- Staat
- -
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 27.12.2023
- Impfdatum
- 21.01.2022
- Beginn
- 30.10.2023
- Tage bis Beginn
- 647,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Anticoagulation drug level above therapeutic
Aortic aneurysm
Aortic dilatation
Arteriosclerosis
Asthenia
Bradycardia
Brain natriuretic peptide increased
COVID-19
COVID-19 pneumonia
Catheterisation cardiac abnormal
Cerebral atrophy
Cerebral small vessel ischaemic disease
Computerised tomogram head abnormal
Computerised tomogram thorax abnormal
Condition aggravated
Conduction disorder
Coronary artery disease
Symptomtext
79 y.o. male patient of MD with history of DMII (HgbA1C 13.3), CAD, HFrEF w/EF 25%, Prostate Cancer w/ bone mets, Hx of LV thrombus, AAA, DDD. Presents with Fall, weakness. Found to have acute hypoxic respiratory failure secondary COVID pneumonia. Improving with remdesivir and dexamethasone. PT consulted to evaluate patient, benefit from outpatient PT. Acute Hypoxic Respiratory Failure, improved COVID Pneumonia Symptoms started a few days ago, no home O2 requirements, AF Found COVID+ 10/31, hypoxic, started on 4L NC CT w/patchy airspace opacities, worst in lingula and LLL Completed remdesivir course 5d Discharged to complete last 5 of dexamethasone 10d course O2 walk test on RA decrease to 86%, discharged on 1L NC Wean supplemental O2 as able outpatient Encouraged continued IS at home Fall Likely 2/2 weakness and hypoxia in setting of COVID infection CT T/L w/ multifocal PNA, multifocal osseous metastasis, similar to prior, severe atherosclerosis w/aneurysmal dilatation of abdominal aorta 3.1 cm CT scans without acute trauma CT head noted small vessel ischemic dx, cerebral atrophy XR Knee Right w/no osseous or soft tissue abnormality PT/OT consulted; PT AMPAC 18 Hyperglycemia, stable DMII with diabetic neuropathy Likely will worsen w/oral steroid treatment Has hx of diabetic wounds, home wound care UA w/ketones, elevated glucose BHB 1.3 > 0.4 S/p Non-DKA insulin gtt, transitioned to lantus 11/1 While admitted Lantus 40u qAM, lispro 14u TID + SSI Consult to diabetic educator Discharged with Rx for Trulicity in addition to home metformin Consider addition of SGLT2i as well HFrEF, not in acute exacerbation HLD Elevated Trops Hx of STEMI Elevated trops likely in setting of demand ischemia Follows with cards, CHF clinic Trop 61 (b/l 55), BNP 821 (b/l 1100s) EKG w/ sinus rhythm, intraventricular conduction delay Last echo 11/2021 EF 25%, Grade I diastolic dysfunction L Heart Cath w/ 70% lesion in circumflex, 90%lesion in RCA, LVEF 25% w/abnormal wall motion Continue lipitor, plavix, coumadin Held on discharge PO lasix, metoprolol, entresto given hypotension and bradycardia Consider restart metoprolol at lower dose at follow up Prostate Cancer w/ bone metastasis Follows with Dr. Last PSA 0.08 Imaging with diffuse sclerotic osseous metastatic disease that has been stable Treated with Lupron, Zytiga, has had good response Pain treated with oxy 7.5mg, diclofenac gel Discussed with Dr., held lupron and zytiga during admission Hx of LV mural thrombus INR supratherapeutic initially Follows with coumadin clinic Continued coumadin while admitted
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 5,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 09.11.2023
- Impfdatum
- 10.02.2022
- Beginn
- 25.07.2023
- Tage bis Beginn
- 530,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Acute respiratory failure
Asthenia
COVID-19
COVID-19 pneumonia
Cough
Hypoxia
SARS-CoV-2 test positive
Symptomtext
BRIEF OVERVIEW: Admission Date: 7/25/2023 Discharge Date: Jul 28, 2023 Discharge Disposition: home health care svc DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Acute respiratory failure with hypoxia COVID-19 HOSPITAL COURSE: Patient is a 82 y.o. male with past medical history significant for history of ESRD with renal transplant and now CKD stage 3, hypertension, paroxysmal AFib on Coumadin, Alzheimer's disease, depression, chronic diastolic CHF, type 2 diabetes, hypothyroidism who presented to the emergency department from home with complaints cough and generalized weakness. Patient was found to be hypoxic and placed on 6 L nasal cannula to maintain oxygenation. Patient was admitted to General Medicine for acute hypoxic respiratory failure. Viral testing revealed COVID pneumonia. Patient was initially started on Rocephin and azithromycin for concerns for community-acquired pneumonia, though quickly taken off this as COVID was determined to be the cause of his respiratory failure. Given his history of renal transplant nephrology was consulted. And assisted with care while he was hospitalized. Patient was started on dexamethasone for COVID pneumonia. He quickly improved and was able to decrease oxygen back to room air. Patient was monitored at on room air without additional desaturations. Given the improvement patient was discharged home in stable condition on 07/28. Given that he was no longer on dexamethasone he was started on 5 mg of prednisone at the recommendation Nephrology given his history of renal transplant.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Paroxysmal atrial fibrillation Primary hypertension Acquired hypothyroidism Type 2 diabetes mellitus with kidney complication, without long-term current use of insulin Presence of permanent cardiac pacemaker Kidney transplant status, living related donor Personal history of colonic polyps Chronic diastolic heart failure Gastroesophageal reflux disease without esophagitis Gout Mixed hyperlipidemia Immunocompromised state due to drug therapy Moderate major depression Alzheimer's disease Monoclonal gammopathy of unknown significance (MGUS) Nonrheumatic aortic valve insufficiency Non-rheumatic mitral regurgitation Pulmonary hypertension Secondary hyperparathyroidism Sick sinus syndrome Vitamin D deficiency Stage 3a chronic kidney disease Coronary artery disease involving native coronary artery of native heart without angina pectoris Hypertensive kidney disease Venous insufficiency
- Andere Medikamente
- acetaminophen (TYLENOL) 500 mg tablet amiodarone (PACERONE) 200 mg tablet amLODIPine (NORVASC) 10 MG tablet calcitRIOL (ROCALTROL) 0.5 MCG capsule cholecalciferol (VITAMIN D3) 25 MCG (1000 UT) capsule donepezil (ARICEPT) 10 MG tablet escita
- Allergien
- Cyclobenzaprine VoriconazoleAnaphylaxis TamsulosinDizziness, Fatigue
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 04.05.2023
- Impfdatum
- 07.01.2022
- Beginn
- 06.03.2022
- Tage bis Beginn
- 58,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Chronic respiratory failure
Pulmonary embolism
Respiratory failure
Symptom recurrence
Symptomtext
PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ACUTE RESPIRATORY FAILURE ACUTE PULMONARY EMBOLISM CHRONIC HYPOXEMIC RESPIRATORY FAILURE HYPOXEMIC RESPIRATORY FAILURE, UNSPECIFIED ACUITY 4/3/2022, 5/1/2022, 5/2/2022 -- RECURRENCE OF SAME SYMPTOMS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 95,0
- Geschlecht
- M
- Eingang
- 23.03.2023
- Impfdatum
- 29.04.2022
- Beginn
- 16.12.2022
- Tage bis Beginn
- 231,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Asthenia
COVID-19
COVID-19 pneumonia
Dyspnoea
Hypoxia
Pneumococcal bacteraemia
SARS-CoV-2 test positive
Symptomtext
Patient was seen in the ED on 12/16/22 for evaluation of shortness of breath. He reported a recent COVID diagnosis ~one week prior. Of note, he was previously hospitalized at another healthcare facility 12/8/22 - 12/13/22 for COVID-19 infection. Repeat COVID PCR testing preformed 12/16/22 was also positive. He was admitted 12/16/22 for worsening hypoxia, and generalized weakness. He was found to have acute hypoxic respiratory failure secondary to COVID-19 pneumonia with concurrent bacteremia pneumonia. Patient required 2 L supplemental O2 but was weaned down to room air. He was discharged 12/13/22. Patient has received the primary COVID vaccine series and two boosters.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 19.01.2023
- Impfdatum
- 29.03.2022
- Beginn
- 02.11.2022
- Tage bis Beginn
- 218,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
COVID-19
Dyspnoea
Positive airway pressure therapy
SARS-CoV-2 test positive
Symptomtext
Patient brought to the ED by EMS on 11/2 with sudden onset of shortness of breath. She was brought in. EMS placed patient on high flow O2 and she was satting at 93%. In the ED, patient tested positive for COVID-19 by PCR. She was ultimately admitted 11/2 - 11/9 with acute on chronic respiratory failure and COVID-19. Patient initially required BiPAP, and at discharge was on CPAP and required about 3-4 L of oxygen. At baseline she uses 2-3L O2. Patient has received the COVID-19 primary vaccine series and one booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 87,0
- Geschlecht
- M
- Eingang
- 26.10.2022
- Impfdatum
- 27.09.2022
- Beginn
- 06.10.2022
- Tage bis Beginn
- 9,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Angiopathy
Chest tube insertion
Computerised tomogram thorax abnormal
Death
Depressed level of consciousness
Dyspnoea
Fatigue
Haemothorax
Hypopnoea
Intrapericardial thrombosis
Pericardial effusion
Pericardial haemorrhage
Pleural effusion
Productive cough
Pulse absent
Red blood cell transfusion
Resuscitation
Sputum discoloured
Symptomtext
Patient previously tested positive on 8/13/22. Patient was brought to local Hospital ED on 10/6 with unknown onset of shortness of breath and productive cough with yellow sputum. He also reported feeling "very very tired". During this visit, CT scan showed concern for blood and blood clots in the pericardium, and the patient was found to have a systolic blood pressure in the 100s. Bedside ultrasound showed fluid around the heart. He was given a unit of blood and started on Levophed, and was transferred to alternate Hospital ED. Within minutes of arrival, the patient became obtunded and unresponsive with shallow respirations. The provider was unable to palpate a pulse so CPR was started immediately. Patient was given multiple rounds of epinephrine, bicarb, calcium and volume resuscitation with IV fluid and packed red blood cells. The provider was concerned for aortic dissection or other catastrophic vascular cause for the patient's presentation. Further ultrasound revealed an apparent pleural effusion on the left. Needle thoracostomy and tube thoracostomy was performed with a large volume of blood from the left hemithorax. Early in the resuscitation, ready pulses were felt with rhythm checks, however pulses were lost and were not regained. per the provider, given the prolonged downtime, likely catastrophic vascular event and the patient's advanced age, further resuscitation efforts appeared futile. Patient passed on 10/6 at 2:28pm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Pt history of asthma, type II diabetes, ESRD, dementia.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 27.09.2022
- Impfdatum
- 14.04.2022
- Beginn
- 25.09.2022
- Tage bis Beginn
- 164,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Death
Symptomtext
Patient expired 9/25/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Cirrhosis, incomplete L3 paraplegia, chronic pain, severe malnutrition, chronic diarrhea, chronic sacral wounds, cervical cancer and hepatitis C
- Andere Medikamente
- Unknown
- Allergien
- Iodinated diagnostic agents, acetaminophen, blood-group specific substance Anti-Duffy a (Fya) antibody, naproxen
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 27.09.2022
- Impfdatum
- 21.12.2020
- Beginn
- 13.09.2022
- Tage bis Beginn
- 631,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Death
SARS-CoV-2 test positive
Symptomtext
Pt was admitted to hospital 9/13, tested positive for covid 9/17, and died on 9/26.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- 14,0
- Labordaten
- Positive covid test 9/17
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Coronary artery disease, gastric and duodena AV malformation, NASH, diabetes, OSA with Bipap, chronic anemia, HTN
- Andere Medikamente
- Unknown
- Allergien
- Chloramphenicol, NSAIDs, statins, Vancomycin
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 31.08.2022
- Impfdatum
- 27.01.2022
- Beginn
- 26.08.2022
- Tage bis Beginn
- 211,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
COVID-19 pneumonia
Fall
SARS-CoV-2 test positive
Symptomtext
Patient received Pfizer COVID vaccine on 5/21/21 (lot # EW0183), 6/11/21 (lot # EW0183), and 1/27/22 (lot # FJ5682). Patient admitted to our inpatient hospital (med/surg unit) on 8/26/22 s/p a fall with acute hypoxemic respiratory failure due to COVID-19 pneumonia. As of today (8/31/22), patient is still admitted in the med/surg unit.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 5,0
- Labordaten
- COVID status positive on 8/27/22.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- history of hidradenitis suppurativa followed by rheumatology, hypertension, pulmonary anemia, GERD, and gout
- Andere Medikamente
- adalimumab inj, allopurinol, atorvastatin, vitamin d3, dicyclomine, furosemide, gabapentin, hydroxyzine, metoprolol er, oxycodone/acetaminophen, pantoprazole, topiramate, trazodone
- Allergien
- sulfa
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 16.08.2022
- Impfdatum
- 12.04.2022
- Beginn
- 14.07.2022
- Tage bis Beginn
- 93,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Asthenia
COVID-19
Gait inability
Nausea
SARS-CoV-2 test positive
Sepsis
Vomiting
Symptomtext
Patient brought to the ED via EMS on 7/14 for evaluation of COVID exacerbation. Patient has been unable to walk due to weakness, has been feeling nauseated and has been vomiting. Patient had a positive COVID home test on 7/10. Additional COVID-19 PCR swab taken in the ED on 7/14 was also positive. Patient admitted from 7/14-7/18 with acute hypoxic operatory failure in the setting of COVID-19 infection and possible pneumonia as well as severe sepsis in the setting of possible pneumonia. Patient has been vaccinated against COVID-19. This meets criteria for vaccine breakthrough case review.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 01.06.2022
- Impfdatum
- 31.01.2022
- Beginn
- 11.05.2022
- Tage bis Beginn
- 100,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Acute kidney injury
Asthenia
Blood albumin decreased
COVID-19
Clostridium test negative
Coagulopathy
Decreased appetite
Fall
Hepatic function abnormal
Hypotension
Hypovolaemia
Infection
Laboratory test normal
Malnutrition
Organ failure
Red blood cell transfusion
SARS-CoV-2 test positive
Septic shock
Symptomtext
Admission Date: 5/11/2022 Discharge Date: 05/30/2022 PRESENTING PROBLEM: Generalized weakness Acute kidney injury (nontraumatic) Multiple falls Laceration of multiple sites of lower extremity, unspecified laterality, initial encounter Hypotension due to hypovolemia Septic shock HOSPITAL COURSE: Patient is a 61 year old female who presented to the ED with complaints of frequently falling and had sustained another fall prior to admission in which she denied striking her head or losing consciousness but did suffer lacerations to her left upper thigh and bilateral medial calves which were sutured in the ED. She had been discharged the previous day from rehab in which she had reported to being stronger but endorsed that she was not back to her baseline. After admission she became hypotensive despite fluid resuscitation, requiring vasopressors to maintain blood pressure. She was treated for septic shock with organ dysfunction. Labs did reveal an intermediate c diff result on 5/12 but subsequent c diff PCR was negative. Source of infection was unclear but she did receive a 7 day course of Zosyn with concern for colitis. She did have significant third spacing on admission felt to be due to poor nutrition status with low albumin. Dietary did speak with her and did discuss proper nutritional goals. We have started her on marinol to improve appetite. During her stay she did have significant coagulopathy felt secondary to liver dysfunction and did receive 3 units of FFP. She also did receive 2 units of PRBCs during this hospital stay. Physical therapy did consult when she stabilized and felt patient would benefit from rehab. Unfortunately, a covid 19 screen was done which was positive; although, she did not have any respiratory symptoms. Due to being positive COVID 19 placement was difficult which caused a prolonged hospital stay. With continued physical therapy the patient's mobility did improve and it was felt that patient could be safely discharged home with family and home physical therapy on 5/29. Patient also expressed eagerness to go home and was agreeable with the plan. She is ambulating in the room independently including feeding, dressing and going to the restroom. We will arrange for home health. We are discharging her on potassium supplementation but would recommend a BMP including magnesium to be checked in the next 5-7 days. Patient is being discharged in stable condition and was agreeable with discharge plans.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Septic shock
- Hospital-Tage
- 19,0
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Anemia Protein-calorie malnutrition, moderate Hypoalbuminemia Bilateral lower extremity edema OSA (obstructive sleep apnea) DJD (degenerative joint disease) Hypertension Hypothyroidism Back pain Depression Ex-smoker Eczema H/O bariatric surgery 2010 Kidney stone Restless legs syndrome (RLS) Medical marijuana use Depression, unspecified depression type Folate deficiency Macrocytosis T wave inversion in EKG Bilateral hip joint arthritis Tibial plateau fracture, left Lesion of spleen Lumbar degenerative disc disease Generalized weakness Copper deficiency Copper deficiency myelopathy Weakness with frequent falls Multiple falls Laceration of multiple sites of lower extremity, unspecified laterality, initial encounter (HFpEF) heart failure with preserved ejection fraction Hypovolemia Hypotension Hypotension due to hypovolemia C. difficile diarrhea Acute diastolic heart failure
- Andere Medikamente
- acetaminophen (TYLENOL) 500 MG tablet aspirin 81 MG chewable tablet Blood Pressure Monitoring (BLOOD PRESSURE CUFF) MISC busPIRone (BUSPAR) 10 MG tablet Carboxymethylcellulose Sodium (ARTIFICIAL TEARS OPTH) Cholecalciferol (VITAMIN D-3
- Allergien
- Adhesive TapeRash LatexRash MorphineNausea Only ValiumNausea Only Vicodin [Hydrocodone-acetaminophen]Nausea Only
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 11.04.2022
- Impfdatum
- 17.02.2022
- Beginn
- 07.03.2022
- Tage bis Beginn
- 18,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Acute respiratory failure
Chest discomfort
Chronic obstructive pulmonary disease
Condition aggravated
Cough
Viral upper respiratory tract infection
Symptomtext
Patient presented to the ED on 3/7/22 for chest discomfort. Patient presented to the ED on 3/15/22 for Viral URI with cough. Patient presented to the ED on 3/17/22 for COPD exacerbation, Acute hypoxemic respiratory failure. These visits are within 6 weeks of receiving covid vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 10,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 08.04.2022
- Impfdatum
- 07.02.2022
- Beginn
- 15.02.2022
- Tage bis Beginn
- 8,0
- Dosis
- 2
- Route/Site
- IM / UN
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cardiac arrest
Death
Inappropriate schedule of product administration
Infection
SARS-CoV-2 test positive
Unresponsive to stimuli
Symptomtext
o 19yr old female experienced cardiac arrest at home, transported by EMS in cardiac arrest, was unresponsive to medical intervention, and was declared deceased shortly after arriving in the ED. o Patient declared deceased 02/15/2022 after failure to develop sustained perfusing rhythm. o COD: cardiac arrest Patient had multiple admissions in the weeks prior to death. 12/22/2021-12/26/2021: fever/pneumonia/ARDS/sepsis. Negative for COVID-19 during this hospitalization. Received first COVID vaccine on day of discharge. 1/28/2022-2/7/2022: fever/UTI/pyelo/dental caries; Negative for COVID-19 during this hospitalization. Received second COVID vaccine on day of discharge. 2/15/2022: cardiac arrest and death; SARS CORONAVIRUS 2 RNA detected in NP swab (acute infection)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cardiac arrest
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- See below inborn error of metabolism GM gangliosidosis type 2, hx of ENT issues, Tonsillectomy/Adenoidectomy, failure to thrive, cognitive impairment, chronic diffuse cerebral volume loss, underweight, dysphagia, scoliosis, acute kidney injury in Sept 2021, chromosomal anomaly, developmental delay, urinary incontinence, anemia, chronic wounds and chronic lung disease
- Vorgeschichte
- inborn error of metabolism GM gangliosidosis type 2
- Andere Medikamente
- -
- Allergien
- None known
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 02.03.2022
- Impfdatum
- 28.01.2022
- Beginn
- 02.02.2022
- Tage bis Beginn
- 5,0
- Dosis
- 3
- Route/Site
- SYR / AR
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Cardiac arrest
Death
Symptomtext
Patient died on 2/2/2022, just 4-5 days after receiving his booster of the COVID-19 Injection from Pfizer. He was feeling just fine that day and had gone out for his daily walk. He had been seen by his cardiologist a week before (roughly) and was said to be doing well without any immediate concerns that would consider him at risk of a spontaneous cardiac event.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cardiac arrest
- Hospital-Tage
- -
- Labordaten
- The patient DIED of cardiac arrest after receiving the booster of the COVID-19 injection 4-5 days prior.
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- AFib, HBP, CAD, Chronic Hypernatremia, BPH
- Andere Medikamente
- Apixaban, Celecoxib, Cetirizine, Cholecalciferol, Metoprolol tartrate, Omega 3, pramipexole, rOpiniRole, rosuvastatin, torsemide
- Allergien
- NA
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 21.02.2022
- Impfdatum
- 03.02.2022
- Beginn
- 18.02.2022
- Tage bis Beginn
- 15,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Death
Symptomtext
Patient found deceased on 2.18.22. Law enforcement investigating death.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- CVA
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 15.02.2022
- Impfdatum
- 28.01.2022
- Beginn
- 30.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Angiogram
Chest X-ray
Dyspnoea
Pulmonary embolism
Ultrasound Doppler
Ultrasound pelvis
Symptomtext
Pt developed a pulmonary embolism, symptoms developed late in the evening of 1/30/2022. She went to Urgent care on the morning of 2/1/2022 for acute shortness of breath. Oxygen saturation was 82-84%. She was taken by ambulance to the ER and admitted for 7 days. She was diagnosed with acute pulmonary embolism.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary embolism
- Hospital-Tage
- 7,0
- Labordaten
- CTA - 2/1/2022 Xray, chest 2/1/2022 LE doppler - 2/2/2022 Pelvic US - 2/2/2022
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- HTN, elevated cholesterol, obesity, chronic sinusitis
- Andere Medikamente
- Lipitor 40 mg; Wllbutrin 300 mg, enalapril 20 mg, chlorthalidone 25 mg, mobic 15 mg
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 04.08.2023
- Impfdatum
- 15.03.2022
- Beginn
- 30.01.2023
- Tage bis Beginn
- 321,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Ischaemic stroke
Symptomtext
ACUTE STROKE DUE TO ISCHEMIA, UNSPECIFIED TYPE AND ARTERY
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ischaemic stroke
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 12.06.2023
- Impfdatum
- 28.01.2022
- Beginn
- 03.11.2022
- Tage bis Beginn
- 279,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Deep vein thrombosis
Symptomtext
PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ACUTE DVT OF RIGHT POPLITEAL VEIN
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Deep vein thrombosis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 06.06.2023
- Impfdatum
- 18.01.2022
- Beginn
- 30.03.2023
- Tage bis Beginn
- 436,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cirrhosis alcoholic
Facial paralysis
Facial paresis
Ischaemic stroke
Lacunar stroke
Symptomtext
LEFT FACIAL PALSY 3/30/2023 ALCOHOLIC CIRRHOSIS ACUTE LACUNAR STROKE, UNSPECIFIED TYPE AND ARTERY 3/29/2023 ALCOHOLIC CIRRHOSIS ACUTE STROKE DUE TO ISCHEMIA, UNSPECIFIED TYPE AND ARTERY 3/31/2023 ALCOHOLIC CIRRHOSIS LEFT FACIAL MUSCLE WEAKNESS 3/29/2023 ALCOHOLIC CIRRHOSIS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Facial paralysis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 22.12.2022
- Impfdatum
- 31.01.2022
- Beginn
- 16.12.2022
- Tage bis Beginn
- 319,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Acute respiratory distress syndrome
COVID-19
Hypotonia
Symptomtext
DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Acute respiratory disease due to COVID-19 virus [U07.1, J06.9] HOSPITAL COURSE: Patient is a 15 year old male with a history of Duchenne muscular dystrophy who was admitted after being diagnosed with COVID as well as influenza. He required close monitoring due to his chronic conditions that carry increased risk of morbidity including acute respiratory failure. Patient was started on both remdesivir as well as Tamiflu. He did not require supplemental O2 or pressure support while admitted. Of note, he is supposed to be on CPAP with sleep but does not tolerate it and so never wears it, and it was decided to not put him on while here. Because patient also has adrenal insufficiency, he was placed on stress dose steroids on admission until day prior to discharge. Nurse care manager worked with mom to help set up home nursing, physical therapy, and occupational therapy. His mom is also going to set up virtual learning because she is nervous having him exposed to germs at school. CONSULTS/RECOMMENDATIONS: None Physical Examination: GENERAL ASSESSMENT: active, alert, no acute distress, well hydrated, well nourished MOUTH: mucous membranes moist LUNGS: Respiratory effort normal, clear to auscultation, normal breath sounds bilaterally HEART: Regular rate and rhythm, normal S1/S2, no murmurs, normal pulses and capillary fill ABDOMEN: Normal bowel sounds, soft, nondistended, no mass, no organomegaly. NEURO: hypotonia 35 minutes were spent coordinating patient's discharge. More than 50% of this time was counseling family on the need for close follow-up with patient's primary care physician, review of medication risks and benefits as indicated, signs of worsening illness, and reasons to return to the primary care physician or Emergency Department for reevaluation. Patient's primary care physician's office was updated of discharge via message.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory distress syndrome
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Respiratory Snoring Obstructive sleep apnea, pediatric Allergic rhinitis Acute respiratory disease due to COVID-19 virus Influenza A Digestive Nausea and vomiting Diarrhea of presumed infectious origin Vitamin D deficiency Infectious/Inflammatory COVID-19 Hematologic Anemia Leukopenia Endocrine/Metabolic Dehydration Hypoxemia Steroid-induced adrenal suppression Other Restless sleeper ADHD (attention deficit hyperactivity disorder) Duchenne muscular dystrophy Complex care coordination Mixed anxiety and depressive disorder Transaminitis
- 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 carvedilol (COREG) 3.125 MG tablet cholecalciferol (VITAMIN D
- Allergien
- Penicillins Amoxicillin Sulfa Drugs
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 08.12.2022
- Impfdatum
- 08.02.2022
- Beginn
- 30.11.2022
- Tage bis Beginn
- 295,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Chest X-ray normal
Computerised tomogram thorax normal
Dyspnoea
Intensive care
Obstructive airways disorder
Post procedural haemorrhage
SARS-CoV-2 test positive
Symptomtext
Patient with 2 COVID vaccines who admitted with COVID complications and positive COVID PCR. Provider d/c note: "Hospital Course: Young man with prior traumatic tracheostomy who recently underwent tracheal reconstruction surgery and was recently placed on anticoagulation for superficial thrombosis presents with tracheostomy bleeding and dyspnea from partial airway obstruction. He was admitted to the PCU and treated with cool mist and nebulized therapy; his anticoagulation was stopped. He was found to have acute COVID; CXR and CT chest were negative for PE or respiratory disease. Given his airway threatening bleeding on anticoagulation for superficial thrombosis without evidence of deep thrombosis, it was recommended that his anticoagulation be stopped. Patient improved and requested discharge to home to follow up with ENT in the next several days."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Intensive care
- Hospital-Tage
- 2,0
- Labordaten
- COVID Detected PCR on 11/30/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Cardiovascular Essential hypertension Superficial thrombophlebitis of lower extremity Integumentary Hidradenitis suppurativa Psychological Anxiety and depression Respiratory Acute viral tracheitis Other Tracheostomy status History of suicide attempt Normocytic anemia Hx of hidradenitis suppurativa Pain at surgical site Iron deficiency anemia secondary to inadequate dietary iron intake Actinomyces infection Elevated alkaline phosphatase level Chronic abscess of areola Abscess of neck Bleeding from Tracheostomy Anticoagulated COVID-19 virus infection
- Andere Medikamente
- -
- Allergien
- Vancomycin
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 08.12.2022
- Impfdatum
- 08.02.2022
- Beginn
- 30.11.2022
- Tage bis Beginn
- 295,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Chest X-ray normal
Computerised tomogram thorax normal
Dyspnoea
Intensive care
Obstructive airways disorder
Post procedural haemorrhage
SARS-CoV-2 test positive
Symptomtext
Patient with 2 COVID vaccines who admitted with COVID complications and positive COVID PCR. Provider d/c note: "Hospital Course: Young man with prior traumatic tracheostomy who recently underwent tracheal reconstruction surgery and was recently placed on anticoagulation for superficial thrombosis presents with tracheostomy bleeding and dyspnea from partial airway obstruction. He was admitted to the PCU and treated with cool mist and nebulized therapy; his anticoagulation was stopped. He was found to have acute COVID; CXR and CT chest were negative for PE or respiratory disease. Given his airway threatening bleeding on anticoagulation for superficial thrombosis without evidence of deep thrombosis, it was recommended that his anticoagulation be stopped. Patient improved and requested discharge to home to follow up with ENT in the next several days."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Intensive care
- Hospital-Tage
- 2,0
- Labordaten
- COVID Detected PCR on 11/30/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Cardiovascular Essential hypertension Superficial thrombophlebitis of lower extremity Integumentary Hidradenitis suppurativa Psychological Anxiety and depression Respiratory Acute viral tracheitis Other Tracheostomy status History of suicide attempt Normocytic anemia Hx of hidradenitis suppurativa Pain at surgical site Iron deficiency anemia secondary to inadequate dietary iron intake Actinomyces infection Elevated alkaline phosphatase level Chronic abscess of areola Abscess of neck Bleeding from Tracheostomy Anticoagulated COVID-19 virus infection
- Andere Medikamente
- -
- Allergien
- Vancomycin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 04.09.2022
- Impfdatum
- 21.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Facial paralysis
Hypoaesthesia
Magnetic resonance imaging
Neurological symptom
Paralysis
Scan with contrast
Symptomtext
Patient 16 years old presented with facial and ear numbness/paralysis and received evaluation at facility. Physician referred patient to Hospital where she was prescribed Barium MRI for brain/vascular evaluation. No known causes were determined aside from recent vaccination and Neurology follow-up determined no known existing conditions were determined.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Facial paralysis
- Hospital-Tage
- -
- Labordaten
- Barium MRI. Persistent neuro-behavior has been identified but no life-threatening so no immediate care plan.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Facial and ear numbness / paralysis on left side. Verified/treated by Hospital
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 14.05.2022
- Impfdatum
- 20.01.2022
- Beginn
- 22.04.2022
- Tage bis Beginn
- 92,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: ja
ER: unbekannt
Erholt: unbekannt
Angiogram cerebral normal
Angiogram normal
Biopsy brain
CSF pressure increased
Computerised tomogram abdomen normal
Computerised tomogram head abnormal
Computerised tomogram thorax normal
Craniotomy
Culture
Dizziness
Ear pain
Facial paralysis
Leukoencephalopathy
Lumbar puncture abnormal
Magnetic resonance imaging head abnormal
Magnetic resonance imaging spinal normal
Nausea
Spinal cord drainage
Symptomtext
Patient was complaining of left ear pain, nausea, vomiting and dizziness. Since admission to Hospital, patient has had a lumbar drain placed and she has experienced now right Cranial Nerve VII and left Cranial Nerve VI palsy. She has been hospitalized for 22 days so far. Recently on 5/13 Patient had a right frontal craniotomy for open bx and clx. Now recommending IVIG.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Facial paralysis
- Hospital-Tage
- 22,0
- Labordaten
- CT head: nonspecific hypodensity throughout the cerebral white matter - most prominent in the frontal lobes and temperal lobes. CTA brain: normal CTA neck: normal MRI brain: There are diffuse symmetric T2 FLAIR hyperintensities visualized involving the periventricular and subcortical white matter with sparing of the subcortical U fibers. There is also diffuse white matter signal abnormality noted within the bilateral temporal lobes, left greater than right. There has been interval progression of the diffuse white matter signal when compared to the MRI dated 11/06/2021. MRV brain: normal Lumbar Puncture: elevated opening pressure measuring greater than 73 cm of CSF. CT chest/abd/pelvis: negative Lumbar Puncture #2: opening pressure greater than 55cm of water. Lumbar drain placement. Lumbar Drain inserted MRI Brain: unchanged from 4/23/2022 MR cervical/thoracic/lumbar spine: negative. VR cerebral angiogram: no significant intracranial vascular irregularity to suggest vasculitis. NO evidence of AVM or dural fistula. MR brain: no definitive cranial nerve enhancement abnormality. Leukoencephalopathy stable. MR CSF flow study: normal craniocaudal flow of CSF through the cerebral aqueduct and around foramen magnum.
- Aktuelle Erkrankungen
- HIV and hypertension
- Vorgeschichte
- HIV and hypertension
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 10.05.2022
- Impfdatum
- 18.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Back pain
Dizziness
Gait inability
Musculoskeletal stiffness
Neck pain
Pain in extremity
Peripheral swelling
Presyncope
Walking aid user
Symptomtext
I received the vaccine on the 18th of April. I started to have stiffness throughout my body around April 23, 2022. It got to the point where I was unable to walk. My neck, knees, back and shoulder hurt. I am just getting to where I can step down on my right foot, but it is still really swollen. I received my vaccine in the left arm. The doctor gave me a shot of steroids and a prednisone pack. I am slowly getting better. I called my doctor yesterday because my foot was so sore. I am going in today to have blood work completed. I am currently using a walker to get around. I tried to make it to my vehicle one day and when I got in, I felt like I was going to pass out. I was lightheaded and in a lot of pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Kidney Failure Heart Stent Blood Pressure Pulmonary Embolism
- Andere Medikamente
- Alopurinol Trazadone Dapsone Tamsulosin Clonazepam Tizanidine Metoprolol Warfarin Lovastatin Furosemide Metformin Doxycycline Vitamin D2 Symbicort Albuterol
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 21.04.2022
- Impfdatum
- 07.04.2022
- Beginn
- 10.04.2022
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Anticoagulant therapy
Deep vein thrombosis
Electrocardiogram
Pain
Peripheral swelling
Ultrasound Doppler abnormal
Symptomtext
Patient went to ER on 4/12/2022 with swelling in RLE for two days. Pfizer vaccine administered on 4/7/2022, developed symptoms on 4/10/2022. No prior history of DVT, no recent trauma or no recent trips. Doppler showed (R) leg DVT, patient started on Eliquis from ER. Office visit 4/20/2022 with PCP, continues to have swelling and some pain, relieved with Tylenol. Denies any SOB or chest pain. Patient provided prescription for Xarelto 20 mg, insurance will not cover Eliquis. Discussion with patient to follow up with Dr. (vascular), keep already established appointment for May. Patient also instructed to report to VSAFE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Deep vein thrombosis
- Hospital-Tage
- -
- Labordaten
- Ultrasound lower extremity venous duplex (R), EKG 12 lead
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- hypertension, Type 2 DM, Gout, Hyperlipidemia, CAD, ED, OAS, Vitamin D deficiency, Chronic Kidney Disease, CHF, OA
- Andere Medikamente
- ASA, Bumetanide, Cetirizine, Colchicine, Vitamin D, Spironolactone, Sotalol, Entresto, metformin, Amaryl
- Allergien
- iodine, wasp
- Vorherige Impfungen
- -
- Staat
- ND
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 12.04.2022
- Impfdatum
- 26.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Presyncope
Symptomtext
Patient presented to the ED on 1/28/22 for near syncope. Patient presented to the ED on 2/2/22 for syncope. These visits are within 6 weeks of receiving covid vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 21.03.2022
- Impfdatum
- 18.02.2022
- Beginn
- 04.03.2022
- Tage bis Beginn
- 14,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Bell's palsy
Facial paralysis
Symptomtext
Patient developed left sided Bell's Palsy on 3/4/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bell's palsy
- Hospital-Tage
- -
- Labordaten
- Patient was seen at Hospital emergency department on 3/4/2022 for left-sided facial droop without other neurological deficits. She did not have labs or imaging done. She was diagnosed with Bell's palsy. Was prescribed prednisone and valacyclovir.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Coronary artery disease; methamphetamine induced cardiomyopathy; hypertension; history CVA; GERD; hyperlipidemia; general anxiety disorder; patent foramen ovale; prediabetes; iron deficiency; and recent diagnosis of middle cerebral artery aneurysm.
- Andere Medikamente
- Albuterol HFA; Atorvastatin;Benzonatate;Buspirone;Carvedilol;Losartan; Omeprazole
- Allergien
- Penicillin-- rash; Lisinopril-- cough.
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 15.03.2022
- Impfdatum
- 11.03.2022
- Beginn
- 15.03.2022
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest X-ray
Chest discomfort
Cough
Dyspnoea
Headache
Hypoxia
Influenza virus test negative
Nausea
Oropharyngeal pain
Pain
Pleurisy
Respiratory distress
SARS-CoV-2 test negative
Upper respiratory tract infection
Symptomtext
21-year-old male presents to emergency department with complaints of left-sided chest discomfort since last night. Complains of a dry cough as well as nausea, sore throat and a mild frontal headache. He denies any fevers or chills. He is not taking any medications for cough. States that he has been drinking Pedialyte. Has not taken any medications for pain. Describes the chest discomfort as a dull ache but tolerable. He denies any known exposure to Covid. States that he took 2 at home Covid test this morning which were negative. He denies any vomiting 1. Acute URI J06.9 Afebrile, nontoxic-appearing. Respiratory distress or hypoxia noted. Patient does have a dry cough. No wheezing or adventitious breath sounds noted on examination. Patient describes some mild left lower chest wall discomfort. Triplex Covid/flu test performed, negative for Covid and influenza. Suspect viral URI. Discussed supportive measures at length with the patient. Instructed the patient that he may take over-the-counter Mucinex or Robitussin as needed for cough. May take over-the-counter Tylenol or ibuprofen as needed for pain. Advised to return back to the emergency department for fever to the 101, coughing up blood or any new or worsening symptoms. Patient verbalized understanding and agreed to plan of care. 2. Pleurisy R09.1 Orders: XR Chest 1 View Portable, 03/15/22 9:50:00, Routine, 03/15/22 9:50:00, SOB, No, Transport Mode: Walk, , Yes, , No, Rad Type
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Respiratory distress
- Hospital-Tage
- -
- Labordaten
- CXR
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- No home medications
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 12.03.2022
- Impfdatum
- 24.01.2022
- Beginn
- 09.02.2022
- Tage bis Beginn
- 16,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bell's palsy
Facial paralysis
Swelling face
Symptomtext
Bell's palsy: patient woke up with one-side of face droopy and swollen. Called doctor. Rule-out stroke. They determined it was Bell's palsy. Given a steroid dose pack and Valtrex.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bell's palsy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None known
- Vorgeschichte
- Diabetes, stroke, heart attack
- Andere Medikamente
- Cialis, Simvastatin, Omeprazole, Furosemide, Carvedilol, Spironolactone, Metformin, Lexapro, Entresto
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 09.03.2022
- Impfdatum
- 04.03.2022
- Beginn
- 04.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Electric shock sensation
Hypoaesthesia
Paraesthesia
Radiculopathy
Symptomtext
Felt like a current of electricity from Left elbow down to Left wrist and numbness in same location plus also from Left knee down to Left foot; went to ER per advise of health center; diagnosed with radiculopathy affecting upper extremity and paresthesia of Left upper and lower extremity; has been taking ibuprofen and acetaminophen - symptoms lasted 48 hours then resolved.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Electric shock sensation
- Hospital-Tage
- -
- Labordaten
- Physical exam by medical provider
- Aktuelle Erkrankungen
- Scalp tingling/numbness of unknown origin
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- Penicillin (rash)
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 08.03.2022
- Impfdatum
- 19.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bell's palsy
Facial paralysis
Symptomtext
Patient reports received vaccine 1/19/2022 approximately at 3:00pm and on 1/20/2022 approximately at noon- had developed facial drooping/bell's palsy
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bell's palsy
- Hospital-Tage
- -
- Labordaten
- Unknonw
- Aktuelle Erkrankungen
- Covid 9/2021
- Vorgeschichte
- None
- Andere Medikamente
- unknown
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 24.02.2022
- Impfdatum
- 19.02.2022
- Beginn
- 21.02.2022
- Tage bis Beginn
- 2,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal distension
Diarrhoea
Electrocardiogram ST segment elevation
Myocarditis
Rash maculo-papular
Tachycardia
Troponin increased
Vomiting
Symptomtext
Vomiting and diarrhea for the past 7 days. NBNB emesis (multiples times) and watery diarrhea (>5 times per day). Abdominal distension and a maculopapular rash (non-pruritic or painful) in the back and torso since 2 days ago.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocarditis
- Hospital-Tage
- -
- Labordaten
- Tachycardia (initial HR 140s) and ST elevations on ECG, found to have rising troponin, consistent with a diagnosis of myocarditis.
- Aktuelle Erkrankungen
- SLE
- Vorgeschichte
- SLE
- Andere Medikamente
- Mycophenolate, Plaquenil and Prednisone
- Allergien
- Acetaminophen and Albuterol
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 13.02.2022
- Impfdatum
- 05.01.2022
- Beginn
- 07.02.2022
- Tage bis Beginn
- 33,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injected limb mobility decreased
Injection site induration
Injection site reaction
Injection site swelling
Pain
Thrombosis
Symptomtext
Not sure if this qualifies under vaers but just trying to ensure he is alright and unsure to see if he needs medical attention. However, we are certain and concerned with a swollen clot at the area of vaccination ( lateral side of Left Arm below shoulder) , limiting his limb movement such as ability to lift, move, rotate, pain to touch. it's hard in the spot. We are gonna wait for 2 more days before visiting primary care physician.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Thrombosis
- Hospital-Tage
- -
- Labordaten
- none taken, this reporting is just raising a concern and precautionary..
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- diabetes, blood thinner.
- Andere Medikamente
- Blood thinner, diabetes medication.
- Allergien
- none yet
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 11.02.2022
- Impfdatum
- 20.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Generalised tonic-clonic seizure
Seizure
Symptomtext
PATIENT HAD GENERALIZED TONIC CLONIC SEIZURES 36 HOURS AFTER VACCINATION
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Generalised tonic-clonic seizure
- Hospital-Tage
- -
- Labordaten
- EEG OBTAINED AFTER HIS FIRST EPISODE OF SEIZURE WAS NORMAL. NEUROLOGY CONSULT WAS REQUESTED AND PATIENT WAS DIAGNOSED WITH SEIZURE DISORDER DUE TO THE REPEATED NATURE OF SEIZURE. AN ADVERSE REACTION TO THE VACCINE COULD NOT BE RULED OUT HOWEVER. PATIENT WAS NOT STARTED ON ANTICONVULSANTS AT THE TIME BUT WAS STARTED ON KEPPRA AFTER A THIRD SEIZURE 1/31/2022
- Aktuelle Erkrankungen
- NONE. PATIENT WAS SEEN IN THE ED FOR FIRST EPISODE OF SEIZURE 3 DAYS AFTER GETTING HIS FIRST COVID VACCINE; PFIZER BIONTECH. PATIENT DID NOT HAVE SEIZURES AFTER THE SECOND DOSE.
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 11.02.2022
- Impfdatum
- 11.02.2022
- Beginn
- 11.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Syncope
Symptomtext
She let the immunizer know as she sat down in the lobby, she felt lightheaded. The pharmacist came out to check on her. She fainted and he caught her before she could hit the floor. The pharmacist and another staff member helped her to sit her upright in the chair. She finally came to. I ran to get her room temp water. She was able to call her dad to come pick her up instead of driving. We all stayed with her until she felt better, and her dad arrived.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Day before may have taken Aspirin.
- Allergien
- Amoxicillin
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 06.02.2022
- Impfdatum
- 13.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 6,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Angiogram cerebral normal
Arteriogram carotid normal
Asthenia
CSF protein increased
Computerised tomogram head normal
Dizziness
Dysphagia
Eating disorder
Endotracheal intubation
Eyelid ptosis
General physical health deterioration
Headache
Immunoglobulin therapy
Intensive care
Lumbar puncture abnormal
Magnetic resonance imaging normal
Neck pain
Obstructive airways disorder
Symptomtext
Patient vaccinated with 2nd dose of Pfizer. 6 days later patient began having dizziness, blurred vision, headache, neck pain, ptosis, and difficulty eating, swallowing and speaking. CT head 1/23 negative. CTA head/neck 1/23 negative. MRI 2/5 negative. Lumbar puncture found to contain protein in CSF. Was originally worked up for AIDP and started on IVIG. After 3 infusions, no improvement. Patient then on 2/5 began worsening and was unable to swallow at all and unable to protect his airway. He was intubated in Neuro Critical Care Unit. Now being worked up for Guillian Barre Syndrome due to increased bulbar weakness. 4 more doses of IVIG will be infused.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Intensive care
- Hospital-Tage
- 13,0
- Labordaten
- -
- Aktuelle Erkrankungen
- HTN
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Shellfish
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 10,0
- Geschlecht
- F
- Eingang
- 04.02.2022
- Impfdatum
- 14.01.2022
- Beginn
- 31.01.2022
- Tage bis Beginn
- 17,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Loss of consciousness
Symptomtext
Frequent HA's and passed out 1/31/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Ibuprofen
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 01.02.2022
- Impfdatum
- 18.01.2022
- Beginn
- 25.01.2022
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Brain natriuretic peptide increased
Cardiac failure
Cardiogenic shock
Echocardiogram abnormal
Endotracheal intubation
Hepatic enzyme increased
Multiple organ dysfunction syndrome
Myocarditis
Renal failure
Troponin increased
Symptomtext
Pt developed fulminant myocarditis. No other etiology other than recent booster vaccine has been identified. Appears to be improving at this time but is still requiring inotropic support and is intubated
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cardiogenic shock
- Hospital-Tage
- 3,0
- Labordaten
- Marked elevation in troponins, BNP, echo with heart failure, and other organ system dysfunction likely related to cardiogenic shock including liver enz elevations and renal failure
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Overweight
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 01.02.2022
- Impfdatum
- 19.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Loss of consciousness
Symptomtext
Approximately 5 minutes after receiving the vaccine, the client called out for help. He reported feeling like he was going to faint. He then did lose consciousness while seated in the chair. He remained upright with minimal assistance and regained consciousness after approximately 30 seconds. No injury to the client. He remained in clinic for another 10 minutes, drank juice and water, and left clinic independently.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- none reported
- Vorherige Impfungen
- Fainted after shots/blood draws in the past.
- Staat
- NM
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 31.01.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Presyncope
Symptomtext
Pt. experienced vasovagal response 10 minutes post vaccine administration. Recovered and had 2nd episode approximately 15 minute later.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- none reported
- Andere Medikamente
- not known
- Allergien
- none reported
- Vorherige Impfungen
- Pt. states post HPV vaccine vasovagal episode
- Staat
- AL
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 29.01.2022
- Impfdatum
- 29.01.2022
- Beginn
- 29.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Drooling
Paraesthesia
Seizure like phenomena
Symptomtext
Patient was given a booster dose of Pfizer Covid-19 vaccine in the the left arm. Patient was seated and responsive upon initial administration of vaccine. Within 2 to 3 minutes of administration, patient began to have seizure like symptoms with noticeable saliva coming out of mouth. Patient was unresponsive for roughly 1 to 2 minutes while the healthcare team stabilized the patient. Patient regained consciousness after 2 minutes and described feeling tingling all over their body. Patient's vital signs were checked. Their blood pressure was 114/78 mmHg and heart rate was 77 bpm. There were no signs of anaphylaxis or rash noted. Patient was given some water and monitored for several minutes. Patient was feeling better after about 20 minutes. They were able to walk around unassisted after roughly 30 minutes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure like phenomena
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No known illnesses
- Vorgeschichte
- No known chronic health conditions
- Andere Medikamente
- Unknown
- Allergien
- None known allergies
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 28.01.2022
- Impfdatum
- 19.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Condition aggravated
Seizure
Symptomtext
generalized seizure, prolonged course, paramedics called, treated with Lorazepam
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- none currently, evaluated by paramedics after seizures resolved
- Aktuelle Erkrankungen
- complex partial seizures, weekly
- Vorgeschichte
- epilepsy
- Andere Medikamente
- Levetiracetam, Phenobarbital, Lamotrigine, Oxcarbazepine, Lorazepam
- Allergien
- Zonisamide
- Vorherige Impfungen
- fever, swollen lymph nodes, joint pain, Pfizer Covid-19, primary series
- Staat
- IL
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 27.01.2022
- Impfdatum
- 19.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Activated partial thromboplastin time shortened
Blood creatine phosphokinase normal
Blood lactic acid
C-reactive protein decreased
Chest X-ray normal
Computerised tomogram head normal
Diarrhoea
Drug screen negative
Dysarthria
Electrocardiogram normal
Full blood count normal
Gait inability
Headache
Human chorionic gonadotropin negative
Hypoaesthesia
Influenza virus test negative
International normalised ratio decreased
Metabolic function test normal
Symptomtext
One day following administration of vaccine developed pruritic, erythematous rash over upper chest, upper back, upper arms, as well as body aches, diarrhea, nausea and headache. On days 2-4 following vaccination, myalgias, nausea, and diarrhea resolved. Rash continued to be erythematous and pruritic. Intermittent headaches, becoming severe on day 4 with syncopal event, dysarthria, bilateral lower extremity numbness in non-dermatomal pattern, bilateral calf pain, and bilateral quadriceps & hamstring weakness resulting in inability to ambulate.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- 3,0
- Labordaten
- Head CT without contrast 1/24/22: unremarkable Chest XR 1/24/22: unremarkable EKG 1/24/22: normal sinus rhythm, intervals within normal ranges Orthostatic vitals x2 (1/24/22, 1/26/22): normal CMP 1/24/22: within normal limits CBC 1/24/22: within normal limits CRP 1/24/22: 0.0 Lactic acid 1/24/22: 0.8 PT 1/24/22: 10.1 (wnl) INR 1/24/22: 1.0 (wnl) APTT 1/24/22 : 24.5 (wnl) Urine drug screen 1/24/22: wnl RSV/Flu/COVID PCR 1/24/22: negative Procal 1/24/22: <0.07 HCG 1/24/22: negative Creatinine kinase 1/25/22: 67 IU/L (wnl) NT proBNP 1/25/22: 29.98 pg/mL (wnl) troponin 1/25/22: 0.008 ng/mL (wnl) ESR 1/26/22: 12 mm/hr (wnl) CRP 1/26/22: <0.3 mg/dL (wnl)
- Aktuelle Erkrankungen
- Infection with SARS-CoV-2 with positive test on 1/05/2022.
- Vorgeschichte
- none. Previously healthy
- Andere Medikamente
- none
- Allergien
- no known allergies
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 26.01.2022
- Impfdatum
- 26.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Amnesia
Chills
Eye movement disorder
Loss of consciousness
Seizure
Symptomtext
Before administering vaccine, pt was nervous and taking deep breaths prior to administration. After administering vaccine, patient was experiencing chills. Pt remained seated for about 4 minutes after administering vaccine. Pt then stood and walked over to the waiting area after vaccine. As soon as pt sat down, pt began to seize. Lasting about 35-45 seconds, pt has no recollection of what happened. Eyes rolled back, no conciousness. Immediately called emergency number and EMS arrived shortly. Pt vitals were checked by EMS and highly advised to check into hopsital as it is pts first seiuzure.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Escitalopram 20mg, Adderall 30mg, zaleplon 10mg
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 26.01.2022
- Impfdatum
- 25.01.2022
- Beginn
- 25.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal pain
Confusional state
Dyspnoea
Flushing
Hyperhidrosis
Pallor
Seizure
Syncope
Tremor
Unresponsive to stimuli
Symptomtext
Systemic: Allergic: Difficulty Breathing-Medium, Systemic: Abdominal Pain-Medium, Systemic: Confusion-Medium, Systemic: Fainting / Unresponsive-Medium, Systemic: Flushed / Sweating-Medium, Systemic: Seizure-Medium, Systemic: Shakiness-Medium, Additional Details: patient developed symptoms about 5 minutes after receiving vaccine. She started looking very pale and looked like she was about to faint. pt started having seizures soon after. paramedics were called.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VT
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 25.01.2022
- Impfdatum
- 24.01.2022
- Beginn
- 25.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Head injury
Loss of consciousness
Symptomtext
When I woke up the morning after get my third dose, I went to urinate and passed out while I was washing my hands. I hit my head on the tile floor. I lost consciousness for a few seconds.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- None yet.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 22.01.2022
- Impfdatum
- 18.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Electrocardiogram
Myocarditis
Troponin increased
Symptomtext
Myocarditis. Treatment and outcome have yet to be determined at the time of this note.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocarditis
- Hospital-Tage
- -
- Labordaten
- EKG, positive troponin 1/21/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Gender dysphoria
- Andere Medikamente
- Estradiol, spironolactone, sertraline
- Allergien
- Augmentin
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 21.01.2022
- 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: ja
Dizziness
Presyncope
Symptomtext
Approximately 8-10 minutes after vaccine was given, patient became very dizzy, light-headed and nearly passed out. He was taken to clinic exam room and laid down on an exam table. Cool compresses applied and water given. Patient had no food for almost 8 hours prior to the vaccine. Patient recovered in less than 30 minutes and felt fine and discharged to home with parent.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- ADHD
- Andere Medikamente
- Aderall XR, Catapres
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 20.01.2022
- Impfdatum
- 15.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Brain natriuretic peptide normal
Chest discomfort
Chest pain
Echocardiogram normal
Electrocardiogram ST segment elevation
Myocarditis
Pain
Sinus bradycardia
Troponin I increased
Troponin increased
Symptomtext
chest pain in the right upper chest that felt pressure-like without radiation. Was persistent through the night at around a pain of 5/10. This started 2 days after COVID-19 vaccine booster. Patient had elevated troponin and anterior and inferior ST segment elevations on EKG. He was admitted to the hospital for treatment of COVID-19 vaccine associated myocarditis
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocarditis
- Hospital-Tage
- 2,0
- Labordaten
- Troponin:Results as of 1/20/2022 12:21 1/18/2022 13:05 Troponin I, High Sensitivity: 3,706 (HH) 1/18/2022 19:56 Troponin I, High Sensitivity: 2,687 (HH) 1/19/2022 04:30 Troponin I, High Sensitivity: 4,416 (HH) 1/19/2022 12:44 B-TYPE NATRIURETIC PEPTIDE: 19 Troponin I, High Sensitivity: 3,766 (HH) 1/20/2022 06:00 Troponin I, High Sensitivity: 2,943 (HH) Echocardiogram: normal on 1/18/2021 EKG 1/18/2021: "Normal sinus rhythm ST elevation in Anterolateral leads ST elevation in Inferior leads No previous ECGs available EKG 1/19/2021:Sinus bradycardia ST elevation in Inferolateral leads
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- multivitamin vitamin C
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 20.01.2022
- Impfdatum
- 20.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Head injury
Syncope
Symptomtext
pt fainted within 5 mins after shot. Head hit the floor. Instucted pt to lay down and feet up at least 15-30 mins or until feeling better. Pt can sit up after 20 mins and requested protein bar bc he was in the middle of intermetten fasting (no eating for 18 hours and eating within the 6 hours). Blood pressure 141/87 with pulse 75. Pt felt fine , forehead not hurting unless touch the area .
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- no
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 19.01.2022
- Impfdatum
- 11.01.2021
- Beginn
- 11.01.2022
- Tage bis Beginn
- 365,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anaphylactic reaction
Dizziness
Fall
Hypotension
Seizure
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Allergic: Anaphylaxis-Medium, Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Severe, Systemic: Hypotension-Medium, Systemic: Seizure-Mild, Additional Details: Per Nurse: Patient was given Pfizer and flu shot two minutes later. Fifteen seconds later patient fell. He stood up and sat down but fainted a second time. Nurse stated she thought patient may have had seizure. BP was 84/89. Was given Epipen. Paramedics soon arrived. Patient stated he felt faint and was taken to Hospital on gurney. Called mother and she states patient has receovered and is being monitored by MD. Mother stated MD stated that patient was doing well.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anaphylactic reaction
- Hospital-Tage
- 1,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 18.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Loss of consciousness
Tremor
Symptomtext
Patient passed out and was shaking. She regained consciousness. The paramedics were called and monitored her. She was able to leave on her own.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 18.01.2022
- Impfdatum
- 11.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Aspartate aminotransferase increased
Blood bilirubin increased
Blood chloride decreased
Blood creatine phosphokinase MB increased
Blood creatine phosphokinase increased
Blood creatinine increased
Blood glucose normal
Blood lactic acid increased
Blood potassium decreased
Blood smear test abnormal
Blood sodium decreased
Blood urea increased
Brain natriuretic peptide increased
C-reactive protein increased
Carbon dioxide increased
Computerised tomogram head abnormal
Condition aggravated
Confusional state
Symptomtext
Patient received booster Covid-19 vaccine on 1/11/2022. Patient has no prior history of illness which we are aware of. Patient presented to the Emergency Department complaining of a headache since 9/2021. On this day states the headache is worse and not going away. Some nausea and vomiting with shortness of breath. Patient was admitted to the hospital on 1/14/2022 with a hypertensive crisis of 240/120. Patient with BMI of 33. Patient was admitted to the ICU and placed on Cardene drip. He was also given labetalol 100 mg every 8 hours. His blood pressure came down to a systolic in the 160s. He was seen the next morning by nephrology, hematology, and attending physician. He was still somewhat confused. His platelet count was 117,000. He did have an MRI of his brain which did not show any bleed but showed changes consistent with severe hypertension. It was found out that the patient received the COVID-19 vaccine about 5 days previous to his admission. This may be a reaction to the vaccine. He is thought to have TTP. His blood smear was seen by the hematologist and showed evidence of schistocytes and helmet cells consistent with TTP. Patient was transferred to a tertiary care facility for possible plasmapheresis. Patient was transferred on a Cardene drip. He has been given 2 units of FFP and steroids per recommendations from hematology.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Intensive care
- Hospital-Tage
- 1,0
- Labordaten
- CT Head - Scattered areas of subcortical white matter hypoattenuation involving both cerebral hemispheres, nonspecific Renal Ultrasound - Hyperechogenic renal cortex parenchyma bilaterally. This pattern suggests chronic medical renal disease. There is no hydronephrosis or advanced renal atrophy. 5 mm non-obstructing right renal calculus. Labs - WBC 11, RBC 3.44, Hgb 9.4, Hct 27.8, Schistocytes 1+, Na 131, K 2.5, Cl 89, Co2 31, BUN 77, Creat 9.9, Gluc 146, Bili 2.2, AST 107, CK 5468, CKMB 13.3, Trop 1.320, BNP 51,000, Lactate 2359, CRP 4.1
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- ACETAMINOPHEN 500MG PRN
- Allergien
- ZIPRASIDONE
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 15.01.2022
- Impfdatum
- 15.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Feeling cold
Nausea
Syncope
Tremor
Symptomtext
The patient received her first Pfizer vaccine. She left the pharmacy right after the shot and was at a yard sale. She started to feel dizzy and very cold within 10 minute of getting the vaccination. She had a yellowish color. She passed out for an unknown time. Helpers gave her water and drove her home. The patient called me from the yard sale and described what happened, she was still dizzy and shaking. I checked in on her 3 hours later. She was still feeling very cold, light headed and a little nauseous.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 14.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Contusion
Fall
Loss of consciousness
Symptomtext
Patient noted falling off from chair 5 minutes after he sat down in the observation area. loss of consciousness noted for about 30 seconds. Assistance provided immediately. Vital signs initiated (please refer to VS below). Bruise noted on right forehead. Patient verbalized, "I saw everything black, it's possibly from my anxiety." Denied chest pain, shortness of breath, dizziness. Patient asked to be sat up on the chair and then loss consciousness for second time at around 1607. EMS was activated. Patient regained consciousness after a few seconds but again lost consciousness at 1609. Patient remained on the floor, was positioned to the side. Patient regained consciousness in a few seconds. EMS arrived at site, assessed patient. Patient reported feeling "fine." Patient was transported out of observation site via wheelchair to the ambulance. Patient was transported to hospital by EMS. Vital Signs: Time: 1607, P: 38, R: was not able to obtain, B/P: was not able to obtain, O2: 99% Time: 1607, P: 56, R: 18, B/P: 100/60, O2: 99% Time: 1614, P: 90, R: 20, B/P: 120/82, O2: 99% Time: 1631, P: 86, R:16, B/P: 120/62, O2: 99%
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE REPORTED
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 10.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Seizure
Symptomtext
Per patient, she had a 15 minute seizure about 13 hours after the booster pfizer shot. She had the shot between 9:30-9:50am that same day. She said it only occurred the one time and now she feels ok.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Codeine, epinephrine
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 11.01.2022
- Impfdatum
- 11.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood glucose normal
Heart rate increased
Hypotension
Loss of consciousness
Seizure
Symptomtext
Patient was counseled before vaccine. Patient had not previously had any reaction to any other vaccine. Patient was nervous as it had been years since receiving a vaccine. Patient received vaccine and felt okay right afterwards. Was instructed to wait 15 minutes. As patient was in observation area talking with attendant he passed out. He hit the floor and had a seizure that lasted 1 minute. Pharmacist and store manager responded and 911 was called. Patient came to but kept going in a out of consciousness. While waiting on EMS a cold rag was placed on his neck and it seemed to help. EMS arrived and patient has low blood pressure and fast pulse. Blood sugar was normal. Patient declined ambulance ride to hospital . Patient parent picked him up. Store manager filled out an accident report.
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
- 16,0
- Geschlecht
- F
- Eingang
- 11.01.2022
- Impfdatum
- 11.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Nausea
Syncope
Vomiting
Symptomtext
After receiving vaccine, pt began to get light headed and stated "I fainted." Pt was placed in a supine position, with legs elevated. Ice packs placed under neck and legs. Pt proceeded to vomit 4 times in the span of 15 minutes. Pt stated after vaccine they did not eat anything prior to vaccine and are afraid of needles. Pt still dizzy and nauseous when legal guardian, against medical advice, removed her from the vaccination site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- Impfdatum
- 08.01.2022
- Beginn
- 09.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fall
Head injury
Hyperpyrexia
Pain in extremity
Syncope
Symptomtext
Patient woke up the next morning and said her arm really hurt. She went to the bathroom and then fainted, fell to the ground, and hit her head. She had a very, very high fever. I treated the fever with Tylenol. I noted she was menstruating.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 24.03.2023
- Impfdatum
- 15.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Chest discomfort
Dizziness
Dyspnoea
Heart rate
Heart rate increased
Palpitations
Tinnitus
Symptomtext
A even more rapid and pronounced pounding in my chest and ears, accompanied by cold air in the center of my chest; A even more rapid and pronounced pounding in my chest and ears, accompanied by cold air in the center of my chest; A even more rapid and pronounced pounding in my chest and ears, accompanied by cold air in the center of my chest; My heart rate which was normally mid 60's/minute would suddenly become 80-100/minute; Shortness of breath; Periodic dizziness; Also I began having a consistently harder & harder time climbing the 17 stairs to my condo without stopping for a break; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 73-year-old female patient received BNT162b2 (BNT162B2), on 15Apr2022 as dose 4 (booster), single (Lot number: FJ5682) at the age of 72 years for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: BNT162b2 (DOSE 1, SINGLE, Lot number: EL9269), administration date: 13Feb2021, when the patient was 71-year-old, for COVID-19 immunization; BNT162b2 (DOSE 2, SINGLE, Lot number: EN6198), administration date: 06Mar2021, when the patient was 71-year-old, for COVID-19 immunization, reaction(s): "following my second initial COVID shot, I have developed atrial fib and have been put on Eliquis", "Rapid, thumping pulse in the back of my neck at the base of the skull", "Alternating episodes of rapid heartbeat in my chest and throat that were so strong, I felt them without using my hand or an instrument", "A lump in my left breast that was the shape and size of a new erase on a #2 pencil. Even though it had gone away before the scan, the local breast center said it probably was a result of my second COVID shot"; BNT162b2 (DOSE 3 (BOOSTER), SINGLE, Lot number: FE3590), administration date: 04Oct2021, when the patient was 72-year-old, for COVID-19 immunization, reaction(s): "By early 2022, the thumping pulse in the back of my neck became less and less frequent". The following information was reported: PALPITATIONS (non-serious), TINNITUS (non-serious), CHEST DISCOMFORT (non-serious) all with onset 2022, outcome "unknown" and all described as "A even more rapid and pronounced pounding in my chest and ears, accompanied by cold air in the center of my chest"; ASTHENIA (non-serious) with onset 2022, outcome "unknown", described as "Also I began having a consistently harder & harder time climbing the 17 stairs to my condo without stopping for a break"; HEART RATE INCREASED (non-serious) with onset 2022, outcome "unknown", described as "My heart rate which was normally mid 60's/minute would suddenly become 80-100/minute"; DIZZINESS (non-serious) with onset 2022, outcome "unknown", described as "Periodic dizziness"; DYSPNOEA (non-serious) with onset 2022, outcome "unknown", described as "Shortness of breath". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: By mid-fall 2022 after taking both boosters, patient's symptoms changed to an even more rapid and pronounced pounding in chest and ears, accompanied by cold air in the center of chest. The patient's heart rate which was normally mid 60's/minute suddenly become 80-100/minute. Patient had periodic dizziness and shortness of breath, but it was not constant. The only consistent trigger was drinking ice water. Also, patient began having a consistently harder and harder time climbing the 17 stairs to condo without stopping for a break. For the last 20 plus years, patient had never even been winded when rapidly climbing them. At this point, patient had to lie down afterwards.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300122458 same patient and different drug dose/events;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Test Name: Heart rate; Result Unstructured Data: Test Result:60's/minute; Comments: normally mid 60's/minute; Test Name: Heart rate; Result Unstructured Data: Test Result:80-100/minute; Comments: suddenly become 80-100/minute
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 20.03.2023
- Impfdatum
- 24.01.2022
- Beginn
- 16.03.2023
- Tage bis Beginn
- 416,0
- Dosis
- 3
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Chronic obstructive pulmonary disease
Condition aggravated
Hypoxia
SARS-CoV-2 test positive
Symptomtext
Brief Summary of Hospital Stay: 80-year-old female with a history of chronic obstructive pulmonary disease, HTN, T2DM who was admitted for acute hypoxia 2/2 to COVID-19 infection and likely COPD exacerbation. She was given a course of Remdesivir for 2 days, Ceftriaxone, and Prednisone. She was feeling better at time of discharge. She was sent home on 2L of oxygen. She was discharged to finish 2 more days of antibiotics with Cefdinir, and 7 more days of Prednisone. She was found to have soft BP's inpatient and was told to hold HCTZ until she sees PCP. She was discharged on home oxygen. She needs to follow with PCP for management of care after inpatient stay.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- 3,0
- Labordaten
- Positive COVID PCR test 3/16/23
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 31.01.2023
- Impfdatum
- 28.01.2022
- Beginn
- 25.10.2022
- Tage bis Beginn
- 270,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Dyspnoea
Heart valve incompetence
Laboratory test abnormal
Symptomtext
Mid October he began complaining about random chest pains. He could be watching TV and have random chest pain. They lasted 30 seconds to a minute. After the pain would subside he would have difficulty breathing for another minute or two. This would occur 3-4 times a day for 2-3 weeks. Took him to a PCP in the same clinic. Was referred to cardiologist. Went to cardiologist in November and ran several tests. It was determined that there was a 1% leakage in one of his valves and that it was normal for children his age.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Ran several tests but I am not sure which ones
- Aktuelle Erkrankungen
- COVID-19 the month prior
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 30.01.2023
- Impfdatum
- 21.01.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 11,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Atrial fibrillation
Condition aggravated
Electrocardiogram ambulatory abnormal
Supraventricular extrasystoles
Symptomtext
I had my vaccination on 01/21/2022. I started to experience atrial fibrillation 02/2022. I was administered the Holter monitor and diagnosed with Premature atrial contractions (PACs). I was prescribed medication for the Premature atrial contractions (PACs) and currently followed by cardiology. I had the last Atrial Fibrillation 11/2022 and scheduled for ablation surgery 2023.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- 02/2022 Holter monitor results showed Premature atrial contractions (PACs)
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Meniscus in knee; Diverticulitis; Hypertension
- Andere Medikamente
- Lisinopril; diltiazem; multivitamins; joint supplements; fish oil; glucosamine
- Allergien
- Topical betadine; DEMEROL; cats
- Vorherige Impfungen
- COVID-19 Moderna; A fibrillation
- Staat
- WA
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 11.01.2023
- Impfdatum
- 10.01.2022
- Beginn
- 01.09.2022
- Tage bis Beginn
- 234,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood thyroid stimulating hormone normal
Condition aggravated
Full blood count normal
Gastrointestinal disorder
Metabolic function test normal
Thyroxine free normal
Symptomtext
The vaccination exacerbated existing digestive tract issues. It had to change diet to low FODMAP Diet. I now, potentially, have IBS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- 10/11/2022 Comprehensive Metabolic Panel, normal; 10/11/2022 Complete Blood Count, no differential, normal; 10/11/2022 TSH Reflex to FT4 IF indicated, normal
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Chronic Migraines; Anxiety; Post Concussive Depressive Disorder; Generalized Depression; Insomnia
- Andere Medikamente
- Venlafaxine; topiramate; prazosin; hydroxyzine; FOCALIN
- Allergien
- Quetiapine; cats
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- F
- Eingang
- 17.10.2022
- Impfdatum
- 10.02.2022
- Beginn
- 21.03.2022
- Tage bis Beginn
- 39,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Asthenia
Injection site pain
Mobility decreased
Urticaria
Symptomtext
Reports Right shoulder pain Then pain in knees, ankles, hives Hip weakness Hard to get out of bed in AM
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- chronic pain after MVA 2013, reactive airway disease
- Andere Medikamente
- Kirklans Multivitamin
- Allergien
- fentanyl, gabapentin, naproxen
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 05.10.2022
- Impfdatum
- 01.03.2022
- Beginn
- 05.04.2022
- Tage bis Beginn
- 35,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anxiety
Bundle branch block left
Cardiac ablation
Cardiac electrophysiologic study abnormal
Cardiac monitoring abnormal
Dyspnoea
Electrocardiogram abnormal
Heart rate increased
Heart rate irregular
Palpitations
Supraventricular tachycardia
Symptomtext
A few months after the initial two Covid vaccines that I received in March of 2021 I noticed I had times of irregular heartbeats, high pulse, palpations to a point I had to stop what I was doing until I could catch my breath and compose myself. Then a month after receiving the booster in March of 2022 these conditions had increased in the number of episodes and the magnitude of them to a point I was very concerned. I saw my Primary Care Physician on 5/13/22 and wore an iRhythm Zio 14 day heart monitor from 5/29/22 to 6/12/22, 33 page report. Due the severity of the data from this monitor I was immediately seen by my Cardiologist on 6/30/22 who immediately turned me over to an Electrophysiologist. I had an EKG and an Echocardiogram run. I saw the Electrophysiologist on July 7, 2022 who noted I had a past history of First Degree AV Delay, but the monitor revealed I had Supraventricular Tachycardia (SVT) runs (over 1200 episodes) in 14 days along with pulse rates as high a 250. I also had Ventricular Tachycardia and something new that did not show up in my October 2021 cardiology annual checkup which included an ECG and Echocardiogram which was Left Bundle Branch Block (LBBB). On July 25, 2022 I was admitted to the hospital for a Electrophysiology Study in which an ablation was performed. Currently I am feeling better than I have in the last year or more. Just so you understand I cannot prove 100% the Covid Vaccines had anything to do with my heart conditions that took place over the past year but looking back at the timeline of what took place and when I had gotten the vaccines, especially the Booster in March of 2022, I believe there is some correlation. None of my doctors, my Primary Care Physician, my Cardiologist, nor the Electrophysiologist have an opinion on how these heart conditions came about, but to me I feel there is very good possibility the vaccines brought these things on in some manner or form especially after the booster in which case the severity of the condition increased immediately along with the magnitude of the episodes as they were not all there prior.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Wore an iRhythm Zio 14 day heart monitor from 5/29/22 to 6/12/22. Had an EKG and Electrocardiogram in early July, by July 25, 2022 was admitted to the hospital for a Electrophysiology Study in which an ablation was performed.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Mitral valve repair in 2008, Monoclonal B Cell Lymphocytosis
- Andere Medikamente
- Valsartan 20mg, Vit D, Zinc, Prostatrol Forte, Magnesium
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 23.09.2022
- Impfdatum
- 22.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Interchange of vaccine products
Lymph node pain
Lymphadenopathy
Mobility decreased
Off label use
Peripheral swelling
Symptomtext
gland under both my arms swelled to larger than golfball size//right lump/left lump; painful; could not lower arms to side; feet swelled a bit/foot swelling lasted 3 weeks; had beging 2 dose moderna/switch to pfizer; had beging 2 dose moderna/switch to pfizer; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 63-year-old female patient received BNT162b2 (BNT162B2), on 22Jan2022 as dose 3 (booster), single (Lot number: FJ5682) at the age of 63 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Hysterectomy" (ongoing); "High BP" (ongoing); "Migraine" (ongoing); "Asthma" (ongoing); "weakened immune system." (unspecified if ongoing), notes: Booster dose due to a weakened immune system. Concomitant medication(s) included: PREMARIN oral taken for hysterectomy (ongoing); ATENOLOL oral taken for hypertension, migraine (ongoing); ALVESCO oral taken for asthma (ongoing). Vaccination history included: moderna (DOSE 1, Lot number: unknown), administration date: 10Mar2021, when the patient was 62-year-old, for COVID-19 Immunization, reaction(s): "I was unable to walk", "severe pain", "extremely swelling of feet & legs", "extremely swelling of feet & legs"; moderna (DOSE 2, Lot number: unknown), administration date: 07Apr2021, when the patient was 62-year-old, for COVID-19 Immunization, reaction(s): "I was unable to walk", "severe pain", "extremely swelling of feet & legs", "extremely swelling of feet & legs". The following information was reported: OFF LABEL USE (non-serious), INTERCHANGE OF VACCINE PRODUCTS (non-serious) all with onset 22Jan2022, outcome "unknown" and all described as "had beging 2 dose moderna/switch to pfizer"; LYMPHADENOPATHY (non-serious), outcome "recovering", described as "gland under both my arms swelled to larger than golfball size//right lump/left lump"; LYMPH NODE PAIN (non-serious), outcome "recovering", described as "painful"; MOBILITY DECREASED (non-serious), outcome "unknown", described as "could not lower arms to side"; PERIPHERAL SWELLING (non-serious), outcome "recovering", described as "feet swelled a bit/foot swelling lasted 3 weeks". The events "gland under both my arms swelled to larger than golfball size//right lump/left lump", "painful", "could not lower arms to side" and "feet swelled a bit/foot swelling lasted 3 weeks" required physician office visit. Additional information: Patient had beginning 2 doses Moderna (10Mar2021 & 07Apr2021). I was unable to walk due to extremely swelling of feet & legs accompanied by severe pain. Went down after 6 months of second shot. Reason she switched to Pfizer. Dr checked- No heart issue. Both 1st & 2nd Pfizer boosters, her glands under both her arms swelled to larger than golfball size, Painful but no fever, she couldn't lower arms to side. Feet swelled a bit-Nothing like before. Right lumb went away first both Pfizer vaccination times- 13 days left lump took 21 days 1st time & 17 days 2nd shot. Foot swelling lasted 3 weeks both times & reoccurs from time to time but not unbearable. Pain yes, swelling yes but improves. Did not seek medical attention with Pfizer. 1st time Dr. said it was a normal reaction to contact if continues past 21 days. Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Asthma; Blood pressure high; Hysterectomy; Migraine
- Vorgeschichte
- Medical History/Concurrent Conditions: Immune system disorder (Booster dose due to a weakened immune system.)
- Andere Medikamente
- PREMARIN; ATENOLOL; ALVESCO
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 15.09.2022
- Impfdatum
- 08.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest discomfort
Chest pain
Electrocardiogram normal
Symptomtext
-June 2021 Covid vaccine #2, c/o chest pain and tightness for 2-3d. -January 8, 2022 Booster given - c/o chest pain and tightness for 2-3d similar to June 2021 event.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- EKG done 1/21/22 which was normal
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- NO
- Andere Medikamente
- UNKNOWN
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 13.09.2022
- Impfdatum
- 20.01.2022
- Beginn
- 08.09.2022
- Tage bis Beginn
- 231,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute kidney injury
Ageusia
Asthenia
COVID-19
Decreased appetite
Dizziness
Fatigue
Gastritis
Hypotension
Nausea
SARS-CoV-2 test positive
Vaccine breakthrough infection
Vomiting
Symptomtext
Patient seen in the ED on 9/8 for hypotension. She reported being diagnosed with COVID about 3 weeks prior (8/18/22). For the past 3 weeks she has been experiencing dizziness, generalized weakness, fatigue, decreased appetite, nausea, and vomiting. While in the ED, patient tested positive again for COVID by PCR. She was admitted to the hospital from 9/8-9/11 with discharge diagnoses including nausea, vomiting, and loss of taste, suspect related to COVID gastritis; hypotension; and AKI, improving. Patient has received vaccine and 1 booster for COVID-19. This meets criteria for COVID vaccine breakthrough case review.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Patient with history of rheumatoid arthritis.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 13.09.2022
- Impfdatum
- 10.01.2022
- Beginn
- 05.09.2022
- Tage bis Beginn
- 238,0
- Dosis
- 3
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Dyspnoea
Myalgia
Symptomtext
SOB, myalgias
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 07.09.2022
- Impfdatum
- 29.12.2021
- Beginn
- 07.08.2022
- Tage bis Beginn
- 221,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal X-ray
Abdominal distension
Abdominal pain
Aggression
Agitation
COVID-19
Condition aggravated
Cough
Crying
Culture stool negative
Decreased appetite
Diarrhoea
Endoscopy upper gastrointestinal tract abnormal
Exposure to SARS-CoV-2
Faeces discoloured
Head banging
Intentional self-injury
Quarantine
Symptomtext
13y.o. male with PMH of cerebral palsy, ARID1B-related (Coffin-Siris) syndrome-spectrum neurodevelopmental disorder, developmental delay, agitation/self-injurious behavior requiring protective helmet, encopresis with constipation and overflow incontinence of stool, aerophagia, and hx of GI perforation in 2020 who presented with worsening agitation, self-injurious behavior and mother's concern that this was secondary to abdominal pain. Patient was going to go to camp today, but mother was too concerned about his behavior and so brought him to the ED. Mother says that patient has worsening agitation and self-injurious behavior (crying excessively, banging head on items, hitting mother, etc.) in the past that has been a sign of abdominal pain. She say that these behaviors have increased recently. Per mother, patient is nonverbal and has not been able to demonstrate abdominal tenderness in the past. Mother says that his last BM was early yesterday (08/07/2022). She says that he typically has a lot of flatulence, but has not had much recently. She states that his appetite has been decreased for the last 6 weeks. Patient has a long history of encopresis with constipation and overflow incontinence of stool. He typically will use a diaper, however can sometimes sit on the toilet with assistance by his caretaker. Mother says that a few months ago, although previously he would produce occasional hard pebble balls, he was now experiencing explosive diarrhea. Mother says that she cut down his bowel regimen, stopping Colace, and decreasing Dulcolax to 15 from 30, while continuing Miralax. Diarrhea is brown/yellow in color. Patient was last seen by GI on 04/15/2022. There they recommended use of milk of mag, periactin, Levsin, speaking with a GI dietitian and trial of pecid. Currently patient is not taking of any of those medications. An abdomen XR on that same date, did show moderate gaseous distention. Their next appointment with GI is in 2 weeks. Patient has had previous GI scopes. Patient had an EGD and colonoscopy in Feb 2021 that only showed duodenitis. Of note, family had COVID start of July, ended quarantine more than 2 weeks ago. Family tested positive, patient was assumed positive (not tested due to agitation), had sneezing/coughing. Family did have diarrhea as one of their symptoms. Patient's diarrhea does predate family's symptoms. Patient has a long psychiatry related history. Patient has had multiple psych admissions at facility. Patient has been previously taken olanzapine, valproic acid, clonidine and risperidone. Per mother, they follow with Dr. who 1 month ago began a med washout as none of the medications have been helping. Mother says that currently, she administers medical grade THC solution that she gets from a dispensary that is mixed in juice and given twice a day. Further chart review shows that patient was seen in 03/10/2021 for a similar presentation of worsening behavior. At the time, patient received an extensive work-up that included a dental examination, rheumatology and neurology consultation for autoimmune encephalitis and psychiatry consult who had started the patient on some of his previous anti-psychiatry medications. Per the note, it appears that the diagnosis most favored was that this behavior was most consistent with early pubertal changes. Patient is a 13y.o. male with PMH of cerebral palsy, ARID1B-related (Coffin-Siris) syndrome-spectrum neurodevelopmental disorder, developmental delay, agitation/self-injurious behavior requiring protective helmet, encopresis with constipation and overflow incontinence of stool, aerophagia, and hx of GI perforation in 2020 who presented with worsening agitation, self-injurious behavior and mother's concern that this was secondary to abdominal pain. Patient was going to go to camp today, but mother was too concerned about his behavior and so brought him to the ED. Mother says that patient has worsening agitation and self-injurious behavior (crying excessively, banging head on items, hitting mother, etcc..) in the past that has been a sign of abdominal pain. She say that these behaviors have increased recently. Per mother, patient is nonverbal and has not been able to demonstrate abdominal tenderness in the past. Mother says that his last BM was early yesterday (08/07/2022). She says that he typically has a lot of flatulence, but has not had much recently. She states that his appetite has been decreased for the last 6 weeks. Patient has a long history of encopresis with constipation and overflow incontinence of stool. He typically will use a diaper, however can sometimes sit on the toilet with assistance by his caretaker. Mother says that a few months ago, although previously he would produce occassional hard pebble balls, he was now experiencing explosive diarrhea. Mother says that she cut down his bowel regimen, stopping colace, and decreasing dulcolax to 15 from 30, while continuing Miralax. Diarrhea is brown/yellow in color. Patient was last seen by GI on 04/15/2022. There they recommended use of milk of mag, periactin, Levsin, speaking with a GI dietitian and trial of pecid. Currently patient is not taking of any of those medications. An abdomen XR on that same date, did show moderate gaseous distention. Their next appointment with GI is in 2 weeks. Patient has had previous GI scopes. Patient had an EGD and colonoscopy in Feb 2021 that only showed duodenitis. Of note, family had COVID start of July, ended quarantine more than 2 weeks ago. Family tested positive, patient was assumed positive (not tested due to agitation), had sneezing/coughing. Family did have diarrhea as one of their symptoms. Patient's diarrhea does predate family's symptoms. Patient has a long psychiatry related history. Patient has had multiple psych admissions. Patient has been previously taken olanzapine, valproic acid, clonidine and risperidone. Per mother, they follow with Dr. who 1 month ago began a med washout as none of the medications have been helping. Mother says that currently, she administers medical grade THC solution that she gets from a dispensary that is mixed in juice and given twice a day. Further chart review shows that patient was seen in 03/10/2021 for a similar presentation of worsening behavior. At the time, patient received an extensive work-up that included a dental examination, rheumatology and neurology consultation for autoimmune encephalitis and psychiatry consult who had started the patient on some of his previous anti-psychiatry medications. Per the note, it appears that the diagnosis most favored was that this behavior was most consistent with behavioral changes due to early pubertal changes. During his hospital admission, Pt was started on Zyprexa and we noticed a decrease it the number of aggressive outburst. He was also evaluated by GI and had upper endoscopy that showed mild duodenitis therefore patient was started on Lansoprazole. Patient also had stool culture which returned negative. He was also started on Levsin and home bowel regimen was restarted. Patient was also evaluated by surgery who recommended a CT abdomen with PO and IV contrast. After discussion with anaesthesilogy and GI team and due to patient needed to be intubated for imaging decision was made to hold of on any additional imaging. Patient follows with GI clinic and as an appointment scheduled for next Friday. Since we do not have a GI motility clinic, it was advised that mother establish care there. Mother in agreement with plan.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- 8/7 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC --detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 10,0
- Geschlecht
- F
- Eingang
- 01.09.2022
- Impfdatum
- 07.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Heart rate
Heart rate increased
Limb discomfort
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 10-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 07Jan2022 at 11:30 as dose 3 (booster), single (Lot number: FJ5682) at the age of 10 years, in left arm for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. Past drug history included: Amoxicillin, reaction(s): "Known allergies: Amoxicillin". Vaccination history included: BNT162b2 (Dose 2 in left arm; lot number=EW0183; administration time=09:45 AM), administration date: 03Jun2021, when the patient was 9-year-old, for Covid-19 immunization; BNT162b2 (Dose 1 in left arm; lot number=FJ5682; administration time=11:30 AM), administration date: 13May2021, when the patient was 9-year-old, for COVID-19 Immunization. The following information was reported: CHEST PAIN (non-serious) with onset 10Jan2022 at 08:00, outcome "not recovered"; HEART RATE INCREASED (non-serious) with onset 10Jan2022 at 08:00, outcome "not recovered", described as "rapid heart rate"; LIMB DISCOMFORT (non-serious) with onset 26Jan2022, outcome "not recovered", described as "heaviness in left arm and left leg". The events "chest pain", "rapid heart rate" and "heaviness in left arm and left leg" required physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of chest pain. Additional information: There were no other vaccine in four weeks. Treatment included ibuprofen for chest pain.; Sender's Comments: Linked Report(s) : 202200802375 same patient/drug, different dose/event;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220110; Test Name: Heart rate; Result Unstructured Data: Test Result:Rapid
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 12.08.2022
- Impfdatum
- 08.03.2022
- Beginn
- 07.08.2022
- Tage bis Beginn
- 152,0
- Dosis
- 3
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Cough
Dyspnoea
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 29.07.2022
- Impfdatum
- 29.07.2022
- Beginn
- 29.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest discomfort
Chills
Cough
Dysphagia
Dyspnoea
Immediate post-injection reaction
Nausea
Symptomtext
Patient started having an immediate reaction to the vaccine, he started shivering, coughing and complained of a hot sensation in his chest. We took him to the ER and in route he had c/o SOB and nausea and difficulty swallowing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Patient was taken to our ER
- Aktuelle Erkrankungen
- No medical History
- Vorgeschichte
- He stated after the fact that he had a history of 2 CVA's
- Andere Medikamente
- Not on file
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 14.07.2022
- Impfdatum
- 12.01.2022
- Beginn
- 30.03.2022
- Tage bis Beginn
- 77,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Chest pain
Fatigue
Nasal congestion
Oropharyngeal pain
Pain in extremity
Pyrexia
SARS-CoV-2 test positive
Vomiting
Symptomtext
She had a fever, fatigue and sore arm for a few hours for Dose 3. She tested positive for COVID-19 via a home test on May 12. On May 10 her symptoms: stuffy nose, sore throat and we thought it was seasonal allergies. She threw-up after eating her breakfast one morning before school. She has had extreme fatigue since having COVID-19. I contacted the health department to report her having COVID-19. I gave her MUCINEX to help her with her symptoms. Her oxygen level remained within normal range. She had chest pains with Dose 2 that went away within 24 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Home test COVID-19 positive on May 12.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- ZOLOFT; LO-ESTROGEN; CENTRUM vitamin
- Allergien
- Seafood; gluten intolerance
- Vorherige Impfungen
- October 2016 she got a flu vaccine and had an adverse reaction. She felt sick with headaches, nauseous and tired.
- Staat
- SC
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 13.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 16.06.2022
- Tage bis Beginn
- 65,0
- Dosis
- 4
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Dyspnoea
Fatigue
Rhinorrhoea
SARS-CoV-2 test positive
Sinus congestion
Throat irritation
Vaccine breakthrough infection
Symptomtext
On 6-12-2022, I started having shortness of breath. On 6-13, I noticed a scratchy throat, head congestion, runny nose, a cough and temp of 99.5. On 6-15, I noticed extreme fatigue. On 6-16, I performed a home Covid 19 test with positive results. I called the doctor the same day and they prescribed Paxlovid. I am feeling fine now. I am reporting a breakthru case of Covid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 6-16-2022 home Covid 19 test with positive result
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Migraines, Pituitary tumor
- Andere Medikamente
- Vit D3, Centrum, Vit B12, Vit C, Fish Oil, Vit B2, Magnesium, Calcium, Nurtec
- Allergien
- Topamax
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 08.07.2022
- Impfdatum
- 07.04.2022
- Beginn
- 28.05.2022
- Tage bis Beginn
- 51,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Chest discomfort
Cough
Dyspnoea
Nasal congestion
SARS-CoV-2 test positive
Symptomtext
I thought I had a cold-stuffy nose and cough, around the 30th of May, while I was traveling. I was tested for COVID-19 before we flew home on the 1st of June and it was negative. On June 2nd I started feeling worse, my chest was tight and trouble breathing and couldn't breathe out of my nose. On the same day, I took a home and it was positive. So, I went to the clinic and was tested there and it was also, positive. June 2nd or 3rd I texted my doctor and she prescribed me PAXLOVID. I picked up my prescriptions and the mediation began working right away and helped a lot. My symptoms lasted 6 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 30MAY202- COVID-19 negative; 02JUNE2022- at home COVID-19- positive; 02JUNE2022- COVID-19- positive.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Multivitamin; calcium; magnesium; zinc with vitamin D; fish oil.
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 25.01.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Dysgeusia
Fatigue
Nausea
Oropharyngeal pain
Palpitations
Pruritus
SARS-CoV-2 test negative
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 40-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 23Feb2021 at 13:00 as dose 1, single (Lot number: EN6200), in right arm, on 16Mar2021 at 13:00 as dose 2, single (Lot number: EN6206), in right arm and on 25Jan2022 at 18:00 as dose 3 (booster), single (Lot number: FJ5682) at the age of 39 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Asthma" (unspecified if ongoing). There were no concomitant medications. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Unknown Result; (20Jun2022) Negative; (21Jun2022) Negative; (22Jun2022) Positive. Therapeutic measures were taken as a result of covid-19. Clinical course: The patient had no known allergies. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- Test Name: covid test; Result Unstructured Data: Test Result:Unknown Result; Test Date: 20220620; Test Name: covid test; Test Result: Negative ; Test Date: 20220621; Test Name: covid test; Test Result: Negative ; Test Date: 20220622; Test Name: covid test; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Asthma
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 25.01.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Dysgeusia
Fatigue
Nausea
Oropharyngeal pain
Palpitations
Pruritus
SARS-CoV-2 test negative
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 40-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 23Feb2021 at 13:00 as dose 1, single (Lot number: EN6200), in right arm, on 16Mar2021 at 13:00 as dose 2, single (Lot number: EN6206), in right arm and on 25Jan2022 at 18:00 as dose 3 (booster), single (Lot number: FJ5682) at the age of 39 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Asthma" (unspecified if ongoing). There were no concomitant medications. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Unknown Result; (20Jun2022) Negative; (21Jun2022) Negative; (22Jun2022) Positive. Therapeutic measures were taken as a result of covid-19. Clinical course: The patient had no known allergies. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- Test Name: covid test; Result Unstructured Data: Test Result:Unknown Result; Test Date: 20220620; Test Name: covid test; Test Result: Negative ; Test Date: 20220621; Test Name: covid test; Test Result: Negative ; Test Date: 20220622; Test Name: covid test; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Asthma
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 30.06.2022
- Impfdatum
- 17.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest pain
Dyspnoea
Fatigue
Palpitations
Symptomtext
Onset 1 day after booster. Chest pain, palpitations, shortness of breath, fatigue lasting 4 days, plus residual chest pain on day 5. Treated at home by mom. Self resolved. (Treatments included electrolytes and Prussian Blue).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- headaches resolved by eating and hydrating
- Andere Medikamente
- vitamin D, magnesium, fish oil
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 26.06.2022
- Impfdatum
- 09.02.2022
- Beginn
- 14.02.2022
- Tage bis Beginn
- 5,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Atrial fibrillation
Back pain
Blood magnesium normal
Cardiac flutter
Chest pain
Dyspnoea
Echocardiogram normal
Electrocardiogram abnormal
Electrocardiogram ambulatory
Glomerular filtration rate normal
Heart rate increased
Metabolic function test normal
Pain
Palpitations
Symptomtext
Adverse events: Rapid/racing heartbeat, extended heart flutters (longer than a minute per event), chest pain that radiated to the back, heart palpitations, shortness of breath, and first time AFib event with RVR. Caught on ECG. Was prescribed a beta blocker (metoprolol), which I didn't start because I wanted a diagnosis by my cardiologist after holter monitor results came back.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Cardiologist was booked, so I saw her NP. Received an ECG, which showed that I was in AFib with RVR. Had two faulty heart monitors with only about an hour of data. Blood work: comprehensive metabolic panel, magnesium level and estimated GFR. All results came back normal. Had and echocardiogram, which came back normal. After seeing my cardiologist for a follow-up I learned that the NP did not order the appropriate tests to diagnose myocarditis. An blood enzyme test and or Cardio MRI was needed. Cardiologist reported that it was too late to have these tests by the time I was able to see her on 4/20/22.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Mitral valve prolapse
- Andere Medikamente
- None
- Allergien
- Sulfa based drugs
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 21.06.2022
- Impfdatum
- 20.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 8,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
Blood potassium decreased
Chills
Cough
Dizziness
Dyspnoea
Feeling abnormal
Impaired work ability
Laboratory test normal
Symptomtext
Brain fog, SOB, lightheadedness, dizziness, cough, chills, and weakness that lasts for 2 days. It's like having COVID symptoms every couple of weeks without losing taste. It keeps me out of work a lot lately.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 05/2022: Lab Work at ER - Normal except that potassium was low.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Pulmonary Embolism, Hypertension, High Cholesterol, Prediabetes
- Andere Medikamente
- HCTZ, Lipitor, Amlodipine, Vitamin D3, Zinc, Vitamin C, Omega 3
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 13.06.2022
- Impfdatum
- 22.03.2022
- Beginn
- 22.05.2022
- Tage bis Beginn
- 61,0
- Dosis
- 4
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthma
COVID-19
Laryngitis
Mobility decreased
SARS-CoV-2 test positive
Symptomtext
I spent 17 days in country (May1-17) and then three and a half days in country. I tested negative on Friday, May 20 at 2:30PM in country, the country so I was able to board my plane to return home, and awoke at 3:30AM on Sunday, May 23 in my bed barely able to move my body and with significant asthma. I tested positive on an at-home antigen test and on a PCR test at a testing center. My doctor put me on Paxlovid for five days and I was mostly symptom free until the Paxlovid ended (May 27, 2022). Since then, I have had asthma and laryngitis, despite being on inhaled steroids since May 24, 2022. And, I'm still testing positive on at-home antigen tests..
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- 5/22/22- PCR test
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma, but it has been in control for over 15 years. This was NOT an adverse reaction to the vaccine or booster - I had NO reaction to either vaccine or the boosters. I am submitting this report because I contracted Covid, despite two vaccinations, two boosters, a 96.1% antibody test and aggressive masking.
- Andere Medikamente
- Nexium, Rosuvastatin, Singulaire, Mybetriq, Zioptan, Allegra, Ceentrum Silver, Calcium+D, Flax Lignans
- Allergien
- Penicillin, Eythromicin, bananas
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 19.05.2022
- Impfdatum
- 28.03.2022
- Beginn
- 02.04.2022
- Tage bis Beginn
- 5,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cardiovascular evaluation
Dyspnoea
Fatigue
Heart rate increased
Loss of personal independence in daily activities
Supraventricular tachycardia
Symptomtext
Increased heart rate while resting (SVT), extreme fatigue after increased heart rate, shortness of breath with daily normal activities,
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Have had a cardiac evaluation completed by Dr.; Being referred to new cardiologist for further evaluation. New cardiologist is M.D.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- None
- Allergien
- Augmentin
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 18.05.2022
- Impfdatum
- 18.01.2022
- Beginn
- 21.03.2022
- Tage bis Beginn
- 62,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Dysphagia
Dyspnoea
Headache
Immunisation reaction
Lymphadenopathy
Oropharyngeal pain
Pain
SARS-CoV-2 test positive
Speech disorder
Streptococcus test negative
Tonsillar hypertrophy
Symptomtext
Severe headaches and rapidly worsening sore throat and severely swollen tonsils, especially on right side. Visited Clinic on 3/30/2022 due to pain severity increasing dramatically over the course of the week. Became unable to swallow. Having difficulty talking and even breathing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Strep test negative. Advised by NP that swelling of Lymph Nodes and tonsils is likely a reaction to COVID-19 vaccination. I had issues with the second dose last summer with a rash on my left arm that appeared a few months after the vaccination. Was advised to take large dose of Advil and went on an Advil & Tylenol regimen for the next 7-10 days. Swelling subsided after about a week and pain lessened. Tonsils continue to this day to appear slightly swollen (right side).
- Aktuelle Erkrankungen
- COVID-19 positive on 2/3/2022.
- Vorgeschichte
- None
- Andere Medikamente
- IUD Mirena, Multi-Vitamin
- Allergien
- NKA
- Vorherige Impfungen
- Age 29, Second COVID vaccine Pfizer administered 3/26/2021, that summer (June) developed severed rash down left arm- lasted in s
- Staat
- PA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 12.05.2022
- Impfdatum
- 15.04.2022
- Beginn
- 16.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Ageusia
Anosmia
Balance disorder
Chest discomfort
Chest pain
Dyspnoea
Ear pain
Headache
Lymphadenopathy
Pharyngeal erythema
Pharyngeal swelling
Rhinorrhoea
SARS-CoV-2 test
Stress
Weight
Weight abnormal
X-ray
Symptomtext
Chest pain; Trouble breathing; Her equilibrium is off, and her balance; Taste is off; Smell is off; Lymph nodes in her neck; Her throat is swollen and red; Her ears hurt; Her weight keeps going up and down between 134-136lbs; Her throat is swollen and red; Head has been hurting which may be stress related; Head has been hurting which may be stress related; Sniffles; She had pressure in her chest; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 60-year-old female patient received BNT162b2 (BNT162B2), on 15Apr2022 as dose 4 (booster), single (Lot number: FJ5682) at the age of 60 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Post high blood pressure" (unspecified if ongoing), notes: Post high blood pressure - been maintained. Concomitant medication(s) included: SHINGRIX taken for immunisation, on 21Mar2022 as dose number unknown, single. Vaccination history included: BNT162b2 (Dose 1, EL3982 or EZ3982), administration date: 18Feb2021, when the patient was 59-year-old, for COVID-19 Immunization; BNT162b2 (Dose 2, Lot number: EN8301), administration date: 11Mar2021, when the patient was 59-year-old, for COVID-19 Immunization; BNT162b2 (Dose 3, Vaccine lot: FC3181), administration date: 19Aug2021, when the patient was 59-year-old, for COVID-19 Immunization. The following information was reported: CHEST PAIN (non-serious) with onset 16Apr2022 at 01:00, outcome "not recovered"; BALANCE DISORDER (non-serious) with onset 16Apr2022 at 01:00, outcome "not recovered", described as "Her equilibrium is off, and her balance"; ANOSMIA (non-serious) with onset 16Apr2022 at 01:00, outcome "not recovered", described as "Smell is off"; AGEUSIA (non-serious) with onset 16Apr2022 at 01:00, outcome "not recovered", described as "Taste is off"; DYSPNOEA (non-serious) with onset 16Apr2022 at 01:00, outcome "not recovered", described as "Trouble breathing"; HEADACHE (non-serious), STRESS (non-serious) all with onset 2022, outcome "unknown" and all described as "Head has been hurting which may be stress related"; EAR PAIN (non-serious) with onset 2022, outcome "unknown", described as "Her ears hurt"; PHARYNGEAL SWELLING (non-serious), PHARYNGEAL ERYTHEMA (non-serious) all with onset 2022, outcome "unknown" and all described as "Her throat is swollen and red"; WEIGHT ABNORMAL (non-serious) with onset 2022, outcome "unknown", described as "Her weight keeps going up and down between 134-136lbs"; LYMPHADENOPATHY (non-serious) with onset 2022, outcome "not recovered", described as "Lymph nodes in her neck"; CHEST DISCOMFORT (medically significant) with onset 2022, outcome "unknown", described as "She had pressure in her chest"; RHINORRHOEA (non-serious) with onset 2022, outcome "not recovered", described as "Sniffles". The events "lymph nodes in her neck", "her throat is swollen and red", "her ears hurt" and "her weight keeps going up and down between 134-136lbs" required physician office visit. The events "she had pressure in her chest", "chest pain", "trouble breathing", "her equilibrium is off, and her balance", "taste is off", "smell is off", "head has been hurting which may be stress related" and "sniffles" required physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (2022) Unknown results; Weight: (unspecified date) 134-136 lbs, notes: Her weight keeps going up and down between 134-136lbs; X-ray: (2022) Unknown results. Therapeutic measures were taken as a result of chest discomfort, chest pain, dyspnoea, balance disorder, ageusia, anosmia, lymphadenopathy, pharyngeal swelling, ear pain, weight abnormal, pharyngeal erythema, headache, stress, rhinorrhoea and she was treated with antibiotics and steroids and another antibiotic has been added as well as prednisone. Additional information: She has had a side effect with her ears too. She said agent was loud. That same night after her second booster, she had to go to the Emergency room at 1 o'clock am. She had chest pain and she was having trouble breathing. It came to her attention when someone later asked if the Emergency room reported it to Pfizer. She doesn't know if they did. She is still having side effects. She still has the sniffles it is like her body is still trying to fight this. When this happened, she went to the emergency room. Her equilibrium is off, and her balance. He taste is off and her smell is off. She had an ENT doctor look at her because her throat is swollen and red. She has lymph nodes in her neck. The doctor said he had never seen anything like it. Her head has been hurting which may be stress related. Her ears hurt. Her chest still feels tight which has been an ongoing issue. The doctor put her on some antibiotics to get the lymph nodes in her neck down. The lymph nodes were making her airway feel like it was blocked. At first the pharmacist said don't take prednisone because it could lower the strength. So she had to suffer for the first two weeks. At the emergency room they did IVs, x-rays, and a COVID test.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Test Date: 2022; Test Name: COVID test; Result Unstructured Data: Test Result:Unknown results; Test Name: Weight; Result Unstructured Data: Test Result:134-136 lbs; Comments: Her weight keeps going up and down between 134-136lbs; Test Date: 2022; Test Name: X-rays; Result Unstructured Data: Test Result:Unknown results
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Blood pressure high (Post high blood pressure - been maintained)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 11.05.2022
- Impfdatum
- 08.02.2022
- Beginn
- 09.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acupuncture
Chiropractic
Oesophageal disorder
Oesophagram
Paraesthesia
Sensation of foreign body
Sensory disturbance
Vibratory sense increased
Symptomtext
13 hours after getting the booster, I had this nervy wave feeling coming over me. It felt like a nerve thing going up and down my body. I had pins and needles on both arms and hands. The scar on my left side had the feeling of pins and needles. A few hours later it progressed to sharp prickles on my back, neck, thighs, pubic area, and ankles. I also had buzzing and vibrating in my arms and hands through the next night. I had an undulating vibration in feet 3 days later. It felt like ocean waves. On the 16th I found a chiropractor who did a lot of different techniques. After her treatment all symptoms went away except for the pins and needles in my arms and hand. The symptoms returned on March 11, 2022, but were milder. On March 21, I went back to the chiropractor who did additional techniques and 5 days later, I woke up with no symptoms. On March 28, while eating pita chips, I felt like something was stuck in my esophagus. I had to have my husband get off to get hot water in order to break down the particles. I have an appointment with an ENT and he had me to do a Esophagram and indicated I had transient resistance in my esophagus. I am seeing an acupuncturist now as well. I am having an EGD test done to look at my esophagus function.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- Esophagram: Transient Resistance
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Fibromyalgia Eczema
- Andere Medikamente
- Fish Oil Minerals C-complex Magnesium Vitamin D Vitamin C Zinc Mitochondrial Function Supplements
- Allergien
- Penicillin Mango
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 05.05.2022
- Impfdatum
- 22.04.2022
- Beginn
- 22.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Paraesthesia oral
Pruritus
Rash
Symptomtext
Approximately one hour after vaccine administration, the patient reported itchiness on her upper extremities, as well as a localized rash on the right inner forearm and tingling on the tongue. Symptoms improved with a cold pack and cetirizine. The patient was monitored for one hour.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia oral
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Metformin, semaglutide, insulin glargine, dapagliflozin, triam cinolone, latnoprost, pregabalin, zolpidem, atorvastatin, albuterol
- Allergien
- Swordfish
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 04.05.2022
- Impfdatum
- 21.02.2022
- Beginn
- 22.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Musculoskeletal disorder
Neuralgia
Pain
Pain in extremity
Paraesthesia
Symptomtext
C/o persistent R arm pain >2mos after vaccine, worst at injection site radiating down humerus and into forearm, worse with movement/ feels like 'any movement stretches muscles', tingling / neuropathic pain, describes R arm as 'useless'
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- type 2 diabetes, peptic ulcer disease, COPD
- Andere Medikamente
- wixela, metformin, lisinopril, atorvastatin, ASA, albuterol
- Allergien
- Reglan
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 27.04.2022
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dizziness
Electrocardiogram
Headache
Nausea
Neurological examination
Rash
Tremor
Symptomtext
On April 05/2022 received booster and my adverse event started on the same day within 20 minutes) dizziness, headache, nauseas, rash, right arm tremor. I was in my PCP's office that day and she call the ambulance I was sent to the ER. They kept me there and monitored me there. They gave me medications and after 8 hours they let me go home. They did neurological exams. Medication for nausea. I still have headache and dizziness and still seeking care for it.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- EKG
- Aktuelle Erkrankungen
- On going Dizziness; Migraine
- Vorgeschichte
- None
- Andere Medikamente
- Zyrtec; Allegra
- Allergien
- Bacitracin; Clindamycin; Nortriptyline 20 mg; Pineapple
- Vorherige Impfungen
- Moderna vaccine, dizziness, rash, headache and nausea.
- Staat
- IN
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 21.04.2022
- Impfdatum
- 01.04.2022
- Beginn
- 02.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Atrial fibrillation
Condition aggravated
Symptomtext
I used to have occasional Atrial Fibrillation but after this 4th dose my this has become been constant. My PCP recommended that I see a Cardiologist for my heart condition, I have an upcoming appointment on 5/13/2022 at a local medical facility. My doctor also wants me to have a sleep study.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- My Doctors: PCP, ENT, Urologist, Pain Management, Cardiologist.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Nasal; Chronic Back Pain; Hypertrophic; Cardiomyopathy; Blood Thinner condition
- Andere Medikamente
- Lorazepam 1 mg; Acetaminophen 500mg; Budesonide .5mg; Cetirizine 10mg; Diltiazem 120mg; Gabapentin 300mg; Fluticasone 50mg; Hydrocodone 7.5/325mg; Irbesartan hydro 150/1.5mg; Ketoconazole 5micrograms shampoo; Krill Oil 350mg; Melatonin 10m
- Allergien
- Mold; Dander; Tree Bark; Cigarettes
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 20.04.2022
- Impfdatum
- 24.01.2022
- Beginn
- 25.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Amnesia
COVID-19
Decreased appetite
Dyspnoea
Fatigue
Feeling abnormal
Frequent bowel movements
Hypersomnia
Hypophagia
Nausea
Pain
Pyrexia
SARS-CoV-2 test positive
Weight decreased
Symptomtext
01/25/2022 Woke up running a fever 105.4. Took 3 Advil and it knocked it down to 104.8. I emptied my entire colon in several bowel movements. I had general aches and pains I had no appetite and bad nausea. I drove myself to the pharmacy 2 days later to get a COVID test and results came back positive. Basically, the next 2 weeks were blank. I don't remember anything, and you were unable to eat much. I could only eat rice, apple sauce and toast. I lost over 20 pounds. I still do not feel good. I am out of breath and very tired, sleep a lot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- COVID test, positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Multi Vitamin generic version of Centrum
- Allergien
- Pollen
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 18.04.2022
- Impfdatum
- 24.02.2022
- Beginn
- 25.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Heart rate increased
Heart rate irregular
Pain in extremity
Peripheral swelling
Symptomtext
A day after the vaccine I woke up with a sore arm and swelling under my arm, It started to go down after 3-4 days but my chest was really sore. I then noticed that my heart rate was 10-15 more than normal, I then went to the doctor a week and they said I had a irregular heart beat and I'm now awaiting my appointment for my mammogram in May.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 07.04.2022
- Impfdatum
- 27.01.2022
- Beginn
- 19.02.2022
- Tage bis Beginn
- 23,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Anaemia
Asthenia
COVID-19
Chest pain
Dizziness
SARS-CoV-2 test positive
Upper gastrointestinal haemorrhage
Vision blurred
Symptomtext
Patient is a direct admission from ED with chest pain x2 days, dizziness, transient left eye blurry vision this morning and general body weakness. He was managed for: Acute Upper GI Bleed, acute Symptomatic anemia in the setting of Above, Hx of bleeding gastritis and duodenal ulcers, and Hx of Uncomplicated diverticulosis. Positive COVID-19 infection. Treated for all hospital problems and discharged home. ED visit and hospital admission within 6 weeks of receiving the COVID vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 07.04.2022
- Impfdatum
- 01.03.2022
- Beginn
- 12.03.2022
- Tage bis Beginn
- 11,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood pressure increased
Blood test
Cardiac discomfort
Cardiac failure congestive
Cardiospasm
Chest X-ray
Chest pain
Dyspnoea
Fatigue
Peripheral swelling
Symptomtext
Two days after pt received Pfizer COVID 19 vaccine he received a MMR vaccine and a Flu vaccine from a doctor. He is unable to recall the name of the doctor. Pt reports he started having SOB, chest pain, heart spasms, swelling of feet and legs, and his blood pressure was rising. Was seen by a Dr. at the hospital on 3/14/2022. Pt said he had blood work and a CXR. Pt was Dx with congestive heart failure. Pt said he was prescribed Furosemide 20 mg one tablet a day for 30 days. Since ER visit pt said his feet and legs remain swollen and he feels like he has fluid around his heart. He continues to hav SOB and is fatigued. He is having frequent urine output with the Furosemide medication. Pt has a follow up appointment with his PCP on 4/5/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- blood work and a CXR at ER visit on 3/14/22
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- hypertension
- Andere Medikamente
- Amlodipine and Losartan
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 29.03.2022
- Impfdatum
- 14.02.2022
- Beginn
- 07.03.2022
- Tage bis Beginn
- 21,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Pneumonia
Respiratory syncytial virus infection
Symptomtext
RSV - treated and released in ER. Admission 3 days later for Pneumonia of right lung due to infectious organism. He was started on empiric ceftriaxone and doxycycline for possible superimposed bacterial pneumonia along with RSV infection and was also treated with oral steroids and nebulizers. Patient received 5 days of IV ceftriaxone, and was continued on doxycycline here instead of azithromycin due to concern for prolonged QTc (therapy completed). From a respiratory standpoint is continuing to improve and the plan was to discharge him home. ED visit and hospital admission within 6 weeks of receiving the COVID vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pneumonia
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 23.03.2022
- Impfdatum
- 14.03.2022
- Beginn
- 15.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Back pain
Hypoaesthesia
Impaired work ability
Mobility decreased
Pain
Pain in extremity
Symptomtext
Received vaccine on 3/14/22. On 3/15/22, I noticed pain in my right arm radiating to my mid back and assumed it would go away. The next morning, I woke up and couldn't move my arm due to extreme pain. I went to the doctor and was prescribed a muscle relaxer and told to take ibuprofen and tylenol. I tried this with no relief. On 3/18/22, I started having numbness in my fingers and increased pain so I went to the ED. I was prescribed pain medication and started a prednisone taper. The pain and numbness have not subsided. I am unable to work and followed up with my doctor on 3/22/22. I have been placed on a medical leave since I can't perform my duties as a registered nurse,
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- tests pending scheduling (EMG with NCV)
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- hashimoto's thyroiditis
- Andere Medikamente
- omeprazole, dicyclomine
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 18.03.2022
- Impfdatum
- 18.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Mobility decreased
Paraesthesia
Pruritus
Renal pain
Ultrasound liver
Vaccination site mass
Vaccination site paraesthesia
Symptomtext
pain on the left side kidney area; hard place on her left arm where she got the inject which made it hard to move; hard place on her left arm where she got the inject which made it hard to move; tingling on her left arm that went all the way to her ring finger; tingling on her left arm that went all the way to her ring finger; uncomfortable ithcing; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 41 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 18Jan2022 12:30 (Lot number: FJ5682) at the age of 40 years as dose 1 , single for covid-19 immunisation. Relevant medical history included: "Lyme disease", start date: Jul2015 (unspecified if ongoing); "Liver Disease", start date: Jun2018 (unspecified if ongoing); "Hashimoto's disease", start date: 2013 (unspecified if ongoing); "allergies to bees" (unspecified if ongoing); "allergies to pollen" (unspecified if ongoing); "allergies to mold" (unspecified if ongoing); "allergies to wool" (unspecified if ongoing); "Stomach acid issues" (unspecified if ongoing). Concomitant medication(s) included: JUNEL FE taken for contraception; OMEPRAZOLE taken for abdominal discomfort. Past drug history included: Percocet, reaction(s): "itchiness". The following information was reported: VACCINATION SITE MASS (non-serious), MOBILITY DECREASED (non-serious) all with onset 19Jan2022, outcome "recovering" and all described as "hard place on her left arm where she got the inject which made it hard to move"; VACCINATION SITE PARAESTHESIA (non-serious), PARAESTHESIA (non-serious) all with onset 19Jan2022, outcome "recovering" and all described as "tingling on her left arm that went all the way to her ring finger"; PRURITUS (non-serious) with onset 19Jan2022, outcome "recovering", described as "uncomfortable ithcing"; RENAL PAIN (non-serious) with onset 21Jan2022, outcome "recovering", described as "pain on the left side kidney area". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: Caller stated that she got the 1st dose of the Pfizer Covid 19 vaccine on 18Jan2022. Stated that she experienced the following adverse reactions after getting the dose, hard place on her left arm where she got the inject which made it hard to move, tingling on her left arm that went all the way to her ring finger, uncomfortable ithcing, and pain on the left side kidney area. Caller also noted that she had pre-existing lyme and liver disease prior to the vaccination. Caller was asking if there would be any recommendations regarding her getting the second dose. Received call from consumer regarding the Pfizer COVID vaccine. She got it, and then pharmacist who issued told her she should call and does not know if she should continue with 2nd one. Maybe it was a known side effect or an allergy. It was kind of like when you get a Tetanus shot and it is hard, and her arm was hard to move. She did not provide any information or clarify if she had had this happen to her after a Tetanus shot or not. She also had tingling up left arm and into ring finger. She got uncomfortably itchy and said the tingling lasted 3-4 days and itching, where she had to soothe self in cool baths, happened for 48 hours. She had liver disease and did feel in her kidney area some pain and does not know if related. This last part occurred 5 days after she got the shot. This occurred 2 weeks from her 41st birthday. Every now and then, her arm will still tingle. She confirmed that she had liver disease prior to getting the vaccine. She had been hesitant to get it because of this. She had no other symptoms, and then said none that would be related to this. No further details provided. She is supposed to have it for work. She wonders what would happen if people were allergic to it, and what happens then. If it was supposed to be a reaction, she does not know what she can do and work does not know how long they can prolong it. This sucks having all these people who require it. She would like to know if she should attempt 2nd dose. There was some mixed reviews she was getting. Her Pharmacist said no, but her doctor's nurses said it would be ok. No other vaccines were administered on the same date of Pfizer vaccine administration. There was no emergency room and physician office visit. No other vaccine administered within four weeks prior to the first administration date of the suspect vaccine. AE(s) following prior vaccinations: She does get some itchiness with Percocet twice in her life. She does not have a lot or expiration. It has been years ago and she no longer had it. She does not take it if they prescribe it for her now. Medical history details included: Hashimoto's disease diagnosed in 2013. She was a mixed bag and counts a lot of it for the Lyme. She had allergies to bees, pollen, mold and mildew and wool. Diagnosis dates are all unknown. When she was sick she was diagnosed with allergy to wool where she gets fevers and headaches. That started in 1986. Regarding lab test it was reported: She could pull up Lyme titers and liver ultrasound results, if needed, but she did not have those results at the time of call. She had a lot of blood work done. Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- Test Name: blood work; Result Unstructured Data: Test Result:Unknown results; Test Name: Liver Ultrasound; Result Unstructured Data: Test Result:Unknown results
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Allergic reaction to bee sting; Allergy to molds; Allergy to wool; Hashimoto's disease; Liver disorder; Lyme disease; Pollen allergy; Stomach discomfort
- Andere Medikamente
- JUNEL FE; OMEPRAZOLE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 17.03.2022
- Impfdatum
- 21.02.2022
- Beginn
- 23.02.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Asthenia
Balance disorder
Extra dose administered
Infection
Laboratory test abnormal
Malaise
Mobility decreased
Urinary tract infection
Symptomtext
She got her vaccine, she checked with her PCP and her pharmacist and was told that she could get the 4th one as she is immunocompromised. She had a mammogram a day after the 1st vaccine and told her to look at the pictures and that the Pfizer vaccine had changed her lymph nodes, and that they had seen a pattern with the Pfizer vaccine. She did not feel well that day and then by Wednesday she was completely laid out. Her joints hurt, had no equilibrium, no balance, and stayed in bed for a week or so. she called her PCP a couple of times and was informed it was probably a reaction to her vaccine. Tuesday a week ago she saw a doctor and ran tests, and had a pretty severe UTI and some other infections as well. She was put on antibiotics and did not help. She went back on Monday for the FU and she had told her that her GI doctor had a special IV to combat a really strong UTI like she had, had this for 3 weeks. She went to see her GI doctor who admitted her and was on 2 days of IV antibiotics, and got out yesterday and is very weak right now. The infection has now cleared.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- 2,0
- Labordaten
- As above.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Crohn's disease, renal tubular acidosis, Thyroid disease, high blood pressure. Had colon resection due to Crohn's disease and ilium is gone, as well as 95% of her intestines.
- Andere Medikamente
- Has extensive list available upon request.
- Allergien
- PCP is trying to determine if she is still having problems, not the case of these reactions.
- Vorherige Impfungen
- 1st one was informed it had changed her lymph glands and lymph nodes.
- Staat
- -
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 16.03.2022
- Impfdatum
- 28.02.2022
- Beginn
- 01.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Adnexa uteri pain
Axillary mass
Back pain
Chest pain
Dizziness
Dyspnoea
Headache
Oropharyngeal pain
Pain
Panic attack
Symptomtext
Symptoms - ?LUMP IN RIGHT ARMPIT, LOWER BACK PAIN/ KIDNEY AREA, PAIN IN OVARY AREAS, BODYACHES, PANIC ATTACKS, SHORTNESS OF BREATH, DIZZINESS, CHEST PAIN, HEADACHES, THROAT PAIN. SAW PCP IN REGARDS TO SYMPTOMS AND PCP SAID IT WAS A BAD REACTION TO THE BOOSTER VACCINE. HAS HX OF OTHER ALLERGIES TO FOOD AND VACCINATIONS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NO.
- Vorgeschichte
- YES.
- Andere Medikamente
- -
- Allergien
- YES.
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 14.03.2022
- Impfdatum
- 14.03.2022
- Beginn
- 14.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cough
Dysphagia
Electrocardiogram abnormal
Paraesthesia oral
Pharyngeal paraesthesia
Sinus tachycardia
Urticaria
Symptomtext
Vaccine administered at 11:45 AM. At 12:05 associate reported "tingling in tongue and at back of throat". B/P 130/82, Heart Rate 122. Associate then complained of " a little difficulty swallowing". Associate also began a small cough. Associate advised to go to ED. Escorted to ED. Associate started breaking out in hives.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia oral
- Hospital-Tage
- -
- Labordaten
- EKG- sinus tach.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- No
- Allergien
- No Known Allergies
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 14.03.2022
- Impfdatum
- 21.02.2022
- Beginn
- 22.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Hypoaesthesia
Joint range of motion decreased
Pain
Pain in extremity
Paraesthesia
Symptomtext
Pain, limited range of motion in left shoulder. Numbness, pain and tingling radiating from left shoulder down arm to left hand. Pain, numbness to left shin area radiating down to foot on left side only.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- None done at time of reporting. Waiting for employer response to address issue.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- OTC multivitamin
- Allergien
- Augmentin
- Vorherige Impfungen
- Frozen left shoulder, 51 year old, date vaccine given: 06/03/2021, COVID vaccine, Johnson & Johnson
- Staat
- TX
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 08.03.2022
- Impfdatum
- 22.02.2022
- Beginn
- 23.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Diarrhoea
Hypoaesthesia
Pain in extremity
Symptomtext
Pain in arm, morning after injection 2/23/2022 continuing till 3/8/2022, still occurring Intermittent right Finger tips Numbness starting on 3/6/2022, still occurring Complete right arm numbness intermittent starting 3/7/2022, still occurring Diarrhea 2/23/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Bisoprolol/HCTZ 5Mg/6.25MG tabs Naproxen sodium 220 mg Acetaminophen Extended-release tablets 8HR (Tylenol)
- Allergien
- Peaches Penicillin Lisinopril
- Vorherige Impfungen
- diarrhea, extreme fatigue
- Staat
- CT
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 08.03.2022
- Impfdatum
- 22.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood pressure increased
Chest discomfort
Condition aggravated
Immediate post-injection reaction
Symptomtext
Immediate Tightness in chest, Blood Pressure Spike, Arm Pain, general muscular pain, exhaustion. Chest Tightness and Blood Pressure spike lasted 4 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- High Blood Pressure, Weight
- Andere Medikamente
- Amlodipine Besylate, Hydralazine, Carvedilol, Spironolactone, Rosuvastatin, Montelukast, Losartain, Cetirizine, Aspirin
- Allergien
- none
- Vorherige Impfungen
- All Covid 19 Vaccinations, same issues, age 55, 4/21/21 and 5/12/21. Both Pfizer
- Staat
- CO
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 08.03.2022
- Impfdatum
- 11.02.2022
- Beginn
- 23.02.2022
- Tage bis Beginn
- 12,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
Blood test normal
Dizziness
Fatigue
Head discomfort
Headache
Injection site pain
Nausea
Tremor
Symptomtext
I had fatigue, headache, and pain at injection site. Then two later, I had major fatigue, dizziness, and tired. I was serve nausea, headache, and head pressure. I am very weak and shaky. These symptoms have lasted for about 2 weeks. I went to my doctor and a hospital. The hospital did a bunch of blood work. They could not found anything wrong.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- Blood work
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Lamotrigine, Propranolol
- Allergien
- Sofia
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 05.03.2022
- Impfdatum
- 16.02.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Cold sweat
Dizziness
Fatigue
Feeling cold
Gait disturbance
Headache
Hypoaesthesia
Limb discomfort
Nausea
Nerve injury
Pain
Pain in extremity
Paraesthesia
Somnolence
Symptomtext
Dizzy; Nauseous; my legs they feel very heavy, they also feel like tingling and numbness and its kind of little hard for me to walk/her left foot go downwards and cannot straighten her toes; my legs they feel very heavy, they also feel like tingling and numbness and its kind of little hard for me to walk; my legs they feel very heavy, they also feel like tingling and numbness and its kind of little hard for me to walk; my legs they feel very heavy, they also feel like tingling and numbness and its kind of little hard for me to walk; nerve damage in my left leg; was very tired; sleepy; headache; chills; cold sweats; body aches/pain was excruciating/shooting pain in her leg/pain in her leg; feet got real cold; severe arm pain; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. Other Case identifier(s): US-PFIZER INC-202200313418 (Pfizer). A 70 year-old female patient received bnt162b2 (BNT162B2), administration date 16Feb2022 (Lot number: FJ5682) at the age of 70 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Asthma" (unspecified if ongoing), notes: Verbatim: Asthma. The patient took concomitant medications. The following information was reported: DIZZINESS (non-serious) with onset Feb2022, outcome "unknown", described as "Dizzy"; NAUSEA (non-serious) with onset Feb2022, outcome "unknown", described as "Nauseous"; LIMB DISCOMFORT (non-serious) with onset Feb2022, outcome "unknown", described as "my legs they feel very heavy, they also feel like tingling and numbness and its kind of little hard for me to walk/her left foot go downwards and cannot straighten her toes"; HYPOAESTHESIA (non-serious), PARAESTHESIA (non-serious), GAIT DISTURBANCE (non-serious) all with onset Feb2022, outcome "unknown" and all described as "my legs they feel very heavy, they also feel like tingling and numbness and its kind of little hard for me to walk"; NERVE INJURY (non-serious) with onset Feb2022, outcome "unknown", described as "nerve damage in my left leg"; FATIGUE (non-serious) with onset Feb2022, outcome "unknown", described as "was very tired"; SOMNOLENCE (non-serious) with onset Feb2022, outcome "unknown", described as "sleepy"; HEADACHE (non-serious) with onset Feb2022, outcome "unknown", described as "headache"; CHILLS (non-serious) with onset Feb2022, outcome "unknown", described as "chills"; COLD SWEAT (non-serious) with onset Feb2022, outcome "unknown", described as "cold sweats"; PAIN (non-serious) with onset Feb2022, outcome "unknown", described as "body aches/pain was excruciating/shooting pain in her leg/pain in her leg"; FEELING COLD (non-serious) with onset Feb2022, outcome "unknown", described as "feet got real cold"; PAIN IN EXTREMITY (non-serious) with onset Feb2022, outcome "recovered" (2022), described as "severe arm pain". Therapeutic measures were not taken as a result of dizziness, nausea, limb discomfort, hypoaesthesia, paraesthesia, gait disturbance, nerve injury. Additional information: Consumer stated, "I was calling because I just, I got my vaccine (clarified as Pfizer COVID vaccine) about 3 days ago. Now, I find out this is normal, if you are supposed to be getting this kind of symptoms that I have, I think I got just about every symptom here is but I got first the pain was excruciating and then I got really dizzy, I got nauseous, I got like pain in my body but now what I have this really bothering me is my legs they feel very heavy, they also feel like tingling and numbness and it's kind of little hard for me to walk because of the 'bothers behind my leg'(Not clear), I was wondering if that was normal. When probed for the LOT#: Consumer stated, "I think this is two NO or NV, I am not sure. I don't know the handwriting. Its N2, two N I think then its 10. Her handwriting is really bad I don't understand that. I think its two N10 dose. Yes, that's what I am thinking because she is kind of, her handwriting is not really good. The madam said that the due date is 21 days I have to wait. When probed for the date of the first dose: Consumer stated, "16Feb of this year. I am sorry, on the back it says, 09Mar2022, Mar 09th of 2022, it says in the back. She got one date in the form and what the other date is it says dose 1 date, I think it must be 2/16Feb2022, on the back I think the back is for another vaccine that I am supposed to be getting." Per caller, she had her 1st dose of the vaccine last 16Feb2022 and it was horrible, the effects on her were really bad she stated. Caller stated, she got all the side effects as soon as she got the vaccine, caller got really dizzy, got nauseous, started to get numbness and heaviness and a tingle, with pain in her leg and feet got real cold, caller started to get shooting pain in her leg that makes her difficult to walk, it was really heavy and got a lot of joint pains and weakness, caller also got severe arm pain that lasted for 4 days, got muscle pain, was very tired and sleepy, headache, chills, cold sweats, body aches. Caller also added, last night when she was sleeping, she woke up with a very bad pain on her left leg, her left foot goes downwards and cannot straighten her toes, the pain was so bad that she can't straighten her toes at all. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Asthma (Verbatim: Asthma)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 04.03.2022
- Impfdatum
- 10.02.2022
- Beginn
- 10.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Neuralgia
Restless legs syndrome
Symptomtext
Pt notes sudden and significant increase in bilateral neuropathic pain and increasing restless leg syndrome symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- n/a.
- Aktuelle Erkrankungen
- Later discovered he had Primary/Early Syphilis (not known at time of vaccination).
- Vorgeschichte
- Uncontrolled Diabetes with weight loss, hypertension; restless leg syndrome; chronic pain syndrome; Major Depressive Disorder.
- Andere Medikamente
- Albuterol; Aspirin; Dulaglutide; Gabapentin; Insulin Glargine; Lisinopril; Dulera; Oxycodone/Acetaminophen; Pantoprazole; Paroxetine; Tizanidine; Influenza vaccination.
- Allergien
- Reported Prednisone allergy (though doubtful).
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 03.03.2022
- Impfdatum
- 25.02.2022
- Beginn
- 25.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Feeling abnormal
Hypersensitivity
Oedema peripheral
Peripheral swelling
Pyrexia
Swelling
Symptomtext
I felt weird and off. I ran a slight fever. Then my right arm started swelling up really bad. I took Benadryl 25mg. The doctors think it is an allergic reaction. I also have swelling in the area that's under my arm at the upper right quadrant of my chest. My arm is still swollen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma
- Andere Medikamente
- Zyrtec 10mg; Benadryl 25mg; Tamoxifen 20mg; Albuterol Inhaler
- Allergien
- Iodine; Gadolinium; Cipro; Sulfa; Latex
- Vorherige Impfungen
- Covid Vaccine (1st & 2nd)- My arm, collar bone, and all across my whole chest was swollen. (3/1/2021) I had a swollen arm (9/1/2
- Staat
- WA
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 28.02.2022
- Impfdatum
- 28.02.2022
- Beginn
- 28.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Eye movement disorder
Fatigue
Hyperhidrosis
Tremor
Vomiting
Symptomtext
Within 4 minutes of vaccine administration- (post well care) pt's grandmother was yelling for help from the exam room. Grandma reports patient complained he was dizzy and thought he might pass out but thought it was due to fear of needles. Within a couple seconds of saying that he started having body shakes and eyes rolled back in his head for about 1-2 seconds. He then snapped out of it according to grandma and started vomiting. Patient's vitals were then checked- within normal for his age and NP performed exam. Diaphoresis noted and some fatigue but was responsive and alert. Ice pack placed to chest, vitals and physical exam completed x2 after that at 15 minute intervals and within normal findings. Patient's mom was at the clinic by then and was able to be sent home with strict instructions regarding ER protocols. Printed information about myocardititis and MIS-C. Instructed patient he may not participate in tennis or any strenuous activity.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- Will have him follow up in 1 month for EKG and MISC-C labs as needed.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- ASthma Allergic rhinitis
- Andere Medikamente
- Prozac
- Allergien
- doxycyline cats
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 28.02.2022
- Impfdatum
- 20.02.2022
- Beginn
- 21.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain
Asthenia
Chills
Confusional state
Feeling abnormal
Flushing
Headache
Hyperhidrosis
Hypoaesthesia
Injection site swelling
Lymphadenopathy
Muscle spasms
Nausea
Pain
Paraesthesia
Pyrexia
Symptomtext
Site: Swelling at Injection Site-Medium, Systemic: Abdominal Pain-Medium, Systemic: Body Aches Generalized-Severe, Systemic: Chills-Severe, Systemic: Confusion-Medium, Systemic: Fever-Severe, Systemic: brain fog, left eye spasms, severe headache. swollen left armpit lymph node-Severe, Systemic: Flushed / Sweating-Medium, Systemic: Headache-Severe, Systemic: Lymph Node Swelling-Severe, Systemic: Nausea-Medium, Systemic: Numbness (specify: facial area, extremities)-Medium, Systemic: Tingling (specify: facial area, extemities)-Medium, Systemic: Weakness-Medium, Additional Details: Patient had a virtual consult with provider on February 23rd at 11:52am. Was instructed to rest, take acetaminophen for fever and report any additional symptoms that persist/worsen. Pateint also reports he had similar adverse effects after the 2nd vaccination but did not report to pharmacy or provider at that time (mainly severe headache, fever/chills, brain fog and tender left armpit lymphnode).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 28.02.2022
- Impfdatum
- 23.02.2022
- Beginn
- 23.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Chest pain
Chills
Cold sweat
Feeling abnormal
Extremity contracture
Hypoaesthesia
Incomplete course of vaccination
Paraesthesia
Injected limb mobility decreased
Pyrexia
Vomiting
Symptomtext
Pt reports, chills, fever, perfuse vomiting for 24 hours. After 24 hours continued with fever and "hands curling with numbness and tingling" for 15 minutes. Declines 2nd vaccine. Patient called PCP and HD to report. No treatment
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 28.02.2022
- Impfdatum
- 23.02.2022
- Beginn
- 23.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Chest pain
Chills
Cold sweat
Feeling abnormal
Extremity contracture
Hypoaesthesia
Incomplete course of vaccination
Paraesthesia
Injected limb mobility decreased
Pyrexia
Vomiting
Symptomtext
Pt reports, chills, fever, perfuse vomiting for 24 hours. After 24 hours continued with fever and "hands curling with numbness and tingling" for 15 minutes. Declines 2nd vaccine. Patient called PCP and HD to report. No treatment
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 27.02.2022
- Impfdatum
- 18.01.2022
- Beginn
- 23.01.2022
- Tage bis Beginn
- 5,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Gait inability
Inflammation
Joint swelling
Pain in extremity
Paraesthesia
Symptomtext
Patient states inflammatory reaction requiring hospitalization; leg pain could not lift leg or walk; leg pain could not lift leg or walk; Swelling in joints; pins and needles feeling; This is a spontaneous report received from a contactable reporter(s) (Pharmacist). A 63 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm right, administration date 18Jan2022 09:30 (Lot number: Fj5682) at the age of 63 years as dose 1 (tris), single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: INFLAMMATION (hospitalization) with onset 23Jan2022, outcome "unknown", described as "Patient states inflammatory reaction requiring hospitalization"; PAIN IN EXTREMITY (non-serious), GAIT INABILITY (non-serious) all with onset 23Jan2022, outcome "unknown" and all described as "leg pain could not lift leg or walk"; JOINT SWELLING (non-serious) with onset 23Jan2022, outcome "unknown", described as "Swelling in joints"; PARAESTHESIA (non-serious) with onset 23Jan2022, outcome "unknown", described as "pins and needles feeling". The events "patient states inflammatory reaction requiring hospitalization", "leg pain could not lift leg or walk", "leg pain could not lift leg or walk", "swelling in joints" and "pins and needles feeling" were evaluated at the physician office visit. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Based on the description given in the narrative, there is reasonable possibility of causal association between the serious event and the suspect BNT162B2 cannot be excluded. The impact of this report on the benefit/risk profile of the Pfizer drug is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 27.02.2022
- Impfdatum
- 24.01.2022
- Beginn
- 24.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal pain
Chest discomfort
Chest pain
Dyspnoea
Electrocardiogram
Investigation
Nausea
Oxygen saturation
Oxygen saturation decreased
Pain
SARS-CoV-2 test
Vomiting
Symptomtext
short of breath; aching/hurting all over; abdominal pain; chest discomfort; nausea; vomiting several times; oxygen saturation went down in the 70's; chest pain; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. An 81 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 24Jan2022 17:00 (Lot number: FJ5682) at the age of 81 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "CAD" (unspecified if ongoing); "Prostate cancer" (unspecified if ongoing); "Kidney disease" (unspecified if ongoing); "Diabetic" (unspecified if ongoing); "Interstitial lung disease" (unspecified if ongoing); "hypertension" (unspecified if ongoing); "hypothyroidism" (unspecified if ongoing); "sleep apnea" (unspecified if ongoing); "Known allergies: IVP dye" (unspecified if ongoing); "Known allergies: Ace Inhibitors" (unspecified if ongoing). Concomitant medication(s) included: AMIODARONE; LEVOTHYROXIN; METOPROLOL; LASIX [FUROSEMIDE]; ASA. Past drug history included: Iv lidocaine, reaction(s): "Drug Allergy"; Tricor, reaction(s): "Drug Allergy"; Tamiflu, reaction(s): "Drug Allergy"; Niacin, reaction(s): "Drug Allergy"; Amlodipine, reaction(s): "Drug Allergy". Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: EN3247, Location of injection: Arm Left), administration date: 28Jan2021, when the patient was 80 years old, for COVID-19 immunization; Bnt162b2 (Dose Number: 2, Batch/Lot No: EN531B, Location of injection: Arm Right), administration date: 18Feb2021, when the patient was 80 years old, for COVID-19 immunization. The following information was reported: DYSPNOEA (hospitalization) with onset 24Jan2022 21:00, outcome "recovering", described as "short of breath"; PAIN (hospitalization) with onset 24Jan2022 21:00, outcome "recovering", described as "aching/hurting all over"; ABDOMINAL PAIN (hospitalization) with onset 24Jan2022 21:00, outcome "recovering", described as "abdominal pain"; CHEST DISCOMFORT (hospitalization) with onset 24Jan2022 21:00, outcome "recovering", described as "chest discomfort"; NAUSEA (hospitalization) with onset 24Jan2022 21:00, outcome "recovering", described as "nausea"; VOMITING (hospitalization) with onset 24Jan2022 21:00, outcome "recovering", described as "vomiting several times"; OXYGEN SATURATION DECREASED (hospitalization) with onset 24Jan2022 21:00, outcome "recovering", described as "oxygen saturation went down in the 70's"; CHEST PAIN (hospitalization) with onset 24Jan2022 21:00, outcome "recovering", described as "chest pain ". The patient was hospitalized for dyspnoea, pain, abdominal pain, chest discomfort, nausea, vomiting, oxygen saturation decreased, chest pain (hospitalization duration: 4 day(s)). The events "short of breath", "aching/hurting all over", "abdominal pain", "chest discomfort", "nausea", "vomiting several times", "oxygen saturation went down in the 70's" and "chest pain " were evaluated at the emergency room visit. The patient underwent the following laboratory tests and procedures: electrocardiogram: (unspecified date) unknown results; investigation: (unspecified date) unknown results; oxygen saturation: (26Jan2022) 70, notes: oxygen saturation went down in the 70's; sars-cov-2 test: (26Jan2022) negative. Therapeutic measures were taken as a result of dyspnoea, pain, abdominal pain, chest discomfort, nausea, vomiting, oxygen saturation decreased, chest pain. The evening he received the Covid Booster vaccine (24Jan), he began aching/hurting all over. The next day (25Jan) he continued with the aching & hurting all over. He was in bed most of the day. That evening, he began to have abdominal pain, chest discomfort & nausea. He began vomiting several times & also became short of breath. He thought these symptoms would resolve. On 26Jan he really became short of breath, his oxygen saturation went down in the 70's. His abdominal pain & chest pain became worse. His wife then took him to the Emergency Room. He was admitted to PCU. Several tests, IV Lasix, heart monitoring.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- 4,0
- Labordaten
- Test Name: heart monitoring; Result Unstructured Data: Test Result:Unknown results; Test Name: Several tests; Result Unstructured Data: Test Result:Unknown results; Test Date: 20220126; Test Name: oxygen saturation; Result Unstructured Data: Test Result:70; Comments: oxygen saturation went down in the 70's; Test Date: 20220126; Test Name: Nasal Swab; Test Result: Negative
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Coronary artery disease; Diabetic; Drug allergy; Hypertension; Hypothyroidism; Interstitial lung disease; Kidney disorder; Prostate cancer; Sleep apnea
- Andere Medikamente
- AMIODARONE; LEVOTHYROXIN; METOPROLOL; LASIX [FUROSEMIDE]; ASA
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 25.02.2022
- Impfdatum
- 25.02.2022
- Beginn
- 25.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dysphagia
Dyspnoea
Eye swelling
Mouth swelling
Pruritus
Rash
Swelling face
Swollen tongue
Throat tightness
Symptomtext
Systemic: Allergic: Difficulty breathing-Medium, Systemic: Allergic: Difficulty swallowing, throat tightness-Medium, Systemic: Allergic: Itch generalized-Medium, Systemic: Allergic: Rash generalized-Medium, Systemic: Allergic: Swelling of face/eyes/mouth/tongue-Medium.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 24.02.2022
- Impfdatum
- 22.02.2022
- Beginn
- 23.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test normal
Chest pain
Electrocardiogram normal
Heart rate increased
Tachycardia
Symptomtext
Acute Tachycardia accompanied by chest pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- EKG, blood tests. EKG and blood panels were normal, heart rate was high.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- hormone/ period related migraines
- Andere Medikamente
- none
- Allergien
- penicillin
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 21.02.2022
- Impfdatum
- 15.02.2022
- Beginn
- 15.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dyspnoea
Pharyngeal swelling
Swelling face
Symptomtext
Difficulty breathing and swelling of the face/throat (not within 4 hours).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- N/A.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- COPD, asthma, GERD, acquired hypothyroidism, anxiety disorder, arthritis with multiple joint involvement, chronic CHR, malignant neoplasm of breast, dizziness, colon polyps, decreased renal function, osteoporosis
- Andere Medikamente
- Albuterol HFA, Fosamax, Xanax, Arimidex, Aspirin, Bevespi Aerosphere, Flovent HFA, Synthroid, Hyzaar, Mobic, Nitroglycerin, Nystatin oral suspension, Nystatin cream, Prilosec
- Allergien
- Adhesive, Azithromycin, Cefuroxime, Codeine, Levofloxacin, Prednisone, Sulfamethoxazole W-trimethoprim
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 20.02.2022
- Impfdatum
- 11.02.2022
- Beginn
- 13.02.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Asthenia
Dyspnoea
Dysstasia
Fatigue
Injection site pain
Laboratory test
Nodule
Pain
Pyrexia
Symptomtext
Fatigue, trouble standing, shortness of breath, weakness, body aches, low-grade fever, knot in the armpit, pain below where initial shot was given, and pain all the way down the left side to the hip area.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- respiratory panel performed on 02/16/2022
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- high blood pressure asthma acid reflex cancer(previously)
- Andere Medikamente
- Losartan Potassium 50 mg Hydrochlorothiazide 12.5 mg Proair Omeprazole 40 mg Mometasome Furoate Monohydrate nasal spray Fexofenadine HCL 180 mg
- Allergien
- potatoes Almonds Citrus Fruit Pork Penicillin
- Vorherige Impfungen
- Pfizer 04/05/2021 muscle aches and Pfizer 04/23/2021 extreme fatigue age at both shot was 50 yrs old
- Staat
- IN
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 19.02.2022
- Impfdatum
- 27.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anxiety
Blindness
Blood test
Dizziness
Dyspnoea
Feeling abnormal
Hyperventilation
Insomnia
Tremor
Viral infection
Vision blurred
X-ray
Symptomtext
had some vision loss for just a short period of time; labored breathing; heavy breathing; extremely dizzy; It was the worst feeling she ever had and it was just weird; didn't sleep; little anxiety; She was just shaking and shaking, like she was starting to have Parkinson''s or something/still wobbly; blurry than vision loss; might have had a little virus; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 72 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 27Jan2022 (Lot number: FJ5682, Expiration Date: 31Aug2022) at the age of 72 years as dose 3 (booster), single for covid-19 immunisation; cortisone (CORTISONE), first regimen details not provided (Batch/Lot number: unknown) and second regimen from 28Jan2022 (Batch/Lot number: unknown) to 28Jan2022 at one in each shoulder for pain. Relevant medical history included: "diabetes, type 2" (unspecified if ongoing); "high blood pressure/Hypertension" (unspecified if ongoing); "cholesterol" (unspecified if ongoing); "bone spurs" (unspecified if ongoing). Concomitant medication(s) included: LOSARTAN taken for high blood pressure; ATORVASTATIN (ongoing); HYDROCHLOROTHIAZIDE taken for blood pressure (ongoing); TRULICITY taken for Diabetes (ongoing). Vaccination history included: Bnt162b2 (Dose Number:01, LOT: EW0191 , EXP: 30Sep2021, Route, Anatomical Location: left arm), administration date: 21Jun2021, when the patient was 71 years old, for Covid-19 Immunization, reaction(s): "No AE(s) "; Bnt162b2 (Dose Number:02, LOT: EW0181 , EXP: 31Aug2021, Route, Anatomical Location: left arm), administration date: 12Jul2021, when the patient was 71 years old, for Covid-19 Immunization, reaction(s): "No AE(s) "; Flu shot (in the 70s), for immunization, reaction(s): "No AE(s) ". No Additional Vaccines Administered on Same Date of the Pfizer Suspect. No Prior Vaccinations (within 4 weeks). Caller states the only vaccine she has had all these years besides this, for Covid, was probably the flu shot in the 70s. No AE(s) following prior vaccinations. No Family Medical History Relevant to AE(s). The following information was reported: BLINDNESS (medically significant) with onset 28Jan2022, outcome "recovered" (2022), described as "had some vision loss for just a short period of time"; DYSPNOEA (non-serious) with onset 28Jan2022, outcome "unknown", described as "labored breathing"; HYPERVENTILATION (non-serious) with onset 28Jan2022, outcome "unknown", described as "heavy breathing"; DIZZINESS (non-serious) with onset 28Jan2022, outcome "unknown", described as "extremely dizzy"; FEELING ABNORMAL (non-serious) with onset Jan2022, outcome "unknown", described as "It was the worst feeling she ever had and it was just weird"; INSOMNIA (non-serious) with onset Jan2022, outcome "unknown", described as "didn't sleep"; ANXIETY (non-serious) with onset Jan2022, outcome "unknown", described as "little anxiety"; TREMOR (non-serious) with onset Jan2022, outcome "not recovered", described as "She was just shaking and shaking, like she was starting to have Parkinson''s or something/still wobbly"; VISION BLURRED (non-serious) with onset Jan2022, outcome "unknown", described as "blurry than vision loss"; VIRAL INFECTION (non-serious) with onset Jan2022, outcome "unknown", described as "might have had a little virus". The patient underwent the following laboratory tests and procedures: blood test: (2021) unknown results; x-ray: (unspecified date) unknown results. The action taken for cortisone was unknown. Therapeutic measures were not taken as a result of blindness, dyspnoea, hyperventilation, dizziness, feeling abnormal, insomnia, anxiety, tremor, vision blurred, viral infection. Additional information: Caller stated she was calling regarding the Pfizer booster shot. Further clarified that she was referring to the Pfizer Covid vaccine booster shot. She stated that she called (withheld) and they advised her to call Pfizer. She stated that she got her booster shot last Thursday and had a doctors appointment the next day. The doctor gave her 2 shots of Cortisone in her shoulder. She was not aware that the doctor was going to do it that day or not. Caller states that Friday, she had heavy breathing, labored breathing and was extremely dizzy. She had some vision loss for just a short period of time. She wasn't sure if it was the booster shot or a combination with the Cortisone shot, that kind of bumped against each other. She had not had any kind of problem with the Pfizer shot prior to that. She had all ready contacted her orthopedic doctor and they had not returned the call yet. She did not know if this had happened to anybody else and knows that any reaction should be reported to the company. All of Friday and about half of Saturday, she didn't know. It was the worst feeling she ever had and it was just weird. She also didn't sleep and she had a little anxiety. She was really concerned because she had 2 Cortisone shots in her knees, like 3 weeks before that. Caller stated she was not aware that her doctor was going to give her the Cortisone shot because she was just there getting an X-ray. They suggested that she had the 2 Cortisone shots. Caller stated she had not had any adverse reactions to Cortisone shots before. She has had Cortisone shots before, in her life and she did not know if the 2 collided, the Cortisone shot and the Covid booster shot. Caller stated she gave it the weekend because she did not want to jump on the phone or jump into the doctors office. She tried to see if it could be a food allergy or who knows. She waited and carried it through. When it started, she didn't think it started until 7:00m or 8:00pm that night. It went on the whole night that Friday. She made sure she had her other medicines, she had other medical problems. She made sure she had all her medicines for her diabetes, her blood pressure and her cholesterol. She made sure she had taken them. She had gotten the shot that, kind of calmed down a little. She thought and stated she had never felt it but, people had told her then when the blood sugar spikes, they would have these problems. That was what it felt like. She calmed down a little when she took the shot but it kept going on all night. She stated she finally dozed off about maybe 2:00am or 3:00am the next morning and was still wobbly. She was just shaking and shaking, like she was starting to have Parkinsons or something. Then, the hands were shaking a little and she was trying to control them. It wasn't severe if she could keep her head still. She stated she was a little shocked because she hadn't ever had problems with Cortisone before. Saturday, she kind of mellowed out and had some place to go on Sunday. She stated that yesterday, she made the call to the orthopedic doctor and left them a message. She tried calling (withheld) yesterday but something was happening with the phone. She called today and today was the first day she had reported this. Clarified that when the caller previously mentioned she had experienced vision loss, she stated that it was more blurry than vision loss. She stated she had diabetes, type 2 and had gotten shaky but, nothing like this. She felt fine with the booster shot the day before. Clarified that she had the Covid booster shot the day before the Cortisone shot. Clarified that the caller had the Pfizer Covid booster 27Jan2022 at 11:30am or 12:00pm. She had her Cortisone shot around 2:00pm or 3:00pm, Friday, 28Jan2022. Clarified these as the dates she had the booster shot and Cortisone shot and not the dates the caller previously stated. Clarified that when the caller previously mentioned she got the shot and calmed down a little, she was referring to when she got her booster shot. She stated that she felt fine after she got her booster shot. No Treatment. She states that the only medicine she had was the medicine she has been taking daily or weekly. Caller stated that there was probably absolutely nothing but there might be something going on. If she told something, they can put this in the data for further information, or someone else may have the same problems. Caller states her body was falling apart. She had 2 injections of Cortisone shot, one in each knee, about a month ago, within the last month. When she went to see this doctor, to get an X-ray done, it was in her shoulder, because she was having pains. They told her she had some bone spurs in both sides and that she had the option for them to go in there and grind the bone down or give her the Cortisone shot. She states she just had some Cortisone shots in her knees. She was told that it didn't matter if it were in another part of her body, that they could put Cortisone in different places. She stated she had one shot in each shoulder. She wanted to report this because it was absolutely weird. It was probably nothing and she might have had a little virus but, she did not know, it was strange. She stated that now it was reported and she felt comfortable. The adverse events didn't require a visit to Emergency Room and Physician Office. Caller states she had blood (Tests) taken for her annual last Sep2021 or Nov2021, it was between Sep2021 and Nov2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Test Date: 2021; Test Name: blood; Result Unstructured Data: Test Result:Unknown results; Test Name: X-ray; Result Unstructured Data: Test Result:Unknown results
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Bone spur; Cholesterol; Hypertension; Type 2 diabetes mellitus
- Andere Medikamente
- LOSARTAN; ATORVASTATIN; HYDROCHLOROTHIAZIDE; TRULICITY
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 19.02.2022
- Impfdatum
- 14.02.2022
- Beginn
- 14.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Chest pain
Diarrhoea
Headache
Myalgia
Palpitations
Pyrexia
Symptomtext
Chest pain, heart palpitations, crippling joint pain, muscle pain and daily fever (from 103.5 first 3 days to 101 daily since). Headaches won't go away even with Imitrex. Diarrhea. No treatments given. I'm scheduled for blood work and EKG next week. I was told to go to hospital if it escalates prior to my appointment. My rheumatologist was upset I got the vaccine, because I am so sensitive to all vaccines. I had COVID-19 1 month ago. PCP didn't want me to get booster. As of today, I received the vaccination. I had to decide between this outcome or losing my job. Now vaccination not mandated. And now I'm ignored because it's just a side effect.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- COVID-19 positive January 18th.
- Vorgeschichte
- Mixed connective tissue disease (2018)
- Andere Medikamente
- Plaquenil 200mg BID; Adderall 30mg QD; Tylenol 1000mg (after vaccination)
- Allergien
- None
- Vorherige Impfungen
- Pfizer COVID-19.
- Staat
- CA
- Alter
- -
- Geschlecht
- F
- Eingang
- 16.02.2022
- Impfdatum
- 11.02.2022
- Beginn
- 12.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Electrocardiogram
Headache
Nausea
Palpitations
Symptomtext
Patient developed headache, nausea and palpitations 02/12/22. Palpitations continue intermittently lasting 5-10 min.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- EKG.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Cephalexin, Sulfa, NSAID's
- Vorherige Impfungen
- chest pain
- Staat
- NC
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 16.02.2022
- Impfdatum
- 25.01.2022
- Beginn
- 25.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Paraesthesia
Symptomtext
Site: Pain at Injection Site-Mild, Systemic: Tingling (specify: facial area, extremities)-Mild, Additional Details: Patient reported back for 2nd dose today. Her left arm, where she received the 1st dose on 1/25/2022, has been tingling since the 1st administration.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 10.02.2022
- Impfdatum
- 07.02.2022
- Beginn
- 07.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Dyspnoea
Tonsillar disorder
Symptomtext
COVID19 (Pfizer-BioNTech)Patient began experiencing difficulty breathing with visible tonsilar swelling upon oral evaluation 20 minutes post 2nd pfizer injection. Epi 0.3mg was administered IM to left thigh at 1125 and patient was transferred to ER for further evaluation at 1130. Spoke with patient at 4pm and states he was discharged home in stable condition after receiving steroid and benadryl injections.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- Pt reported "white spots" appeared on arm after first pfizer dose was given.
- Staat
- MO
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 09.02.2022
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood magnesium normal
Blood phosphorus normal
Condition aggravated
Differential white blood cell count normal
Electrocardiogram QT prolonged
Full blood count normal
Headache
Human chorionic gonadotropin negative
Metabolic function test normal
Symptomtext
3rd COVID vaccine dose given on 2/4/22. Severe headache, onset 4 hours following vaccine administration, initially relived by Compazine, Benadryl and Toradol. Headache recurred 48 hours later and did not improve with Compazine, Benadryl and Toradol, which was repeated, followed by Prednisone. The patient was seen in the ER on 2/7/22 and given a third round of Compazine, Benadryl and Toradol. She was admitted to hospital and received 4 doses of DHE after which her headache improved. She was discharged from hospital on 2/9/22. She had similar symptoms following doses 1 and 2 and Pfizer vaccine in May and June 2021, VAERS report completed July 2021. CDC CISA consult performed prior to administration of dose 3, recommendations for Neurology consult and mitigation plan followed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- 2,0
- Labordaten
- Normal CBC with diff, CMP, phosphorus and magnesium, negative urine beta HCG EKG with slight prolongation of QTc obtained after administration of Compazine, Benadryl and Toradol
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- History of headaches following doses 1 and 2 of Pfizer COVID vaccine, hospitalized both times
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- Severe headache requiring hospital admission, Pfizer COVID vaccination 5/15/21 and 6/5/21
- Staat
- IN
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 08.02.2022
- Impfdatum
- 01.02.2022
- Beginn
- 02.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Headache
Hypoaesthesia
Muscle spasms
Muscular weakness
Pain in extremity
Paraesthesia
Symptomtext
I started to experience extreme leg and back pain the day after the vaccine. I have since been experiencing muscle spasms throughout the entire headache. I am still experiencing back pain. My legs and hands feel very weak and I feel sharp shoot pains, numbness, and tingling through all extremities. I also experience stomach spasms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- I have not received any tests so far, I will be contacting a doctor tomorrow!
- Aktuelle Erkrankungen
- I have just been diagnosed with PCOS and a possible thyroid issue. I was advised I was ok to take this vaccine.
- Vorgeschichte
- I have been having issues with my health for a few years. I found that I have a torn labrum, I had a mild bulging disc at c6-c7 and I also have a torn right hip labrum. I was just diagnosed with PCOS in December and I have very small nodules on my Thyroid. I have not started medication because I am being tested for Insulin resistance due to PCOS.
- Andere Medikamente
- No
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- ND
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 08.02.2022
- Impfdatum
- 19.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Bronchospasm
Chest discomfort
Cough
Dyspnoea
Feeling abnormal
Productive cough
Pyrexia
Rhinorrhoea
SARS-CoV-2 test negative
Sputum discoloured
Wheezing
Symptomtext
She got the vaccine, on Friday she was running a light fever, coughing, tightness in her chest. Friday she called the clinic and they told her to take cough drops, and OTC medications for the symptoms. On 1/22/22 she called them again and she was advised to go to the office on 1/24/22 for COVID test, did so and was a 48 test, got the results on 1/26/22 that they were negative. By then she was not doing good, you had coughing green sputum, running out of her nose like water (green), light fever of 99, trouble breathing with shortness of breath, and went to the ER. They did a breathing treatment, they gave her a Ventolin inhaler, a steroid shot, they advised her to see her PCP in 7 days. While in the ER she had a 2nd COVID test that was negative also. They told her that they did not have the reason for her symptoms, but if they continue to return to the ER or go to the PCP. Diagnosed with acute bronchial spasm. She had to go out of town to bury her nephew who was killed. On 2/2/22 she went to CHC and was given a Z-Pak, and a cough syrup Promethezine DM. She was afraid that she had gotten COVID as she felt bad. She saw doctor at the clinic. This did help her, but she still has wheezing when she takes a deep breath, and still coughing up sputum.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Hypertension, fibromyalgia.
- Andere Medikamente
- Valsartan 320 mg, Amlodipine 10 mg, Vitamin D 4000 units.
- Allergien
- Dilaudid, Norco, narcotic pain medications.
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 06.02.2022
- Impfdatum
- 04.02.2022
- Beginn
- 05.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Headache
Lymph node pain
Pain in extremity
Symptomtext
Was the booster shot Left Arm pain - starting within 8 hrs (lasting > 24 hrs) Left Lymph node pain - starting within 12 hrs after arm pain (lasting > 24 hrs) Headache - starting within 12 hrs (lasting > 24 hrs)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Migraines Osteoarthritis High blood pressure Low thyroid Structural and muscular issues (handicapped)
- Andere Medikamente
- High blood pressure (Losartan Potassium, Amlodapine) Thyroid (Levothyroxine) NoRco for pain Multi vitamin Biotine B12 (Rizatriptin as needed for migraines) Vitamin D
- Allergien
- Iodine
- Vorherige Impfungen
- Arm pain
- Staat
- FL
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 05.02.2022
- Impfdatum
- 22.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anxiety
Condition aggravated
Dyspnoea
Heart rate
Heart rate increased
Chest discomfort
Wheezing
Oxygen saturation
Oxygen saturation decreased
Symptomtext
at rest heart rate up to 101-102; O2 saturations at 94%; maybe it was anxiety; shortness of breath; shortness of breath/progressively getting worse/states she has been short of breath with talking and walking; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 54 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 22Jan2022 16:00 (Batch/Lot number: unknown) at the age of 54 years as dose 1, single for covid-19 immunisation at Pharmacy. Relevant medical history included: "Sarcoidosis", start date: 2012 (ongoing), notes: where the majority of the lymph nodes are effected; "autoimmune disease" (unspecified if ongoing), notes: have effects lymph nodes in center of chest; "so many allergies" (unspecified if ongoing). There were no concomitant medications. Family Medical History Relevant to AE(s): None. History of all previous immunization with the Pfizer vaccine considered as suspect: none. Additional Vaccines administered on Same Date of the Pfizer Suspect: None. Prior Vaccinations (within 4 weeks): None. The following information was reported: DYSPNOEA (medically significant) with onset 22Jan2022, outcome "not recovered", described as "shortness of breath"; CONDITION AGGRAVATED (medically significant) with onset 22Jan2022, outcome "not recovered", described as "shortness of breath/progressively getting worse/states she has been short of breath with talking and walking"; HEART RATE INCREASED (non-serious), outcome "unknown", described as "at rest heart rate up to 101-102"; OXYGEN SATURATION DECREASED (non-serious), outcome "unknown", described as "O2 saturations at 94%"; ANXIETY (non-serious), outcome "unknown", described as "maybe it was anxiety". After the vaccine it was just really hard to take a deep breath. AE(s) require a visit to: Emergency Room: No and Physician Office: No. The patient underwent the following laboratory tests and procedures: heart rate: elevated to 101-102; oxygen saturation: 94 %, notes: her O2 saturations has been fine around 94% but for her that is a little low. Investigation Assessment: No. The lot number for bnt162b2 was not provided and will be requested during follow up.; Sender's Comments: Based on the information currently available,The casual association between the reported events and suspected vaccine BNT162B2 cannot be completely excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Test Name: heart rate; Result Unstructured Data: Test Result:elevated to 101-102; Test Name: O2 saturations; Test Result: 94 %; Comments: her O2 saturations has been fine around 94% but for her that is a little low
- Aktuelle Erkrankungen
- Sarcoidosis (where the majority of the lymph nodes are effected)
- Vorgeschichte
- Medical History/Concurrent Conditions: Allergy; Autoimmune disorder (have effects lymph nodes in center of chest)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 04.02.2022
- Impfdatum
- 18.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Dyspnoea
Fatigue
Heart rate increased
Symptomtext
Accelerated heart rate, dizziness, out of breath and fatigue feeling.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Cannot get in until March to see my doctor to request EKG and stress test.
- Aktuelle Erkrankungen
- None. This was the booster for the Pfizer COVID vaccine.
- Vorgeschichte
- Slight high blood pressure.
- Andere Medikamente
- Accelerated heart rate, dizziness, out of breath and fatigue.
- Allergien
- Codeine
- Vorherige Impfungen
- 2nd COVID dose I had a slight rash that lasted a couple hours.
- Staat
- MN
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 02.02.2022
- Impfdatum
- 01.02.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoaesthesia
Injection site pain
Paraesthesia
Symptomtext
Vaccine injection hurt more than expected, more than previous vaccines. One hour after shot describes whole arm "pins and needles", that lasted a couple hours then changed to "numb feeling" in upper arm and right palm. Exam with normal strength, ROM
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Type 1 Diabetes Mellitus
- Andere Medikamente
- Insulin pump
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 28.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Injection site erythema
Injection site pain
Injection site warmth
Palpitations
Symptomtext
Patient reported pain and redness around injection site. Patient also reported it was warm to the touch. She tried a few courses of bendryl and over the counter pain relievers to aid but it did not change. Patient also reported heart palpitations. She went to emergency/urgent care and was prescribed a course of antibiotics.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NOT REPORTED
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 27.01.2022
- 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: nein
Injection site pain
Insomnia
Malaise
Pain
Pain in extremity
Paraesthesia
Symptomtext
Site: Pain at Injection Site-Mild, Systemic: Body Aches Generalized-Severe, Systemic: Unable to Sleep-Severe, Additional Details: PATIENT STATED SYMPTOMS STARTED LATER THAT DAY OF THE VACCINATION. SYMPTOMS INCLUDED "NOT FEELING WELL, TINGLING SENSATION AND TOSSING AND TURNING WHEN TRYING TO SLEEP". PT ALSO COMPLAINED OF A SORE ARM BUT IT WAS GETTING BETTER. PT ON 01/26 COMPLAINED OF BODY ACHES WHICH SHE DID NOT PREVIOUSLY MENTION.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 25.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test abnormal
Chest pain
Dizziness
Fatigue
Headache
Heart rate
Heart rate increased
Lymphadenopathy
Nausea
Pain
Rash
Hypersensitivity
Immunisation
SARS-CoV-2 test
Swelling face
Throat tightness
Urinary tract infection
Wheezing
Symptomtext
fatigue; Allergic reaction day after booster; soreness; headache; nausea; pain in chest; rapid heartbeat; swelling in face; lymph nodes in neck and jaw; tight throat; booster; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 13 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 14Jan2022 18:30 (Lot number: FJ5682) at the age of 13 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Possible diagnosis of Mast Cell Syndrome" (unspecified if ongoing), notes: Possible diagnosis of Mast Cell Syndrome; "Multiple allergies" (unspecified if ongoing), notes: Name of Drug as Reported: Multiple allergies as yet unsubstanciated by allergist. , Reaction: Allergy. Concomitant medication(s) included: MIDOL [IBUPROFEN]. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: EW0167), administration date: 15May2021, when the patient was 12 years old, for COVID-19 Immunization; Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0167), administration date: 05Jun2021, when the patient was 12 years old, for COVID-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 14Jan2022 18:30, outcome "unknown", described as "booster"; FATIGUE (non-serious) with onset 15Jan2022 07:00, outcome "not recovered", described as "fatigue"; HYPERSENSITIVITY (non-serious) with onset 15Jan2022 07:00, outcome "not recovered", described as "Allergic reaction day after booster"; PAIN (non-serious) with onset 15Jan2022 07:00, outcome "not recovered", described as "soreness"; HEADACHE (non-serious) with onset 15Jan2022 07:00, outcome "not recovered", described as "headache"; NAUSEA (non-serious) with onset 15Jan2022 07:00, outcome "not recovered", described as "nausea"; CHEST PAIN (non-serious) with onset 15Jan2022 07:00, outcome "not recovered", described as "pain in chest"; HEART RATE INCREASED (non-serious) with onset 15Jan2022 07:00, outcome "not recovered", described as "rapid heartbeat"; SWELLING FACE (non-serious) with onset 15Jan2022 07:00, outcome "not recovered", described as "swelling in face"; LYMPHADENOPATHY (non-serious) with onset 15Jan2022 07:00, outcome "not recovered", described as "lymph nodes in neck and jaw"; THROAT TIGHTNESS (non-serious) with onset 15Jan2022 07:00, outcome "not recovered", described as "tight throat". The events "fatigue", "allergic reaction day after booster", "soreness", "headache", "nausea", "pain in chest", "rapid heartbeat", "swelling in face", "lymph nodes in neck and jaw" and "tight throat" were evaluated at the physician office visit and emergency room visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of fatigue, hypersensitivity, pain, headache, nausea, chest pain, heart rate increased, swelling face, lymphadenopathy, throat tightness. Additional Information: Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Treatment received for the adverse event were Anyphylaxis ER treatment, prednisone, cephalexin.Prior to vaccination, the patient was not diagnosed with COVID-19. Follow-Up (20Jan2022): Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220115; Test Name: heartbeat; Result Unstructured Data: Test Result:Rapid; Test Date: 20220107; Test Name: Binax Now; Test Result: Negative; Comments: Nasal Swab.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Mast cell activation syndrome (Possible diagnosis of Mast Cell Syndrome); Multiple allergies (Name of Drug as Reported: Multiple allergies as yet unsubstanciated by allergist. Reaction: Allergy.)
- Andere Medikamente
- MIDOL [IBUPROFEN].
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 25.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test abnormal
Chest pain
Dizziness
Fatigue
Headache
Heart rate
Heart rate increased
Lymphadenopathy
Nausea
Pain
Rash
Hypersensitivity
Immunisation
SARS-CoV-2 test
Swelling face
Throat tightness
Urinary tract infection
Wheezing
Symptomtext
fatigue; Allergic reaction day after booster; soreness; headache; nausea; pain in chest; rapid heartbeat; swelling in face; lymph nodes in neck and jaw; tight throat; booster; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 13 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 14Jan2022 18:30 (Lot number: FJ5682) at the age of 13 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Possible diagnosis of Mast Cell Syndrome" (unspecified if ongoing), notes: Possible diagnosis of Mast Cell Syndrome; "Multiple allergies" (unspecified if ongoing), notes: Name of Drug as Reported: Multiple allergies as yet unsubstanciated by allergist. , Reaction: Allergy. Concomitant medication(s) included: MIDOL [IBUPROFEN]. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: EW0167), administration date: 15May2021, when the patient was 12 years old, for COVID-19 Immunization; Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0167), administration date: 05Jun2021, when the patient was 12 years old, for COVID-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 14Jan2022 18:30, outcome "unknown", described as "booster"; FATIGUE (non-serious) with onset 15Jan2022 07:00, outcome "not recovered", described as "fatigue"; HYPERSENSITIVITY (non-serious) with onset 15Jan2022 07:00, outcome "not recovered", described as "Allergic reaction day after booster"; PAIN (non-serious) with onset 15Jan2022 07:00, outcome "not recovered", described as "soreness"; HEADACHE (non-serious) with onset 15Jan2022 07:00, outcome "not recovered", described as "headache"; NAUSEA (non-serious) with onset 15Jan2022 07:00, outcome "not recovered", described as "nausea"; CHEST PAIN (non-serious) with onset 15Jan2022 07:00, outcome "not recovered", described as "pain in chest"; HEART RATE INCREASED (non-serious) with onset 15Jan2022 07:00, outcome "not recovered", described as "rapid heartbeat"; SWELLING FACE (non-serious) with onset 15Jan2022 07:00, outcome "not recovered", described as "swelling in face"; LYMPHADENOPATHY (non-serious) with onset 15Jan2022 07:00, outcome "not recovered", described as "lymph nodes in neck and jaw"; THROAT TIGHTNESS (non-serious) with onset 15Jan2022 07:00, outcome "not recovered", described as "tight throat". The events "fatigue", "allergic reaction day after booster", "soreness", "headache", "nausea", "pain in chest", "rapid heartbeat", "swelling in face", "lymph nodes in neck and jaw" and "tight throat" were evaluated at the physician office visit and emergency room visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of fatigue, hypersensitivity, pain, headache, nausea, chest pain, heart rate increased, swelling face, lymphadenopathy, throat tightness. Additional Information: Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Treatment received for the adverse event were Anyphylaxis ER treatment, prednisone, cephalexin.Prior to vaccination, the patient was not diagnosed with COVID-19. Follow-Up (20Jan2022): Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220115; Test Name: heartbeat; Result Unstructured Data: Test Result:Rapid; Test Date: 20220107; Test Name: Binax Now; Test Result: Negative; Comments: Nasal Swab.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Mast cell activation syndrome (Possible diagnosis of Mast Cell Syndrome); Multiple allergies (Name of Drug as Reported: Multiple allergies as yet unsubstanciated by allergist. Reaction: Allergy.)
- Andere Medikamente
- MIDOL [IBUPROFEN].
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 24.01.2022
- Impfdatum
- 19.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Symptomtext
Chest pain 48 hours after vaccine. I was at rest. Symptoms went away with Motrin 400 mg, but come back when the Motrin wears off.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- seasonal allergies
- Vorgeschichte
- OA
- Andere Medikamente
- Allegra, Motrin, Tylenol
- Allergien
- Compazine
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 22.01.2022
- Impfdatum
- 22.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Cold sweat
Grip strength decreased
Hypoaesthesia
Mobility decreased
Paraesthesia
Symptomtext
Client complained of numbness/tingling to left arm, unable to move, weak grips, resp even unlabored, skin cool, clammy, pupils reactive, EMS called, reassessed with weakness moving to right arm. Vitals stable 120/80, HR 76.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None reported
- Vorgeschichte
- Mother reports tremors, neuro deficits after motor vehicle accident 6 months ago
- Andere Medikamente
- None reported
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 21.01.2022
- Impfdatum
- 18.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Dizziness
Electrocardiogram
Pain in extremity
Palpitations
Vision blurred
Symptomtext
Intermittent dizziness since received vaccine and blurry vision. Heart racing daily since received shot. Soreness in right arm where received shot. Internal pain in mid to back of upper left arm (arm not with injection)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- EKG, blood pressure, 1/21/22
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma, Eczema
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 21.01.2022
- Impfdatum
- 19.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Heart rate increased
Nausea
Palpitations
Vertigo
Symptomtext
My heart was beating very hard and fast while laying down. I took ibuprofin and it helped but I thought you should know. My heart felt like it would explode and I was very dizzy and was experiencing intense vertigo as well. Playing a video game I turned the camera and nearly vomited.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- None because the US has a PROFIT based health system and I cannot afford to have doctor...like millions of us, because we are a capitalist hellscape.
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- Post gonadectomy arthrosis, osteoporosis, intersex, congenital hip dysplasia
- Andere Medikamente
- no
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 21.01.2022
- Impfdatum
- 18.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoaesthesia
Paraesthesia
Symptomtext
Systemic: numbness and tingling in the arm-Severe, Systemic: Tingling (specify: facial area, extemities)-Severe
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 20.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 5,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Chest pain
Electrocardiogram
Electrocardiogram ambulatory
Heart rate increased
Tachycardia
Symptomtext
On January 17,2022 had a fast heart rate known as Tachycardia. My heart rate was very high and I experienced chest pain. The next day my heart rate stayed high. I went to my doctor on January 19, 2022 had EKG, 2 week Holter monitor.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- EKG (waiting results), Holter Monitor (wear 2 weeks), Blood work (waiting results)
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Panic Disorder, Asthma (haven't had any trouble past month)
- Andere Medikamente
- Vit D, Vit C, Magnesium, Quercetin
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 19.01.2022
- Impfdatum
- 17.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Injection site swelling
Lymphadenopathy
Migraine
Mouth ulceration
Nausea
Oral candidiasis
Pyrexia
Tonsillar disorder
Symptomtext
Severe lymph node swelling under left armpit (left arm injection site), mouth ulcers, thrush/white patches on both tonsils, migraine, fever, nausea, severe fatigue - still continuous 49 hours later (current time)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- pharmacy facility refused to provide testing for adverse side effects.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 18.01.2022
- Impfdatum
- 15.01.2022
- Beginn
- 16.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Agitation
Chills
Hallucination
Pain
Pyrexia
Crying
Palpitations
Screaming
Suicidal ideation
Suicide attempt
Symptomtext
pt with fever, hallucinations/agitation approximately 15 hrs after injection - started to feel achy and chilled around 12 hrs, went to bed, then woke up told father he needed to die and tried to jump off the bannister of the stairs. Parents had to restrain him and asked questions - took about 4-5 minutes for him to return to baseline - no memory of episode. fine for rest of night and day. Then about 36 hrs post injection, woke again after ~90 min asleep with agitation, said, "dad you need to kill me", said he had jumped off a ledge or cliff earlier in day. after 4-5 minutes of calming he returned to baseline, no memory of episode. Was afebrile at this time. No prior h/o psychosis/mood disorder/SI, night terrors, hallucinations with fevers .
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- 2nd COVID pfizer vaccine, 12 yr, 6/11/21, lot EW0187; similar response ~18 hrs after vaccine woke up with fever, agitation, sayi
- Staat
- WA
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 18.01.2022
- Impfdatum
- 15.01.2022
- Beginn
- 16.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Agitation
Chills
Hallucination
Pain
Pyrexia
Crying
Palpitations
Screaming
Suicidal ideation
Suicide attempt
Symptomtext
pt with fever, hallucinations/agitation approximately 15 hrs after injection - started to feel achy and chilled around 12 hrs, went to bed, then woke up told father he needed to die and tried to jump off the bannister of the stairs. Parents had to restrain him and asked questions - took about 4-5 minutes for him to return to baseline - no memory of episode. fine for rest of night and day. Then about 36 hrs post injection, woke again after ~90 min asleep with agitation, said, "dad you need to kill me", said he had jumped off a ledge or cliff earlier in day. after 4-5 minutes of calming he returned to baseline, no memory of episode. Was afebrile at this time. No prior h/o psychosis/mood disorder/SI, night terrors, hallucinations with fevers .
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- 2nd COVID pfizer vaccine, 12 yr, 6/11/21, lot EW0187; similar response ~18 hrs after vaccine woke up with fever, agitation, sayi
- Staat
- WA
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 17.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abnormal dreams
Axillary pain
Chest pain
Discomfort
Fatigue
Injection site erythema
Injection site pain
Injection site swelling
Peripheral swelling
Pruritus
Rash
Symptomtext
RECEIVED THE VACCINE Friday at work. Normal arm soreness after. That night started having severe arm pain with pain into chest and left arm pit as well as itching. Woke up Saturday AM with rash across body worse on both arms, large amount of swelling/redness/pain around the size of a palm at injection site. Continued severe pain in arm/armpit into Sunday. As of Monday arm is still swollen. Took Benedryl 3X to get rash to go away, also took Tylenol 500MG to help with pain discomfort. Extreme fatigue/vivid dreams
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Chronic Neck pain, iron deficient anemia
- Andere Medikamente
- Iron, Vitamin D 50,000 IUs, Vitamin C
- Allergien
- Penicillin
- Vorherige Impfungen
- Flu vaccine 09/2021 no idea brand
- Staat
- OH
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 15.01.2022
- 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: ja
Erholt: nein
Anxiety
Dyspnoea
Feeling hot
Flushing
Tremor
Symptomtext
36 yo patient received her Pfizer booster at Covid clinic on 01/15/2022. Vaccine given at 1407 in left deltoid. Lot number was FJ5682, expiration 04/01/2022. Patient had no reaction after first 2 pfizer vaccines.Patient wanted to stay for 15 minute observation. Within the first 2-4 minutes after vaccine she developed warm feeling all over and was flushed, she felt she had a hard time taking a deep breath. She was given water and she said she felt better. At 2:25 she said she was feeling shaky and appeared very anxious.She was laid down on the cart and her BP was 144/84, pulse ox 100, HR 140. She was encouraged to take slow deep breaths and sips of water. She denied itchy feeling or difficulty swallowing.She continued to have feelings of not getting enough breath and emergency was called at 2:45.The squad came at 2:50 and placed her on gurney to transport to ER. She called her mother prior to leaving Covid Clinic. She has allergy to Penicillin. No present illness. She has a history of depression and Anxiety but has been off medication x 1 year. She took no medication earlier today.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- history of depression and anxiety - no medications x1 year
- Andere Medikamente
- none
- Allergien
- penicillin
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 13.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Chest pain
Echocardiogram normal
Headache
Myalgia
Pyrexia
Troponin increased
Symptomtext
Patient experienced myalgias close after vaccine booster. Began to have fever (100.8) and headache on day 2 post-vaccine. Presented to Emergency Department on day 5 post vaccine with chest pain and was found to have elevated troponins. Patient was hemodynamically stable and ultimately discharged after an echocardiogram had normal ventricular function. Mother also mentions mild substernal/epigastric pain after the 2nd administration. (Had gotten an ECG and GI cocktail in the ED at that time).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- Please see prior portion of documentation.
- Staat
- IN
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 12.01.2022
- Impfdatum
- 11.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Injection site pain
Musculoskeletal chest pain
Musculoskeletal disorder
Pain
Pain in extremity
Symptomtext
Decreased function of right extremity. Radiating pain and aches from injection site, down to lower extremity, through the vertebrae, and into rib cage.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Musculoskeletal chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- Phentermine and Escitalopram
- Allergien
- NA
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 11.01.2022
- Impfdatum
- 11.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Electrocardiogram abnormal
Palpitations
Sinus tachycardia
Symptomtext
Approximately 10 minutes after vaccine injection patient reported symptoms of heart pounding, apple watch showed heart rate at 177. Patient vitals obtained BP 169/105, pulse 177. No chest pain, shortness of breath, lightheadedness, nausea. After about 5 minutes vitals improved to BP 163/105 and P 135. Patient monitored for about 2 hours, took 20 mg of propranolol that was given to her after similar reaction to moderna vaccine - dose 2(about 15 hours later). Patient seen by clinician. 2 hours after procedure vitals imprved to BP 123/82 and pulse 97. Patient went home in personal vehicle.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- EKG 1/11/22 - Sinus tachycardia - rate 127 BPM
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- clindamycin
- Vorherige Impfungen
- Moderna Covid vaccine - date 2/23/21, reaction 2/24/21
- Staat
- CA
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- Impfdatum
- 10.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Dyspnoea
Erythema
Symptomtext
Pt had minor shortness of breath and redness after vaccination. Pt was monitored by both Pharmacist and Pharmacist in Charge. Informed pt that if necessary, epinephrine would be administered and EMS would be contacted. Pt refused treatment and did not want to contact EMS. Grandmother (legal guardian) did not disagree with her. Pt and grandmother were advised to go to Urgent Care. Pt went to a local urgent care where they administered fluids, O2 and epinephrine. Pt went home in good health per grandmother.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Per pt, she has Tourette
- Vorgeschichte
- Tourette
- Andere Medikamente
- N/A
- Allergien
- "Unidentified" per grandmother
- Vorherige Impfungen
- 2nd Pfizer vaccination on 6/9/21 where pt states she had a minor rash
- Staat
- MD
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 06.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest pain
Consciousness fluctuating
Fall
Symptomtext
Shortly after vaccination in the observation area, EMT noticed her starting to fall over from her seat. EMT and Friend where able to lay her on the ground. Pt. was in and out of consciousness. Pt complained of chest pain at times. Pt was placed on a NRB supine with legs elevated. Vitals were stable.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 11.12.2023
- Impfdatum
- 13.01.2022
- Beginn
- 10.12.2023
- Tage bis Beginn
- 696,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Cough
Malaise
Pyrexia
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test
Symptomtext
General malaise, fevers/chills, congestion, rhinorrhea, cough
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- IDNOW
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 04.08.2023
- Impfdatum
- 15.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Cardiac disorder
Diabetes insipidus
Endocrine disorder
Inflammation
Malaise
Nail ridging
Onycholysis
Raynaud's phenomenon
Weight decreased
Symptomtext
Systemic inflammation Weight loss Raynaud's Heart issues Beau's lines / Onycholysis Her heart continues to have issues
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- 25,0
- Labordaten
- She was in the hospital for 25 days from Feb 2022 to March 2022
- Aktuelle Erkrankungen
- Severe reactions from vaccines May and June 2021. Never recovered then the booster shot on 1/15/22 caused her to become very ill.
- Vorgeschichte
- In process of genetic testing for connective tissue disorder Osteochondritis dissecans (OCD) Central Diabetes Insipidus diagnosis May of 2022 - pituitary gland
- Andere Medikamente
- None - hospitalized on 2/10/22
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- F
- Eingang
- 09.06.2023
- Impfdatum
- 13.01.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Crying
Dysgraphia
Gait disturbance
Hypersomnia
Pain in extremity
Symptomtext
having trouble walking; legs hurt/hands hurt/Her legs and her hands worsen every week, every month; crying; She can't write now anyway; They go to sleep all the time; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP), Program ID. The reporter is the patient. A 60-year-old female patient received BNT162b2 (BNT162B2), on 13Jan2022 as dose 3 (booster), single (Lot number: FJ5682), in left arm for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: BNT162b2 (DOSE 1, SINGLE, Lot Number: EP7533, Anatomical location: right arm), administration date: 29Mar2021, for Covid-19 immunization; BNT162b2 (DOSE 2, SINGLE, Lot Number: EP7533, Anatomical location: left arm), administration date: 19Apr2021, for Covid-19 immunization. The following information was reported: GAIT DISTURBANCE (non-serious), outcome "not recovered", described as "having trouble walking"; PAIN IN EXTREMITY (non-serious), outcome "unknown", described as "legs hurt/hands hurt/Her legs and her hands worsen every week, every month"; CRYING (non-serious), outcome "unknown"; DYSGRAPHIA (non-serious), outcome "unknown", described as "She can't write now anyway"; HYPERSOMNIA (non-serious), outcome "unknown", described as "They go to sleep all the time". Additional information: She said that she took the COVID Pfizer vaccine booster, and since she received it her health became worse. She was having trouble walking and getting out of bed, including sitting up. She was crying. Her legs hurt all the time. She cannot write any-way. Her hands hurt too bad. They go to sleep all the time. This is all since the vaccine. Before the vaccine she was able to paint her walls with a brush. Now she cannot even paint a fingernail now. After the booster, she started to experience it within 30 days. Her problems were bilateral, and more in her legs than her arms. She has had no other vaccines. Prior Vaccinations within 4 weeks were none. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Back disorder NOS (She has always had back trouble, but could still walk); Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other Conditions: No
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 06.03.2023
- Impfdatum
- 30.01.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Dizziness
Headache
Pruritus
Rash
Rash vesicular
Symptomtext
I had my vaccination on 01/30/2022. A couple of weeks later in 02/2022 I started to experience dizziness and bad headache. I started to have a rash located on my abdomen and down my lower extremities and inner thighs. My doctor put me on a steroid cream that did end up making it worse. I had the headache for a couple of months. I had the dizziness for a couple of weeks. The rash lasted for about 6 months and started to blister. I did go to the emergency room for further evaluation in 08/2022. They prescribed me an ointment for the rash and blisters which reduced the itching and blisters.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Type II Diabetes
- Andere Medikamente
- Metformin; glipizide
- Allergien
- Aspirin; egg whites; melons
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 17.01.2023
- Impfdatum
- 12.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bursitis
Pain in extremity
Symptomtext
Starting shortly after receiving the vaccine, I developed soreness in the right arm. It has remained sore, achy and, even with recent steroid injection for Bursitis in the shoulder, the soreness did not resolve. Therefore, I feel its more related to the vaccine/injection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Amlodipine; Flomax; Baby Aspirin; Saw Palmetto; Red Rice Yeast
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 05.01.2023
- Impfdatum
- 13.01.2022
- Beginn
- 25.10.2022
- Tage bis Beginn
- 285,0
- Dosis
- 3
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Lethargy
Pain
Respiratory tract congestion
Symptomtext
I received my Covid-19 vaccine on 01/13/2022. On the morning of 10/25/2022 I woke up with extreme lethargy, extremely sore and really congested. I reached out to my doctor on 10/27/2022 and was prescribed Paxlovid. Symptoms lasted about two weeks.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Welbutrin;
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 11.08.2022
- Impfdatum
- 09.02.2022
- Beginn
- 29.07.2022
- Tage bis Beginn
- 170,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Cough
Feeling abnormal
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test negative
Upper-airway cough syndrome
Symptomtext
During the middle of night, I started having nasal dripping. I took a COVID-19 test and it was negative. By the afternoon I had a fever and congestion. I felt very bad. I had a fever for a couple of days. I was giving bebtelovimab treatment. I still have a lingering cough and congestion. My head feel a little better. On 8/5/2022, I tested for negative for COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- COVID-19
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Monoclonal gammopathy of undetermined significance
- Andere Medikamente
- Estradiol; rosuvastatin; multivitamin
- Allergien
- KEFLEX
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 25.07.2022
- Impfdatum
- 24.01.2022
- Beginn
- 19.05.2022
- Tage bis Beginn
- 115,0
- Dosis
- 3
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain
Back pain
Computerised tomogram abnormal
Dysmenorrhoea
Heavy menstrual bleeding
Menstrual disorder
Ultrasound scan
Symptomtext
I received my 3rd dose on 01/24/2022 and my symptoms started on the 05/19/2022. Around 6:00PM I had mild pain in my abdominal and lower back pain. It was shifting from back and abdominal and I couldn't even sit. The pain became more severe on the following day early morning around 1:30-2;00AM until 05:00AM on 05/20/2022. My husband took me to the local ER. I waited 2 and half hours but I wasn't allowed so we went to another hospital. They took me in. They gave me an IV and ibuprofen. I started feeling better, they also did a cat scan. They said I had severe dysmenorrhea (a lot of blood clots). I never experienced it before. Now I have excessive blood flow. My period stopped for menopause in December. On May 19/2022 it came back. I wasn't expecting it to be like this but after the 3rd dose this is what happened with me. I did a ultrasound yesterday 07/24/2022 but haven't gotten the result yet. I am going to OBGYN on 08/08/2022 for pap smear and LEEP procedure. I am recovering as of now. I am still experiencing the excessive period flow but not like before. I am just concerned how long will this keep happening for.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- Cats scan
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Multivitamins; aloe vera drink; vitamins
- Allergien
- Environmental; pollen
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 19.07.2022
- Impfdatum
- 18.04.2022
- Beginn
- 18.06.2022
- Tage bis Beginn
- 61,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Fatigue
Oropharyngeal pain
SARS-CoV-2 test positive
Symptomtext
On 06/18/2022 and 06/19/2022 I took a home test and both were negative. I retested on 06/20/2022 and was positive. The only thing I had was a really sore throat, dry cough and felt tired for the first day or so. I received a prescription for PAXLOVID 06/20/2022 and started taking it the same day. I was symptom free by Wednesday morning and tested negative the following Sunday the 26th.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Home COVID-19 06/20/2022 positive.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma
- Andere Medikamente
- SYNTHROID; CYTOMEL; VASCEPA; rosuvastatin; ZOLOFT
- Allergien
- Sulfa
- Vorherige Impfungen
- Dose 1 COVID-19 vaccine, slight fever; headache; fatigue.
- Staat
- MI
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 18.07.2022
- Impfdatum
- 17.01.2022
- Beginn
- 13.07.2022
- Tage bis Beginn
- 177,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Cough
Delivery
Exposure during pregnancy
Fatigue
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
Patient was seen at urgent care on 7/13/22 for cough, congestion, and fatigue and tested positive. She presented to the hospital on 7/16/22 to deliver her baby at 38 weeks 5 days. The baby was born on 7/17/22 and weighed 3.74 kg. During pregnancy, the patient had gestational diabetes and hypothyrodism
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID+ by PCR on 7/13/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 13.07.2022
- Impfdatum
- 11.04.2022
- Beginn
- 17.06.2022
- Tage bis Beginn
- 67,0
- Dosis
- 4
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Decreased appetite
Fatigue
Malaise
Oropharyngeal pain
Pain
SARS-CoV-2 test positive
Symptomtext
I had a sore throat, cough, body aches, malaise, fatigue, loss of appetite. I took an at-home COVID-19 on 06/18/2022 which came back positive. I called my doctor and was prescribed PAXLOVID and began the prescription a couple of days after. Once the prescription almost finished, I began feeling better. Currently, I'm doing fine and better than before.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 test: 06/18/2022.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Anxiety; Depression; High Cholesterol; Hypothyroidism
- Andere Medikamente
- Sertraline; atorvastatin; SYNTHROID; aspirin; LATUDA; calcium; vitamin D; vitamin E
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 13.07.2022
- Impfdatum
- 10.02.2022
- Beginn
- 10.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Rash
Symptomtext
Rash all over body, happened within hours of shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Doxcycline
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 12.07.2022
- Impfdatum
- 11.04.2022
- Beginn
- 25.06.2022
- Tage bis Beginn
- 75,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Headache
Oropharyngeal pain
SARS-CoV-2 test positive
Sleep disorder
Symptomtext
During the night of June 23, 2022, I awoke with a really bad headache, took TYLENOL and it subsided. I awoke on the next night with headache and sore throat. I took a COVID-19 that came up positive. I decided to go to the local hospital testing site to confirm my positive result. I was advised to contact my primary care physician to get PAXLOVID, I contacted them once I got home. I got a call back and they let me know they had prescribed the PAXLOVID and I could pick it up and start it immediately. I took a reduced amount of PAXLOVID per NP instruction as there could be side effects with my heart medication.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Home COVID-19 test. Rapid COVID-19 test.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Hypothyroid; High Blood Pressure; High Cholesterol
- Andere Medikamente
- Diltiazem ER; levothyroxine; metoprolol ER succinate; losartan; atorvastatin; senior multivitamin; aspirin EC; stool softener
- Allergien
- Sulfa; hydrochlorothiazide; MACROBID
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 29.06.2022
- Impfdatum
- 31.05.2022
- Beginn
- 22.06.2022
- Tage bis Beginn
- 22,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Fatigue
Headache
SARS-CoV-2 test positive
Throat irritation
Symptomtext
Starting 06/22/2022, I developed a scratchy throat and mild cough. I took at home tests on 06/22 and 06/23 which were negative. I took another at home test on 06/25/2022 which was positive. From 06/24/2022 until the 27th I had a dry cough in my chest, dull headache and some fatigue. Yesterday 06/28/2022 I still had some fatigue. Today, 06/29/2022 I still have fatigue but better than yesterday. The fatigue from 06/25/2022-06/27/2022 was very extreme.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- At home tests (06/22/2022 and 06/23/2022): negative; At home test (06/25/2022): positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Vitamin D; Gingko; Calcium
- Allergien
- Iodine contrast media
- Vorherige Impfungen
- Rabies booster - 21 days after booster I broke out into hives and had swelling which were treated with steroids.
- Staat
- CT
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 26.06.2022
- Impfdatum
- 16.01.2022
- Beginn
- 14.06.2022
- Tage bis Beginn
- 149,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Headache
Pyrexia
SARS-CoV-2 test
Symptomtext
fever, headache, fatigue
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Home rapid 6/14/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 06.06.2022
- Impfdatum
- 06.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 13,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain upper
Diarrhoea
Loss of personal independence in daily activities
Nausea
Sleep disorder
Vomiting
Symptomtext
He started with stomach pain two weeks after getting the vaccine. He had nausea, vomiting and diarrhea for about 2-3 times a week. It caused him to missed a lot of school because of this. Sometimes he can't sleep because of his stomach be hurting and he be in a lot of pain a lot of the time. It hurts me to see my son hurting. Before the vaccine my son was a healthy child. The doctor prescribe him some Banophen 25mg x2 every 6 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 19.05.2022
- Impfdatum
- 16.02.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 63,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Fatigue
Nasal congestion
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
Started with late afternoon fatigue on 4/20. Nasal congestion on 4/20 as well. 4/21 symptoms were worse, and sinus drainage caused coughing. 4/22 Monoclonal Antibody treatment received. 5/1 there was a deep cough in the chest. Antibiotics caused deep cough to resolve within 48 hours. About 4 weeks total the fatigue resolved.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Home covid test was positive and
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- ankylosing spondylitis
- Andere Medikamente
- Cosentix, Celebrex, multivitamin, melatonin, diclofenac gel, lidocaine, probiotics, Tylenol,
- Allergien
- Naprosyn, vancomycin, iodine
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 11.05.2022
- Impfdatum
- 11.04.2022
- Beginn
- 07.05.2022
- Tage bis Beginn
- 26,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Cough
Dizziness
Headache
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test
Vaccine breakthrough infection
Symptomtext
Breatkthrough case of COVID. Fever, cough, fatigue, headache, congestion, dizziness
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- BinaxNow at-home rapid antigen test
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- High cholesterol, Bow Hunter's Syndrome
- Andere Medikamente
- Atorvastatin, Pentoxifylline
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 10.05.2022
- Impfdatum
- 28.04.2022
- Beginn
- 05.05.2022
- Tage bis Beginn
- 7,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Swelling face
Urticaria
Symptomtext
Body hives swelling face
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 09.05.2022
- Impfdatum
- 08.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blister
Burning sensation
Rash
Rash erythematous
Rash papular
Rash pruritic
Symptomtext
Red raised fluid filled itchy burning rash to bilateral chest, upper abdomen, right neck area and rightmedial shoulder.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- 1st degree av block, palpitations, arthritis,
- Andere Medikamente
- Atorvastatin, Zyrtec, fish oil, multi vitamins , calcium supplement, Magnesium, ibuprofen, tylenol arthritis,
- Allergien
- Penicillin, Cephalosporins.
- Vorherige Impfungen
- Zostavax
- Staat
- MN
- Alter
- 46,0
- Geschlecht
- F
- 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
Arthralgia
Injection site pain
Limb discomfort
Pain
Symptomtext
After her COVID vaccine she had a sore spot distal to the injection site near her elbow. She continues to have some discomfort in her left arm. COVID booster was 3/9/22. She feels like her strength is normal but when she carries something she has significant pain in her left elbow. She denies any trauma to the elbow. Left elbow is not swollen or tender to touch. No joint effusion. No erythema. Full range of motion present in the left elbow without discomfort. Muscle strength is 5 out of 5 and equal in bilateral upper extremities. Extremities: No clubbing or cyanosis. No peripheral edema.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- watchful waiting
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- HTN, dyslipidemia, hyperlipidemia, hypothyroidism, Type 2 DM, Vit D deficiency, GERD, CKD, bipolar, peripheral neuropathy
- Andere Medikamente
- alprazolam, Apri, atenolol, strattera, atorvastatin, vit D3, duloxetine, diflucan, gabapentin, glipizide, levothyroxine, losartan, multivitamin, omeprazole, trileptal, ozempic, triazolam
- Allergien
- trulicity, medroxyprogesterone, ability, lisinopril, rexulti, temazepam
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 21.04.2022
- Impfdatum
- 12.02.2022
- Beginn
- 19.02.2022
- Tage bis Beginn
- 7,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Arthralgia
Symptomtext
new onset joint pain in knees, then other parts of body
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 20.04.2022
- Impfdatum
- 04.02.2022
- Beginn
- 05.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Erythema
Injection site bruising
Injection site erythema
Pain in extremity
Skin irritation
Tenderness
Symptomtext
I woke up and my left arm was red from my shoulder to my wrist and it hurt. At my injection site there was a large bruise. I was in pain just at the touch. It was just red and irritated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High Blood Pressure
- Andere Medikamente
- Labetalol
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 19.04.2022
- Impfdatum
- 22.03.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 21,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pruritus
Injection site urticaria
Symptomtext
Itching around injection site after getting vaccine, hives around injection site x3 weeks after vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pruritus
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Grave's Disease
- Andere Medikamente
- NA
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 98,0
- Geschlecht
- F
- Eingang
- 13.04.2022
- Impfdatum
- 25.01.2022
- Beginn
- 17.03.2022
- Tage bis Beginn
- 51,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Housebound
Pemphigoid
Rash vesicular
Symptomtext
In mid March, approximately six weeks after vaccination, patient developed a blistering skin rash in axilla and groin, clinically consistent with Bullous a pemphigoid. She has no prior history of similar condition. She is homebound so did not have a skin biopsy done. She has required prednisone, topical steroids, and follow up. I do not know the ultimate outcome of this condition in her.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash vesicular
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hyperlipidemia
- Andere Medikamente
- Zocor
- Allergien
- Flu shot- rash
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 07.04.2022
- Impfdatum
- 23.03.2022
- Beginn
- 01.03.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Chills
Dizziness
Pain
Pain in extremity
Symptomtext
body ache; chills; dizzy; arm was a little sore; Joint pain; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 51 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 23Mar2022 11:00 (Lot number: FJ5682) at the age of 51 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Blood pressure high" (ongoing), notes: Blood pressure high Diagnosed years ago; "allergic to penicillin" (unspecified if ongoing), notes: allergic to penicillin. Concomitant medication(s) included: NORVASC. The following information was reported: DIZZINESS (non-serious) with onset 24Mar2022, outcome "recovered" (24Mar2022), described as "dizzy"; PAIN (non-serious) with onset 26Mar2022 07:00, outcome "recovering", described as "body ache"; CHILLS (non-serious) with onset 26Mar2022 07:00, outcome "unknown", described as "chills"; ARTHRALGIA (non-serious) with onset Mar2022, outcome "unknown", described as "Joint pain"; PAIN IN EXTREMITY (non-serious) with onset 23Mar2022, outcome "recovered" (23Mar2022), described as "arm was a little sore". Therapeutic measures were taken as a result of arthralgia. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Blood pressure high (Blood pressure high Diagnosed years ago)
- Vorgeschichte
- Medical History/Concurrent Conditions: Penicillin allergy (allergic to penicillin)
- Andere Medikamente
- NORVASC
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 04.04.2022
- Impfdatum
- 18.12.2021
- Beginn
- 19.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Injection site reaction
Rash
Skin texture abnormal
Urticaria
Vaccine positive rechallenge
Symptomtext
After both shots, had reaction with bumps and hives. Took benadryl. Started having pain in area of arm where shots were given. Still today pain is consistent and when patient feels the area where shot was given, it has a spongy feeling, per patient
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 01.04.2022
- Impfdatum
- 23.03.2022
- Beginn
- 25.03.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Abdominal pain
Alanine aminotransferase increased
Aspartate aminotransferase increased
Blood glucose normal
Laboratory test normal
Lipase increased
Pancreatitis acute
Vomiting
Symptomtext
Pfizer COVID Vaccine EUA: Adverse Drug Reaction of Pancreatitis Patient received Pfizer Vaccine on 3/22/22. Pt presented to ED with severe abdominal pain with associated vomiting. Pt was recently restarted on ozempic 6 weeks ago and has no other new medications besides her regular metformin. Upon admission, Glu 155, SGOT 75, SGPT 58,lipase of >9k, all other labs wnl. Admitted for acute pancreatitis without gallstones or necrosis. Ozempic was d/c. As of 3/31/22 acute pancreatitis has resolved.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- 6,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- DM, morbid obesity
- Andere Medikamente
- ibuprofen, metformin, semaglutide
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 30.03.2022
- Impfdatum
- 21.03.2022
- Beginn
- 21.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Nausea
Pyrexia
Vomiting
Symptomtext
nausea, vomiting, extreme fatigue, fever starting on night of vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Ewing sarcoma (in remission) age 12 years
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 19.03.2022
- Impfdatum
- 02.02.2022
- Beginn
- 05.02.2022
- Tage bis Beginn
- 3,0
- Dosis
- 2
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Muscle twitching
Muscular weakness
Pain in extremity
Restlessness
Symptomtext
Upper right arm and shoulder area feel weak, painful, keeps twitching, feels restless; Upper right arm and shoulder area feel weak, painful, keeps twitching, feels restless; Upper right arm and shoulder area feel weak, painful, keeps twitching, feels restless; Upper right arm and shoulder area feel weak, painful, keeps twitching, feels restless; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 40 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 02Feb2022 17:45 (Lot number: FJ5682) at the age of 40 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Major depressive disorder" (unspecified if ongoing); "anxiety" (unspecified if ongoing); "hypothyroidism" (unspecified if ongoing). Concomitant medication(s) included: LEVOTHYROXINE SODIUM; PROZAC. Past drug history included: Meloxicam, reaction(s): "Allergy: Meloxicam", notes: Allergy: Meloxicam. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: 33025BD, Location of injection: Arm Right, Vaccine Administration Time: 05:45 PM), administration date: 12Jan2022, when the patient was 40 years old, for COVID-19 immunization. The following information was reported: MUSCULAR WEAKNESS (non-serious), PAIN IN EXTREMITY (non-serious), MUSCLE TWITCHING (non-serious), RESTLESSNESS (non-serious) all with onset 05Feb2022, outcome "not recovered" and all described as "Upper right arm and shoulder area feel weak, painful, keeps twitching, feels restless". Additional information: The onset time of adverse event was 12:00 AM. The patient had not received any other vaccine within 4 weeks. Patient had not been diagnosed with COVID prior to vaccination and had not been tested COVID post the vaccination. Other medications in two weeks: Levothyroxine, Prozac. Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Anxiety; Hypothyroidism; Major depressive disorder
- Andere Medikamente
- LEVOTHYROXINE SODIUM; PROZAC
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- U
- Eingang
- 18.03.2022
- Impfdatum
- 27.01.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 5,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Back pain
Cough
Hypoaesthesia
Illness
Oropharyngeal pain
Pain
Productive cough
Rhinorrhoea
Symptomtext
I feel like sick; I have like cough/ cough and the phlegm; I have like cough/ cough and the phlegm; I have like sore throat; Runny nose; I have this symptoms in my face, I feel that my face is numb; My body is weak; Pain in my back; Body is sore; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A patient (no qualifiers provided) received bnt162b2 (BNT162B2), administration date 27Jan2022 (Lot number: FJ5682) as dose 1, single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: ILLNESS (non-serious) with onset Feb2022, outcome "recovered", described as "I feel like sick"; COUGH (non-serious), PRODUCTIVE COUGH (non-serious) all with onset Feb2022, outcome "recovered" and all described as "I have like cough/ cough and the phlegm"; OROPHARYNGEAL PAIN (non-serious) with onset Feb2022, outcome "recovered", described as "I have like sore throat"; RHINORRHOEA (non-serious) with onset Feb2022, outcome "recovered", described as "Runny nose"; HYPOAESTHESIA (non-serious) with onset Feb2022, outcome "recovered", described as "I have this symptoms in my face, I feel that my face is numb"; ASTHENIA (non-serious) with onset Feb2022, outcome "recovered", described as "My body is weak"; BACK PAIN (non-serious) with onset Feb2022, outcome "recovered", described as "Pain in my back"; PAIN (non-serious) with onset Feb2022, outcome "recovered", described as "Body is sore". No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 17.03.2022
- Impfdatum
- 16.03.2022
- Beginn
- 16.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Abdominal discomfort
Arthralgia
Decreased appetite
Fatigue
Musculoskeletal stiffness
Neck pain
Pain in extremity
Symptomtext
Booster. 2nd Hour noticed stiffness and mild pain in shoulders and neck accompanied by tightness in abdomen. Those issues diminished over following 6 hrs while joint pain in elbows, knees particularly left hip socket and left foot appeared, Loss of appetite. 2nd day feeling fatigue and left side arthritic like pain in left elbow, hip , knee and foot. Note: First shot in series (Mar/2021 ) resulted in similar neck and shoulder stiffness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- Covid vac 1st shot. neck and shoulder stiffness
- Staat
- FL
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 17.03.2022
- Impfdatum
- 19.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Body temperature
Fatigue
Headache
Pain
Pyrexia
Symptomtext
Fever for 2 days (100 F); body ache; Headache; fatigue; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 13 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 19Jan2022 (Lot number: FJ5682) at the age of 13 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. Vaccination history included: Bnt162b2 (COVID 19, Pfizer, lot number=EW0168, administration date=11Jun2021, dose number=2, vaccine location=Right arm), administration date: 11Jun2021, when the patient was 13 years old, for Covid-19 immunization; Bnt162b2 (COVID 19, Pfizer, lot number=EW0173, administration date=21May2021, dose number=1, vaccine location=Left arm), administration date: 21May2021, when the patient was 13 years old, for Covid-19 immunization. The following information was reported: PYREXIA (non-serious) with onset 20Jan2022 08:00, outcome "recovered", described as "Fever for 2 days (100 F)"; PAIN (non-serious) with onset 20Jan2022 08:00, outcome "recovered", described as "body ache"; HEADACHE (non-serious) with onset 20Jan2022 08:00, outcome "recovered", described as "Headache"; FATIGUE (non-serious) with onset 20Jan2022 08:00, outcome "recovered", described as "fatigue". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of pyrexia, pain, headache, fatigue. Additional information: Patient had received treatment for events was Tylenol. No covid prior vaccination. No Known allergies. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Test Name: Fever; Result Unstructured Data: Test Result:100 Fahrenheit; Comments: for 2 days
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 17.03.2022
- Impfdatum
- 26.01.2022
- Beginn
- 27.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest discomfort
Chills
Fatigue
Lymphadenopathy
Pyrexia
Symptomtext
fever; Chills; chest discomfort; fatigue; lymph node swelling; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 46 year-old male patient received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 26Jan2022 13:15 (Lot number: FJ5682) at the age of 46 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "known allergies: eggs" (unspecified if ongoing). There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose 1, Lot number: EN6203, Location of injection: Arm left, Route of Administration: Intramuscular), administration date: 21Mar2021, when the patient was 45 years old, for COVID-19 Immunization; Bnt162b2 (Dose 2, Lot number: ER8730, Location of injection: Arm left, Route of Administration: Intramuscular), administration date: 22Apr2021, when the patient was 45 years old, for COVID-19 immunization. The following information was reported: PYREXIA (non-serious) with onset 27Jan2022 06:00, outcome "recovering", described as "fever"; CHILLS (non-serious) with onset 27Jan2022 06:00, outcome "recovering", described as "Chills"; CHEST DISCOMFORT (non-serious) with onset 27Jan2022 06:00, outcome "recovering", described as "chest discomfort"; FATIGUE (non-serious) with onset 27Jan2022 06:00, outcome "recovering", described as "fatigue"; LYMPHADENOPATHY (non-serious) with onset 27Jan2022 06:00, outcome "recovering", described as "lymph node swelling". Therapeutic measures were not taken as a result of pyrexia, chills, chest discomfort, fatigue, lymphadenopathy. Additional information: The patient did not receive any other medications in two weeks. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The device date was reported as 29Jan2022. The case was assessed as non-serious. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Egg allergy
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 11.03.2022
- Impfdatum
- 22.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Diarrhoea
Fatigue
Lymphadenopathy
Pain in extremity
Symptomtext
I experienced pain under my left arm, lymph nodes swollen under my left breast, fatigue, diarrhea, and weakness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Lupus, High blood pressure
- Andere Medikamente
- Edarbyclor, Metformin and Prednisone
- Allergien
- Antibiotics
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 08.03.2022
- Impfdatum
- 07.03.2022
- Beginn
- 07.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Blood pressure increased
Feeling hot
Flushing
Nausea
Peripheral coldness
Symptomtext
Approximately 5 - 6 minutes after receiving the Pfizer vaccine she began to complain of feeling very hot and sudden onset nausea. Her skin was noted to be cool and her ears and face were flushed. Her blood pressure was elevated 180/90. She denied any pain or tingling in her chest or extremities. She was escorted to the emergency room for further evaluation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- Continued vital signs : BP 197/116, 197, 116, 169/81, 158/90 ......(0.1 mg Clonidine PO once) Temp: 99.2, 992, 98.5 HR: 99, 99, 78, 70 Pulse Ox: 100, 100, 98 room air
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- -
- Andere Medikamente
- N/A
- Allergien
- Codeine
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 07.03.2022
- Impfdatum
- 04.03.2022
- Beginn
- 05.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Arthritis
Asthenia
Headache
Lymph node pain
Lymphadenitis
Pain
Pain in extremity
Pain of skin
Sensitive skin
Symptomtext
Severe headache, painful inflamed left lymph nodes, painful inflamed joints specially fingers and knees, body aches throughout, legs? skin painful when clothes rubbed and lack of energy. Today is the 3rd after the booster and I still woke up with an headache which I rarely get and lymph nodes are still very sore and inflamed.
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
- TN
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 05.03.2022
- Impfdatum
- 31.01.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Breast pain
Fatigue
Lymphadenopathy
Myalgia
Symptomtext
Swollen Lymph Nodes; Pain in Left Axilla/ Breast; Pain in Left Axilla/ Breast; mild muscle aches; fatigue; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 60 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 31Jan2022 11:30 (Lot number: FJ5682) at the age of 60 years as dose 2 (booster), single for covid-19 immunisation. Relevant medical history included: "Osteopenia" (unspecified if ongoing); "Elevated BP" (unspecified if ongoing). Concomitant medication(s) included: PROZAC; LISINOPRIL; CALCIUM;VITAMIN D. Vaccination history included: Janssen covid 19 (Dose Number: 1, Batch/Lot No: 045A21A, Location of injection: Arm Left, administration date=17May2021), administration date: 17May2021, when the patient was 59 years old, for Covid-19 immunization, reaction(s): "no adverse events". The following information was reported: LYMPHADENOPATHY (non-serious) with onset 01Feb2022, outcome "recovering", described as "Swollen Lymph Nodes"; AXILLARY PAIN (non-serious), BREAST PAIN (non-serious) all with onset 01Feb2022, outcome "recovering" and all described as "Pain in Left Axilla/ Breast"; MYALGIA (non-serious) with onset 01Feb2022, outcome "recovering", described as "mild muscle aches"; FATIGUE (non-serious) with onset 01Feb2022, outcome "recovering", described as "fatigue". Therapeutic measures were not taken as a result of lymphadenopathy, axillary pain, breast pain, myalgia, fatigue. Additional Information: The patient did not receive any other vaccines within 4 weeks prior to the covid vaccine. Prior to vaccination, the patient was not diagnosed with covid-19. Since the vaccination, the patient not been tested with covid-19. The patient had no known allergies. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Elevated BP; Osteopenia
- Andere Medikamente
- PROZAC; LISINOPRIL; CALCIUM;VITAMIN D
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 04.03.2022
- Impfdatum
- 01.03.2022
- Beginn
- 02.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Headache
Pain
Pyrexia
Rash erythematous
Symptomtext
Fever chills severe headache severe body aches full body bright red rash
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Hypothyroidism
- Vorgeschichte
- -
- Andere Medikamente
- Tirasint 100mcg po daily
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 03.03.2022
- Impfdatum
- 03.03.2022
- Beginn
- 03.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Dermatitis acneiform
Headache
Injection site pain
Nausea
Pain
Pyrexia
Rash erythematous
Rash papular
Symptomtext
patient experienced pounding headache, severe body aches, nausea, chills, fever, burning on injection site notable: patient has SEVERE rash all over front and back of her body - red, puffy, not itchy
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown - pt does not usually fill at our pharmacy
- Allergien
- sulfa
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 47,0
- Geschlecht
- M
- Eingang
- 01.03.2022
- Impfdatum
- 26.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Pruritus
Throat irritation
Symptomtext
Systemic: Allergic: Itch (specify: facial area, extremities)-Mild, Additional Details: at 5:15pm pt was coughing and complained of itchy throat, gave 25mg Benadryl and monitored pt ofr another 20 minutes, bp1:146/101 hr:55 at 5:23pm, bp2: 151/106 hr:53 at 5:30pm. pt left at 5:35pm advised pt to monitor for symptoms of allergic reaction and seek medical help if increased in swelling or and airway issues. advised pt to take another 25mg Benadryl in 4 hrs
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 01.03.2022
- Impfdatum
- 03.02.2022
- Beginn
- 10.02.2022
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cardiac discomfort
Cellulitis
Discomfort
Dizziness
Erythema
Fatigue
Gait disturbance
Headache
Heart rate increased
Herpes zoster
Skin warm
Swelling
Symptomtext
Patient presented with 2 shingles / zoster blisters on 2/10/22 on right buttocks and upper right leg Shingles blisters expanded on buttocks, leg and torso. Original shingles blisters became infected and patient was treated with Bactrim antibiotic on 2/17/2022. Pt was seen by Dr who diagnosed a cellulitis infection (a life-threatening infection if left untreated) which was treated with Prednisone steroids on 2/18/22. Steroid topical. Valtrex 2/19 Pt was unable to walk normally and limped while walking. Discomfort with red, swollen, painful and warm to touch 10?x8? area on right upper leg and buttocks. Headache. Pt was dizzy, extremely exhausted and unable to care for kids (her job) for more than 3 hours 2/20/22 through 2/27/22 Pt seen 2/24/22 by Dr., cellulitis resolved, shingles blisters present. Elevated heart rate and heart pressure.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- Shingles / zoster onset 2/10/22 Cellulitis diagnosed 2/2/18/22 Elevated heart rate and blood pressure 2/24/22
- Aktuelle Erkrankungen
- No illnesses at time of vaccination or one month prior.
- Vorgeschichte
- None. Hypothyroidism within normal range.
- Andere Medikamente
- Levothyroxin, Xyzal
- Allergien
- Allergic to mangos. No medication allergies. No previous AEs after vaccination.
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 25.02.2022
- Impfdatum
- 11.02.2022
- Beginn
- 11.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site urticaria
Urticaria
Symptomtext
Arm began to break out from injection site all the way to my wrist. Then hives all over my neck.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NO
- Vorgeschichte
- NO
- Andere Medikamente
- Lamotrigine, Buspar, Buspirone
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 24.02.2022
- Impfdatum
- 01.02.2022
- Beginn
- 03.02.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blister
Lymph node pain
Lymphadenopathy
Symptomtext
On 2/3/2022 patient woke with blisters on R breast and bilateral painful and sswollen lymph nodes
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymph node pain
- Hospital-Tage
- -
- Labordaten
- Seen by oncologist
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Breast cancer survivor
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 22.02.2022
- Impfdatum
- 20.02.2022
- Beginn
- 21.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymph node pain
Lymphadenopathy
Lymphoedema
Symptomtext
Lymphedema of the left arm. Swelling and tenderness in the underarm area of the left arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymph node pain
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 22.02.2022
- Impfdatum
- 10.02.2022
- Beginn
- 10.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Full blood count normal
Headache
Nasal congestion
Nausea
Pyrexia
Rash
SARS-CoV-2 test negative
Streptococcus test negative
Urticaria
Vomiting
Symptomtext
Fever/chills, vomiting, nauseous, severe clogged nose, headache, (all started within 4-6 hours after vaccine) Hives/rash all over body appeared at day 5, while all other symptoms were still active. Duration: Fever- 6 days, vomiting-6 days, hives 4 days, mucus membranes on going at day 12.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- 02/14/22-urgent care visit, rapid covid test negative 02/15/22-ER visit, cbc preformed, results negative Strep test, negative
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 22.02.2022
- Impfdatum
- 16.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Confusional state
Dizziness
Heavy menstrual bleeding
Polymenorrhoea
Symptomtext
light headed/dizzy; a little confused sometimes; monthly cycle started 2 weeks early, was much worse than usual, experienced excessive blood clots with the first round; monthly cycle started 2 weeks early, was much worse than usual, experienced excessive blood clots with the first round; This is a spontaneous report received from a contactable consumer. The reporter is the patient. A 29 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 16Jan2022 10:30 (Lot number: FJ5682) at the age of 29 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Bipolar 2" (unspecified if ongoing); "depression" (unspecified if ongoing); "GAD" (unspecified if ongoing); "PMDD" (unspecified if ongoing); "arthritis" (unspecified if ongoing); "allergies to Avocado" (unspecified if ongoing). Prior to vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Concomitant medication(s) included: LAMICTAL. The following information was reported: POLYMENORRHOEA (non-serious), HEAVY MENSTRUAL BLEEDING (non-serious) all with onset 17Jan2022, outcome "recovering" and all described as "monthly cycle started 2 weeks early, was much worse than usual, experienced excessive blood clots with the first round"; DIZZINESS (non-serious), outcome "not recovered", described as "light headed/dizzy"; CONFUSIONAL STATE (non-serious), outcome "not recovered", described as "a little confused sometimes". The patient reported that monthly cycle started 2 weeks early, was much worse than usual, experienced excessive blood clots with the first round. The second round was 3 days ago, and she was still light headed, dizzy, and a little confused sometimes. Therapeutic measures were not taken as a result of polymenorrhoea, heavy menstrual bleeding, dizziness, confusional state. Since the vaccination, the patient has not been tested for COVID-19. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Arthritis; Bipolar II disorder; Depression; Fruit allergy; Gadolinium deposition disease; Premenstrual dysphoric disorder
- Andere Medikamente
- LAMICTAL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 21.02.2022
- Impfdatum
- 18.02.2022
- Beginn
- 19.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Injection site swelling
Symptomtext
Site: Pain at injection site-medium; Site: Swelling at injection site-medium.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 20.02.2022
- Impfdatum
- 18.02.2022
- Beginn
- 19.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Discomfort
Lymph node pain
Lymphadenopathy
Symptomtext
Swollen lymph nodes in left armpit, pain and discomfort from swelling.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymph node pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Multi vitamin, calcium supplement, vitamin D supplement, Zyrtec, bladder control medicine
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 19.02.2022
- Impfdatum
- 17.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Hypoaesthesia
Inappropriate schedule of product administration
Pain
Pruritus
Sinus disorder
Vaccination site erythema
Vaccination site pruritus
Vaccination site reaction
Vaccination site swelling
Symptomtext
numbness from shoulder to elbow; Sinuses have been an issue too; Pain in my left shoulder to my elbow; Inject site swelled about 5 inches around, red and itchy; Inject site swelled about 5 inches around, red and itchy; Inject site swelled about 5 inches around, red and itchy; Inject site swelled about 5 inches around, red and itchy; sever itching from left shoulder to my elbow; Pain in my left shoulder to my elbow; Inappropriate schedule of vaccine administered; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 53 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 17Jan2022 17:00 (Lot number: fj5682) at the age of 53 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Covid-19" (unspecified if ongoing). The patient's concomitant medications were not reported. Past drug history included: Sulfa and narcotics, reaction(s): "Allergy"; Narcotics, reaction(s): "Allergy". Vaccination history included: Bnt162b2 (Product=COVID 19, Brand= Pfizer, Lot number=fj5682, administration time=10:30 AM, dose number=1, vaccine location=Left arm), administration date: 03Jan2022, when the patient was 53 years old, for COVID-19 immunization. The following information was reported: INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (non-serious) with onset 17Jan2022, outcome "unknown", described as "Inappropriate schedule of vaccine administered"; VACCINATION SITE SWELLING (non-serious), VACCINATION SITE REACTION (non-serious), VACCINATION SITE ERYTHEMA (non-serious), VACCINATION SITE PRURITUS (non-serious) all with onset 19Jan2022 12:00, outcome "not recovered" and all described as "Inject site swelled about 5 inches around, red and itchy"; PRURITUS (non-serious) with onset 19Jan2022 12:00, outcome "not recovered", described as "sever itching from left shoulder to my elbow"; ARTHRALGIA (non-serious), PAIN (non-serious) all with onset 19Jan2022 12:00, outcome "not recovered" and all described as "Pain in my left shoulder to my elbow"; HYPOAESTHESIA (non-serious) with onset 19Jan2022 12:00, outcome "not recovered", described as "numbness from shoulder to elbow"; SINUS DISORDER (non-serious) with onset 19Jan2022 12:00, outcome "not recovered", described as "Sinuses have been an issue too". Therapeutic measures were not taken as a result of inappropriate schedule of product administration, vaccination site swelling, vaccination site reaction, vaccination site erythema, vaccination site pruritus, pruritus, arthralgia, pain, hypoaesthesia. Therapeutic measures were taken as a result of sinus disorder. Additional Information: The patient was not tested for Covid post vaccination. The patient did not take any other vaccine in four weeks and no other medications in two weeks. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 17.02.2022
- Impfdatum
- 27.01.2022
- Beginn
- 27.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Depression
Feeling abnormal
Headache
Inappropriate schedule of product administration
Interchange of vaccine products
Symptomtext
Pfizer given instead of the Moderna 21 days from the dose of Moderna as described above. A dose of Moderna was given on 01/06/2022 followed by a dose of Pfizer on 01/27/2022. Client was contacted and expressed feeling "funky and depressed", she also referred headache, no other complaints other than those previously stated. She was vaccinated at a homeless shelter where she is currently living.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No known
- Vorgeschichte
- No known
- Andere Medikamente
- No known
- Allergien
- No known
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 15.02.2022
- Impfdatum
- 19.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Herpes zoster
Rash
Symptomtext
Allergy in the form of a skin rash on my Ches, neck, belly and thighs. Appearance of shingles like sores in my groin area.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- None.
- Allergien
- Amoxicillin.
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 14.02.2022
- Impfdatum
- 26.01.2022
- Beginn
- 29.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Myalgia
Symptomtext
left shoulder joint/muscle aching and pain with abduction and internal and external rotation-- with no history of prior trauma or joint issues. Symptoms are still present three weeks later and hinder normal activities of daily living
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- F
- Eingang
- 12.02.2022
- Impfdatum
- 12.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cough
Dysphonia
Pyrexia
Shoulder operation
Wheezing
Symptomtext
she developed hoarseness; coughing; fever; treatments take away the wheezing; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 67 year-old female patient received bnt162b2 (BNT162B2), administration date 12Jan2022 (Batch/Lot number: unknown) as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose: 1, I didn't have any of this with the first 2 doses of the PBCV (purple formula)), for COVID-19 immunization; Bnt162b2 (Dose: 2, I didn't have any of this with the first 2 doses of the PBCV (purple formula)), for COVID-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 12Jan2022, outcome "unknown", described as "received a PBCV Booster dose"; DYSPHONIA (non-serious) with onset 13Jan2022, outcome "unknown", described as "she developed hoarseness"; COUGH (non-serious) with onset 13Jan2022, outcome "unknown", described as "coughing"; PYREXIA (non-serious) with onset 13Jan2022, outcome "unknown", described as "fever"; WHEEZING (non-serious) with onset Jan2022, outcome "recovered" (Jan2022), described as "treatments take away the wheezing". Therapeutic measures were taken as a result of dysphonia, cough, pyrexia, wheezing. Additional information: Patient stated that she received a PBCV Booster dose on 12Jan2022. On 13Jan2022 she developed hoarseness, coughing and fever. Patient asked whether these are normal and should she still be experiencing them one week later. Also stated that "she had an appt with her HCP yesterday via telemedicine, she was taking Tylenol, Robitussin and her Ventolin Inhaler, she also started her breathing treatments at home." She stated these treatments take away the wheezing, "but her voice was still hoarse. She didn't have any of this with the first 2 doses of the PBCV (purple formula), She asked that how long this will last. The lot number for bnt162b2 was not provided and will be requested during follow up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 11.02.2022
- Impfdatum
- 08.02.2022
- Beginn
- 09.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Fatigue
Headache
Lymph node pain
Lymphadenopathy
Pain
Pyrexia
Symptomtext
Fever, chills, body aches, fatigue, head ache all have subsided as of 02/11/2022 sore & swollen lymph node under left armpit still persisting as of 02/11/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension, High cholesterol
- Andere Medikamente
- Benadryl , Actaminophen
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 09.02.2022
- Impfdatum
- 07.02.2022
- Beginn
- 08.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abnormal dreams
Constipation
Feeling hot
Musculoskeletal stiffness
Nausea
Pain
Salivary hypersecretion
Symptomtext
Body aches, vivid dreams, nauseous, warm sensation at neck and down shoulder , stiff neck , I felt like I had to poop but could not go, my mouth had more salvia then normal
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Migraine headache
- Vorgeschichte
- None
- Andere Medikamente
- Zyrtec, Zoloft, Wellbutrin
- Allergien
- Penicillin Sulfa drugs She?ll fish
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 09.02.2022
- Impfdatum
- 08.02.2022
- Beginn
- 09.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pyrexia
Vomiting
Symptomtext
Fever and severe vomiting, onset at 2:37 am. Treatment of Zofran, ginger ale, and Tylenol.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Lamictal, buspirone, Wellbutrin, birth control, hair/nail vitamins
- Allergien
- Penicillin/sulfa drugs, oxycodone, coconut, mushrooms
- Vorherige Impfungen
- 27, Covid, 6/3/21, shot/injection, Pfizer.
- Staat
- OR
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 07.02.2022
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Pain
Symptomtext
I started having a sharp, shooting pain in my left armpit about 3 hours after receiving the vaccination. The pain would happen every few minutes, then increased to constant pain by about 9:30pm. I took tylenol and started using an icepack at about midnight to be able to sleep. The pain decreased enough to sleep from about 3am to 10am. The pain has continued to be constant since Friday evening with tylenol and ice helping enough to let me sleep.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- high cholesterol, chronic low back pain, chronic pain syndrome, mood disorder, obesity
- Andere Medikamente
- rosuvastatin, GABA, turmeric, vitamin k, vitamin d, monolaurin, boswellia extract, melatonin, glucosamine, chondroitin, hyaluronic acid, antacid, vitamin c, bromelain, cranberry,
- Allergien
- aspirin/ibuprophen: bleeding spicy peppers (jalepeno): throat closing sulpha drugs: red rash
- Vorherige Impfungen
- -
- Staat
- DE
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 07.02.2022
- Impfdatum
- 27.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Symptomtext
Daily headache.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- Covid-19
- Vorgeschichte
- n/a
- Andere Medikamente
- over the counter vitamins
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 07.02.2022
- Impfdatum
- 04.02.2022
- Beginn
- 06.02.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Injection site erythema
Injection site warmth
Pyrexia
Symptomtext
Two days after receiving booster dose, patient reported feeling chills and fever on Sunday 2/6/22 at 3 AM. Patient returned to facility on Monday 2/7/22 to report side effects. In addition, clinician noted the site where injection was administered (left arm) showed a large area of redness as well as being hot to the touch.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A.
- Vorgeschichte
- N/A.
- Andere Medikamente
- N/A.
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 07.02.2022
- Impfdatum
- 04.02.2022
- Beginn
- 05.02.2022
- 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 erythema
Injection site pain
Injection site swelling
Injection site warmth
Symptomtext
swelling, warmth, redness and tenderness at injection site
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 06.02.2022
- Impfdatum
- 04.02.2022
- Beginn
- 05.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Axillary pain
Chills
Decreased appetite
Headache
Malaise
Musculoskeletal stiffness
Myalgia
Pain
Pain in extremity
Pyrexia
Swelling
Symptomtext
Teeth-chattering chills Complete loss of appetite Alternating slight fevers Headache Injection arm pain: stiffness, pain when raising arm, pain and swelling in the armpit General feeling of unwellness Muscle aches on left (injection) side of body (above complaints continued all day Saturday 2/5/22 and into Sunday 2/6/22)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 05.02.2022
- Impfdatum
- 13.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Headache
Lethargy
Vaccination site pain
Symptomtext
lethargy; headache; injection site pain; exhaustion; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 30 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 13Jan2022 18:00 (Lot number: fj5682) at the age of 30 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "neuropathy" (unspecified if ongoing); "ocd" (unspecified if ongoing); "narcolepsy" (unspecified if ongoing); "sulfa drugs allergy" (unspecified if ongoing). Concomitant medication(s) included: LUVOX CR; OMEPRAZOLE; NUVIGIL; XYREM. Past drug history included: Codeine, reaction(s): "allergy"; Ceclor, reaction(s): "allergy"; Hydrocodone, reaction(s): "allergy". Vaccination history included: Bnt162b2 (Dose 2, Batch/Lot No: ew0196, Location of injection: Arm Left, Vaccine Administration Time: 07:00 PM, Route of Administration: Intramuscular), administration date: 25Jun2021, when the patient was 30 years old, for COVID-19 immunization; Bnt162b2 (Dose 1, Batch/Lot No: ew0180, Location of injection: Arm Left, Vaccine Administration Time: 07:00 PM, Route of Administration: Intramuscular), administration date: 04Jun2021, when the patient was 29 years old, for COVID-19 immunization. The following information was reported: LETHARGY (non-serious) with onset 14Jan2022, outcome "recovering", described as "lethargy"; HEADACHE (non-serious) with onset 14Jan2022, outcome "recovering", described as "headache"; VACCINATION SITE PAIN (non-serious) with onset 14Jan2022, outcome "recovering", described as "injection site pain"; FATIGUE (non-serious) with onset 14Jan2022, outcome "recovering", described as "exhaustion". Therapeutic measures were not taken as a result of lethargy, headache, vaccination site pain, fatigue. Additional information: The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Narcolepsy; Neuropathy; Obsessive-compulsive disorder; Sulfonamide allergy
- Andere Medikamente
- LUVOX CR; OMEPRAZOLE; NUVIGIL; XYREM
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 05.02.2022
- Impfdatum
- 12.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Headache
Pain
Pain in extremity
Pyrexia
SARS-CoV-2 test negative
Symptomtext
Fever; fatigue; body aches; sore arm; headache; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A 16 year-old male patient received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 12Jan2022 15:00 (Lot number: FJ5682) at the age of 16 years as dose 3 (booster) , single for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0187, Route of Administration: Intramuscular), administration date: 13Jun2021, when the patient was 15 years old, for COVID-19 Immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EW0178, Route of Administration: Intramuscular), administration date: 23May2021, when the patient was 15 years old, for COVID-19 immunization. The following information was reported: PYREXIA (non-serious) with onset 13Jan2022, outcome "not recovered", described as "Fever"; FATIGUE (non-serious) with onset 13Jan2022, outcome "not recovered", described as "fatigue"; PAIN (non-serious) with onset 13Jan2022, outcome "not recovered", described as "body aches"; PAIN IN EXTREMITY (non-serious) with onset 13Jan2022, outcome "not recovered", described as "sore arm"; HEADACHE (non-serious) with onset 13Jan2022, outcome "not recovered", described as "headache". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of pyrexia, fatigue, pain, pain in extremity, headache. Additional information: The patient did not received any other vaccine with 4 weeks prior to vaccine. The patient did not received any other vaccine with 2 weeks prior to vaccine. The patient did not had COVID prior to vaccine. No known allergies. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220113; Test Name: Rapid Test; Test Result: Negative ; Comments: Nasal Swab
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 04.02.2022
- Impfdatum
- 03.02.2022
- Beginn
- 03.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Nausea
Vomiting
Symptomtext
Pt came for Pfizer covid booster. With in 5 mins of injection patient became nauseated and vomited twice. Had patient lie on cot. Patient states this happened after other 2 covid vaccines and only last a few minutes. Pt declined going to ER. Pt left with her mother at 10: 50am stating she felt better and wanted to leave. Vitals - BP - 110/74, P - 76, O2 - 9
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- COVID-19 DIAGNOSED ON 1/17/2022
- Vorgeschichte
- N/A
- Andere Medikamente
- UNKNOWN
- Allergien
- GRASS
- Vorherige Impfungen
- UNKNOWN DATES - VOMITING
- Staat
- AZ
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 04.02.2022
- Impfdatum
- 03.02.2022
- Beginn
- 03.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Symptomtext
Chills causing teeth to chatter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Diabetes.
- Andere Medikamente
- None.
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 24,0
- Geschlecht
- F
- 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: ja
Erholt: nein
Abdominal pain upper
Symptomtext
Patient complained about having stomach pain after vaccination observation period.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- All vitals normal per EMS team
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 03.02.2022
- Impfdatum
- 02.02.2022
- Beginn
- 03.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypersensitivity
Urticaria
Symptomtext
Patient phoned pharmacy on 2/3/2022 at 12:45 pm stating that he had an allergic reaction to the 2nd dose he received the day before. Patient states he had hives under arms. Patient states he took Allegra and Pepcid to alleviate side effects.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- None noted.
- Aktuelle Erkrankungen
- none noted
- Vorgeschichte
- none noted
- Andere Medikamente
- unknown
- Allergien
- none noted
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 03.02.2022
- Impfdatum
- 14.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Headache
Lymphadenopathy
Pain in extremity
Pharyngeal swelling
Pruritus
Rash
Urinary tract infection
Symptomtext
I woke up Saturday morning and my throat was swollen, my armpits were hurting, my legs were killing me, and my head was aching. I called my doctor who told me to take 10mg Zyrtec and 125mg Benadryl every 4 hours. That helped for some days. On 01/18/2022, my lymph nodes had been swelling and I had a bad rash that kept itching and spread from my lower torso and up my back. I called my doctor who told me to continue taking the allergy medication and to contact him if things progressively got worse. When I went in for a follow-up appointment, I was given Fluconazole 150mg (1 tablet every 72 hours) to help reduce the rash and to help with my UTI.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Hemochromatosis, Gastroparesis, Enlarged liver and spleen
- Vorgeschichte
- Type 2 diabetes
- Andere Medikamente
- Jardiance 25mg, Glipizide 10mg, Nitrofurantoin Mono 100mg, Tylenol 500mg
- Allergien
- Iodine, Sulfur, fish products, Betadine
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 03.02.2022
- Impfdatum
- 01.02.2022
- Beginn
- 02.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Chills
Erythema
Headache
Oedema peripheral
Tenderness
Symptomtext
Headache and Chills 4am. By morning, patient noticed significant pain of Axilla with Right axillary swelling, redness and tenderness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Obesity
- Andere Medikamente
- Mirena iud
- Allergien
- Sulfa Adhesives
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 01.02.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Fatigue
Myalgia
Pyrexia
Respiratory tract congestion
Symptomtext
Patient states that after receiving the 2nd dose of Pfizer 01/28/2022, started experiencing symptoms that evening of fever, chills, muscle aches, fatigue, and congestion. Primary communications with recommendations of hydration, antibiotics, and Tylenol.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Penicillin, Cipro, Sulfa
- Vorherige Impfungen
- 1st dose of Pfizer 3/10/2021 (flu-like symptoms lasting 7 days).
- Staat
- NY
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 31.01.2022
- Impfdatum
- 08.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Injection site urticaria
Pain
Peripheral swelling
Symptomtext
About an hour after she started having hives around the vaccine sight. It started to move up her arm and her arm swell. Fainting feeling and in overall pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- no
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- no
- Allergien
- raspberries, blueberries, msg, codienem, aspirin, flagyl
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 29.01.2022
- Impfdatum
- 19.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Body temperature
Chills
Fatigue
Influenza virus test
Lymphadenopathy
Pain
Pyrexia
SARS-CoV-2 test
Vaccination site pain
Symptomtext
Felt achy/ aches; Tired; Injection site hurting; He had a fever above 102F by 24 hours post injection; Chills; His lymph nodes under the arm on the injection side were very raised and swollen.; This is a spontaneous report from a contactable reporter (consumer or other non HCP). A 12-year-old male patient received bnt162b2 (BNT162B2), intramuscular, administered in right arm, administration date 19Jan2022 at 19:45 (Lot number: FJ5682) at the age of 12 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "Asthma" (unspecified if ongoing) and "Eczema" (unspecified if ongoing), notes: ezcema. There were no concomitant medications. Past drug history included: Cephalexin, reaction: "Drug allergy", notes: Known allergies: cephalexin. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE; Lot Number: FA7484; Route of Administration: Intramuscular), administration date: 26Jul2021, when the patient was 12 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE; Lot Number: FA7485; Route of Administration: Intramuscular), administration date: 16Aug2021, when the patient was 12 years old, for COVID-19 immunisation. The following information was reported: PAIN (non-serious) with onset 20Jan2022, outcome "recovered" (20Jan2022), described as "Felt achy/ aches"; FATIGUE (non-serious) with onset 20Jan2022, outcome "recovered" (20Jan2022), described as "Tired"; VACCINATION SITE PAIN (non-serious) with onset 20Jan2022, outcome "recovered" (20Jan2022), described as "Injection site hurting"; PYREXIA (non-serious) with onset 20Jan2022, outcome "recovered" (20Jan2022), described as "He had a fever above 102F by 24 hours post injection"; CHILLS (non-serious) with onset 20Jan2022, outcome "recovered" (20Jan2022), described as "Chills"; LYMPHADENOPATHY (non-serious) with onset 20Jan2022, outcome "recovered" (20Jan2022), described as "His lymph nodes under the arm on the injection side were very raised and swollen". The events "Felt achy/ aches", "Tired", "Injection site hurting", "He had a fever above 102F by 24 hours post injection", "Chills" and "His lymph nodes under the arm on the injection side were very raised and swollen." were evaluated at the physician office visit and emergency room visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of pain, fatigue, vaccination site pain, pyrexia, chills and lymphadenopathy. Additional information: The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had been tested for COVID-19. It was reported that although the reporter was aware of the adverse event, it had been waited to report until received a negative PCR Covid test, as the patient's soccer teammates had recently tested positive for Covid. The doctor stated his symptoms were consistent with Covid and she was not certain if there was an adverse event reaction.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220120; Test Name: COVID-19 virus test; Test Result: Negative ; Comments: tested negative for rapid flu and covid; Test Date: 20220120; Test Name: Body temperature; Result Unstructured Data: Test Result:Above 102F; Comments: fever above 102F by 24 hours post injection; Test Date: 20220120; Test Name: Rapid flu; Test Result: Negative ; Test Date: 20220120; Test Name: PCR; Test Result: Negative ; Comments: Nasal swab, tested negative for rapid flu and covid and then later covid pcr
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Asthma; Eczema (ezcema)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 28.01.2022
- Impfdatum
- 24.01.2022
- Beginn
- 25.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Lymph node pain
Lymphadenopathy
Myalgia
Pain
Pyrexia
Symptomtext
Fever over 100 degrees, extreme muscular pain, lymph node swelling and pain in armpits and groin, slight joint pain, body aches
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- Temperature taken at home
- Aktuelle Erkrankungen
- COVID on 1/1/2021
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 28.01.2022
- Impfdatum
- 20.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Breast swelling
Erythema
Lymphadenopathy
Pain in extremity
Physical examination
Rash
Tenderness
Symptomtext
On the evening of January 20, 2022 I started experiencing pain in my left arm. The next morning (1/21/22) while applying deodorant I noticed a raised area in my left armpit. I took photos and contacted my doctor. I took Allegra and ibuprofen for pain/allergic reaction management. In addition to the pain I was experiencing tenderness and some redness. The next morning (1/22/22) I noticed more swelling in my armpit and down my inner left arm into my antecubital area. There was pain in my inner arm and shoulder joint. I continued Allegra and ibuprofen. The morning of 1/24/22 I noticed my left breast was significantly larger than my right and it felt somewhat engorged. I was concerned that the swelling kept getting worse so I contacted my doctor again and told him I wanted to be seen. I was seen that afternoon, given a PE and prescribed prednisone and clindamycin. The next day 1/25/22 I noticed the swelling in my left breast was reducing and as of today 1/28/22 is almost completely resolved. There is still a small area of swelling under my left arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- 1/24/22 Physical exam.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- hypertension, depression and anxiety, acne
- Andere Medikamente
- losartan, propranolol, fluoxetine, Valtrex, vitamin D, multivitamin, isotretinoin
- Allergien
- hair glue
- Vorherige Impfungen
- Pfizer COVID-19 vaccine 2nd dose (4/18/21) age 46; fever, chills, muscle aches, fatigue, and malaise.
- Staat
- MD
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 26.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Pain
Pain in extremity
Temperature intolerance
Symptomtext
After the 1st dose on Dec 7, 2021 constant aching in every finger and toe started. Two days after the second shot, got noticeably worse. The shoulder, elbow and knee pain remained the same. Fingers and toes have very low tolerance to cold. Just a few minutes exposure results in excruciating pain. Occasionally have shooting pains through forearms and lower legs. Taking 2 aspirin and 2 Advil every day to ease the pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- Severe illness after small pox vaccine as a child.
- Staat
- OH
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 26.01.2022
- Impfdatum
- 21.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Injection site pain
Symptomtext
Site: Pain at Injection Site-Severe
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 24.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain upper
Diarrhoea
Fatigue
Headache
Impaired work ability
Loss of personal independence in daily activities
Pain
Pyrexia
SARS-CoV-2 test negative
Symptomtext
A persistent or significant incapacity or substantial disruption of the ability to conduct normal life functions. I was in bed for 10 days, I could not function to work even. Fatigue, fever up to 100.6, body aches, diarrhea, stomachache, and headaches are what I experienced.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- 2 COVID tests that were negative, 1/18 and 1/19.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Lyrica, Xanax
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 24.01.2022
- Impfdatum
- 20.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Back pain
Computerised tomogram abnormal
Electroencephalogram
Neck pain
Pain
Pain in extremity
Peripheral swelling
Swelling
X-ray
Symptomtext
My armpit and arm were hurting the night of my booster. The next day, my torso, back, neck and left arm were all painfully swollen. I called the pharmacy and advised them of my symptoms and they recommend I go to urgent care. They advised I go the the ER. They found swelling during a cat scan. They gave me Benadryl and antibiotics. My swelling is starting to go down.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- EEG, cat scan, x-ray.
- Aktuelle Erkrankungen
- Ear infection
- Vorgeschichte
- Bone disorder
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 24.01.2022
- Impfdatum
- 17.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Malaise
Vaccine breakthrough infection
Symptomtext
Fully vaccinated, boosted on 1/17/22. Symptomatic COVID breakthrough infection with inpatient hospital stay.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 22.01.2022
- Impfdatum
- 17.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Rash
SARS-CoV-2 test negative
Urticaria
Symptomtext
Within 20 hours of shot, developed severe rash/hives over both arms, legs and ankles. I went to urgent care 24 hours later, received an injection of Medrol 125mg and prescriptions for Medrol Pak, Benadryl and Pepcid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- Negative for COVID-19.
- Aktuelle Erkrankungen
- Unknown. Had minimal rash on both arms 1 week prior to the shot. Never read nor heard that was a possible symptom of COVID -19.
- Vorgeschichte
- Throat cancer survivor, 2 years after treatments.
- Andere Medikamente
- Levothyroxine
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 22.01.2022
- Impfdatum
- 22.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Pyrexia
Symptomtext
PATIENT REPORTED DIZZINESS, LIGHT-HEADEDNESS, AND FEELING FEVERISH FIVE MINUTES AFTER VACCINATION. EMS ARRIVED TO CHECK ON PATIENT; AFTER EXAMINATION THEY DID NOT FIND ANY CONCERNING SYMPTOMS AND CLEARED HER TO DEPART THE PHARMACY.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- BLOOD PRESSURE AND HEART RATE NORMAL.
- Aktuelle Erkrankungen
- NONE KNOWN
- Vorgeschichte
- HEART MURMER
- Andere Medikamente
- NONE KNOWN
- Allergien
- PENICILLINE, AMOXICILLIN, CODEINE, MORPHINE, BACTRIM
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 21.01.2022
- Impfdatum
- 19.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pruritus
Pruritus
Rash
Symptomtext
Site: Itching at Injection Site-Medium, Site: Redness at Injection Site-Medium, Systemic: Allergic: Itch Generalized-Medium, Systemic: Allergic: Rash Generalized-Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 20.01.2022
- Impfdatum
- 17.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Pruritus
Urticaria
Symptomtext
Pt developed Generalized hives all over his body and itching. Hives continue to present time requiring Benadryl after receiving booster shot of Pfizer. First two vaccines were Moderna and were well tolerated
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Covid positive 12/26/2021
- Vorgeschichte
- Childhood asthma
- Andere Medikamente
- None
- Allergien
- Amoxicillin -rash
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 19.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Headache
Insomnia
Pyrexia
Vomiting
Symptomtext
Fever, chills, insomnia, headache, vomiting (2 times)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- PCOS
- Andere Medikamente
- Prenatal
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- 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
Chills
Decreased appetite
Feeling hot
Hyperhidrosis
Injection site pain
Nodule
Symptomtext
Pain and soreness at the injection site, knot under arm, knot on shoulder near the base of neck, chills, felt extremely hot, extreme sweating, no appetite. Took Tylonol.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 18.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Back pain
Fatigue
Lymph node pain
Lymphadenopathy
Muscle tightness
Myalgia
Neuralgia
Pain in extremity
Symptomtext
exhaustion, joint aches, swollen and sore lymph node in left armpit, tightness in lifting left arm in arm pit area, sore muscles in back, nerve pain in left arm between bicep and tricep on inside of arm down just past elbow joint. very distinct line of pain. treatment (no insurance): rest, water, acetaminophen, strong symptoms day after shot, 50% better 2nd day after, mostly recovered by the following monday.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- hypertension
- Andere Medikamente
- Hydrochlorothiazide
- Allergien
- keflex, penicillin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 16.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Illness
Mass
Pain in extremity
Symptomtext
Sick next day then arm got very sore and red and a big lump
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- None yet
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Copd
- Andere Medikamente
- Nicotine patch
- Allergien
- Sulfa drugs
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 10.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Chapped lips
Ear pain
Fatigue
Feeling abnormal
Lip pain
Lip swelling
Lymphadenopathy
Malaise
Neck pain
Pain
Pain in extremity
Pyrexia
SARS-CoV-2 test negative
Swelling
Symptomtext
On 01/10/2022- she was feeling ill by 2:30 in the afternoon had a fever at about 6:30pm - 101.5. She had a sore arm, fatigue, fever that day and the next day. 01/11/2021, early in the evening before bed she felt her bottom lip on the left side was swelling up. It was swollen, it was the size of a big grape tomato and painful and she was absolutely miserable. The next morning it progressed to her left jaw line, swollen gland on her left side and swollen lymph nodes on her left side and her pain was from the bottom of her neck on left side going from her lip to the left side and she was saying that her left ear hurt. She was all swollen . We started giving her Benadryl and the swelling would go down a little bit, after 5 hrs it would wear off and the swelling would continue. The doctor told us to keep her on Benadryl, and ibuprofen. By 4 in the afternoon, she was in a lot of pain. I was getting worried. The APRN told us to take her to the ER, that she need to be seen in the emergency Hospital. 01/12/2021- We took her to the ER. They gave her Benadryl and ibuprofen and we waited an 1 1/2 before she was seen . The doctor gave her one dose or oral steroids, dexamethasone. Originally the APRN, thought it was possibly and allergy, This doctor felt it was an overly strong immune response. Her lip was so swollen, that it actually cracked. She was miserable. The steroids really worked, It helped the swelling go down. She was a lot more comfortable on the way home and she did not have a fever. On Thursday and Friday, she was completely exhausted. She was complaining about her lip hurting . She finally left the house on Saturday. She felt fine to go back to school today, 01/18/2022. She did get considerably better after the steroid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ear pain
- Hospital-Tage
- -
- Labordaten
- 01/13/2022- COVID 19 test- negative
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- no
- Allergien
- no
- Vorherige Impfungen
- Pfizer dose 2,07/12/2021, and her 1st flu shot as a baby, 2009 or 2010
- Staat
- IL
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 17.01.2022
- Impfdatum
- 16.01.2022
- Beginn
- 16.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal discomfort
Blood glucose
Gait disturbance
Hypotonia
Malaise
Unresponsive to stimuli
Symptomtext
Manager came to pharmacy to report that a customer was not feeling well after her booster shot. Went up front and found her slumped in a chair and nonresponsive. Family member stated that she complained of an upset stomach right before collapsing. Paramedics were called, and patient started to respond a little. Every time she tried to sit up she would fall over again though. Her vitals seemed ok, but she had great difficulty walking to the bathroom. Paramedics advised that she be transported to the hospital, but she opted to return home with a family member.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- Paramedics tested blood glucose, blood pressure and pulse ox.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 15.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Hallucination
Headache
Muscular weakness
Pyrexia
Swelling
Symptomtext
Hallucinations, swollen arm pit, fever and headache, muscle weakness, fatigue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Sinus infection 2 weeks before
- Vorgeschichte
- Hypertension, obesity, PCOS
- Andere Medikamente
- Amlodipine, metformin
- Allergien
- Ibuprofen, Bactrim
- Vorherige Impfungen
- Same symptoms except swollen painful armpit, 32, 3/13/21 and 4/2/21 , Pfizer for both
- Staat
- NY
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 13.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Fatigue
Headache
Incorrect dose administered
Symptomtext
Patient inappropriately received adult dose Pfizer at a vaccination clinic. The patient, who is currently 11 years and 11 months old, should have received the pediatric dose of Pfizer. The date of birth was incorrectly added to the patient's chart at registration and was not confirmed prior to the vaccination being provided. The patient's mother was present for the vaccination. The error was discovered while the patient and his mother were still at the vaccination station. The error was discussed with the patient and his mother, and they both understood to look for adverse events and to call with any symptoms. We reached out to the patient's mother on 1/13. She stated the patient was feeling fatigued, had a headache and chills. She was instructed to encourage fluids and to contact us with new or worsening symptoms. She was also told to seek emergency care for severe symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 11.01.2022
- Impfdatum
- 10.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Breast discomfort
Chest discomfort
Hypoaesthesia
Pyrexia
Symptomtext
I received a Pfizer booster yesterday 1/10/22 and today have a low temp with 5/10 pain in my axilla at rest and my left arm is numb with radiating discomfort into my left breast, tightness in my chest and numbness into my left jaw.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- We recommended she go visit her primary care physician.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Diarrhoea
Fatigue
Pain in extremity
Swelling
Symptomtext
Pt. states that after receiving the 3rd dose of Phizer 01/07/2022, started experiencing symptoms 01/10/2021 of left arm pain, loose stool, fatigue, and a "Lump" swelling on the left side of the collarbone. Primary communications 01/10/2021 (waiting for recommendations). Pt. still experiencing symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- HBP
- Andere Medikamente
- Levothroyxm, Losartan, Metaphorim, Vitamin D3, Super B Complex, Simavistatin
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 18.12.2023
- Impfdatum
- 13.01.2022
- Beginn
- 14.12.2023
- Tage bis Beginn
- 700,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
SARS-CoV-2 test
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- SARS-CoV-2 test
- Hospital-Tage
- -
- Labordaten
- IDNOW
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Metastatic small cell caarcinoma
- Andere Medikamente
- -
- Allergien
- Hydrocodone, Nsaids, Oxycodone
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 13.10.2023
- Impfdatum
- 18.01.2022
- Beginn
- 26.09.2022
- Tage bis Beginn
- 251,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Audiogram
Deafness unilateral
Electronystagmogram
Magnetic resonance imaging head
Vertigo
Symptomtext
Right ear hearing loss, vertigo
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Audiogram
- Hospital-Tage
- -
- Labordaten
- Audiogram: 10/4/2022, 10/13/2022, 9/18/2023 Brain MRI with contrast: 10/27/2022 ENG/VNG: 9/26/2023
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 96,0
- Geschlecht
- F
- Eingang
- 08.08.2023
- Impfdatum
- 25.01.2022
- Beginn
- 10.01.2023
- Tage bis Beginn
- 350,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Hypoxia
Symptom recurrence
Symptomtext
HYPOXIA 1/15/2023 -- RECURRENCE OF HOSPITALIZATION WITH SAME SYMPTOMS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypoxia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 98,0
- Geschlecht
- F
- Eingang
- 01.08.2023
- Impfdatum
- 02.02.2022
- Beginn
- 12.03.2023
- Tage bis Beginn
- 403,0
- Dosis
- 2
- Route/Site
- - / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Vaccine breakthrough infection
Symptomtext
Covid Breakthrough Infection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Not listed
- Andere Medikamente
- Atorvastatin, Bumex, Desvenlafaxine, Diclofenac Enoxaparin, Famotidine, Flecainide, Hydroxyzine, Insulin, Vit- C&D, Albuterol, Atrovent,
- Allergien
- Betadine, Doxycycline, Embrel, Etanercept, Povidone Iodine
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 09.06.2023
- Impfdatum
- 27.01.2022
- Beginn
- 04.11.2022
- Tage bis Beginn
- 281,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Chronic respiratory failure
Epilepsy
Obstructive sleep apnoea syndrome
Respiratory failure
Sleep apnoea syndrome
Symptomtext
EPILEPSY, UNSPECIFIED SLEEP APNEA OBSTRUCTIVE SLEEP APNEA CHRONIC HYPOXEMIC RESPIRATORY FAILURE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chronic respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 12.05.2023
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product administration error
Product expiration date issue
Symptomtext
Reporting administration error per Agency. We contacted Pfizer for expiration dates, pfizer vaccine specialist advised expiration dates and deemed vaccines viable at the time of vaccine administration. Pfizer vaccine vials only include manufactuarer dates on the box and vials. Therefore, we contacted pfizer to attain expiration dates directly from them. No adverse reaction reported from the patient at the time of vaccination and no adverse reaction reported since given the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 12.05.2023
- Impfdatum
- 21.03.2022
- Beginn
- 21.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product administration error
Symptomtext
Reporting administration error. We contacted Pfizer for expiration dates, pfizer vaccine specialist advised expiration dates and deemed vaccines viable at the time of vaccine administration. Pfizer vaccine vials only include manufacturer dates on the box and vials. Therefore, we contacted pfizer to attain expirations dates directly from them. No adverse reaction reported from the patient at the time of vaccination and no adverse reaction reported since given the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- -
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 12.05.2023
- Impfdatum
- 28.03.2022
- Beginn
- 28.03.2022
- 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 administration error
Product expiration date issue
Symptomtext
Reporting administration error. We contacted Pfizer for expiration dates, pfizer vaccine specialist advised expiration dates and deemed vaccine viable t the time of vaccine administration. Pfizer vaccine vials only include manufacturer dates on the box and vials. Therefore, we contacted pfizer to attain expirations dates directly from them. No adverse reaction reported from the patient at the time of vaccination and no adverse reaction reported since given the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 12.05.2023
- Impfdatum
- 31.03.2022
- Beginn
- 31.03.2022
- 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 administration error
Symptomtext
Reporting administration error. We contacted Pfizer for expiration dates, pfizer vaccine specialist advised expiration dates and deemed vaccines viable at the time of vaccine administration. Pfizer vaccine vials only include manufacturer dates on the box and vials. Therefore, we contacted pfizer to attain expirations dates directly from them. No adverse reaction reported from the patient at the time of vaccination and no adverse reaction reported since given the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 83,0
- Geschlecht
- F
- Eingang
- 10.04.2023
- Impfdatum
- 08.04.2022
- Beginn
- 01.01.2023
- Tage bis Beginn
- 268,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Atrial fibrillation
Electrocardiogram abnormal
Symptomtext
I experienced A-fib around January 2023 but do not know if it related. I went for a yearly check up in late October 2022 and my doctor gave me an EKG and there was a glitch on my EKG and she sent me to a cardiovascular doctor. I did not have any symptoms after my vaccine. I feel better today but have not gotten back to where I used to be.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Atrial fibrillation
- Hospital-Tage
- -
- Labordaten
- OCT 2022 EKG
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Arthritis; PMR
- Andere Medikamente
- CELEBREX; amlodipine; atorvastatin; CYMBALTA
- Allergien
- Penicillin; crab meat; shellfish; fluoride
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 13.03.2023
- Impfdatum
- 05.04.2022
- Beginn
- 07.02.2023
- Tage bis Beginn
- 308,0
- Dosis
- 5
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Adenoma benign
Symptomtext
Nothing happened after the vaccine. The problem is that I have a growth in my mouth (Adenoma), it was confirmed by a 2nd physician, in a regular visit to the dentist. They sent me to a specialist, and I will have an extraction next month.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Adenoma benign
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Bronchitis
- Vorgeschichte
- Epilepsy; Hypothyroidism; GRUD
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 04.02.2023
- Impfdatum
- 21.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Heart rate increased
Symptomtext
Rapid heart beat; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 54-year-old male patient received BNT162b2 (BNT162B2), on 21Jan2022 as dose 3 (booster), single (Lot number: FJ5682) at the age of 54 years, in left arm for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: HYDROCHLOROTHIAZIDE; TAMSULOSIN. Vaccination history included: BNT162b2 (DOSE 1, SINGLE, Batch/Lot No: ER8737, Location of injection: Arm Right), administration date: 10Apr2021, when the patient was 53-year-old, for Covid-19 immunization; BNT162b2 (DOSE 2, SINGLE, Batch/Lot No: EW0171, Location of injection: Arm Left), administration date: 01May2021, when the patient was 53-year-old, for Covid-19 immunization. The following information was reported: HEART RATE INCREASED (non-serious) with onset 22Jan2022, outcome "not recovered", described as "Rapid heart beat". The event "rapid heart beat" required physician office visit. Therapeutic measures were not taken as a result of heart rate increased. Additional information: Facility type was vaccine pharmacy or drug store. The patient did not received other vaccine in four weeks. The patient had COVID prior vaccination and COVID tested post vaccination was reported as no. Adverse event resulted in doctor or other healthcare professional office/clinic visit. The patient also received Dose 4 vaccine on 09Jan2023 at 07:00 PM, lot number was GJ6796 and vaccine location was left arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Heart rate increased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- HYDROCHLOROTHIAZIDE; TAMSULOSIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 30.01.2023
- Impfdatum
- 08.02.2022
- Beginn
- 31.12.2022
- Tage bis Beginn
- 326,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
12/31/22 presents to ED for "corona virus concern". PMHx of "CAD status post four-vessel CABG, numerous stents, diabetes, hypertension, and CHF"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- 12/31/22 SARS-CoV-2 (COVID-19) by NAA detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 15.01.2023
- Impfdatum
- 13.01.2022
- Beginn
- 23.03.2022
- Tage bis Beginn
- 69,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Tinnitus
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tinnitus
- Hospital-Tage
- -
- Labordaten
- Hearing Test - May 10, 2022 by Dr. M.D.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Ubiquinol, Fish oil, Vitamin B12, Vitamin D
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 04.01.2023
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Interchange of vaccine products
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; Interchange of vaccine product; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). A 53-year-old male patient received BNT162b2 (BNT162B2), on 08Apr2022 as dose 4 (booster), single (Lot number: FJ5682) at the age of 53 years, in left arm for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 18Feb2021 as dose 1, single (Lot number: 006M20A), in left arm, on 18Mar2021 as dose 2, single (Lot number: 038A21A), in left arm, on 31Oct2021 as dose 3 (booster), single (Batch/Lot number: unknown), in left arm and on 16Sep2022 as dose 5 (booster), single (Lot number: 017AOC), in left arm for covid-19 immunisation. The patient's relevant medical history included: "cardiovascular disease" (unspecified if ongoing); "obesity" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 08Apr2022, outcome "unknown", described as "Interchange of vaccine product"; DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 27Dec2022, outcome "unknown" and all described as "COVID 19 Treatment". Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: Patient received COVID 19 treatment with Paxlovid, treatment start date: 18Dec2022, treatment stop date: 23Dec2022. Patient had no known allergies.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Cardiovascular disease, unspecified; Obesity
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 14.12.2022
- Impfdatum
- 12.12.2022
- Beginn
- 12.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Wrong product administered
Symptomtext
The patient came into the doctor's office to receive the Pfizer Covid - 19 Bivalent vaccine. The regular Pfizer Covid-19 vaccine was administered in error.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 07.12.2022
- Impfdatum
- 11.07.2022
- Beginn
- 10.08.2022
- Tage bis Beginn
- 30,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Immunisation reaction
Magnetic resonance imaging
Optic ischaemic neuropathy
Vision blurred
Symptomtext
Pt woke up while on vacation with blurred vision. Sought out treatment from optometry who referred her to neurology. Pt was diagnosed with anterior ischemic optic neuropathy. While this is not uncommon with MS, pt reports that neurologist felt like this was not related to her MS and given the proximity of the incident to her vaccine, was suspicious this could have contributed to this.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Immunisation reaction
- Hospital-Tage
- -
- Labordaten
- MRI- results available from neurology
- Aktuelle Erkrankungen
- Vit. D deficiency MS
- Vorgeschichte
- Vit. D deficiency MS
- Andere Medikamente
- N/A
- Allergien
- Penicillin Sulfa
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 21.10.2022
- Impfdatum
- 01.04.2022
- Beginn
- 01.08.2022
- Tage bis Beginn
- 122,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bundle branch block left
Electrocardiogram abnormal
Symptomtext
I had my vaccination on 04/01/2022. In 08/2022 I had an abnormal EKG. This indicated I had a Left Posterior Vesicular Block. I was asymptomatic. I have a follow up with my cardiologist in 11/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bundle branch block left
- Hospital-Tage
- -
- Labordaten
- EKG 08/2022 Abnormal
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Breast CA survivor 2016
- Andere Medikamente
- Vitamin C; Vitamin D; Vitamin K2; Magnesium; Krill Oil; Probiotic
- Allergien
- NSAIDS
- Vorherige Impfungen
- COVID-19 Vaccination slight fever 09/24/2021
- Staat
- -
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 28.09.2022
- Impfdatum
- 13.01.2022
- Beginn
- 19.09.2022
- Tage bis Beginn
- 249,0
- Dosis
- 2
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Cough
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cough
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 24.09.2022
- Impfdatum
- 16.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Symptomtext
This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 69-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 05Feb2022 as dose 3 (booster), single (Batch/Lot number: unknown), in left arm and on 16Apr2022 at 14:00 as dose 4 (booster), single (Lot number: FJ5682) at the age of 69 years, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown) and as dose 2, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 2022, outcome "unknown" and all described as "Treatment of COVID-19". Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: It was reported that the patient had no known allergies and no other medical history. The patient also do not have other medication in 2 weeks. The information on the batch/lot number for BNT162b2 has been requested and will be submitted if and when received.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other medical history: No
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 21.09.2022
- Impfdatum
- 01.04.2022
- Beginn
- 04.09.2022
- Tage bis Beginn
- 156,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
COVID-19; COVID-19; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 60-year-old male patient received BNT162b2 (BNT162B2), in Mar2021 as dose 1, single (Lot number: en6204), in Apr2021 as dose 2, single (Lot number: er8727) and in Apr2022 as dose 3 (booster), single (Lot number: fj5682) at the age of 59 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "high blood pressure" (unspecified if ongoing), notes: Other medical history: High blood pressure; "Known allergies: minor food allergies" (unspecified if ongoing), notes: Known allergies: minor food allergies. Concomitant medication(s) included: OLMESARTAN, start date: Jan2015. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 04Sep2022, outcome "not recovered" and all described as "COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (04Sep2022) Positive, notes: Tested positive 04Sep; (10Sep2022) Positive, notes: on 10Sep still tested positive (faint line); (12Sep2022) Negative, notes: negative test; (13Sep2022) Positive, notes: test positive with faint line; (14Sep2022) Positive, notes: test positive with solid line (not faint); (16Sep2022) Positive, notes: 16Sep faint line on test for positive. Therapeutic measures were taken as a result of drug ineffective, covid-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220904; Test Name: Covid-19; Test Result: Positive ; Comments: Tested positive 04Sep.; Test Date: 20220910; Test Name: Covid-19; Test Result: Positive ; Comments: on 10Sep still tested positive (faint line).; Test Date: 20220912; Test Name: Covid-19; Test Result: Negative ; Comments: negative test.; Test Date: 20220913; Test Name: Covid-19; Test Result: Positive ; Comments: test positive with faint line.; Test Date: 20220914; Test Name: Covid-19; Test Result: Positive ; Comments: test positive with solid line (not faint).; Test Date: 20220916; Test Name: Covid-19; Test Result: Positive ; Comments: 16Sep faint line on test for positive.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Blood pressure high (Other medical history: High blood pressure); Food allergy (Known allergies: minor food allergies)
- Andere Medikamente
- OLMESARTAN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 12.09.2022
- Impfdatum
- 09.06.2022
- Beginn
- 26.08.2022
- Tage bis Beginn
- 78,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Dermatitis contact
SARS-CoV-2 test positive
Sinus disorder
Symptomtext
COVID-19 was mild and all in my nose and was like a sinus infection. And lasted about 6 days. I took Mucinex. I also got posin ivy the very next week after having COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID-19 - positive
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Fenofibrate; Atenolol; Triamterene-HCTZ; Vitamin C; Vitamin D; Multivitamin; Accuvite; Fish oil; Flaxseed; Low dose Aspirin; Famotidine
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 26.08.2022
- Impfdatum
- 14.07.2022
- Beginn
- 26.08.2022
- Tage bis Beginn
- 43,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Symptomtext
Fully vaccinated and boosted twice
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 26.08.2022
- Impfdatum
- 07.01.2022
- Beginn
- 21.08.2022
- Tage bis Beginn
- 226,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Symptomtext
Fully vaccinated and boosted once
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 16.08.2022
- Impfdatum
- 13.01.2022
- Beginn
- 15.08.2022
- Tage bis Beginn
- 214,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient partially vaccinated and then tested positive for COVID19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 10.08.2022
- Impfdatum
- 29.03.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Symptomtext
COVID-19; COVID-19; This is a spontaneous report received from a non-contactable reporter(s) (Nurse). A 69-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 29Mar2022 as dose 4 (booster), single (Lot number: FJ5682) at the age of 69 years for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 3 (booster), single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 1, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history was not reported. The patient took concomitant medications. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID-19". Therapeutic measures were taken as a result of drug ineffective and covid-19 with Paxlovid (Oral) from 27Jul2022 to 31Jul2022. No follow-up attempts are possible. No further information is expected.; Sender's Comments: As there is limited information in the case provided, the causal association between the reported events with the suspect drug BNT162B2 cannot be excluded. The case will be reassessed once new information is available.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 05.08.2022
- Impfdatum
- 08.02.2022
- Beginn
- 14.07.2022
- Tage bis Beginn
- 156,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Disease recurrence
SARS-CoV-2 test
Vaccination failure
Symptomtext
tested + on 22Jul; Covid-19; Covid-19; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 63-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 13Jan2021 as dose 1, single (Lot number: EK9231), in left arm, on 05Feb2021 as dose 2, single (Lot number: EL3247), in left arm, on 30Aug2021 as dose 3 (booster), single (Lot number: EW1087), in left arm and on 08Feb2022 as dose 4 (booster), single (Lot number: FJ5682) at the age of 63 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Complex regional pain syndrome" (unspecified if ongoing); "s/p lyme disease" (unspecified if ongoing); "Known allergies: sulfa" (unspecified if ongoing); "Known allergies: contrast iodine" (unspecified if ongoing); "known allergies: nightshade allergy" (unspecified if ongoing), notes: known allergies: nightshade allergy. Concomitant medication(s) included: OXYCODONE, start date: Jan2011; TRAZODONE, start date: Jan2011, stop date: 13Jul2022; ESTRADIOL, start date: Sep2001, stop date: 16Jul2022; ACYCLOVIR [ACICLOVIR], start date: Feb2009, stop date: 16Jul2022; ADDERALL, start date: 13Jun2022, stop date: 14Jul2022. Past drug history included: Morphiene, reaction(s): "Known allergies: Morphine"; Ativan, reaction(s): "adverse response", notes: adverse response to ativan & gabapentin; Gabapentin, reaction(s): "adverse response", notes: adverse response to ativan & gabapentin; Ativan, reaction(s): "Known allergies: Ativan", notes: adverse response to ativan & gabapentin; Gabapentin, reaction(s): "Known allergies: Gabapentin", notes: adverse response to ativan & gabapentin. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 14Jul2022, outcome "recovered" (19Jul2022) and all described as "Covid-19"; DISEASE RECURRENCE (medically significant) with onset 22Jul2022, outcome "recovered" (27Jul2022), described as "tested + on 22Jul". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (14Jul2022) Positive, notes: Initially tested + on PCR 14Jul; (19Jul2022) Negative, notes: Tested - on 19Jul; (22Jul2022) Positive, notes: tested + on 22Jul and 25Jul; (25Jul2022) Positive, notes: tested + on 22Jul and 25Jul; (27Jul2022) Negative, notes: Tested - on 27Jul. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical Course: Other medication received in 2 weeks. Paxlovid received as a treatment. Treatment Indication: Treatment of COVID-19. Adverse event: Had strong, bad taste, slight dizziness within 30 minutes of first dose. This waned after about 10 hrs. Worse side effects with 2nd dose plus nausea. Covid Sx of mild sore throat, tight chest & low O2 greatly improved. Mostly feeling the medication effects. Nausea slightly better after 11 hrs. 3rd dose had significant dizziness, nausea and bad taste plus vomiting. Unable to tolerate another dose and discontinued with PCP consult. It took two days for side effects to improve. Still have some fuzzy headedness. Initially tested + on PCR 14Jul. Tested - on 19Jul. Slight return of sniffles & tested + on 22Jul and 25Jul. Tested - on 27Jul. Started having chest pain and diaphragmatic spasms on 26Jul which has continued. O2 sat are normal. Still feeling mild nausea and GI discomfort. I may have better tolerated a lower dose better? I weigh 137 lbs. Every person I know of that has taken Paxlovid has had a rebound but have not reported it to my knowledge. Likely this is under reported. No follow-up attempts are needed. No further information is expected.; Sender's Comments: Based on the information available , a possible contributory role of the suspect BNT162B2 cannot be excluded for the reported events of covid-19 and vaccination failure.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220714; Test Name: tested; Test Result: Positive ; Comments: Initially tested + on PCR 14Jul; Test Date: 20220719; Test Name: tested; Test Result: Negative ; Comments: Tested - on 19Jul; Test Date: 20220722; Test Name: tested; Test Result: Positive ; Comments: tested + on 22Jul and 25Jul; Test Date: 20220725; Test Name: tested; Test Result: Positive ; Comments: tested + on 22Jul and 25Jul; Test Date: 20220727; Test Name: tested; Test Result: Negative ; Comments: Tested - on 27Jul
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Allergy (known allergies: nightshade allergy); Complex regional pain syndrome; Iodine contrast media allergy; Lyme disease; Sulfonamide allergy
- Andere Medikamente
- OXYCODONE; TRAZODONE; ESTRADIOL; ACYCLOVIR [ACICLOVIR]; ADDERALL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 03.08.2022
- Impfdatum
- 29.07.2022
- Beginn
- 29.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
No adverse event
Symptomtext
Pt came to clinic requesting 3rd dose of COVID vaccine be given as mandatory requirement to work in nursing home. As per patient, she was "emailed and called by her facility to have booster completed by the end of this week or she will not be able to start". 3rd dose of Pfizer COVID vaccine was administered to healthcare professional on 7/29. 2nd COVID dose 6/3/22. 3rd COVID dose given 2 MONTHS after 2nd dose. As per CDC guideline, administered too early. 3rd vaccine not considered booster for her series and consider this 3rd vaccine as additional 2nd dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- Pt denies s/s of adverse effects.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 01.08.2022
- Impfdatum
- 31.01.2022
- Beginn
- 21.03.2022
- Tage bis Beginn
- 49,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Oedema peripheral
Swelling
Symptomtext
I started getting edema in my feet and ankles. I am not for sure if it is due to the vaccine. I went to my doctor and I do have further testing with an Hepatology and Endocrinologist. The swelling comes and goes. This still persists even yesterday.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oedema peripheral
- Hospital-Tage
- -
- Labordaten
- None yet
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- CVID; Undifferentiated Connective Tissue Disease
- Andere Medikamente
- N/A
- Allergien
- Penicillin; Ceclor; Apresoline; Multiple food allergies
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 91,0
- Geschlecht
- F
- Eingang
- 01.08.2022
- Impfdatum
- 31.01.2022
- Beginn
- 29.07.2022
- Tage bis Beginn
- 179,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asthenia
Symptomtext
Began feeling weak yesterday, daughter came to check on her today and had trouble lifting her. Vaccinated for covid, currently oxygenating well on room air. Remdesivir x3 days, D5% 0.45% NaCl + KCl 20mEq/L 100/hr
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asthenia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 29.07.2022
- Impfdatum
- 04.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 66-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 30Jan2021 as dose 1, single (Lot number: EL3249), in right arm, on 20Feb2021 as dose 2, single (Lot number: EN6200), in right arm, on 28Sep2021 as dose 3 (booster), single (Lot number: FF2578), in right arm and on 04Apr2022 as dose 4 (booster), single (Lot number: FJ5682) at the age of 65 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Sleep apnea" (unspecified if ongoing); "high blood pressure" (unspecified if ongoing); "Penicillin allergy" (unspecified if ongoing); "shellfish allergy" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "recovering" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (19Jul2022) Positive, notes: Tested positive again 6 days after finishing Paxlovid prescription. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical information: Patient received anti-viral Paxlovid (Lot number: 1917017A) from 11Jul2022 to 16Jul2022 for COVID 19 treatment. Rebound of virus after Paxlovid. Tested positive again 6 days after finishing Paxlovid prescription.; Sender's Comments: Based on the available information in the case, the causal association between the events Vaccination failure, COVID-19 and the suspect drug cannot be excluded.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220719; Test Name: Covid-19 test; Test Result: Positive ; Comments: Tested positive again 6 days after finishing Paxlovid prescription
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Blood pressure increased; Penicillin allergy; Shellfish allergy; Sleep apnea
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 27.07.2022
- Impfdatum
- 09.04.2022
- Beginn
- 01.06.2022
- Tage bis Beginn
- 53,0
- Dosis
- 4
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Neck mass
Thyroid disorder
Ultrasound scan abnormal
Symptomtext
In the middle of June I've noticed that there was a lump in the front of my neck I called my doctor and scheduled an appointment for July 07/03/2022. The same day I was referred to the endocrinologist and did an ultrasound. On 07/21/2022 my doctor reviewed the results and told me that I was diagnosed with a large thyroid condition. I have an appointment with the endocrinologist on 08/16/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Neck mass
- Hospital-Tage
- -
- Labordaten
- Ultrasound
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High Blood Pressure; Border line Cholesterol; Type 2 Diabetics
- Andere Medikamente
- Hydrochlorothiazide; metformin HCL
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 21.07.2022
- Impfdatum
- 19.04.2022
- Beginn
- 19.04.2022
- 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 administration error
Symptomtext
Reporting administration error as per Agency. We contacted Pfizer for expiration dates, Pfizer vaccine specialist advised that the expiration dates were deemed viable at the time of vaccine administration. Pfizer vaccine vials only include manufacturer dates on the box and vials. Therefore, we contacted Pfizer to obtained expiration dates directly from them. No adverse reactions were reported from the patient at the time of vaccination. No adverse reactions were reported since the administration of vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- no known allergies
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 21.07.2022
- Impfdatum
- 29.03.2022
- Beginn
- 29.03.2022
- 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 administration error
Symptomtext
Reporting administration error as per Agency. We contacted Pfizer for expiration dates, Pfizer vaccine specialist advised that the expiration dates were deemed viable at the time of vaccine administration. Pfizer vaccine vials only include manufacturer dates on the box and vials. Therefore, we contacted Pfizer to obtained expiration dates directly from them. No adverse reactions were reported from the patient at the time of vaccination. No adverse reactions were reported since the administration of vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 20.07.2022
- Impfdatum
- 20.07.2022
- Beginn
- 20.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Inappropriate schedule of product administration
Symptomtext
Patient self- scheduled for COVID vaccination. Patient completed consent for booster dose Pfizer covid vaccine form and attested that he meets the vaccine eligibility criteria to receive booster. Author confirmed his full name and birthday. Also confirmed if this was a 2nd booster dose and patient verbalized "yes, it is 2nd booster" Author verified with patient for any previous side effects. Patient denied any side effects. Patient did not bring vaccination card. Second booster was administered. Patient tolerated well, waited for 15 minutes observation. No side effects noted. Upon reviewing the immunization record, author found that patient had 4th dose of Pfizer vaccine on April 27, 2022 which is less than 4 months of recommended time frame.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- contrast dye allergy
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.07.2022
- Impfdatum
- 06.02.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ageusia
Symptomtext
I can't always taste salt, sometimes I can smell the food but can't taste what I smell. Coffee is a toss up; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A patient (no qualifiers provided) received BNT162b2 (BNT162B2), on 06Feb2022 as dose 3 (booster), single (Lot number: FJ5682) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: BNT162b2 (Dose 1, EW0162), administration date: 13Apr2021, for Covid-19 Immunization, reaction(s): "lost my sense of taste and smell"; BNT162b2 (Dose 2, EE0169), administration date: 04May2021, for Covid-19 Immunization, reaction(s): "sense of smell and taste has never returned". The following information was reported: AGEUSIA (non-serious), outcome "unknown", described as "I can't always taste salt, sometimes I can smell the food but can't taste what I smell. Coffee is a toss up".; Sender's Comments: Linked Report(s) : US-PFIZER INC-202200926528 same reporter/patient, different dose, similar event;US-PFIZER INC-PV202200016058 same reporter/patient, different dose, similar event;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ageusia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 08.07.2022
- Impfdatum
- 08.01.2022
- Beginn
- 03.07.2022
- Tage bis Beginn
- 176,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
Covid Positive Illness; Covid Positive Illness; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non-healthcare professional). The reporter is the patient. A 48-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 04Feb2021 as dose 1, single (Lot number: EL3247), on 23Feb2021 as dose 2, single (Lot number: EL3247) and on 08Jan2022 as dose 3 (booster), single (Lot number: FJ5682) at the age of 48 years for covid-19 immunisation. The patient relevant medical history was not reported. There were no concomitant medications. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 03Jul2022, outcome "not recovered" and all described as "Covid Positive Illness". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (03Jul2022) Positive, notes: COVID test type post vaccination: Nasal Swab. Therapeutic measures were not taken as a result of vaccination failure, covid-19. Clinical Information: No other medications in two weeks and no other vaccination in four weeks. No covid prior vaccination. Tested for covid post vaccination. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220703; Test Name: covid test; Test Result: Positive ; Comments: COVID test type post vaccination: Nasal Swab
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 06.07.2022
- Impfdatum
- 11.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Symptomtext
COVID-19; COVID-19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). An 80-year-old male patient received BNT162b2 (BNT162B2), on 11Apr2022 as dose number unknown, single (Lot number: FJ5682) at the age of 80 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Type 2 diabetics" (unspecified if ongoing); "Shellfish Allergy" (unspecified if ongoing), notes: Known allergies: Shellfish; "latex gloves Allergy" (unspecified if ongoing), notes: Known allergies: latex gloves. There were no concomitant medications or other medication in 2 weeks. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 2022, outcome "unknown" and all described as "COVID-19". Therapeutic measures were taken as a result of drug ineffective, covid-19 which included Paxlovid 15Jun2022 to 20Jun2022. On 29Jun2022, the patient had COVID rebound.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Latex allergy (Known allergies: latex gloves); Shellfish allergy (Known allergies: Shellfish); Type 2 diabetes mellitus
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Drug ineffective
SARS-CoV-2 test
Suspected COVID-19
Symptomtext
COVID-19; COVID-19; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 51-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 12Apr2022 at 09:00 as dose 4 (booster), single (Lot number: FJ5682) at the age of 51 years, in right arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 3 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Asthma" (unspecified if ongoing); "Penicillin" (unspecified if ongoing), notes: Known allergies: Penicillin; "Yeast infection treatment" (unspecified if ongoing). Concomitant medication(s) included: MONISTAT 3 taken for fungal infection, start date: 12Jun2022, stop date: 14Jun2022. Past drug history included: Tetracycline, reaction(s): "Known allergies: tetracycline", notes: Known allergies: tetracycline. The following information was reported: DRUG INEFFECTIVE (medically significant), SUSPECTED COVID-19 (medically significant), outcome "unknown" and all described as "COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Unknown Results, notes: Full rebound of covid symptoms. Therapeutic measures were taken as a result of drug ineffective, suspected covid-19. Clinical information: She had other medication in 2weeks. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Drug ineffective
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID 19 Treatment; Result Unstructured Data: Test Result:Unknown Results; Comments: Full rebound of covid symptoms
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Asthma; Penicillin allergy (Known allergies: Penicillin); Yeast infection
- Andere Medikamente
- MONISTAT 3
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- M
- Eingang
- 03.07.2022
- Impfdatum
- 03.02.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a contactable reporter(s) (Physician). A 69-year-old male patient received BNT162b2 (BNT162B2), on 03Feb2022 as dose 4 (booster), single (Lot number: FJ5682), in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 3 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Known allergies: NSAIDs" (unspecified if ongoing). Concomitant medication(s) included: SILDENAFIL oral, start date: Dec2017. Past drug history included: Sudafed, reaction(s): "Known allergies: sudafed". The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Unknown Result. Therapeutic measures were taken as a result of drug ineffective, covid-19. No follow-up attempts are possible. No further information is expected.; Sender's Comments: The efficacy of a drug varies from patient to patient and can be affected by different factors; however, a contributory role of the suspect product bnt162b2 to the reported drug ineffective / COVID-19 cannot be ruled out
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID-19 test; Result Unstructured Data: Test Result:Unknown Result
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Allergy to NSAIDs
- Andere Medikamente
- SILDENAFIL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 27.06.2022
- Impfdatum
- 21.04.2022
- Beginn
- 19.06.2022
- Tage bis Beginn
- 59,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Nasopharyngitis
Rhinorrhoea
SARS-CoV-2 test positive
Sneezing
Symptomtext
I started having sniffles, coughing, sneezing on the plane trip back from vacation. It felt more like a summer cold. Once I arrived home I took a home COVID 19 test that came back positive. I called my doctor and he referred me to the COVID 19 provider. Doctor and I spoke about my symptoms and conditions, he prescribed Paxlovid that I started taking that night. Five days later I felt much better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Home COVID 19
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Esophageal Cancer Stage III Kidney Disease
- Andere Medikamente
- Omeprazole, Vitamin D, Baby Aspirin, Multivitamin
- Allergien
- Statins
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 24.06.2022
- Impfdatum
- 27.01.2022
- Beginn
- 15.06.2022
- Tage bis Beginn
- 139,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against and then tested positive for COVID19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 07.06.2022
- Impfdatum
- 19.01.2022
- Beginn
- 01.06.2022
- Tage bis Beginn
- 133,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
Developed COVID, tested positive; Developed COVID, tested positive; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A 62-year-old male patient received BNT162b2 (BNT162B2), on 27Mar2021 as dose 1, single (Lot number: EP6955), on 17Apr2021 as dose 2, single (Lot number: EP6955) and on 19Jan2022 as dose 3 (booster), single (Lot number: FJ5682) at the age of 62 years, all intramuscular for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 01Jun2022, outcome "unknown" and all described as "Developed COVID, tested positive". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (01Jun2022) Positive, notes: Nasal swab. Therapeutic measures were not taken as a result of vaccination failure, covid-19. Clinical course: Patient had no known allergies. Facility type vaccine: Public Health Clinic/Administration facility. Patient did not receive any other vaccines within 4 weeks or 2 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Patient tested positive for covid post vaccination. Covid test type post vaccination=Nasal swab, Covid test name post vaccination= BinaxNOW.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220601; Test Name: BinaxNOW; Test Result: Positive ; Comments: Nasal swab
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: none
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 02.06.2022
- Impfdatum
- 15.04.2022
- Beginn
- 26.05.2022
- Tage bis Beginn
- 41,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
I had a runny nose and cough that persisted for some days. So I decided to take an at-home COVID-19, and it came back positive; hours later, I went to a pharmacy and got a PCR COVID-19 test done as well on 05/26/2022 which came back positive. I contacted my doctor and prescribed me Paxlovid to help with my COVID-19. I feel the prescription because my cough and runny nose has gone away.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID-19 Test: 05/29/2022
- Aktuelle Erkrankungen
- N/a
- Vorgeschichte
- N/a
- Andere Medikamente
- Rosuvastatin Tamsulosin Losartan Vitamin D3
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 94,0
- Geschlecht
- F
- Eingang
- 02.06.2022
- Impfdatum
- 13.01.2022
- Beginn
- 31.05.2022
- Tage bis Beginn
- 138,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asthenia
COVID-19
Chronic kidney disease
Computerised tomogram head normal
Inappropriate schedule of product administration
Laboratory test abnormal
Pyuria
SARS-CoV-2 test positive
Somnolence
Tachypnoea
Unresponsive to stimuli
Urinary tract infection
Vaccine breakthrough infection
Wheezing
Symptomtext
COVID breakthrough first dose 5/20/2021 EW0179 second dose 1/13/2022 FJ5682. 94y.o. female with a h/o dementia on aricept and memantine, HTN on metoprolol, mitral regurgitation, hyperlipidemia who was diagnosed with COVID yesterday and taking keflex at home for UTI. Per ED physician, daughter concerned that she has become weaker and more drowsy and thus brought her to the ED. Labs in the ED are c/w previously diagnosed CKD. She does have pyuria. As patient has been weak and rolled out of bed, ED requests admission. Upon my evaluation in the ED, she does appear slightly tachypneic with occ wheezing. She is verbally unresponsive and is lying on her left lateral side. Her vital signs are wnl with an oxygen saturation of 98% on room air. No CXR has been obtained by the ED. Head CT without any acute changes. Per d/w daughter via telephone as patient was unable to provide history. She rolled out of her bed on Sunday morning (5/29). She needed assistance to get back into bed. She was diagnosed with coronavirus this morning
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asthenia
- Hospital-Tage
- -
- Labordaten
- Reported test positive 5/31/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- DCIS, diabetes, HTN, hyperlipidemia
- Andere Medikamente
- -
- Allergien
- sulfdiazine
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 26.05.2022
- Impfdatum
- 25.05.2022
- Beginn
- 25.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Vaccine administered has been at refrigerator temperature for over 10 weeks
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asthma, Seasonal Allergies, GERD
- Andere Medikamente
- BACLOFEN10MG 2 TAB BY MOUTH TWICE DAILY AS NEEDED 08/17/2022 MAR NORTRIPTYLINE10MG 1 CAP BY MOUTH TWICE DAILY AS NEEDED 08/17/2022 MAR IBUPROFEN600MG 1 TAB BY MOUTH TWICE DAILY *TAKE WITH FOOD*MAY CAUSE BLEEDING* 08/17/2022 MAR
- Allergien
- No Known Drug Allergies
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 26.05.2022
- Impfdatum
- 24.05.2022
- Beginn
- 24.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Pt received a covid vaccine that was 8 hours expired. Manufacturer is being contacted to see what the stability and recommendations are for this type of error.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 26.05.2022
- Impfdatum
- 23.03.2021
- Beginn
- 15.05.2022
- Tage bis Beginn
- 418,0
- Dosis
- 1
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Interchange of vaccine products
Symptomtext
ADMITTED TO HOSPITAL
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 26.05.2022
- Impfdatum
- 25.05.2022
- Beginn
- 25.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Vaccine administered has been at refrigerator temperature for over 10 weeks
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- no known drug allergies
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 26.05.2022
- Impfdatum
- 25.05.2022
- Beginn
- 25.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Vaccine administered has been at refrigerator temperature for over 10 weeks
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Chronic lower extremity swelling
- Vorgeschichte
- Seizures, Asthma, Hypertension
- Andere Medikamente
- SERTRALINE25MG 1 TAB BY MOUTH DAILY 11/03/2022 MAR ALBUTEROL 3ML U/D0.083% 75ML 1 SOL BY INHALATION TWICE DAILY 06/13/2022 MAR AMLODIPINE10MG 1 TAB BY MOUTH DAILY 06/13/2022 MAR CETIRIZINE10MG 1 TAB BY MOUTH EVERY NIGHT AT BEDT
- Allergien
- Seafood
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 26.05.2022
- Impfdatum
- 25.05.2022
- Beginn
- 25.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Vaccine administered has been at refrigerator temperature for over 10 weeks
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- none known
- Vorgeschichte
- Intermittent Asthma, seasonal allergies
- Andere Medikamente
- ALBUTEROL 3ML U/D0.083% 75ML 1 SOL By Inhalation BID 07/13/2022 MAR LORATADINE (CLARITIN)10MG 1 TAB By Mouth QD 07/13/2022 MAR buPROPion75MG 1 TAB BY MOUTH TWICE DAILY ; BRIDGED 06/03/2022 MAR PRAZOSIN2MG 1 CAP BY MOUTH EVERY
- Allergien
- No known drug allergies
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 13.04.2022
- Beginn
- 12.05.2022
- Tage bis Beginn
- 29,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 68-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 30Jan2021 as dose 1, single (Lot number: EL9264), in left arm, on 19Feb2021 as dose 2, single (Lot number: EN6203), in left arm, on 25Sep2021 as dose 3 (booster), single (Lot number: 301308A), in left arm and on 13Apr2022 at 15:45 as dose 4 (booster), single (Lot number: FJ5682) at the age of 68 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Idiopathic peripheral neuropathy" (unspecified if ongoing); "Bee venom" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 12May2022, outcome "not recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Positive; (12May2022) Positive, notes: Tested positive with home Binax test. Therapeutic measures were taken as a result of vaccination failure, covid-19 which included Paxlovid. Treatment start date was May2022 and treatment stop date was May2022. The patient finished Paxlovid with morning dose on 07May2022. Symptoms started returning 11May2022. Tested 12May2022 as symptoms seemed to get worse (sore throat, runny nose, slight cough). Tested positive with home Binax test. Other medication in 2 weeks was unknown. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: Covid test; Test Result: Positive ; Test Date: 20220512; Test Name: Covid test; Test Result: Positive ; Comments: Tested positive with home Binax test
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Bee sting; Peripheral neuropathy
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 16.05.2022
- Impfdatum
- 09.02.2022
- Beginn
- 14.05.2022
- Tage bis Beginn
- 94,0
- Dosis
- 3
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Nasopharyngitis
SARS-CoV-2 test positive
Symptomtext
cold symptoms , tested positive covid
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Binex now rapid test
- Aktuelle Erkrankungen
- none declared
- Vorgeschichte
- none declared
- Andere Medikamente
- flecainide, lisinopril, metoprolol tartrate, vitamins
- Allergien
- sulfates, formaldehyde
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 16.05.2022
- Impfdatum
- 07.05.2022
- Beginn
- 07.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Patient was given the Pfizer Covid vaccine that expired 23 days prior. Patient and physician have been notified
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 16.05.2022
- Impfdatum
- 07.05.2022
- Beginn
- 07.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Patient was given the Pfizer Covid vaccine that expired 23 days prior. Patient and physician have been notified
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 16.05.2022
- Impfdatum
- 07.05.2022
- Beginn
- 07.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Patient was given the Pfizer Covid vaccine that expired 23 days prior. Patient and physician have been notified
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 16.05.2022
- Impfdatum
- 07.05.2022
- Beginn
- 07.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Patient was given the Pfizer Covid vaccine that expired 23 days prior. Patient and physician have been notified
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 16.05.2022
- Impfdatum
- 07.05.2022
- Beginn
- 07.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Patient was given the Pfizer Covid vaccine that expired 23 days prior. Patient and physician have been notified
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 16.05.2022
- Impfdatum
- 07.05.2022
- Beginn
- 07.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Patient was given the Pfizer Covid vaccine that expired 23 days prior. Patient and physician have been notified
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 16.05.2022
- Impfdatum
- 07.05.2022
- Beginn
- 07.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Patient was given the Pfizer Covid vaccine that expired 23 days prior. Patient and physician have been notified
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 16.05.2022
- Impfdatum
- 07.05.2022
- Beginn
- 07.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Patient was given the Pfizer Covid vaccine that expired 23 days prior. Patient and physician have been notified
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 16.05.2022
- Impfdatum
- 07.05.2022
- Beginn
- 07.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Patient was given the Pfizer Covid vaccine that expired 23 days prior. Patient and physician have been notified
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 16.05.2022
- Impfdatum
- 04.03.1942
- Beginn
- 07.05.2022
- Tage bis Beginn
- 29.284,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Patient was given the Pfizer Covid vaccine that expired 23 days prior. Patient and physician have been notified
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 16.05.2022
- Impfdatum
- 07.05.2022
- Beginn
- 07.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Patient was given the Pfizer Covid vaccine that expired 23 days prior. Patient and physician have been notified
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 16.05.2022
- Impfdatum
- 07.05.2022
- Beginn
- 07.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Patient was given the Pfizer Covid vaccine that expired 23 days prior. Patient and physician have been notified
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 16.05.2022
- Impfdatum
- 07.05.2022
- Beginn
- 07.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Patient was given the Pfizer Covid vaccine that expired 23 days prior. Patient and physician have been notified
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 16.05.2022
- Impfdatum
- 07.05.2022
- Beginn
- 07.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Patient was given the Pfizer Covid vaccine that expired 23 days prior. Patient and physician have been notified
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 13.05.2022
- Impfdatum
- 07.05.2022
- Beginn
- 07.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Patient received a Covid vaccine that was expired 23 days prior to injection. The patient will be contacted for revaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 13.05.2022
- Impfdatum
- 07.05.2022
- Beginn
- 07.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Patient received a Covid vaccine that was expired 23 days prior to injection. The patient will be contacted for revaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 13.05.2022
- Impfdatum
- 07.05.2022
- Beginn
- 07.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Patient received a Covid vaccine that was expired 23 days prior to injection. The patient will be contacted for revaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 13.05.2022
- Impfdatum
- 07.05.2022
- Beginn
- 07.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Patient received a Covid vaccine that was expired 23 days prior to injection. The patient will be contacted for revaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 13.05.2022
- Impfdatum
- 07.05.2022
- Beginn
- 07.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Patient received a Covid vaccine that was expired 23 days prior to injection. The patient will be contacted for revaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 13.05.2022
- Impfdatum
- 07.05.2022
- Beginn
- 07.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Patient received a Covid vaccine that was expired 23 days prior to injection. The patient will be contacted for revaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 13.05.2022
- Impfdatum
- 07.05.2022
- Beginn
- 07.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Patient received a Covid vaccine that was expired 23 days prior to injection. The patient will be contacted for revaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 13.05.2022
- Impfdatum
- 07.05.2022
- Beginn
- 07.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Patient received a Covid vaccine that was expired 23 days prior to injection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 13.05.2022
- Impfdatum
- 07.05.2022
- Beginn
- 07.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Patient received a Covid vaccine that was expired 23 days prior to injection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 13.05.2022
- Impfdatum
- 07.05.2022
- Beginn
- 07.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was given a vaccine that was expired 23 days prior
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 5,0
- Geschlecht
- M
- Eingang
- 06.05.2022
- Impfdatum
- 15.03.2022
- Beginn
- 15.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
Symptomtext
patient received the 12+ dosage of 0.3ml/ 30mcg rather than the 5-11 dosage of 0.2ml/10mcg
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 21.04.2022
- Impfdatum
- 07.04.2022
- Beginn
- 07.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Trigeminal neuralgia
Symptomtext
Trigeminal Neuralgia, left side of jaw, face, teeth, face.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Trigeminal neuralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None known
- Vorgeschichte
- hypothyroid
- Andere Medikamente
- Unithroid; Vitamin C; Vitamin D-3; Rosuvastatin; Zyrtec; Flonaise nasal spray; Excedrin;
- Allergien
- Latex
- Vorherige Impfungen
- Hives and Trigeminal Neuralgia after a flu shot.
- Staat
- TX
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 20.04.2022
- Impfdatum
- 31.01.2022
- Beginn
- 31.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
Incorrect formulation given
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 9,0
- Geschlecht
- M
- Eingang
- 19.04.2022
- 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
No adverse event
Symptomtext
no adverse effects
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 16.04.2022
- Impfdatum
- 13.04.2022
- Beginn
- 14.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Breast swelling
Musculoskeletal stiffness
Peripheral swelling
Tenderness
Symptomtext
Left arm swelling, under arm swelling, armpit swelling and excruciating tenderness, left breast swelling and tenderness, left neck stiffness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Breast swelling
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- Pfizer COVID
- Staat
- MN
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 14.04.2022
- Impfdatum
- 19.01.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 13,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Colorectal cancer
Ileostomy
Laparoscopic surgery
Proctectomy
Postoperative care
Symptomtext
Hospital admission within 6 weeks of COVID vaccination. Admitted: 2/1/2022 for post op care.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Colorectal cancer
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 14.04.2022
- Impfdatum
- 19.01.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 13,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Colorectal cancer
Ileostomy
Laparoscopic surgery
Proctectomy
Postoperative care
Symptomtext
Hospital admission within 6 weeks of COVID vaccination. Admitted: 2/1/2022 for post op care.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Colorectal cancer
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 13.04.2022
- Impfdatum
- 13.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
The patient was scheduled for her 2nd Pfizer vaccine today at 8:10 am. I administered the vaccine in the patients left deltoid. After I asked the patient to wait 15 minutes in our waiting area in case of any adverse reaction. I went to talk to the patient to document the lot number and todays date on her COVID card. When I read the documentation of the first vaccination I noticed the date read 3/30/2022. Then did I realize I had administered the 2nd vaccine earlier than the recommended 28 days in between vaccinations.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Latex, Pollen
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 12.04.2022
- Impfdatum
- 25.03.2022
- Beginn
- 25.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 12.04.2022
- Impfdatum
- 24.03.2022
- Beginn
- 24.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 12.04.2022
- Impfdatum
- 21.03.2022
- Beginn
- 21.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Beyond Use Date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 12.04.2022
- Impfdatum
- 11.03.2022
- Beginn
- 11.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 12.04.2022
- Impfdatum
- 24.02.2022
- Beginn
- 24.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 12.04.2022
- Impfdatum
- 18.02.2022
- Beginn
- 18.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 12.04.2022
- Impfdatum
- 17.02.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 12.04.2022
- Impfdatum
- 16.02.2022
- Beginn
- 16.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 12.04.2022
- Impfdatum
- 14.02.2022
- Beginn
- 14.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 12.04.2022
- Impfdatum
- 11.02.2022
- Beginn
- 11.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 12.04.2022
- Impfdatum
- 08.02.2022
- Beginn
- 08.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Beyond Use Date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 12.04.2022
- Impfdatum
- 07.02.2022
- Beginn
- 07.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 12.04.2022
- Impfdatum
- 07.02.2022
- Beginn
- 07.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 12.04.2022
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 12.04.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 12.04.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 12.04.2022
- Impfdatum
- 26.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 12.04.2022
- Impfdatum
- 26.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Beyond Use Date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 12.04.2022
- Impfdatum
- 21.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 12.04.2022
- Impfdatum
- 21.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 12.04.2022
- Impfdatum
- 19.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 12.04.2022
- Impfdatum
- 19.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Beyond Use Date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 12.04.2022
- Impfdatum
- 18.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 12.04.2022
- Impfdatum
- 17.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 12.04.2022
- Impfdatum
- 13.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 12.04.2022
- Impfdatum
- 13.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 12.04.2022
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 12.04.2022
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 12.04.2022
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 12.04.2022
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 12.04.2022
- Impfdatum
- 11.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Beyond Use Date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 12.04.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 12.04.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 12.04.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 12.04.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 12.04.2022
- Impfdatum
- 06.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 12.04.2022
- Impfdatum
- 06.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 12.04.2022
- Impfdatum
- 01.02.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 12.04.2022
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 12.04.2022
- Impfdatum
- 04.01.2022
- Beginn
- 04.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 11.04.2022
- Impfdatum
- 25.01.2022
- Beginn
- 10.02.2022
- Tage bis Beginn
- 16,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Fracture debridement
Open reduction of fracture
Tibia fracture
Wound treatment
Symptomtext
Admission for open fracture of proximal end of right tibia. Procedure(s) - Right - debridement and irrigation of open fracture, open reduction internal fixation of bicondylar tibial plateau fracture. The hospitalization was necessary for pain control, therapy, medical care and discharge placement. Ultimately, the patient was discharged to group home under satisfactory medical and post-operative condition. ED visit to hospital admission within 6 weeks of receiving the COVID vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fracture debridement
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 07.04.2022
- Impfdatum
- 27.03.2021
- Beginn
- 01.04.2021
- Tage bis Beginn
- 5,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dysmenorrhoea
Loss of personal independence in daily activities
Symptomtext
started having severe cramping with menstral cycles . never had cramps before first started 4/21/2021 has been in the clinic multiple times and has also missed school at least 4 days over the last 6 months
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dysmenorrhoea
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- hereditary high cholesterol
- Andere Medikamente
- crestor 10 mg
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 06.04.2022
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Symptomtext
0.5ml given instead of 0.3ml dose
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 06.04.2022
- Impfdatum
- 21.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 5,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Amputation
Diabetic foot infection
Incisional drainage
Magnetic resonance imaging abnormal
Osteomyelitis
Walking aid user
Symptomtext
Diabetic foot infection (left) with osteomyelitis. MRI was not definitive for osteo but infection did not improve on IV antibiotics so he was taken to OR for I&D and amputations. He did very well post op and was discharged home with cane. ED visit and hospital admission within 6 weeks of receiving the COVID vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Amputation
- Hospital-Tage
- 5,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 05.04.2022
- Impfdatum
- 15.02.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Symptomtext
Hospitalization within 6 weeks of COVID vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 05.04.2022
- Impfdatum
- 02.02.2022
- Beginn
- 11.03.2022
- Tage bis Beginn
- 37,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Caesarean section
Delivery
Exposure during pregnancy
Rhesus antigen positive
Streptococcus test negative
Symptomtext
Patient hospitalized for repeat low transverse cesarean section within 6 weeks of receiving covid vaccination. "She delivered a viable male infant weighing 3460gm, with APGARs of 8 and 8 at 1 and 5 minutes, respectively; in NICU for management of NAS. Patient is Rh (+) blood type, GBS negative."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Caesarean section
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 04.04.2022
- Impfdatum
- 19.01.2022
- Beginn
- 29.01.2022
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Overdose
Symptomtext
Patient presented to the emergency room on January 28th after taking an overdose of a variety of pills. Behavioral health admission and treatment. Hospital admission within 6 weeks of receiving the COVID vaccine. Additional ED visit for overdose on 2/21/2022 - treated and released.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Overdose
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 01.04.2022
- Impfdatum
- 21.01.2022
- Beginn
- 03.02.2022
- Tage bis Beginn
- 13,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Unevaluable event
Symptomtext
ED visit/Hospitalization within 6 weeks of COVID vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- 8,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 31.03.2022
- Impfdatum
- 04.02.2022
- Beginn
- 27.02.2022
- Tage bis Beginn
- 23,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Delivery
Exposure during pregnancy
Normal labour
Symptomtext
Normal labor and delivery on 2/27/2022. Hospital admission within 6 weeks of receiving the COVID vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Delivery
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 29.03.2022
- Impfdatum
- 24.03.2022
- Beginn
- 26.03.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Blood test
Feeling abnormal
Gait disturbance
Monoplegia
Urine analysis
Symptomtext
Felt funny and legs quit working and she couldn't walk. Went to ER. The ER doctor couldn't find anything and she still couldn't walk so they told her it was a bad reaction to the booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood test
- Hospital-Tage
- -
- Labordaten
- yes blood work and urine samples
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- hypothyroidism, pre diabetic
- Andere Medikamente
- esomeprazole, advair inhaler, toprylamate, metformin, synthroid
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 83,0
- Geschlecht
- F
- Eingang
- 28.03.2022
- Impfdatum
- 03.02.2022
- Beginn
- 10.03.2022
- Tage bis Beginn
- 35,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Aspiration pleural cavity
Pulmonary alveolar haemorrhage
Symptomtext
Diffuse pulmonary alveolar hemorrhage - Right thoracocentesis 750 ml pleural fluid consistent with transudate. Recovery in hospital. Hospital admission within 6 weeks of receiving the COVID vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Aspiration pleural cavity
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 28.03.2022
- Impfdatum
- 04.02.2022
- Beginn
- 14.02.2022
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Symptomtext
Patient had an ED visit and/or hospitalization within 6 weeks of receiving COVID vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- 1,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 25.03.2022
- Impfdatum
- 26.01.2022
- Beginn
- 18.02.2022
- Tage bis Beginn
- 23,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Asthenia
Symptomtext
Patient presented to the ED and was subsequently hospitalized for weakness within 6 weeks of receiving covid vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asthenia
- Hospital-Tage
- 5,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 6,0
- Geschlecht
- F
- Eingang
- 22.03.2022
- 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: nein
Incorrect dose administered
Symptomtext
The patient was receiving their second dose in the primary Pfizer series. She should have received the pediatric dose of Pfizer (0.2ml), however the adult 12+ dose was documented (0.3ml grey cap). The employee no longer works at Clinic and it is unknown if the patient received the wrong dose or if the wrong dose was documented.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 18.03.2022
- Impfdatum
- 15.03.2022
- Beginn
- 15.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Interchange of vaccine products
No adverse event
Symptomtext
Prior to the pt's administration of the 1st Covid vaccine shot (Moderna- Not administered by nurse) she had intermittent tremors. Following administration, they became more frequent (being addressed by PCP). Due to this the patient did not want to get Moderna as the second shot to complete the series but requested that she received Pfizer. nurse discussed this with nurse practitioner who said that she could get the Pfizer as the second but a VAERS would need to be completed after. Pt waited 30 minutes after administration of Pfizer vaccination without any adverse reactions.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Unknown
- Allergien
- Ciprofloxacin
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 16.03.2022
- Impfdatum
- 16.03.2022
- Beginn
- 16.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient came in for her covid pfizer vaccine booster. Staff called pharmacy asking for an unopened covid pfizer vaccine vial since the only one we had had been punctured on 3/14/22 at 1400 and today is 3/16/22 @ 0730. Opened vial had been refrigerated since 3/14/22.Pharmacy attendant misunderstood what exp date we were talking about and said we need to go with the thaw expiration date. Therefore, patient was given a dose of the covid pfizer vaccine which actually expired @ 2000 on 3/14/22. Patient did not have any adverse reaction to the injection. I called patient at 1500 on 3/16/22 and shared what happened and told her that a repeated dose was recommended at the timing of her choice. She states she will come back on 3/22/22 @ 0810 to receive her repeated booster vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none known
- Andere Medikamente
- none known
- Allergien
- nkda
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 16.03.2022
- Impfdatum
- 10.02.2022
- Beginn
- 15.03.2022
- Tage bis Beginn
- 33,0
- Dosis
- 3
- 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 Moderna 3/29/21 017B21A dose 2 Moderna 4/26/21 048B21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Covid+ test 3/15/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 15.03.2022
- Impfdatum
- 15.03.2022
- Beginn
- 15.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
This patient received a fourth dose of Covid-19 vaccine (a 2nd Pfizer dose) 0.3 ml LD IM . She knew that it was her fourth dose but did not disclose that fact to nursing staff, but did disclose that fact to N P during the visit after being vaccinated. Patient disclosed that she was afraid of contracting Covid-19 and wanted the fourth dose to protect her from getting it. She had received her booster dose on 11/29/21 Pfizer Covid-19 vaccine. She received the 1st dose Moderna vaccine 12/23/2020, and 2nd dose of Moderna 1/27/2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Skin Rash
- Vorgeschichte
- Depression, anxiety, allergic rhinitis
- Andere Medikamente
- N/A
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 15.03.2022
- Impfdatum
- 12.03.2022
- Beginn
- 12.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
patient was given her booster dose of Pfizer on 3/12/2022 which was 7 days prior to the due date of 3/19/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 11.03.2022
- Impfdatum
- 03.03.2022
- Beginn
- 03.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
Symptomtext
Patient came to office site to receive 2nd Covid vaccine. She completed consent form evaluated by nurse concerning consent form questions (Allergies, Health history) explained side possible side effects pt verbalized understanding administered vaccine IM/RA & advised pt to proceed next door to be monitored for 15 mins in which the pt started verbalizing she received previous vaccine a certain date which made her ineligiable to receive 2nd dose due to vaccine was given in error to soon (should have been 03/17/22) but info wasn't stated on consent form or vaccine card by registration person. Pt was then advised by a healthcare professional who monitored her that she would not received incentive card today because of this error and that she got could return om 03/17/2022 to obtain incentive card upon approval of staff. Pt Verbalized understanding and exited office in satisfactory condition with updated/correct vaccine care
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- None (verbalized by pt)
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 11.03.2022
- Impfdatum
- 11.03.2022
- Beginn
- 11.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient came in for a covid booster, I went and drew up the vaccine and gave patient 0.3 ml. After patient left I realized the vial was/had expired. No symptoms at time of immunization was given. Informed/called patient after he left & informed him what happened. Informed PCP as well, & we rescheduled patient to come back in 4 days to provide patient w/ correct dose & up to date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 02.03.2022
- Impfdatum
- 01.03.2022
- Beginn
- 01.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administration error
Product preparation error
Symptomtext
Float staff unfamiliar with workflow in clinic, pulled Pfizer vial and didn't dilute, gave too concentrated dose to patient. Per guidance on administration errors, dose does not need to be repeated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administration error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 28.02.2022
- Impfdatum
- 23.02.2022
- Beginn
- 23.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Wrong product administered
Symptomtext
Patient Received a Pfizer Covid-19 Vaccine when they should of received a Moderna. Moderna vaccine was given first before the Pfizer.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- Diabetic
- Vorgeschichte
- Diabetic
- Andere Medikamente
- Glyburide, Metformin
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 28.02.2022
- Impfdatum
- 15.03.2021
- Beginn
- 17.03.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Antinuclear antibody negative
Blood calcium
Blood iron
Full blood count
Glycosylated haemoglobin
International normalised ratio
Joint noise
Lipids
Metabolic function test
Muscular weakness
Prothrombin time
Vitamin D
Symptomtext
3 days after receiving the 2nd vaccine I began experiencing muscle weakness and joint popping, the joint popping happens with every movement I do. It has not subsided and has become worse since my booster. Now the joint popping and cracking are louder and have gone to my fingers and toes. After numerous supplementations and trial and errors with exercises, the popping of the joints and muscle weakness have not stopped. I am not vitamin deficient and have had blood work and am not anemic. I have no pain or swelling of the joints, but the joint popping has reached my spine and chest, I can now pop my chest as if a person can crack their knuckles. I was told by my doctor to continue with calcium and vitamin D supplementation. I work in healthcare and absolutely none of my older patients have any popping or cracking in their joints like I do. Nothing seems to alleviate this symptom, I stretch, I do cardio, I am physically fit for my age, I weigh 125 lbs. with muscle. I have even checked if I had rheumatoid arthritis, ANA was negative. Please, I urge whoever handles these messages is able to provide me with some resolution. It is so bad that my bones sound they are about to pop out of the socket or their placement in the joint, again, no pain or swelling, but very loud and with every movement I make they pop.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Antinuclear antibody negative
- Hospital-Tage
- -
- Labordaten
- CBC, CMP, ANA, Vitamin D, Calcium levels, Iron levels, Lipid panel, PT INR, A1c all done 12/15/2021.
- Aktuelle Erkrankungen
- No other illnesses.
- Vorgeschichte
- Past history of Non-Hodgkin's Lymphoma 2011. No other medical conditions.
- Andere Medikamente
- Multivitamins, no medications.
- Allergien
- NKDA, lactose intolerant.
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 25.02.2022
- Impfdatum
- 24.02.2022
- Beginn
- 24.02.2022
- 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
Patient given a booster dose too early. Received pediatric dose on 11/18/2021, a second adult dose on 01/10/2022 and his booster dose on 02/24/2022. After review of CDC guidance the parent was instructed no further booster is needed at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- -
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 23.02.2022
- Impfdatum
- 01.04.2021
- Beginn
- 05.02.2022
- Tage bis Beginn
- 310,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Symptomtext
covid-19 illness
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 1,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 22.02.2022
- Impfdatum
- 22.02.2022
- Beginn
- 22.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Symptomtext
unknown at this time
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Femynor
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 21.02.2022
- Impfdatum
- 27.01.2022
- Beginn
- 02.02.2022
- Tage bis Beginn
- 6,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Immediate post-injection reaction
Lacrimation increased
Ocular hyperaemia
Photophobia
Symptomtext
Both eyes turned red immediately after my vaccine shot and was watering. Seen my PCP doctor on Feb 18th and she referred me to a eye doctor. Doctor prescribed Flarex, antibiotics and Tobranyzin bexamethasone. I follow up with my doctor in two weeks but my eyes are still watering a pink color as soon as I come outside. I now have to get my eyes cleaned every two weeks and still an on going issue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Immediate post-injection reaction
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- Diabetes High cholesterol Herpes
- Vorgeschichte
- Seasonal asthma
- Andere Medikamente
- Vitamin one a day complete Multi vitamins Vitamin C & D
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 16.02.2022
- Impfdatum
- 09.02.2022
- Beginn
- 09.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Electrocardiogram
Laboratory test
Peripheral swelling
Ultrasound Doppler
Symptomtext
This was only after booster done the pt developed swollen up of loiter LE. Venous US as well as EKG and labs symptoms improved over the next few weeks
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Electrocardiogram
- Hospital-Tage
- -
- Labordaten
- LABS, EKG, US Duplex venous study Bilat
- Aktuelle Erkrankungen
- Hypertrichosis, ADHD, prolong menstruation, Iron def-anemia
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 16.02.2022
- Impfdatum
- 08.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Acoustic stimulation tests abnormal
Deafness
Tinnitus
Symptomtext
Tinnitis, hearing loss
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acoustic stimulation tests abnormal
- Hospital-Tage
- -
- Labordaten
- Hearing Test
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Low T
- Andere Medikamente
- Celecoxid, ipratropium Bromide, Testosterone Injection, Multi Vitamin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 16.02.2022
- Impfdatum
- 14.02.2022
- Beginn
- 14.02.2022
- 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
Incorrect dose administered
Symptomtext
Patient was incorrectly given 5-11yo vaccine as a booster (LOT# FL8094) instead of 12+ vaccine. Patient was redosed immediately with Pfizer 12+ vaccine as booster (LOT# FJ5682)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 15.02.2022
- Impfdatum
- 20.01.2022
- Beginn
- 12.02.2022
- Tage bis Beginn
- 23,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Menstrual disorder
Menstruation irregular
Polymenorrhoea
Symptomtext
Irregular menstrual cycle. I started menstruation a week early. Blood was light in volume and dark in color, as if it had already clotted. I have been on birth control since 2017, and always have my period during my placebo week. This time it started while I was on week 3 of my birth control.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Menstrual disorder
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Tri-Lo-Marzia, combination oral contraceptive Lorazepam, 0.5 mg, PRN Trazodone, 50 mg, nightly
- Allergien
- Tree nut allergies
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 14.02.2022
- Impfdatum
- 11.02.2022
- Beginn
- 12.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hypoaesthesia
Symptomtext
Numbness to left arm, shoulder, jaw, that radiated to right arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypoaesthesia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- migraines, hypothyroidism, nodule of left lung, add, depressive disorder, prediabetes
- Vorgeschichte
- as previously noted
- Andere Medikamente
- lexapro, levothyroxine, methylprednisone
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 11.02.2022
- Impfdatum
- 09.02.2022
- Beginn
- 09.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoaesthesia oral
Lip swelling
Symptomtext
Lip numbness and swelling
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypoaesthesia oral
- Hospital-Tage
- -
- Labordaten
- Medrol Dosepack, Benadryl, Pepcid
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- No
- Andere Medikamente
- Tylenol
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 11.02.2022
- Impfdatum
- 11.02.2022
- Beginn
- 11.02.2022
- 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
No adverse event
Symptomtext
No adverse event. But patient received Moderna 1st COVID Vaccine dose and unfortunately got Pfizer, as a second dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 5,0
- Geschlecht
- F
- Eingang
- 11.02.2022
- Impfdatum
- 11.02.2022
- Beginn
- 11.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Symptomtext
Five year old female child in clinic for Covid-19 and Flu vaccine, Child was mistakenly given 12yrs and up vaccine. She was kept in observation for over 15 minutes nurse and doctors were notified no symptoms developed during observation period and no treatments had to be given.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- NKDA, food allergies, or other products
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 11.02.2022
- Impfdatum
- 24.01.2022
- Beginn
- 31.01.2022
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Tinnitus
Symptomtext
Tinnitus got increasingly louder in both ears
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tinnitus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Vitamin D Vitamin C Multivitamin
- Allergien
- Hydrocodone
- Vorherige Impfungen
- After first dose of Pfizer on 3/20/2021 tinnitus in both ears started for the first time. It got slightly reduced over time, bu
- Staat
- OH
- Alter
- 86,0
- Geschlecht
- F
- Eingang
- 11.02.2022
- Impfdatum
- 10.02.2022
- Beginn
- 10.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
No adverse event
Symptomtext
No adverse events at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 10.02.2022
- Impfdatum
- 10.02.2022
- Beginn
- 10.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest discomfort
Symptomtext
Client reported chest pressure rated 1/10 in quality at 3:53PM. EMS was called. Client reported that the pressure went away and did not leave with EMS. Denied difficulty breathing, blurred vision.Vital signs BP 116/75, O2 98%, HR 88, T 98.3 F. Client advised to call EMS if symptoms of chest pressure or difficulty breathing return. She verbalized understanding.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest discomfort
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Asthma
- Vorgeschichte
- Asthma
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 09.02.2022
- Impfdatum
- 07.02.2022
- Beginn
- 08.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Lip swelling
Symptomtext
Patient experienced upper and lower lip swelling within 24-hours of injection. Has recent history of receiving dermal fillers to area in december 2021
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lip swelling
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 07.02.2022
- Impfdatum
- 04.02.2022
- Beginn
- 05.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Oedema peripheral
Swelling
Tenderness
Symptomtext
Next morning noticed swelling to the front of her chest, over collar bone, that has been spreading up to her left neck and left axillary area, very tender no itching no rash.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oedema peripheral
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- GERD, seasonal allergies
- Andere Medikamente
- bupropion, protonix
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 06.02.2022
- Impfdatum
- 06.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Adverse event
Symptomtext
The adverse event is still taking place I?m currently still looking into treatment from the reaction my body is having.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- I have asthma periodically
- Vorgeschichte
- I have asthma periodically and had a part of my thyroid removed years ago
- Andere Medikamente
- At the time of vaccination nothing
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 05.02.2022
- Impfdatum
- 05.02.2022
- Beginn
- 05.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
Symptomtext
PT RECEIVED HER BOOSTER 13 DAYS EARLY
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 04.02.2022
- Impfdatum
- 03.02.2022
- Beginn
- 03.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Vial was unlabeled. In the future I will check for label before administration. Patient was notified and declined to return return for repeat dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Contour Strips; Glimepiride; Lidocaine Topical; DME-MEDI HONEY; Tramadol Hydrochloride; Ipratropium Nasal; Tamsulosin; Sevelamer Carbonate; Mupirocin; Metoprolol; Ketorolac; Ferric Cltrate; Doxazosin; Co-Q10; Bumetanide; Atorvastatin; DME M
- Allergien
- Codeine: N/V; Morphine: N/V; Lantus: SOB; Levernir: Cough, Vomiting
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 04.02.2022
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
Patient was given her 2nd dose on 02/04/2022 and the first dose was on 02/02/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asthma, Ovarian cyst, Obesity, prediabetes, Anxiety,
- Andere Medikamente
- no
- Allergien
- Azithromycin, & Ondansetron
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 04.02.2022
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
Patient given his second dose of Pfizer vaccine one week too early.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 41,0
- 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: nein
Inappropriate schedule of product administration
Symptomtext
PT RECEIVED HER SECOND DOSE OF VACCINE ONE WEEK EARLY
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 15,0
- 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: nein
Inappropriate schedule of product administration
Symptomtext
PT GIVEN SECOND DOSE OF VACCINE ONE WEEK EARLY
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 02.02.2022
- Impfdatum
- 09.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Postmenopausal haemorrhage
Vaginal haemorrhage
Symptomtext
24 hours after receiving Pfizer Booster shot I experienced menstal bleeding from my vagina after 15 years from onset of early menopause. bleeding last for a few hours and then stopped.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Postmenopausal haemorrhage
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- treated for major depression for past 10 years
- Andere Medikamente
- hydrochloride 12.5mg, amlodipine 10mg, oxcarbazepine 300mg
- Allergien
- bee stings
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 02.02.2022
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product preparation issue
Symptomtext
A pre-diluted grey-top Pfizer covid vaccine vial (adult) was diluted with 1.8 mL of normal saline. Subsequently, an over-diluted 0.3 mL vaccine was administered to the patient for their booster. The patient was notified of this and the CDC recommendation that they are to repeat the dose immediately. He was able to return to the clinic the same day and receive the correct dose. No adverse events or clinical consequences were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 02.02.2022
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product preparation issue
Underdose
Symptomtext
A pre-diluted grey-top Pfizer covid vaccine vial (adult) was diluted with 1.8 mL of normal saline. Subsequently, an over-diluted 0.3 mL vaccine was administered to the patient for their booster. The patient was called and notified of this and the CDC recommendation that they are to repeat the dose immediately. The patient stated that she prefers to not repeat the dose. No adverse events or clinical consequences were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 02.02.2022
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product preparation issue
Underdose
Symptomtext
A pre-diluted grey-top Pfizer covid vaccine vial (adult) was diluted with 1.8 mL of normal saline. Subsequently, an over-diluted 0.3 mL vaccine was administered to the patient for their booster. The patient was called and notified of this and the CDC recommendation that they are to repeat the dose immediately. The patient stated that they will go to a pharmacy near their home to receive the booster. No adverse events or clinical consequences were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 02.02.2022
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product preparation issue
Symptomtext
A pre-diluted grey-top Pfizer covid vaccine vial (adult) was further diluted with 1.8 mL of normal saline. Subsequently an over-diluted 0.3 mL vaccine was administered to the patient for her booster. The patient was notified of this, and informed that the CDC recommendation is to receive an additional dose of the vaccine immediately. She was not able to return to the clinic the same day, and a follow-up phone call was made to check on the patient and her vaccination status. During this phone call she stated that she is planning to go to a pharmacy near her home to receive the booster. There were no adverse events or clinical consequences reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 02.02.2022
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Multiple use of single-use product
Product preparation issue
Symptomtext
A pre-diluted grey-top Pfizer covid vaccine vial (adult) was further diluted with 1.8 mL of normal saline. Subsequently an over-diluted 0.3 mL vaccine was administered to the patient for her first vaccine. The patient was notified of this, and informed that the CDC recommendation is to receive an additional dose of the vaccine immediately. She returned to the clinic on the same day and received the correct dose/concentration of the vaccine. There were no adverse events or clinical consequences reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Multiple use of single-use product
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 02.02.2022
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product preparation issue
Underdose
Symptomtext
A pre-diluted grey-top Pfizer covid vaccine vial (adult) was further diluted with 1.8 mL of normal saline. Subsequently an over-diluted 0.3 mL vaccine was administered to the patient for his first vaccine. The patient was notified of this, and informed that the CDC recommendation is to receive an additional dose of the vaccine immediately. He returned to the clinic on the same day and received the correct dose/concentration of the vaccine. There were no adverse events or clinical consequences reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 02.02.2022
- Impfdatum
- 11.05.2021
- Beginn
- 10.12.2021
- Tage bis Beginn
- 213,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Appendicectomy
Appendicitis
Computerised tomogram abdomen abnormal
Symptomtext
COVID Vaccine x2 in May 2021, appendicitis Dec 2021, appendectomy required, COVID booster Jan 2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Appendicectomy
- Hospital-Tage
- -
- Labordaten
- CT Scan Saturday 12/11/2021, Appendectomy 12/11/2021
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Prenatal vitamin
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 31.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 29.01.2022
- Tage bis Beginn
- 16,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Vaccine breakthrough infection
Symptomtext
Fully vaccinated, boosted on 1/13/22. COVID breakthrough infection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 31.01.2022
- Impfdatum
- 22.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Adverse event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Adverse event
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 29.01.2022
- Impfdatum
- 28.01.2022
- Beginn
- 29.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Costochondritis
Heart rate increased
Symptomtext
Higher heart rate, 100 bpm while standing. Heartrate at least 10 beats higher than average. Started 24 hours after shot and continues. Costochondritis started about 24 hours after shot and continues.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Costochondritis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma
- Andere Medikamente
- Vitamin D
- Allergien
- Penicillin, wine, beer
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 29.01.2022
- Impfdatum
- 28.01.2022
- Beginn
- 29.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Somnolence
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Somnolence
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 28.01.2022
- 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: unbekannt
Erholt: nein
Inappropriate schedule of product administration
No adverse event
Symptomtext
Patient received second dose exactly 14 days from the first dose. Patient did not have any adverse reaction.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/an/a
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 28.01.2022
- Impfdatum
- 22.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
Symptomtext
A booster shot given 1 month earlier (4 months after the 2nd shot). The immunizer contacted the patient's mom. No abnormal symptoms developed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 28.01.2022
- Impfdatum
- 22.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
No adverse event
Symptomtext
a booster shot was given 1 month earlier, which was 4 month after the 2nd shot. The immunizer contacted the mom, and the patient does not have any abnormal symptoms developed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 10,0
- Geschlecht
- F
- Eingang
- 28.01.2022
- Impfdatum
- 26.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asymptomatic COVID-19
Incorrect dose administered
Symptomtext
Patient 2 (PT2) inadvertently received an age-inappropriate vaccine dose due to mistaken identity on behalf of the patient's mother and sister. EMT, alongside Patient Registrar (PR), confirmed the identity of (PT1) when screening with the mother and (PT1). After vaccinating PT2, PT1 stated they were suppose to receive a vaccine as well and EMT asked PT2 her name, questioned who was PT1 then since they confirmed that PT1 was indeed her name. PT2 stated that it was her sister. EMT asked for PT2 DOB where she discovered was 10 years old and not 14. EMT reached out for guidance immediately. Dr. spoke with the mother of the patient and had translate via teleconference. Dr. informed the mother that, due to mistaken identity, PT2 had inadvertently received an age-inappropriate vaccine dose. In accordance with CDC guidelines, and previous guidelines, advice was given for PT2 to be monitored regularly for any adverse reactions that may occur in the next 21 days, and that a second dose should be an age appropriate pediatric dose. PT2 was asymptotic at the time of the call.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asymptomatic COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 27.01.2022
- Impfdatum
- 27.01.2022
- Beginn
- 27.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Interchange of vaccine products
Symptomtext
Client may have received Pfizer as her second dose instead of Moderna. Client was originally vaccinated on April 23rd, 2021 with Moderna vaccine. When asked about the second vaccine she stated that she did not have her card so they gave her a paper but she could not find it. I asked her when she received the vaccine and she stated that it was not on the day on the back of the card but was on the day after or near. The vaccine was delivered. Over the course of 15 minutes the client said she received the vaccine in the mouth. This made me doubt the veracity of the previous statements about the second dose. I further asked the client about the clinic she received the vaccine from and the doctor and she was very vague.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 27.01.2022
- Impfdatum
- 26.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Patient was given a dose of Pfizer that was administered past the 12 hour time frame of the vials first puncture. Per Pfizer there is data to support the stability of the vaccine up to 24 hours if stored in 2-8 Celsius which vaccine was.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 27.01.2022
- 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
Incorrect dose administered
No adverse event
Symptomtext
Patient received Pfizer Covid-19 vaccine gray cap for ages 12 and up, patient is currently age 11. No symptoms noted at time of administration.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 26.01.2022
- Impfdatum
- 24.01.2022
- Beginn
- 24.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
Symptomtext
Second dose given 7 days early
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- NA
- Allergien
- NA
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 26.01.2022
- Impfdatum
- 18.01.2022
- Beginn
- 24.01.2022
- Tage bis Beginn
- 6,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Heavy menstrual bleeding
Menstruation irregular
Symptomtext
Started my period on day 20 of my cycle. This is very unusual for me. I'm usually on day 32-35. It was also much heavier than normal and lasted longer.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Heavy menstrual bleeding
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Armour Thyroid
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 25.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 23.01.2022
- Tage bis Beginn
- 18,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product preparation issue
Symptomtext
PHARMACIST RECONSTITUTED PFIZER GRAY CAP VACCINE WITH 1.8 ML 0.9% NACL . ADMINISTERED 0.3 ML IM TO PATIENT. SUB THERAPUETIC DOSE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product preparation issue
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- NO
- Vorgeschichte
- NO
- Andere Medikamente
- NO
- Allergien
- NO
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 25.01.2022
- Impfdatum
- 23.01.2022
- Beginn
- 23.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product preparation issue
Underdose
Symptomtext
PHARMACIST RECONSTITUTED GRAY CAP PFIZER VACCINE WITH 1.8 ML OF 0.9% NACL. AND ADMINISTERED 0.3 ML IM TO PATIENT. GIVING SUB A THERAPUETIC DOSE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product preparation issue
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- NO
- Vorgeschichte
- NO
- Andere Medikamente
- NO
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 25.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product preparation issue
Underdose
Symptomtext
Clinic lead diluted gray top Pfizer with diluent. Client received diluted vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product preparation issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 25.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product preparation issue
Symptomtext
Vaccination Administration error. Team lean diluted gray top Pfizer with diluent and administer the diluted Pfizer vaccine to the Client.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product preparation issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 25.01.2022
- Impfdatum
- 19.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Constipation
Suicidal ideation
Symptomtext
Extreme constipation, suicidal ideations
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Constipation
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Anxiety, Depression, IBS, Lactose Intolerance
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 25.01.2022
- Impfdatum
- 16.01.2022
- Beginn
- 16.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Immunisation
Lymphadenopathy
Symptomtext
Enlarged lymph node by clavical; Dose received: 3; This is a spontaneous report from a contactable reporter (consumer or other non-HCP). The reporter is the patient. A 16-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 16Jan2022 (Lot number: FJ5682) at the age of 16 years as dose 3 (booster), single for COVID-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE; Lot number: ER8735; Route of administration: Unspecified; Anatomical location: Right arm), administration date: 08May2021, when the patient was 16 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE; Lot number: EW0178; Route of administration: Unspecified; Anatomical location: Right arm), administration date: 29May2021, when the patient was 16 years old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 16Jan2022, outcome "unknown", described as "Dose received: 3"; LYMPHADENOPATHY (non-serious) with onset 17Jan2022, outcome "recovering", described as "Enlarged lymph node by clavical". Therapeutic measures were not taken as a result of lymphadenopathy. Additional information: Prior to vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the COVID-19 vaccine. The event did not result in doctor or other healthcare professional office/clinic visit, emergency room or urgent care. Since the vaccination, the patient had not been tested for COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Immunisation
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 11,0
- Geschlecht
- F
- Eingang
- 24.01.2022
- Impfdatum
- 24.01.2022
- Beginn
- 24.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
No adverse event
Symptomtext
This 11 years old client received Covid-19 Pfizer Vaccine for +12 years. Did not presented any symptoms during the 15 minutes observation after the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- No Known Allergies.
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 24.01.2022
- Impfdatum
- 21.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Booster dose given 3 months too early. Patient received second COVID-19 shot in November, and given booster in January.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 10,0
- Geschlecht
- M
- Eingang
- 21.01.2022
- Impfdatum
- 21.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
No adverse event
Product administered to patient of inappropriate age
Symptomtext
No Adverse Event - patient filled out form and marked age as 12 and category for Pfizer as 12+ (vs 5-11). Upon documentation of the given vaccine, the vaccinator realized his age was 10 and not 12.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 10,0
- Geschlecht
- F
- Eingang
- 21.01.2022
- 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: ja
Incorrect dose administered
Symptomtext
Patient should have been given 0.2mL of Pfizer, but she received 0.3mL of Pfizer. Patient waited for 15 minutes afterward and she felt fine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 21.01.2022
- Impfdatum
- 21.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Hypoaesthesia
Muscle twitching
Symptomtext
Right side facial numbness, right side eye Twitch
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypoaesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Escitalopram
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 21.01.2022
- Impfdatum
- 20.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dysgeusia
Symptomtext
Persistent taste of metal in mouth
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dysgeusia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- COVID-19
- Vorgeschichte
- ASTHMA, MORBIDLY OBESE, HIGH BLOOD PRESSURE
- Andere Medikamente
- Metoprolol, omeproazole
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 21.01.2022
- Impfdatum
- 20.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Underdose
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 20.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
patient mom came in to get shot with daughter. mom had print out of daughter's shot history but didn't have her own. While Pharmacy was looking up mom's shot history nurse administered shot to daughter. Pharmacy noted mom was too soon and then noticed daughter too soon too but was too late and nurse already administered shot. daughter received booster only after 3 months instead of 5 months. mom said daughter needed booster for school and school told them to come get shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Vaccine breakthrough infection
Symptomtext
Fully vaccinated, and boosted 1/14/22. 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
- TX
- Alter
- 7,0
- Geschlecht
- M
- Eingang
- 19.01.2022
- Impfdatum
- 17.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Symptomtext
Error: Wrong Dose of Vaccine - Too High-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 18.01.2022
- Impfdatum
- 16.01.2022
- Beginn
- 16.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Underdose
Symptomtext
Child came into the clinic with guardian to have 2nd dose administered. Vaccine card was given to RN who then passed the card to the scribe and RN did not verify DOB. Scribe then located patient in the adult clinic. Once verified that patient was in the system, RN gave pediatric dose but was not informed that patient was listed to received adult dose and not pediatric dose. Patient stayed in the observation area for 15 min and no adverse reactions noted and left with guardian.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- unknonw
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 11.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
THERE WAS NO ADVERSE EVENT. *******THIS WAS A VACCINE ADMINISTRATION ERROR.******* THE PATIENT COMPLETED THE ASTRA ZENECA SERIES AND REQUESTED A PFIZER BOOSTER. THE BOOSTER WAS GIVEN TOO SOON. THE ASTRA ZENECA SERIES WAS COMPLETED ON 10/06/2021. PATIENT WAS INFORMED AND GIVE THE APPROPRIATE INFORMATION FROM THE VACCINE ERRORS AND DEVIATIONS GUIDELINE RESOURCE: WILL NOT REPEAT DOSE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 13.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
Received COVID - 19 booster dose too early. Notified patient of early dose, not having any symptoms. She will contact her doctor if she started having any side effects.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 13.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
Symptomtext
VACCINE WAS GIVEN IN THE 4 MONTH INSTEAD OF THE 5TH MONTH
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- NA
- Allergien
- NA
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 12.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
No adverse event
Symptomtext
Patient received booster dose early . Patient received second dose of Pfizer on September 20, 2021 and booster on 01/07/2022. Patient was monitored and no adverse event occured. Follow up call was made to patient and they are fine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 12.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Symptomtext
patient's vaccination card was scanned-- this copy only showed only first two doses that were administered (both in March 2021). when the 3rd dose was given, she handed in the actual vaccination card for me to write on and at the back of the card, was the 3rd dose she had in October. I asked her if she already received her 3rd dose and she denied receiving it. I checked immunet and discovered she did receive her 3rd dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 10.01.2022
- Impfdatum
- 10.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Patient received booster dose too soon after 2nd dose. 2nd dose was given on September 3, 2021, and patient got booster on 01/10/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -