis
- Andere Medikamente
- Citalopram 20mg PO daily Dextroamphetamine-amphetamine 30mg PO daily Atrovent 42 mcg nasal spray daily Loratidine 10mg PO daily
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 21.11.2021
- Impfdatum
- 20.11.2021
- Beginn
- 20.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Chills
Feeling abnormal
Heart rate increased
Hyperhidrosis
Throat irritation
Symptomtext
About 10 minutes after administration, patient said he had a scratchy throat. It was not that way prior to administration. No difficulty breathing. I gave him water and asked him to sit for an additional 15 minutes. I explained that typical allergic reactions occur within 15-30 minutes. Patient then said his heart started raising and he did not feel good. He also started sweating and got chills. At that time he agreed to have EMS called.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Patient taken to hospital for observation and antihistamine.
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Seasonal allergies
- Andere Medikamente
- Unknown
- Allergien
- Unknown- listed as yes on immunization statement
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 21.11.2021
- Impfdatum
- 21.11.2021
- Beginn
- 21.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Hyperhidrosis
Immediate post-injection reaction
Symptomtext
As soon as a 49-year-old female patient is immunized by the nurse, she verbalizes that she feels dizzy and patient observes her sweaty. Immediately afterwards, patient proceeds to call the EMT to evaluate it. At 1:42 pm, the patient was evaluated and her vital signs were: 60/40 B / P, 54 Pulse, 103 DXT and 100% Saturation. At 1:49 pm, the case was consulted with Doctor and she recommended leaving the patient under observation for 30 minutes and in the Trendelenburg position and then re-evaluate the vital signs. At 2:15 am, the patient was evaluated again and the vital signs were: 110/80 B / P, 60 Pulse, 103 DXT and 100% Saturation and then she reported feeling good for what she was discharged.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NO
- Vorgeschichte
- NO
- Andere Medikamente
- NO
- Allergien
- NO
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 20.11.2021
- 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: nein
Dizziness
Dysstasia
Fall
Hyperhidrosis
Impaired work ability
Symptomtext
Patient was told to wait in the waiting area for 15 minutes before leaving. He tried to stand 5 minutes after vaccination & he fell to his knees upon standing. I asked the patient what symptoms was he feeling & he said he felt dizzy. He also started to sweat. Patient was told to remain seated. I asked the patient if the wanted me to call 9-1-1 or an ambulance & he said no. I asked if he wanted he to call someone & he said his friend was in the work truck. I asked if he wanted me to have someone to get him, he said no. A few minutes later he called his friend to come in the pharmacy & I asked his friend to sit with him. Patient drank some water while remaining seated & used paper towels to wipe his forehead. After 20 minutes from the adverse event the patient said he was ok to walk & got up by himself. His friend & I walked him out the store & his friend walked him to the truck. His friend said he will be driving the patient home & the patient said he would not be going back to work that day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- HE DOESN'T KNOW OF HAVING ANY LONG-TERM HEALTH PROBLEMS
- Andere Medikamente
- N/A
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 19.11.2021
- Impfdatum
- 19.11.2021
- Beginn
- 19.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoaesthesia
Swollen tongue
Urticaria
Symptomtext
TONGUE SWELLING, JAW NUMBING, HIVES IN MOUTH. TOOK BENEDRYL
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- ASTHMA, SEASONAL ALLERGIES
- Andere Medikamente
- SMARTY PANTS MULTIVITAMINS, 81 MG ASPRIN, BREZTRI, ALLERGRA, FLONASE, VITAMIN D3
- Allergien
- SHELFISH, PEANUTS, FLU VACCINE, TDAP VACCINE, PESTICIDES
- Vorherige Impfungen
- FLU, SEVERE, SHORTNESS OF BREATH, TONGUE SWELLING,INTERNAL HIVES. TDAP SAME REACTION, AGE 37
- Staat
- MN
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 19.11.2021
- Impfdatum
- 03.11.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Headache
Livedo reticularis
Pain
Pruritus
Symptomtext
- itchiness on neck and torso starting at 7:30 pm following injection 3 hours earlier lasting 12 hours - mottled skin on forearms and inner thighs lasting 7 days - headache beginning 12 hours after injection and lasting 48 hours - overall body aches beginning 24 hours after injection and lasting 48 hours
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- none
- Allergien
- PCN; zithromax
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 19.11.2021
- Impfdatum
- -
- Beginn
- 12.11.2021
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain upper
Chills
Diarrhoea
Fatigue
Feeling abnormal
Hyperhidrosis
Pyrexia
Symptomtext
INTERMITTENT STOMACH PAIN/STOMACH PAIN ON AND OFF; DIARRHEA; SWEATING; GONE TO THE WORLD; CHILLS; FATIGUE; FEVER; This spontaneous report received from a consumer concerned a 36 year old male. The patient's height, and weight were not reported. The patient's concurrent conditions included: stomach ulcer, and bee stings allergy. The patient experienced drug allergy when treated with cefaclor for bee stings allergy. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211D21A, and expiry: UNKNOWN) dose was not reported, administered on 12-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 12-NOV-2021, the patient experienced sweating. On 12-NOV-2021, the patient experienced gone to the world. On 12-NOV-2021, the patient experienced chills. On 12-NOV-2021, the patient experienced fatigue. On 12-NOV-2021, the patient experienced fever. On 15-NOV-2021, the patient experienced diarrhea. On 16-NOV-2021, the patient experienced intermittent stomach pain/stomach pain on and off. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from sweating, gone to the world, chills, fatigue, and fever on 14-NOV-2021, was recovering from diarrhea, and had not recovered from intermittent stomach pain/stomach pain on and off. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Allergic reaction to bee sting; Stomach ulcer (hereditary, not sure what kind of ulcer)
- Vorgeschichte
- Comments: Unknown
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 17.11.2021
- 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
Diarrhoea
Flatulence
Symptomtext
Mild Diarrhea and severe gas
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 16.11.2021
- Impfdatum
- 02.11.2021
- Beginn
- 02.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain
Arthralgia
Chills
Diarrhoea
Dizziness
Headache
Pyrexia
Thirst
Symptomtext
wicked headache, extreme dizziness, abdominal pain, diarrhea, chills, fever, extreme thirst. left wrist pain. Treatment: boneset herbal tea, lots of fluid Time: started around 9PM, day of injection and all day next day
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- allergy rhinitis
- Andere Medikamente
- multi vitamins
- Allergien
- Amoxicillin, Sulfa, Percocet, Allegra, apples, lactose intolerant
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 16.11.2021
- 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: nein
Arthralgia
Chills
Headache
Insomnia
Nausea
Swelling
Swelling face
Tinnitus
Symptomtext
I received my vaccine at 1400 and developed my first symptom of severe joint pain in all my joints at 1600. The symptoms progressed to loud ringing in both ears, sharp headache, swelling feeling in neck and lower face, uncontrollable chills and inability to sleep with nausea.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None at this time. Very hesitant to go to over crowded emergency department. Will if symptoms persist
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 15.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 11.11.2021
- Tage bis Beginn
- 6,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain upper
Irritable bowel syndrome
Nausea
Symptomtext
Stomach pain, cramps, nausea, IBS - occurred beginning at approximately 2:00 AM Thursday, Nov. 11th. Communicated by email to PCP, who advised to monitor symptoms and offered rx if needed. Requested RX via email to PCP Friday, Nov. 12th. PCP prescribed Hyoscyamine Sulfate 0.125 mg tablet. Taking as prescribed, symptoms have subsided almost completely.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- N/AP
- Aktuelle Erkrankungen
- Allergies, Gastroesophageal Reflux, Headache
- Vorgeschichte
- Allergies, Gastroesophageal Reflux, Headache
- Andere Medikamente
- Pantoprazole 40 mg, Vitafusion Women's Multi, Vitamin D3; Nature's Bounty Hair, Skin & Nails Gummies, Loratadine, Flonase, Nature's Bounty Sleep 3, Extra Strength Tylenol
- Allergien
- Trazadone, Welbutrin
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 15.11.2021
- 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: ja
Erholt: nein
Dizziness
Headache
Nausea
Pyrexia
Rash
Vomiting
Symptomtext
SEVERE FEVER OVER 103 FOR 2 + DAYS, FULL BODY RASH, DIZZINESS, NAUSEA, HEADACHES, VOMITING
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- UNKNOWN AT THIS TIME
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 14.11.2021
- 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
Adnexa uteri pain
Back pain
Chills
Fatigue
Headache
Lethargy
Pain
Pyrexia
Rash pruritic
Somnolence
Symptomtext
Fever of 102 Chills Headache Body aches Lower back pain Left ovarian pain Itchy bumps on palm of hand Extreme fatigue Lethargy Sleeping all day for 3 days
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Adnexa uteri pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- No
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 14.11.2021
- Impfdatum
- 02.11.2021
- Beginn
- 06.11.2021
- Tage bis Beginn
- 4,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal discomfort
Abdominal distension
Decreased appetite
Discomfort
Muscle fatigue
Vomiting
Symptomtext
Day 1 within four hours I developed random vomiting, I was fine one moment then all of a sudden vomiting. Day 2 was muscle fatigue which continued to Day 3 and subsided on the 11/6/21 I developed severe stomach upset and symptoms of a gastric ulcer. I can't afford the cost of the tests to prove I have an ulcer, but I can't drink a glass of water or eat without belching. I have abdominal bloating and haven't felt hungry since four days after the covid shot. Discomfort has become my norm, haven't lost any weight, but don't eat much either.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Muscle fatigue
- Hospital-Tage
- -
- Labordaten
- Can't afford them. Insurance is the worst. I need to see a doctor, but don't have the money to do so.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 13.11.2021
- Impfdatum
- -
- Beginn
- 09.11.2021
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Deafness unilateral
Ear discomfort
Ear pain
Insomnia
Otorrhoea
Symptomtext
HEARING LOSS IN LEFT EAR; PAIN IN LEFT EAR; PRESSURE IN LEFT EAR; WETNESS IN THE LEFT EAR; DISRUPTING SLEEP; This spontaneous report received from a patient concerned a 47 year old female. The patient's height, and weight were not reported. The patient's past medical history included: anaphylaxis, and concurrent conditions included: allergies undefined, non smoker, and non alcoholic. The patient had 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: 211D21A expiry: UNKNOWN) dose was not reported, 1 total, administered at left arm on 09-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 09-NOV-2021 within 15 minutes of vaccination, the patient experienced pressure in her left ear like it needed to pop as if she was in an elevator and had pressure which got worse with time. On 09-NOV-2021 (last night), the patient went to the emergency room, they examined and told there was wetness in her left ear and recommended to make an appointment with an eye, ear, throat specialist. The patient reported ringing in her ear along with a muffling sound where the patient cannot hear clearly. She reported sound was muffled and ringing was disrupting her sleep. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from hearing loss in left ear, pain in left ear, pressure in left ear, and the outcome of wetness in the left ear and disrupting sleep was not reported. This report was serious (Other Medically Important Condition).; Sender's Comments: V0: 20211125661-COVID-19 VACCINE AD26.COV2.S-hearing loss in left ear. 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
- Ear pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Abstains from alcohol; Allergy NOS (Undefined but can lead to anaphylaxis); Non-smoker
- Vorgeschichte
- Medical History/Concurrent Conditions: Anaphylaxis; Comments: The patient had no drug abuse or illicit drug usage
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 12.11.2021
- Impfdatum
- 08.11.2021
- Beginn
- 08.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Feeling drunk
Sleep terror
Symptomtext
Over-tiredness;Drunk feeling; Night Terror.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- hyperthyroid w/ poss Graves Disease.
- Andere Medikamente
- Claritin, Flonase.
- Allergien
- methylprednisolone.
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 09.11.2021
- Impfdatum
- 09.11.2021
- Beginn
- 09.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Hyperhidrosis
Symptomtext
Patient became diaphoretic and faintness, assisted to floor with semi-responsive EMS activated. Lower extremities raised on chair, B/P 115/70, pulse 68.. 1052 ambulance arrived b/p 108/71 pulse 76, 02 sat 100 % Blood glucose 84. Patient refused further treatment , released from ambulance. 1108 left with spouse, no further treatment requested, encouraged follow up with primary MD if symptoms persist.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- Headaches
- Andere Medikamente
- Norco and Vicodin
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 43,0
- Geschlecht
- F
- 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
Dizziness
Feeling hot
Hypoacusis
Malaise
Nausea
Symptomtext
PATIENT WAS BEING MONITORED FOR THE 15 MINUTE TIMEFRAME POST VACCINATION. 5 MINUTES INTO MONITORING PATIENT STATES THEY WERE NOT FEELING WELL. FELT NAUSEOUS, HOT, DIZZY, AND THEIR HEARING WAS MUFFLED. WE USED AN ICE PACK PLACED ON THE BACK OF THE NECK FOR THE NEXT 20 MINUTES AND TALKED TO THE PATIENT AND PROVIDED HER A BOTTLE OF WATER. THE SIGNS AND SYMPTOMS SLOWLY RESOLVED OVER THE 20 MINUTES AND PATIENT LEFT ON THEIR OWN ACCORD.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 03.11.2021
- 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: unbekannt
Dizziness
Symptomtext
He experienced lightheadedness within the first 5 minutes up until 20 minutes after. We urged him to stay for another 15 minutes after the symptom subsided. Recommended him for any other emergencies to call 911 or seek immediate medical attention for other symptoms such as fainting, chest pain, difficulty breathing, etc.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 01.11.2021
- Impfdatum
- 29.10.2021
- Beginn
- 31.10.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Oedema peripheral
Pain
Symptomtext
Swelling in right arm pit, showed up Sun morning. Size of a tennis ball. ER doctor advised to watch and follow up with primary care. Take advil for pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- None so far.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Allopurinol, rosuvastatin, metoprolol er, omeprazole
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 02.09.2023
- Impfdatum
- 19.05.2021
- Beginn
- 01.09.2023
- Tage bis Beginn
- 835,0
- Dosis
- 2
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
SARS-CoV-2 test positive
Symptomtext
COVID-19 POSITIVE; No signs and symptoms
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- + Rapid COVID-19 nasal swab
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- hypothyroidism, hemiplegia, GERD, actinic keratosis, osteoarthritis, calculus in bladder, osteopenia, hyperlipidemia, hyperglycemia, atherosclerosis, Raynaud's, fibromyalgia, urinary incontinence, constipation, carpal tunnel syndrome
- Andere Medikamente
- Colace, Flax Oil Xtra caps, Miralax, Multivitamin, Oxybuynin, Probiotic, Senna
- Allergien
- Amoxicillin, Chamomile flower, ciprofloxacin, clindamycin, macrobid, penicillins, risendronate sodium, spironolactone, sulfa antibiotics
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 22.02.2023
- Impfdatum
- 12.08.2022
- Beginn
- 12.08.2022
- 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
Patient received an unauthorized dose of Janssen (under 18, only approved for 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
- IA
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 26.01.2023
- Impfdatum
- 15.11.2021
- Beginn
- 11.02.2022
- Tage bis Beginn
- 88,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Acoustic stimulation tests abnormal
Deafness unilateral
Magnetic resonance imaging
Tinnitus
Symptomtext
Severe tinnitus in right ear with severe hearing loss. I qualify for a cochlear implant. I was diagnoses by the ENT department, Dr. Oral steroids, Steroid injection into the inner ear.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acoustic stimulation tests abnormal
- Hospital-Tage
- -
- Labordaten
- MRI, March 10th, 2022. Several hearing tests. First one, February 14, 2022.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- none
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- ND
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 22.01.2023
- Impfdatum
- 13.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Anxiety
Blood copper increased
COVID-19
Change in sustained attention
Confusional state
Electroencephalogram
Epstein-Barr virus test positive
Eye movement disorder
Fear
Gait disturbance
Immunology test
Incoherent
Magnetic resonance imaging
Neurological examination
Paranoia
Psychotic disorder
SARS-CoV-2 test positive
Speech disorder
Symptomtext
One day following vaccination, patient became confused, fearful, anxious, and paranoid. This progressed until hospitalization within one week. After ER visit, spent one week in hospital. Rapid eye movement, inability to focus, incoherrent speech, unable to walk up flight of stairs. Was placed on heavy doses of psychotic drugs which seemed to make situation worse and had psychotic episode. No prior history for patient and no family history of psychosis or any other relevant diagnosis. Upon release to parental care and appointment with providers in home town, psychotic medicines were immediately tapered resulting in improvement to condition. After six weeks was able to return to college.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anxiety
- Hospital-Tage
- 7,0
- Labordaten
- Covid test in ER was positive so it is believed she was vaccinated while having covid. EBV positive. High copper levels of unknown origin. EEG, MRI, auto immune testing, neurology testing.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Tri-Sprintec Flovent
- Allergien
- Cats and shedding animals
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 92,0
- Geschlecht
- F
- Eingang
- 28.12.2022
- Impfdatum
- 22.12.2021
- Beginn
- 14.12.2022
- Tage bis Beginn
- 357,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against then tested positive for COVID-19 and hospitalized
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 13,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 22.12.2022
- Impfdatum
- 14.12.2021
- Beginn
- 21.10.2022
- Tage bis Beginn
- 311,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Hyponatraemia
Influenza virus test positive
Respiratory syncytial virus test positive
SARS-CoV-2 test positive
Symptomtext
Date of Admission: 10/21/2022 Date of Discharge: 10/28/2022 Admission Diagnosis: Hyponatremia COVID 19 Hospital Principal Problem (Discharge Diagnoses): COVID-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- 10/20 Covid-19, Flu, RSV by NAA, Detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 15.12.2022
- Impfdatum
- 09.04.2022
- Beginn
- 09.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Heart rate irregular
Off label use
Symptomtext
IRREGULAR HEARTBEAT; OFF LABEL DOSING FREQUENCY; This spontaneous report received from a patient concerned a 74 year old female. The patient's height, and weight were not reported. The patient's past medical history included: sudden cardiac death (in 2011), and concurrent conditions included: tachycardia (heart issues), premature ventricular contractions (Pre-ventricular compression (PVCs)), sulpha allergy (Sulfonamide allergy), drug allergy (Steroids (unspecified)), no alcohol use, and non smoker, and other pre-existing medical conditions included: The patient had no drug abuse or illicit drug usage. The patient had previously received elasomeran (Moderna covid-19 vaccine) (Dose number in series 1) (form of admin, route of admin and batch number were not reported, expiry: Unknown) dose was not reported, dose 1 administered on 27-JAN-2021 for covid-19 prophylaxis. On an unspecified date following vaccination with elasomeran (Moderna covid-19 vaccine), the patient experienced allergic reaction (Dose number in series 1). The outcome of allergic reaction was not reported. The patient had previously received covid-19 vaccine ad26.cov2.s (Dose number in series 2) (suspension for injection, route of admin not reported, batch number: 207A21A and expiry: Unknown) dose was not reported, 1 total, dose 2 (first booster) administered in left arm on 13-SEP-2021 for covid-19 prophylaxis which was an off label dosing frequency associated with Off label use and revaccination with different covid-19 vaccine (Dose number in series 2). The outcome of the off label dosing frequency and revaccination with different covid-19 vaccine was not reported. The patient had previously received covid-19 vaccine ad26.cov2.s (Dose number in series 3) (suspension for injection, route of admin not reported, batch number: 1822809 and expiry: Unknown) dose was not reported, 1 total, dose 3 (second booster) administered in left arm on 19-NOV-2021 for covid-19 prophylaxis. It was unknown whether patient had any adverse events following vaccination with second booster of covid-19 vaccine ad26.cov2.s (Dose number in series 3). The patient received covid-19 vaccine ad26.cov2.s (Dose number in series 4) (suspension for injection, route of admin not reported, batch number: 211D21A and expiry: Unknown) dose was not reported, 1 total, dose 4 (third booster) administered in left arm on 09-APR-2022 for covid-19 prophylaxis which was an off label dosing frequency (Off label use) (Dose number in series 4). Age at time of vaccination 74 years old. No concomitant medications were reported. On an unspecified date following vaccination with third booster dose of covid-19 vaccine ad26.cov2.s, the patient experienced irregular heartbeat (Dose number in series 4). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from irregular heartbeat, and the outcome of off label dosing frequency was not reported. This report was non-serious. This case, involving the same patient is linked to 20221225921.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Heart rate irregular
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Abstains from alcohol; Drug allergy (Steroids (unspecified)); Non-smoker; Premature ventricular contractions (pre-ventricular compression (PVCs)); Sulfonamide allergy (Sulfonamide allergy); Tachycardia (heart issues).
- Vorgeschichte
- Medical History/Concurrent Conditions: Sudden cardiac death; Comments: The patient had no drug abuse or illicit drug usage.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 18.11.2022
- Impfdatum
- 12.08.2022
- Beginn
- 01.09.2022
- Tage bis Beginn
- 20,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lichen planus
Symptomtext
I was diagnosed with Lichen Planus, a autoimmune related skin disorder that I never had before.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lichen planus
- Hospital-Tage
- -
- Labordaten
- Observation
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Prenatal vitamin
- Allergien
- PCN
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 25.10.2022
- Impfdatum
- 23.11.2021
- Beginn
- 30.08.2022
- Tage bis Beginn
- 280,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Computerised tomogram
Hemiplegia
Magnetic resonance imaging
X-ray
Symptomtext
RIGHT SIDE PARALYSIS, EMERGENCY, REHABILITATION CARE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood test
- Hospital-Tage
- 30,0
- Labordaten
- MRI XRAYS CAT SCAN BLOODWORK
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 22.10.2022
- Impfdatum
- 09.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Immediate post-injection reaction
Tinnitus
Symptomtext
I have had extreme ringing in the ears. This began one hour after the vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Immediate post-injection reaction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 29.09.2022
- Impfdatum
- 29.07.2021
- Beginn
- 01.10.2021
- Tage bis Beginn
- 64,0
- Dosis
- 2
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Abortion spontaneous
Blood immunoglobulin A
Coeliac disease
Heavy menstrual bleeding
Laboratory test
Maternal exposure before pregnancy
Menstruation delayed
Polymenorrhoea
Symptomtext
Menstrual cycle disruption (delayed, shortened, heavy) Miscarriage Celiac?s disease
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abortion spontaneous
- Hospital-Tage
- 1,0
- Labordaten
- 09/20/2022 Tissue Transglutaminase IgA (tTg-IgA) 3.56
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Bipolar Hypothyroidism Hipersomnia
- Andere Medikamente
- Lithium, synthroid
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 82,0
- Geschlecht
- M
- Eingang
- 27.09.2022
- Impfdatum
- 12.11.2021
- Beginn
- 26.09.2022
- Tage bis Beginn
- 318,0
- 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 dose 1 Janssen 4/9/21 041A21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- covid+ on 9/26/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 20.09.2022
- Impfdatum
- 12.09.2022
- Beginn
- 12.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Client was administered Janssen vaccine with an expiration date of 09/08/2022. Lot # 211D214 on 09/12/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- -
- Geschlecht
- U
- Eingang
- 17.09.2022
- Impfdatum
- 12.09.2022
- Beginn
- 12.09.2022
- 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
EXPIRED VACCINE ADMINISTERED; 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: 211D21A expiry: 08-SEP-2022) dose was not reported, administered on 12-SEP-2022 for covid-19 prophylaxis. The drug was associated with Drug taken beyond expiry date. No concomitant medications were reported. On 12-SEP-2022, the patient experienced expired vaccine administered. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of expired vaccine administered was not reported. This report was non-serious. This report was associated with product quality complaint: 90000251570, 90000251571.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 12.09.2022
- Impfdatum
- 13.04.2022
- Beginn
- 06.09.2022
- Tage bis Beginn
- 146,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against then tested positive for COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 08.09.2022
- Impfdatum
- 05.04.2021
- Beginn
- 29.08.2022
- Tage bis Beginn
- 511,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Device occlusion
Gastrostomy
Symptomtext
08/29/22 presents to EC ED for "Blocked J tube". PMHx of "esophageal cancer s/p chemotherapy and G-tube placement on 8/17" "HTN, recent COVID infection 8/21/2022"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 29.08.2022
- Impfdatum
- 24.08.2022
- Beginn
- 24.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
Presented for J&J COVID vaccine. Pt States she is an emancipated minor, received documentation of emancipation. Educated on preference of MRNA vaccine. Pt confirmed desire for J&J vaccine. Pt waited in lobby 15 minutes per policy. After administration realized patient did not qualify for J&J due to her age. Notified patient, supervisor and Agency.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- UNK
- Vorgeschichte
- UNK
- Andere Medikamente
- UNK
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 15.08.2022
- Impfdatum
- 15.03.2022
- Beginn
- 15.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Symptomtext
Possibly received extra dose. Uncertain if patient is immunocompromised as this was not noted on consent form. Timeline: 1st dose Janssen 03/19/2021, 2nd dose Moderna 04/20/2021 and 3rd dose Janssen 03/15/2022. If patient is immunocompromised this would be an appropriate timeline.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 09.08.2022
- Impfdatum
- 02.01.2022
- Beginn
- 08.08.2022
- Tage bis Beginn
- 218,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Respiratory tract congestion
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Respiratory tract congestion
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- HI
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 04.08.2022
- Impfdatum
- 11.12.2021
- Beginn
- 01.05.2022
- Tage bis Beginn
- 141,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Influenza like illness
SARS-CoV-2 antibody test
Symptomtext
FLU LIKE SYMPTOMS; This spontaneous report received from a patient concerned a 74 year old male. The patient's height, and weight were not reported. The patient's past medical history included: ascorbic acid over dose, myocarditis, and pericarditis, and concurrent conditions included: hay fever, sulfa allergy, non smoker, alcohol user (occasionally red wine), and drug abuse/illicit drug usage. The patient was previously treated with cortisone. The patient had experienced guillain-barre syndrome when treated with influenza vaccine for prophylactic vaccination The patient received covid-19 vaccine ad26.cov2.s (dose number in series 1) (suspension for injection, route of admin not reported, batch number: 1805025 expiry: 20-JAN-2022) dose was not reported, 1 total administered on 26-MAR-2021 to the right arm for covid-19 prophylaxis. On an unspecified date the patient experienced a bump 2-3 inches below the top shoulder joint at the injection site, a little feverish, discomfort in arm, headache, not feeling well and soreness at the injection site (dose number in series 1). The soreness at the injection site, a little feverish and headache was for a week only. The patient received booster dose of covid-19 vaccine ad26.cov2.s (dose number in series 2) (suspension for injection, route of admin not reported, batch number: 211D21A, expiry: 08-SEP-2022) dose was not reported, 1 total administered on 11-DEC-2021 to the right arm for covid-19 prophylaxis. Age at time of vaccination 74 years old. No concomitant medications were reported. On MAY-2022, the patient experienced flu like symptoms (dose number in series 2). On 27-JUL-2022, Laboratory data included: SARS-CoV-2 antibody test spike antibodies was high around 250 and mentioned SARS /cov/ 2 spike protein total AB semi-quantitative exceeding 250U/mL (less then 0.80 u/ml negative for Anti SARS antibody). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from flu like symptoms. This report was non-serious. This case, from the same reporter is linked to 20211240426 (dose number in series 1).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Influenza like illness
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220727; Test Name: SARS COV-2 ANTIBODY; Result Unstructured Data: spike antibodies high around 250, SARS /cov/ 2 spike protein total AB semi-quantitative exceeding 250U/mL (less then 0.80 u/ml negative for Anti SARS antibody)
- Aktuelle Erkrankungen
- Alcohol use (occasionally red wine); Drug abuse; Hay fever; Non-smoker; Sulfonamide allergy
- Vorgeschichte
- Medical History/Concurrent Conditions: Drug overdose; Myocarditis; Pericarditis
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 01.08.2022
- Impfdatum
- 29.07.2022
- Beginn
- 29.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Incorrect dose administered
Symptomtext
Administered patient with a third dose of J&J COVID-19 vaccine, which is not recommended. J&J dosing is 0.5mL. The wrong dose of 0.3mL was given to patient. Patient should have received a third dose of Pfizer or Moderna vaccine as recommended.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 25.07.2022
- Impfdatum
- 17.12.2021
- Beginn
- 23.07.2022
- 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
Confirmed Breakthrough Case COVID-19 (Janssen) 1 03/12/2021 Janssen 1802068 COVID-19 (Janssen) 2 12/17/2021 Janssen 211D21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Positive Lab COVID test 7/23/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 30.06.2022
- Impfdatum
- 30.06.2022
- Beginn
- 30.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Wrong product administered
Symptomtext
Today, 06/30/2022 at approximately 10:30 AM, the patient was administered 0.3 mL of the Janssen vaccine. The patient should have received 0.3 mL of the Pfizer vaccine. The doctor called the patient personally to inform her of the mistake that was made by the medical assistant who administered the vaccine. The patient was informed that she received the Janssen vaccination rather than the Pfizer vaccine and she indicated understanding. She did not have any adverse side effects to the vaccination and she is feeling well.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Tuberculosis pneumonia; Cough.
- Vorgeschichte
- Tuberculosis pneumonia, type II diabetes mellitus, DVT, asthma
- Andere Medikamente
- Pyridoxine; Isoniazid; Rifabutin; Benzonatate; Albuterol; Dulo; Duloxetine; Gabapentin; Fluticasone; Trazodone; Apixaban; Sacubitril; Metoprolol; Methimazole.
- Allergien
- House dust mite allergen extract.
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 25.06.2022
- Impfdatum
- 19.01.2022
- Beginn
- 13.06.2022
- Tage bis Beginn
- 145,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drainage
SARS-CoV-2 test
Vaccination failure
Symptomtext
CONFIRMED CLINICAL VACCINATION FAILURE; CONFIRMED COVID-19 INFECTION; DRAINAGE ISSUES; This spontaneous report received from a patient concerned a 52 year male. The patient's height, and weight were not reported. The patient's concurrent conditions included: non-smoker, and non-alcoholic, and other pre-existing medical conditions included: The patient had no known allergies. The patient had no any drug abuse or illicit drug usage. The patient received 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 04-MAY-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 covid-19 vaccine ad26.cov2.s (Dose number in series 2) (suspension for injection, route of admin not reported, batch number: 211D21A, expiry: unknown) dose was not reported, 1 total, administered on 19-JAN-2022 in right arm for prophylactic vaccination. Age at time of vaccination 52 years old. No concomitant medications were reported. On 13-JUN-2022, the patient was not feeling well and had some drainage issues and itchy throat. On 14-JUN-2022 and 15-JUN-2022, he had a fever and did not felt well. On 16-JUN-2022 he did covid test and got result as he had covid. On 18-JUN-2022, the patient had head congestion. Thus patient had confirmed clinical vaccination failure and confirmed covid-19 infection. Patient reported that, he was still sick with covid (dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from confirmed covid-19 infection, and the outcome of drainage issues and confirmed clinical vaccination failure was not reported. This report was serious (Other Medically Important Condition). This report was associated with product quality complaint number: 90000236384.; Sender's Comments: V0: 20220638632- 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: 20220616; Test Name: COVID-19 VIRUS TEST; Result Unstructured Data: He had covid
- Aktuelle Erkrankungen
- Abstains from alcohol; Non-smoker
- Vorgeschichte
- Comments: The patient had no known allergies. The patient had no any drug abuse or illicit drug usage.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 11.06.2022
- Impfdatum
- 23.11.2021
- Beginn
- 01.05.2022
- Tage bis Beginn
- 159,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood cholesterol
Blood pressure measurement
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 64 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included: sports induced asthma, high blood pressure, high bad cholesterol, penicillin allergy, and fish, shellfish, pork, egg yolk allergy, and other pre-existing medical conditions included: Patient was non-pregnant at the time of vaccination. Patient was previously experienced drug allergy when treated with clindamycin. 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: 1805025 and expiry date: unknown) dose was not reported, 1 total, dose number 1, administered on 06-APR-2021;11:00 on left arm 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 covid-19 vaccine ad26.cov2.s (dose number in series 2) (suspension for injection, route of admin not reported, batch number: 211D21A and expiry: unknown) dose was not reported, 1 total, dose number 2, administered on 23-NOV-2021;11:00 on left arm for prophylactic vaccination. Age at time of vaccination 63 years old. Concomitant medications included clonazepam, linum usitatissimum seed oil, olmesartan medoxomil, rosuvastatin calcium, supple and salvia hispanica. The patient received non company co-suspect Paxlovid (form of admin and route of admin were not reported, batch number: unknown and expiry: unknown) dose not reported, administered from 17-MAY-2022 to 21-MAY-2022 for treatment of COVID-19. On an unspecified date in MAY-2022, the patient experienced confirmed clinical vaccination failure, and confirmed covid-19 infection (dose number in series 2). The patient was doing great had absolutely no symptoms starting day 3 of Paxlovid. On 20-MAY-2022, Took a test on day 4 (Friday) of dosage and seemed negative. On 25-MAY-2022, patient started again with symptoms of itchy nose, eyes and a little cough on Wednesday (25-MAY-2022) morning (dose number in series 2). On 26-MAY-2022, the patient underwent test again and very positive. Patient do not feel bad but it felt like a full blown hay fever attack with a little dry cough. Have taken Mucinex to control nose discharge and cough. Laboratory data (dates unspecified) included: Blood pressure high, and Cholesterol High bad cholesterol. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. 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 a product quality complaint.; Sender's Comments: V0: 20220610716-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
- Blood cholesterol
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220520; Test Name: COVID TEST; Test Result: Negative ; Test Date: 20220526; Test Name: COVID TEST; Test Result: Positive ; Test Name: CHOLESTEROL; Result Unstructured Data: High bad cholesterol; Test Name: BLOOD PRESSURE; Result Unstructured Data: high
- Aktuelle Erkrankungen
- Blood pressure high; Exercise induced asthma; Food allergy; High cholesterol; Penicillin allergy
- Vorgeschichte
- Comments: Patient was non-pregnant at the time of vaccination.
- Andere Medikamente
- ZICAM [CLONAZEPAM]; CRESTOR; BENICAR; FLAX SEED OIL; SALVIA HISPANICA
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 11.06.2022
- Impfdatum
- 21.11.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
SARS-CoV-2 test
Suspected COVID-19
Vaccination failure
Symptomtext
SUSPECTED CLINICAL VACCINATION FAILURE; SUSPECTED COVID-19 INFECTION; This spontaneous report received from a patient concerned a 52 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included: metastatic breast cancer, and other pre-existing medical conditions included: Patient was non-pregnant at the time of vaccination. The patient previously experienced drug allergy when treated with rifaximine. 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: 1805029 and expiry: UNKNOWN) dose was not reported, 1 total, dose number 1, administered on 17-MAR-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 covid-19 vaccine ad26.cov2.s (dose number in series 2) (suspension for injection, route of admin not reported, batch number: 211D21A expiry: UNKNOWN) dose was not reported, 1 total, dose number 2, administered on 21-NOV-2021 for prophylactic vaccination. Age at time of vaccination 52 years old. Concomitant medications included letrozole, and palbociclib. The patient received paxlovid (form of admin, route of admin were not reported, batch number: unknown and expiry: UNKNOWN) dose was not reported, administered from 01-MAY-2022 to 05-MAY-2022 for treatment of COVID-19. On an unspecified date in 2022, the patient experienced suspected clinical vaccination failure, and suspected covid-19 infection (dose number in series 2). Patient was getting better, including fainter and fainter positive rapid test, then had a flare up and strong positive rapid test 7 days after completing Paxlovid. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient was recovering from suspected covid-19 infection, 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: 90000234202.; Sender's Comments: V0: 20220607763-covid-19 vaccine ad26.cov2.s-Suspected 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
- SARS-CoV-2 test
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220513; Test Name: RAPID TEST; Test Result: Positive ; Test Name: RAPID TEST; Test Result: Positive
- Aktuelle Erkrankungen
- Metastatic breast cancer
- Vorgeschichte
- Comments: Patient was non pregnant at the time of vaccination
- Andere Medikamente
- PALBOCICLIB; LETROZOLE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 10.06.2022
- Impfdatum
- 23.11.2021
- Beginn
- 30.05.2022
- Tage bis Beginn
- 188,0
- 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
Confirmed Breakthrough COVID-19 (Janssen) 1 03/20/2021 Hospital Janssen 1802068 COVID-19 (Janssen) 2 11/23/2021 County Health Department Janssen 211D21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Positive COVID Lab test 5/30/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 09.06.2022
- Impfdatum
- 07.06.2022
- Beginn
- 07.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
Patient received Janssen vaccine for his second booster in error at mass vaccination clinic. In all, he has received now 3 doses of JJ which is not authorized. The patient has been informed of this error and reports no adverse reaction or outcome from receiving.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none known
- Vorgeschichte
- none known
- Andere Medikamente
- unknown
- Allergien
- none known
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 02.06.2022
- Impfdatum
- -
- Beginn
- 25.03.2022
- 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
INCORRECT PRODUCT STORAGE; ADMINISTRATION OF EXPIRED AND IMPROPERLY STORED VACCINE; This spontaneous report received from a physician concerned a 45 year old female. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: The patient was not pregnant at the time of vaccination. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211D21A, expiry: 08-SEP-2022) .5 ml, administered on 25-MAR-2022 for prophylactic vaccination. Age at time of vaccination 45 years old. No concomitant medications were reported. On 25-MAR-2022, the patient experienced administration of expired and improperly stored vaccine. On an unspecified date, the patient experienced incorrect product storage. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the administration of expired and improperly stored vaccine and incorrect product storage was not reported. This report was non-serious. This case, from the same reporter is linked to 20220558497, 20220558479, 20220558475, 20220558436, 20220558469 and 20220558482.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Poor quality product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: The patient was not pregnant at the time of vaccination.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 02.06.2022
- Impfdatum
- -
- Beginn
- 25.03.2022
- 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
INCORRECT PRODUCT STORAGE; ADMINISTERED PATIENTS USING AN EXPIRED AND IMPROPERLY STORED VIAL OF THE J&J COVID-19 VACCINE; This spontaneous report received from a physician concerned a 40 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: 211D21A, expiry: 08-SEP-2022) .5 ml, administered on 25-MAR-2022 for prophylactic vaccination. Age at time of vaccination 40 years old. No concomitant medications were reported. On 25-MAR-2022, the patient experienced administered patients using an expired and improperly stored vial of the j&j covid-19 vaccine. On an unspecified date, the patient experienced incorrect product storage. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the administered patients using an expired and improperly stored vial of the j&j covid-19 vaccine and incorrect product storage was not reported. This report was non-serious. This report was associated with product quality complaint: 90000233203. This case, from the same reporter is linked to 20220558497, 20220558479, 20220558475, 20220558469, 20220558498 and 20220558436.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Poor quality product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 02.06.2022
- Impfdatum
- -
- Beginn
- 30.11.2021
- 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
INCORRECT PRODUCT STORAGE; ADMINISTERED PATIENT USING AN EXPIRED VACCINE AND IMPROPERLY STORED VIAL OF THE J AND J COVID-19 VACCINE; This spontaneous report received from a physician concerned a 54 year old female. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: The patient was not pregnant. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211D21A, expiry: 08-SEP-2022) .5 ml, administered on 30-NOV-2021 for prophylactic vaccination. Age at time of vaccination 54 years old. No concomitant medications were reported. On 30-NOV-2021, the patient experienced administered patient using an expired vaccine and improperly stored vial of the j and j covid-19 vaccine. On an unspecified date, the patient experienced incorrect product storage. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the incorrect product storage and administered patient using an expired vaccine and improperly stored vial of the j and j covid-19 vaccine was not reported. This report was non-serious. This case, from the same reporter is linked to 20220558497, 20220558479, 20220558475, 20220558498, 20220558469 and 20220558482. This report was associated with product quality complaint: 90000233203.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Poor quality product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: The patient was not pregnant.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 02.06.2022
- Impfdatum
- -
- Beginn
- 10.12.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product storage error
Poor quality product administered
Symptomtext
INCORRECT PRODUCT STORAGE; ADMINISTRATION OF EXPIRED AND IMPROPERLY STORED VACCINE; This spontaneous report received from a physician concerned a 39 year old female. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: The patient was not pregnant at the time of vaccination. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211D21A, expiry: 08-SEP-2022) .5 ml, administered on 10-DEC-2021 for prophylactic vaccination. Age at time of vaccination 39 years old. No concomitant medications were reported. On 10-DEC-2021, the patient experienced administration of expired and improperly stored vaccine. On an unspecified date, the patient experienced incorrect product storage. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the administration of expired and improperly stored vaccine and incorrect product storage was not reported. This report was non-serious. This report was associated with product quality complaint: 90000233203. This case, from the same reporter is linked to 20220558497, 20220558436, 20220558479, 20220558482, 20220558498 and 20220558469.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: The patient was not pregnant at the time of vaccination.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 02.06.2022
- Impfdatum
- -
- Beginn
- 10.12.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product storage error
Poor quality product administered
Symptomtext
INCORRECT PRODUCT STORAGE; ADMINISTRATION OF EXPIRED AND IMPROPERLY STORED VACCINE; This spontaneous report received from a physician concerned a 39 year old female. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: The patient was not pregnant at the time of vaccination. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211D21A, expiry: 08-SEP-2022) .5 ml, administered on 10-DEC-2021 for prophylactic vaccination. Age at time of vaccination 39 years old. No concomitant medications were reported. On 10-DEC-2021, the patient experienced administration of expired and improperly stored vaccine. On an unspecified date, the patient experienced incorrect product storage. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the administration of expired and improperly stored vaccine and incorrect product storage was not reported. This report was non-serious. This report was associated with product quality complaint: 90000233203. This case, from the same reporter is linked to 20220558497, 20220558436, 20220558479, 20220558482, 20220558498 and 20220558469.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: The patient was not pregnant at the time of vaccination.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 31.05.2022
- Impfdatum
- 18.11.2021
- Beginn
- 27.05.2022
- Tage bis Beginn
- 190,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Vaccine breakthrough infection
Symptomtext
Fully vaccinated with one booster. COVID infection breakthrough
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 31.05.2022
- Impfdatum
- -
- Beginn
- 25.03.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Off label use
Poor quality product administered
Product administered to patient of inappropriate age
Symptomtext
VACCINE ADMINISTERED AFTER 6 HOURS OF VIAL PUNCTURE; OFF LABEL USE; INAPPROPRIATE AGE AT VACCINE ADMINISTRATION; This spontaneous report received from a physician concerned a 13 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: 211D21A, expiry: 08-SEP-2022) .5 ml, administered on 25-MAR-2022 for prophylactic vaccination. Age at time of vaccination 13 years old. No concomitant medications were reported. On 25-MAR-2022, the patient experienced vaccine administered after 6 hours of vial puncture, off label use, and inappropriate age at vaccine administration. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the vaccine administered after 6 hours of vial puncture, off label use and inappropriate age at vaccine administration was not reported. This report was non-serious. This report was associated with a product quality complaint: 90000233206. This case, from the same reporter is linked to 20220558436, 20220558469, 20220558475, 20220558479, 20220558482, 20220558498 and 20220558436.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Off label use
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 31.05.2022
- Impfdatum
- -
- Beginn
- 30.11.2021
- 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
INCORRECT PRODUCT STORAGE; ADMINISTRATION OF INCORRECTLY STORED VACCINE; This spontaneous report received from a physician concerned a 54 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: 211D21A, expiry: 08-SEP-2022) .5 ml, administered on 30-NOV-2021 for prophylactic vaccination. Age at time of vaccination 54 years old. No concomitant medications were reported. On 30-NOV-2021, the patient experienced administration of incorrectly stored vaccine. On an unspecified date, the patient experienced incorrect product storage. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the administration of incorrectly stored vaccine and incorrect product storage was not reported. This report was non-serious. This report is associated with a product quality complaint: 90000233203. This case, from the same reporter is linked to 20220558497, 20220558479, 20220558436, 20220558475, 20220558482 and 20220558498.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Poor quality product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 31.05.2022
- Impfdatum
- -
- Beginn
- 14.02.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Poor quality product administered
Product storage error
Symptomtext
INCORRECT PRODUCT STORAGE; VACCINE ADMINISTERED AFTER 6 HOURS OF VIAL PUNCTURE; This spontaneous report received from a physician concerned a 33 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: 211D21A, expiry: 08-SEP-2022) .5 ml, administered on 14-FEB-2022 for prophylactic vaccination. Age at time of vaccination 33 years old. No concomitant medications were reported. On 14-FEB-2022, the patient experienced vaccine administered after 6 hours of vial puncture. On an unspecified date, the patient experienced incorrect product storage. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the vaccine administered after 6 hours of vial puncture and incorrect product storage was not reported. This report was non-serious. This report was associated with a product quality complaint: 90000233203. This case, from the same reporter is linked to 20220558497, 20220558436, 20220558469, 20220558482, 20220558498 and 20220558436.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 31.05.2022
- Impfdatum
- -
- Beginn
- 14.02.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Poor quality product administered
Product storage error
Symptomtext
INCORRECT PRODUCT STORAGE; VACCINE ADMINISTERED AFTER 6 HOURS OF VIAL PUNCTURE; This spontaneous report received from a physician concerned a 33 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: 211D21A, expiry: 08-SEP-2022) .5 ml, administered on 14-FEB-2022 for prophylactic vaccination. Age at time of vaccination 33 years old. No concomitant medications were reported. On 14-FEB-2022, the patient experienced vaccine administered after 6 hours of vial puncture. On an unspecified date, the patient experienced incorrect product storage. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the vaccine administered after 6 hours of vial puncture and incorrect product storage was not reported. This report was non-serious. This report was associated with a product quality complaint: 90000233203. This case, from the same reporter is linked to 20220558497, 20220558436, 20220558469, 20220558482, 20220558498 and 20220558436.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 27.05.2022
- Impfdatum
- 25.03.2022
- Beginn
- 25.03.2022
- 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
Symptomtext
ADMINISTRATION ISSUES: The vial was previously punctured on 11/30/2021. The patient does not have any side effects. The patient was informed and will re-vaccinate with the pediatric Pfizer dosage as soon as possible.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 27.05.2022
- Impfdatum
- 25.03.2022
- Beginn
- 25.03.2022
- 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 storage error
Symptomtext
ADMINISTRATION ISSUES: The vial was previously punctured on 11/30/2021. The patient does not have any side effects. The patient was informed and will re-vaccinate as soon as possible.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 27.05.2022
- Impfdatum
- 25.03.2022
- Beginn
- 25.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
ADMINISTRATION ISSUES: The vial was previously punctured on 11/30/2021. The patient does not have any side effects. The patient was informed and will re-vaccinate as soon as possible.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 99,0
- Geschlecht
- F
- Eingang
- 27.05.2022
- Impfdatum
- 12.04.2022
- Beginn
- 25.05.2022
- Tage bis Beginn
- 43,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Tested positive 5/25/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 26.05.2022
- Impfdatum
- -
- Beginn
- 18.05.2022
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
SARS-CoV-2 test
Suspected COVID-19
Vaccination failure
Symptomtext
SUSPECTED COVID-19 INFECTION; SUSPECTED CLINICAL VACCINE FAILURE; This spontaneous report received from a patient concerned a 40 year old female of unspecified race and ethnicity Initial information was processed along with the additional information received on 24-MAY-2022. The patient's weight was 155 pounds, and height was 161.5 centimeters. 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, intramuscular, batch number: 043A21A, expiry: unknown) dose was not reported, 1 total, administered on 25-APR-2021 12:00 to left arm for prophylactic vaccination. On 01-MAY-2021, the patient experienced itchy rash all over the body (but not at injection site), left eye became red, left eye became itchy, and hives all over the body (but not at injection site) (all events in dose number in Series 1). The patient recovered from itchy rash all over the body (but not at injection site), left eye became red, left eye became itchy, and hives all over the body (but not at injection site) on 02-MAY-2021. The patient additionally received booster dose of covid-19 vaccine ad26.cov2.s (dose number in series 2) (suspension for injection, route of admin not reported, batch number: 211D21A, and expiry: unknown) dose was not reported, 1 total, administered on 01-NOV-2021 for prophylactic vaccination. Age at time of vaccination 39 years old. No concomitant medications were reported. On 18-MAY-2022, Laboratory data included: COVID-19 antigen test (NR: not provided) positive and the patient experienced suspected clinical vaccine failure (dose number in series 2). On an unspecified date, the patient experienced suspected covid-19 infection (dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the suspected clinical vaccine failure and suspected covid-19 infection was not reported. This report was serious (Other Medically Important Condition). This case, involving the same patient is linked to 20210502244. This report was associated with product quality complaint: 90000232582.; Sender's Comments: V0.20220546376-covid-19 vaccine ad26.cov2.s -suspected clinical vaccine 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
- SARS-CoV-2 test
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220518; Test Name: COVID-19 antigen test; Result Unstructured Data: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 18.05.2022
- Impfdatum
- 11.01.2022
- Beginn
- 16.01.2022
- Tage bis Beginn
- 5,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Received Janssen booster then tested positive for COVID-19 four days later.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Covid-19 test
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 14.05.2022
- Impfdatum
- 07.05.2022
- Beginn
- 07.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Product administered to patient of inappropriate age
No adverse event
Wrong product administered
Symptomtext
The clinic called to verify what booster patient should receive given she just turned 12. They verified they were giving her Pfizer. Wrote on her vaccination card that it was Pfizer and called 3 hours later saying they accidentally gave her Johnson and Johnson, which is not approved for children. No adverse affects so far, but we are furious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 14.05.2022
- Impfdatum
- 07.05.2022
- Beginn
- 07.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Product administered to patient of inappropriate age
No adverse event
Wrong product administered
Symptomtext
The clinic called to verify what booster patient should receive given she just turned 12. They verified they were giving her Pfizer. Wrote on her vaccination card that it was Pfizer and called 3 hours later saying they accidentally gave her Johnson and Johnson, which is not approved for children. No adverse affects so far, but we are furious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 13.05.2022
- Impfdatum
- 12.05.2022
- Beginn
- 12.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Interchange of vaccine products
Symptomtext
Patient presented to health department to receive J&J covid vaccine. She told the clerk that this would be her first dose. The nurse verified with the patient that this was a first dose vaccine while reviewing all paperwork. J&J vaccine administered. The nurse was submitting the information into web roster and noted what she thought to be an error on the patient's social security number. The nurse went to verify the correct social and noticed that a pfizer vaccine was documented for this same patient on this same day. The nurse then questioned the patient asking if the patient received a pfizer dose at the location documented and the patient stated "no." The nurse responded " ok, that's fine. I will just notify the location and let them know that they documented in error." the patient responded "I lied. I went this morning and got it at walmart" the patient then elaborated that she would not have time to receive the second dose before leaving for her cruise, so she came here to receive the J&J. Nurse manager notified as well as the district medical director. Patient observed for 15 min- no signs and symptoms or adverse events noted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 09.05.2022
- Impfdatum
- 26.01.2022
- Beginn
- 27.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Skin odour abnormal
Symptomtext
Immediately my sweat, urine, and all bodily odor has sweet foul smell. Covid vaccine given 1/26/22 and as of today 5/9/22 I still have strange bodily odor that won't go away. Never have I smelled this way.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Skin odour abnormal
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 09.05.2022
- Impfdatum
- 09.05.2022
- Beginn
- 09.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Symptomtext
patient received a 2nd booster shot he received his 1st dose and booster was verified and received his 2nd booster today 05/09/22 at a location. Patient stayed for 15 mins observation with no obvious reaction noted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- Demerol tabs
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- M
- Eingang
- 07.05.2022
- Impfdatum
- 19.11.2021
- Beginn
- 30.04.2022
- Tage bis Beginn
- 162,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
SARS-CoV-2 test
Suspected COVID-19
Vaccination failure
Symptomtext
SUSPECTED CLINICAL VACCINATION FAILURE; SUSPECTED COVID-19 INFECTION; This spontaneous report received from a patient concerned a male of unspecified age, race and ethnic origin. Initial information processed with additional information received from reporter on 05-MAY-2022. The patient's height, and weight were not reported. The patient's concurrent conditions included: alcohol user (1 beer a week), and non smoker, and other pre-existing medical conditions included: Patient did not had any medical condition and was not on any medication other than the supplements of Aspirin, Vitamin C, Vitamin D3 and Zinc which he started after testing positive for COVID. Patient did not had any known allergies. There was no drug abuse or illicit drug usage. The patient previously treated with covid-19 vaccine ad26. cov2. s (dose number in series 1) (suspension for injection, route of admin not reported and batch number: 204A21A, expiry date: unknown) dose was not reported, 1 total, administered in left arm on 14-MAY-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 additionally received covid-19 vaccine ad26.cov2.s (dose number in series 2) (suspension for injection, route of admin not reported, batch number: 211D21A expiry: 11-APR-2022) dose was not reported, 1 total administered in left arm on 19-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 30-APR-2022, the patient experienced fever of 37.8 degree Celsius (dose number in series 2). On 01-MAY-2022, the fever was resolved and patient experienced mild symptoms of sore throat and runny nose (dose number in series 2). On the same day patient tested positive for covid via two self tests, one test was I-health brand and another was Abbott (suspected covid-19 infection and suspected clinical vaccination failure) (dose number in series 2). Patient stated that, he was not clinically diagnosed and had not taken any PCR (Polymerase Chain Reaction) tests, the patient was self medicating with Aspirin, Vitamin C, Vitamin D3, Zinc and consulted with his doctor over the phone for advice on medication to take after testing positive via the self tests and the doctor asked him to continue taking these supplements. Patient stated that his symptoms were mild because he had taken janssen COVID-19 vaccine. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient was recovering from suspected covid-19 infection, and the outcome of suspected clinical vaccination failure was not reported. This report was serious (Other Medically Important Condition). This report was associated with product quality complaint: 90000229509.; Sender's Comments: V0: 20220506411-COVID-19 VACCINE AD26.COV2.S-Suspected clinical vaccination failure. This event is considered not related. 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 than the drug. Specifically: SPECIAL SITUATIONS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Body temperature
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220430; Test Name: Body temperature; Result Unstructured Data: 37.8 C; Comments: fever of 37.8 degree Celsius; Test Date: 20220501; Test Name: COVID-19 virus test; Result Unstructured Data: Positive; Comments: i-health brand Covid-19 self test; Test Date: 20220501; Test Name: COVID-19 virus test; Result Unstructured Data: Positive; Comments: Abbott Covid-19 self test
- Aktuelle Erkrankungen
- Alcohol use (1 beer a week); Non-smoker
- Vorgeschichte
- Comments: Patient did not had any medical condition and was not on any medication other than the supplements of Aspirin, Vitamin C, Vitamin D3 and Zinc which he started after testing positive for COVID. Patient did not had any known allergies. There was no drug abuse or illicit drug usage.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 27.04.2022
- Impfdatum
- 25.04.2022
- Beginn
- 25.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Underdose
Wrong product administered
Symptomtext
HEALTH CARE PROFESSIONAL ACCIDENTALLY GAVE 0.3 ML INSTEAD OF 0.5 ML; HEALTH CARE PROFESSIONAL ACCIDENTALLY GAVE 0.3 ML DOSE TAKEN FROM A JANSSEN VIAL INSTEAD OF A PFIZER VIAL.; This spontaneous report received from a pharmacist concerned a 49 year old female. 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 was previously treated with tozinameran for prophylactic vaccination. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211D21A expiry: 08-SEP-2022) dose was not reported, administered on 25-APR-2022 for prophylactic vaccination. Age at time of vaccination 49 years old. No concomitant medications were reported. On 25-APR-2022, the patient experienced health care professional accidentally gave 0.3 ml instead of 0.5 ml, and health care professional accidentally gave 0.3 ml dose taken from a janssen vial instead of a pfizer vial. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the health care professional accidentally gave 0.3 ml instead of 0.5 ml and health care professional accidentally gave 0.3 ml dose taken from a janssen vial instead of a pfizer vial. was not reported. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: The patient had no known allergies.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 25.04.2022
- Impfdatum
- 25.04.2022
- Beginn
- 25.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
Symptomtext
Patient was incorrectly given an incomplete dose (0.3ml) of Janssen shot instead of her 2nd Pfizer shot. Pt not reporting adverse effects at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- none per pt
- Andere Medikamente
- -
- Allergien
- None per pt
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 99,0
- Geschlecht
- F
- Eingang
- 21.04.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
No adverse event
Symptomtext
Client received a second booster dose of Janssen. There were no adverse reactions, no treatment required. Outcome of client is stable with no adverse reaction.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Unknown
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 08.04.2022
- Impfdatum
- 31.03.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 8,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Symptomtext
Patient education was given prior to vaccine administration. Patient refused mRNA vaccine and only wanted Janssen for a booster. After reviewing teaching given by Nursing Manager, nurse went ahead and administered the Janssen vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- Unknown
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 07.04.2022
- Impfdatum
- 22.03.2021
- Beginn
- 22.03.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Interchange of vaccine products
Product dose omission issue
Pharyngeal swelling
Symptomtext
11/22/21 PATIENT CAME IN FOR A BOOSTER DOSE AFTER ONLY RECEIVING ONE PFIZER DOSE ON 3/22/21, SHE HAD A BAD REACTION ANAPHLAYXIS, HIVES, AND ITCHING, SO HER DOCTOR ADVISED AGAINST THE SECOND DOSE, BUT TO WAIT FOR AN ALTERNATIVE. SHE CAME IN FOR A JOHNSON&JOHNSON. AFTER SPEAKING WITH INDIVIDUAL AND GETTING APPROVAL SHE IS ABLE TO GET THE J&J VACCINE, CHARTED AS A SECOND DOSE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pharyngeal swelling
- Hospital-Tage
- -
- Labordaten
- UNKNOWN
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- Bactrim Demerol hydrocodone lisinopril
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 06.04.2022
- Impfdatum
- -
- Beginn
- 01.12.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Ultrasound scan
Vein rupture
Symptomtext
VEIN BURST IN LEG; This spontaneous report received from a patient concerned a 71 year old white female. The patient's height, and weight were not reported. The patient's past medical history included: 2 bowel surgeries/resection and 3 heart stents and concurrent conditions included: heart problem, bladder problem and allergies. The patient received covid-19 vaccine ad26.cov2.s (Dose number in series 1) (suspension for injection, route of administration, batch number and expiry not reported) dose was not reported, 1 total administered on 07-MAR-2021 on right arm 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 additionally received booster of covid-19 vaccine ad26.cov2.s (Dose number in series 2) (suspension for injection, route of administration not reported, batch number: 211D21A and expiry: 10-JUL-2022) dose was not reported, 1 total administered at right arm on 29-OCT-2021 for prophylactic vaccination. Concomitant medications included acetylsalicylic acid for drug used for unknown indication, amlodipine for drug used for unknown indication, metoprolol tartrate for drug used for unknown indication, potassium for drug used for unknown indication, rosuvastatin for drug used for unknown indication, and glyceryl trinitrate for heart problem. The patient also takes bladder medication. On an unspecified date in DEC-2021, about one and half months after the booster dose, the patient started having a vein issue (a vein burst in her right leg, on the outer side of her leg, behind the kneecap), in late November or early December (Dose number in series 2). The patient went to the emergency room on a weekend. She underwent an ultrasound to make sure it was not a blood clot passing and the results were fine. She was told to relax, take it easy, and to prop up her feet. When she sat for too long the vein did hurt and she had to get up and move. Once the vein burst, the pain went away. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of vein burst in leg was not reported. This report was serious (Other Medically Important Condition).; Sender's Comments: V0- 20220404440-Covid-19 vaccine ad26.CoV-2.s-Vein burst in leg. 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
- Ultrasound scan
- Hospital-Tage
- -
- Labordaten
- Test Name: Diagnostic ultrasound; Result Unstructured Data: Fine
- Aktuelle Erkrankungen
- Allergy multiple; Bladder disorder; Heart disorder
- Vorgeschichte
- Medical History/Concurrent Conditions: Bowel resection; Coronary stent placement
- Andere Medikamente
- NITROGLYCERIN; AMLODIPINE; METOPROLOL TARTRATE; ROSUVASTATIN; POTASSIUM; ASPIRIN [ACETYLSALICYLIC ACID]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 05.04.2022
- Impfdatum
- 02.04.2022
- Beginn
- 02.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
BOOSTER GIVEN EARLY
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- UNKNOWN
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 05.04.2022
- Impfdatum
- 15.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Incorrect dose administered
Symptomtext
PATIENT WAS GIVEN 3 J&J'S & ALSO RECEIVED A SECOND BOOSTER BEFORE SECOND BOOSTERS WERE AVAILABLE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- UNKNOWN
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- HYDROCHLOROTHIAZIDE, PCN
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 05.04.2022
- Impfdatum
- 15.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Incorrect dose administered
Symptomtext
PATIENT WAS GIVEN 3 J&J'S & ALSO RECEIVED A SECOND BOOSTER BEFORE SECOND BOOSTERS WERE AVAILABLE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- UNKNOWN
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- HYDROCHLOROTHIAZIDE, PCN
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 01.04.2022
- Impfdatum
- 01.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product administered to patient of inappropriate age
Symptomtext
shot was given to patient and she's under 18. No adverse reaction
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 30.03.2022
- Impfdatum
- 18.03.2022
- Beginn
- 18.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Interchange of vaccine products
Symptomtext
Janssen vaccine was administered as 2nd dose instead of Pfizer vaccine. Client had received 1st Pfizer vaccine 2/18/22 and was given Janssen 3/18/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 28.03.2022
- Impfdatum
- -
- Beginn
- 24.03.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Off label use
Product administered to patient of inappropriate age
Symptomtext
OFF-LABEL USE; VACCINE ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE; This spontaneous report received from a health care professional concerned a 17 year old female. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: The patient had no known allergies. Patient was not pregnant at the time of reporting. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 211D21A, and expiry: 11-APR-2022) dose was not reported, administered on 24-MAR-2022 11:35 for prophylactic vaccination. No concomitant medications were reported. On 24-MAR-2022, the patient experienced off-label use, and vaccine administered to patient of inappropriate age. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the off-label use and vaccine administered to patient of inappropriate age was not reported. This report was non-serious. This case, from the same reporter is linked to 20211052091 and 20211051934.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Off label use
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: The patient had no known allergies. Patient was not pregnant at the time of reporting.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 24.03.2022
- Impfdatum
- 24.03.2022
- Beginn
- 24.03.2022
- 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 verbally reported age of 18 years old, staff did not catch that patient was only 17 years old. When filling out the vaccine paperwork the patient put 17 on the front of the sheet but marked that she was between 18 and 49 years old on the back of the sheet. She was administered a Johnson and Johnson vaccine dose without our staff realizing she had not yet turned 18 years old this year.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- NONE KNOWN
- Vorgeschichte
- NONE REPORTED
- Andere Medikamente
- NONE KNOWN
- Allergien
- NONE KNOWN
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 24.03.2022
- Impfdatum
- -
- Beginn
- 18.03.2022
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Off label use
Symptomtext
OFF LABEL USE; INAPPROPRIATE SCHEDULE OF VACCINE ADMINISTERED; This spontaneous report received from a health care professional concerned a 71 year old. 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) (first dose) (suspension for injection, route of admin and batch number were not reported) dose was not reported, 1 total, administered on 15-MAR-2021 for prophylactic vaccination. Patient did not experience any adverse events following vaccination (dose number in series 1). The patient received second dose of covid-19 vaccine ad26. cov2.s (dose number in series 2) (booster dose) (suspension for injection, route of admin and batch number were not reported) dose was not reported, 1 total, administered on 16-NOV-2021 for prophylactic vaccination. The batch number was not reported and has been requested. The patient received third dose of covid-19 vaccine ad26.cov2.s (dose number in series 2) (suspension for injection, route of admin not reported, batch number: 211D21A and expiry: 11-APR-2022) dose was not reported, 1 total, administered on 18-MAR-2022 at left deltoid for prophylactic vaccination which was off label use (without adverse event), and inappropriate schedule of vaccine administered (dose number in series 2). The nurse explained that patient came in to get Janssen Covid 19 booster shot. Her vaccination card had the initial shot (given 15-MAR-2021) on one side of card and the first booster (second dose) of Janssen Covid 19 vaccine (given 16-NOV-2021) on other side of card. This led to confusion about the booster shot and a third dose was given. The nurse stated, they asked patient if she was here for her second and she said yes. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the off label use and inappropriate schedule of vaccine administered was not reported. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 18.03.2022
- Impfdatum
- 18.03.2022
- Beginn
- 18.03.2022
- 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
No adverse event
Symptomtext
PATIENT CAME FOR JANSSEN BOOSTER AND AFTER THE NURSE ADMINISTERED THE VACCINE AND TOLD THE PATIENT THAT MAKES HER 2ND DOSE THE PATIENT SAID NO THIS IS MY 3RD DOSE. SUPERVISOR NOTIFIED AND REVIEW OF VACCINE CARD REVEALED THAT 1ST DOSE WAS ON FRONT OF CARD AND GIVEN 03/21 AND ON THE BACK OF THE CARD A DOSE WAS GIVEN 11/21. PATIENT MONITORED A TOTAL OF 25 MINUTES WITH NO ADVERSE REACTION NOTED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- SAME AS BELOW
- Vorgeschichte
- COPD, ASTHMA, HYPERTENSION, ANOREXIA
- Andere Medikamente
- BONIVA, METOPROLOL, POTASSIUM, ALBUTEROL, VITAMIN C AND D , CALCIUM, IBUPROFEN.
- Allergien
- ASA, HYDROCODONE, LATEX, EGGS, FISH, CAFFEINE
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 16.03.2022
- Impfdatum
- 05.11.2021
- Beginn
- 16.03.2022
- Tage bis Beginn
- 131,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
Patient came to pharmacy on 3/16/22 and made an appointment for a booster dose of the J&J vaccine. Upon looking over the patients information, we noticed that the patient was not 18 when he got his first vaccine on 11/05/2021. Patient did not disclose the information on where he got the vaccine. J&J is not indicated for anyone younger than 18. He came into the pharmacy on 3/16/22 looking to get the booster but since he is now 18, I gave him the vaccine as if this was his first dose since now he is eligible.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 10.03.2022
- Impfdatum
- 09.03.2022
- Beginn
- 09.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dysphonia
Hypersensitivity
Swollen tongue
Throat tightness
Symptomtext
At 17:10, client began experiencing an allergic reaction. Client began experiencing tight throat, tongue swelling, and a raspy voice. (RN), stayed with client until 17:45. RN educated client if symptoms got worse, go to urgent care or the ER. Client was able to talk with no problem with no shortness of breath. RN walked with client to her car, which she able to do no problem.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dysphonia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Banana, kiwi, pineapple, and latex
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- -
- Geschlecht
- U
- Eingang
- 05.03.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Off label use
Poor quality product administered
Product storage error
Symptomtext
PRODUCT PLACED INTO FREEZER SINCE 03-NOV-2021; OUT OF SPECIFICATION PRODUCT USE; OFF LABEL USE; This spontaneous report received from a pharmacist 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: 211D21A, expiry: Unknown) dose, start therapy date were not reported for prophylactic vaccination. No concomitant medications were reported. On an unspecified date, the patient experienced product placed into freezer since 03-nov-2021, out of specification product use, and off label use. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the product placed into freezer since 03-nov-2021, out of specification product use 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
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 28.02.2022
- Impfdatum
- 16.11.2021
- Beginn
- 16.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Tenderness
Symptomtext
Arm sore to touch only
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tenderness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Salicylates
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 26.02.2022
- Impfdatum
- -
- Beginn
- 23.02.2022
- Tage bis Beginn
- -
- Dosis
- 1
- 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 POSITIVE; This spontaneous report received from a patient concerned a 52 year old white male of unspecified ethnicity.. 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: 211D21A, and expiry: 11-APR-2022) dose was not reported, 1 total administered to left arm on 04-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 23-FEB-2022, the patient mentioned having tested positive for Covid with a rapid test after receiving the vaccine. Laboratory data included: COVID-19 rapid POC test (NR: not provided) Positive. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of covid-19 positive was not reported. This report was non-serious. This report was associated with product quality complaint (PQC): 90000218866.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- SARS-CoV-2 test
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220223; Test Name: COVID-19 rapid POC test; Result Unstructured Data: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 23.02.2022
- Impfdatum
- 10.12.2021
- Beginn
- 04.01.2022
- Tage bis Beginn
- 25,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Blindness unilateral
Magnetic resonance imaging head abnormal
Neuro-ophthalmological test abnormal
Optic ischaemic neuropathy
Symptomtext
On April 29, 2021 I received the J&J Janssen Covid vaccine at pharmacy. On December 10, 2021 I received the J&J Janssen Covid Booster vaccine at Pharmacy. On the morning of January 4, 2022 I awoke with what turned out to be an eye stroke in my right eye - a rare condition called NAION - that has resulted in significant and permanent vision loss in my right eye.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blindness unilateral
- Hospital-Tage
- -
- Labordaten
- Numerous neuro opthalmic tests conducted by Eye Doctor on January 7, January 20 and February 3 have confirmed the NAION diagnosis. These tests included an MRI of my eyes and brain.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 22.02.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Cold sweat
Eye movement disorder
Pallor
Symptomtext
Mom was present but left to look at some products in a nearby aisle while patient sat quietly after getting her vaccine. Pharmacist and Mom heard her phone drop and mom started talking to her daughter to get her attention. Daughters eyes wanted to roll back in her head and her color was very pale. Patient could speak but took awhile for her thoughts to form and answer questions. She was able to answer simple questions correctly. Mom and Pharmacist removed patient's jacket and lowered her safely to the floor as she was very clammy. 911 was called. Kept patient's head upright as she had a hard time not slumping over. Patient was evaluated at the hospital and sent home the same night. Pharmacist followed up the next day and patient said they told her to follow up with a neurologist.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cold sweat
- Hospital-Tage
- -
- Labordaten
- Patient went to nearby hospital but I am unaware of what specific tests were performed
- Aktuelle Erkrankungen
- NONE. THIS WAS HER BOOSTER DOSE. MOM STATES THAT SHE DID FINE WITH THE FIRST DOSE
- Vorgeschichte
- NONE
- Andere Medikamente
- unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 22.02.2022
- Impfdatum
- 22.05.2021
- Beginn
- 08.09.2021
- Tage bis Beginn
- 109,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Acoustic stimulation tests
Ear, nose and throat examination
Endoscopy
Hypoacusis
Tinnitus
Symptomtext
Continuous TINNITUS that turned on beginning of September 2021 and has not subsided. 1st VACCINATION 05/22/2021 2nd VACCINATION 12/14/2021 Both ears but most prevalent in the right. Also has caused a symmetric reduction of hearing in the higher frequency range . Never experienced TINNITUS throughout life span. Learned of the side affects only after receiving the second vaccination of the same vaccine J&J in 14,DEC of 2021. with disclosure info of medication . Slightly subsided months later ,only to increase once again upon vaccination "booster" of the same kind. ( dosage administered was equivalent in both shots )
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acoustic stimulation tests
- Hospital-Tage
- -
- Labordaten
- ENT specialist 15,NOV 2021 , Camera inspection of the sinuses , ear , and hearing exam.
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE , HEALTHY
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 21.02.2022
- Impfdatum
- 09.12.2021
- Beginn
- 24.12.2021
- Tage bis Beginn
- 15,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anaemia
Blood follicle stimulating hormone
Blood luteinising hormone
Blood testosterone
Blood thyroid stimulating hormone
Full blood count
Menstrual disorder
Menstruation irregular
Oestradiol
Progesterone
Symptomtext
i don't know if this lot is correct, because I can barely read what she wrote... My cycle is only 14 days long now. I get a full period every 2 weeks, and because of it, I have developed anemia. My cycle will not go back to normal. My last normal cycle was December 5th. then on December 9th i was vaccinated. my next period came 2 weeks later, and I have continued to have periods every 2 weeks. the gynecologist tested via ultra sound, and I am still ovulating. These are true periods, not some type of spotting or breakthrough bleeding. She doesn't know why it's happening for any reason beyond the vaccine. My last physical was in October. I was not anemic at that time. Please help.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anaemia
- Hospital-Tage
- -
- Labordaten
- DIF Estradiol DHEAS CBC TSH Testosterone Prolactic Progesterone LH FSH all on february 2nd 2022
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- ADHD CCCA
- Andere Medikamente
- vitamin D probiotic zinc dextroamphetamine 10XR
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 21.02.2022
- Impfdatum
- 20.02.2022
- Beginn
- 20.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product administered to patient of inappropriate age
Symptomtext
No adverse reactions. Patient received Johnson & Johnson vaccine at 0.3mL dose vs 0.3mL Pfizer as requested.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 21.02.2022
- Impfdatum
- 20.02.2022
- Beginn
- 20.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
Patient received 0.3ml Johnson and Johnson dose instead of Pfizer 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
- WI
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 21.02.2022
- Impfdatum
- 11.02.2022
- Beginn
- 11.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Interchange of vaccine products
No adverse event
Symptomtext
Patient received dose of Janssen vaccine after receiving only one dose of Pfizer on 7/10/2021. No adverse effects were reported by client during her time within the vaccine clinic.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 21.02.2022
- Impfdatum
- 19.11.2021
- Beginn
- 18.02.2022
- Tage bis Beginn
- 91,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Vaccine breakthrough infection
Symptomtext
Hospitalized with breakthrough COVID infection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 0,2
- Geschlecht
- F
- Eingang
- 12.02.2022
- Impfdatum
- -
- Beginn
- 09.01.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Epistaxis
Haemoglobin
Symptomtext
NOSE BLEED; This spontaneous report received from a patient concerned an 81-year-old female. 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: 211D21A, and expiry: 11-APR-2022) dose was not reported, 1 total, administered at right arm on 06-JAN-2022 for prophylactic vaccination. No concomitant medications were reported. On 09-JAN-2022, patient experienced nose bleed and called 911, ambulance came and transported her to the ER (emergency room). The hospital kept her overnight and the treatment was packing in both nostrils and was put on put on Cephalexin 250mg 1 capsule by mouth four times daily for 5 days. The patient was released from hospital on 10-JAN-2022, the patient hospitalized for 2 days and was advised to call 911 immediately, if the event recur. The packing was left in for 5 days, the packing was removed by ENT (ears, nose and throat) on 14-JAN-2022. The patient stated it occurred again on 17-JAN-2022, 911 call was placed and the patient was taken to the hospital emergency room via ambulance. She was not admitted and the hospital administered packing on the right side of her nostril. This remained for another 5 days, removed on the 21-Jan-2022 by doctor from ENT and the doctor also catharized her right nostril. The patient stated that it seems to start on both sides and blood also comes out of the mouth. The patient also reported that her hemoglobin dropped to 10.3 (units unspecified) on 10-JAN-2022. The nose bleed occurred again on 26-JAN-2022 with another 911 call placed and was taken to the emergency room. The treatment consisted of no packing. The patient was sent to ENT (after 5-hour emergency room stay). The patient saw doctor and was catharized again and was sent consumer home. The 4th occurrence was on 02-FEB-2022. The patient was able to stop the bleeding herself and went to the ENT immediately. Doctor did catharized the right nostril again which led to bleeding then she had to have balloon packing. The patient was started, again on Cephalexin 500mg 1 capsule by mouth twice daily for 5 days. The balloon packing was removed 08-FEB-2022 and was replaced with a soluble packing that will dissolve on its own. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from nose bleed. This report was serious (Hospitalization Caused / Prolonged).; Sender's Comments: V0: 20220224843-covid-19 vaccine ad26.cov2.s-Nose bleed. 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
- Epistaxis
- Hospital-Tage
- 2,0
- Labordaten
- Test Date: 20220110; Test Name: Hemoglobin; Result Unstructured Data: 10.3
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 10.02.2022
- Impfdatum
- 07.12.2021
- Beginn
- 07.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Hypoaesthesia oral
Swollen tongue
Symptomtext
Symptoms: left side of lips numbing, throat and tongue swelling Treatment: Sent to Urgent Care and was moved from there to the hospital by ambulance. Given EPI Pen and Benadryl intervenosly, Admitted to the Summit ER Outcome: Stayed in ER for 4-1/2 hours, symptoms went away then sent home
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypoaesthesia oral
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Type II diabetes mellitus, S/P PTCA, Subacute combined degeneration of spinal cord, Syncope and collapse; Depression Anxiety Cercicalgia GERD Insulin Resistance Urinary incontinence Folate Deficiency Elevated liver enzymes S/P PTCA (percutaneous transluminal coronary angieplasty Post coronary artery stent replacement Mixed hyperlipidemia Chronic kidney disease, Stage 3b
- Andere Medikamente
- 2x DULoxetine 60 MG capsule 1x lamotrigine 200 MG tablet 2x metoPROLOL tartrate 50 MG tablet 2x pregabalin 75 MG capsule 1x ezetimibe 10 MG tablet 1x clopidogrel 75 MG tablet 1x folic acid 1 MG tablet 1x isosorbide mononitrate 30 MG 24 hr t
- Allergien
- Tetanus Toxoid (Rash), CT Contrast Media (ANAPHYLAXIS) Niacin Tramadol Lantus Naproxen Metformin Albuterol Gadodiamide
- Vorherige Impfungen
- Tetanus Toxoid, Rash
- Staat
- UT
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 04.02.2022
- Impfdatum
- 12.11.2021
- Beginn
- 25.11.2021
- Tage bis Beginn
- 13,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Acoustic stimulation tests
Deafness
Ear tube insertion
Ear, nose and throat examination
Hearing aid user
Respiratory syncytial virus infection
Symptomtext
4 trips to urgent care Diagnosed with RSV Tubes in both ears Now I?m wearing hearing aides praying my hearing might be restored.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acoustic stimulation tests
- Hospital-Tage
- -
- Labordaten
- Hearing tests performed by audiologist. Multiple exams by ENT and Primary Physician.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 04.02.2022
- Impfdatum
- -
- Beginn
- 01.12.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Tinnitus
Symptomtext
RINGING IN THE EARS; This spontaneous report received from a patient concerned a 66 year old female. 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: 1820095, expiry: 01-OCT-2021) dose was not reported, 1 total, administered on 07-AUG-2021 at left deltoid for prophylactic vaccination. It was reported that patient was fine following vaccination with first dose 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: 211D21A, expiry: unknown) dose was not reported, 1 total, administered on 08-NOV-2021 at left deltoid for prophylactic vaccination. No concomitant medications were reported. On an unspecified date in DEC-2021, (a little bit after thanksgiving) she began to experience ringing in both ears, but left one was louder. She stated that the ringing was all the time, the ringing did not sound like a bell but more like crickets or peepers. She stated that the symptom was not going away or subsiding. She noticed the ringing at night first when it was quiet, and since then it had progressed and she was experiencing at the time of reporting while she was on the call. She also mentioned that she had not brought that issue up with her physician yet, but planned to bring that up in the future if she still had it in 6 months (event with dose number series 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from ringing in the ears. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tinnitus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 03.02.2022
- Impfdatum
- 03.02.2022
- Beginn
- 03.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fall
Hypophagia
Pallor
Symptomtext
About two minutes after vaccination, patient became pale and asked for water. He then collapsed to the floor. We got him water and asked if he had eaten anything that day. He stated "no." We got him some chips. He said he was ok and feeling better with chips and water. Meanwhile, paramedics were on the way. Paramedics took his vital signs. He was feeling better and did not leave with paramedics, but rather went home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fall
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 03.02.2022
- Impfdatum
- 03.02.2022
- Beginn
- 03.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest discomfort
Dysphagia
Erythema
Hypersensitivity
Interchange of vaccine products
Swollen tongue
Symptomtext
Patient is a 43 year old woman who presented to the vaccine clinic to receive her booster dose. Patient stated she had a previous mild reaction to the second dose of the Pfizer vaccine. Per Dr. was cleared to receive the J&J booster. The J&J Booster vaccine was administered at 1405. Patient began to exhibit symptoms at 1415. Upon assessment patient was A&Ox4. Respirations were even with non audible wheezes upon auscultation. Notable erythema on face and chest. Patient expressed having difficulty swallowing with severe increased swelling of the tongue. Unable to assess palate and uvula due to increased swelling of the tongue. Patient expressed feeling tightness of the chest. EpiPen Auto-Injector 0.3mg was administered at 1416. Patient expressed mild relief. Patient was transported to the ER via wheelchair. COVID Vaccine Worksheet Did the patient have an immediate allergic reaction of any severity such as urticaria, angioedema, respiratory distress, or anaphylaxis (<4 hours following administration of the COVID vaccine)? Yes Did the patient previously have an immediate allergic reaction of any severity to polysorbate or polyethylene glycol? No Has the patient had prior anaphylactic reactions from another vaccine, medication or any other cause? Yes Did the patient have an allergic reaction >4 hours after administration? OR have an expected side effect of the COVID vaccine? Yes
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest discomfort
- Hospital-Tage
- -
- Labordaten
- Unknown
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- ASTHMA, UNSPECIFIED MIGRAINE W AURA GERD (GASTROESOPHAGEAL REFLUX DISEASE) MAJOR DEPRESSIVE DISORDER, RECURRENT EPISODE, IN FULL REMISSION *OTHER MR # EXISTS URETERAL CALCULUS HX OF CORONAVIRUS COVID-19 DISEASE ADVERSE EFFECT OF CORONAVIRUS COVID-19 VACCINE DEVIATED NASAL SEPTUM CLUSTER HEADACHE POLYCYSTIC OVARIAN SYNDROME PREDIABETES RENAL CALCULUS HX OF CHOLECYSTECTOMY RIGHT NIPPLE DISCHARGE HX OF PITUITARY TUMOR CONTRACEPTIVE SURVEILLANCE HX OF SEVERE NAUSEA VOMITING DUE TO ANESTHESIA PREMATURE VENTRICULAR BEATS FATTY LIVER
- Andere Medikamente
- Patient premediated with Zyrtec 10 mg prior to vaccine .
- Allergien
- Clotrimazole Not Specified Rash 2003-10-01;rash with vaginal prep Darvocet-n 100 [acetaminophen + Propoxyphene Napsylate] Not Specified Itching Diflucan [fluconazole] Erythromycin Base Fentanyl Hydrocodone-acetaminophen Oxycodone-acetaminophen Reglan [metoclopramide] Septra [co-trimoxazole] Vantin [cefpodoxime] Versed [midazolam] Clindamycin Hydrochloride Amoxicillin
- Vorherige Impfungen
- Second dose of Pfizer vaccine, 1/11/21 42 years of age
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 03.02.2022
- Impfdatum
- -
- Beginn
- 22.01.2022
- 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 ADMINISTERED FROM A VIAL THAT WAS EXPOSED TO A TEMPERATURE OF 35 DEGREE FAHRENHEIT FOR 4 HOURS; 5 DOSES FROM THE SAME VIAL WERE ADMINISTERED TO 5 PATIENTS; This spontaneous report received from a consumer concerned multiple patients 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: 211D21A, and expiry: 11-APR-2022) dose was not reported, administered on 22-JAN-2022 for prophylactic vaccination. No concomitant medications were reported. On 22-JAN-2022, the patient experienced vaccine was administered from a vial that was exposed to a temperature of 35 degree Fahrenheit for 4 hours. On 22-JAN-2022, the patient experienced 5 doses from the same vial were administered to 5 patients. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the vaccine was administered from a vial that was exposed to a temperature of 35 degree Fahrenheit for 4 hours and 5 doses from the same vial were administered to 5 patients 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
- TN
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 02.02.2022
- Impfdatum
- 11.11.2021
- Beginn
- 22.01.2022
- Tage bis Beginn
- 72,0
- Dosis
- 1
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Vaccine breakthrough infection
Symptomtext
Breakthrough hospitalization due to COVID-19 in fully vaccinated patient
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 10,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asthma; GERD; Hyperlipidemia
- Andere Medikamente
- Albuterol; diclofenac; doxycycline; gemfibrozil; medrol dose pak; singulair
- Allergien
- Penicillin, sulfa, demerol; cinnamon; mushrooms; almonds; coconut
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- -
- Geschlecht
- U
- Eingang
- 29.01.2022
- Impfdatum
- -
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Off label use
Poor quality product administered
Product storage error
Symptomtext
ADMINISTERED VACCINE AFTER IT WAS RE-FROZEN AND THEN THAWED; INCORRECT PRODUCT STORAGE; OFF LABEL USE; This spontaneous report received from a health care professional 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: 211D21A, and expiry: 11-APR-2022) dose was not reported, administered on JAN-2022 for prophylactic vaccination. No concomitant medications were reported. On JAN-2022, the patient experienced administered vaccine after it was re-frozen and then thawed, incorrect product storage, and off label use. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the administered vaccine after it was re-frozen and then thawed, off label use and incorrect product storage was not reported. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Off label use
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 28.01.2022
- Impfdatum
- 15.11.2021
- Beginn
- 22.11.2021
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Flatulence
Tinnitus
Symptomtext
1. Tinnitus 2.Bad gas (smell was very bad for about 2 months)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Flatulence
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 28.01.2022
- Impfdatum
- 15.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 12,0
- Dosis
- UNK
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Atrial fibrillation
Electrocardiogram
Inflammation
Symptomtext
Atrial fibrillation. Possible inflammation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Atrial fibrillation
- Hospital-Tage
- -
- Labordaten
- EKG 1/27/2022.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 27.01.2022
- Impfdatum
- 17.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
Individual received a second dose of J&J (1/17/2022) 12 days after she received her first dose of J&J (1/5/2022). Individual used different last names for both shots but used same address, phone number, date of birth and first name of mother. She was called and confirmed that she received both shots.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- DENIES
- Vorgeschichte
- DENIES
- Andere Medikamente
- UNKNOWN
- Allergien
- UNKNOWN
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 27.01.2022
- Impfdatum
- 18.11.2021
- Beginn
- 26.01.2022
- Tage bis Beginn
- 69,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Vaccine breakthrough infection
Symptomtext
Hospitalized with breakthrough COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 26.01.2022
- Impfdatum
- 15.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Symptomtext
Patient received 1st dose Covid -19 Janssen 03/24/2021 Patient received 2nd dose (Booster) Covid-19 Janssen 10/25/2021 at Pharmacy Patient received a 3rd dose Covid-19 Janssen 01/15/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- unknown
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 25.01.2022
- Impfdatum
- 08.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Vaccine was administered to a 13 y/o child. J & J vaccine is not approved for individuals under age 18 years. Mother was contacted to determine if the child experienced any adverse effects from the vaccine on 1) the day of the clinic, and post vaccine day 1 and 2. Mother denied that the child experienced any adverse effects from the J and J vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 25.01.2022
- Impfdatum
- 09.12.2021
- Beginn
- 24.01.2022
- Tage bis Beginn
- 46,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Vaccine breakthrough infection
Symptomtext
Fully vaccinated with J&J, not boosted. COVID infection breakthrough with inpatient hospital stay.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 24.01.2022
- Impfdatum
- 12.12.2021
- Beginn
- 22.01.2022
- Tage bis Beginn
- 41,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Hospitalized with a breakthrough case of COVID 19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- 1/22/22-SARS Coronavirus-2, PCR detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 24.01.2022
- Impfdatum
- 20.12.2021
- Beginn
- 25.12.2021
- Tage bis Beginn
- 5,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Parosmia
Symptomtext
5 days after the covid vaccination some smells permanently changed. Some meals that used to smell pleasing now have a pungent repulsive smell. Have not identified what ingredients cause the smell but have smelled the same repulsive odor frequently in different meals and restaurants and stores. It's as if ~15% of my smell receptors have been replaced with this odor; like they've been reprogrammed to tell me it's a repulsive smell instead of pleasing like it used to be.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Parosmia
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- bee stings
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 24.01.2022
- Impfdatum
- 07.12.2021
- Beginn
- 07.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Interchange of vaccine products
Product preparation issue
Symptomtext
27 yo female pt received one vaccination with 0.3 mL of Pfizer vaccine and 0.2 mL of Janssen vaccine components instead of intended 0.5 mL of Janssen vaccine. Immunizer drew up 0.5 mL of Janssen vaccine, labeled it, and set it down. Immunizer then went through information with patient and picked up a syringe nearby, realized there were only 0.3 mL in it, then added another 0.2 mLs for a total of 0.5 mL. Administered this immunization to the patient. Later, immunizer realized the Janssen vaccine was still sitting where it was left earlier. Immunizer had picked up a Pfizer vaccine (0.3 mL) and added Janssen (0.2 mL) to this syringe before giving it to patient. Patient has since been contacted and made aware of the situation. Plan to schedule second appointment for Pfizer vaccination dose 2.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 22.01.2022
- Impfdatum
- 21.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Interchange of vaccine products
Symptomtext
patient had requested the Moderna booster and was given the Janssen instead
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- muscle pain and nerve pain following Janssen dose 1 covid vaccine
- Staat
- WI
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 21.01.2022
- Impfdatum
- 20.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
Symptomtext
Client presented his vaccination card the showed the second dose of a Pfizer primary series being administered on 9/19/2021. Client presented for booster a month early but received a booster of Janssen due to a clerical error of only counting 4 rather than 5 months out from the second dose of the primary series.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- -
- Beginn
- 17.01.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Off label use
Product administered to patient of inappropriate age
Symptomtext
PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE; OFF LABEL USE; This spontaneous report received from a pharmacist concerned a 16 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: 211D21A, expiry: UNKNOWN) dose was not reported, administered on 17-JAN-2022 for prophylactic vaccination. No concomitant medications were reported. On 17-JAN-2022, the patient experienced product administered to patient of inappropriate age, and off label use. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the product administered to patient of inappropriate age 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
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 04.12.2021
- Beginn
- 04.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Symptomtext
Patient was given a dose of Johnson & Johnson Covid -19 vaccine at a vaccine clinic by RN, on 12/04/2021. She was 16 years of age at time of vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- unknown
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 25.03.2021
- Beginn
- 25.03.1973
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Symptomtext
Patient received 1st dose of J&J Lot # 1805018, 3/25/2021, Returned to vaccine clinic 6/17/2021 received dose J&J Lot # 203A21A. Charted as 1st dose. Returned 12/11/2021 received another dose J&J lot #211D21A. charted as booster. (Received 3 doses of J&J from SCHD from )3/25/2021 to 12/11/2021
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- unknown
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 18.01.2022
- 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: unbekannt
Erholt: unbekannt
Product administered to patient of inappropriate age
Symptomtext
No signs or symptoms during the 15-minute recommended wait time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- -
- Beginn
- 17.01.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Off label use
Product administered to patient of inappropriate age
Symptomtext
VACCINE ADMINISTERED TO 17 YEAR OLD; OFF LABEL USE; This spontaneous report received from a pharmacist concerned a 17 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, intramuscular, batch number: 211D21A, expiry: 11-APR-2022) dose was not reported, administered on 17-JAN-2022 for prophylactic vaccination. No concomitant medications were reported. On 17-JAN-2022, the patient experienced vaccine administered to 17 year old, and off label use. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the vaccine administered to 17 year 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
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Moaning
Muscle tightness
Tension
Symptomtext
Patient described previously that she had muscle tightening with the 1st J & J prior to receiving her 2nd J & and J today and knew she would be experiencing the same adverse reaction. She was lead into a quieter room and laid on a gurney for comfort and safety. Upon receiving her J & J dose today after about 15 seconds, she experienced muscle tightening with both her arms, legs and her head lifted from the gurney and let out a groan. This continued for about 10-15 seconds every 2 to 3 minutes for about 10-15 minutes all during the time she was fully conscious. VS was stable throughout.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Moaning
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Please see item 10
- Andere Medikamente
- -
- Allergien
- The patient states that same type of reaction also happened when she received her 1st J & J vaccine. While she was conscious, she experienced muscle tightness throughout her body for bout 15 seconds every 2 to 3 minutes for about 15 minutes. This includes, arms clenching, head elevated and legs elevated due to tension with a random groan. When asked if she lost consciousness, she said she did not and heard everything I was saying. She replied that there is something going on with her body for the past 2 year but did not know how to pinpoint her actions.
- Vorherige Impfungen
- Same as dose #1
- Staat
- NV
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 13.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Interchange of vaccine products
Symptomtext
Patient came to the pharmacy and said she had an appointment for the J&J vaccine. She said it was her first covid vaccine dose, and that she had not received any covid vaccines prior. When the dose was administered and it came time to enter the information, there was a Pfizer dose from 1/3/22 (10 days ago). When the patient was asked why she asked for a J&J vaccine after she got one dose of Pfizer last week, she admitted that she lied to us because she wanted to be fully vaccinated 14 days before going on a cruise.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 12.01.2022
- Impfdatum
- 26.11.2021
- Beginn
- 23.12.2021
- Tage bis Beginn
- 27,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Angiogram
Computerised tomogram abdomen
Liver function test normal
Metabolic function test
Metabolic function test normal
Renal infarct
Ultrasound kidney
Ultrasound pelvis
Urine analysis normal
Symptomtext
Renal infarct--admit 12/23/21 to 12/24/21 at Hospital Re-eval ER 12/29/21
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Angiogram
- Hospital-Tage
- -
- Labordaten
- CT Abd/Pelvic 12/23/21, US Pelvis 12/25/21, US Renal 12/29/21, CT Angio 1/10/22. Zio Patch Pending, MRI Abd Pending, Urinalysis 1/10/22 Normal, BMP 1/10/22 Normal, LFT 1/4/22 NORMAL. cardiolipid AB 1/10/22 Normal
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 08.01.2022
- 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: nein
Incorrect dose administered
Symptomtext
no adverse reactions. Due to the worker who talked to her being a friend and her not putting age just DOB on form we didn't know she was 17 instead of 18. So she is a bit outside of recommended dose rage
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- not sure
- Allergien
- not sure
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 05.01.2022
- Impfdatum
- 17.11.2021
- Beginn
- 18.12.2021
- Tage bis Beginn
- 31,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Tinnitus
Symptomtext
I began with ringing in my ears about one month after the booster dose of the vaccine. It is constant 24/7. Sounds like crickets are in my ears.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tinnitus
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- a little high blood pressure was maintained with blood pressure meds. Had Gout but is under control.
- Andere Medikamente
- blood pressure meds. Gout med.
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 04.01.2022
- Impfdatum
- 04.01.2022
- Beginn
- 04.01.2022
- 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
Client is only 16 years of age and was given Janssen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 03.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Symptomtext
Patient brought in vaccine card with one dose of J&J in June of 2021- gave her booster 1-3-2022. After I finished she informed me she had one dose of Moderna in march or April 2021 ( ended up being March 10, 2021) but it caused her hearing issues. She did not complete that series and instead was told by her md to get a J&J dose - she went to a pharmacy for that
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- patient got a dose of moderna in march 2021 that caused her issues with hearing, then got a J&J in 6/2021 and a booster of J&J 01-03-2022
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 30.12.2021
- 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 ADMINISTERED 13 HOURS AFTER INITIAL PUNCTURE; INCORRECTLY STORED VACCINE ADMINISTRATED; This spontaneous report received from a health care professional 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, and batch number: 211D21A expiry: 11-APR-2022) dose was not reported, administered on 28-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. On 28-DEC-2021, the patient experienced vaccine administered 13 hours after initial puncture, and incorrectly stored vaccine administrated. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the vaccine administered 13 hours after initial puncture and incorrectly stored vaccine administrated 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
- PR
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 30.12.2021
- Impfdatum
- -
- Beginn
- 08.12.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Contusion
Symptomtext
BRUISING IN VARIOUS PARTS OF THE BODY; This spontaneous report received from a consumer concerned a 60 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included: alcohol user (very unusual maybe a glass of wine), and non smoker. The patient had no known allergy. The patient previously received covid-19 vaccine ad26. cov2.s (Janssen, Dose number in series 1)(suspension for injection, route of admin not reported, batch number:1805029, expiry: UNKNOWN) dose was not reported, 1 total, administered on 16-MAR-2021 for prophylactic vaccination. The patient had no issues with series 1. The patient received covid-19 vaccine ad26.cov2.s (Janssen, Dose number in series 2) (suspension for injection, route of admin not reported, batch number: 211D21A, expiry: UNKNOWN) dose was not reported, 1 total, administered on 20-NOV-2021 for prophylactic vaccination. No concomitant medications were reported. On 08-DEC-2021 (Post 4 weeks of vaccination), the patient experienced bruising in various parts of the body. The reporter saw 2 on right arm and patient stated she had bruising in various part of body covered by clothing. The reporter stated that bruising appeared after booster dose. The reporter stated that bruising was noticed after doing exercise. (Dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from bruising in various parts of the body. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Contusion
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Alcohol use (very unusual maybe a glass of wine); Non-smoker
- Vorgeschichte
- Comments: The patient had no known allergy
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -