- Staat
- -
- Alter
- 92,0
- Geschlecht
- F
- Eingang
- 21.09.2023
- Impfdatum
- 29.12.2021
- Beginn
- 29.08.2023
- Tage bis Beginn
- 608,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Angiogram pulmonary abnormal
Asthenia
Blood culture negative
C-reactive protein increased
COVID-19
COVID-19 pneumonia
Chest X-ray abnormal
Dyspnoea
Hypersomnia
Hypophagia
Laboratory test
Lung opacity
Mental status changes
Pneumonia
Staphylococcus test positive
Toxic encephalopathy
Urine analysis normal
Symptomtext
Patient is a 93 y.o. female patient of MD with history of Alzheimer Dementia, Anemia, Seizure disorder on Keppra, CKD 3a, CAD, and HLD presented on 8/29/2023 with SOB. Agency consulted by Hospitalists, Generic for medical management. Acute respiratory failure with hypoxia Covid 19 PNA Multifocal PNA Pneumonia DNR CC Presented with weakness, SOB CXR 8/26 showed no acute cardiopulmonary process CXR 8/29 showed bibasilar airspace opacity CTPA 8/29 show bilateral lower lobe pneumonia AF, WBC normal, CRP 308.4, PCT 6.14, Blood culture NGTD, MRSA detected, Urine Ag negative ID and Pulm following; was needing HHF but now on RA since not keeping NC on Resumed remdesivir (Stop 9/2), dexamethasone (stop 9/9) Rocephin and azithromycin stopped, now po Pt's mental status is waxing and waining Palliative care consulted, DNR CC, All labs, IV have been discontinued Plan to discharge to SNF then home Acute toxic encephalopathy Likely d/t COVID and pneumonia with dementia baseline UA without infection Continues to wax and wane Generalized weakness Decreased oral intake Likely secondary to COVID and pneumonia PT/OT/CM History of seizures Continued home Keppra Dementia Holding home Remeron due to hypersomnolence and AMS Hyperlipidemia Holding home statin History of CVA Continue home aspirin; holding statin since risks outweigh benefits
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 8,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 02.06.2023
- Impfdatum
- 06.01.2022
- Beginn
- 15.09.2022
- Tage bis Beginn
- 252,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Deep vein thrombosis
Pulmonary embolism
Symptomtext
PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE SADDLE PULMONARY EMBOLISM ACUTE DVT OF RIGHT LEG, UNSPECIFIED VEIN
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary embolism
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 26.05.2023
- Impfdatum
- 31.01.2022
- Beginn
- 25.05.2023
- Tage bis Beginn
- 479,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Death
Symptomtext
Patient expired 5/25/2023.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- CAD, HTN, DM2
- Andere Medikamente
- Unknown
- Allergien
- Penecillins
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 25.05.2023
- Impfdatum
- 16.12.2021
- Beginn
- 14.11.2022
- Tage bis Beginn
- 333,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute myocardial infarction
Anaemia
Hypotension
Symptomtext
I21.4 ACUTE NON ST ELEVATION MI 11/14/2022 ACUTE NON ST ELEVATION MI I95.9 HYPOTENSION 2/8/2023 ACUTE NON ST ELEVATION MI I21.4 ACUTE NON ST ELEVATION MI 11/14/2022 ANEMIA I95.9 HYPOTENSION 2/8/2023 ANEMIA I21.4 ACUTE NON ST ELEVATION MI 11/14/2022 ACUTE NON ST ELEVATION MI I95.9 HYPOTENSION 2/8/2023 ACUTE NON ST ELEVATION MI I21.4 ACUTE NON ST ELEVATION MI 11/14/2022 ACUTE NON ST ELEVATION MI I95.9 HYPOTENSION 2/8/2023 ACUTE NON ST ELEVATION MI
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 23.05.2023
- Impfdatum
- 21.12.2021
- Beginn
- 24.09.2022
- Tage bis Beginn
- 277,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute coronary syndrome
Acute myocardial infarction
Symptom recurrence
Symptomtext
PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ACUTE NON ST ELEVATION MI ACUTE CORONARY SYNDROME, UNSPECIFIED 9/28/2022 -- RECURRENCE OF SAME SYMPTOMS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 17.05.2023
- Impfdatum
- 22.12.2021
- Beginn
- 14.02.2023
- Tage bis Beginn
- 419,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Asthenia
COVID-19
Confusional state
Death
Dyspnoea
Fatigue
General physical health deterioration
Hypoxia
Pancytopenia
Positive airway pressure therapy
SARS-CoV-2 test positive
Symptomtext
The patient has a history of multiple myeloma and is currently undergoing therapy. He was brought to the ED by EMS on 2/14/23 for evaluation of shortness of breath, weakness, fatigue, and confusion that began two days prior. A COVID PCR test done in the ED resulted positive. He was admitted to the hospital on 2/14 for acute respiratory failure with hypoxia and pancytopenia. During admission, he was treated with steroids and on BIPAP. He continued to worsen and could no longer oxygenate with noninvasive support. The patient passed away on 2/22/23. Discharge diagnosis was acute hypoxic respiratory failure, pneumonitis likely due to combination of med toxicity (isatuximab/carfilozamab for multiple myeloma) and COVID infection. Of note, the patient has received the primary COVID vaccine series and one booster. The most recent booster was administered 12/22/21.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 25.04.2023
- Impfdatum
- 20.12.2021
- Beginn
- 22.03.2022
- Tage bis Beginn
- 92,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute respiratory failure
Symptomtext
J96.00 ACUTE RESPIRATORY FAILURE 3/15/2022 HX OF INTRACEREBRAL HEMORRHAGE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 19.04.2023
- Impfdatum
- 22.12.2021
- Beginn
- 15.02.2022
- Tage bis Beginn
- 55,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute myocardial infarction
Symptomtext
ACUTE NON ST ELEVATION MI
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 10.02.2023
- Impfdatum
- 14.12.2021
- Beginn
- 15.01.2023
- Tage bis Beginn
- 397,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Anticoagulant therapy
COVID-19
Chronic respiratory failure
Dyspnoea
Hypoxia
Pneumonia staphylococcal
Pulmonary embolism
Respiratory syncytial virus infection
SARS-CoV-2 test positive
Superinfection
Symptomtext
01/15/23 presents to ED for "SOB". PMHx of "CKD stage III, PE on Eliquis (December 2022), chronic hypoxic respiratory failure status post RSV with superimposed MRSA pneumonia (November 2022), asthma, bronchiectasis, IgA deficiency, CVA with PFO, HFpEF, COVID-19 pneumonia"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary embolism
- Hospital-Tage
- -
- Labordaten
- 01/15/23 SARS-CoV-2 (COVID-19) by NAA detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 27.12.2022
- Impfdatum
- 29.01.2021
- Beginn
- 22.12.2022
- Tage bis Beginn
- 692,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
COVID-19
Productive cough
Rhinorrhoea
Syncope
Symptomtext
Pt with PMH of CAD s/p remote CABG, type II NIDDM, presents after multiple syncopal episodes at home. Has had a cough with intermittent phlegm production and new rhinorrhea. Pt admitted with acute hypoxic respiratory failure and COVID infection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 20.11.2022
- Impfdatum
- 22.12.2021
- Beginn
- 15.11.2022
- Tage bis Beginn
- 328,0
- Dosis
- 3
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Acute respiratory failure
Alanine aminotransferase normal
Angiogram pulmonary normal
Anion gap
Anticoagulant therapy
Aspartate aminotransferase normal
Aspiration
Bacterial test positive
Base excess
Basophil count decreased
Basophil percentage decreased
Bilirubin urine
Bladder catheterisation
Blood albumin normal
Blood alkaline phosphatase normal
Blood bicarbonate
Blood bilirubin decreased
Blood calcium decreased
Symptomtext
Document Type: History and Physical Document Subject: History & Physical Note Encounter Info: Hospital, Inpatient, 11/15/22 - * Final Report * Chief Complaint respiratory arrest History of Present Illness/Subjective 53-year-old male with a past medical history of Charcot-Marie-Tooth and diaphragmatic paralysis who was supposed to use Trelegy at night, among other conditions listed below who was intubated in the field for respiratory arrest and inability to protect his airway as per EMS. The patient is following with pulmonology outpatient who he saw last month, and according to chart review of the visit note, the patient has been experiencing worsening difficulty breathing due to his diaphragmatic dysfunction/paralysis and the plan was to follow-up with a neurologist for his progressively worsening condition. According to the ED provider, his mother stated he was not wearing his trilogy device when she found him not breathing, she states that some nights he enjoys falling asleep without having to use it. She also notes it has been increasingly difficult for him to ambulate independently. In the ED the patient was found to have high lactate, elevated troponin, however CT head and CTA of chest were negative. He was also found to have mild leukocytosis as well as a anion gap of 18 and elevated glucose in the 250s. Patient is being accepted to ICU for continued ventilatory support, close monitoring, and possible initiation of insulin drip. Patient may need a neurology evaluation in the a.m., if the neurologist feels an in person evaluation is passed then patient may need to be transferred to another facility at that time however patient is currently appropriate for our ICU. Mother is at bedside and states she is not aware of an active advanced directive and believes her son would want cpr and mechanical vent if required and therefore patient is full code. This patient is critically ill due to metabolic, hemodynamic and/or respiratory instability. They require high complexity evaluation, decision making, and care. They require ICU level of care and monitoring due to high risk of clinical decompensation with high risk of morbidity and mortality. Critical care time includes, but is not limited to, bedside assessment, review of medical record, radiographic and laboratory results, ventilator and/or respiratory management, review of ekg and/or cardiac monitoring, critical decision making, coordination of care with consultants and/or care team, and documentation of critical intervention/plans, and consultation with patient and/or family. Time excludes any procedural time. I spent greater than 65 minutes in the evaluation and management of this patient with more than 50% of the time spent counseling and/or coordinating care. I counseled the patient and/or family about the findings, differential diagnoses, my assessment, recommendations, and plan. I coordinated care with the multidisciplinary healthcare team. Review of Systems Unable to assess due to patient being intubated and sedated on ventilator Physical Exam/Objective Vital Signs (most recent and range for last 24 hours) Temp (CEL) 36.5 (36.5-36.5) Temp (FAHR) 97.7 (97.7-97.7), BP 130/76 (121-191)/(73-101), HR 75 (75-83), RR 18 (18-20), O2Sat 92 (90-92) Patient Weight Current Daily Weight: 82.6 kg 11/15/22 Previous Daily Weight: 82.6 kg 11/15/22 Patient Height General: Intubated, eyes spontaneously open, not following commands Eye: no conjunctival injection Pupils 2 mm and minimally reactive Cardiovascular: rhythm regular, S1S2 within normal limits Respiratory: Mechanical breath sounds bilaterally with good air entry, tolerating vent, no obvious wheezes or rales Gastrointestinal: soft, non-distended, nontender, no guarding Msk: NC/AT, extremities without deformity Skin: warm, dry Psych: Unable to assess Neurological: Eyes are spontaneously open, moving upper extremities symmetrically, not following commands Assessment/Plan 1. Respiratory arrest R09.2 likely 2/2 #6 and #5, possibly some underlying pna but exam and imaging did not suggest pneumonia and hx supports noncompliance with night time Trelegy device at time of arrest 2. Severe sepsis R65.20 3. Elevated lactic acid level R79.89 met severe sepsis criteria but likely explained by demand ischemia from resp failure rather than infectious etiology however will panculture and cont broad spectrum abx for now iv hydration, serial lactates trend procal, maintain map >65 4. Acute respiratory failure J96.00 5. Chronic respiratory failure J96.10 6. Diaphragmatic paresis J98.6 7. Charcot-Marie-Tooth disease G60.0 #4 and #5 likely related to #6 and #7, will likely need neurology evaluation and possibly pulm opinion on ventillatory weaning in the setting of diaphragmatic paresis/dysfunction made need evaluation for trach if not able to wean from vent trend abd, adjust vent prn cont fentanyl and propofol for now to rass -1 8. Hyperglycemia R73.9 9. DM (diabetes mellitus), type 2 E11.9 q2h poc glucose checks, iss hold oral meds for now long acting insulin as needed anion gap initially elevated, will repeat bmp stat and determine if initiation of insulin drip is required vs subcu insulin 10. Elevated troponin R77.8 likely related to hypoxic event and subsequent demand ischemia 11. Hyperlipidemia E78.5 resume home meds when able to 12. Hypertension I10 resume home meds as able to Orders: acetaminophen, 650 mg, Orally, Tablet, Q4H, PRN, Pain, Mild PO (1-3 out of 10)/Fever, 11/15/22 6:06:00 cefePIME, 1 GM, IVPB, Injection, Q8H, Indication: Sepsis (Update Indication in 36-48 hrs), 11/15/22 15:00:00, 12.5 mL/hr, Infuse Over 4 Hours, Total Volume (mL) = 50 Dextrose 10% in Water 500 mL, Total Volume (mL) = 500, IV, 11/15/22 7:19:00, PRN - See Comments fentaNYL 2,500 mCg + Sodium Chloride 0.9% 250 mL, Total Volume (mL) = 250, IV, 11/15/22 6:32:00, Titrate - See Comments glucagon, 1 mg, IM, Injection, Unscheduled, PRN, Hypoglycemia, 11/15/22 7:19:00 glucose, Per Glucose Level, IV Push, Injection, Unscheduled, PRN, Low Blood Sugar, 11/15/22 7:19:00 heparin, 5,000 Units, Subcutaneous, Injection, Q8H, Routine, 11/15/22 7:00:00 insulin lispro, Sliding Scale, Subcutaneous, Injection, With Glucose Testing, PRN, Serum Glucose, 11/15/22 7:19:00 Lactated Ringers 1,000 mL, Total Volume (mL) = 1,000, IV, 11/15/22 6:07:00, 75 mL/hr, Clinical Weight metroNIDAZOLE, 500 mg, IVPB, Infusion, Q8H, 11/15/22 15:00:00, 100 mL/hr, Infuse Over 60 minutes, Total Volume (mL) = 100 polyethylene glycol 3350, 17 GM, Orally, Powder, Daily, PRN, Constipation - Use First, 11/15/22 6:06:00 propofol 1,000 mg + Premix Solution 100 mL, Total Volume (mL) = 100, IV, 11/15/22 6:48:00, Titrate - See Comments propofol infusion bolus dose, 10 mg, Via Infusion Pump, Infusion, Q5min, PRN, Agitation, 11/15/22 6:48:00 vancomycin, 2 GM, IVPB, Injection, ONCE, Indication: Sepsis (Update Indication in 36-48 hrs), 11/15/22 7:00:00, 11/15/22 7:00:00, 250 mL/hr, Infuse Over 2 Hours, Total Volume (mL) = 500 Admit to Inpatient CAH Aspiration Precautions Basic Metabolic Panel Call (Specify) Call (Specify) Call Blood Glucose Call Blood Glucose Call Diastolic Blood Pressure Call Heart Rate Call Mean Arterial Pressure Call Mental Status Changes Call O2 Saturation Call Respiratory Distress Call Respiratory Rate Call Systolic Blood Pressure Call Temperature Call Urine Output Call Urine Output CBC w/Differential Comp Metabolic Panel Continuous Oxygen Saturation Conventional Ventilator DC SIRS Alert and Sepsis Screen Do Not (Specify) Document per Nursing (Specify) Dysphagia Screen by RN End Tidal CO2 Monitor Continuous Fall Precautions Fluid Intake Requirement Gluc-Strip POC Gluc-Strip POC Glucose POC Hgb A1C HPLC Bld QN Initiate IV Care Protocols As Appropriate Initiate Mobility Protocol Initiate Oxygen Protocol Initiate Respiratory Protocol Initiate Skin and Wound Care Protocol Intake + Output Strict L pneumophila Ag Ur QL Lactate Pl Venous QN Level of Care Lipid Panel SerPl QN Magnesium SerPl QN Maintain (Specify) Medical Service Medication Message to Nursing Message to Nursing Message to Nursing Notify Provider Notify Provider Notify Provider NPO Except Medications Peripheral IV Insertion Peripheral IV Insertion Pharmacy Review/Follow-Up Phosphorus SerPl QN Procalcitonin Procalcitonin RCP Airway Assessment Resp CX + Stn Resp Evaluation or Assessment Resuscitation Status Sequential Compression Device Strep pneumoniae Ag Urine Telemetry Class III 24hr Recommendation Titrate FiO2 to Keep O2 Sat Troponin-I High Sensitivity TSH w FreeT4 reflex Urinary Catheter Routine Care Vancomycin Pharmacy Dosing Consult Vital Signs Weight Weight Code Status Resuscitation Status - Ordered -- 11/15/22 6:06:00, Full Code Chronic Problem List Charcot-Marie-Tooth atrophy Chronic respiratory failure Diabetic neuropathy DM (diabetes mellitus), type 2 Foot pain, bilateral Hyperlipidemia Hypertension Neuropathy Onychogryphosis Onychomycosis of toenail Paralysis, diaphragm Schizophrenia Seasonal allergies Procedure/Surgical History ?Unknown Medications Home Medications (10) Active acetaminophen 325 mg oral tablet 650 mg = 2 Tablet, PRN, Orally, Q4H Basaglar (insulin glargine) KwikPen 100 units/mL subcutaneous solution See Instructions, 40 units in the AM60 units in the PM fluticasone 50 mCg/inh nasal spray 1 Spray, intraNASAL, BID, pt needs annual for further refills Geodon 40 mg oral capsule 40 mg = 1 Capsule, Orally, BID Januvia 100 mg oral tablet lisinopril 5 mg oral tablet 5 mg = 1 Tablet, Orally, Daily loratadine 10 mg oral tablet 10 mg = 1 Tablet, Orally, Daily metFORMIN 1, Orally, BID, unsure of dose omega-3 polyunsaturated fatty acids 1200 mg oral capsule 2,400 mg = 2 Capsule, Orally, QAM simvastatin 40 mg oral tablet 40 mg = 1 Tablet, Orally, At Bedtime Active Scheduled Inpatient Medications cefePIME, Injection, 1 GM, IVPB, Q8H, Indication: Sepsis (Update Indication in 36-48 hrs), Start: 11/15/22 15:00:00 heparin (heparin 5,000 units/0.5 mL injectable solution), Injection, 5,000 Units, Subcutaneous, Q8H, Start: 11/15/22 07:00:00 metroNIDAZOLE, Infusion, 500 mg, IVPB, Q8H, Start: 11/15/22 15:00:00 vancomycin, Injection, 2 GM, IVPB, ONCE, Indication: Sepsis (Update Indication in 36-48 hrs), Start: 11/15/22 07:00:00 fentaNYL PREMIX + Sodium Chloride 0.9% PREMIX IV Titrate - See Commnets 50 mCg/hr 11/15/22 Propofol + Solution PREMIX IV Titrate - See Comments 40.008 mCg/kg/min 11/15/22 NORepinephrine PREMIX + Sodium Chloride 0.9% PREMIX IV Titrate - See Comments 0 mCg/min 11/15/22 Lactated Ringers 1,000 mL IV 75 mL/hr fentaNYL PREMIX + Sodium Chloride 0.9% PREMIX IV Titrate - See Comments Propofol + Solution PREMIX IV Titrate - See Comments 39.9919 mCg/kg/min Dextrose 10% in Water 500 mL IV PRN - See Comments One-Time Medications Given 11/14/22 00:00:00 TO 11/15/22 07:39:15 None Reported PRN Medications (0600 - 0559) from 11/14 - 11/15 acetaminophen, 650 mg, Orally, Q4H, 0 Dose(s) glucagon, 1 mg, IM, Unscheduled, 0 Dose(s) glucose, Per Glucose Level , IV Push, Unscheduled, 0 Dose(s) insulin lispro, Sliding Scale , Subcutaneous, With Glucose Testing, 0 Dose(s) polyethylene glycol 3350, 17 GM, Orally, Daily, 0 Dose(s) propofol infusion bolus dose, 10 mg, Via Infusion Pump, Q5min, 0 Dose(s) Allergies Seldane aspirin Social History Electronic Cigarette/Vaping E-Cigarette Use Never. Home/Environment Lives with Mother. Tobacco Tobacco Use: Never (less than 100 in lifetime). Family History Family history is negative Lab Results All Labs Last 24 hours (No Micro or Pathology) Hematology: WBC: 13.5 k/cumm High (11/15/22 02:52:00) RBC: 4.2 million/cumm (11/15/22 02:52:00) Hgb: 10.9 GM/dL Low (11/15/22 02:52:00) Hct: 35.3 % Low (11/15/22 02:52:00) MCV: 84 fL (11/15/22 02:52:00) MCH: 25.9 pg Low (11/15/22 02:52:00) MCHC: 30.7 GM/dL Low (11/15/22 02:52:00) RDW: 16.9 % High (11/15/22 02:52:00) Platelet: 238 k/cumm (11/15/22 02:52:00) MPV: 8.3 fL (11/15/22 02:52:00) Neutrophils %: 90 % (11/15/22 02:52:00) Lymphocytes %: 5 % (11/15/22 02:52:00) Monocytes %: 5 % (11/15/22 02:52:00) Eosinophils %: 0 % (11/15/22 02:52:00) Basophils %: 0 % (11/15/22 02:52:00) Absolute Neutrophil: 12.1 k/cumm High (11/15/22 02:52:00) Absolute Lymphocyte: 0.6 k/cumm Low (11/15/22 02:52:00) Absolute Monocyte: 0.7 k/cumm (11/15/22 02:52:00) Absolute Eosinophil: 0.1 k/cumm (11/15/22 02:52:00) Absolute Basophil: 0 k/cumm (11/15/22 02:52:00) Chemistry: Sodium SerPl QN: 149 mmol/L High (11/15/22 06:59:00) Potassium SerPl QN: 4 mmol/L (11/15/22 06:59:00) Chloride SerPl QN: 100 mmol/L (11/15/22 06:59:00) Carbon Dioxide SerPl QN: 30 mmol/L High (11/15/22 06:59:00) Anion Gap: 19 mmol/L High (11/15/22 06:59:00) BUN SerPl QN: 31 mg/dL High (11/15/22 06:59:00) Creatinine SerPl QN: 1.14 mg/dL (11/15/22 06:59:00) Estimated GFR (CKD-EPI, no race): 77 mL/min/1.73m2 (11/15/22 06:59:00) Estimated CRCL (CG): 83 mL/min (11/15/22 06:59:00) Glucose SerPl QN: 133 mg/dL High (11/15/22 06:59:00) Calcium Total SerPl QN: 8.8 mg/dL (11/15/22 06:59:00) Alkaline Phos SerPl QN: 70 Units/L (11/15/22 02:52:00) ALT SerPl QN: 21 Units/L (11/15/22 02:52:00) AST SerPl QN: 25 Units/L (11/15/22 02:52:00) Bilirubin Total SerPl QN: 0.2 mg/dL (11/15/22 02:52:00) Total Protein SerPl QN: 6 GM/dL Low (11/15/22 02:52:00) Albumin SerPl QN: 3.7 GM/dL (11/15/22 02:52:00) Troponin-I High Sensitivity: 475 ng/L High (11/15/22 04:38:00) BNP Pl QN: 51 pg/mL (11/15/22 02:52:00) Lactate Venous Pl QN: 8.4 mmol/L High (11/15/22 02:52:00) Gluc-Strip, POC: 121 mg/dL High (11/15/22 06:53:00) pH Bld Arterial QN: 7.44 (11/15/22 04:36:00) PCO2 Bld Arterial QN: 37 mmHg (11/15/22 04:36:00) PO2 Bld Arterial QN: 100 mmHg (11/15/22 04:36:00) Base Excess Bld Arterial: 1 mmol/L (11/15/22 04:36:00) Bicarb Bld Arterial Calc: 25 mmol/L (11/15/22 04:36:00) O2 Sat Bld Arterial Calc: 98 % (11/15/22 04:36:00) FIO2: 50% vent (11/15/22 04:36:00) Patient Temperature: 37 DegC (11/15/22 04:36:00) Coagulation: PT: 10.8 seconds (11/15/22 02:52:00) INR: 0.95 (11/15/22 02:52:00) Urine Studies: Color: Yellow (11/15/22 04:38:00) Clarity: Clear (11/15/22 04:38:00) Specific Gravity: 1.015 (11/15/22 04:38:00) pH: 6.0 (11/15/22 04:38:00) Protein: 30 Abnormal (11/15/22 04:38:00) Glucose: 500 Abnormal (11/15/22 04:38:00) Ketones: NEGATIVE (11/15/22 04:38:00) Bilirubin: NEGATIVE (11/15/22 04:38:00) Hgb Ur: TRACE. Abnormal (11/15/22 04:38:00) Nitrite: NEGATIVE (11/15/22 04:38:00) Urobilinogen: NormalUro (11/15/22 04:38:00) Leukocyte Esterase Ur: TRACE. Abnormal (11/15/22 04:38:00) WBC: 21-50 Abnormal (11/15/22 04:38:00) RBC: 3-5 Abnormal (11/15/22 04:38:00) Bacteria: Many Abnormal (11/15/22 04:38:00) Squamous Epithelial: Few (11/15/22 04:38:00) Granular Casts: 0-2 Abnormal (11/15/22 04:38:00) All Other Labs: COVID 19 Specimen Source: Nasopharyngeal (11/15/22 04:24:00) Coronavirus SARS-CoV2 Rapid: Not Detected (11/15/22 04:24:00) Diagnostics Radiology Results - Last 24 hours Across Visits 11/15/2022 03:20 - XR Chest PA or AP Portable IMPRESSION:1. Endotracheal tube as described above.2. Low lung volumes. No focal pulmonary consolidation, pleuraleffusion or pneumothorax. Thank you for consulting our team of subspecialty radiologists. 11/15/2022 04:02 - CT Head W/o IV Contrast IMPRESSION: 1. No acute intracranial hemorrhage or obvious infarct.2. No skull fracture or pneumocephalus.3. Mastoid air cells are clear.Thank you for consulting our team of subspecialty radiologists. 11/15/2022 04:06 - CTA Chest Pulm Embolism W/IV Contrast IMPRESSION:1. Negative for pulmonary embolism.2. No focal pulmonary consolidation, pleural effusion orpneumothorax.Thank you for consulting our team of subspecialty radiologists. 11/15/2022 04:53 - XR Chest PA or AP Portable IMPRESSION:1. Lines and tubes as Described Above.2. Otherwise, No Significant Interval Change When Compared to priorstudy.Thank you for consulting our team of subspecialty radiologists. Signature Line Electronically Signed on 11/15/22 07:43 ________________________________________________________
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 18.11.2022
- Impfdatum
- 23.12.2021
- Beginn
- 23.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abscess limb
Blood albumin decreased
Blood creatine phosphokinase decreased
Blood creatinine increased
Blood gases
Blood lactic acid
Blood potassium decreased
Blood potassium increased
Blood sodium increased
Blood urea increased
Carbon dioxide decreased
Computerised tomogram abnormal
Death
Eating disorder
Erythema
Condition aggravated
Renal cell carcinoma
Glycosylated haemoglobin normal
Symptomtext
Antibiotics were continued per recommendations 10/27 1 PRBC transfused, pt declined COVID vaccine 10/28 increased swelling and erythema proximal LLE and suprapubic area, no fever, vanc added for possible superimposed cellulitis 10/31 f/u appt, not a candidate for further cancer treatment, hospice recommended 11/3 1 PRBC Overall patient continued to worsen with respect to mental status. His CT last week was most c/w progressive CNS metastatic disease. He was not eating much at all and became unable to take PO medications now. He was clear with NP last week that he did not want a feeding tube. Hospice care was offered but his wife was not ready yet. He died peacefully 11/14/22, his 41st wedding anniversary. I spoke with the wife this afternoon. She expressed gratitude for the care he received throughout this illness. Cause of death: Renal cell carcinoma Other contributing factors: Left hip, gluteal, and thigh abscesses and osteomyelitis Severe protein calorie malnutrition
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- Antibiotics were continued per recommendations 10/27 1 PRBC transfused, pt declined COVID vaccine 10/28 increased swelling and erythema proximal LLE and suprapubic area, no fever, vanc added for possible superimposed cellulitis 10/31 f/u appt, not a candidate for further cancer treatment, hospice recommended 11/3 1 PRBC Labs: 11/14 Na 148, K 3.2, CO2 17, BUN 37, Cr 1.1, WBC 15, Hgb 6.7, PLT 384 11/12 Na 151, K 3.8, CO2 15, BUN 39, Cr 1.2 11/9 Na 152, BUN 35, Cr 0.9, WBC 15.5, Hgb 7, PLT 423 11/7 Na 147, Hgb 7.4 11/4 Na 142, K 4.2, CO2 18, BUN 32, Cr 0.9, Hgb 7.2 11/3 Na 143, K 4.7, CO2 16, BUN 29, Cr 0.9, WBC 12.5, Hgb 6.6, PLT 508 11/1 vanc 10.6 10/31 Na 137, K 4.5, CO2 17, BUN 19, Cr 0.8, WBC 13, Hgb 7.1, PLT 486 10/30 Na 140, K 4.4, CO2 19, BUN 20, Cr 0.8 10/28 Na 136, K 4.9, CO2 19, BUN 18, Cr 0.9, Hgb 8 10/27 Na 138, K 5.1, CO2 21, BUN 18, Cr 0.9, WBC 9, Hgb 6.7 then 8.3, PLT 537 10/26 Na 138, K 5.5, CO2 14, BUN 17, Cr 0.8, Hgb 7.3, ABG 7.44/30/81. LA 1, CPK 47 10/25 Na 139, K 5.5, CO2 17, BUN 21, Cr 0.9, Hgb 7 10/24 Na 137, K 5.2, CO2 21, BUN 22, Cr 1, WBC 4.2, Hgb 13.2 (suspect spurious), PLT 331 10/21 Na 142, K 5.1, CO2 22, BUN 21, Cr 0.9, alb 2.4, LFTs OK, WBC 11, Hgb 8.5, PLT 619, A1c 5.1
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HTN, hyperlipidemia, chronic afib,
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 85,0
- Geschlecht
- M
- Eingang
- 14.11.2022
- Impfdatum
- 06.01.2022
- Beginn
- 03.11.2022
- Tage bis Beginn
- 301,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Death
Symptomtext
Death on 11/03/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Alzheimer's disease; OSC: COVID-19
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 10.10.2022
- Impfdatum
- 16.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: ja
ER: unbekannt
Erholt: nein
Computerised tomogram head abnormal
Dizziness
Drain of cerebral subdural space
Haemorrhagic stroke
Headache
Hypoaesthesia
Immediate post-injection reaction
Loss of personal independence in daily activities
Magnetic resonance imaging
Malaise
Medical induction of coma
Mobility decreased
Wheelchair user
Symptomtext
As soon as I received the Pfizer booster I was immediately sick. I was suffering severe headaches, dizziness etc. I followed up 5 days later with my ENT and expressed what I was feeling. He assured me that it had nothing to do with my sinuses, etc. The headaches did not go away and 7 weeks later I suffered a hemorrhagic stroke. On February 27, 2022 my left side went completely numb and I was rushed to the hospital and put into a CT scan where I heard the techs talking about my serious bleed. That was the last thing I remember until mid April. I was sedated and in an induced coma. A bolt was placed in my head and then a drain to try to relieve the pressure. I have been in extensive rehabilitation since April 1, 2022 but I have not regained any function of my left side and I am in a wheelchair. My wife and children take care of me on a daily basis. I have had several CT scans and MRI's as well as having been seen by many Neurologists and Neuosurgeons looking for answers. Before Feb 27, I was in great shape. I exercised, ate right and never once ever had High BP until the day I was given the Pfizer booster injection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Medical induction of coma
- Hospital-Tage
- 31,0
- Labordaten
- I have several scans
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Lipitor
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 21.09.2022
- Impfdatum
- 14.12.2021
- Beginn
- 04.09.2022
- Tage bis Beginn
- 264,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Asthenia
COVID-19
Chest X-ray
Confusional state
Constipation
Diarrhoea
Fall
Hepatic encephalopathy
SARS-CoV-2 test positive
Treatment noncompliance
Urinary tract infection
Viral infection
Symptomtext
The patient is a 68 y.o. female patient with history of nonalcoholic liver cirrhosis, history of gastric bypass 1998, peptic ulcer disease presented with confusion COVID-positive Acute hypoxemic respiratory failure Covid-19 Virus Infection Date of onset of symptoms: 9/2/2022 Symptoms present on admission: Yes Date of covid positive test: 9/4/2022 Vaccination status: vaccinated Imaging: Chest x-ray Oxygen requirements on admission: Yes Current oxygen requirements: She was weaned off to room air before discharge Medical therapy: steroids and remdesivir Consultants following: ID Anticipated special isolation end date: 9/13/2022 Acute encephalopathy, likely hepatic in the setting of lactulose noncompliance and viral infection, resolved Nonalcoholic liver cirrhosis Ongoing diarrhea Lactulose 30 mg 3 times daily, she did not have a bowel movement yesterday, up titrate to 3 bowel movements a day Supportive care Pain management History of gastric bypass History of peptic ulcer disease Protonix IV Urinary tract infection, ceftriaxone Weakness and frequent falls She was provided with home health
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 13.09.2022
- Impfdatum
- 13.01.2022
- Beginn
- 21.08.2022
- Tage bis Beginn
- 220,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Acute respiratory failure
Asthenia
Benign prostatic hyperplasia
COVID-19
Chest X-ray abnormal
Computerised tomogram thorax abnormal
Cough
Echocardiogram normal
Ejection fraction normal
Insomnia
Ischaemic cardiomyopathy
Liver function test normal
Physical deconditioning
Pulmonary mass
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
A 76 y.o. male admitted to the hospital on 8/21/2022 for weakness after testing positive for COVID. History of anoxic brain injury from cardiac arrest in 1998 and limited mobility at home. D/C 8/25/2022. Discharge Diagnosis and Associated Hospital Course. Acute hypoxemic respiratory failure -Secondary to COVID. Some chronic lung changes on CT, history of pulmonary sarcoid years ago that has been stable. Also component of general debility and deconditioning. -Initially hypoxic to 86-87% on RA, currently on 3L NC to maintain O2 sat > 90% but no increased work of breathing. -Treatment of COVID as below. Incentive spirometer. Wean O2 for goal spO2 88-92%. COVID-19 infection- Presented with: cough, weakness, rhinorrhea- Symptom onset: 8/20- Positive COVID-19: 8/20 on home test and 8/21 - Vaccination status: Vaccinated with Pfizer and boosted x 2 with Pfizer. - CXR on admission showed possible edema and/or bronchitis, but may also be chronic changes (post inflammatory scar and bronchitis noted on prior CT scans)- Oxygen status: 3L- Decadron: Yes. Expected end date 8/29/22- Remdesivir: started 8/21, completed 5 days of treatment. LFT's stable. - DVT prophylaxis:Currently on full anticoagulation- Serial COVID labs ordered: Yes- Case Management/Social Services consulted: Yes; History of PE -Bilateral PE in July 2021 -Continue Eliquis 5 BID -wife reports Dr. recommended he stay on eliquis indefinitely; CAD -With cardiac arrest in 1998. PCI to LAD in Apr 1998. -Continue ASA, statin, BB. Ischemic cardiomyopathy -Prior EF 40-45% but most recent echo 6/30/22 with EF 55% -Continue BB. BPH -Continue bethanechol, finasteride, Flomax. Insomnia -Continue home Remeron and nightly Klonopin. Pulmonary nodules -Follows with Dr. -Repeat CT chest in May 2022 stable if not improved so pulm recommended repeat CT chest in one year (May 2023).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 4,0
- Labordaten
- As above
- Aktuelle Erkrankungen
- History of anoxic brain injury s/p cardiac arrest 1988.
- Vorgeschichte
- CAD; CHF; Hyperlipidemia; HTN; Hypothyroidism; History of PE; Sarcoidosis
- Andere Medikamente
- Apixaban; Aspirin; Atorvastatin; Bethanechol;Carvedilol;Vitamin D3; Clonazepam; Famotidine; Finasteride; Levothyroxine; Mirtazapine; Polyethylene glycol; Tamsulosin.
- Allergien
- Phenytoin; Quinidine
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 08.09.2022
- Impfdatum
- 19.03.2021
- Beginn
- 17.08.2022
- Tage bis Beginn
- 516,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Acidosis
Acute kidney injury
Acute myocardial infarction
Alanine aminotransferase increased
Alcohol test
Anaemia
Analgesic drug level
Angiopathy
Aspartate aminotransferase increased
Blood bilirubin increased
Blood creatine phosphokinase increased
Blood creatinine increased
Blood potassium increased
Blood urea increased
COVID-19
Condition aggravated
Creatinine renal clearance
Diarrhoea
Symptomtext
50M presented 8/17/22 with hx sarcoidosis, NICM/HFrEF s/p ICD, AF, CKD5, current smoking came to the EC 8/17 with fever and intractable nausea/NBNB vomiting/watery NB diarrhea. He tested COVID positive 2 days prior and is vaccinated against COVID x3 with this being his first COVID infection. He denied respiratory complaints. In the EC he was AFVSNL and examination noted scleral icterus. Labs revealed only mildly elevated PT/INR but AST 6520, ALT 2444, T bili 1.7, BUN/Cr 91/6.2, and hyperkalemia 5.8. MICU and GI were consulted and further imaging and labs were ordered with consideration for transaminitis secondary to shock, viral hepatitis, congestion, drug-induced etiologies. Ultimately he was admitted to Facility acute COVID infection c/b significant transaminitis in the thousands, rhabdomyolysis, AKI on CKD5, and hyperkalemia 5.8. His acetaminophen and EtOH levels were undetectable and he was not hypotensive though tachycardic on presentation. He had normal hepatic morphology on MRI abdomen 2022. GI's current leading diagnosis is acute viral hepatitis with transaminitis compounded by rhabdomyolysis versus shock liver versus AI liver disease versus vascular pathology. GI recommended BCx, viral serologies, ANA/ASMA/AMA/LKM/ceruloplasmin, empiric IV NAC, hydration for rhabdo, doppler US to r/o vascular pathology, echo, tending LFT's/PT/INR/daily MELD labs, neurochecks. His acetaminophen and EtOH levels were undetectable and he was not hypotensive though tachycardic on presentation. He had normal hepatic morphology on MRI abdomen 2022. GI's current leading diagnosis is acute viral hepatitis with transaminitis compounded by rhabdomyolysis versus shock liver versus AI liver disease versus vascular pathology. GI recommended BCx, viral serologies, ANA/ASMA/AMA/LKM/ceruloplasmin, empiric IV NAC, hydration for rhabdo, doppler US to r/o vascular pathology, echo, tending LFT's/PT/INR/daily MELD labs, neurochecks. Nephrology consulted for AKI on CKD5 and rhabdomyolysis c/b hyperkalemia, hyperphosphatemia, hypocalcemia. Cardiology consulted for NSTEMI with troponin 0.51 and ST-T abnormalities. He had elevated d-dimer 9753 with thrombocytopenia 121. His home bumex and metoprolol were held while hydralazine continued and coreg initiated given his HFrEF. He was noted to have chronic anemia around Hb 9-11 for which outpatient iron studies should be considered. ID was consulted given his COVID infection: Paxlovid precluded by CrCl <30, remdesivir not recd 2/2 transaminitis, no currently available mAb, ideally vax prevent declining resp disease in this setting; liver damage could be COVID, consider hypovolemia/hypotension; consider babesiosis, ehrlichiosis, anaplasmosis, RMSF; check parasite smears and RMSF serology, started doxy 100 mg IV q12 8/18.His CK was ~4500 and declined on repeat. For electrolyte abnormalities in context of his CKD5 he was continued on Renvela 800 mg TID. He was discharged in stable condition with renal function at baseline, acidosis significantly improved, liver function tests down-trending, and appetite adequate without further nausea/vomiting/diarrhea.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- 4,0
- Labordaten
- 8/17 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC --detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 19.08.2022
- Impfdatum
- 24.12.2021
- Beginn
- 09.08.2022
- Tage bis Beginn
- 228,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
COVID-19 pneumonia
Hypotension
Metabolic encephalopathy
Symptomtext
Patient admitted for COVID-19 pneumonia, hypotension, metabolic encephalopathy, acute hypoxemic respiratory failure. Treated with decadron and remdesivir and inhalers. Once stable pt d/c home
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- hypertension, hyperlipidemia, coronary artery disease status post 5 stents, status post CABG x5, 3 years ago, depressi
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 02.08.2022
- Impfdatum
- 14.12.2021
- Beginn
- 25.07.2022
- Tage bis Beginn
- 223,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Bacterial infection
Blood culture negative
Blood lactic acid normal
COVID-19
Catheter removal
Catheter site infection
Chest X-ray normal
Condition aggravated
Culture positive
Dialysis
Hypotension
Intensive care
Klebsiella test positive
Pyrexia
SARS-CoV-2 test positive
Sepsis
Septic shock
Ultrasound Doppler normal
Symptomtext
Admission Date: 7/25/2022 Discharge Date: 8/1/2022 PRESENTING PROBLEM: Septic shock Sepsis HOSPITAL COURSE: DATE OF ADMISSION: 07/25/2022 BRIEF HISTORY OF PRESENTING ILLNESS: 75-year-old male with a past medical history significant for end-stage renal disease on Monday Wednesday Friday dialysis as well as history of diabetes and coronary artery disease with known aortic stenosis who presented due to hypotension fever noted after dialysis. In the emergency department the patient was hypotensive despite fluid. He was found have a normal white blood cell count and lactic acid level. Chest x-ray showed no acute infiltrate. COVID-19 testing was found to be positive although he has tested positive for COVID-19 in the past. He was empirically started on piperacillin/tazobactam and was started on vasopressors as well and moved to the intensive care unit. Patient had quick resolution in regards to his hypotension and was able to wean off of vasopressors and move out of the intensive care unit. Etiology behind his infection was uncertain but it was suspected that it was related to his dialysis catheter. IR was consulted to remove his tunneled dialysis catheter and although the patient had been on Zosyn and vancomycin, after blood cultures show no growth and with the thought that MRSA would have grown or at least been isolated by now, vancomycin was discontinued on 07/28/2022 and dialysis catheter was removed on the same day. Patient's dialysis catheter tip was cultured and this came back growing Gram-negative rods. He was continued on Zosyn and ID was consulted. Id recommended repeating blood culture morning 07/30/2022 and also recommended 7 days of antibiotic therapy based on sensitivities with route to be determined. His cultures came Klebsiella arginine ease. This was pansensitive. Infectious Disease is okay with giving an oral antibiotic today and tomorrow and then following up with blood cultures on 08/08, which they will order. Patient is feeling very well. He has no fevers or chills. Ultrasound was done of his right upper extremity rule out septic thrombus which was negative. Patient was getting ready to get discharged today on oral antibiotics however it would appear that his dialysis bed tomorrow at 06:00 at Fresenius has been given up and he is scheduled for a.m. here. If this cannot be arranged to have him have dialysis as an outpatient tomorrow unfortunately he will have to stay overnight, get dialysis and then discharged immediately after that. He can go back on his torsemide, hydralazine and home dose of insulin.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Septic shock
- Hospital-Tage
- 8,0
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Generalized anxiety disorder Obesity, morbid (HCC) OSA (obstructive sleep apnea) Diverticular disease Hypertension Pulmonary nodule BPH (benign prostatic hypertrophy) ASHD (arteriosclerotic heart disease) Type 2 diabetes mellitus, with long-term current use of insulin (HCC) Mixed hyperlipidemia Gross hematuria Adrenal adenoma Benign lipomatous tumor Ganglion of left wrist Hyperglycemia due to type 2 diabetes mellitus (HCC) Nephrotic syndrome Polycystic kidney disease Status post total shoulder arthroplasty Anemia due to chronic kidney disease, on chronic dialysis (HCC) Iron deficiency anemia VT (ventricular tachycardia) (HCC) Long term current use of insulin (HCC) ICD (implantable cardioverter-defibrillator) in place COVID-19 Chronic diastolic heart failure (HCC) Aortic stenosis Hypertensive heart and chronic kidney disease stage 5 (HCC) Renal osteodystrophy Stage 5 chronic kidney disease (HCC) Diabetic renal disease (HCC) Statin intolerance Coagulation defect, unspecified (HCC) Disorder of phosphorus metabolism, unspecified End stage renal disease (HCC) Secondary hyperparathyroidism of renal origin (HCC) Septic shock (resolved) due to suspected central line infection Coronary artery disease involving native coronary artery
- Andere Medikamente
- acetaminophen (TYLENOL) 325 MG tablet allopurinol (ZYLOPRIM) 100 MG tablet aspirin 81 MG tablet calcitriol (ROCALTROL) 0.25 MCG capsule carvedilol (COREG) 12.5 MG tablet carvedilol (COREG) 25 MG tablet ciprofloxacin (CIPRO) 500 MG tab
- Allergien
- Crestor [Rosuvastatin Calcium]Myalgia Hmg-coa-r InhibitorsMyalgia Lipitor [Atorvastatin Calcium]Myalgia No Known Iodine AllergyOther No Known Latex AllergyOther Vytorin [Ezetimibe-simvastatin]Myalgia
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 84,0
- Geschlecht
- M
- Eingang
- 27.07.2022
- Impfdatum
- 16.12.2021
- Beginn
- 16.07.2022
- Tage bis Beginn
- 212,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Death
SARS-CoV-2 test positive
Symptomtext
Death on 07/16/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- Tested positive for Covid-19 07/14/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- OSC; Hx of CVA; CKD Stage 3; DM2; HTN; HLD; CAD
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 84,0
- Geschlecht
- M
- Eingang
- 06.07.2022
- Impfdatum
- 18.12.2021
- Beginn
- 29.06.2022
- Tage bis Beginn
- 193,0
- Dosis
- 3
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Acute respiratory failure
Atrial fibrillation
COVID-19
COVID-19 pneumonia
Fall
Rib fracture
SARS-CoV-2 test positive
Thoracic vertebral fracture
Symptomtext
Provider summary "84 YO male with history of hypertension, Alzheimer's, BPH, recent diagnosis of atrial fibrillation presented to the hospital after fall from stairs Brief Summary of Hospital Stay: (Include Significant Findings and Invasive Procedures) found to have COVID pneumonia, acute respiratory failure overnight, has acute T2 fracture and nondisplaced left rib 5th and 7th fractures, had AFib with RVR"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 5,0
- Labordaten
- Positive COVID PCR 6/29/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Closed wedge compression fracture of T2 vertebra 6/29/2022 HYPERTENSION, BENIGN ESSENTIAL (401.1) Unknown INJURY NOS, CHEST WALL (959.11) Unknown Sensorineural hearing loss, asymmetrical (Chronic) 10/19/2012 Closed fracture of multiple ribs of left side 6/29/2022 Alzheimer's dementia 6/30/2022 COVID-19 6/29/2022
- Andere Medikamente
- amoxicillin/potassium clav 875-125 mg 875 mg Oral 2 times daily benzonatate 100 mg Oral 3 TIMES DAILY PRN calcium carbonate 1,000 mg Oral EVERY 8 HOURS PRN dexamethasone 4 mg Oral DAILY WITH BREAKFAST diltiazem HCl 60 mg Oral 2 times da
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 95,0
- Geschlecht
- F
- Eingang
- 20.06.2022
- Impfdatum
- 30.12.2021
- Beginn
- 09.06.2022
- Tage bis Beginn
- 161,0
- Dosis
- 3
- Route/Site
- - / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute respiratory failure
Angiogram pulmonary abnormal
Anticoagulant therapy
Apnoea
Atrial fibrillation
Back pain
Bradypnoea
Brain natriuretic peptide increased
Breath sounds abnormal
COVID-19
Cardiac failure congestive
Chest X-ray abnormal
Chest pain
Condition aggravated
Confusional state
Death
Dyspnoea
Fibrin D dimer increased
Symptomtext
Admission Date: 6/9/2022 PRESENTING PROBLEM: Atrial fibrillation with RVR [I48.91] Acute on chronic respiratory failure with hypoxia [J96.21] Acute on chronic congestive heart failure, unspecified heart failure type [I50.9] COVID-19 virus infection [U07.1] HOSPITAL COURSE: The patient is a 96 yo female with PMH which includes HTN, HLD, DM II, hypothyroidism, osteoporosis, arthritis and chronic back pain, b/l cataracts, recent bouts of community-acquired pneumonia and recently diagnosed (5/4/22) Atrial fibrillation with RVR, started on diltiazem and Eliquis the day prior to presentation. She came in with a chief complaint of worsening back pain and shortness of breath/respiratory distress. Patient was found to have severe sepsis and acute on chronic hypoxic hypercapneic respiratory failure likely secondary to acute COVID 19 infection, A fib with RVR, and concern for acute heart failure (no prior history, but elevated BNP). Patient tachycardic, tachypneic (initially, now some intermittent apnea/bradypnea), worsening confusion/AMS with periods of lethargy/minimal responsiveness, consistent with severe sepsis at the time of admission. Mental status improved, although still some mild intermitt confusion. Continued to require increased respiratory support with HFNC/Non-breather at times with CXR showing worsening effusions and colidations.Patient had some intermittent improvement with IV steroids and lasix. However, CTA thorax was obtained on 6/11 due to concern PE with worsening chest pain, tachycardia, and elevated D-dimer (b/l doppler US negative). CTA showed no evidence of PE, but worsening bilateral pleural effusions, including her chronic complex R pleural effusion with thickening and concern for possible exudative process. Bilateral lower lobe consolidations were significantly worse as well, especially on the left. On 6/12/22, patient asked to stop aggressive cares and transition to hospice. Team spoke with patient's activated DPOA (son) and he was in agreement with patient's desire to become comfort care/hospice. Palliative care was consulted, active treatment was discontinued and comfort meds initiated. Paged by nursing that patient had passed on evening of 6/14. On my evaluation, patient not responsive to verbal stimuli or sternal rub. Pupils fixed and nonreactive. No heart or lung sounds heard after a full minute of auscultation. Peripheral pulses not present. Death pronounced at 7:25pm. Personally notified patient's son and DPOA, of death. All questions answered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 5,0
- Labordaten
- -
- Aktuelle Erkrankungen
- 12/3/2021- ED Visit for Fatigue/Dizziness
- Vorgeschichte
- Double vision Hypertensive emergency Small vessel disease, cerebrovascular Clear cell adenocarcinoma of uterus Osteoporosis Back pain, unspecified back pain laterality, unspecified chronicity, unspecified location Acute on chronic respiratory failure with hypoxia Acute congestive heart failure Pneumonia due to COVID-19 virus Atrial fibrillation with RVR End of life care
- Andere Medikamente
- acetaminophen (TYLENOL) 325 MG tablet albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler apixaban (ELIQUIS) 2.5 MG tablet aspirin 81 MG chewable tablet atorvastatin (LIPITOR) 40 MG tablet Calcium Carb
- Allergien
- Fentanyl Other PenicillinsRash
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 87,0
- Geschlecht
- F
- Eingang
- 27.05.2022
- Impfdatum
- 21.12.2021
- Beginn
- 21.05.2022
- Tage bis Beginn
- 151,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Aspiration
COVID-19
COVID-19 pneumonia
Pneumonia bacterial
SARS-CoV-2 test positive
Sepsis
Symptomtext
Patient received Pfizer COVID vaccine on 1/29/21 (lot # EL3302), 2/19/21 (lot # EI3302), and 12/21/21 (lot # FD7218). Patient tested positive for COVID on 5/21/22 and was admitted to our inpatient facility on 5/22/22 with severe sepsis due to COVID-19 pneumonia +/- secondary bacterial pneumonia/aspiration and acute respiratory failure due to COVID-19 and likely secondary bacterial pneumonia/aspiration. Patient was admitted in our med/surg unit and discharged back to her AFH on 5/26/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 4,0
- Labordaten
- COVID status positive 5/21/22.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- AFH resident with a history of CVA and currently bedbound with total care and nonverbal, permanent A. fib, coronary artery disease, chronic systolic heart failure, asthma, and schizophrenia
- Andere Medikamente
- acetaminophen, cetrizine, vitamin d3, docusate, furosemide, gabapentin, guaifenesin PRN, haloperidol, Xopenex inh, lisinopril, melatonin, metoprolol, polyethylene gycol, potassium chloride, rivaroxaban, sennosides
- Allergien
- morphine, penicillins
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 11.05.2022
- Impfdatum
- 26.12.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 5,0
- Dosis
- UNK
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anticoagulant therapy
Blood test
Chest X-ray
Computerised tomogram
Dyspnoea
Dyspnoea exertional
Feeling abnormal
Gait disturbance
Oxygen saturation decreased
Pulmonary embolism
SARS-CoV-2 test negative
Symptomtext
"heavy load pulmonary emboli all lobes" On Saturday 1/31/2021 I felt poorly while exercising so I stooped on Thursday 1/6/2022 in the evening I felt very poorly and out of breath. My wife took me to Hospital. They tested me for COVID and it was negative and they discharged me despite low oxygen (95 -I was very fit). On Saturday morning 1/8/2022 I could barely walk without becoming extremely out of breath so my wife took me back to the hospital. At triage my oxygen level was 88. They did tests and told me that I had pulmonary emboli. I was hospitalized and am now on Eliquis.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary embolism
- Hospital-Tage
- 2,0
- Labordaten
- Need records - CT scan and chest xray blood work
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Forgot which ones; would need to check
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 26.04.2022
- Impfdatum
- 09.12.2021
- Beginn
- 14.01.2022
- Tage bis Beginn
- 36,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Laboratory test abnormal
Myocardial infarction
Symptomtext
Heart attack; I am in recovery.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocardial infarction
- Hospital-Tage
- 2,0
- Labordaten
- Labs to confirm heart attack.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 09.04.2022
- Impfdatum
- 03.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Angina pectoris
Chest pain
Electrocardiogram
Feeling abnormal
Inappropriate schedule of product administration
Blood test
Echocardiogram
Lung disorder
Limb discomfort
Myocardial infarction
Pain
Sensory disturbance
Symptomtext
high lung pressure; heart attack; chest pain; feeling weird little sensations in my arms & legs; This is a spontaneous report received from contactable Consumers (including patient). A 32 year-old female patient received BNT162b2 (PFIZER-BIONTECH COVID-19 VACCINE), intramuscular, administered in deltoid right, administration date 03Jan2022 (Lot number: FD7218) at the age of 32 years as dose 2, single for COVID-19 immunisation. Relevant medical history included: ongoing immune system disorder (reported as "Immunity"); ongoing loss of energy (reported as "Energy"); "depression" (ongoing). Concomitant medications included: VITAMIN D [VITAMIN D NOS] taken for immune system disorder (ongoing); ASHWAGANDHA taken for asthenia (ongoing); FISH OIL taken for depression (ongoing); VITAMIN B12 [CYANOCOBALAMIN] taken for asthenia (ongoing). Vaccination history included: BNT162b2 (Dose 1, Anatomical site of injection: rt deltoid, Route of administration: Intramuscular, Batch/lot number: 30155BA), administration date: 12Nov2021, for COVID-19 Immunization, reaction(s): "She has inflammation around her heart and has been seeing a doctor for about a month now". The patient stated she started feeling weird little sensations in her arms & legs (in Jan2022) and then a few days later chest pain (on 13Jan2022), especially after exercise, clarifying this had continued for about 2 months to varying degrees and had lessened over time but was still present. The patient considered the event chest pain was life-threatening and required physician office visit. The patient underwent the following laboratory tests and procedures: blood test: (25Jan2022) normal; echocardiogram: (09Feb2022) almost normal, notes: showed high lung pressure; electrocardiogram: (25Jan2022) abnormal, notes: showed heart attack; (27Jan2022) abnormal, notes: showed heart attack. Therapeutic measures were taken as a result of the events which included anti inflammatory & heart meds. The outcome of the events was not recovered. Follow-Up (08Apr2022): Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocardial infarction
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220125; Test Name: Blood test; Result Unstructured Data: Test Result:Normal; Test Date: 20220209; Test Name: Echocardiogram; Result Unstructured Data: Test Result:Almost normal; Comments: showed high lung pressure; Test Date: 20220125; Test Name: EKG; Result Unstructured Data: Test Result:Abnormal; Comments: showed heart attack; Test Date: 20220127; Test Name: EKG; Result Unstructured Data: Test Result:Abnormal; Comments: showed heart attack
- Aktuelle Erkrankungen
- Depression; Immune system disorder; Loss of energy
- Vorgeschichte
- -
- Andere Medikamente
- VITAMIN D [VITAMIN D NOS]; ASHWAGANDHA; FISH OIL; VITAMIN B12 [CYANOCOBALAMIN]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 09.04.2022
- Impfdatum
- 03.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Angina pectoris
Chest pain
Electrocardiogram
Feeling abnormal
Inappropriate schedule of product administration
Blood test
Echocardiogram
Lung disorder
Limb discomfort
Myocardial infarction
Pain
Sensory disturbance
Symptomtext
high lung pressure; heart attack; chest pain; feeling weird little sensations in my arms & legs; This is a spontaneous report received from contactable Consumers (including patient). A 32 year-old female patient received BNT162b2 (PFIZER-BIONTECH COVID-19 VACCINE), intramuscular, administered in deltoid right, administration date 03Jan2022 (Lot number: FD7218) at the age of 32 years as dose 2, single for COVID-19 immunisation. Relevant medical history included: ongoing immune system disorder (reported as "Immunity"); ongoing loss of energy (reported as "Energy"); "depression" (ongoing). Concomitant medications included: VITAMIN D [VITAMIN D NOS] taken for immune system disorder (ongoing); ASHWAGANDHA taken for asthenia (ongoing); FISH OIL taken for depression (ongoing); VITAMIN B12 [CYANOCOBALAMIN] taken for asthenia (ongoing). Vaccination history included: BNT162b2 (Dose 1, Anatomical site of injection: rt deltoid, Route of administration: Intramuscular, Batch/lot number: 30155BA), administration date: 12Nov2021, for COVID-19 Immunization, reaction(s): "She has inflammation around her heart and has been seeing a doctor for about a month now". The patient stated she started feeling weird little sensations in her arms & legs (in Jan2022) and then a few days later chest pain (on 13Jan2022), especially after exercise, clarifying this had continued for about 2 months to varying degrees and had lessened over time but was still present. The patient considered the event chest pain was life-threatening and required physician office visit. The patient underwent the following laboratory tests and procedures: blood test: (25Jan2022) normal; echocardiogram: (09Feb2022) almost normal, notes: showed high lung pressure; electrocardiogram: (25Jan2022) abnormal, notes: showed heart attack; (27Jan2022) abnormal, notes: showed heart attack. Therapeutic measures were taken as a result of the events which included anti inflammatory & heart meds. The outcome of the events was not recovered. Follow-Up (08Apr2022): Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocardial infarction
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220125; Test Name: Blood test; Result Unstructured Data: Test Result:Normal; Test Date: 20220209; Test Name: Echocardiogram; Result Unstructured Data: Test Result:Almost normal; Comments: showed high lung pressure; Test Date: 20220125; Test Name: EKG; Result Unstructured Data: Test Result:Abnormal; Comments: showed heart attack; Test Date: 20220127; Test Name: EKG; Result Unstructured Data: Test Result:Abnormal; Comments: showed heart attack
- Aktuelle Erkrankungen
- Depression; Immune system disorder; Loss of energy
- Vorgeschichte
- -
- Andere Medikamente
- VITAMIN D [VITAMIN D NOS]; ASHWAGANDHA; FISH OIL; VITAMIN B12 [CYANOCOBALAMIN]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 25.03.2022
- Impfdatum
- 21.12.2021
- Beginn
- 02.02.2022
- Tage bis Beginn
- 43,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Chest discomfort
Coronary arterial stent insertion
Dizziness
Dyspnoea
Electrocardiogram abnormal
Laboratory test
Musculoskeletal discomfort
Myocardial infarction
Nausea
Symptomtext
I felt a great deal of pressure on my chest and discomfort underneath both shoulders with slight shortness of breath. I was lightheaded and became nauseous. I went to the urgent care locally where I had an EKG performed and was transported by ambulance to a HCF. I experienced a heart attack where I had 2 stents placed in my heart. I was in recovery where I remained overnight and was released after 2 days. I am now on several medications to address the issues. I returned home and have a new cardiologist. After the initial visit and confirmation of the heart attack, I have to follow up with the provider in June. I did contract covid 1 week after my booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocardial infarction
- Hospital-Tage
- 2,0
- Labordaten
- EKG, several unknown heart related test.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Simvastatin; hydrochlorothiazide; alprazolam; daily vitamin; vitamin C; vitamin D
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 15.03.2022
- Impfdatum
- 29.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Autopsy
Chest discomfort
Chills
Death
Feeling abnormal
Blood immunoglobulin E normal
Blood pressure increased
Body temperature increased
Hypertension
Loss of consciousness
Pulse absent
Pyrexia
Resuscitation
Seizure like phenomena
Tryptase
Unresponsive to stimuli
Seizure
Tachycardia
Symptomtext
Awoke at approximately 1230 hours on 12/30/2021 with chills, elevated blood pressure, and temperature of 101F. Took Tylenol and nitroglycerin. Had seizure-like activity then went unresponsive. CPR attempted to no avail. Death pronounced at 0424 hours on 12/30/2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- Immunoglobulin E (IgE) 48.2 IU/mL. (reference range: <114.0 IU/mL) Tryptase 7 ug/L (reference range: <11 ug/L
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hypertension, coronary artery disease, hyperlipidemia, polymyalgia rheumatica, BPH, h/o statin induced rhabdomyolysis
- Andere Medikamente
- prednisone, Lopressor, nitroglycerin, fluticasone
- Allergien
- Lipitor, Crestor, niacin, tamsulosin
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 13.03.2022
- Impfdatum
- 15.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anticoagulant therapy
Arrhythmia
Asthenia
Blood potassium increased
Bronchitis
COVID-19
Central venous catheterisation
Chest X-ray normal
Death
Decreased appetite
Dyspnoea
Dysstasia
Endotracheal intubation
Fatigue
Gastrointestinal tube insertion
Haematology test normal
Immunisation reaction
Infection
Symptomtext
12/17/21: malaise 12/18-12/25/21: progressing gray pallor, malaise, loss of appetite 12/26/21: mild shortness of breath, worsening color. Previous symptoms continued. 12/29/21: exam by PCP. Listened to patients lungs. Dx "bronchitis". No testing. No imaging. Rx Augmentin 875/125 2x/d. Benzonatate 200mg 3x/d. No improvement. 1/2/22. About 7pm, patient too weak to stand, SOB. EMS called. O2Sat 70%. Rx O2, IV and steroid. Admitted via ED Hospital. Dx: blood clots lungs/legs; double pneumonia (type not specified). Negative for COVID 19; no fever, no evidence of infection. Rx oxygen(non-invasive ventilation: NIV), antibiotics, blood thinners and steroids. Response: O2Sat up to 94% on high flow oxygen. 1/3/22: admitted from ED to TCU. Central IV started. 1/3/22: second negative COVID-19 test. Cardiac arrhythmia due to "fluid on his heart". No prior history. Rx diuretics and anti-arrhythmic. Changed to anticoagulant (abdominal injections). Response: arrhythmia resolved in 24 hrs. No improvement in blood clots. 1/4/22: Hematology consult-no origin of clots identified. Platelets reportedly normal. 1/5/22: third negative COVID-19 test. No fever, alert, oxygen NIV continues, O2 Sat mid-90's. 1/6/22: Hematology work-up negative for malignancy. Cardiologist off record "these are COVID clots". 1/7/22: DAY 6 of hospitalization. FIRST positive COVID-19 test. Family told only possible Rx was Remdesivir because patient was already hospitalized. Began Remdesivir and cont'd anticoagulants, antibiotics and steroids. 1/8/22: transferred from TCU to ICU, breathing worsened. Patient more fatigued, mentally clear, clots unchanged. O2 Sat in upper 80s on NIV at highest oxygen flow. 1/9/22: early afternoon: intubated, sedated, and placed on ventilator. High pressure of "12" required using "a gas" to expand his lungs. Able to follow simple commands. Cont'd anticoagulants, antibiotics and steroids. 1/10/22: "poor kidney function". CXR unchanged. Rx for elevated K+, no other change in medications. NG tube insertion attempt failed. 1/11/22: NG tube successfully inserted. Given liquid nutrition. Last day Remdesivir. Sedated, restrained, but follows commands. No other Rx changes. 1/12-1/15/22: Remains on ventilator, attempts to wean not successful. Unable to reduce oxygen requirements. CXRs unchanged. Cont'd anticoagulants, antibiotics and steroids. Rx plan: "try again to wean off ventilator in 3-5 days". 1/16/22: low grade fever. Rx: IV antibiotic changed. 1/17/22: port at neck identified as source of infection. Port line changed. Antibiotic continued; fever resolved. 1//18/22: clots persisting on maximum anticoagulants. CXR unchanged. Day 9 on ventilator. Medical team advised tracheotomy, PEG and acute care rehab. Family requested DNR. 1/21/22. Patient unresponsive. Spouse observation: "the life went out of him". 1/22/22: Pneumonia and blood clots not responding to anticoagulants and kidneys failing. Family chose Comfort Care. 1/24/22: Life support withdrawn and patient died minutes after.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- see #18
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Acid reflux, high blood pressure, high cholesterol (all controlled)
- Andere Medikamente
- Centrum Silver, Omeprazole, Simvastatin, Rampril
- Allergien
- No known
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 11.03.2022
- Impfdatum
- 22.12.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 9,0
- Dosis
- 3
- Route/Site
- UN / UN
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Acute pulmonary oedema
Acute respiratory failure
Death
Symptomtext
Patient was fully vaccinated Pfizer on 4/5/21, 4/26/21 and received booster on 12/22/21. Facility received death abstract. confirmed Patient was admitted on 12/28/21 to Hospital. Patient Died 12/31/21 at 00:20 due to Acute Hypoxic Respiratory failure and flash pulmonary edema. No further information provided to facility.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 2,0
- Labordaten
- unknown
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 28.02.2022
- Impfdatum
- 23.12.2021
- Beginn
- 28.02.2022
- Tage bis Beginn
- 67,0
- Dosis
- 3
- Route/Site
- - / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Death
Vaccine breakthrough infection
Symptomtext
COVID RELATED DEATH; BREAKTHROUGH CASE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 01.02.2022
- Impfdatum
- 06.01.2022
- Beginn
- 23.01.2022
- Tage bis Beginn
- 17,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Death
Symptomtext
Death related to COVID-19 infection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Other significant conditions: Alzheimer's dementia
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 20.01.2022
- Impfdatum
- 10.12.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 22,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Death
Mechanical ventilation
SARS-CoV-2 test positive
Symptomtext
case tested positive on 1/1/22 at hospital . ventilated on 1/4. died 1/15
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- 14,0
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- CLL (leukemia)
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 83,0
- Geschlecht
- F
- Eingang
- 07.01.2022
- Impfdatum
- 20.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 9,0
- Dosis
- 3
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Accessory spleen
Acute respiratory failure
Alanine aminotransferase increased
Angiogram pulmonary abnormal
Arteriosclerosis coronary artery
Aspartate aminotransferase increased
Blood culture negative
COVID-19
COVID-19 pneumonia
Chills
Cough
Culture urine positive
Diarrhoea
Dyspnoea
Dysuria
Escherichia test positive
Exposure to SARS-CoV-2
Fatigue
Symptomtext
Patient was seen in the ED 12/29/21 and discharged with COVID-19. Patient returned for care 1/1/22 and discharged for COVID 19. Patient was admitted on 1/4/22 for acute respiratory failure and still hospitalized. Pt. is a 83 y.o. female with a past medical history of mixed anxiety and depressive disorder, migraines, obstructive sleep apnea, mixed urge and stress incontinence, hypertension, GERD, CKD stage 3 who presented to the emergency department due to worsening of shortness of breath and cough. Patient started experiencing nasal congestion sore throat and cough along with shortness of breadth 1 week ago after she had an exposure from a family member. She also has been experiencing diarrhea along with urinary urgency frequency and dysuria that started few days ago. She was prescribed Ceftin for urinary tract infection but she was not able to pick up the prescription and eventually only took 1 dose of antibiotic prior to this presentation for her urinary tract infection. Patient continues to have rigors chills fatigue. In the emergency department patient was hemodynamically stable. Due to hypoxia was placed on 2 L of oxygen. AST and ALT were elevated at 80 and 41. Procalcitonin was high at 3.29. UA positive for urinary tract infection. Cultures consistent with E coli due to elevated D-dimer patient also underwent CT angiogram which was negative for PE. Patient was started on Decadron in the emergency department due to concern for acute hypoxic respiratory failure secondary to COVID and admitted for further management of COVID pneumonia and urinary tract infection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 3,0
- Labordaten
- USV Venous Lower Extremity Duplex Bilateral [362101418] Resulted: 01/05/22 1609 Order Status: Completed Updated: 01/05/22 1611 Narrative: EXAMINATION: Complete Right and Left Lower Extremity Venous Duplex Doppler Ultrasound EXAM DATE: 1/5/2022 4:04 PM TECHNIQUE: Real-time B-mode imaging with and without compression was used to evaluate the right and left lower extremity for deep venous thrombosis (DVT). Duplex Doppler with color and spectral Doppler was used. INDICATION: Covid with elevated D-dimer COMPARISON: None _____________________ Right Lower Extremity Findings: Right Common Femoral Vein: No DVT. Right Femoral Vein: No DVT. Right Popliteal Vein: No DVT. Right Posterior Tibial Veins: No DVT. Right Peroneal Veins: No DVT. Right proximal Greater Saphenous Vein: No thrombus. Left Lower Extremity Findings: Left Common Femoral Vein: No DVT. Left Femoral Vein: No DVT. Left Popliteal Vein: No DVT. Left Posterior Tibial Veins: No DVT. Left Peroneal Veins: No DVT. Left proximal Greater Saphenous Vein: No thrombus. Duplex Doppler: Spectral Doppler demonstrates bilateral normal respirophasic waveforms in the common femoral veins. Additional Findings: None. _____________________ Impression: There is no deep venous thrombosis in the visualized deep veins of the right or left lower extremity. CT ANGIO THORAX WITH IV CONTRAST [362018135] Resulted: 01/04/22 1605 Order Status: Completed Updated: 01/04/22 1607 Narrative: EXAMINATION: CT Angiography of the Thorax EXAM DATE: 1/4/2022 3:11 PM TECHNIQUE: Standard protocol CT angiogram images were obtained through the chest following the administration of intravenous contrast. Coronal and axial MIP 3-D reformations were performed. IV Contrast: The amount and type of contrast are recorded in the medical record. QPP DOCUMENTATION: At least one of the following dose reduction techniques was utilized: Iterative reconstruction, and/or Automatic Exposure Control, and/or mA/kV adjustment based on body size. INDICATION: PE suspected, low/intermediate prob, positive D-dimer COMPARISON: CTs between 10/15/2011 and 9/4/2020 ENCOUNTER: Not applicable ____________________ CHEST FINDINGS: Base of Neck & Axillae: There is no adenopathy. Mediastinum & Hila: There is no mediastinal or hilar adenopathy. Cardiovascular: The heart has a normal size and atherosclerotic plaque is present on the coronary arteries. There is no pericardial effusion. The thoracic aorta is normal in caliber. Pulmonary Arteries: No pulmonary embolism is present. Lungs and Airways: There are bilateral groundglass opacities involving portions of all lobes. Pleural Space: There are no pleural effusions. There is no pneumothorax. Upper Abdomen: There is a small accessory spleen. Chest Wall & Musculoskeletal: There is a large L1 Schmorl's node. There are no concerning osseous or soft tissue lesions. ____________________ Impression: 1. No evidence of an acute pulmonary embolism. 2. Bilateral pulmonary opacities are consistent with COVID-19 pneumonia in this COVID-19 positive patient. Peripheral Blood Culture [362101086] Collected: 01/04/22 2051 Order Status: Completed Specimen: Blood, Venous Updated: 01/06/22 2202 Cult Blood Peripheral No Growth 48 hours Peripheral Blood Culture [362101087] Collected: 01/04/22 2052 Order Status: Completed Specimen: Blood, Venous Updated: 01/06/22 2202 Cult Blood Peripheral
- Aktuelle Erkrankungen
- Anxiety - 11/17/2021
- Vorgeschichte
- Lumbar stenosis Fatigue Mixed anxiety and depressive disorder Migraine OSA (obstructive sleep apnea) Pelvic pressure in female Mixed incontinence urge and stress (male)(female) Essential hypertension OAB (overactive bladder) Gastroesophageal reflux disease with esophagitis Age-related osteoporosis without current pathological fracture Chronic renal insufficiency, stage III (moderate) Septic shock
- Andere Medikamente
- albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler ALPRAZolam (XANAX) 0.5 MG tablet Ascorbic Acid (VITAMIN C) 500 MG tablet aspirin 81 MG tablet Calcium Carbonate-Vit D-Min (CALTRATE 600+D PLUS PO) choleca
- Allergien
- Duragesic Disc Transdermal System Environmental Lexapro Morphine Sertraline Zoloft
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 27.12.2021
- Impfdatum
- 10.12.2021
- Beginn
- 19.12.2021
- Tage bis Beginn
- 9,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Acute kidney injury
Acute myocardial infarction
Acute respiratory failure
Anticoagulant therapy
Atrial fibrillation
Blood creatinine increased
Blood culture positive
Blood gases
Blood glucose normal
Blood lactic acid normal
Blood pH normal
Blood urea increased
Brain natriuretic peptide increased
Bundle branch block right
COVID-19
Chronic kidney disease
Chronic obstructive pulmonary disease
Computerised tomogram head normal
Symptomtext
Hospitalized (12.19.21 - still currently admitted); COVID-19 positive (12.19.21); fully vaccinated PLUS booster CHIEF COMPLAINT Lethargy, fatigue, confusion, fever HISTORY OF PRESENT ILLNESS Pt is a 81 y.o. male with past medical history significant for coronary artery disease, essential hypertension, type 2 diabetes mellitus, chronic obstructive pulmonary disease, prior history of DVT, OSA, persistent atrial fibrillation on Eliquis, CKD 4 who presented to the ED on 12/19 for evaluation of confusion, fever, and shortness of breath which started in the middle of the night on 12/18-12/19. Throughout the day of 12/19 the patient tells me he has not wanted to do anything but sleep, which was concerning to his wife. He was recently admitted 12/15 through 12/18/2021 at a local Hospital for AKI which was thought to be secondary to a combination of over-diuresis and hypotension. Medications were adjusted; he stopped losartan and started torsemide 20mg daily. He reports compliance with this on the one day he has been home for. His main complaints are severe fatigue, fever and dyspnea. He is oriented x 4 at the time of my exam, but does fall asleep frequently. He reports increased thirst and poor intake. Denies diarrhea/nausea/vomiting. Denies chest pain or palpitations. Making urine and denies dysuria. He does tell me he has not been compliant with his CPAP. He expresses frustration that he is here with COVID. Tells me he has done everything right, got his vaccines earlier this year, wears a mask. He is understandably frustrated that he got COVID, as he probably got it in the hospital. COVID 19 infection - Symptom onset 12/19 - Vaccination status: vaccinated with pfizer 1/26/21, 3/8/21, has not been boosted - Currently requiring 1 L O2 - CXR independently reviewed, with stable cardiomegaly and pulmonary vascular congestion - Received decadron in the ED, continue for now - Monitor daily covid immunology labs - VTE prophylaxis with home eliquis - IS q 1hr while awake, prone positioning prn Metabolic encephalopathy, improving Suspect due to combination of fever and hypoxia in the setting of covid 19/volume overload vs. Accumulation of home pain medications in the setting of poor renal function - CT head independently reviewed, negative for acute intracranial process - Blood cultures x 2 obtained - Oriented x 4 on my exam, but quite somnolent - VBG on presentation with pCO2 36, will repeat on a.m. draw - Encourage cpap compliance, patient states he has not been wearing at home - Neuro checks q 4 hours Mild acute hypoxemic respiratory failure, resolved - Patient was in respiratory distress and hypoxic to the 80s when picked up by EMS, requiring 4L NC - He has since been weaned to room air - Unclear cause. COPD vs. covid 19 vs. CHF ? - Only had 350ml out with lasix, but on my exam looks euvolemic, no wheezing on exam... feel it's reasonable to continue decadron for now Chronic systolic CHF EF 44% 6/14/21 - CXR independently reviewed, with stable cardiomegaly, mild-moderate persistent CHF, actually improved from 12/17 - BNP 15147 - S/p 40mg IV lasix in ED with only 350ml UOP - Reports compliance with 20mg PO torsemide at home - Wean oxygen as tolerated - Telemetry, continuous pulse ox - Daily weights, strict I/O, 2g Na/2L fluid restriction Troponin elevation Type 2 MI in setting of demand ischemia - Hstnt 171-- >168 - EKG independently reviewed, with atrial fibrillation, rate 74, stable RBBB, unchanged from 5 days ago - Suspect troponin elevation is related to demand ischemia in setting of volume overload/CHF exacerbation - Denies chest pain - Telemetry AKI on CKD 4 - Patient was hospitalized 12/15-12/18 and nephrology was consulted at that time - Losartan d/c'd on recent admission - Creatinine 3.01, (recent baseline appears to be 2.5) - Nephro - trend BMP - hold home torsemide for now
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- 9,0
- Labordaten
- The patient arrived in the emergency department hemodynamically stable, febrile to 103.1 and hypoxic to 85% on room air. Hypoxia improved with initiation of 2 L nasal cannula. CBC was remarkable for hgb 9.7, plt 111. CMP was remarkable for BUN 83, creatinine 3.01, glucose 153. VBG showed pH 7.45, pCO2 36. NT proBNP elevated to 15,000. Troponin baseline 171, 2 hour troponin 168, delta -3. Blood cultures x2 were obtained. UA with 10 protein, otherwise unremarkable. CT head without contrast was obtained and independently reviewed, negative for acute intracranial process. Chest x-ray was obtained and independently reviewed, with stable/slightly improved mild to moderate findings of congestive heart failure. EKG was obtained and independently reviewed, with atrial fibrillation, stable right bundle branch block, rate 73, no acute changes from prior. In the emergency department, he was given 1 g oral Tylenol, 40 mg IV Lasix and 6 mg IV Decadron. The patient was admitted to the hospitalist service for further workup and management. Progress note from 12.27.21: COVID-19 pneumonia Acute respiratory failure Chronic obstructive pulmonary disease Altered mentation CT head with contrast showing no acute intracranial abnormality Vaccinated COVID positive - placed in severe respiratory isolation Continue dexamethasone 6 mg IV for total of 10 days (12/19-12/29) No remdesivir due to elevated creatinine Continue nebs as needed Continue supportive treatment as needed Chest x-ray on 12/22 showing slightly increased right perihilar infiltrates Lactate within normal limits Procal elevated, started on ceftriaxone on 12/23 x 5d - will stop on 12/28 Blood cultures showing stap epidermis in 1 vial, likely contaminate, will repeat BCX repeated, NGTD x 24 hours Likely respiratory failure multifactorial & related to CHF exacerbation as well Currently on high-flow oxygen at 95%/40, slightly worsened from yesterday Will obtain CXR to eval for possible pleural effusion vs COVID Maintain goal O2 sats greater than 88% PT/OT consulted, appreciate recs AKI on CKD Baseline creatinine prior to admission approximately 2.2 per Nephro Creatinine stable, high Avoid nephrotoxic agents Continue 2 G sodium diet Continue daily BMPs - labs pending still for 12/27 Dose medications at estimated GFR of less than 20 Nephrology consult, appreciate recommendations Continue holding torsemide May consider restarting based on CXR ordered above Congestive heart failure with reduced ejection fraction of 45% CHF exacerbation, BNP 15, 147 Coronary artery disease, history of stenting of LAD in May 2021 Hypertension Atrial fibrillation Normocytic anemia Started on torsemide 20mg (held on 12/25 given worsening kidney function) Admission weight of 89 kg, stable for last 2 days at 84kg Elevated troponin, downtrended - believe 2/2 nonischemic myocardial injury from CHF and CKD Cardiology consulted, appreciate recommendations Continuing Amlodipine and Metoprolol, holding losartan Continuing home Eliquis Continue high potency statin therapy, long-acting nitrate, and clopidogrel H&H stable
- Aktuelle Erkrankungen
- Admitted to hospital 12.14.21 - 12.18.21: acute kidney injury superimposed on CKD; HOSPITAL COURSE: Pt is a 81 y.o. male with past medical history of coronary artery disease, hypertension, type II DM, CODP, hx of DVT's, OSA, persistent Afib on Xarelto, and gout who presented to the hospital at the direction of his nephrologist due to an AKI on his CKD. His AKI was felt to be due to a combination of over-diuresis and hypotension. He was seen by nephrology in the hospital. His losartan and torsemide were held with improvement in his kidney function tests. He was also seen by palliative care for management of his chronic pain regimen. He was changed to DNR after a goals of care discussion this visit. Patient was noted to be hypoxic and repeat chest x-ray was obtained, which showed worsening pulmonary edema. Torsemide was restarted at 20 mg daily. Patient's renal function was monitored with restarting Torsemide. Creatinine trending down upon discharge. Discharged in stable condition with instructions to follow up with PCP and Nephrology.
- Vorgeschichte
- ASHD (arteriosclerotic heart disease) Coronary artery disease involving native coronary artery of native heart without angina pectoris Deviated nasal septum OSA (obstructive sleep apnea) Wide-complex tachycardia DVT of lower extremity (deep venous thrombosis) Dyslipidemia Essential hypertension Type 2 diabetes mellitus with stage 4 chronic kidney disease, with long-term current use of insulin Back pain Chronic combined systolic and diastolic congestive heart failure Carotid stenosis COPD (chronic obstructive pulmonary disease) Spinal stenosis of lumbar region with neurogenic claudication Right bundle branch block (RBBB) LBBB (left bundle branch block)-noted during dobutamine stress test-testing was cancelled. NM MPI ordered instead Chronic ITP (idiopathic thrombocytopenia) Persistent atrial fibrillation Heart failure Acute kidney injury superimposed on CKD Ischemic cardiomyopathy Subclinical hyperthyroidism Elevated sedimentation rate Iron deficiency anemia, unspecified Chest pain Gout Cervical myelopathy Dehydration Fall Elevated troponin Nail disorder Vitamin B12 deficiency Hypomagnesemia GERD (gastroesophageal reflux disease) Colon polyp Depression Muscle weakness (generalized) Medication management contract agreement Other constipation Acute kidney injury
- Andere Medikamente
- acetaminophen (TYLENOL) 500 MG tablet amLODIPine (NORVASC) 5 MG tablet apixaban (ELIQUIS) 2.5 MG tablet atorvastatin (LIPITOR) 40 MG tablet bisacodyl (DULCOLAX) 10 MG suppository budesonide/formoterol (SYMBICORT) 80-4.5 MCG/ACT inhaler calc
- Allergien
- LotrisoneRash
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 16.11.2021
- Beginn
- 19.11.2021
- Tage bis Beginn
- 3,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Blood test
Cerebrovascular accident
Computerised tomogram
Echocardiogram
Electrocardiogram
Electroencephalogram
Magnetic resonance imaging
Symptomtext
suffered a stroke
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- 3,0
- Labordaten
- MRI, CAT scans, EEG, EKG, Blood work, Echo Cardiogram (12/20 - 12/22)
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 22.12.2021
- Impfdatum
- 22.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Cardio-respiratory arrest
Throat tightness
Symptomtext
on 12/22/2021 patient came into office for Pfizer Booster, Patient had already received First dose on 04/21/2021 and Second Dose on 05/12/2021. After Vaccine was administered at 2pm patient was advised to stay in waiting area for 15 minutes. Before administering Vaccine patient was given a pre vaccination questionnaire where patient selected no to all questions regarding allergic reaction to previous vaccine this information was verified with patient before administering the vaccine. At 2:25 patient expressed that she felt like her throat was closing so code blue was called and help was on the way. At 2:30 patient was given an Epi pen to try and open airway which patient stated felt like it was closing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cardio-respiratory arrest
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 20.12.2021
- Impfdatum
- 20.12.2021
- Beginn
- 20.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Erythema
Respiratory arrest
Symptomtext
Patient tilted her head back and her face turned red and actually stopped breathing, then woke back up when i prepared to start cpr procedures. Patient woke back up and seemed fine and actually drank water and laid on the floor until EMS came to store. Patient spoke with us the whole time and stated she ate a small snack this morning. Patient is now doing okay and is shopping in our store at the moment and has been cleared by EMS. Patient may have passed out due to excitement of the shot itself.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Respiratory arrest
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- NO JUST STATED SHE GETS NERVOUS BEFORE VACCINES.
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 01.07.2023
- Impfdatum
- 20.04.2020
- Beginn
- 20.04.2020
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Ageusia
Angina pectoris
Asthenia
Atrial fibrillation
Balance disorder
Computerised tomogram
Electrocardiogram
Electromyogram
Epistaxis
Eye pain
Fall
Gait disturbance
Guillain-Barre syndrome
Haemoptysis
Headache
Hypoaesthesia
Insomnia
Joint range of motion decreased
Symptomtext
Arm swollen pain, arm motion range couldn't lift arm, heart palpation nosebleed, spit up blood clotes fallen neuropathy, cane, thrombocytopenia, nerves attacted (AFib) heart pain musle loss Gullain Bar Syndrome Patient given Pfizer shot 4/2020. Patient began 1 1/2 hour later arm swollen legs num/needle pins in feet and legs. Coughing up bloot clots, lost muscle mas, weakness lost balance to walk, headaches, nauseous at stomach couldn't sleep heart paltation! Nosebleeds, arm range motion lost! Nerves attacted. Muscle mass lost, weight gain Brain to go blood clots in legs. Long Covid. Taste gone. Shots 4/16/21 Eye Sight low Pfizer Lot ER8732 5/07/21 Pfizer Lot EW0179 01/18/22 Pfizer Lot FD7218 7/04/22 PFR-BNT 30mcg/0.3mL Lot FM0173 11/15/22 Pfizer Bivalent 30mcg/0.3mL Lot GJ3277 Uptic Neuritis-Pain in eyes. I have Thrombocytopenia
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Guillain-Barre syndrome
- Hospital-Tage
- -
- Labordaten
- MRI 04/20/2023 EKG EMG, Ct
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Long Covid reaction to vaccine
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 23.05.2023
- Impfdatum
- 21.09.2022
- Beginn
- 06.10.2022
- Tage bis Beginn
- 15,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hepatic mass
Hypovolaemic shock
Symptomtext
R57.1 HYPOVOLEMIC SHOCK 10/6/2022 LIVER MASS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypovolaemic shock
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 05.05.2023
- Impfdatum
- 12.12.2021
- Beginn
- 11.07.2022
- Tage bis Beginn
- 211,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Embolic stroke
Embolism arterial
Symptomtext
PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ACUTE STROKE DUE TO EMBOLISM OF UNSPECIFIED ARTERY
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Embolic stroke
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 11.04.2023
- Impfdatum
- 12.12.2021
- Beginn
- 07.02.2022
- Tage bis Beginn
- 57,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Adenocarcinoma gastric
Blood alkaline phosphatase increased
Embolic stroke
Subdural haemorrhage
Symptomtext
I63.9 ACUTE STROKE DUE TO EMBOLISM OF UNSPECIFIED ARTERY 2/11/2022 ACUTE NONTRAUMATIC SUBDURAL HEMORRHAGE I63.9 ACUTE STROKE DUE TO EMBOLISM OF UNSPECIFIED ARTERY 2/11/2022 ELEVATED ALKALINE PHOSPHATASE I63.9 ACUTE STROKE DUE TO EMBOLISM OF UNSPECIFIED ARTERY 2/11/2022 ADENOCARCINOMA, CARDIA OF STOMACH I63.9 ACUTE STROKE DUE TO EMBOLISM OF UNSPECIFIED ARTERY 2/11/2022 ELEVATED ALKALINE PHOSPHATASE I63.9 ACUTE STROKE DUE TO EMBOLISM OF UNSPECIFIED ARTERY 2/11/2022 ADENOCARCINOMA, CARDIA OF STOMACH
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Embolic stroke
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 28.03.2023
- Impfdatum
- 05.01.2022
- Beginn
- 27.03.2023
- Tage bis Beginn
- 446,0
- Dosis
- 3
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Alanine aminotransferase normal
Angiopathy
Anion gap
Aspartate aminotransferase normal
Atrial flutter
Basophil count increased
Basophil percentage
Blood albumin decreased
Blood alkaline phosphatase normal
Blood bilirubin normal
Blood calcium decreased
Blood chloride normal
Blood creatinine normal
Blood glucose normal
Blood magnesium normal
Blood phosphorus normal
Blood potassium normal
Blood sodium decreased
Symptomtext
Document Type: History and Physical Document Subject: History & Physical Note Inpatient, 03/27/23 - * Final Report * Chief Complaint Shortness of breath History of Present Illness/Subjective This is a 54-year-old female with a past medical history of a flutter, CHF, stasis dermatitis of her lower extremities who presented to ED with a chief complaint of shortness of breath. She states that her shortness of breath has been worsening over the past few weeks as well as increasing leg swelling. She was recently started on levothyroxine and Eliquis went when she was diagnosed last week with atrial flutter. She is a 1.5 pack/day smoker. She states she does not drink alcohol. She notes her legs are chronically swollen but were worse over the last few weeks. In the ED she was found to be in A-fib flutter with rapid ventricular response she was given Cardizem push and responded to a degree. Patient was taking Toprol, will change to Lopressor to better control heart rate. Her lab work was relatively benign other than leukocytosis. Review of Systems A complete, 13-system review was performed and was negative except for as noted in the HPI. Physical Exam/Objective Vitals & Measurements most recent past 24 hours T: 36.8 ?C (Oral) HR: 110 (Monitored) HR: 92 (Peripheral) RR: 19 BP: 108/73 SpO2: 92% WT: 138 kg BMI: 40.1 Oxygen Therapy: Room air Oxygen Flow Rate: 0 (L/min) Hemodynamics Neurologic Glasgow Coma Score: 15 Patient Weight Current Daily Weight: 138 kg 03/27/23 Previous Daily Weight: 138 kg 03/27/23 BMI: 40.1 03/27/23 Morbid Obesity (BMI > = 40) Patient Height Current Height: 185.4 cm 03/27/23 Constitutional: No acute distress, well-nourished Eyes: PERRL, EOMI, normal conjunctiva, no scleral icterus ENMT: Moist oral mucosa Neck: Supple, non-tender, intact range of motion Respiratory: diffuse crackles b/l with minor wheezing Cardiovascular: Tachycardic, a flutter, no murmur appreciated Gastrointestinal: Soft, non-tender, non-distended, obese abdomen Musculoskeletal: No joint swelling, no deformity, intact ROM Integumentary: B/l LE edema with erythema and tenderness as well exudative slough on the left leg Neurologic: Alert & Oriented x 3, no cognitive impairment, no focal deficits Psychiatric: Cooperative, appropriate mood and affect Assessment/Plan This is a 54-year-old female with past medical history of CHF and recently diagnosed atrial flutter started on Eliquis who presents with chief complaint of shortness of breath found to have a flutter with RVR and sepsis likely due to lower extremity cellulitis admitted to ICU for further management. 1. Atrial flutter with rapid ventricular response I48.92 Switch Toprol to Lopressor for better rate control, maintain telemetry monitoring, tropes negative, EKG not concerning for ACS, cardio as needed if rate control is not achieved with the switch of medications 2. CHF (congestive heart failure) I50.9 Continue other home medications Stop torsemide and start Lasix 40 mg IV daily, titrate as needed 3. Stasis dermatitis I87.2 4. Sepsis A41.9 5. Leukocytosis D72.829 6. Cellulitis of lower extremity L03.119 Given patient's allergy to vancomycin we will start linezolid, monitor CBC, and cefepime to cover for cellulitis with risk factors for MRSA Wound care per nursing Additional imaging as needed Obtain CRP and procalcitonin Orders: acetaminophen, 650 mg, Orally, Tablet, Q4H, PRN, Pain, Mild PO (1-3 out of 10)/Fever, 03/27/23 19:51:00 EDT apixaban, 5 mg, Orally, Tablet, BID, 03/28/23 9:00:00 EDT cefePIME, 1 GM, IVPB, Injection, Q8H, Indication: Other (MUST specify in Comments), 03/28/23 0:00:00 EDT, 12.5 mL/hr, Infuse Over 4 Hours, Total Volume (mL) = 50 furosemide, 40 mg, IV Push, Injection, Daily, 03/28/23 9:00:00 EDT hydroCODONE-acetaminophen, 1 Tablet, Orally, Tablet, Q6H, PRN, Pain, Moderate (4-6 out of 10), 03/28/23 2:56:00 EDT levothyroxine, 50 mCg, Orally, Tablet, Daily, 03/28/23 6:00:00 EDT linezolid, 600 mg, IVPB, Infusion, Q12H, Indication: Other (MUST specify in Comments), 03/27/23 23:00:00 EDT, 150 mL/hr, Infuse Over 2 Hours, Total Volume (mL) = 300 metoPROLOL, 25 mg, Orally, Tablet, BID, 03/27/23 22:10:00 EDT polyethylene glycol 3350, 17 GM, Orally, Powder, Daily, PRN, Constipation - Use First, 03/27/23 19:51:00 EDT Sodium Chloride 0.9% 500 mL, Total Volume (mL) = 500, IV, 03/27/23 23:56:00 EDT, Other - See Comments, Clinical Weight 2000 mg Sodium, 20 gm Saturated Fat Diet Admit to Inpatient Auto Diff Blood CX Blood CX Call Blood Glucose Call Diastolic Blood Pressure Call Heart Rate Call Mental Status Changes Call O2 Saturation Call Respiratory Distress Call Respiratory Rate Call Systolic Blood Pressure Call Temperature Call Urine Output Care Management Consult CBC w/Differential cefePIME Pharmacy Dosing Consult Comp Metabolic Panel Creatinine SerPl QN CRP High Sensitiv SerPl QN Diagnosis Hgb Initiate IV Care Protocols As Appropriate Initiate Mobility Protocol Initiate Skin and Wound Care Protocol Intake + Output Strict Level of Care Magnesium SerPl QN Medical Service Phosphorus SerPl QN Procalcitonin Resp Evaluation or Assessment Resuscitation Status Sequential Compression Device Single Oxygen Saturation T4 Free Direct SerPl QN Telemetry Class III 24hr Recommendation Troponin-I High Sensitivity TSH w FreeT4 reflex Vital Signs Weight This patient is critically ill due to metabolic, hemodynamic and/or respiratory instability. They require high complexity evaluation, decision making, and care. They require ICU level of care and monitoring due to high risk of clinical decompensation with high risk of morbidity and mortality. Critical care time includes, but is not limited to, bedside assessment, review of medical record, radiographic and laboratory results, ventilator and/or respiratory management, review of ekg and/or cardiac monitoring, critical decision making, coordination of care with consultants and/or care team, and documentation of critical intervention/plans, and consultation with patient and/or family. Time excludes any procedural time. I spent greater than 50 minutes in the evaluation and management of this patient with more than 50% of the time spent counseling and/or coordinating care. I counseled the patient and/or family about the findings, differential diagnoses, my assessment, recommendations, and plan. I coordinated care with the multidisciplinary healthcare team. Code Status Resuscitation Status - Ordered -- 03/27/23 19:51:00 EDT, Full Code Chronic Problem List Atrial flutter with rapid ventricular response CHF (congestive heart failure) Elevated d-dimer Pleural effusion Severe obesity Stasis dermatitis Tobacco use Procedure/Surgical History ?Displaced Fx ?Laproscopy Medications Home Medications (6) Active Eliquis 5 mg oral tablet 5 mg, Orally, BID ibuprofen 600 mg oral tablet 600 mg = 1 Tablet, Orally, TID levothyroxine 50 mCg (0.05 mg) oral tablet 50 mCg = 1 Tablet, Orally, Daily metoPROLOL Succinate ER 25 mg oral tablet, extended release 25 mg, Orally, Daily ocular lubricant solution 1 Drop, Eye, Left, Q2H torsemide 20 mg oral tablet 20 mg, Orally, Every Other Day Active Scheduled Inpatient Medications apixaban, Tablet, 5 mg, Orally, BID, Start: 03/28/23 09:00:00 cefePIME, Injection, 1 GM, IVPB, Q8H, Indication: Other (MUST specify in Comments), Start: 03/28/23 00:00:00 furosemide (Lasix), Injection, 40 mg, IV Push, Daily, Start: 03/28/23 09:00:00 levothyroxine, Tablet, 50 mCg, Orally, Daily, Start: 03/28/23 06:00:00 linezolid, Infusion, 600 mg, IVPB, Q12H, Indication: Other (MUST specify in Comments), Start: 03/27/23 23:00:00 metoPROLOL (metoPROLOL tartrate), Tablet, 25 mg, Orally, BID, Start: 03/27/23 22:10:00 Sodium Chloride 0.9% 500 mL IV Other - See Comments One-Time Medications Given 03/27/23 00:00:00 TO 03/28/23 06:32:37 None Reported PRN Medications (0600 - 0559) from 03/27 - 03/28 acetaminophen, 650 mg, Orally, Q4H, 0 Dose(s) hydroCODONE-acetaminophen, 1 Tablet, Orally, Q6H, 1 Dose(s) polyethylene glycol 3350, 17 GM, Orally, Daily, 0 Dose(s) Allergies vancomycin (Hives) Neosporin cortisone Social History Alcohol Denies Electronic Cigarette/Vaping E-Cigarette Use Never. Substance Abuse Denies Tobacco Tobacco Use: 10 or more cigarettes (1/2 pack or more)/day in last 30 days. Lab Results All Labs Last 24 hours (No Micro or Pathology) Hematology: WBC: 14.7 k/cumm High (03/28/23 02:44:00) RBC: 4.78 million/cumm (03/28/23 02:44:00) Hgb: 12.9 GM/dL (03/28/23 02:44:00) Hct: 38 % (03/28/23 02:44:00) MCV: 79 fL Low (03/28/23 02:44:00) MCH: 27.1 pg (03/28/23 02:44:00) MCHC: 34.1 GM/dL (03/28/23 02:44:00) RDW: 15.7 % High (03/28/23 02:44:00) Platelet: 364 k/cumm (03/28/23 02:44:00) MPV: 7.6 fL (03/28/23 02:44:00) Neutrophils %: 72 % (03/28/23 02:44:00) Lymphocytes %: 12 % (03/28/23 02:44:00) Monocytes %: 12 % (03/28/23 02:44:00) Eosinophils %: 3 % (03/28/23 02:44:00) Basophils %: 1 % (03/28/23 02:44:00) Absolute Neutrophil: 10.5 k/cumm High (03/28/23 02:44:00) Absolute Lymphocyte: 1.7 k/cumm (03/28/23 02:44:00) Absolute Monocyte: 1.7 k/cumm High (03/28/23 02:44:00) Absolute Eosinophil: 0.5 k/cumm High (03/28/23 02:44:00) Absolute Basophil: 0.2 k/cumm (03/28/23 02:44:00) Chemistry: Sodium SerPl QN: 134 mmol/L Low (03/28/23 02:44:00) Potassium SerPl QN: 3.9 mmol/L (03/28/23 02:44:00) Chloride SerPl QN: 100 mmol/L (03/28/23 02:44:00) Carbon Dioxide SerPl QN: 25 mmol/L (03/28/23 02:44:00) Anion Gap: 9 mmol/L (03/28/23 02:44:00) BUN SerPl QN: 18 mg/dL (03/28/23 02:44:00) Creatinine SerPl QN: 0.79 mg/dL (03/28/23 02:44:00) Estimated GFR (CKD-EPI, no race): 89 mL/min/1.73m2 (03/28/23 02:44:00) Estimated CRCL (CG): >120 (03/28/23 02:44:00) Glucose SerPl QN: 111 mg/dL High (03/28/23 02:44:00) Calcium Total SerPl QN: 8.8 mg/dL (03/28/23 02:44:00) Phosphorus SerPl QN: 3.8 mg/dL (03/28/23 02:44:00) Alkaline Phos SerPl QN: 77 Units/L (03/28/23 02:44:00) ALT SerPl QN: 8 Units/L (03/28/23 02:44:00) AST SerPl QN: 10 Units/L Low (03/28/23 02:44:00) Bilirubin Total SerPl QN: 0.7 mg/dL (03/28/23 02:44:00) Total Protein SerPl QN: 6.4 GM/dL (03/28/23 02:44:00) Albumin SerPl QN: 3 GM/dL Low (03/28/23 02:44:00) Magnesium SerPl QN: 1.9 mg/dL (03/28/23 02:44:00) Troponin-I High Sensitivity: 10 ng/L (03/28/23 02:44:00) BNP Pl QN: 276 pg/mL High (03/27/23 09:24:00) TSH 3rd Gen SerPl QN: 5.34 mcU/mL High (03/27/23 20:19:00) Coagulation: D-Dimer Pl QN: 506 ng/mL DDU High (03/27/23 09:24:00) All Other Labs: COVID 19 Specimen Source: Nasopharyngeal (03/27/23 12:03:00) Coronavirus SARS-CoV2 Rapid: Not Detected (03/27/23 12:03:00) Diagnostics Radiology Results - Last 24 hours Across Visits 03/27/2023 09:28 - XR Chest PA or AP Portable Impression:1. Interval development of cardiomegaly and vascular congestioncompared with prior study. There are also subtle interstitialopacities suspicious for early pulmonary edema.2. There is new asymmetric elevation left hemidiaphragm and adjacentsmall left effusion, of uncertain significance. 03/27/2023 11:38 - Venous Duplex Scan LE Bilateral Impression:1. No evidence for deep or superficial venous thrombosis of thebilateral lower extremities.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Intensive care
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 23.01.2023
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Angiogram normal
Arrhythmia
Cardiac assistance device user
Cardiac failure acute
Echocardiogram abnormal
Ejection fraction decreased
Syncope
Symptomtext
Acute Heart Failure diagnosed 3/3/22, after 2 months of gradually worsening symptoms including collapse from arrhythmia 2 weeks prior to hospitalization. 3 months of wearing mobile defibrillator vest, very expensive heart failure medications.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- 2,0
- Labordaten
- Echocardiogram initial Ejection Fraction 23% Angiogram normal
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 09.08.2022
- Impfdatum
- 23.12.2021
- Beginn
- 25.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest discomfort
Chest pain
Hypoaesthesia
Myopericarditis
Paraesthesia
Troponin
Symptomtext
Patient admitted from the ED with complaint of chest pain, chest heaviness, numbness and tingling sensation. Patient was diagnosed with myopericarditis secondary to COVID vaccination. No treatment was indicated. Patient already receiving aspirin 81mg for stroke treatment. Patient was monitored outpatient. Symptoms resolved by 1/10/21 cardiology outpatient visit.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myopericarditis
- Hospital-Tage
- 1,0
- Labordaten
- 12/25/21- Troponin 12,402pg/ml (Ref <30.9pg/ml)
- Aktuelle Erkrankungen
- None noted
- Vorgeschichte
- PMHx of Ischemic Stroke in Feb 2021 Klinefletcher Syndrome GERD
- Andere Medikamente
- Aspirin 81mg - 1 tablet daily Calcium Carbonate0- As needed for heart burn
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 26.05.2022
- Impfdatum
- 06.12.2021
- Beginn
- 25.12.2021
- Tage bis Beginn
- 19,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Blindness unilateral
Chest X-ray
Computerised tomogram
Hypoaesthesia
Ischaemic stroke
Laboratory test
Magnetic resonance imaging
Symptomtext
Ischemic stroke affecting right side of body. Left partial numbness on right side limbs. body and face. Most numbness has subsided. Caused blind spot in right eye, which has been corrected/healed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ischaemic stroke
- Hospital-Tage
- 7,0
- Labordaten
- CAT scan, MRI, chest X-ray, cardia studies
- Aktuelle Erkrankungen
- Nausea. dizziness, fatigue
- Vorgeschichte
- Type 2 diabetes, hypertensives
- Andere Medikamente
- Metformin Metoprolol Amlopidine Advil Sertraline
- Allergien
- Verapamil, Dilantin, Flagyl, Depakote, Tegretol, Penicillin, Rybelsus. Jardiance
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 21.05.2022
- Impfdatum
- 12.12.2021
- Beginn
- 01.02.2022
- Tage bis Beginn
- 51,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pericarditis
Symptomtext
Pericarditis; 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 65-year-old female patient received BNT162b2 (BNT162B2), on 12Dec2021 as dose 3 (booster), single (Lot number: FD7218) at the age of 65 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Hypothyroidism" (unspecified if ongoing); "Parathyroid", start date: 2019 (unspecified if ongoing), notes: Treated for parathyroid in 2019. Removed 2 parathyroid glands. That was before COVID. Concomitant medication(s) included: LEVOTHYROXINE taken for hypothyroidism. Vaccination history included: BNT162b2 (Dose 1, single; Lot: EW0158 expiration: Unknown, anatomical location: Injected in right arm), administration date: 20Apr2021, when the patient was 65-year-old, for Covid-19 immunization; BNT162b2 (Dose 1, single; Lot: EW0158 expiration: unknown, anatomical location: Injected in right arm), administration date: 21May2021, when the patient was 65-year-old, for Covid-19 immunization. The following information was reported: PERICARDITIS (medically significant) with onset Feb2022, outcome "not recovered". Therapeutic measures were taken as a result of pericarditis. Caller stated that she received her first booster shot of the Pfizer-BioNTech Covid 19 Vaccine on 12Dec2021 and after that she has been suffered with pericarditis and she still has it. She wants to know if this side effect has been reported due to the vaccine because she can't get rid of it. Caller stated that it is a disgrace that Pfizer does not have information on how to treat pericarditis due to the vaccine. She also mentioned that this side effect should be a headline and Pfizer must disclose it, also saying that "this is bad and not good". Caller wanted to verify if this call is being recorded, so she can have evidence that she spoke to us. Additional information on drug: Additional Information for Other medicines Levothyroxine: Taking 20 years. Dosage and Relevant Information: Dosage text: Unknown Dose. 0.75 mcg. once daily. Case narrative including clinical course, therapeutic measures, outcome, and additional relevant information: Dates when patient was in hospital for Heart Operation: 27Jan2022 to 30Jan2022. Warm transfer from (name withheld), Pfizer Global Switchboard. She has a lady who had reaction to Pfizer COVID booster. Patient confirmed information above. She would like to know if we have any data that this is happening to people that they are getting Pericarditis from the booster. She does not know if it came from the booster. She first started providing address, then changed to the address where she is currently. She also had an operation. She took the booster when she was 65. Her aunt was reading things and said she thinks the reason she is not getting rid of it is because of the booster. They kept her on steroids for 30 days. She gets off and gets sick again in 3 days and then is on for another 30 days. Unknown lot and expiration and names of the steroids. She just knows the dosage and was prescribed through #. When she was on it, it was good, but when off, it came back. She does not know where inflammation is coming from. She will see a specialist. It gets worse when it is not being treated with medication. When she was diagnosed with it, the only medication she was taking prior was Levothyroxine. She takes supplements. Treated for parathyroid in 2019. Removed 2 parathyroid glands. That was before COVID. Description of Product Complaint: Description of complaint: They kept her on steroids for 30 days. She gets off and gets sick again in 3 days and then is on for another 30 days. Unknown lot and expiration and names of the steroids. She just knows the dosage and was prescribed through. When she was on it, it was good, but when off, it came back. Product strength and count size dispensed: not provided. No follow up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pericarditis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Hypothyroidism; Parathyroid gland excision (Treated for parathyroid in 2019. Removed 2 parathyroid glands. That was before COVID.)
- Andere Medikamente
- LEVOTHYROXINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 29.04.2022
- Impfdatum
- 21.12.2020
- Beginn
- 23.02.2021
- Tage bis Beginn
- 64,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Dizziness
Echocardiogram abnormal
Electrocardiogram ST segment depression
Electrocardiogram abnormal
Hypertransaminasaemia
Laboratory test abnormal
Myopericarditis
Palpitations
Pericardial effusion
Petechiae
SARS-CoV-2 test positive
Symptomtext
Patient developed palpitations, lightheadedness, with heart rate in the 140's on 2-23-21. Echocardiogram revealed pericardial effusion. She also developed petechiae and mild transaminitis around this time, but the petechiae and transaminitis resolved quickly. Pericardial effusion did resolve per repeat echo. Of note, she tested positive for COVID infection on 8-7-21. She has experienced numerous episodes of palpitations between April 2021 and April 2022. Cardiology visit on 4-18-22 revealed diffuse ST segment depressions on EKG. The cardiologist diagnosed her with myopericarditis.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myopericarditis
- Hospital-Tage
- -
- Labordaten
- Echo 3-2-21 showed pericardial effusion. She also had an echo on 6-14-21 and 4-25-22. Mild transaminitis on labs on 4-7-21 and 4-16-21.
- Aktuelle Erkrankungen
- N/A (none known)
- Vorgeschichte
- Meniere's Disease, allergic rhinitis, history of colon polyps
- Andere Medikamente
- Estradiol 1mg per day, Triamterene/HCTZ 37.5mg/25mg per day, Vitamin D 2000 units per day, Zyrtec 10mg pe rday, Glucosamine, Chondroitin
- Allergien
- Penicillin, Hydrocodone
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 20.04.2022
- Impfdatum
- 23.12.2021
- Beginn
- 24.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arrhythmia
Condition aggravated
Dizziness
Fall
Fatigue
General physical condition abnormal
Heart rate increased
Hypertension
Loss of consciousness
Mobility decreased
Nausea
Palpitations
Symptomtext
On 12/23/2021, I received my Pfizer booster. Almost 24 hours later on 12/24/2021, I started having persistent cardiac arrhythmias. I felt nauseous and fatigued. I checked my O2 saturation, which was normal. However, my blood pressure was high and my heart rate fast. I wasn't able to do anything without feeling faint. At about 4 PM, I blacked out while walking through my house and fell. My adult son came over to have Christmas dinner, and he expressed concern, because I didn't look well. I would move from one room to another and immediately have to sit down, because I would get dizzy. My blood pressure was up, and I kept checking it; it was 170/120 with no exertion. My elevated blood pressure and dizziness lasted for about 10 days. The blood pressured dropped to about 140/95 after about 5 days. I was hesitant to call my doctor, because I was sure I would be told to go to the ER. I was terrified to go to the ER, because I knew they were swamped, plus I was afraid I would contract COVID. Instead, I ate healthy food, drank plenty of water, and I got up to walk through the house about once every hour. I slowly got better, but at the time of this writing, I still have occasional episodes of rapid heart rate without exertion and a feeling of faintness. Whenever I climb the stairs, my heart intermittently starts pounding; this never happened until I got the booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Depression; Anxiety; PTSD.
- Andere Medikamente
- Vitamin D; Vitamin B12.
- Allergien
- Sensitivity to eggs and dairy; Maxalt; Red dye #40 food coloring.
- Vorherige Impfungen
- I had shingles and heart flutters after the first Pfizer vaccine. After the second Pfizer vaccine, I had heart arrhythmias.
- Staat
- SC
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 16.03.2022
- Impfdatum
- 27.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Electric shock sensation
Paraesthesia
Symptomtext
Intermittent electric shock sensations and pricks all over; Pricks all over/a pricking sensation; 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 39 year-old female patient received bnt162b2 (BNT162B2), administered in arm right, administration date 27Dec2021 18:40 (Lot number: FD7218) at the age of 39 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "WPW: Wolf Parkinsons White Syndrome", start date: 2012 (ongoing), notes: Verbatim: WPW: Wolf Parkinsons White Syndrome. The patient's concomitant medications were not reported. The following information was reported: ELECTRIC SHOCK SENSATION (non-serious) with onset 27Dec2021, outcome "not recovered", described as "intermittent electric shock sensations and pricks all over"; PARAESTHESIA (non-serious) with onset 27Dec2021, outcome "unknown", described as "pricks all over/a pricking sensation". Additional Information: Patient got her first Pfizer covid vaccine on 27Dec and about 3 to 4 hours later, started experiencing intermittent electric shock sensations and pricks all over. The first occurred in her stomach, then in other parts like her arms, legs, right shoulder and it is a singular electric shock sensation. Patient is frustrated that there is no information on the side effect she is having. Pfizer is pushing the vaccine and there are mandates all over so she is forced to get it. She sees people reporting it on the internet. She took the vaccine because the government is mandating the vaccine for all private workers. Patient described the sensation similar to a belt that is used in physical therapy to decompress muscles and provides electric shocks. Patient describes as random and intermittent. Patient asked if this effect been reported. She needs concrete assistance because this is a problem. She said here is no level of accountability because the vaccine is mandated. She feels like a guinea pig, taking this vaccine. Patient did not receive additional vaccines on the same day of suspect. The events did not require emergency room or physician office visit. Patient did not receive any vaccinations within four weeks and there were no adverse events following prior vaccinations. Patient did not underwent any relevant test. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Electric shock sensation
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- WPW syndrome
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 01.03.2022
- Impfdatum
- 15.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Angiogram abnormal
Anticoagulant therapy
Chest pain
Dizziness
Hypertension
Jugular vein thrombosis
Pain
Rash
Ultrasound Doppler abnormal
Symptomtext
starting on 12/17/2021, patient experienced light headness, dizzy, rash, hypertension, severe chest pain that moved down to right side. Approximately, on 2/9/2022, patient was placed on lisinopril for hypertension. On 2/22/2022, patient was admitted to hospital with nonocclusive thrombosis of distal aspect of internal jugular. Per history, patient is a chronic smoker. Patient was discharged on 2/26/2022 with a new prescription for Eliquis 5 mg BID.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Jugular vein thrombosis
- Hospital-Tage
- 4,0
- Labordaten
- 2/22/2022 - CTA Chest - thrombus in the left jugular vein 2/22/2022 - US Ven Dop - nonocclusive thrombosis of the distal aspect of the internal jugular vein 2/23/2022 - US Ven Dop - bilateral nonocclusive thrombus with flow remaining.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- None
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 21.02.2022
- Impfdatum
- 12.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Angiogram pulmonary
Axillary pain
Chest X-ray
Chest discomfort
Chest pain
Chills
Echocardiogram abnormal
Ejection fraction
Electrocardiogram normal
Fatigue
Myocarditis
Palpitations
Pericardial effusion
Pyrexia
Specialist consultation
Troponin normal
Unevaluable event
Symptomtext
Patient received Pfizer COVID vaccine on 1/12/22. This was a booster dose for her. She received Moderna COVID vaccine for her first two doses. The day following her Pfizer booster, she developed chills and fever, soreness in her armpit, fatigue, and heart palpitations. She had chest pain which she described as pressure in the left middle chest. Cardiology was consulted and determined patients? picture to be consistent with acute myocarditis likely secondary to her COVID vaccine. ECG was without acute injury pattern, echocardiogram showed preserved ejection fraction and normal wall motion throughout. Trace amount of fluid was noted on follow-up limited echo and then repeat showed resolution of pericardial effusion. Troponin remained stable from admission at 0.08. Of note, patient does have history of lupus nephritis so could not be excluded that myocarditis could be lupus induced. Cardiology recommended patient be treated with ibuprofen 600 mg three times daily for 1-2 weeks and colchicine 0.6mg twice daily for the next 90 days. Was determined to be stable and discharged home. Follow up appointment with cardiology after discharge showed patient to be improving with some occasional chest pains but no constant or persistent pains at this time. She continued to take ibuprofen as needed for intermittent pain and remains on colchicine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocarditis
- Hospital-Tage
- 3,0
- Labordaten
- XR Chest- 1/15/22 CTA Chest- 1/15/22 ECHO TTE- 1/15/22, 1/17/22, 1/24/22 Troponin- 1/15/22, 1/16/22, 1/17/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Stage III Lupus nephritis ADHD Depression Hashimoto's disease Hypothyroidism
- Andere Medikamente
- B-complex with vitamin C
- Allergien
- Lamictal Latex Plaquenil
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 12.02.2022
- Impfdatum
- 16.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Hyperhidrosis
Myelitis
Pain in extremity
Presyncope
Renal disorder
Renal pain
Urinary tract disorder
Symptomtext
the pain is migrating towards legs; describes the pain in her back as spinal acute myelitis in which it affects the nerves; Starting to mess up kidneys; The caller's kidneys are starting to hurt also.; On the second day, 17Dec2021, the caller almost passed out.; The caller doesn't know has to go to bathroom and all a sudden feels nothing just comes.; next day she started sweating really bad; After receiving booster dose vaccine back started hurting/ Felt like ripping spine out of body, like just pulling spine out.; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team for a Pfizer sponsored program (159558). The reporter is the patient. A 57 year-old female patient received bnt162b2 (BNT162B2), administered in arm right, administration date 16Dec2021 16:00 (Lot number: FD7218, Expiration Date: 28Feb2022) at the age of 57 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Asthma" (ongoing), notes: Has had asthma since the patient was young or little; "COVID-19", start date: 03Feb2021 (unspecified if ongoing); "pretty sick" (unspecified if ongoing), notes: pulmonologist said the patient should get the vaccine because the patient was pretty sick. Concomitant medication(s) included: XOLAIR taken for asthma (ongoing). Began taking 7 years ago, takes Xolair shots every other week. Vaccination history included: Bnt162b2 (lot: EW0153, Route of administration: right arm), administration date: 05Apr2021, when the patient was 56 years old, for COVID-19 immunization; Bnt162b2 (lot: EW0167, route of administration: right arm), administration date: 06May2021, when the patient was 57 years old, for COVID-19 immunization. The following information was reported: MYELITIS (non-serious), outcome "unknown", described as "describes the pain in her back as spinal acute myelitis in which it affects the nerves"; BACK PAIN (non-serious) with onset 16Dec2021 18:00, outcome "not recovered", described as "After receiving booster dose vaccine back started hurting/ Felt like ripping spine out of body, like just pulling spine out". The patient states that her spine feels like it did when she had COVID; RENAL DISORDER (non-serious) with onset 17Dec2021, outcome "unknown", described as "Starting to mess up kidneys"; PAIN IN EXTREMITY (non-serious), outcome "unknown", described as "the pain is migrating towards legs"; RENAL PAIN (non-serious) with onset 17Dec2021, outcome "unknown", described as "The caller's kidneys are starting to hurt also."; PRESYNCOPE (non-serious) with onset 17Dec2021, outcome "unknown", described as "On the second day, 17Dec2021, the caller almost passed out."; URINARY TRACT DISORDER (non-serious) with onset 17Dec2021, outcome "unknown", described as "The caller doesn't know has to go to bathroom and all a sudden feels nothing just comes."; HYPERHIDROSIS (non-serious) with onset 17Dec2021, outcome "unknown", described as "next day she started sweating really bad". The patient provided that she has consulted with her HCP yesterday and they plan to prescribe her IV steroids, run blood work, and have an MRI next Thursday. The patient states this was pretty serious. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Asthma (Has had asthma since the patient was young or little)
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19; Sickness (pulmonologist said the patient should get the vaccine because the patient was pretty sick.)
- Andere Medikamente
- XOLAIR
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 12.02.2022
- Impfdatum
- 15.12.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Abdominal pain
Axillary pain
Blood test
Body temperature
Breast pain
Arthralgia
Bundle branch block right
Cardiac monitoring
Burning sensation
Chest discomfort
Chest pain
Dizziness
Computerised tomogram normal
Dyspnoea
Echocardiogram normal
Echocardiogram
Electrocardiogram
Exercise tolerance decreased
Symptomtext
Peripheral neuropathy; Developed shortness of breath; a squeezing/tightness in the chest; Substantial exercise intolerance; cannot tolerate walking; Severe injection site and left arm pain; Severe injection site and left arm pain; Pain spread to the armpit, left breast,and chest; Pain spread to the armpit, left breast,and chest; Pain spread to the armpit, left breast,and chest; Fever of 101.9; pins and needles in the feet; burning calves; abdominal pain; lightheadedness; orthostatic tachycardia; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A 32-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 15Dec2021 (Lot number: FD7218) at the age of 32 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Acid reflux" (unspecified if ongoing); "Gall bladder removal" (unspecified if ongoing); "Endometriosis" (unspecified if ongoing); "Medication: Plan B pill" (unspecified if ongoing). There were no concomitant medications. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE, Batch/Lot No: EL1283, Location of injection: Arm Left, Route of Administration: Intramuscular), administration date: 2021, for COVID-19 Immunization; Bnt162b2 (DOSE 2, SINGLE, Batch/Lot No: EN5318, Location of injection: Arm Left, Route of Administration: Intramuscular), administration date: 2021, for COVID-19 Immunization. The following information was reported: PARAESTHESIA (disability), outcome "unknown", described as "pins and needles in the feet"; BURNING SENSATION (disability), outcome "unknown", described as "burning calves"; ABDOMINAL PAIN (disability), outcome "unknown", described as "abdominal pain"; DIZZINESS (disability), outcome "unknown", described as "lightheadedness"; TACHYCARDIA (disability), outcome "not recovered", described as "orthostatic tachycardia"; VACCINATION SITE PAIN (hospitalization, disability) with onset Dec2021, outcome "unknown", PAIN IN EXTREMITY (hospitalization, disability) with onset Dec2021, outcome "not recovered" and all described as "Severe injection site and left arm pain"; NEUROPATHY PERIPHERAL (hospitalization, disability, medically significant) with onset 16Dec2021 08:00, outcome "not recovered", described as "Peripheral neuropathy"; AXILLARY PAIN (hospitalization, disability), BREAST PAIN (hospitalization, disability), CHEST PAIN (hospitalization, disability) all with onset Dec2021, outcome "not recovered" and all described as "Pain spread to the armpit, left breast, and chest"; PYREXIA (hospitalization, disability) with onset Dec2021, outcome "recovered" (Dec2021), described as "Fever of 101.9"; DYSPNOEA (hospitalization, disability) with onset 16Dec2021 08:00, outcome "unknown", described as "Developed shortness of breath"; CHEST DISCOMFORT (hospitalization, disability) with onset 16Dec2021 08:00, outcome "unknown", described as "a squeezing/tightness in the chest"; EXERCISE TOLERANCE DECREASED (hospitalization, disability) with onset 16Dec2021 08:00, outcome "unknown", described as "Substantial exercise intolerance"; GAIT DISTURBANCE (hospitalization, disability) with onset 16Dec2021 08:00, outcome "unknown", described as "cannot tolerate walking". The patient was hospitalized for vaccination site pain, pain in extremity, neuropathy peripheral, axillary pain, breast pain, pyrexia, dyspnoea, chest discomfort, exercise tolerance decreased, gait disturbance (start date: 20Dec2021, discharge date: 20Dec2021, hospitalization duration: 1 day(s)); for chest pain (start date: 20Dec2021, discharge date: Dec2021, hospitalization duration: 1 day(s)). The events "pins and needles in the feet", "burning calves", "abdominal pain", "lightheadedness", "orthostatic tachycardia", "severe injection site and left arm pain", "severe injection site and left arm pain", "peripheral neuropathy", "pain spread to the armpit, left breast, and chest", "pain spread to the armpit, left breast, and chest", "pain spread to the armpit, left breast, and chest", "fever of 101.9", "developed shortness of breath", "a squeezing/tightness in the chest", "substantial exercise intolerance" and "cannot tolerate walking" were evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: blood test: (Dec2021) unknown results; body temperature: (Dec2021) 101.9; cardiac monitoring: (Dec2021) unknown results; echocardiogram: (Dec2021) unknown results; electrocardiogram: (Dec2021) unknown results; heart rate: (Dec2021) 120-130, notes: bpm, upon standing; troponin: (Dec2021) unknown results. Therapeutic measures were taken as a result of chest pain, dyspnoea. The patient had not received any other vaccines within 4 weeks prior to the COVID vaccine. There were no list of any other medications the patient received within 2 weeks of vaccination. The patient experienced severe injection site and left arm pain 12 hours post vaccination. Pain spread to the armpit, left breast, and chest by 24 hours post vaccination. The patient experienced fever of 101.9 at 24 hours post vaccination, and fever lasted about 6 hours. Chest pain increased in severity as arm, armpit, and breast pain decreased. First Emergency room (ER) visit on 17Dec2021 with complaints of chest pain. The patient developed shortness of breath and a squeezing/tightness in the chest in addition to sharp chest pain. The patient was admitted to the hospital on 20Dec2021 for observation. The patient developed additional symptoms following release from the hospital, including orthostatic tachycardia (120-130 bpm upon standing), lightheadedness, burning calves, abdominal pain, and pins and needles in the feet. Chest pain and shortness of breath were controlled with colchicine 0.6 mg 2x/day and bed rest but return within hours of the medication wearing off. Peripheral neuropathy and orthostatic tachycardia persist. The patient experienced substantial exercise intolerance and could not tolerate walking etc. Prior to vaccination, the patient was not diagnosed as COVID-19. Since the vaccination, the patient had not been tested for COVID-19. No follow-up attempts are needed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pericarditis
- Hospital-Tage
- 1,0
- Labordaten
- Test Date: 202112; Test Name: blood work; Result Unstructured Data: Test Result:Unknown results; Test Date: 202112; Test Name: Body temperature; Result Unstructured Data: Test Result:101.9; Test Date: 202112; Test Name: 24 heart monitoring; Result Unstructured Data: Test Result:Unknown results; Test Date: 202112; Test Name: Echocardiogram; Result Unstructured Data: Test Result:Unknown results; Test Date: 202112; Test Name: EKG; Result Unstructured Data: Test Result:Unknown results; Test Date: 202112; Test Name: Heart rate; Result Unstructured Data: Test Result:120-130; Comments: bpm, upon standing; Test Date: 202112; Test Name: troponin; Result Unstructured Data: Test Result:Unknown results
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Acid reflux (oesophageal); Drug allergy; Endometriosis; Gallbladder removal
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 12.02.2022
- Impfdatum
- 15.12.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Abdominal pain
Axillary pain
Blood test
Body temperature
Breast pain
Arthralgia
Bundle branch block right
Cardiac monitoring
Burning sensation
Chest discomfort
Chest pain
Dizziness
Computerised tomogram normal
Dyspnoea
Echocardiogram normal
Echocardiogram
Electrocardiogram
Exercise tolerance decreased
Symptomtext
Peripheral neuropathy; Developed shortness of breath; a squeezing/tightness in the chest; Substantial exercise intolerance; cannot tolerate walking; Severe injection site and left arm pain; Severe injection site and left arm pain; Pain spread to the armpit, left breast,and chest; Pain spread to the armpit, left breast,and chest; Pain spread to the armpit, left breast,and chest; Fever of 101.9; pins and needles in the feet; burning calves; abdominal pain; lightheadedness; orthostatic tachycardia; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A 32-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 15Dec2021 (Lot number: FD7218) at the age of 32 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Acid reflux" (unspecified if ongoing); "Gall bladder removal" (unspecified if ongoing); "Endometriosis" (unspecified if ongoing); "Medication: Plan B pill" (unspecified if ongoing). There were no concomitant medications. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE, Batch/Lot No: EL1283, Location of injection: Arm Left, Route of Administration: Intramuscular), administration date: 2021, for COVID-19 Immunization; Bnt162b2 (DOSE 2, SINGLE, Batch/Lot No: EN5318, Location of injection: Arm Left, Route of Administration: Intramuscular), administration date: 2021, for COVID-19 Immunization. The following information was reported: PARAESTHESIA (disability), outcome "unknown", described as "pins and needles in the feet"; BURNING SENSATION (disability), outcome "unknown", described as "burning calves"; ABDOMINAL PAIN (disability), outcome "unknown", described as "abdominal pain"; DIZZINESS (disability), outcome "unknown", described as "lightheadedness"; TACHYCARDIA (disability), outcome "not recovered", described as "orthostatic tachycardia"; VACCINATION SITE PAIN (hospitalization, disability) with onset Dec2021, outcome "unknown", PAIN IN EXTREMITY (hospitalization, disability) with onset Dec2021, outcome "not recovered" and all described as "Severe injection site and left arm pain"; NEUROPATHY PERIPHERAL (hospitalization, disability, medically significant) with onset 16Dec2021 08:00, outcome "not recovered", described as "Peripheral neuropathy"; AXILLARY PAIN (hospitalization, disability), BREAST PAIN (hospitalization, disability), CHEST PAIN (hospitalization, disability) all with onset Dec2021, outcome "not recovered" and all described as "Pain spread to the armpit, left breast, and chest"; PYREXIA (hospitalization, disability) with onset Dec2021, outcome "recovered" (Dec2021), described as "Fever of 101.9"; DYSPNOEA (hospitalization, disability) with onset 16Dec2021 08:00, outcome "unknown", described as "Developed shortness of breath"; CHEST DISCOMFORT (hospitalization, disability) with onset 16Dec2021 08:00, outcome "unknown", described as "a squeezing/tightness in the chest"; EXERCISE TOLERANCE DECREASED (hospitalization, disability) with onset 16Dec2021 08:00, outcome "unknown", described as "Substantial exercise intolerance"; GAIT DISTURBANCE (hospitalization, disability) with onset 16Dec2021 08:00, outcome "unknown", described as "cannot tolerate walking". The patient was hospitalized for vaccination site pain, pain in extremity, neuropathy peripheral, axillary pain, breast pain, pyrexia, dyspnoea, chest discomfort, exercise tolerance decreased, gait disturbance (start date: 20Dec2021, discharge date: 20Dec2021, hospitalization duration: 1 day(s)); for chest pain (start date: 20Dec2021, discharge date: Dec2021, hospitalization duration: 1 day(s)). The events "pins and needles in the feet", "burning calves", "abdominal pain", "lightheadedness", "orthostatic tachycardia", "severe injection site and left arm pain", "severe injection site and left arm pain", "peripheral neuropathy", "pain spread to the armpit, left breast, and chest", "pain spread to the armpit, left breast, and chest", "pain spread to the armpit, left breast, and chest", "fever of 101.9", "developed shortness of breath", "a squeezing/tightness in the chest", "substantial exercise intolerance" and "cannot tolerate walking" were evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: blood test: (Dec2021) unknown results; body temperature: (Dec2021) 101.9; cardiac monitoring: (Dec2021) unknown results; echocardiogram: (Dec2021) unknown results; electrocardiogram: (Dec2021) unknown results; heart rate: (Dec2021) 120-130, notes: bpm, upon standing; troponin: (Dec2021) unknown results. Therapeutic measures were taken as a result of chest pain, dyspnoea. The patient had not received any other vaccines within 4 weeks prior to the COVID vaccine. There were no list of any other medications the patient received within 2 weeks of vaccination. The patient experienced severe injection site and left arm pain 12 hours post vaccination. Pain spread to the armpit, left breast, and chest by 24 hours post vaccination. The patient experienced fever of 101.9 at 24 hours post vaccination, and fever lasted about 6 hours. Chest pain increased in severity as arm, armpit, and breast pain decreased. First Emergency room (ER) visit on 17Dec2021 with complaints of chest pain. The patient developed shortness of breath and a squeezing/tightness in the chest in addition to sharp chest pain. The patient was admitted to the hospital on 20Dec2021 for observation. The patient developed additional symptoms following release from the hospital, including orthostatic tachycardia (120-130 bpm upon standing), lightheadedness, burning calves, abdominal pain, and pins and needles in the feet. Chest pain and shortness of breath were controlled with colchicine 0.6 mg 2x/day and bed rest but return within hours of the medication wearing off. Peripheral neuropathy and orthostatic tachycardia persist. The patient experienced substantial exercise intolerance and could not tolerate walking etc. Prior to vaccination, the patient was not diagnosed as COVID-19. Since the vaccination, the patient had not been tested for COVID-19. No follow-up attempts are needed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pericarditis
- Hospital-Tage
- 1,0
- Labordaten
- Test Date: 202112; Test Name: blood work; Result Unstructured Data: Test Result:Unknown results; Test Date: 202112; Test Name: Body temperature; Result Unstructured Data: Test Result:101.9; Test Date: 202112; Test Name: 24 heart monitoring; Result Unstructured Data: Test Result:Unknown results; Test Date: 202112; Test Name: Echocardiogram; Result Unstructured Data: Test Result:Unknown results; Test Date: 202112; Test Name: EKG; Result Unstructured Data: Test Result:Unknown results; Test Date: 202112; Test Name: Heart rate; Result Unstructured Data: Test Result:120-130; Comments: bpm, upon standing; Test Date: 202112; Test Name: troponin; Result Unstructured Data: Test Result:Unknown results
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Acid reflux (oesophageal); Drug allergy; Endometriosis; Gallbladder removal
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 01.02.2022
- 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: ja
Dizziness
Loss of consciousness
Symptomtext
Within about 5 minutes of receiving the vaccine, Pt. Began feeling lightheaded and briefly lost consciousness. Pt was helped to the floor with assistance per mom and RN. She was out for approximately 45 seconds and quickly regained consciousness. Legs were elevated and pt began to feel better and sat up quickly.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- BP: 124/79 HR: 78 R: 18 02 sat= 100%
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 31.01.2022
- Impfdatum
- 21.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Condition aggravated
Dyspnoea
Heart rate increased
Paraesthesia
Paraesthesia oral
Generalised tonic-clonic seizure
Petit mal epilepsy
Presyncope
Seizure
Symptomtext
After receiving the booster shot (maybe after 5 minutes), I started feeling my lips and arms tingling, felt an increased heart rate, shortness in the breath and about to faint. Then, my seizures started. The medical staff took good care of me. I have not been diagnosed with epilepsy (yet!) but I have a history having seizures since I was a child.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Generalised tonic-clonic seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 31.01.2022
- Impfdatum
- 21.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Condition aggravated
Dyspnoea
Heart rate increased
Paraesthesia
Paraesthesia oral
Generalised tonic-clonic seizure
Petit mal epilepsy
Presyncope
Seizure
Symptomtext
After receiving the booster shot (maybe after 5 minutes), I started feeling my lips and arms tingling, felt an increased heart rate, shortness in the breath and about to faint. Then, my seizures started. The medical staff took good care of me. I have not been diagnosed with epilepsy (yet!) but I have a history having seizures since I was a child.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Generalised tonic-clonic seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 27.01.2022
- Impfdatum
- 29.12.2021
- Beginn
- 02.01.2022
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Activated partial thromboplastin time shortened
Alanine aminotransferase increased
Angiogram normal
Anion gap
Antidepressant drug level
Aspartate aminotransferase increased
Basophil count decreased
Basophil percentage decreased
Benzodiazepine drug level
Bilirubin urine
Blood albumin normal
Blood alkaline phosphatase normal
Blood bilirubin normal
Blood calcium normal
Blood chloride normal
Blood creatinine normal
Blood glucose normal
Blood magnesium normal
Symptomtext
booster; myalgia; chest pain, particularly with lying flat; EKG showed right bundle branch block; Cardiology performed a cardiac catheterization; mildly elevated left-sided filling pressures; mild anterolateral hypokinesis; suggestive of myocarditis; Increased WBC; Elevated D-dimer; Elevated LFT; Troponin 26.600; This is a spontaneous report received from a contactable reporter (Physician). A 19-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE),intramuscular, administered in arm left, administration date 29Dec2021 (Lot number: FD7218) at the age of 18 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. The patient did not have any allergies to medications, food, or other products. The patient did not receive any other vaccine within 4 weeks prior to the vaccine.There were no concomitant medications. Vaccination history included: Bnt162b2 (prev dose brand=Pfizer,, prev dose brand unknown=False, prev dose lot number=EN6205,, prev dose lot unknown=False,, prev dose administration date=16Mar2021, prev dose dose number=2), administration date: 16Mar2021, when the patient was 18 years old, for COVID-19 immunization; Bnt162b2 (prev dose product=COVID 19,, prev dose brand=Pfizer,, prev dose brand unknown=False,, prev dose lot number=EN6198,, prev dose lot unknown=False,, prev dose administration date=22Feb2021, prev dose dose_number=1), administration date: 22Feb2021, when the patient was 18 years old, for COVID-19 immunization. The following information was reported: IMMUNISATION (hospitalization) with onset 02Jan2022, outcome "recovering", described as "booster"; MYALGIA (hospitalization) with onset 02Jan2022, outcome "recovering", described as "myalgia"; CHEST PAIN (hospitalization) with onset 02Jan2022, outcome "recovering", described as "chest pain, particularly with lying flat"; BUNDLE BRANCH BLOCK RIGHT (hospitalization) with onset 02Jan2022, outcome "recovering", described as "EKG showed right bundle branch block"; CATHETERISATION CARDIAC (hospitalization) with onset 02Jan2022, outcome "recovering", described as "Cardiology performed a cardiac catheterization"; LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED (hospitalization) with onset 02Jan2022, outcome "recovering", described as "mildly elevated left-sided filling pressures"; VENTRICULAR HYPOKINESIA (hospitalization) with onset 02Jan2022, outcome "recovering", described as "mild anterolateral hypokinesis"; MYOCARDITIS (hospitalization) with onset 02Jan2022, outcome "recovering", described as "suggestive of myocarditis"; WHITE BLOOD CELL COUNT INCREASED (hospitalization) with onset 02Jan2022, outcome "recovering", described as "Increased WBC"; FIBRIN D DIMER INCREASED (hospitalization) with onset 02Jan2022, outcome "recovering", described as "Elevated D-dimer"; LIVER FUNCTION TEST INCREASED (hospitalization) with onset 02Jan2022, outcome "recovering", described as "Elevated LFT"; TROPONIN INCREASED (hospitalization) with onset 02Jan2022, outcome "recovering", described as "Troponin 26.600". The patient was hospitalized for immunisation, myalgia, chest pain, bundle branch block right, catheterisation cardiac, left ventricular end-diastolic pressure increased, ventricular hypokinesia, myocarditis, white blood cell count increased, fibrin d dimer increased, liver function test increased, troponin increased (hospitalization duration: 1 day(s)). The events "booster", "myalgia", "chest pain, particularly with lying flat", "ekg showed right bundle branch block", "cardiology performed a cardiac catheterization", "mildly elevated left-sided filling pressures", "mild anterolateral hypokinesis", "suggestive of myocarditis", "increased wbc", "elevated d-dimer","elevated lft" and "troponin 26.600" were evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: cardiac catheterization: (02Jan2022) normal coronaries but features of, notes: Cardiac catheterization showed normal coronaries but features of some mildly elevated left-sided filling pressures and mild anterolateral hypokinesis, ejection fraction 55%, suggestive of myocarditis, and the patient was admitted for further evaluation and treatment; ejection fraction: (02Jan2022) 55 %; electrocardiogram: (02Jan2022) right bundle branch block, notes: showed right bundle branch block and Cardiology performed a cardiac catheterization; fibrin d dimer: (02Jan2022) increased; liver function test: (02Jan2022) raised; mildly elevated left-sided filling pressures: (02Jan2022) increased; SARS-CoV-2 RNA Rapid Abbott: (02Jan2022) negative, notes: Nasal Swab; troponin: (02Jan2022) 26.600; white blood cell count: (02Jan2022) increased. Therapeutic measures were taken as a result of immunisation, myalgia, chest pain, particularly with lying flat, EKG showed right bundle branch block, Cardiology performed a cardiac catheterization, mildly elevated left-sided filling pressures, mild anterolateral hypokinesis, suggestive of myocarditis, white blood cell count increased, Elevated D-dimer, Elevated LFT (liver function test), Troponin 26.600. Treatment included Tylenol 1000 mg q.6 p.r.n. (as needed), Aspirin 81 mg daily, Colcrys 0.6 mg p.o (per oral) b.i.d (twice a day) for 1 week per "C" . Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient was covid tested post vaccination. Clinical course There is no history of any fever, rigors or chills. No history of headache, loss of consciousness, seizures. The troponins were elevated. ASSESSMENT: Chest pain, status post cardiac catheterization showing normal coronaries and possibly myocarditis with mild anterolateral hypokinesis. Recent COVID-19 booster vaccination, Pfizer.; Sender's Comments: Based on the information currently available, a possible contributory role of the suspect drug in the reported serious events cannot be completely ruled out given the known suspect drug profile and/or implied temporal association. 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 Regul atory Authorities, Ethics Committees and Investigators, as appropriate.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocarditis
- Hospital-Tage
- 1,0
- Labordaten
- Test Date: 20220102; Test Name: cardiac catheterization; Result Unstructured Data: Test Result:normal coronaries but features of; Comments: Cardiac catheterization showed normal coronaries but features of some mildly elevated left-sided filling pressures and mild anterolateral hypokinesis, ejection fraction 55%, suggestive of myocarditis, and the patient was admitted for further evaluation and treatment.; Test Date: 20220102; Test Name: ejection fraction; Test Result: 55 %; Test Date: 20220102; Test Name: EKG; Result Unstructured Data: Test Result:right bundle branch block; Comments: showed right bundle branch block and Cardiology performed a cardiac catheterization.; Test Date: 20220102; Test Name: D-dimer; Result Unstructured Data: Test Result:Increased; Test Date: 20220102; Test Name: LFT; Result Unstructured Data: Test Result:Raised; Test Date: 20220102; Test Name: mildly elevated left-sided filling pressures; Result Unstructured Data: Test Result:increased; Test Date: 20220102; Test Name: SARS-CoV-2 RNA Rapid Abbott; Test Result: Negative ; Comments: Nasal Swab; Test Date: 20220102; Test Name: Troponin; Result Unstructured Data: Test Result:26.600; Test Date: 20220102; Test Name: WBC; Result Unstructured Data: Test Result:Increased
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 27.01.2022
- Impfdatum
- 29.12.2021
- Beginn
- 02.01.2022
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Activated partial thromboplastin time shortened
Alanine aminotransferase increased
Angiogram normal
Anion gap
Antidepressant drug level
Aspartate aminotransferase increased
Basophil count decreased
Basophil percentage decreased
Benzodiazepine drug level
Bilirubin urine
Blood albumin normal
Blood alkaline phosphatase normal
Blood bilirubin normal
Blood calcium normal
Blood chloride normal
Blood creatinine normal
Blood glucose normal
Blood magnesium normal
Symptomtext
booster; myalgia; chest pain, particularly with lying flat; EKG showed right bundle branch block; Cardiology performed a cardiac catheterization; mildly elevated left-sided filling pressures; mild anterolateral hypokinesis; suggestive of myocarditis; Increased WBC; Elevated D-dimer; Elevated LFT; Troponin 26.600; This is a spontaneous report received from a contactable reporter (Physician). A 19-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE),intramuscular, administered in arm left, administration date 29Dec2021 (Lot number: FD7218) at the age of 18 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. The patient did not have any allergies to medications, food, or other products. The patient did not receive any other vaccine within 4 weeks prior to the vaccine.There were no concomitant medications. Vaccination history included: Bnt162b2 (prev dose brand=Pfizer,, prev dose brand unknown=False, prev dose lot number=EN6205,, prev dose lot unknown=False,, prev dose administration date=16Mar2021, prev dose dose number=2), administration date: 16Mar2021, when the patient was 18 years old, for COVID-19 immunization; Bnt162b2 (prev dose product=COVID 19,, prev dose brand=Pfizer,, prev dose brand unknown=False,, prev dose lot number=EN6198,, prev dose lot unknown=False,, prev dose administration date=22Feb2021, prev dose dose_number=1), administration date: 22Feb2021, when the patient was 18 years old, for COVID-19 immunization. The following information was reported: IMMUNISATION (hospitalization) with onset 02Jan2022, outcome "recovering", described as "booster"; MYALGIA (hospitalization) with onset 02Jan2022, outcome "recovering", described as "myalgia"; CHEST PAIN (hospitalization) with onset 02Jan2022, outcome "recovering", described as "chest pain, particularly with lying flat"; BUNDLE BRANCH BLOCK RIGHT (hospitalization) with onset 02Jan2022, outcome "recovering", described as "EKG showed right bundle branch block"; CATHETERISATION CARDIAC (hospitalization) with onset 02Jan2022, outcome "recovering", described as "Cardiology performed a cardiac catheterization"; LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED (hospitalization) with onset 02Jan2022, outcome "recovering", described as "mildly elevated left-sided filling pressures"; VENTRICULAR HYPOKINESIA (hospitalization) with onset 02Jan2022, outcome "recovering", described as "mild anterolateral hypokinesis"; MYOCARDITIS (hospitalization) with onset 02Jan2022, outcome "recovering", described as "suggestive of myocarditis"; WHITE BLOOD CELL COUNT INCREASED (hospitalization) with onset 02Jan2022, outcome "recovering", described as "Increased WBC"; FIBRIN D DIMER INCREASED (hospitalization) with onset 02Jan2022, outcome "recovering", described as "Elevated D-dimer"; LIVER FUNCTION TEST INCREASED (hospitalization) with onset 02Jan2022, outcome "recovering", described as "Elevated LFT"; TROPONIN INCREASED (hospitalization) with onset 02Jan2022, outcome "recovering", described as "Troponin 26.600". The patient was hospitalized for immunisation, myalgia, chest pain, bundle branch block right, catheterisation cardiac, left ventricular end-diastolic pressure increased, ventricular hypokinesia, myocarditis, white blood cell count increased, fibrin d dimer increased, liver function test increased, troponin increased (hospitalization duration: 1 day(s)). The events "booster", "myalgia", "chest pain, particularly with lying flat", "ekg showed right bundle branch block", "cardiology performed a cardiac catheterization", "mildly elevated left-sided filling pressures", "mild anterolateral hypokinesis", "suggestive of myocarditis", "increased wbc", "elevated d-dimer","elevated lft" and "troponin 26.600" were evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: cardiac catheterization: (02Jan2022) normal coronaries but features of, notes: Cardiac catheterization showed normal coronaries but features of some mildly elevated left-sided filling pressures and mild anterolateral hypokinesis, ejection fraction 55%, suggestive of myocarditis, and the patient was admitted for further evaluation and treatment; ejection fraction: (02Jan2022) 55 %; electrocardiogram: (02Jan2022) right bundle branch block, notes: showed right bundle branch block and Cardiology performed a cardiac catheterization; fibrin d dimer: (02Jan2022) increased; liver function test: (02Jan2022) raised; mildly elevated left-sided filling pressures: (02Jan2022) increased; SARS-CoV-2 RNA Rapid Abbott: (02Jan2022) negative, notes: Nasal Swab; troponin: (02Jan2022) 26.600; white blood cell count: (02Jan2022) increased. Therapeutic measures were taken as a result of immunisation, myalgia, chest pain, particularly with lying flat, EKG showed right bundle branch block, Cardiology performed a cardiac catheterization, mildly elevated left-sided filling pressures, mild anterolateral hypokinesis, suggestive of myocarditis, white blood cell count increased, Elevated D-dimer, Elevated LFT (liver function test), Troponin 26.600. Treatment included Tylenol 1000 mg q.6 p.r.n. (as needed), Aspirin 81 mg daily, Colcrys 0.6 mg p.o (per oral) b.i.d (twice a day) for 1 week per "C" . Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient was covid tested post vaccination. Clinical course There is no history of any fever, rigors or chills. No history of headache, loss of consciousness, seizures. The troponins were elevated. ASSESSMENT: Chest pain, status post cardiac catheterization showing normal coronaries and possibly myocarditis with mild anterolateral hypokinesis. Recent COVID-19 booster vaccination, Pfizer.; Sender's Comments: Based on the information currently available, a possible contributory role of the suspect drug in the reported serious events cannot be completely ruled out given the known suspect drug profile and/or implied temporal association. 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 Regul atory Authorities, Ethics Committees and Investigators, as appropriate.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocarditis
- Hospital-Tage
- 1,0
- Labordaten
- Test Date: 20220102; Test Name: cardiac catheterization; Result Unstructured Data: Test Result:normal coronaries but features of; Comments: Cardiac catheterization showed normal coronaries but features of some mildly elevated left-sided filling pressures and mild anterolateral hypokinesis, ejection fraction 55%, suggestive of myocarditis, and the patient was admitted for further evaluation and treatment.; Test Date: 20220102; Test Name: ejection fraction; Test Result: 55 %; Test Date: 20220102; Test Name: EKG; Result Unstructured Data: Test Result:right bundle branch block; Comments: showed right bundle branch block and Cardiology performed a cardiac catheterization.; Test Date: 20220102; Test Name: D-dimer; Result Unstructured Data: Test Result:Increased; Test Date: 20220102; Test Name: LFT; Result Unstructured Data: Test Result:Raised; Test Date: 20220102; Test Name: mildly elevated left-sided filling pressures; Result Unstructured Data: Test Result:increased; Test Date: 20220102; Test Name: SARS-CoV-2 RNA Rapid Abbott; Test Result: Negative ; Comments: Nasal Swab; Test Date: 20220102; Test Name: Troponin; Result Unstructured Data: Test Result:26.600; Test Date: 20220102; Test Name: WBC; Result Unstructured Data: Test Result:Increased
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 24.01.2022
- Impfdatum
- 14.12.2021
- Beginn
- 22.01.2022
- Tage bis Beginn
- 39,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Anticoagulant therapy
Dyspnoea exertional
Electrocardiogram
Laboratory test
Magnetic resonance imaging
Pain in extremity
Pulmonary thrombosis
Thrombosis
Symptomtext
Began having pain in right leg by 12/22/2021. On 01/21/2022 began having severe shortness of breath when walking. On 1/22, taken to Emergency Room at Hospital and admitted for blood clot in lung. Also, many blood clots found in right leg. Doctors could find no reason for the blood clots. After thinking about it, realized that the pain in the leg had begun shortly after receiving the third COVID Vaccine. Currently still in Hospital receiving Heparin and Oxygen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary thrombosis
- Hospital-Tage
- -
- Labordaten
- 01/22/2022 - Hospital ER - EKG, MRI, etc.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Amoxicillin
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 18.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 16.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Chest pain
Echocardiogram abnormal
Myocarditis
Pericardial effusion
Tachycardia
Troponin I increased
Symptomtext
chest pain after 2 days of injection, diagnosed to be myopericarditis.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocarditis
- Hospital-Tage
- 2,0
- Labordaten
- raised Troponin I; Echocardiogram shows pericardial effusion; persisting tachycardia;
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 18.01.2022
- Impfdatum
- 14.12.2021
- Beginn
- 14.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood bilirubin normal
Blood creatinine normal
Blood glucose normal
Blood potassium normal
Blood sodium normal
Blood urea normal
Haematocrit normal
Haemoglobin decreased
Loss of consciousness
Platelet count normal
White blood cell count normal
Symptomtext
Passed Out, Ambulance, Hospital (four days)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- hemoglobin 13.2 gm/dL, hematocrit 42.5, WBC Count 5.36 thou cummin, platelet count -267 thou cummin, sodium level - 138 mEqL potassium level - 4.4/ mEq/L, Creatinine 0.83 mg/dl, BuN 14 mg/dL, Total Bilirubin 0.5 mg/dl. Glucose Level 92 mg/dL
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- allopurinol,, aspirin, losartan, atorvastatin
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 17.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Loss of consciousness
Nausea
Tremor
Symptomtext
Patient passed out within minutes of receiving Pfizer Covid booster and flu immunization. Patient became nauseous and light headed and then started to shake. She quickly became unconscious and was lowered to the ground without incident. Patient regained consciousness within 30 seconds. Patient's feet were elevated and she remained in a lying position until nausea and lightheadedness subsided. Patient was offered lemonade once she sat up. She was monitored in the store for 45 minutes and fully recovered. Patient denied the need to call 911. Patient has a history of fainting and did so with her 1st COVID vaccine as well.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Anxiety disorder
- Andere Medikamente
- Escitalopram 20mg
- Allergien
- NONE
- Vorherige Impfungen
- Passed out after 1st Pfizer vaccine at a different facility, exact date unknown.
- Staat
- TX
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 12.01.2022
- Impfdatum
- 29.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Condition aggravated
Echocardiogram
Electrocardiogram
Implantable defibrillator insertion
Resuscitation
Syncope
Troponin
Ventricular tachycardia
Symptomtext
The day following the third COVID vaccine, the patient had a syncopal episode at home. This is presumeably secondary to ventricular tachycardia secondary to the patient's prolonged QT syndrome. The patient responded to a sharp cardiac thump and 911 was activated. The patient had not had a syncopal episode in two years since initial diagnosis until this event occurred a day following her booster. The patient was admitted and had a AICD placed
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- 6,0
- Labordaten
- ECHO cardiac Serial EKGs Troponin
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Prolonged QT Interval
- Andere Medikamente
- Nadolol 60 mg QD Paxil 10 mg QD
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 08.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dysarthria
Muscle rigidity
Musculoskeletal stiffness
Nausea
Paraesthesia
Seizure
Syncope
Symptomtext
Approximately 5 minutes following his vaccine, patient began signs of fainting or possible seizure activity due to rigid body, slurred speech, neck stiffening, tingling in fingers, nausea. this lasted approximately 10 minutes. 911 was immediately called. Patient was accessed and had a heart rate of 50 and a blood pressure of 96. It was recommended that he go to the hospital for an evaluation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 08.01.2022
- Impfdatum
- 19.12.2021
- Beginn
- 20.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Adverse event
Dizziness
Nausea
Symptom recurrence
Chills
Dysstasia
Presyncope
Pyrexia
Symptomtext
almost fainted; two episodes of extreme dizziness (almost fainted); low grade fever; Chills; could not stand; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. 34 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 19Dec2021 14:00 (Lot number: Fd7218) at the age of 34 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Gerd" (unspecified if ongoing); "anxiety" (unspecified if ongoing); "covid-19" (unspecified if ongoing), notes: prior vaccination. Concomitant medication(s) included: PROTONIX [OMEPRAZOLE]; PEPCID [FAMOTIDINE]; LEXAPRO. Past drug history included: Bactroban, reaction(s): "Known allergies"; Keflex, reaction(s): "Known allergies"; Amoxicillin, reaction(s): "Known allergies"; Erythromycin, reaction(s): "Known allergies". Vaccination history included: Bnt162b2 (Dose 1, single, at 02:00 PM administered in arm left, Lot Number: Ew0183), administration date: 18Nov2021, when the patient was 34 years old, for COVID-19 Immunization. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The following information was reported: PRESYNCOPE (medically significant) with onset 20Dec2021 05:45, outcome "unknown", described as "almost fainted"; DIZZINESS (non-serious) with onset 20Dec2021 05:45, outcome "unknown", described as "two episodes of extreme dizziness (almost fainted)"; PYREXIA (non-serious) with onset 20Dec2021 05:45, outcome "unknown", described as "low grade fever"; CHILLS (non-serious) with onset 20Dec2021 05:45, outcome "unknown", described as "Chills"; DYSSTASIA (non-serious) with onset 20Dec2021 05:45, outcome "recovered" (20Dec2021 20:45), described as "could not stand". The patient could not stand about 15 hours after 2nd dose. Therapeutic measures were not taken as a result of presyncope, dizziness, pyrexia, chills, dysstasia. The patient was not tested for covid post vaccination. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Anxiety; COVID-19 (prior vaccination); GERD
- Andere Medikamente
- PROTONIX [OMEPRAZOLE]; PEPCID [FAMOTIDINE]; LEXAPRO
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 08.01.2022
- Impfdatum
- 19.12.2021
- Beginn
- 20.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Adverse event
Dizziness
Nausea
Symptom recurrence
Chills
Dysstasia
Presyncope
Pyrexia
Symptomtext
almost fainted; two episodes of extreme dizziness (almost fainted); low grade fever; Chills; could not stand; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. 34 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 19Dec2021 14:00 (Lot number: Fd7218) at the age of 34 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Gerd" (unspecified if ongoing); "anxiety" (unspecified if ongoing); "covid-19" (unspecified if ongoing), notes: prior vaccination. Concomitant medication(s) included: PROTONIX [OMEPRAZOLE]; PEPCID [FAMOTIDINE]; LEXAPRO. Past drug history included: Bactroban, reaction(s): "Known allergies"; Keflex, reaction(s): "Known allergies"; Amoxicillin, reaction(s): "Known allergies"; Erythromycin, reaction(s): "Known allergies". Vaccination history included: Bnt162b2 (Dose 1, single, at 02:00 PM administered in arm left, Lot Number: Ew0183), administration date: 18Nov2021, when the patient was 34 years old, for COVID-19 Immunization. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The following information was reported: PRESYNCOPE (medically significant) with onset 20Dec2021 05:45, outcome "unknown", described as "almost fainted"; DIZZINESS (non-serious) with onset 20Dec2021 05:45, outcome "unknown", described as "two episodes of extreme dizziness (almost fainted)"; PYREXIA (non-serious) with onset 20Dec2021 05:45, outcome "unknown", described as "low grade fever"; CHILLS (non-serious) with onset 20Dec2021 05:45, outcome "unknown", described as "Chills"; DYSSTASIA (non-serious) with onset 20Dec2021 05:45, outcome "recovered" (20Dec2021 20:45), described as "could not stand". The patient could not stand about 15 hours after 2nd dose. Therapeutic measures were not taken as a result of presyncope, dizziness, pyrexia, chills, dysstasia. The patient was not tested for covid post vaccination. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Anxiety; COVID-19 (prior vaccination); GERD
- Andere Medikamente
- PROTONIX [OMEPRAZOLE]; PEPCID [FAMOTIDINE]; LEXAPRO
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 05.01.2022
- Impfdatum
- 29.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Fall
Impaired driving ability
Malaise
Mobility decreased
Muscle spasms
Nausea
Peripheral swelling
Rash macular
Syncope
Vomiting
Symptomtext
Wednesday - 12/29/21 Day of Vaccine - One hour and 20 minutes after vaccine - Nausea and vomiting , muscle spasms to arms and legs Could not drive home from a store - called wife to pick him up. Placed heating pad on at home - drank 2 sport drinks for hydration. Fell asleep. After 2 hours awakened with visible muscle spasms to arms and legs. Right forearm is swollen. Thursday - 12/30/21 - Muscle spasms continue - fell putting pants on. Went to local Emergency room at 0630 - Was given Ativan, Tylenol and Ibuprofen and a nausea med. Friday - 12-31-21 - In bed all day - muscle spasms continue - nausea continues - Saturday 01/01/22 - Out of bed - eating lightly - spasms continue Sunday 01/02/22 - Nausea - eating lightly - spasms less - continue Monday 01/03/22 - Went to work - eating lightly - spasms continue Tuesday 01/04/22 - AT work - eating lightly - spasms continue. 1"-2" red blotchy patches form on arms and legs. Ate a full meal. Wednesday 01/05/22 - At work- faint red patches remain to arms - left swollen forearm is new symptom. Spasms continue. Feeling ill. Recommend going to ER or Personal Physician. Left work in stable condition per self. States he is OK to drive himself home or to the doctors office
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- Unknown
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- Pfizer vaccine #2 - 50 years old
- Staat
- FL
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 03.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Syncope
Symptomtext
Patient stated she had issues in the past with passing out from vaccines. She said she did fine with the first 2 doses of the COVID-19 Pfizer vaccine. After vaccination, patient was lightheaded so we had her remain seated. She took a sip of water from her bottle and was breathing in and out to calm herself. After a few minutes, patient's eyes closed and she fainted in the seat. I was able to get to the patient and hold her. We called for emergency services to come in and evaluate her. I remained with patient until they arrived. They evaluated her and deemed her ok to go home. Patient was able to walk out on her own after being evaluated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- Unknown what was done by EMS.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- Fainting.
- Staat
- NY
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 02.01.2022
- Impfdatum
- 23.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 5,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Abnormal behaviour
Agitation
Blood lactic acid
Chest X-ray
Coagulation test
Computerised tomogram head
Confusional state
Echocardiogram
Electroencephalogram
Fall
Foaming at mouth
Full blood count
Generalised tonic-clonic seizure
Laboratory test
Magnetic resonance imaging head
Magnetic resonance imaging spinal
Patient elopement
Patient restraint
Symptomtext
Seizures I was found wandering naked outside the house at 5:40-6 AM. I was let in the home and said I had to pee repeatedly, going to the bathroom 3-4 times in about 10 minutes. My mother in law called my wife and and she brought me to the bedroom. She saw I was confused and the room I was sleeping in was in disarray. She was concerned but I thought I had probably been sleepwalking. She is a night nurse so she went to sleep but stayed with me due to the strange occurrence. We typically sleep apart right now due to the covid surge. Around 1245 PM my wife awoke to me seizing. I had a tonic clonic seizure. I was foaming into my CPAP mask and wet the bed with urine. My wife pulled off my CPAP and ran into the house to alert her parents to call 911. When she returned 20-30 sec later I had fallen onto the floor and knocked my bed to the side. She held me to the side and I was still seizing when EMS arrived. I did not respond to sternal rub. EMS brought me to the hospital and I needed to be sedated and restrained as I was extremely confused and agitated after the event. They tried versed x2 and finally ketamine IM to sedate me. I received fluids, IV antibiotics, IV keppra, IV tylenol and IV muscle relaxers. I know I had another unwitnessed seizure earlier that morning due to the pattern of disarray in the room after the second witnessed seizure. I had fallen out of the bed both times.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Generalised tonic-clonic seizure
- Hospital-Tage
- 2,0
- Labordaten
- 12/28-12/29 CBC, Coagulation labs, urinalysis, chemistry labs, lactic acid, CXR, cardiac labs, brain CT, brain MRI, spine MRI, EEG, Echocardiogram Lactic acid initially was 7.1 Troponins initially were 496. Trended down to 132 over the hospital stay.
- Aktuelle Erkrankungen
- Chronic persistent neuropathic pain bilateral hips, legs, feet
- Vorgeschichte
- Anxiety, depression, autism spectrum disorder, multi level spinal fusion L4-S1 Sep 2021, spinal fusion L4-L5 Dec 2020, microdiscectomy x2 May and June 2020.
- Andere Medikamente
- Clonidine 0.2mg 3x day, Paroxetine HCL 50 mg daily, Quetiapine Fumarate 100 mg daily, multivitamin, medical marijuana (registered user).
- Allergien
- Ceclor and ciprofloxacin (hives)
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 29.12.2021
- Impfdatum
- 29.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cold sweat
Pallor
Syncope
Symptomtext
PATIENT FAINTED ABOUT 15 FEET FROM WHERE HE WAS SITTING
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- EMT'S WE'RE CALLED. BLOOD PRESSURE WAS TAKEN. CUSTOMER WAS COLD, PALE, AND CLAMMY
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- PENICILLINS
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 28.12.2021
- Impfdatum
- 28.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Agonal respiration
Disorientation
Electrocardiogram
Heart rate decreased
Hypotension
Hypotonia
Loss of consciousness
Mydriasis
Slow speech
Unresponsive to stimuli
Symptomtext
PATIENT WAS SEEN TO BE PASSED OUT ON CHAIR, FLACCID ABOUT 4 MINS POST INJECTION. WHEN ATTEMPTED TO AROUSE, PATIENT WAS NOT RESPONSIVE, STILL BREATHING INDEPENDENTLY. STERNAL RUBBED, NO RESPONSE. REPOSITIONED AND WITNESSED AGONAL BREATHING. JAW-THRUSTED MOUTH. STAT NURSE PAGED OVERHEAD. APPLIED OXYGEN TO PATIENT VIA NASAL CANNULA. 911 CALLED. PT DISORIENTED AND SLOW TO SPEECH WITH EYES DILATED. DURATION OF VASOVAGAL: 30 SECONDS TO 1 MINUTE. PLACED IV, ADMINISTERED 1L OF NORMAL SALINE. CONTINUOUS BLOOD PRESSURE MONITORING AND PULSE OX. OBSERVED LOW BP 60S/30S WITH LOW HR OF 40S. PARAMEDICS PERFORMED EKG. AFTER 500 ML OF NORMAL SALINE ADMINISTERED BP REACHED 100S/70S. PATIENT WAS TRANSFERRED TO HIGH LEVEL OF ACUITY FACILITY WITH CONSENT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- EKG UNKNOWN RESULT.
- Aktuelle Erkrankungen
- patient reported none
- Vorgeschichte
- patient reported none
- Andere Medikamente
- patient reported none
- Allergien
- patient reported none
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 28.12.2021
- Impfdatum
- 13.12.2021
- Beginn
- 13.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anaphylactic reaction
Immunisation
Pain
Symptomtext
Anaphlylactic reaction; booster; Aches and pains; This is a spontaneous report received from a contactable reporter, Consumer. A 57-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 13Dec2021 15:15 (Lot number: FD7218) at the age of 57 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Allergies: Seafood" (unspecified if ongoing); "Allergies: Iodine" (unspecified if ongoing). There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EN6206, Route of Administration: Intramuscular, Location of injection: Arm Left, Vaccine Administration Time: 08:45 AM), administration date: 24Mar2021, when the patient was 57 years old, for COVID-19 Immunization, reaction: body aches; Bnt162b2 (lot number =EN5318,, administration time=09:30 AM,, vaccine location =Left arm., dose number=1), administration date: 02Mar2021, when the patient was 57 years old, for COVID-19 Immunization. The following information was reported: anaphylactic reaction (medically significant) with onset 13Dec2021 15:30, outcome recovered (Dec2021); immunisation (medically significant) with onset 13Dec2021 15:30, outcome recovered (Dec2021); pain (non-serious) with onset 13Dec2021 15:30, outcome recovered (Dec2021), described as "Aches and pains". Therapeutic measures were not taken as a result of anaphylactic reaction, immunisation, pain.; Sender's Comments: Linked Report(s) : PFIZER INC-2021325756 Same patient, different dose and event.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anaphylactic reaction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Iodine allergy; Seafood allergy
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 27.12.2021
- Impfdatum
- 27.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Feeling hot
Loss of consciousness
Symptomtext
Pt felt dizzy and then passed out for approx. 45 seconds then came too and complained of being very hot. EMS was called and she was checked out but refused to go to hospital. She left with her brother.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- prior history of passing out after vaccines
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- augmentin
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 27.12.2021
- Impfdatum
- 27.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syncope
Symptomtext
Patient fainted
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 27.12.2021
- Impfdatum
- 27.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Heart rate increased
Loss of consciousness
Symptomtext
pt waited her 15 minutes. walked outside then returned to take son to the restroom. said her heart started beating fast then she passed out in front of the pharmacy. we were able to wake pt within a minute or 2. Store manager called 911. pt was dizzy but after20 to 30 minutes was able to leave the pharmacy with her husband. pt did not need to go to the hospital
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 22.12.2021
- Impfdatum
- 22.02.2021
- Beginn
- 22.02.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syncope
Symptomtext
patient receive covid-19 pfizer after 15 minutes upon leaving the store patient faint at the front of the entrance
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- Ambulance came & check out patient
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- no
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 22.12.2021
- Impfdatum
- 22.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syncope
Symptomtext
fainted while waiting after vaccination
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 22.12.2021
- Impfdatum
- 22.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Seizure
Symptomtext
on site, she had seizure
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 22.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Feeling hot
Flushing
Hyperhidrosis
Seizure
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Severe, Systemic: extremely hot but temp was not taken during event-Severe, Systemic: Flushed / Sweating-Severe, Systemic: Seizure-Mild, Additional Details: Patient warned of probable fainting. He fainted after his flu shot. He was fine immediately after shot then 6-7 minutes later patient passet out leaning against his father. Within 10 seconds patient began to seize (arched bac and arms and legs drew up. This lastes only a few seconds and patient was immediately able to speak coherently but stated he was very light headed. Patient was very warm. He was given bottle of cold water and an ice pack which was placed on his neck. ems declined
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 21.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Electrocardiogram ST segment depression
Syncope
Symptomtext
01:43 PM: client was seating in seat and fainted, was put on the floor on a mat, director POD, EMS and dr present, Legs elevated on a chair.. V/S:114/74, pls at 45/min and SAT at 99%. 01:47 PM V/S at 125/73 pls at 57/min and SAT at 100%. At 01 53 PM: client seat on a chair, feel better,, V/S at 102/70, pls at 62/min, and SAT at 97%. At 01:56 PM, client eating snack and then start feeling dizzy again. )1 58 PM : patient lay down flat, 4 lead EKG done, pls at 49/min,, 114/66, Sat at 99%. At 02:00PM, 12 lead EKG done, Pls at 53/min, 124/80, SAT at 100%. Doctor notice ST depression in EKG. At 02:10 PM, patient feel better,, seat upwright, 02: 22PM: 121/75, PLS at 55/min and SAT at 98%. client in chair and feel good. At 02 29 PM patient stand up, at 02: 30PM: 115/78, PLS at 66/min and SAT 98%, client is now discharge
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- 12 lead EKG
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- had heart surgery 5 years ago to replace valve
- Andere Medikamente
- Metropolol, Liptor, aspirine
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 21.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Feeling abnormal
Feeling hot
Immediate post-injection reaction
Nausea
Pallor
Posture abnormal
Presyncope
Symptomtext
1222PM nurse approached pt. noted with pallor and uncomfortable posture. Patient reported nausea. Pt reported she felt "weird" after the vaccine administered. MD approached and assessed patient. no diaphoresis, no fever, no chills, no reports of blurry vision, no swelling of throat or arm. 1223 pt was rested on ground with feet up on chair. No past medical history. No more reports of lightheaded when laying down. Reports having food. No history of allergies and Doctor states likely to have vasovagal response. Pt reports taking delaxine 2% ointment. No issues in first 2 vaccines. She experienced nausea and feeling hot immediately following vaccine. 1229 color returning to face while supine. nausea subsided an no dizziness or lightheaded. 1232 sat up with no issues. sat into chair with assistance. reported feeling better. 1236 cleared by doctor. no weakness and color back. left ambulatory.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- delaxin 2% ointment
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 21.12.2021
- Impfdatum
- 14.12.2021
- Beginn
- 14.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hyperhidrosis
Syncope
Symptomtext
Patient received Pfizer booster of COVID vaccine. She had a syncopal episode and diaphoresis
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- Vital signs
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 20.12.2021
- Impfdatum
- 19.12.2021
- Beginn
- 19.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syncope
Symptomtext
NP was alerted that pt had an episode of syncope immediately following Pfizer booster dose while seated on exam chair. Pt regained consciousness immediately. Alert and oriented at this time. Pt denies symptoms or respiratory distress and all other symptoms at this time. She states she has a history of syncopal episodes after vaccination. Vitals stable: Bp 132/80, p 61/ o2 99%. Repeat vitals 10 minutes later: bp 135/75, p 63, o299%. Pt denies dizziness when standing, then when ambulating. Pt assisted to observation area without further incident.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 20.12.2021
- Impfdatum
- 20.12.2021
- Beginn
- 20.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Hyperhidrosis
Loss of consciousness
Seizure
Symptomtext
Dizzy, sweating, seizing, passing out. Administered Epi Pen and called 911. Patient later taken to Hospital by a friend.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- none given
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 20.12.2021
- Impfdatum
- 19.12.2021
- Beginn
- 19.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chills
Confusional state
Dizziness
Flushing
Hyperhidrosis
Nausea
Syncope
Unresponsive to stimuli
Vomiting
Symptomtext
Systemic: Chills-Medium, Systemic: Confusion-Medium, Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Severe, Systemic: Flushed / Sweating-Severe, Systemic: Nausea-Severe, Systemic: Vomiting-Severe, Additional Details: Patient received first dose of Pfizer vaccine by pharmacist with no issues/complaints. During the 15min observation period, patient noted she was dizzy and requested some water. Pharmacist immediately brought her back into the vaccination room to sit down and observe closer, at which point she slumped back in chair, tensed up & did not respond to verbal cues. EMS was called, and patient began vomiting upon coming to.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 19.12.2021
- Impfdatum
- 10.12.2021
- Beginn
- 10.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal pain
Chest pain
Chills
Discomfort
Dizziness
Dyspnoea
Electrocardiogram abnormal
Gait disturbance
Hyperhidrosis
Moaning
Pain
Presyncope
Sinus tachycardia
Syncope
Symptomtext
Narrative: Medical response was called sometime before 1100. Medical response call indicated 1st floor bathroom. Writer arrived to scene to find patient laying on floor of handicap bathroom stall. He was laying on his left side with rt arm over his head.He was diaphoretic and shivering. Moaning in pain. He c/o SOB,dizziness, and abd pain. It was difficult to ask him questions initially due to other patients in the restroom and patient repeating,"I just got my booster! I just got my booster!" Initially said "yes" when asked if he fell. It was undetermined whether he had fallen. Connected patient to pulse oximeter. He was saturating 97% and Hr was fluctuating between 115-130bpm. 911 called immediately. Patient was perspiring profusely. Stated that he had SOB, but denied closing of throat or swelling of tongue. He was unable to describe or rate pain, simply stating, "My stomach hurts really bad." Unable to give health history. Denied being diabetic. Medical Response Note for Clinics with Emergency Response Boxes REASON FOR THE EMERGENCY RESPONSE: [ ] chest pain [X] dyspnea [ ] syncope or near syncope [X] dizziness [X] Possible fall [ ] other (specify) Comments: SITE: SETTING: [ ] Patient care area [ ] Registration area [ ] Lobby [ ] Lab [ ] Parking lot [X] Other (specify)1st floor restroom. VITALS VS were obtatined by FD BP:219/112 Temp: Heart Rate:115 Respirations:22 Pain level:Unable to rate. Severe Pulse Ox: 97 on room air INTERVENTIONS (Enter items which apply): [X] Paramedics called. Time Called:11:10 Time Arrived: [ ] Paramedics called but cancelled by (name of Provider): [ ] Automatic External Defibrillator (AED) used: [ ] OXYGEN [ ] Oxygen by nasal cannula _____liters/min. [ ] Face mask _____liters/min. [X] EKG performed by FD. Sinus tach per paramedics. [ ] IV 500 cc 0.9% Normal Saline ______rate. [X] IV saline lock. #22 left hand inserted by writer. [ ] MEDICATIONS given per Provider Verbal Order: [ ] ALBUTEROL oral inhaler. _____puffs by oral inhalation. [ ] ASPIRIN chewable 81 mg tablets. Administered ___ mg. [ ] Diphenhydramine (BENADRYL) 50 mg/ml IM. Administered _____ mg I.M. [ ] Naloxone (NARCAN) 0.4 mg/ml . Administered ______ mg by ___(route). [ ] Repeated NARCAN _____ mg by ____(route) Times administered: [ ] NITROGLYCERIN Sublingual 0.4 mg. Times administered: 1st dose: ___2nd dose___3rd dose___ [ ] EPINEPHRINE 0.3 mg/0.3 ml. Injection. Administered 0.3 mg I.M. Time administered: [ ] Repeat EPINEPHRINE 0.3 mg/0.3 ml. Administer 0.3 mg I.M. Time administered: ___ [ ] GLUCOSE GEL 37.5 gm tube: administered ____ Tube(s) P.O. Time administered: [X] Accucheck Performed by FD=300+ [ ] Repeat GLUCOSE GEL 37.5 gm tube: Administer _____Tube(s)P.O. Time administered: [ ] Accucheck (prior Blood Sugar value if known) ___mg/dl [ ] GLUCAGON 1 mg. Injected 1 mg by ___(route). Time administered: ______ [ ] Accucheck (prior Blood Sugar valve if known______mg/dl [ ] OTHER INTERVENTIONS: Comments/ including patient response to interventions: PATIENT DISPOSITION: [X] Transferred by paramedics to (location):Hospital [ ] Transfer Coordinator notified if patient transferred to outside facility [ ] Seen in Clinic for further evaluation [ ] Home [ ] Homeless Shelter [ ] other: [ ] Did not want treatment (AMA) Reason: [X] Other :Once FD arrived to seen, they planned to transport patient out via gurney, but patient was able to stand up and walk to lobby. Gait was slightly unsteady. Remained diaphoretic and appeared to be in discomfort at times. Other times, he appeared to have fallen asleep, but was easily aroused. Was able to answer further questioning. He did not fall. Stated that he layed down on the bathroom floor. Still w/ SOB, dizziness, and abd pain when paramedics transferred him to rig. Denied any chest pain or pain to neck/arm/jaw. Transferred to ER. Provider responding to Emergency response:Dr.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 19.12.2021
- Impfdatum
- 18.12.2021
- Beginn
- 18.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Loss of consciousness
Seizure
Symptomtext
After receiving Pfizer booster, patient felt faint and passed-out. Patient experienced some convulsions during the time. Paramedics called to the scene. Patient was fine after a few minutes and left unharmed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 19.12.2021
- Impfdatum
- 19.12.2021
- Beginn
- 19.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fall
Hyperhidrosis
Loss of consciousness
Symptomtext
After vaccine patient was seated in waiting area, patient started falling to the ground and was caught by bystander, patient talking "I'm okay", diaphoretic, pulse 80, BP 140/p. Patient a&ox4, reports he had not eaten yet today, wearing multiple layer/heavy jacket in warm indoor environment. Patient was given juice, denies any pain from fall, denies CP, denies SOB, denies difficult swallowing, no rash/hives present, no nausea/vomiting. Patient reports feeling a warm sensation flush through his body, and feeling himself start to pass out, reports that the same thing happened during a routine blood draw. Patient remained on site for 20 min, patients skin cool/dry, with healthy color, had patient stand for a moment before leaving, patient denies any dizziness/lightheadedness. Patient left with significant other, with plan to have something to eat when he got home. Directed patient to call 911 if he started feeling lightheaded/dizzy, or had new onset chest pain/pressure, back pain, radiating arm pain, SOB, difficulty swallowing or other allergic reaction symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- HISTORY OF SYNCOPE DURING BLOOD DRAW
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 18.12.2021
- Impfdatum
- 18.12.2021
- Beginn
- 18.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Seizure
Symptomtext
Patient received dose #2 of COVID Pfizer. Pt began having seizures while seated ~ five minutes after vaccine. Pt recovered and was talking. EMS was called to scene for assistance. Pt. went home with a caregiver.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 18.12.2021
- Impfdatum
- 18.12.2021
- Beginn
- 18.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Lethargy
Seizure
Symptomtext
Sudden onset of seizure that lasted under 3 minutes. Pt lethargic for 10-15 minutes after but was able to sit up and speak. Alert and oriented post seizure. EMS called and medics checked her out.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- Unknown. Called paramedics for transport to local hospital.
- Aktuelle Erkrankungen
- Unknown?-reported healthy by significant other
- Vorgeschichte
- Unknown?-reported healthy by significant other
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 16.12.2021
- Impfdatum
- 10.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 6,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Electrocardiogram
Pericarditis
X-ray abnormal
Symptomtext
Pericarditis - developed severe burning sensation in the center and across my chest, went to urgent care for a chest x ray and was diagnosed with mild pericarditis.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pericarditis
- Hospital-Tage
- -
- Labordaten
- X ray and ekg - 12/15/2021
- Aktuelle Erkrankungen
- Asthma flare weeks before receiving vaccine
- Vorgeschichte
- Seasonal asthma Bipolar II disorder
- Andere Medikamente
- 100 MG lamictal 150 MG wellbutrin xl 40 MG protonix 1 MG melatonin
- Allergien
- Pollen alleegy
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 15.12.2021
- Impfdatum
- 15.12.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Loss of consciousness
Tremor
Symptomtext
Patient was shaky and passed out about 5 minutes after receiving vaccines. She came to and said she felt fine, but was encouraged to go to the hospital to get checked out.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown, our records show no chronic health conditions
- Andere Medikamente
- unknown
- Allergien
- unknown, our records show no allergies
- Vorherige Impfungen
- Patient stated about a month ago, she received a shot from her dermatologist. She did not pass out, however, she felt shaky.
- Staat
- NY
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 15.12.2021
- Impfdatum
- 15.12.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Syncope
Symptomtext
Patient fainted after vaccination. He came to after about 40-60 seconds and drank some orange juice. He still felt dizzy and sat for about 30 minutes until he felt better. Patient did not want to call EMS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 10.12.2021
- Impfdatum
- 09.12.2021
- Beginn
- 09.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Syncope
Symptomtext
The patient felt lightheaded 8 minutes after the vaccine so he put the seat back ( he was waiting in his car for 15 minutes after the shot) His friend that was waiting with him stated that it appeared that he passed out and his body got tense like a seizure. It only lasted a minute then he sat up and said he felt fine. He called his doctor and stated that he will follow up with him
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none indicated
- Vorgeschichte
- none indicated in profile
- Andere Medikamente
- Unknown
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 09.12.2021
- Impfdatum
- 05.12.2021
- Beginn
- 05.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Chills
Dyspnoea
Fall
Headache
Impaired work ability
Injection site pain
Injection site swelling
Loss of consciousness
Peripheral swelling
Pyrexia
SARS-CoV-2 test negative
Swelling
Swelling face
Vertigo
Symptomtext
Swelling and pain at the injection site, chills, severe headache, shortness of breath, vertigo started within approximately 15-20 of injection. These symptoms continued to get worse as the evening went on till I black out and fell trying to go the bathroom. I doesed myself with 50mg of benadryl and 600mg of ibuprofen and tried to sleep despite the danger because I wasn't think clear and felt feverish. I check my temp once home it was 102.8 then 2 hours later it was 97.1 and continued to bounce up and down for the first 12 hours or so. When I got up the next I realized more than my arm had swelled. My neck and face on the right side had swelled. I called off work the next because the headache and vertigo were horrible. Day 2 I was off and did a little bit of activity but still very weak, vertigo, headache, and short of breath. I went home early from work day 3 and went to be seen because I wasn't getting better. Md ruled out covid and ear problems, but couldn't rule out vaccine lasting affect or other viral possibility. I'm still having issues and can't work as of today day 4.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- covid test=negative and physical exam of ears and throat
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- migraines
- Andere Medikamente
- birth control, sertraline, cetirizine
- Allergien
- codeine, sulfa, thimerosal
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 09.12.2021
- Impfdatum
- 06.12.2021
- Beginn
- 08.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Computerised tomogram
Concussion
Fatigue
Head injury
Headache
Nausea
Skin laceration
Syncope
Ultrasound scan
Symptomtext
Had booster on Monday afternoon. Tuesday felt extreme fatigue and head ache. Tuesday night went to bed and woke up during night with extreme nausea. Made my way to the bathroom. Fainted. Hit head on wall which caused concussion and head laceration. Husband found me unresponsive on the bathroom floor. Due to extreme nausea, went back to bed. I was not aware that I had a head injury until the morning when I found the bed pillow covered in blood. Went to ER in the morning. Had CT scan and ultrasound. Required stitches/staples to scalp.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- Had CT Scan, ultrasound and tetanus shot
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- levoTHYROxine 50 MCG Tab traZODone 50 MG Tab
- Allergien
- pcn
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 94,0
- Geschlecht
- F
- Eingang
- 08.12.2023
- Impfdatum
- 04.01.2022
- Beginn
- 29.11.2023
- Tage bis Beginn
- 694,0
- Dosis
- 2
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute kidney injury
Asymptomatic bacteriuria
Blood creatinine abnormal
Blood folate
Blood iron decreased
Blood thyroid stimulating hormone
COVID-19 pneumonia
Cough
Dehydration
Diarrhoea
Faeces discoloured
Faeces soft
Fluid intake reduced
Glomerular filtration rate decreased
Hypertension
Hypophagia
Hypotension
Hypothyroidism
Symptomtext
Admit date: 11/29/2023 Discharge date: 12/3/23 Admitting Physician: MD Attending Physician at the Time of Discharge: MD Primary Care Physician: MD, Reason for Admission: Amazingly well 96 F. Has been at the terraces for almost 2 years now. (Assisted Living). She walks around with cane assist. Not feeling well after 6 days ago. Could not describe well what exactly ailed her. 3 days PTA noted to be on the toilet for 45 mnutes. ?loose stools. Had dark stools when she wiped. 2 days ago felt unwell again. +sore throat. Stool was soft, no longer dark. No fever or chills. Poor PO and fluid intake. No resp or pain issues. Sore throat resolved. Daughter brought her in for evaluation. ED eval shows unremarkable labwork save for some AKI. Baseline GFR is 40-50's. Current GFR is 17. Hospitalist called to evaluate for admission.Admitting patient for further eval and MGT of AKI. BP noted to be on the soft side (SBP 90's). She is not symptomatic from her low BP. Brief Summary of Hospital Stay: (Include Significant Findings and Invasive Procedures) Principal Problem: COVID pneumonia - with acute hypoxia - Rx with steroids, remdesevir. Need 2L for few days but came off O2 today. Cough+ - no crackles. No wheeze. Robitussin for cough. Finish course of steroids. AKI (acute kidney injury) (HCC) - likely prerenal from dehydration and recent diarrhea. No diarrhea now. Creat has improved Encourage po fluids Asymptomatic bacteriuria - UA abnormal - no urinary Sx. No need to treat. Normocytic anemia - no GI bleed evident. B12, TSh, folate okay. Low on Iron and Fe Def - replaced on DC. . Active Problems: HTN (hypertension) - not on meds. Hypothyroidism - continue supplement. Discharged to Home Health Care.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19 pneumonia
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 05.07.2023
- Impfdatum
- 18.12.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Adrenal insufficiency
Blood test
Cardiac stress test
Catheterisation cardiac
Chronic fatigue syndrome
Chronic inflammatory response syndrome
Decreased ventricular preload
Hypovolaemia
COVID-19
Drug ineffective
SARS-CoV-2 test
Echocardiogram
Electrocardiogram
Gene mutation identification test
General physical health deterioration
Hypobarism
Injection site pain
Laboratory test
Symptomtext
COVID test result=Positive; COVID test result=Positive; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 24-year-old male patient received BNT162b2 (BNT162B2), on 02Apr2021 as dose 1, single (Lot number: ER8737), on 21Apr2021 as dose 2, single (Lot number: EN6207) and on 18Dec2021 as dose 3 (booster), single (Lot number: FD7218) at the age of 24 years for covid-19 immunisation. The patient's relevant medical history included: "Asthma" (unspecified if ongoing); "pelvic floor dysfunction" (unspecified if ongoing); "Known allergies: Dairy" (unspecified if ongoing); "Known allergies: eggs" (unspecified if ongoing); "Known allergies: tree nuts" (unspecified if ongoing). Concomitant medication(s) included: DULERA; GAVILYTE C. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID test result=Positive". The patient underwent the following laboratory tests and procedures: Blood test: Positive; SARS-CoV-2 test: Positive; Negative.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300237581 same patient/product, different dose/event;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Postural orthostatic tachycardia syndrome
- Hospital-Tage
- -
- Labordaten
- Test Name: Blood test; Test Result: Positive ; Test Name: COVID test/Covid-19 virus test; Test Result: Positive ; Test Name: Nasal Swab; Test Result: Negative
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Allergy to nuts; Asthma; Egg allergy; Milk allergy; Pelvic floor dysfunction
- Andere Medikamente
- DULERA; GAVILYTE C
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 05.07.2023
- Impfdatum
- 18.12.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Adrenal insufficiency
Blood test
Cardiac stress test
Catheterisation cardiac
Chronic fatigue syndrome
Chronic inflammatory response syndrome
Decreased ventricular preload
Hypovolaemia
COVID-19
Drug ineffective
SARS-CoV-2 test
Echocardiogram
Electrocardiogram
Gene mutation identification test
General physical health deterioration
Hypobarism
Injection site pain
Laboratory test
Symptomtext
COVID test result=Positive; COVID test result=Positive; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 24-year-old male patient received BNT162b2 (BNT162B2), on 02Apr2021 as dose 1, single (Lot number: ER8737), on 21Apr2021 as dose 2, single (Lot number: EN6207) and on 18Dec2021 as dose 3 (booster), single (Lot number: FD7218) at the age of 24 years for covid-19 immunisation. The patient's relevant medical history included: "Asthma" (unspecified if ongoing); "pelvic floor dysfunction" (unspecified if ongoing); "Known allergies: Dairy" (unspecified if ongoing); "Known allergies: eggs" (unspecified if ongoing); "Known allergies: tree nuts" (unspecified if ongoing). Concomitant medication(s) included: DULERA; GAVILYTE C. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID test result=Positive". The patient underwent the following laboratory tests and procedures: Blood test: Positive; SARS-CoV-2 test: Positive; Negative.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300237581 same patient/product, different dose/event;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Postural orthostatic tachycardia syndrome
- Hospital-Tage
- -
- Labordaten
- Test Name: Blood test; Test Result: Positive ; Test Name: COVID test/Covid-19 virus test; Test Result: Positive ; Test Name: Nasal Swab; Test Result: Negative
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Allergy to nuts; Asthma; Egg allergy; Milk allergy; Pelvic floor dysfunction
- Andere Medikamente
- DULERA; GAVILYTE C
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 13.03.2023
- Impfdatum
- 10.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asthma
Condition aggravated
Dyskinesia
Gait disturbance
Hypersensitivity
Muscular weakness
Neurological examination
Symptomtext
1-Allergic reaction, asthma attacks. Treatments were spariva, budesonide and formoterso fumarate inhallation aerosol, outcome was better after a few weeks 2- would wake up in the morning unable to control my hands, difficulty walking. It was like walking through tar. Left shoulder jerkiing out of control. no treatment. Doctors just watched it closely. Outcome is that eventually I got control of my hands and legs but should still jerks involuntarily although less sever than in the beginning. Since it's been over a year now, I'm guessing it permanent.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Just visit with neurologist who did some basic tests and decided to wait to see what happened since symptoms were improving by the time I was able to get in to the office. Wait times were kind of long.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asthma, Li-Fraumeni Syndrome, Previous Kidney and Breast cancer
- Andere Medikamente
- escitalopram 5mg
- Allergien
- Corn, Pork, Mushrooms, Green Olives, Compazine, Penicillin
- Vorherige Impfungen
- FLU Vaccine, asthma
- Staat
- NY
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 13.03.2023
- Impfdatum
- 31.10.2021
- Beginn
- 08.11.2021
- Tage bis Beginn
- 8,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Back pain
Blindness
Blood test
Burning sensation
Computerised tomogram
Dysstasia
Electroencephalogram
Eye pain
Gait inability
Headache
Hypoaesthesia
Pain in extremity
Pain in jaw
Paraesthesia
Scan brain
Spinal pain
Trigger finger
Vision blurred
Symptomtext
Within 2 weeks and have not stopped. Numbness in legs, pain in legs, pins and needles in legs, burning in legs, pain in lower back, pain in spine, severe headaches, headaches behind eyes, pins and needles in face, blurry vision, temporary loss of vision, jaw pain, locking fingers, unable to stand up, unable to walk, unable to run.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- X-rays, CAT scans, Brain scan, blood tests, EEG,
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 20.02.2023
- Impfdatum
- 17.02.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Feeding disorder
Feeling abnormal
Impaired work ability
Influenza like illness
Mobility decreased
Nausea
Pain
Post-acute COVID-19 syndrome
SARS-CoV-2 test negative
X-ray
Symptomtext
I felt really bad, very achy, had a temperature, felt like I had the flu. I had to take two days off from work could not get out of bed, nausea, could not eat. I took a home a COVID-19 test that came back negative. I made an appointment with my pulmonologist, had x-rays done. He determined that I have long COVID-19 from when I did have COVID-19. I have an appointment scheduled with my primary care physician to be tested for cancer as my sister has now tested positive and getting treated for cancer.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- X-ray
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Levoxyl; Vitamin C; Vitamin D; Sambuca; Multivitamin
- Allergien
- Penicillin; Sulfa; Codeine; Vicodin
- Vorherige Impfungen
- Tdap has caused me to cough more.
- Staat
- MI
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 30.01.2023
- Impfdatum
- 13.12.2021
- Beginn
- 29.12.2022
- Tage bis Beginn
- 381,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Dyspnoea
SARS-CoV-2 test positive
Symptomtext
12/29/22 presents to ED for "shortness of breath". PMHx of "hypertension, CAD, CHF, A. fib on Eliquis, and emphysema"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 12/29/22 SARS-CoV-2 (COVID-19) by NAA detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 16.01.2023
- Impfdatum
- 12.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Amnesia
Blood pressure increased
Blood test
Chest discomfort
Chest pain
Dyspnoea
Exercise tolerance decreased
Fatigue
Feeling abnormal
Frustration tolerance decreased
Headache
Heart rate increased
Muscular weakness
Night sweats
Pain in extremity
Palpitations
Tinnitus
Weight fluctuation
Symptomtext
I was experiencing extreme fatigue, underarm pain, weight fluctuation, ear ringing, headache, rapid heartbeat, night sweats, upper and lower extremities pain, muscle weakness in my legs, and memory loss/brain fog during a span of months after receiving my booster. Everything gradually got worse over time, especially the rapid heartbeat and heart palpitations even during resting. I don't have the stamina I once had; I can no longer run or exercise like I once was able to do. I went from working out 5-6 times a week to now I've only worked out 5-6 times in the last year since receiving the booster. I contacted my doctor in regards to the symptoms I've had and was referred to a rheumatologist. I've had several bloodwork tests completed to try to determine a proper diagnosis for what's happening. I've been hospitalized twice in August and September 2022 as well as December 2022; I had to go the emergency room because the pain and tightness had gotten so bad in my chest, I couldn't breathe. My blood pressure has constantly spiked since then as well. I'm just frustrated with everything that's been happening and no proper diagnosis.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- 1,0
- Labordaten
- Bloodwork
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Lipitor; Vitamin D3; Multivitamin; Turmeric; Ashwagandha
- Allergien
- Certain Antibiotics
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 01.01.2023
- Impfdatum
- 30.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Computerised tomogram head abnormal
Ear pain
Headache
Idiopathic intracranial hypertension
Intracranial pressure increased
Lumbar puncture
Magnetic resonance imaging head
Pain
Swelling
Vision blurred
Symptomtext
Upon receiving the Covid booster I started with nonstop headaches. After 2 months of severe headaches, onset of blurry vision, and shooting pains behind my ears my primary care ordered bloodwork and CT scan. The CT showed an empty sella due to increased intracranial pressure. After following up with a neuro-ophthalmologist who diagnosed idiopathic intracranial hypertension and swollen optic nerves, scheduled a lumbar puncture. I started topiramate, increased the dose then added acetazolamide and increased the dose. The doctors cannot increase the medications because I have neurological side effects so they can not keep the pressure down in my head and have discussed transverse sinus stenting as the next step to relieve the pressure. I did consult with a neurosurgeon in April.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Idiopathic intracranial hypertension
- Hospital-Tage
- -
- Labordaten
- bloodwork 2/17/22, 7/12/22, 11/8/22, CT 2/17/22, MRI 3/17/22, numerous eye exams 3/18/22, 4/1/22, 6/7/22, 7/12/22, 11/16/22, lumbar puncture 5/3/22
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- hypertension well controlled and GERD
- Andere Medikamente
- hydrochlorothiazide, omeprazole, nebivolol, bupropion xl
- Allergien
- cipro, oxycodone
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 29.12.2022
- Impfdatum
- 20.12.2021
- Beginn
- 15.12.2022
- Tage bis Beginn
- 360,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Carotid artery stenosis
Computerised tomogram head abnormal
Condition aggravated
Confusional state
Culture urine positive
Encephalopathy
Klebsiella infection
Mental status changes
SARS-CoV-2 test positive
Urinary tract infection
Urine analysis abnormal
Symptomtext
"Patient with history of 3 COVID vaccines who admitted to hospital with COVID detected PCR. No hypoxia noted during stay. Provider d/c note: ""Brief Summary of Hospital Stay: (Include Significant Findings and Invasive Procedures) The patient per the report of her husband was in her normal mental state earlier in the day and then when he returned after getting some food he found her in the bathroom very confused. As she had an apparently abrupt change in mental status she was evaluated with a code stroke. There were no acute lesions on CT head or perfusion study. There were mild stenoses in the carotids. Patient has a history of frequent urinary tract infections and her urinalysis here was abnormal. Patient admitted for altered mental status.(HPI per Dr) Hospital Course: No notes on file Patient is an 86yr old female with a history of HTN, CAD, CKD, HLD, Osteoporosis on denosumab, Depression, Cognitive decline who presented with confusion AMS and found to have UTI. Today she is seen sitting in chair out of bed. She says she feels ok. Acute Encephalopathy secondary to Klebsiella UTI - CT head unremarkable. Urine culture grew >100,000 CFU. She received 4 days of IV Ceftriaxone. She was switched to nitrofurantoin which was apparently prescribed by her urologists but due to her CKD, I switched it to keflex on discharge. Discharge Exam: General - Elderly female, not in obvious distress HEENT - NC AT Heart - S1 S2 RRR Lung - CTAB Ext - No LE edema Neuro - AAAO to person, partially to place and time. """
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- 6,0
- Labordaten
- COVID Detected PCR on 12/15/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Cardiovascular CAD (coronary artery disease) Essential hypertension Bilateral carotid artery stenosis Left renal artery stenosis, significant (per 9/2008 angio.) Mitral regurgitation Digestive Gastroesophageal reflux disease Endocrine Secondary hyperparathyroidism of renal origin Urinary CKD (chronic kidney disease) stage 4, GFR 15-29 ml/min Urinary, incontinence, stress female Overactive bladder Other Dyslipidemia History of recurrent UTIs Age-related osteoporosis without current pathological fracture Normocytic normochromic anemia Vaginal dryness, menopausal Altered mental status Abnormal urinalysis Hypomagnesemia COVID-19 virus infection Acute encephalopathy
- Andere Medikamente
- -
- Allergien
- Bactrim [Sulfamethoxazole-trimethoprim] Dexilant [Dexlansoprazole] Ranexa [Ranolazine]
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 12.12.2022
- Impfdatum
- 08.02.2022
- Beginn
- 11.10.2022
- Tage bis Beginn
- 245,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Chest pain
Dyspnoea
SARS-CoV-2 test positive
Symptomtext
Patient was experiencing sudden onset chest pain and shortness of breath on 10/11/22 and came to the emergency department. He tested positive for COVID on 10/11/22. He was discharged from the hospital on 10/23/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- 13,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 21.11.2022
- Impfdatum
- 15.12.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Differential white blood cell count normal
Dizziness
Electrocardiogram normal
Full blood count normal
Heart rate increased
Muscle spasms
Speech disorder
Troponin normal
Symptomtext
About 1.5 hours after I received both vaccines, my heart rate spiked, I got extremely dizzy and thought I was going to pass out and was rushed the the hospital. I felt like I was having a heart attack because of the chest pains, muscle spasm and inability to talk.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- 12/15/21 ecg- normal 12/15/21 CBC with differential- normal 12/15/21 troponin high sensitivity- normal
- Aktuelle Erkrankungen
- N/a
- Vorgeschichte
- Depression, anxiety, insomnia
- Andere Medikamente
- Multi vitamin Vitamin D Ginkgo
- Allergien
- N/a
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 25.10.2022
- Impfdatum
- 30.12.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Gait disturbance
Loss of personal independence in daily activities
Orthostatic hypotension
Sitting disability
Symptomtext
Extreme dizziness the morning after receiving the vaccine. As soon as I would try to stand or sit up, I would feel like I was going to pass out and had to immediately lay back down. I had to have assistance getting to the bathroom and was unable to walk to the kitchen or to sit up in a chair except for a recliner. I also had orthostatic hypotension associated with standing. It was severe for 2 full days and gradually got better over the next 5 days. It was my 3rd Pfizer dose. I opted for a Moderna booster 6 months later and had no side effects from that.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Orthostatic hypotension
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- I had a 4 month course of chemotherapy for breast cancer from 8/2021-11/2021. I'd undergone general anesthesia for a mastectomy on 12/9/2021.
- Vorgeschichte
- Invasive Lobular Carcinoma breast cancer diagnoses 07/07/2021.
- Andere Medikamente
- Occasional Acetaminophen or Motrin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 90,0
- Geschlecht
- F
- Eingang
- 26.09.2022
- Impfdatum
- 13.12.2021
- Beginn
- 19.09.2022
- Tage bis Beginn
- 280,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anticoagulant therapy
Asthenia
Atrial fibrillation
Blood bilirubin increased
Blood thyroid stimulating hormone increased
Condition aggravated
Cough
Echocardiogram normal
Electrocardiogram abnormal
Fatigue
COVID-19
COVID-19 pneumonia
Cardiomyopathy
Chest X-ray abnormal
Chest pain
Haemoglobin decreased
Hypertension
Laboratory test
Symptomtext
Discharge Provider: DO Primary Care Provider at Discharge: MD Discharge Date: 9/21/2022 HOSPITAL COURSE: Patient is a 91-year-old female with history of hypertension, hypothyroidism, hyperlipidemia and anxiety who presented to the emergency department with chest pain and palpitations. She reported increasing fatigue and weakness for about 1 week prior to presentation, and developed chest pain on evening of presentation. In the emergency department, she was hypertensive, but otherwise hemodynamically stable. Lab workup showed bilirubin of 1.8 and hemoglobin 9.2 g/dL. Pro-BNP was found to be elevated to 2768 and troponin was 34, then 36. Chest x-ray showed cardiomyopathy without evidence of heart failure. EKG showed sinus tachycardia with PACs. She was found to be positive for COVID-19. She was admitted to the hospitalist service for further evaluation of COVID-19 and chest pain. Upon admission, the patient remained hemodynamically stable on room air. She did not report shortness of breath, but did report sore throat, cough and minimal sputum production. She remained afebrile. Given unclear duration of symptoms and lack of hypoxemia, she was not treated with IV remdesivir or Decadron. She developed acute onset of atrial fibrillation with rapid ventricular response on the afternoon of 9/20. Heart rates reached as high as the 180s. EKG confirmed atrial fibrillation with rapid ventricular response. She was given 2 doses of IV Cardizem, and started on oral Toprol-XL and oral Cardizem for rate control. Later that evening, she converted back to normal sinus rhythm, and was continued on Toprol-XL 50 mg daily. Oral Cardizem was discontinued. She was found to have a CHADS-VASc score of 4, so was recommended to start Eliquis 2.5 mg PO BID for stroke risk reduction. She remained in normal sinus rhythm overnight and into the next day. Echocardiogram was performed, and showed preserved ejection fraction with no wall motion abnormalities. Of note, her TSH returned at 0.02, although this was markedly different from TSH value of 11.8 on 8/5/22. She may benefit from outpatient referral to endocrinology given significant lability in TSH values over the last couple of months. She was felt stable for discharge home on the afternoon of 9/21/2022. She will be discharged on Toprol-XL 50 mg daily and Eliquis 2.5 mg PO BID. Due to addition of Toprol-XL, losartan will be decreased to 50 mg daily (from twice daily). I would recommend outpatient follow-up with Cardiology, given new onset of atrial fibrillation. She should follow-up with her PCP in 1 week. Could consider outpatient referral to endocrinology due to lability in TSH values over the last few months, but will defer to PCP. DISCHARGE DIAGNOSES: 1. COVID-19 pneumonia 2. Atrial fibrillation with RVR 3. Acute on chronic macrocytic anemia 4. Lower extremity edema 5. Benign essential hypertension 6. Hypothyroidism 7. Hyperlipidemia 8. Anxiety
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19 pneumonia
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Essential hypertension Non-recurrent unilateral inguinal hernia without obstruction or gangrene Ganglion cyst of joint of finger of right hand Type 2 diabetes mellitus with diabetic polyneuropathy, without long-term current use of insulin Mixed hyperlipidemia Macrocytic anemia History of right breast cancer Acquired hypothyroidism Age-related osteoporosis without current pathological fracture Sensorineural hearing loss (SNHL) of both ears Valgus deformity of both great toes Persistent insomnia History of recurrent UTI (urinary tract infection) Low-tension glaucoma of both eyes, severe stage History of basal cell carcinoma (BCC) of skin History of fracture of pelvis Type 2 diabetes mellitus with diabetic peripheral angiopathy without gangrene, without long-term current use of insulin Chest pain COVID-19 Acute on chronic anemia Atrial fibrillation with RVR
- Andere Medikamente
- alendronate (FOSAMAX) 70 MG tablet apixaban (ELIQUIS) 2.5 MG tablet atorvastatin (LIPITOR) 10 MG tablet B Complex Vitamins (VITAMIN B COMPLEX) TABS cholecalciferol (VITAMIN D3) 125 MCG (5000 UT) CAPS glucose monitoring kit (FREESTYLE) monit
- Allergien
- BandaidsRash
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 23.09.2022
- Impfdatum
- 30.12.2021
- Beginn
- 16.07.2022
- Tage bis Beginn
- 198,0
- Dosis
- 3
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chills
Diarrhoea
Dyspnoea
SARS-CoV-2 test positive
Symptomtext
Tested COVID positive, symptoms include chills, shortness of breath, and diarrhea.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Nasopharyngeal test collected 7/19/2022 tested positive for SARS-CoV-2 Antigen on 7/19/2022.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Type 2 diabetes mellitus, hypertension, and cardiovascular diseases.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 26.08.2022
- Impfdatum
- 04.05.2021
- Beginn
- 21.08.2022
- Tage bis Beginn
- 474,0
- Dosis
- 3
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Body temperature increased
COVID-19
Chest pain
Dyspnoea
Fatigue
SARS-CoV-2 test positive
Tachycardia
Symptomtext
Pt to ED 8/21 for fatigue x3 days. Pt tachy in triage at 115 with low grade temp. Pt reporting intermittent CP/shortness of breath. COVID+ 8/21. 8/23 bed without any gait disturbances. Pt denies any CP, nausea, vomitng and SOB. Pt discharged 8/23.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- 3,0
- Labordaten
- see above
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Gastroesophageal reflux disease ... Gastroesophageal reflux disease Chronic idiopathic constipation Weight loss Hematochezia Abdominal bloating General weakness
- Andere Medikamente
- Acetaminophen 500 MG PO Cap ... Acetaminophen 500 MG PO Cap Alendronate Sodium 70 MG PO Effer Tab aspirin 81 MG PO Chew Tab atorvastatin (LIPITOR) 20 MG PO Tab hydrocortisone (CORTEF) 10 MG PO Tab Levothyroxine Sodium (SYNTHROID PO) lisinop
- Allergien
- Penicillins
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 86,0
- Geschlecht
- F
- Eingang
- 19.07.2022
- Impfdatum
- 27.04.2021
- Beginn
- 16.07.2022
- Tage bis Beginn
- 445,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Dyspnoea
Productive cough
SARS-CoV-2 test positive
Symptomtext
Pt has a history of HTN, HLD, and CAD s/p stent to RCA. She presented to the ED with shortness of breath and was found to be COVID positive. She had been having shortness of breath for several weeks and a productive cough with sputum.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 02.07.2022
- Impfdatum
- 19.04.2021
- Beginn
- 01.05.2021
- Tage bis Beginn
- 12,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Abnormal loss of weight
Abnormal weight gain
Anxiety
Asthenia
Back pain
Blood test
Bone pain
Computerised tomogram head
Condition aggravated
Depression
Fatigue
Hyponatraemia
Impaired work ability
Influenza like illness
Injection site induration
Injection site mass
Injection site pain
Insomnia
Symptomtext
Hard, painful lumps on and around injection sites, muscle & bone aching, random severe itching all over body, feet and ankles swelling, rashes in several places (feet, hands, lower legs, ankles), hyponatremia (hospitalized), sudden severe weight gain, increase in depression and anxiety levels, insomnia, sudden weight loss, pain all over, low back pain, flu-like symptoms, constant exhaustion.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- 4,0
- Labordaten
- Bloodwork, numerous, don't have dates. X-rays, CT scan of brain, ultrasound, MRI
- Aktuelle Erkrankungen
- Mental health illnesses, osteoarthritis
- Vorgeschichte
- Major Depression, Panic,, GAD, BiPolar, ADD, PTSD, Arthritis
- Andere Medikamente
- Effexor, Wellbutrin, Xanax, Butrans, Propranolol, Metformin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 01.07.2022
- Impfdatum
- 30.12.2021
- Beginn
- 17.06.2022
- Tage bis Beginn
- 169,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Ageusia
Anosmia
COVID-19
Cough
Fatigue
Foreign travel
Headache
Migraine
Nasal congestion
Nausea
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Sinusitis
Vertigo
Vomiting
Symptomtext
Initial I had fever, nausea, vomiting, headache, cough and congestion. On the third or fourth day I lost my sense of taste of smell and taste. I tested positive so I isolated and for two weeks. I flew back home and have now tested negative but still have no sense of taste or smell and I still have a cough and some nasal congestion, vertigo, a bad headache that won't go away. It's like a migraine or sinusitis and fatigue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- COVID-19 Test
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 27.06.2022
- Impfdatum
- 23.12.2021
- Beginn
- 30.05.2022
- Tage bis Beginn
- 158,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
COVID-19
Exposure to SARS-CoV-2
Fatigue
Hyperaesthesia
Paraesthesia
Rhinorrhoea
SARS-CoV-2 test
SARS-CoV-2 test positive
Tenderness
Symptomtext
I thought I was having allergies, I had just gotten back from traveling. I attended two large graduations on May the 23rd and then also on the 27th. I also attended church on the 29th. I noticed a runny nose on that Monday, I called my doctor because I had an appointment the next day on the 31st. I had a scratchy throat, tingly ears and a crazy runny nose throughout that week. When I was at my Doctor on the 31st we thought that I had allergies. On June 5th I got a call from a friend I had just visited that they were positive for COVID-19 so I took a home test which was positive. I then went to a walk in clinic and that test was negative. I then took a PCR test and that was positive. I really had no other symptoms other than being fatigued on June 6th and 7th. The worst symptom was the runny nose. Since getting this booster my arm has been sensitive and has a tingling sensation when I touch it and its just tender. I have also had a pain behind my left knee and its tender and just hurts which is a new thing and only occurred after the booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- COVID-19 Home Test, COVID-19 PCR Test, COVID-19 Rapid Test
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Vitamin C, Omega 3 Fish Oil
- Allergien
- Sensitivity to gluten and dairy
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 21.06.2022
- Impfdatum
- 16.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Chest pain
Chills
Fatigue
Feeling abnormal
Insomnia
Malaise
Pyrexia
Symptomtext
I had the vaccine on Thursday morning, and that night I started to feel really bad, I had COVID a month before after I go the vaccine I felt worse than I did when I had COVID, the COVID symptoms changed over time, I had chills all the time, when I got the vaccine I had a fever and it was so hot that I could not sleep, the next day I was very fatigued and just not feeling well at all. After the next day the fever did break and I was just fatigued for a few days. When I had COVID I had some chest pains after having COVID and it was like someone was sticking a needle through my chest, but they were getting better, but after the booster they came back on the 24th and then on the 28th I went to the hospital to check to see what was going on and they said that this was something that they have seen with people get after they have had COVID. I just felt like my symptoms that I had for COVID just came back but worse. I had a physical exam and they did not give me any medications.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Physical exam
- Aktuelle Erkrankungen
- I had COVID a month prior that started on the 3rd of November and lasted until the beginning of Dec, about a week before I got the vaccine.
- Vorgeschichte
- Sickle Cell Trait
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 15.06.2022
- Impfdatum
- 14.12.2021
- Beginn
- 09.06.2022
- Tage bis Beginn
- 177,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Cough
Dehydration
Exposure to SARS-CoV-2
Fatigue
Headache
Induration
Nasal congestion
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test negative
SARS-CoV-2 test positive
Symptomtext
My parents tested positive for COVID last Tuesday, I tested Negative myself, but Thursday evening I had nasal congestion, throat felt hard, low fever that night, at the middle of the night I have chills and very high feverish, Friday I continued with congestion and coughing and Friday morning I called the doctor, and they prescribed Paxlovid. Friday night I had fever of 103, I was dehydrated, very bad headache, that was my worst night. Fever went away, this morning I finished Paxlovid but I am taking Mucinex, I still feel congested and tired.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dehydration
- Hospital-Tage
- -
- Labordaten
- COVID 19 Test - Negative, PCR - Negative.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Spinal Muscular Atrophy
- Andere Medikamente
- Evrysdi, Multivitamin, Sodium Chloride Nebulizer Solution
- Allergien
- Albuterol
- Vorherige Impfungen
- Flu vaccine, in 2001, I ended with Pneumonia
- Staat
- WA
- Alter
- 92,0
- Geschlecht
- M
- Eingang
- 02.06.2022
- Impfdatum
- 16.12.2021
- Beginn
- 29.05.2022
- Tage bis Beginn
- 164,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
COVID-19 pneumonia
Failure to thrive
Inappropriate schedule of product administration
Lethargy
SARS-CoV-2 test positive
Symptomtext
Patient received Pfizer COVID vaccine on 3/10/21 (lot # EN6208), 4/7/21 (lot # ER8729), and 12/16/21 (lot # FD7218). On 5/29/22, patient was admitted to our inpatient facility (med/surg unit) with lethargy and failure to thrive secondary to COVID-19 pneumonia and possibly bacterial pneumonia. As of today (7/2), patient is still admitted in the med/surg unit.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19 pneumonia
- Hospital-Tage
- 4,0
- Labordaten
- COVID status positive 5/29/22.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- history of known coronary disease with three-vessel CABG in 2004, DES to RCA 2008, recent CVA, type 2 diabetes, hypertension, hyperlipidemia, and squama cell carcinoma status post Mohs intervention
- Andere Medikamente
- acetaminophen, clopidogrel, coenzyme q10, gabapentin, glucosamine/chondroit, krill oil, melatonin, metformin xr, midodrine, mirabegron er, centrum silver for men, rosuvastatin, tamsulosin
- Allergien
- nkda
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 01.06.2022
- Impfdatum
- 25.03.2021
- Beginn
- 28.05.2022
- Tage bis Beginn
- 429,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Chest pain
Cough
Haemoptysis
Pain
SARS-CoV-2 test positive
Symptomtext
Pt states that she tested positive for COVID at home. She had been treated with a course of Paxlovid and presents with sudden onset of chest pain and blood-tinged sputum. Pt has a cough, no fever, but body aches. She did test positive for COVID on PCR at the hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 24.05.2022
- Impfdatum
- 11.12.2021
- Beginn
- 13.05.2022
- Tage bis Beginn
- 153,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
COVID-19
Fatigue
Headache
Mobility decreased
Nasopharyngitis
Oropharyngeal pain
Pyrexia
SARS-CoV-2 test positive
Symptomtext
Cold symptoms and sore throat about 3am, Fever at about 6 pm on 5/13. 11 pm 5/13 at home rapid test positive. 5/14 cold symptoms got worse, and a headache was added. On 5/15 call doctor, provided prescription with Paxlovid. Cold like symptoms improved slowly over the course of the next week and fatigue caused me to stay in bed half of the day. On 5/19 I got a bad headache that lasted until 5/21 that was debilitating. Tylenol did not help the pain of the head ache. Tested Negative on 5/21 on an at home test.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- High blood pressure
- Andere Medikamente
- Lisinopril, cranberry supplement, women's daily care probiotic
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 07.05.2022
- Impfdatum
- 14.12.2021
- Beginn
- 24.12.2021
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Atrial fibrillation
Electrocardiogram abnormal
Palpitations
Symptomtext
Heart palpitations and atrial fibrillation approximately one week after vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- January 3, 2022 exam and ECG 12 by Dr. confirmed persistent atrial fibrillation.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Paroxysmal atrial fibrillation CHADS-VASC=4; Essential hypertension.
- Andere Medikamente
- Pradaxa; Flomax. Dutasteride; Losartan K; Toprol; Centrum Silver vitamin.
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 20.04.2022
- Impfdatum
- 12.12.2021
- Beginn
- 06.03.2022
- Tage bis Beginn
- 84,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal distension
Anxiety
Asthenia
Blood test normal
Eructation
Erythema
Feeling hot
Hyperaesthesia
Influenza
Laziness
Lethargy
Malaise
Mechanical urticaria
Mobility decreased
Nasopharyngitis
Pain
Palpitations
Pruritus
Symptomtext
March 6, 2022, I came down with a very heavy cold. Took OTC medication to try and soothe it but within a very quick span, I felt completely drained of energy. Couldn't get out of bed and had a fever of 100+. Was basically lazy, lethargic, no energy, zero. Never felt this kind of symptoms so the next day, we did a COVID test at home and that came back negative. So that was kind of a relief for a moment. Took me about 3-4 days after that with a lot of hydration to get back to normal. It was the most extreme case of flu. That was this particular episode. A week later after that, I started observing intense itching all over my body from scalp to bottom of feet. Indiscriminate of the location of body, time, and time of day. I could not figure out anything and I wasn't allergic to any food groups. When the itch would come, I would get a sensation that the part was going to itch and I would feel a needle prick then my body would start heating up and that was an indicator that that part of my body would itch, then that's when the itching began. I did wait 7-8 days before finally seeing a doctor. And the itching was what prompted me to go see the doctor. When I was at the doctor's office, in terms of trying to take care of the problem, they told me to shut down 6 food groups, which we did. They also gave me medication, hydroxyzine, and I was asked to take that. I took that and I shut down on the food groups. I was following the doctor's protocol for treatment. It did not bring the itching under control. Something weird would happen at the body part that would itch. It would bring up a lot of heat. Touching my skin would cause like-symptoms of dermatographia. The skin originally looked normal at the initial visit. The 2nd visit and a nurse was taking my blood pressure, and when the cuff puffed up, my skin started flaring up again. The doctor was physically watching me break out as urticaria. Changed the medication to cetirizine to take every day. And put me on a 12 day diminishing dose of prednisone. Asked me to see an allergist and immunologist. The medication is helping slightly, and the itching isn't there all the time. But the redness and flare up are still happening. Instead of the body, the focus is on the neck, face, ears, feels like a fire lit underneath the skin then feels like it cools down. The itching is under control some. It's still happening but not as bad as it was a week ago. Seeing a specialist for these symptoms at some point soon. I've never been allergic to anything or food groups, or anything severe. I've also never been sick like that initial cold. They're not sure if it's a virus or allergy, or anything. I'm not sure if it's directly related to the vaccine but what I've experienced I've never felt before. Two more symptoms: I have never had any form of indigestion. I've had this a couple of times, especially in the morning- seems like a burp that won't expel, heart starts racing, that comes with anxiety, almost a panic attack. Takes 30-40 minutes to expel the burp, then it expels. The feeling at the same time, feels like the throat is being constricted. Once the burp comes out, the tightness goes away. Can't really drink water during this time in the morning because I feel bloated and these symptoms seem to start in the morning. I try to walk around to get my day started to prevent these symptoms and try to take in a small sip of water. They come together and it's a morning event that doesn't happen again until early the next morning. All these symptoms have developed since March 6 or 7 after that initial cold, and before then I've been completely healthy, so I just want to figure out what's wrong.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- At home COVID-19 test - negative, Initial blood work - came back normal
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Penicillin, Sulfa
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 16.04.2022
- Impfdatum
- 08.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Anti-thyroid antibody
Anti-thyroid antibody negative
Anxiety
Blood thyroid stimulating hormone decreased
Chest pain
Disorientation
Disturbance in attention
Fatigue
Hyperhidrosis
Muscular weakness
Palpitations
Restlessness
Scan thyroid gland
Temperature intolerance
Thyroid stimulating immunoglobulin increased
Thyroxine free increased
Weight decreased
Symptomtext
Symptoms slowly developed after 2nd dose March 30, 2021, then significantly worsened within a week after 3rd dose 1/8/2022. Developed debilitating fatigue, rapid weight loss with no other changes, heightened anxiety and restlessness/inability to focus, disorientation, muscle weakness, chest pain and racing heart rate even while at rest. Profuse sweating and heat intolerance.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- TSH (<.01 LOW), FT4 (2.5 HIGH), TSI (.95 HIGH), Thyroid Peroxidase AB (1.9 normal) , Thyroglobulin AB (0.9 normal), Thyroid Uptake Scan (4 hrs 1.63% LOW, 24 hrs 2.82% LOW)
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Raynauds Phenomen
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 11.04.2022
- Impfdatum
- 17.12.2021
- Beginn
- 03.01.2022
- Tage bis Beginn
- 17,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Blood test normal
COVID-19
Chest X-ray normal
Chest pain
Cough
Echocardiogram abnormal
Electrocardiogram normal
Oropharyngeal pain
Rhinorrhoea
SARS-CoV-2 test positive
Supraventricular extrasystoles
Ventricular extrasystoles
Symptomtext
I had sore throat, running nose, and cough that lasted for about 6 or 7 days. On Jan 3rd, I tested positive for COVID-19. Then about a week later, I started having chest pain. I went to Urgent Care. They did blood work, normal result. They also did EKG and chest x-ray, all normal. I was referred to a cardiologist. I had to wear a heart monitor for about a week. They did an heart ultrasound, show that I had infrequent PVC and PAC.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- COVID-19 test; EKG; Chest x-ray; Heart ultrasound.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Levothyroxine; Berotec
- Allergien
- Osmosis
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 31.03.2022
- Impfdatum
- 21.12.2021
- Beginn
- 09.02.2022
- Tage bis Beginn
- 50,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Angiogram
Aphasia
Computerised tomogram
Confusional state
Dizziness
Echocardiogram
Hemiplegia
Hemiplegic migraine
Laboratory test
Magnetic resonance imaging
Neurological examination
Symptomtext
suffered paralysis on her whole right side; suffered a hemiplegic migraine; aphasia; dizziness / acute on chronic dizziness / increased dizziness; confusion; This is a spontaneous report received from a contactable reporter (Nurse). The reporter is the patient. A 41 year-old female patient (not pregnant) received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), intramuscular, administered in arm left, administration date 21Dec2021 (Lot number: FD7218) at the age of 41 years as dose 3 (booster), single for COVID-19 immunization. Relevant medical history included: "Migraines" (unspecified if ongoing), notes: normally had traditional migraines that were not complicated by any auras; "Acne" (unspecified if ongoing); "OAB" (unspecified if ongoing). The patient had no known allergies. Concomitant medications included: ALDACTONE [SPIRONOLACTONE]; AJOVY [FREMANEZUMAB]; ATARAX [ALPRAZOLAM]; EXCEDRIN MIGRAINE; FLONASE ALLERGY RELIEF. Vaccination history included: BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (DOSE 2, SINGLE, Lot number: ER8732, Location of injection: left arm, route of administration: intramuscular), administration date: 27Mar2021, when the patient was 41 years old, for COVID-19 immunization; BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (DOSE 1, SINGLE, Lot number: EN6198, Location of injection: left arm, route of administration: intramuscular), administration date: 03Mar2021, when the patient was 41 years old, for COVID-19 immunization. The vaccination facility type was reported as the hospital. The patient had no COVID-19 prior vaccination. The patient was not tested for COVID-19 post vaccination. The following information was reported: HEMIPLEGIA (hospitalization, medically significant) with onset 09Feb2022 18:15, outcome "recovered with sequelae," described as "suffered paralysis on her whole right side"; HEMIPLEGIC MIGRAINE (hospitalization) with onset 09Feb2022 18:15, outcome "recovered with sequelae," described as "suffered a hemiplegic migraine"; APHASIA (hospitalization) with onset 09Feb2022 18:15, outcome "recovered with sequelae," described as "aphasia"; DIZZINESS (hospitalization) with onset 09Feb2022 18:15, outcome "recovered with sequelae," described as "dizziness / acute on chronic dizziness / increased dizziness"; CONFUSIONAL STATE (hospitalization) with onset 09Feb2022 18:15, outcome "recovered with sequelae," described as "confusion." The patient was hospitalized for hemiplegia, hemiplegic migraine, aphasia, dizziness, confusional state (start date: 09Feb2022, discharge date: 11Feb2022, hospitalization duration: 2 days). The event "dizziness / acute on chronic dizziness / increased dizziness" was evaluated at the emergency room visit. The patient underwent the following laboratory tests and procedures: angiogram (CTA): unknown result; computerised tomogram (CT): unknown result; echocardiogram (TEE): unknown result; laboratory test (basic work-up): normal; magnetic resonance imaging (MRI): unknown result; neurological examination (full neuro workup): all normal. Therapeutic measures were taken as a result of hemiplegia, hemiplegic migraine, aphasia, dizziness, confusional state, which included Plavix and aspirin. Clinical course: The doctors believed the patient suffered a hemiplegic migraine. She suffered paralysis on her whole right side, aphasia, dizziness, and confusion. The hospital did a full neuro workup, which was all normal. The patient had never experienced this type of migraine before, ever. She was also currently experiencing acute on chronic dizziness since the hemiplegic migraine attack. All of these symptoms started a few weeks after her 3rd Pfizer dose. In addition, the patient went to the ER for increased dizziness on 17Mar2022. The hospital did a basic work-up which was normal. She was to follow up with ENT and was prescribed Meclizine. The patient had never experienced any of this in her life.; Sender's Comments: Based on the current available limited information in the case provided, the causal association between the events and the use of suspect product BNT162B2 cannot be fully 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
- Hemiplegic migraine
- Hospital-Tage
- 2,0
- Labordaten
- Test Name: CTA; Result Unstructured Data: Test Result:Unknown Result; Test Name: CT; Result Unstructured Data: Test Result:Unknown Result; Test Name: TEE; Result Unstructured Data: Test Result:Unknown Result; Test Name: basic work-up; Result Unstructured Data: Test Result:normal; Test Name: MRI; Result Unstructured Data: Test Result:Unknown Result; Test Name: full neuro workup; Result Unstructured Data: Test Result:all normal
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Acne; Migraine (normally had traditional migraines that were not complicated by any auras); Overactive bladder
- Andere Medikamente
- ALDACTONE [SPIRONOLACTONE]; AJOVY [FREMANEZUMAB]; ATARAX [ALPRAZOLAM]; EXCEDRIN MIGRAINE; FLONASE ALLERGY RELIEF
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 30.03.2022
- Impfdatum
- 17.12.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 15,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Blood immunoglobulin G
Blood immunoglobulin M
Computerised tomogram
Dizziness
Dyspnoea
Extrasystoles
Fall
Fatigue
Headache
Insomnia
Loss of personal independence in daily activities
Muscular weakness
Symptomtext
lightheaded; shortness of breath when climbing up the stairs; now they find out when she has shortness of breath her heart skips a beat; she can't do daily activities one day; fell; Insomnia; tired more easily; Headache; Dizziness; weakness of her legs; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from product quality group for a Pfizer sponsored program (159558). The reporter is the patient. A 65 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 17Dec2021 (Lot number: FD7218) at the age of 65 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "high blood pressure" (unspecified if ongoing); "Fatty liver" (unspecified if ongoing); "allergy" (unspecified if ongoing). Concomitant medication(s) included: AMLODIPINE taken for hypertension; ROSUVASTATIN taken for hepatic steatosis; LEVOCETIRIZINE taken for hypersensitivity. Vaccination history included: Bnt162b2 (Dose: 1, Lot number: EP7534, Location: Left arm), administration date: 20Mar2021, when the patient was 64 years old, for COVID-19 Immunization; Bnt162b2 (Dose:2, Lot number: ER8731, Location: Left arm, she got really sick), administration date: 10Apr2021, when the patient was 64 years old, for COVID-19 Immunization, reaction(s): "sick", "shaking inside", "feeling cold/felt so cold", "Whole body was aching", "nauseous", "dizzy", "slept in bed all day", "feel warm", "bad headache", "low temperature". The following information was reported: DIZZINESS (hospitalization) with onset Jan2022, outcome "recovered" (18Jan2022), described as "lightheaded"; DYSPNOEA (non-serious), outcome "recovering", described as "shortness of breath when climbing up the stairs"; EXTRASYSTOLES (non-serious), outcome "unknown", described as "now they find out when she has shortness of breath her heart skips a beat"; LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (non-serious), outcome "unknown", described as "she can't do daily activities one day"; DIZZINESS (non-serious) with onset Jan2022, outcome "unknown", described as "Dizziness"; MUSCULAR WEAKNESS (non-serious) with onset Jan2022, outcome "recovering", described as "weakness of her legs"; FALL (non-serious), outcome "unknown", described as "fell"; INSOMNIA (non-serious), outcome "unknown", described as "Insomnia"; FATIGUE (non-serious), outcome "not recovered", described as "tired more easily"; HEADACHE (non-serious), outcome "not recovered", described as "Headache". The patient was hospitalized for dizziness (start date: Jan2022). The event "shortness of breath when climbing up the stairs" was evaluated at the emergency room visit. The patient underwent the following laboratory tests and procedures: blood immunoglobulin g: negative, notes: blood test; blood immunoglobulin m: positive, notes: blood test; computerised tomogram: no signs of pneumonia or embolism. Therapeutic measures were not taken as a result of dizziness, dizziness, muscular weakness, fatigue, headache. Therapeutic measures were taken as a result of dyspnoea. Clinical course: Patient had the COVID-19 booster on 17Dec2021, after the booster shot her reaction was not as severe as after the second shot and cannot remember how many days later after the COVID-19 booster dose she developed shortness of breath, when climbing up the stairs and the shortness of breath gradually builds up more and more and it then it was getting severe until Jan2022 when she went to the Emergency Room. Doctor said she may have had a very mild case of COVID-19 since she never felt sick with covid. Patient reports an acute reaction from the COVID-19 booster, her body is telling her something went wrong after her COVID-19 booster vaccine on 17Dec2021 and shortness of breath began a few days later and was gradually getting heavier and heavier and was getting more severe and shortness of breath was going on persistently and gradually and then it worsened and then this week she started feeling better. Patient states when she lays on the table she gets lightheaded and dizziness as well as, headaches and insomnia, insomnia is not consistent. She reports when her body wants to catch some sleep, she is able to sleep. Patient reports in Jan2022, when trying to turn the steering wheel, she got short of breath, due to her lungs. Patient states this is weakness of her legs, Now its improving but she gets tired easily. Lightheaded began the first 2 weeks in Jan2022 up to the 18Jan2022 when she was admitted to the hospital. frequency of headaches and the headaches started a few days ago, headaches are ongoing and come along periodically. Headaches are not worsening but maybe persisting. Dizziness began the beginning of Jan2022, dizziness could come back and then goes away. Patient reports that the dizziness does not bother her as the dizziness comes back and then goes away quickly. Patient states that lack of exercise may have caused her to be tired more easily. Weakness of legs started sometime in Jan2022 before she went to the emergency room. Regarding Treatment for Shortness of Breath patient reports diclofenac didn't help, the doctors couldn't find out anything and that she must have inflammation in her body, they found IgM was positive and she was placed on prednisone and that didn't help and albuterol sulfate inhalation aerosol 90mcg 2 puffs every 4 hours as needed and the inhaler didn't help, patient was also prescribed budesonide formoterol fumarate dihydrate inhalation aerosol 160/4.5mcg 2 puffs 2 times a day. Patient reports no treatment for the lightheadedness, headache, dizziness, tired more easily, or weakness of legs. Patient reports now they find out when she has shortness of breath her heart skips a beat. patient repots shortness of breath got so severe and she climbed a few steps from her garage to her house and was out of breath. Pharmacy was Vaccination Facility Type. No vaccinations within four weeks prior to the first administration date of the suspect vaccine. Patient reports her first shingles shot last Jan2021 she had an adverse event. Blood work for her IgM was how they told her she was positive for the COVID-19 virus and she doesn't know when she had it. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Test Name: IgG; Test Result: Negative ; Comments: blood test; Test Name: IgM; Test Result: Positive ; Comments: blood test; Test Name: CAT; Result Unstructured Data: Test Result:no signs of pneumonia or embolism
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Allergy; Blood pressure high; Fatty liver
- Andere Medikamente
- AMLODIPINE; ROSUVASTATIN; LEVOCETIRIZINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 26.03.2022
- Impfdatum
- 29.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Headache
Hypoaesthesia
Inappropriate schedule of product administration
Limb discomfort
Paraesthesia
SARS-CoV-2 test
Symptomtext
Dose Number 1/Date of start of drug: 16-MAR-2021/ Dose Number 2/Date of start of drug: 29-DEC-2021; symptoms of sharp pains and numbness in my head; symptoms of sharp pains and numbness in my head; right arm felt dead, listless; left hand tingling and legs are worse; left hand tingling and legs are worse; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 58 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 29Dec2021 17:30 (Lot number: FD7218) at the age of 59 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Type 2 Diabetes" (unspecified if ongoing); "Asthma" (unspecified if ongoing); "Arthritis" (unspecified if ongoing), notes: knees; "high cholesterol" (unspecified if ongoing); "High blood pressure" (unspecified if ongoing), notes: From the mass behind my left optic nerve.; "Morbidly Obese" (unspecified if ongoing); "bulging discs in neck and back" (unspecified if ongoing). The patient's concomitant medications were not reported. Past drug history included: Penicillin, reaction(s): "allergy"; Ampicillin, reaction(s): "Allergy"; Chemicals, reaction(s): "Allergy", notes: Some perfumes,peanuts. Vaccination history included: Bnt162b2 (Dose Number: 1,(11:45 am), Batch/Lot No: EN6205, Location of injection: Arm left), administration date: 16Mar2021, when the patient was 58 years old, for COVID-19 immunization. The following information was reported: INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (non-serious) with onset 29Dec2021 17:30, outcome "unknown", described as "Dose Number 1/Date of start of drug: 16-MAR-2021/ Dose Number 2/Date of start of drug: 29-DEC-2021"; HEADACHE (non-serious), HYPOAESTHESIA (non-serious) all with onset 29Dec2021, outcome "unknown" and all described as "symptoms of sharp pains and numbness in my head"; LIMB DISCOMFORT (non-serious) with onset 29Dec2021, outcome "unknown", described as "right arm felt dead, listless"; PARAESTHESIA (non-serious), CONDITION AGGRAVATED (non-serious) all with onset 29Dec2021, outcome "unknown" and all described as "left hand tingling and legs are worse". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of headache. Additional Information:No other vaccines were received within 4 weeks prior to the COVID vaccine. Patient received some medications in two weeks. Prior to vaccination,patient was not diagnosed with COVID-19.After the vaccination, patient tested negative for COVID-19. Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Test Name: SARS-CoV-2 test; Test Result: Negative ; Comments: Nasal swab
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Arthritis (knees); Asthma; Blood pressure high (From the mass behind my left optic nerve.); Herniated disc; High cholesterol; Obesity; Type 2 diabetes mellitus
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 25.03.2022
- Impfdatum
- 21.01.2022
- Beginn
- 23.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Atrial fibrillation
Blood pressure measurement
Hypertension
Palpitations
Symptomtext
atrial fib; palpitaions; high blood pressure; This is a spontaneous report received from a contactable reporter(s) (Pharmacist). The reporter is the patient. A 82 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 21Jan2022 12:00 (Lot number: FD7218) at the age of 82 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history was not reported. The patient took concomitant medications. Vaccination history included: Bnt162b2 (Prev dose product=COVID 19, Prev dose brand=Pfizer, brand unknown=False,, lot number: EL9262,, lot unknown=False,, administration time: 01:00 PM , number=1, vaccine location=Left arm), administration date: 25Jan2021, when the patient was 81 years old, for Covid-19 immunization; Bnt162b2 (product=COVID 19, brand=Pfizer, brand unknown=False,, lot number: EN6201,, lot unknown: False, dose administration time: 02:00 PM, dose number=2, dose vaccine location=Left arm), administration date: 11Feb2021, when the patient was 81 years old, for Covid-19 immunization, reaction(s): "atrial fib", "high blood pressure", "Palpitations". The following information was reported: ATRIAL FIBRILLATION (disability) with onset 23Jan2022 16:00, outcome "recovered with sequelae", described as "atrial fib"; PALPITATIONS (disability) with onset 23Jan2022 16:00, outcome "recovered with sequelae", described as "palpitaions"; HYPERTENSION (disability) with onset 23Jan2022 16:00, outcome "recovered with sequelae", described as "high blood pressure". The patient underwent the following laboratory tests and procedures: blood pressure measurement: (23Jan2022) high. Therapeutic measures were not taken as a result of atrial fibrillation, palpitations, hypertension.; Sender's Comments: Based on available information, a possible contributory role of BNT162B2 vaccine cannot be excluded for the reported events due to temporal relationship.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220123; Test Name: blood pressure; Result Unstructured Data: Test Result:high
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 17.03.2022
- Impfdatum
- 13.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Dyspnoea
Feeling cold
Gait disturbance
Immunisation reaction
Neck pain
Pain in extremity
Palpitations
Peripheral swelling
Symptomtext
had really hard time breathing; that went for 3 days; I was able to walk outside and it took me like 15 minute to walk back; when I got the vaccine within minute so I felt pain in my hand and it kind of swelled up and then the arm in which I got the injection; base of my neck like it was like crackling back of my neck up to my skull and then I got dizzy; I sit down and my heart started palpitating really fast, it start beating really fast; I started getting really cold; I had the severe reaction; when I got the vaccine within minute so I felt pain in my hand and it kind of swelled up and then the arm in which I got the injection; base of my neck like it was like crackling back of my neck up to my skull; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. Other Case identifier(s): US-PFIZER INC-202200167108. A 63 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 13Jan2022 (Lot number: FD7218) at the age of 63 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Name of Drug as Reported: Latex; Reaction: Allergy" (unspecified if ongoing). There were no concomitant medications. Past drug history included: Codeine, reaction(s): "Name of Drug as Reported: codeine; Reaction: Allergy"; Vitamin c ester lotion, reaction(s): "Name of Drug as Reported: vitamin c ester lotion; Reaction: Allergy". The following information was reported: PAIN IN EXTREMITY (non-serious) with onset 13Jan2022 17:00, outcome "recovered with sequelae", PERIPHERAL SWELLING (non-serious) with onset 13Jan2022, outcome "unknown" and all described as "when I got the vaccine within minute so I felt pain in my hand and it kind of swelled up and then the arm in which I got the injection"; DIZZINESS (non-serious) with onset 13Jan2022 17:00, outcome "recovered with sequelae", described as "base of my neck like it was like crackling back of my neck up to my skull and then I got dizzy"; PALPITATIONS (non-serious) with onset 13Jan2022, outcome "unknown", described as "I sit down and my heart started palpitating really fast, it start beating really fast"; FEELING COLD (non-serious) with onset 13Jan2022, outcome "unknown", described as "I started getting really cold"; VACCINATION COMPLICATION (non-serious) with onset 13Jan2022, outcome "unknown", described as "I had the severe reaction"; DYSPNOEA (non-serious) with onset 14Jan2022, outcome "recovered" (17Jan2022), described as "had really hard time breathing; that went for 3 days"; GAIT DISTURBANCE (non-serious) with onset 14Jan2022, outcome "recovered" (14Jan2022), described as "I was able to walk outside and it took me like 15 minute to walk back"; NECK PAIN (non-serious) with onset 13Jan2022, outcome "unknown", described as "base of my neck like it was like crackling back of my neck up to my skull". Therapeutic measures were not taken as a result of pain in extremity, peripheral swelling, dizziness, palpitations, feeling cold, vaccination complication, dyspnoea, gait disturbance, neck pain. Additional information: On the date when she got the vaccine within minute, so felt pain in her hand and it kind of swelled up and then the arm in which she got the injection. She got the vaccine on 13Jan2022. She felt like this it was like back it was base of her neck like it was like crackling back of her neck up to her skull and then she got dizzy. So, she waited but she went into my car because going home I didn't think I am going to have a problem. I went after work grab my dog and she was sitting in my car, so I went inside my car I felt like little bit dizzy, but I had to get home. I didn't realize that having symptoms that I should mentioned it because people were saying that they side effects. So, I went home, and I started getting really cold so, it turned the heater and then my boss called me and then asked me how I was felling, and I told them I am very dizzy he said oh my gosh you not even sound right, and I need to sit down. So, I sit down, and my heart started palpitating really fast, it starts beating really fast. I sat for a while and then got up and went to bed. The next morning, I woke up and had really hard time breathing. It was cold because we are in withheld. I was able to walk outside, and it took me like 15 minute to walk back and forth to finally be able to take the breath and that went for 3 days. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. There is no list of any other medications the patient received within 2 weeks of vaccination. Prior to vaccination, the patient was not diagnosed with COVID-19 and since the vaccination, patient had not been tested for COVID-19. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Latex allergy
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 15.03.2022
- Impfdatum
- 31.12.2021
- Beginn
- 21.01.2022
- Tage bis Beginn
- 21,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Anxiety
Blood test normal
Cardiac stress test normal
Chest pain
Electrocardiogram ambulatory normal
Electrocardiogram normal
Palpitations
Symptomtext
Heart palpitations (pounding heart), chest pain, anxiety. Taking propranolol 10mg twice daily, symptoms unresolved.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- EKG, electrocardiogram, blood tests, Holter monitor, stress test. All done in mid-February and early-March. All show normal functioning.
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- Asthma, atomic dermatitis
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 28.02.2022
- Impfdatum
- 10.01.2022
- Beginn
- 25.01.2022
- Tage bis Beginn
- 15,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Computerised tomogram
Diarrhoea
Headache
Heart rate increased
Mouth ulceration
Pain
Tachycardia
Symptomtext
I noticed my heart rate was accelerating & it wouldn't stop & I had ulcers in my mouth, so I went to er I was achy had headaches & also diarrhea they gave me meds for Tachycardia.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tachycardia
- Hospital-Tage
- -
- Labordaten
- CT Scan, IV Fluids, Bloodwork
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Melanoma
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 24.02.2022
- Impfdatum
- 18.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 9,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: ja
ER: unbekannt
Erholt: nein
Anxiety
Blood thyroid stimulating hormone
Brain natriuretic peptide
Dizziness
Electrocardiogram
Electrocardiogram ambulatory
Feeding disorder
Full blood count
Heart rate increased
Metabolic function test
Rhinovirus infection
Tachycardia
Tremor
Troponin
Symptomtext
Starting 12/27/2021 developed tachycardia, heart rate up to 180. Ambulance called. Also diagnosed with rhinovirus. Patient has not recovered from tachycardia. HR 90-150?s. Dizziness. Unable to eat, severe anxiety. 3 emergency room visits and admission on 2/21/22 for shaking, tachycardia and severe anxiety. Still hospitalized as of date of this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tachycardia
- Hospital-Tage
- 4,0
- Labordaten
- EKG Holter monitor BNP Troponin CBC CMP TSH
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Eosinophilia (chronic) Mast cell activation syndrome Ehlers-Danlos
- Andere Medikamente
- Nucala 300mg Zoloft 12.5mg Zyrtec 10mg
- Allergien
- Sulfa NSAIDs Amoxicillin Peaches Bananas
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 27,0
- Geschlecht
- U
- Eingang
- 21.02.2022
- Impfdatum
- 30.12.2021
- Beginn
- 02.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Chest X-ray normal
Dyspnoea
Echocardiogram
Electrocardiogram ambulatory
Fatigue
Musculoskeletal chest pain
Rash
Symptomtext
Chest wall tenderness, sided, Shortness of breath on exertion, rash on abdomen, and fatigue. I am writing him up for possible Myocarditis: Echo/ Holter Monitor. Patient is improving, will also monitor for any more symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Chest X-ray, no findings 2/15/2022.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- anxiety
- Andere Medikamente
- N/A
- Allergien
- Amoxicillin & Penicillin
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 21.02.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Chills
Pain
Product storage error
Tremor
Symptomtext
Vaccine stored in freezer too long resulting in a temperature excursion. Patient reported aches, shakes and chills (1-2 days).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 21.02.2022
- Impfdatum
- 06.01.2022
- Beginn
- 14.02.2022
- Tage bis Beginn
- 39,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Cyanosis
Dyspnoea
Ear pain
Erythema
Oxygen saturation decreased
Pain
Pain in extremity
Peripheral swelling
Poverty of speech
Pyrexia
Vomiting
Symptomtext
CHIEF COMPLAINT: pt comes in reporting redness, swelling, pain to left lower leg. also has been vomiting since friday. low O2 on arrival, wears home O2 24/7 that she has not had on PTA. SOB on arrival, cyanotic lips. diff speaking in full sentences. HISTORY OF PRESENT ILLNESS: 57-year-old female with past medical history of COPD, HTN, Pulmonary HTN, and morbid obesity who presents with a chief complaint of right lower extremity pain, redness, and swelling. Patient states that she began experiencing fever, chills, vomiting, and left ear pain on Friday, 2/11/2022. She states that she then began to have right leg pain, redness, and swelling starting on Saturday, 2/12/2022. She rates her pain as 8/10 in severity and throbbing/burning in quality. She denies having the symptoms in the past. She reports shortness of breath, which patient states is chronic and at her current baseline. She reports being on 4 to 6 L of supplemental oxygen at home (pulmonologist). Denies chest pain. Patient states that she saw her PCP, 12 days ago at which time she was told to discontinue her furosemide. Patient states that she has had slight increase in bilateral lower extremities over the past week, but not significantly changed from her baseline. She states that her left ear pain and fever have improved, but is still experiencing chills. Reports no other complaints at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Unknown
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- COPD, Hypertension, Pulmonary hypertension, SOB (shortness of breath)
- Andere Medikamente
- Unknown
- Allergien
- penicillins, Levaquin,
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 19.02.2022
- Impfdatum
- 16.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Antinuclear antibody positive
Biopsy skin
Blood test normal
COVID-19
Chest discomfort
Computerised tomogram coronary artery normal
Electrocardiogram normal
Exposure to SARS-CoV-2
Feeling cold
Illness
Discomfort
Disturbance in attention
Drug ineffective
Interchange of vaccine products
SARS-CoV-2 test
Lymphadenopathy
Magnetic resonance imaging neck
Magnetic resonance imaging spinal normal
Symptomtext
home test-covid test result=Positive; home test-covid test result=Positive; experienced coolness in my legs/ cold feeling spread to my buttocks. My buttocks feel icy. My legs and buttocks feel cool to the touch but extremely cold to me; It is difficult to concentrate on my work and my life because of the cold feeling in my legs and my buttocks.; I am very uncomfortable; Interchange of vaccine products; 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 53 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 16Dec2021 (Lot number: Fd7218) at the age of 53 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Essential tremor" (unspecified if ongoing). There were no concomitant medications. Past drug history included: Erythromycin, reaction(s): "Known allergies: Erythromycin", notes: known allergies: Erythromycin. Vaccination history included: Moderna (Dose Number: 2, Batch/Lot No: 047B21A, Location of injection: Arm Left), administration date: 14Apr2021, when the patient was 52 years old, for COVID-19 Immunization; Moderna (Dose Number: 1, Batch/Lot No: 046A21A, Location of injection: Arm Left), administration date: 17Mar2021, when the patient was 52 years old, for COVID-19 Immunization. The patient did not had other vaccine in four weeks and other medications in two weeks.The patient did not have covid prior vaccination. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 16Dec2021, outcome "unknown", described as "Interchange of vaccine products"; DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 06Jan2022, outcome "unknown" and all described as "home test-covid test result=Positive"; FEELING COLD (disability, medically significant) with onset 18Dec2021 17:00, outcome "not recovered", described as "experienced coolness in my legs/ cold feeling spread to my buttocks. My buttocks feel icy. My legs and buttocks feel cool to the touch but extremely cold to me"; DISTURBANCE IN ATTENTION (disability, medically significant) with onset 18Dec2021 17:00, outcome "not recovered", described as "It is difficult to concentrate on my work and my life because of the cold feeling in my legs and my buttocks."; DISCOMFORT (disability, medically significant) with onset 18Dec2021 17:00, outcome "not recovered", described as "I am very uncomfortable". The events "experienced coolness in my legs/ cold feeling spread to my buttocks. my buttocks feel icy. my legs and buttocks feel cool to the touch but extremely cold to me", "it is difficult to concentrate on my work and my life because of the cold feeling in my legs and my buttocks." and "i am very uncomfortable" were evaluated at the physician office visit. The patient underwent the following laboratory tests and procedures: sars-cov-2 test: (06Jan2022) positive, notes: covid test type post vaccination=Nasal Swab; (19Dec2021) negative, notes: covid test type post vaccination=Nasal Swab; (21Dec2021) negative, notes: covid test type post vaccination=Nasal Swab. Therapeutic measures were not taken as a result of feeling cold, disturbance in attention, discomfort. Clinical course: 2 days after the Pfizer vaccine booster (3rd shot), Patient experienced coolness in her legs. About 2 weeks later the cold feeling spread to her buttocks. Her buttocks feel icy. Her legs and buttocks feel cool to the touch but extremely cold to me. She have had to wear outdoor lined running pants 24/7. She put a heating pad on her desk chair to sit on and drape a blanket over her lap. She was very uncomfortable. It was difficult to concentrate on work and her life because of the cold feeling in her legs and buttocks. It was persistent, relentless and does not let up. No follow-up attempts are needed; information about lot/batch number cannot be obtained. No further information is expected. Amendment (DSU): to allow successful HA submission.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220106; Test Name: At home test; Test Result: Positive ; Comments: covid test type post vaccination=Nasal Swab; Test Date: 20211219; Test Name: PCR; Test Result: Negative ; Comments: covid test type post vaccination=Nasal Swab; Test Date: 20211221; Test Name: PCR; Test Result: Negative ; Comments: covid test type post vaccination=Nasal Swab
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Essential tremor
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 19.02.2022
- Impfdatum
- 16.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Antinuclear antibody positive
Biopsy skin
Blood test normal
COVID-19
Chest discomfort
Computerised tomogram coronary artery normal
Electrocardiogram normal
Exposure to SARS-CoV-2
Feeling cold
Illness
Discomfort
Disturbance in attention
Drug ineffective
Interchange of vaccine products
SARS-CoV-2 test
Lymphadenopathy
Magnetic resonance imaging neck
Magnetic resonance imaging spinal normal
Symptomtext
home test-covid test result=Positive; home test-covid test result=Positive; experienced coolness in my legs/ cold feeling spread to my buttocks. My buttocks feel icy. My legs and buttocks feel cool to the touch but extremely cold to me; It is difficult to concentrate on my work and my life because of the cold feeling in my legs and my buttocks.; I am very uncomfortable; Interchange of vaccine products; 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 53 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 16Dec2021 (Lot number: Fd7218) at the age of 53 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Essential tremor" (unspecified if ongoing). There were no concomitant medications. Past drug history included: Erythromycin, reaction(s): "Known allergies: Erythromycin", notes: known allergies: Erythromycin. Vaccination history included: Moderna (Dose Number: 2, Batch/Lot No: 047B21A, Location of injection: Arm Left), administration date: 14Apr2021, when the patient was 52 years old, for COVID-19 Immunization; Moderna (Dose Number: 1, Batch/Lot No: 046A21A, Location of injection: Arm Left), administration date: 17Mar2021, when the patient was 52 years old, for COVID-19 Immunization. The patient did not had other vaccine in four weeks and other medications in two weeks.The patient did not have covid prior vaccination. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 16Dec2021, outcome "unknown", described as "Interchange of vaccine products"; DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 06Jan2022, outcome "unknown" and all described as "home test-covid test result=Positive"; FEELING COLD (disability, medically significant) with onset 18Dec2021 17:00, outcome "not recovered", described as "experienced coolness in my legs/ cold feeling spread to my buttocks. My buttocks feel icy. My legs and buttocks feel cool to the touch but extremely cold to me"; DISTURBANCE IN ATTENTION (disability, medically significant) with onset 18Dec2021 17:00, outcome "not recovered", described as "It is difficult to concentrate on my work and my life because of the cold feeling in my legs and my buttocks."; DISCOMFORT (disability, medically significant) with onset 18Dec2021 17:00, outcome "not recovered", described as "I am very uncomfortable". The events "experienced coolness in my legs/ cold feeling spread to my buttocks. my buttocks feel icy. my legs and buttocks feel cool to the touch but extremely cold to me", "it is difficult to concentrate on my work and my life because of the cold feeling in my legs and my buttocks." and "i am very uncomfortable" were evaluated at the physician office visit. The patient underwent the following laboratory tests and procedures: sars-cov-2 test: (06Jan2022) positive, notes: covid test type post vaccination=Nasal Swab; (19Dec2021) negative, notes: covid test type post vaccination=Nasal Swab; (21Dec2021) negative, notes: covid test type post vaccination=Nasal Swab. Therapeutic measures were not taken as a result of feeling cold, disturbance in attention, discomfort. Clinical course: 2 days after the Pfizer vaccine booster (3rd shot), Patient experienced coolness in her legs. About 2 weeks later the cold feeling spread to her buttocks. Her buttocks feel icy. Her legs and buttocks feel cool to the touch but extremely cold to me. She have had to wear outdoor lined running pants 24/7. She put a heating pad on her desk chair to sit on and drape a blanket over her lap. She was very uncomfortable. It was difficult to concentrate on work and her life because of the cold feeling in her legs and buttocks. It was persistent, relentless and does not let up. No follow-up attempts are needed; information about lot/batch number cannot be obtained. No further information is expected. Amendment (DSU): to allow successful HA submission.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220106; Test Name: At home test; Test Result: Positive ; Comments: covid test type post vaccination=Nasal Swab; Test Date: 20211219; Test Name: PCR; Test Result: Negative ; Comments: covid test type post vaccination=Nasal Swab; Test Date: 20211221; Test Name: PCR; Test Result: Negative ; Comments: covid test type post vaccination=Nasal Swab
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Essential tremor
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 18.02.2022
- Impfdatum
- 27.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Paraesthesia oral
Pharyngeal paraesthesia
Symptomtext
Shortly after shot, tip of tongue then sides started to tingle. This was about 10-15 minutes after. Then the back of my throat also was tingling. I remained at the clinic for one full hour on my own. This subsided over the next couple days. The tongue tingling has happened with each vaccine from Pfizer (1st, second and now this last booster)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia oral
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Dysautonomia, cardiac arrythmia history
- Andere Medikamente
- Bisoprolol, aspirin, crestor, vitamin B, vitamin D
- Allergien
- Clorox, Bleach, Perfumes, Essential Oils, Amonia - cleaners and seasonal
- Vorherige Impfungen
- I have had tongue tingling and chest pain with the first dose and tingling of tongue and back of throat with the booster
- Staat
- MO
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 13.02.2022
- Impfdatum
- 21.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Feeling hot
Headache
Hypoaesthesia
Influenza like illness
Injection site pain
Joint stiffness
Neck pain
Neuropathy peripheral
Pain
Pain in extremity
Pain in jaw
Paraesthesia
Peripheral swelling
Pruritus
Toothache
Symptomtext
Within 10 minutes I had shooting pain up my right neck into my right jaw. Shortly after I developed frontal headache. I had injection site pain for 4-5 days. My headache lasted almost 3 weeks. I was tired and felt fluish for 5 days leading me to get a covid test on 12/27. It was negative. My entire body ached and I was hot all over starting day 4 through 8 or so. My teeth would hurt at times and so would my jaw. This was intermittent for a few weeks. I developed itching within a couple of hours after the injection that lasted for 3-4 days. I had numbness and tingling in my hands and feet a few days after. It turned into pain and itching. My hands and feet still feel swollen, tight and hurt with occasional itching at times.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- None, I reported it to my doctor but am just dealing with the neuropathy. I don't know if it is permanent at this time.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- hypertension,
- Andere Medikamente
- lisinopril, escitalopram, multi vitamin, vit D
- Allergien
- sulfa, penicillin
- Vorherige Impfungen
- body aches, fatigue, generalized pain from head to toe, headache all for 5 days, lympadenopathy left axilla, injection site pai
- Staat
- NY
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 10.02.2022
- Impfdatum
- 16.12.2021
- Beginn
- 20.12.2021
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Heart rate increased
Heart rate irregular
Palpitations
Symptomtext
Vaccine 3 Heart rate increase 20 beats per minute at rest and walking or exercising for 72 hours. Day 4 post booster - had heart palpitations/irregular beats every 30 seconds for 24 hours , slowly decreased until ending on day 6
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Postural orthotic tachycardia.
- Andere Medikamente
- Midodrine, omeprazole, Zyrtec
- Allergien
- Wheat Percocet
- Vorherige Impfungen
- 2/12/2021 immediately after second Pfizer covid vaccine i inhad a drop in blood pressure and heart rate with dizziness.
- Staat
- WA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 09.02.2022
- Impfdatum
- 07.01.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Injected limb mobility decreased
Insomnia
Migraine
Pain
Pain in extremity
Symptomtext
Severe left arm pain. After receiving injections patient's arm sore. Instead of soreness improving, soreness worsened. No onset date of symptoms. severe pain, unable to lift left arm, difficultly sleeping, migraines. Patient has been seen at medical office and ER for symptoms. Latest ER visit 2/9/22. patient believes she is having a reaction to the TD vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 08.02.2022
- 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: nein
Chest pain
Tinnitus
Symptomtext
chest pain, ear ringing
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 02.02.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal discomfort
Anosmia
Asthenia
Body temperature decreased
Dizziness
Anxiety
Fatigue
Headache
Incorrect dose administered
Nausea
Dyspnoea exertional
Feeding disorder
Gastrooesophageal reflux disease
Hypotension
Inflammation
Influenza like illness
Joint swelling
Malaise
Symptomtext
I went in to get my booster (3rd dose) of the vaccine. The nurse at stroe - gave me 6 doses (overdose) instead of 1 for my booster. -- I got very sick - fever, shakes, low blood pressure, blurred vision, dizzy, hard to maintain body temp. I also got upset stomach, nausea, acid reflux and swelling of joints, inflammation overall. In addition I had flu like symptoms that lasted a week. Also, I got very weak and had a hard time walking very far without getting winded. I had head aches, heart palpitations and overall unwell. I couldn't eat for several days. Also, I had changes in smell and taste. Things would have no smell or an "off" smell. I am still suffering from that depending on the smell. Also my taste isn't back to normal yet. I am still having a hard time with my energy level, aches and pains and inflammation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea exertional
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Septra
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 02.02.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 7+
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal discomfort
Anosmia
Asthenia
Body temperature decreased
Dizziness
Anxiety
Fatigue
Headache
Incorrect dose administered
Nausea
Dyspnoea exertional
Feeding disorder
Gastrooesophageal reflux disease
Hypotension
Inflammation
Influenza like illness
Joint swelling
Malaise
Symptomtext
I went in to get my booster (3rd dose) of the vaccine. The nurse at stroe - gave me 6 doses (overdose) instead of 1 for my booster. -- I got very sick - fever, shakes, low blood pressure, blurred vision, dizzy, hard to maintain body temp. I also got upset stomach, nausea, acid reflux and swelling of joints, inflammation overall. In addition I had flu like symptoms that lasted a week. Also, I got very weak and had a hard time walking very far without getting winded. I had head aches, heart palpitations and overall unwell. I couldn't eat for several days. Also, I had changes in smell and taste. Things would have no smell or an "off" smell. I am still suffering from that depending on the smell. Also my taste isn't back to normal yet. I am still having a hard time with my energy level, aches and pains and inflammation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea exertional
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Septra
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 31.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Chills
Condition aggravated
Fatigue
Full blood count
Injection site erythema
Interchange of vaccine products
Lymphadenopathy
Night sweats
Pain
Vomiting
White blood cell count increased
Symptomtext
The evening after her vaccination, pt developed chills, possible fever but didn't check temperature. The following morning she felt weak, achy, fatigued and vomited x 1. Temp of 99 that day, continued to have chills. Developed bulky left axillary lymphadenopathy on 1/9, "size of an ice cream scoop". Injection site redness up to 4x6 inches which gradually improved. Symptoms improved by 1/13/22 other than lymphadenopathy. I saw her in clinic on 1/22 and she reported feeling nearly back to her baseline, still slightly more tired than usual and had had two nights of night sweats, but had ongoing bulky left axillary lymphadenopathy measuring about 4cm x 7cm - firm, non-tender, mobile node. Of note, the patient had a similar reaction after her second dose of Moderna vaccine during her primary series, and her lymphadenopathy lasted 6 weeks that time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- CBC with WBC count 39.2k (stable from prior - pt has known CLL)
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Chronic Lymphocytic Leukemia (CLL) - stable, asymptomatic Genital HSV Lumbar stenosis Mixed urge and stress incontinence Benign essential tremor
- Andere Medikamente
- Diclofenac 75mg BID Acyclovir 400mg BID Trospium 60mg XR daily
- Allergien
- Amoxicillin
- Vorherige Impfungen
- Similar rxn after Moderna #2 given 4/17/21
- Staat
- NJ
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 28.01.2022
- Impfdatum
- 23.12.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Balance disorder
Bedridden
Condition aggravated
Vertigo
Visual impairment
Headache
Loss of personal independence in daily activities
Mobility decreased
Symptomtext
started experiencing symptoms of vertigo; that the episodes are getting worse; she cannot get out of bed and if she turns her neck a little bit or even slowly she loses her ability to balance; she cannot get out of bed and if she turns her neck a little bit or even slowly she loses her ability to balance; her vision is definitely impaired; 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 48 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 23Dec2021 17:30 (Batch/Lot number: unknown) at the age of 48 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Bnt162b2 (first dose), administration date: 19Jan2021, when the patient was 47 years old, for COVID-19 Immunization; Bnt162b2 (Second dose), administration date: 19Feb2021, when the patient was 47 years old, for COVID-19 Immunization. The following information was reported: VERTIGO (non-serious) with onset 24Dec2021, outcome "not recovered", described as "started experiencing symptoms of vertigo"; CONDITION AGGRAVATED (non-serious) with onset Dec2021, outcome "not recovered", described as "that the episodes are getting worse"; BEDRIDDEN (non-serious), BALANCE DISORDER (non-serious) all with onset Dec2021, outcome "unknown" and all described as "she cannot get out of bed and if she turns her neck a little bit or even slowly she loses her ability to balance"; VISUAL IMPAIRMENT (non-serious) with onset Dec2021, outcome "not recovered", described as "her vision is definitely impaired". Therapeutic measures were not taken as a result of vertigo, condition aggravated, bedridden, balance disorder, visual impairment. Additional information: The side effect she has is concerning her as she has had it a week now and it is a very extensive case of vertigo where she cannot get out of bed and if she turns her neck a little bit or even slowly she loses her ability to balance and her vision is definitely impaired and she knew some of it was possible but this has lasted so long. States the vertigo began for her exactly the next morning.but now the vertigo is happening more and more and it is not going away and it is way worse.she has her 1st dose of the Pfizer Covid vaccine on 19Jan2021 and her second dose a month later on 19Feb2021 and her booster dose just a week ago but can't remember the exact date now but it was right before Christmas so she will say the booster dose was on 23Dec2021.she has no lots, expiry dates or NDC numbers to provide because she does not have her patient card with her as her husband has it and he is not home.Did any AE(s) require a visit to: Emergency Room? No; Physician Office? No;Prior Vaccinations (within 4 weeks): None.AE(s) following prior vaccinations: n/a.Patient's Medical History (including any illness at time of vaccination) None.Family Medical History Relevant to AE(s): None.Relevant Tests: None. Her pharmacist told her to just keep taking Tylenol and laying down and to drink water.she did not take Tylenol because she is not a big fan of medicine and just thought the vertigo would go away so she took it kind of easy and she has kind of quarantined her family anyways because of the pandemic which is a quiet break for them and her vertigo is turning into something a bit concerning. she does not take any medication and is completely healthy otherwise.she was wondering if since both she and her son are both really skinny and she is 120 or 115 pounds and her son is very skinny so maybe the Pfizer Covid booster is maybe a little too strong for her and her son and they both did not have vertigo or did not have the vertigo this severe with at least the first two doses of their Pfizer Covid vaccines and she is not sure what went wrong with her and her son's third doses of the Pfizer Covid vaccine. The lot number for bnt162b2 was not provided and will be requested during follow up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Patient History: No
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- F
- Eingang
- 25.01.2022
- Impfdatum
- -
- Beginn
- 18.12.2021
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthma
Burning sensation
Cellulitis
Condition aggravated
Dizziness
Eczema
Erythema
Immunisation
Nausea
Paraesthesia
Symptomtext
eczema; Cellulitis on arm; burning sensation/ tingling felt like burning all over and inside her body; redness; Asthma attack; Asthma attack; Severe nausea; Dizziness; Tingling all over body; booster; This is a spontaneous report received from a contactable reporter (consumer). The reporter is the patient. A 64 year-old female patient received BNT162b2 (PFIZER-BIONTECH COVID-19 VACCINE), administered in arm right, administration date 2021 (Lot number: FD7218) as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "Asthma" (ongoing), notes: diagnosed at 4 years old. The patient's concomitant medications were not reported. Vaccination history included: BNT162b2 (Dose 1, Lot Number: ER8727, right arm), administration date: 25Mar2021, when the patient was 63 years old, for COVID-19 immunisation, reaction: "Asthma attack"; BNT162b2 (Dose 2, Lot Number: ER8727, right arm), administration date: 15Apr2021, when the patient was 63 years old, for COVID-19 immunisation, reaction: "Asthma attack". The following information was reported: IMMUNISATION (medically significant) with onset 2021, outcome "unknown", described as "booster"; CELLULITIS (medically significant) with onset 20Dec2021, outcome "recovering", described as "Cellulitis on arm"; BURNING SENSATION (medically significant) with onset 20Dec2021, outcome "recovering", described as "burning sensation/ tingling felt like burning all over and inside her body"; ERYTHEMA (medically significant) with onset 20Dec2021, outcome "recovering", described as "redness"; ASTHMA (medically significant), CONDITION AGGRAVATED (medically significant) all with onset 18Dec2021, outcome "not recovered" and all described as "Asthma attack"; NAUSEA (non-serious) with onset 18Dec2021, outcome "recovering", described as "Severe nausea"; DIZZINESS (non-serious) with onset 18Dec2021, outcome "not recovered", described as "Dizziness"; PARAESTHESIA (non-serious) with onset 18Dec2021, outcome "recovered" (2021), described as "Tingling all over body"; ECZEMA (non-serious), outcome "unknown", described as "eczema". The events "cellulitis on arm", "burning sensation/ tingling felt like burning all over and inside her body", "redness", "asthma attack", "asthma attack", "severe nausea", "dizziness", "tingling all over body" and "eczema" were evaluated at the physician office visit. Therapeutic measures were taken as a result of cellulitis, burning sensation, erythema. Additional information: Vaccination facility type was pharmacy/drug store. The patient did not receive other vaccinations within four weeks prior to vaccination with Pfizer. There were no additional vaccines administered on same date of the Pfizer vaccine. There were no relevant tests. The events occurred after the booster dose. Severe nausea on 18Dec2021 and ongoing with outcome of improved. Dizziness on 18Dec2021 and ongoing with outcome of persisting. Tingling all over body on 18Dec2021 with outcome of recovered completely. Asthma attack on 18Dec2021 and ongoing with outcome of persisting. Cellulitis on arm on 20Dec2021 and ongoing with outcome of improved. The patient stated that cellulitis on arm was on the flat side of her arm, described as similar to a burn, the skin bubbled up and it looked like burned skin that had peeled away. She was given Clobetasol cream, a steroid cream and was effective in improving the burning sensation and redness. She said her skin still has texture, like tape across her arm. She also reported severe nausea, dizziness, and tingling all over body. She explained that the tingling felt like burning all over and inside her body, similar to having bad reflux. The events ended a few days after it started. The patient also had an asthma attack after booster. She had previously reported asthma attacks after her first and second vaccines. All events did not require a visit to the Emergency Room but required a visit to the Physician Office. She said the vaccines made her asthma worse. She wanted to report her events so it would be documented for other people. She is wondering if the booster shot activated her eczema and that is why her arm had cellulitis. She has heard of people reporting a lot of rashes with the booster but cannot provide any identifiers of specifics. Her doctor also took a picture of her arm. She said she probably will not receive Covid boosters anymore in the future. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Asthma (diagnosed at 4 years old)
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 24.01.2022
- Impfdatum
- 20.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Computerised tomogram head
Headache
Magnetic resonance imaging
Migraine
Occipital neuralgia
Specialist consultation
Tension headache
Symptomtext
Around 10 days after receiving my booster shot, I developed severe headache, migraines, and burning sensations. Several migraine and pain medications were prescribed to me with no effect. I tried massage, acupuncture, chiropractic work which helped a little. But a month from the time of the shot in 1/20/22 the pain from the band headache got extremely intense. I have received shots in the back of my head from a neurologist and plan to have more treatment to numb the pain for possible Occipital Neuralgia.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- No further imaging was done since I had previously had an MRI and head CT within the last 3 months.
- Aktuelle Erkrankungen
- GERD, IBS, anxiety, headaches, chest and body pains, fatigue
- Vorgeschichte
- None
- Andere Medikamente
- Alprazolam, vitamin D, fish oil, turmeric
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 24.01.2022
- Impfdatum
- 19.12.2021
- Beginn
- 23.12.2021
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypertension
Hypoaesthesia
Nervous system disorder
Paraesthesia
Rash
Tinnitus
Symptomtext
Systemic: Allergic: Rash Generalized-Medium, Systemic: Hypertension-Mild, Systemic: Neurological Disorder (diagnosed by MD)-Medium, Systemic: Numbness (specify: facial area, extremities)-Mild, Systemic: Tingling (specify: facial area, extemities)-Mild, Systemic: Tinnitus-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 22.01.2022
- Impfdatum
- 15.12.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Immunisation
Musculoskeletal stiffness
Pain in extremity
Paraesthesia
Symptomtext
During the week of 12/27/21 I then also developed left knee, ankle, and foot pains; I had severe tenderness and pain in my left hand, mostly in the palm of my hand/ sore in my palm/ I sometimes get jolts pains in my hand/ foot pains/ pain in my leg and foot increases throughout the work week; It was difficult to make a fist; Sometimes a slight tingling that radiates towards my elbow/ some tingling that felt similar to the sensations I get in my hand and forearm/ It sometimes feels like pins and needles on my foot and radiates towards my knee; Dose received: 3; This is a spontaneous report received from contactable reporter (Other healthcare professional). The reporter is the patient. A 41-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in left arm, administration date 15Dec2021 at 15:45 (Lot number: FD7218) at the age of 41 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "Chronic back pain" (unspecified if ongoing) and "Spider vein" (unspecified if ongoing), notes: Spider veins in both legs. There were no concomitant medications. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE; Lot Number: UNKNOWN; Anatomical Location: Left arm; Route of Administration: Unspecified; Administration time: 10:00), administration date: an unknown date in Dec2020, when the patient was 40 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE; Lot Number: UNKNOWN; Anatomical Location: Left arm; Route of Administration: Unspecified; Administration time: 10:00), administration date: an unknown date in Jan2021, when the patient was 40 years old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 15Dec2021 at 15:45, outcome "unknown", described as "Dose received: 3"; PAIN IN EXTREMITY (non-serious) with onset 16Dec2021 at 07:00, outcome "not recovered", described as "I had severe tenderness and pain in my left hand, mostly in the palm of my hand/ sore in my palm/ I sometimes get jolts pains in my hand/ foot pains/ pain in my leg and foot increases throughout the work week"; MUSCULOSKELETAL STIFFNESS (non-serious) with onset 16Dec2021 at 07:00, outcome "not recovered", described as "It was difficult to make a fist"; PARAESTHESIA (non-serious) with onset 16Dec2021 at 07:00, outcome "not recovered", described as "Sometimes a slight tingling that radiates towards my elbow/ some tingling that felt similar to the sensations I get in my hand and forearm/ It sometimes feels like pins and needles on my foot and radiates towards my knee"; ARTHRALGIA (non-serious) with onset 27Dec2021, outcome "not recovered", described as "During the week of 12/27/21 I then also developed left knee, ankle, and foot pains". The events "I had severe tenderness and pain in my left hand, mostly in the palm of my hand/ sore in my palm/ I sometimes get jolts pains in my hand/ foot pains/ pain in my leg and foot increases throughout the work week", "It was difficult to make a fist", "Sometimes a slight tingling that radiates towards my elbow/ some tingling that felt similar to the sensations I get in my hand and forearm/ It sometimes feels like pins and needles on my foot and radiates towards my knee" and "During the week of 12/27/21 I then also developed left knee, ankle, and foot pains" were evaluated at the physician office visit. Therapeutic measures were not taken as a result of pain in extremity, musculoskeletal stiffness, paraesthesia and arthralgia. Additional information: The patient had no known allergies. 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 vaccine. Since the vaccination, the patient had not been tested for COVID-19. It was reported that after several days the tenderness decreased but it still felt sore in her palm to that day (at the time of this report). She stands at work almost all day long so the pain in her leg and foot increases throughout the work week.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Chronic back pain; Spider vein (Spider veins in both legs)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 87,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 05.03.2021
- Beginn
- 18.01.2022
- Tage bis Beginn
- 319,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Dyspnoea
SARS-CoV-2 test positive
Symptomtext
COUGH, SHORTNESS OF BREATH
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- POSITIVE COVID TEST 1/18/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- CKD stage III Endometrial cancer History of colonic polyps HTN Hyperlipidemia Palpitations Hypertriglyceridemia Sick sinus syndrome Osteopenia Restless leg syndrome Atrophic vaginitis Atrial fibrillation Overweight Endometrial cancer
- Andere Medikamente
- calcium-cholecalciferol, D3, (CALCIUM 600 + D) 600 mg(1,500mg) -400 unit Oral Tab diltiazem (CARDIZEM CD) 120 mg oral extended release capsule 24 HR
- Allergien
- Alendronate Atorvastatin
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 19.12.2021
- Beginn
- 19.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Headache
Immunisation
Peripheral swelling
Product use issue
Pruritus
Throat irritation
Vaccination site mass
Vaccination site pain
Vaccination site reaction
Vaccination site swelling
Symptomtext
Large, itchy red swollen bump / on left arm at injection sight; Large, itchy red swollen bump / on left arm at injection sight; Large, itchy red swollen bump / on left arm at injection sight; Large, itchy red swollen bump / on left arm at injection sight; itchy throat; headache; chest pain on right side; pain at injection site; swollen left armpit; Booster; Other vaccine same date vaccine date 19Dec2021; This is a spontaneous report received from contactable reporter(s) (Consumer or other non-HCP). The reporter is the patient. A 27-years-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 19Dec2021 12:00 (Lot number: FD7218) at the age of 27 years as dose 3 (booster), single for covid-19 immunisation; influenza vaccine (FLU), administered in arm right, administration date 19Dec2021 (Batch/Lot number: unknown) as dose number(unknown)single. The patient's relevant medical history was not reported. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0173, Location of injection: Arm Left), administration date: 08May2021, when the patient was 26 years old, for Covid-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EW0164, Location of injection: Arm Left), administration date: 07Apr2021, when the patient was 26 years old, for Covid-19 immunization. The following information was reported: PRODUCT USE ISSUE (non-serious) with onset 19Dec2021, outcome "unknown", described as "Other vaccine same date vaccine date 19Dec2021"; IMMUNISATION (non-serious) with onset 19Dec2021 12:00, outcome "unknown", described as "Booster"; VACCINATION SITE REACTION (non-serious), PRURITUS (non-serious), VACCINATION SITE SWELLING (non-serious), VACCINATION SITE MASS (non-serious) all with onset 20Dec2021 10:00, outcome "not recovered" and all described as "Large, itchy red swollen bump / on left arm at injection sight"; THROAT IRRITATION (non-serious) with onset 20Dec2021 10:00, outcome "not recovered", described as "itchy throat"; HEADACHE (non-serious) with onset 20Dec2021 10:00, outcome "not recovered", described as "headache"; CHEST PAIN (non-serious) with onset 20Dec2021 10:00, outcome "not recovered", described as "chest pain on right side"; VACCINATION SITE PAIN (non-serious) with onset 20Dec2021 10:00, outcome "not recovered", described as "pain at injection site"; PERIPHERAL SWELLING (non-serious) with onset 20Dec2021 10:00, outcome "not recovered", described as "swollen left armpit". The events "large, itchy red swollen bump / on left arm at injection sight", "large, itchy red swollen bump / on left arm at injection sight", "large, itchy red swollen bump / on left arm at injection sight", "large, itchy red swollen bump / on left arm at injection sight", "itchy throat", "headache", "chest pain on right side", "pain at injection site" and "swollen left armpit" were evaluated at the physician office visit. Therapeutic measures were not taken as a result of vaccination site reaction, pruritus, vaccination site swelling, vaccination site mass, throat irritation, headache, chest pain, vaccination site pain, peripheral swelling. Additional Information: The patient had large, itchy red swollen bump (larger than size of golf ball, felt like hard lump) on left arm at injection sight, itchy throat, headache, chest pain on right side, pain at injection site, swollen left armpit. The patient had no known allergies. The patient had no other vaccine in four weeks and no other medications in two weeks. No treatment was received for adverse events. The patient had no COVID-19 prior to vaccination and post the vaccination was not tested for COVID-19. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 19.01.2022
- Impfdatum
- 28.12.2021
- Beginn
- 12.01.2022
- Tage bis Beginn
- 15,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Amblyopia
Condition aggravated
Muscle twitching
Symptomtext
Patient called the vaccine clinic on January 19th to discuss his potential reaction to the vaccine. Patient stated he had a lazy eye and a face twitch after the 2nd Pfizer vaccination, which was later diagnosed as bell's palsy. He stated he was again having a lazy eye and face twitch that began about two days after receiving his booster dose of the covid vaccination. Patient stated one of his other family members had a similar reaction.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asthma. Family history of Bell's Palsy.
- Andere Medikamente
- -
- Allergien
- NKDA
- Vorherige Impfungen
- Covid Pfizer vaccine on 2/4/2021 (Lot: EL1284): patient reports he had a similar reaction with a lazy eye and an eye twitch and
- Staat
- FL
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 15.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Blood creatine phosphokinase normal
C-reactive protein normal
Laboratory test normal
Pain
Pain in extremity
Paraesthesia
Tenderness
Vitamin B12 normal
Symptomtext
The morning after the injection I woke up to severe tenderness and pain in my left hand, mostly in the palm of my hand . After approx 3 days it decreased to a more mild constant ache, slight tingling sensations that radiated towards my elbow, and occasional jolts of pain multiple times throughout the days. Once I returned to my regular work week on 12/27/21, I also developed a similar aching pain in my left knee, ankle, and foot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- On 1/17/22, my phsician performed several test that all came back in "normal" range. (CPK, B12, and C-reactive protien).
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- Minor back pain , spider veins in both legs.
- Andere Medikamente
- NONE
- Allergien
- NONE KNOWN
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 17.01.2022
- Impfdatum
- 30.12.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Burning sensation
Gait disturbance
Headache
Influenza A virus test negative
Influenza B virus test
Lymphadenopathy
Migraine
Movement disorder
Myalgia
Pain
Pain in extremity
SARS-CoV-2 test negative
Sleep disorder
Symptomtext
I woke up on 12/31/2021 in so much pain I could barely walk or move. Every muscle and joint hurt, I walked like I was 90 years old. My lymph nodes swelled so much I ended up having headaches and migraines. I went to the chiropractor 3 times in less than a week for pain and headaches. My arm burned and hurt for at least two weeks.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- Covid and Influenza A and B testing, both negative
- Aktuelle Erkrankungen
- None, possibly bronchitis
- Vorgeschichte
- Chronic pain
- Andere Medikamente
- Lexapro 30 mg once daily, Verapamil 180 mg once daily, prenatal once daily
- Allergien
- Ultram, bentyl, peppermint
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 17.01.2022
- Impfdatum
- 17.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dizziness
Hypertension
Symptomtext
patient reported feeling lightheaded after vaccine. bp 170/100. reports this is her baseline. snacks provided. patient reported symptoms subsided upon discharge. patient advised to contact her provider asap. advised to go to emergency room if symptoms return and or blood pressure continues to be high. she was agreeable.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 15.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- UN / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Breast pain
Chest pain
Lymph node pain
Lymphadenopathy
Pain
Pain in extremity
Pyrexia
Skin warm
Sluggishness
Swelling
Symptomtext
Friday - on and off fever and aches and sluggishness. Saturday fever gone, sluggishness and aches all over but very painful swelling in lymph node under left arm - radiating into left breast and chest. Swelling was easily noticeable visually. The arm and underarm and chest was warm to the touch and very painful. By Monday pain , all other symptoms were gone and the lymph node pain was much decreased to just bothersome and always present. Swelling was still visually noticeable but to a much lesser degree. As of 9 days after vaccine booster, the underarm lymph node is now only sore if touched. Much improved and not visually noticable.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Thyroid medication - levoxyl
- Allergien
- N/A
- Vorherige Impfungen
- Moderna vaccines (2 doses) fever and aches only for 2 days each
- Staat
- AZ
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 15.01.2022
- Impfdatum
- 21.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injected limb mobility decreased
Injection site pain
Pain
Myalgia
Pain in extremity
Symptomtext
The patient reported that his left arm has been sore every since he received his booster. He states it is in the muscle where he received the vaccine and feels like he has over exerted his arm. The pain is so bad that he has been taking 2 aleve per day to help the pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 15.01.2022
- Impfdatum
- 21.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injected limb mobility decreased
Injection site pain
Pain
Myalgia
Pain in extremity
Symptomtext
The patient reported that his left arm has been sore every since he received his booster. He states it is in the muscle where he received the vaccine and feels like he has over exerted his arm. The pain is so bad that he has been taking 2 aleve per day to help the pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 27.12.2021
- Beginn
- 05.01.2022
- Tage bis Beginn
- 9,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Angina pectoris
Palpitations
Rash
Symptomtext
Rash, heart pain, palpitation
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 14.01.2022
- Impfdatum
- 08.01.2022
- Beginn
- 09.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Angioedema
Oedema peripheral
Pruritus
Rash
Lip swelling
Paraesthesia oral
Peripheral swelling
Urticaria
Symptomtext
Patient's mother has written down and kept track to see what patient reacts to. This paperwork shows patient receiving the pfizer booster on 1/8/2022 with no reactions all day. On 1/9/2022 at 11:00 AM patient ended up having minor itching after eating pancakes with raspberry jam and sausage links. that same day patient ended up with moderate itching on his whole body, swelling of his feet and toes as well as the soles of both feet after having mike & Ike candy. Patient had taken 37.5mg of benadryl and the swelling went away. 1800 patient had chili for dinner and had minor itching. At 2300 patient had mint chocolate chip ice cream and ended up having whole body itching and swelling of his lip. The swelling went away within 30 minutes. 1/10/2022 at 1500 patient had a coffee, at 1520 his left hand started swelling, he had a rash / welts to his entire face. 1535 he took 37.5mg of benadryl and the rash to his face went away however the swelling to his left hand was still present. At 1800 patient had chili for dinner with no reaction. 1/11/2022 they called the doctor for suggestions. At 1050 after consuming 2 scoops of mint chocolate chip ice cream patient experienced slight lip tingling that only lasted a couple of minutes. At 1120 he developed a rash on his ankles.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia oral
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- no illness
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- amoxicillin, no food allergies, grasses
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 13.01.2022
- 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
Dizziness
Dyspnoea
Palpitations
Pruritus
Tremor
Urticaria
Symptomtext
Patient received Pfizer booster on 1/8/22, and had reaction hours after injection, Pt broke out in hives on his face, chest, back, and arms. Hives were itchy in nature. Also reports Pt felt dizzy, shaky, short of breath and felt like his heart was racing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Allergies; Gluten intolerance; Premature infant; Reactive airway disease; Asthma; Eczema.
- Andere Medikamente
- Albuterol; Cetirizine; Advair; Florajen 4 kids.
- Allergien
- Codeine; Gluten.
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 11.01.2022
- Impfdatum
- 21.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 6,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Antinuclear antibody positive
Chest pain
Fatigue
Inflammation
Laboratory test
Pain
Pyrexia
Symptomtext
I had regular symptoms of exhaustion, body aches and low-grade fever (nothing over 100.9) for the first 6 days or so. The body aches got worse into the week of Dec 27th - to the point where I could not get out of bed. The body aches continued and so did the exhaustion. On new years eve, I started having chest pains and so I went to the Emergency room. They found that I did not have a heart attack so they sent me home. I followed up with a doctor at Facility (Dr.) and I briefly mentioned that I think this was related to the COVID booster. He told me that it is highly unlikely that it is the vaccine and that adverse reactions are minimal. To this day I am still easily exhausted and have to lie down often. Dr. ordered labwork and it showed some inflammation and tested positive for ANA. Saw rheumatologist today and again, I expressed my concerns that this is all related to the booster shot. He listened and told me there is a chance it could be, but that we are going to rule out everything else first.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Diabetes 2, Bipolar II
- Andere Medikamente
- Rybelsus, metformin, glipizide, lisinopril
- Allergien
- amoxicillin
- Vorherige Impfungen
- Just low-grade fevers for both 3/2021 and 4/2021 Pfizer COVID vaccines.
- Staat
- NJ
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 11.01.2022
- Impfdatum
- 02.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 6,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest X-ray
Chest discomfort
Chest pain
Differential white blood cell count
Dizziness
Dyspnoea
Electrocardiogram
Fatigue
Full blood count
Hepatitis C antibody
Lipase
Metabolic function test
Paraesthesia
Troponin
Symptomtext
Extreme discomfort in chest, going down left arm with tingling in left hand. Fatigue, shortness of breath, dizziness. Patient went to emergency room in case it was a heart attack. Symptoms much less pronounced after 2 hours (started at 6am, up until about 8am). Diagnosis is chest pains. Released from ER after 5 hours. Still experiencing light symptoms two days later.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Lab tests: CBC and differential, CMP, Lipase, Troponin T, Hepatitis C Antibody (includes reflex). Imaging tests: ECG 12 lead performed 2 times. XR chest 2 views. BP 160/90, pulse 78.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Obesity
- Andere Medikamente
- One-A-Day men's health vitamin Zzz=Quill melanin chews w/ elderberry
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Condition aggravated
Fatigue
Feeling abnormal
Headache
Impaired work ability
Pain
Sleep disorder
Tremor
Vomiting
Symptomtext
12 hours after injection, I awoke with horrible chills. I was shaking so violently I woke myself and my husband. I proceeded to vomit four times. Since that time, I had a headache and general body aches. Exhaustion continues. I was unable to go to work today as I am so tired. I feel very foggy-headed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypothyroidism
- Andere Medikamente
- Armour thyroid
- Allergien
- None
- Vorherige Impfungen
- Moderna COVID-19 dose #2 had the same effect but only 36 hours.
- Staat
- NY
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- Impfdatum
- 30.12.2021
- Beginn
- 08.01.2022
- Tage bis Beginn
- 9,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Dyspnoea
Symptomtext
CHIEF COMPLAINT: C/O SOB, cough since Covid Booster on 12/31. Home albuterol tx x5, DuoNeb and decadron x1 vis EMS. HISTORY OF PRESENT ILLNESS: This patient is a 67-year-old female presents emergency department with complaints of cough and shortness of breath. Patient states that she received a Covid booster on 12/31. Patient states that she has been having symptoms since then. Patient states she has a history of asthma and has used her home albuterol treatment 5 times today. Patient called EMS and was given a DuoNeb and Decadron. The patient denies any chest pain but does complain of significant shortness of breath stating that she saw oxygen saturation levels as low as 77%.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Unknown
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Acute bronchitis, Epilepsy, Hypertension, IBS, Osteoarthritis
- Andere Medikamente
- Unknown
- Allergien
- clindamycin, sulfa drugs, Zofran, Lipitor, Crestor, iodine containing compounds, statins,
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 09.01.2022
- Impfdatum
- 28.12.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Chest pain
Electrocardiogram
X-ray
Symptomtext
SEVERE CHEST PAIN
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Blood work, EKG, X-ray 12/31/2021 regional medical center ER, 1/5/2022 medical center ER, 1/9/2022 medical center ER, 1/11/2022 cardiologist Medical center
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Shellfish, eggs
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 08.01.2022
- Impfdatum
- 16.12.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Asthenia
Body temperature
Chest discomfort
Cough
Delirium
Dizziness
Feeling cold
Hypersomnia
Immunisation
Loss of personal independence in daily activities
Pyrexia
Tremor
Vomiting
Wheezing
Symptomtext
fever/ I am now at 97.6. I was at a 102 at one point and it dropped to a 100; Caller reports that she received the Pfizer Covid booster shot; vomited; she became really cold; shaking from how cold she was; She reports having slept for 2 days straight and afterwards was too weak to get up; I ran in and ran back out and now I am dizzy; she feels like mucous is in her chest; she has wheezing in her chest; coughing relentlessly; delirium; She reports having slept for 2 days straight and afterwards was too weak to get up; can't even make anything to eat/ she hasn't worked in 6 days; 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 58 year-old female patient received bnt162b2 (BNT162B2), intramuscular, administered in deltoid right, administration date 16Dec2021 (Lot number: FD7218) at the age of 58 years as dose number unknown (booster), single for covid-19 immunisation. Relevant medical history included: "High blood pressure" (unspecified if ongoing); "stent in my heart" (unspecified if ongoing), notes: I have a stent in my heart; "I have a bad heart" (unspecified if ongoing), notes: I have a bad heart,. The patient's concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Dose number unknown, Manufacturer unknown), for Covid-19 immunization. The following information was reported: IMMUNISATION (disability, medically significant) with onset 16Dec2021, outcome "unknown", described as "Caller reports that she received the Pfizer Covid booster shot"; DELIRIUM (medically significant) with onset Dec2021, outcome "unknown", described as "delirium"; HYPERSOMNIA (disability), ASTHENIA (non-serious) all with onset Dec2021, outcome "unknown" and all described as "She reports having slept for 2 days straight and afterwards was too weak to get up"; PYREXIA (disability) with onset 17Dec2021, outcome "unknown", described as "fever/ I am now at 97.6. I was at a 102 at one point and it dropped to a 100"; LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (disability) with onset Dec2021, outcome "unknown", described as "can't even make anything to eat/ she hasn't worked in 6 days"; VOMITING (non-serious) with onset 16Dec2021, outcome "unknown", described as "vomited"; FEELING COLD (non-serious) with onset Dec2021, outcome "unknown", described as "she became really cold"; TREMOR (non-serious) with onset Dec2021, outcome "unknown", described as "shaking from how cold she was"; DIZZINESS (non-serious) with onset Dec2021, outcome "unknown", described as "I ran in and ran back out and now I am dizzy"; CHEST DISCOMFORT (non-serious) with onset Dec2021, outcome "unknown", described as "she feels like mucous is in her chest"; WHEEZING (non-serious) with onset Dec2021, outcome "unknown", described as "she has wheezing in her chest"; COUGH (non-serious) with onset Dec2021, outcome "unknown", described as "coughing relentlessly". The patient underwent the following laboratory tests and procedures: body temperature: (Dec2021) 102; (Dec2021) 100, notes: dropped; (21Dec2021) 97.6, notes: I am now at 97.6. Therapeutic measures were taken as a result of delirium, pyrexia, chest discomfort, wheezing, cough. Clinical course: Patient has had "every symptom under the sun" reporting that she vomited within 4 hours. Patient vomited "like nobody's business" then she became really cold, drove home and started shaking from how cold she was. She slept for 2 days straight and afterwards was too weak to get up and now can't even make anything to eat. She reports that today was the first day she could drive to get something in the house, she states "I ran in and ran back out and now I am dizzy". Patient reported that while she doesn't have a cough, she feels like mucous is in her chest, she has wheezing in her chest and was taking Mucinex and Advil for the fever. Within the first 24 hours, she developed fever, coughing relentlessly, delirium. She slept literally for 2 days straight and today is the first day that broke the fever. Patient was now at 97.6, was at a 102 at one point and it dropped to a 100. Patient had been bed ridden. She had not been able to work in 6 days. Within a matter of 4-6 hours, she was vomiting, projecting like it came out of nowhere. She was taking Mucinex and just drinking lot of water. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- Test Date: 202112; Test Name: Fever; Result Unstructured Data: Test Result:102; Test Date: 202112; Test Name: Fever; Result Unstructured Data: Test Result:100; Comments: dropped; Test Date: 20211221; Test Name: Fever; Result Unstructured Data: Test Result:97.6; Comments: I am now at 97.6
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Blood pressure high; Cardiac disorder (I have a bad heart,); Coronary stent user (I have a stent in my heart)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 08.01.2022
- Impfdatum
- 17.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Angina pectoris
Blood test normal
Chest X-ray normal
Electrocardiogram normal
Hypertension
Immunisation
Paraesthesia
Symptomtext
I developed pain around my heart; blood pressure was high; tingling pins and needles sensation in my face, starting with the left side of my face and neck and (10 hours later) including my right side of my face as well as parts of my head, my ears and my neck; Booster; This is a spontaneous report received from a contactable reporter (Consumer). The reporter is the patient. A 51-year-old female patient (not pregnant) received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), administered in arm left, administration date 17Dec2021 11:15 (Lot number: FD7218) at the age of 51 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Known allergies: Sulfa" (unspecified if ongoing). The patient's concomitant medications were not reported. The patient did not receive any other vaccine within 4 weeks prior to the vaccine. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0180, Location of injection: Arm Left, Vaccine Administration Time: 10:30 AM), administration date: 16Jun2021, when the patient was 51 years old, for COVID-19 Immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EW0178, Location of injection: Arm Left, Vaccine Administration Time: 11:00 AM), administration date: 26May2021, when the patient was 51 years old, for COVID-19 Immunization. The following information was reported: ANGINA PECTORIS (medically significant) with onset 22Dec2021 01:00, outcome "not recovered", described as "I developed pain around my heart"; IMMUNISATION (non-serious) with onset 17Dec2021 11:15, outcome "unknown", described as "Booster"; HYPERTENSION (non-serious) with onset 22Dec2021 01:00, outcome "not recovered", described as "blood pressure was high"; PARAESTHESIA (non-serious) with onset 22Dec2021 01:00, outcome "not recovered", described as "tingling pins and needles sensation in my face, starting with the left side of my face and neck and (10 hours later) including my right side of my face as well as parts of my head, my ears and my neck". The events "i developed pain around my heart", "blood pressure was high" and "tingling pins and needles sensation in my face, starting with the left side of my face and neck and (10 hours later) including my right side of my face as well as parts of my head, my ears and my neck" were evaluated at the emergency room visit. Therapeutic measures were not taken as a result of angina pectoris, hypertension, paraesthesia. Prior to the vaccination, the patient was not diagnosed with COVID-19. It was also reported that since the vaccination, the patient had not been tested for COVID-19. Follow-Up (27DEC2021): Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Sulfonamide allergy
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 08.01.2022
- Impfdatum
- 17.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Angina pectoris
Blood test normal
Chest X-ray normal
Electrocardiogram normal
Hypertension
Immunisation
Paraesthesia
Symptomtext
I developed pain around my heart; blood pressure was high; tingling pins and needles sensation in my face, starting with the left side of my face and neck and (10 hours later) including my right side of my face as well as parts of my head, my ears and my neck; Booster; This is a spontaneous report received from a contactable reporter (Consumer). The reporter is the patient. A 51-year-old female patient (not pregnant) received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), administered in arm left, administration date 17Dec2021 11:15 (Lot number: FD7218) at the age of 51 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Known allergies: Sulfa" (unspecified if ongoing). The patient's concomitant medications were not reported. The patient did not receive any other vaccine within 4 weeks prior to the vaccine. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0180, Location of injection: Arm Left, Vaccine Administration Time: 10:30 AM), administration date: 16Jun2021, when the patient was 51 years old, for COVID-19 Immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EW0178, Location of injection: Arm Left, Vaccine Administration Time: 11:00 AM), administration date: 26May2021, when the patient was 51 years old, for COVID-19 Immunization. The following information was reported: ANGINA PECTORIS (medically significant) with onset 22Dec2021 01:00, outcome "not recovered", described as "I developed pain around my heart"; IMMUNISATION (non-serious) with onset 17Dec2021 11:15, outcome "unknown", described as "Booster"; HYPERTENSION (non-serious) with onset 22Dec2021 01:00, outcome "not recovered", described as "blood pressure was high"; PARAESTHESIA (non-serious) with onset 22Dec2021 01:00, outcome "not recovered", described as "tingling pins and needles sensation in my face, starting with the left side of my face and neck and (10 hours later) including my right side of my face as well as parts of my head, my ears and my neck". The events "i developed pain around my heart", "blood pressure was high" and "tingling pins and needles sensation in my face, starting with the left side of my face and neck and (10 hours later) including my right side of my face as well as parts of my head, my ears and my neck" were evaluated at the emergency room visit. Therapeutic measures were not taken as a result of angina pectoris, hypertension, paraesthesia. Prior to the vaccination, the patient was not diagnosed with COVID-19. It was also reported that since the vaccination, the patient had not been tested for COVID-19. Follow-Up (27DEC2021): Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Sulfonamide allergy
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 07.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Asthenia
Fatigue
Headache
Mobility decreased
Nausea
Pain
Vomiting
Symptomtext
Vomiting, severe nausea, extreme body and joint pain, headache, weakness, tired, unable to fully lift left arm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- Post COVID Syndrome
- Vorgeschichte
- Post COVID Syndrome
- Andere Medikamente
- atenenol 50 mg gabapentin 300 mg amytryptaline 15 mg riboflavin 400 mg magnesium mulitvitamin
- Allergien
- tramadol
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 07.01.2022
- Impfdatum
- 28.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Back pain
Blood pressure increased
Dyspnoea
Electrocardiogram
Eye pain
Fatigue
Gait disturbance
Headache
Heart rate increased
Heart rate irregular
Nausea
Paraesthesia
Paraesthesia oral
Swelling face
Tremor
Vision blurred
Symptomtext
IRREGULAR RAPID HEARTBEAT, DIFFICULTY BREATHING/SHORTNESS OF BREATH, BLOOD PRESSURE SHOT UP, SWELLING & TINGLING OF FACE, MOUTH INSIDE & OUT LIPS, OUTER EARS, LEGS, DIFFICULTY WALKING, HAND TREMORS, SEVERE HEADACHE AND PAIN BEHIND EYES, NAUSA, SEVERE FATIGUE, UPPER BACK PAIN, BLURRY VISION
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- AT ER ON HEART MONITOR AND CHECKING OF VITALS OVER 5 HOURS, EKG AFTER 4 HOURS WAS GOOD, GIVEN BENEDRYL AND PEPCID
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- LONG-HAUL COVID PATIENT
- Andere Medikamente
- nebivolol 5 mg, eliquis 2,5mg, armour thyroid 15 & 30 mg, ser sertraline 12.5mg
- Allergien
- penicillin, codine, iodine, cefuroxime axetil, sotalol, mexile mexiletine, medrol pack, dairy, gluten
- Vorherige Impfungen
- EGGLESS FLU SHOTS - ARM PAIN, BODY ACHES, FATIQUE OVER YEARS GIVEN
- Staat
- MI
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 05.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest X-ray normal
Chest pain
Dizziness
Haematocrit increased
Haemoglobin increased
Red blood cell count increased
Symptomtext
Approximately 10 minutes following vaccination I began having sharp chest pains in the center of my chest, accompanied by spells of dizziness, on and off. The dizziness subsided the following day on 1/4/22 although the chest pain has not.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- - Chest X-ray 1/4/22 (Negative) - Various Blood Labs done (Showed elevated RBC, Hemoglobin and Hematrocit)
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- - Severe Migraines
- Andere Medikamente
- None
- Allergien
- -Cefzil -Zithromax (Z-pack)
- Vorherige Impfungen
- Severe Aura Migraines, 23 y.o, 8/20/21, Hepatitis B Vaccine
- Staat
- OR
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 03.01.2022
- Impfdatum
- 28.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chills
Decreased appetite
Dehydration
Dyspnoea
Heart rate increased
Symptomtext
Elevated heart rate, trouble breathing, and chills. Pulse of 108, dehydration, no apetite.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dehydration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- None.
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 03.01.2022
- Impfdatum
- 30.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Back pain
Condition aggravated
Induration
Mass
Musculoskeletal pain
Spinal pain
Tenderness
Symptomtext
AFTER RECEIVING THE 2ND DOSE OF PFIZER COVID VACCINE, MY HUSBAND EXPERIENCED A HARD, TENDER/PAINFUL LUMP ON HIS RIGHT SHOULDER, WHICH WE BELIEVED TO BE A SWOLLEN LYMPH NODE BASED ON APPEARANCE AND LOCATION, AND WHICH LASTED APPROXIMATELY 10 DAYS. THE EVENING AFTER RECEIVING THE THIRD/BOOSTER DOSE, HE COMPLAINED OF PAIN IN HIS UPPER BACK/SHOULDER AREA. THAT NIGHT, I NOTICED THAT HE HAD A SLIGHTLY SMALLER BUT SIMILAR-LOOKING HARD LUMP ON HIS SHOULDER. THE NEXT MORNING, HE INITIALLY STATED HE FELT AS IF HE'D "SLEPT WRONG," BECAUSE HIS SHOULDERS/BACK WERE SORE. AS THE DAY PROGRESSED, HE FELT MORE SORENESS MOVING DOWN THE RIGHT SIDE OF HIS BACK, ALONG HIS SPINE. THE NEXT DAY, HE DESCRIBED IT AS FEELING LIKE HE'D "DONE A TON OF SQUATS," BECAUSE HE HAD SORENESS/TENDERNESS ALONG HIS BACK AND INTO HIS RIGHT BUTTOCK. WE CANNOT THINK OF ANY EXPLANATION FOR THESE SYMPTOMS EXCEPT THE VACCINE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NKA
- Vorherige Impfungen
- SAME/SIMILAR ISSUE W/ 2ND DOSE OF COVID VACCINE
- Staat
- FL
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 02.01.2022
- Impfdatum
- 27.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dyspnoea
Skin discolouration
Urticaria
Symptomtext
Per Patients wife, patient experienced Hives throughout all body, labored breathing and black feet. Patient was admitted in the hospital and given steroids. Patient went back to ER on 01/01/22 and administered Decadron shot and was discharged. Patient has a new Epipen prescription. Still has complaints of labored breathing and hives.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Done in ER
- Aktuelle Erkrankungen
- None reported
- Vorgeschichte
- None reported
- Andere Medikamente
- Tamsulosin, Rosuvastatin,
- Allergien
- Plavix
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 01.01.2022
- Impfdatum
- 13.03.2021
- Beginn
- 14.03.2021
- 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
Disturbance in attention
Tinnitus
Symptomtext
I have had tinnitus for many years. It has always sounded like cicadas and the sound was very consistent in rhythm and loudness. Shortly after my initial vax I started noticing the sound I was hearing was louder and inconsistent in rhythm. It's now distracting and affects my ability to focus and concentrate.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Gerd
- Andere Medikamente
- Famotidine 40mg twice daily Bupropion 100mg twice daily
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 31.12.2021
- Impfdatum
- 27.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Chest pain
Feeling of body temperature change
Respiratory rate increased
Symptomtext
About 10 minutes in to the waiting period after the shot was given, the pt started complaining of chest pain. She was breathing really fast and alternated between feeling hot and cold. 911 was called and the EMT's on the scene checked her vitals, all which were normal. Blood pressure, sugar, pulse ox were all in normal range. She responded to commands and turned her head when the light was shined in the eye. Mom was called and was asked about her history of seizures. She remembered a MD saying something about pseudo seizures in her past. EMT's seemed to think that that was the case this time, would not be sure until they did a full work up. Patient said she wanted to go to hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- anxiety, seizures
- Andere Medikamente
- unknown
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 31.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Immunisation
Paraesthesia
Symptomtext
Tingling in left arm and left leg; Headache; Dose number 3; This is a spontaneous report from a non-contactable reporter (consumer or non-HCP). The reporter is the patient. A 33-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in left arm, administration date 21Dec2021 at 16:30 (Lot number: FD7218) at the age of 33 years as dose 3 (booster), single for COVID-19 immunisation. The patient's relevant medical history was not reported. Concomitant medications included: LEXAPRO; TOPAMAX and AMOXICILLIN. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE; Anatomical location: left arm; Lot number: EP7533), administration date: 05Apr2021, when the patient was 32 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE; Anatomical location: left arm; Lot number: EW0171), administration date: 26Apr2021, when the patient was 32 years old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 21Dec2021 at 16:30, outcome "unknown", described as "Dose number 3"; PARAESTHESIA (non-serious) with onset 21Dec2021 at 17:30, outcome "unknown", described as "Tingling in left arm and left leg"; HEADACHE (non-serious) with onset 21Dec2021 at 17:30, outcome "unknown", described as "Headache". Therapeutic measures were not taken as a result of paraesthesia and headache. Additional information: The patient did not receive any other vaccines within four weeks prior to the COVID-19 vaccine. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- LEXAPRO; TOPAMAX; AMOXICILLIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 31.12.2021
- Impfdatum
- -
- Beginn
- 07.12.2021
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary mass
Condition aggravated
Headache
Immunisation
Pain
Swelling
Symptomtext
Booster; I am also experiencing headache pretty bad headache; It seems to be sustaining or worsening; I have got a really large swollen area like a big lump under my arm pit and it''s really painful; I have got a really large swollen area like a big lump under my arm pit and it''s really painful; I have got a really large swollen area like a big lump under my arm pit and it''s really painful; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 27 year-old female patient received bnt162b2 (BNT162B2), administered in arm left (Lot number: FD7218) at the age of 27 years as dose number unknown (booster), single for covid-19 immunisation. Relevant medical history included: "Depression" (unspecified if ongoing); "sleeping" (unspecified if ongoing), notes: I have a sleeping medication Zolpidem. Concomitant medication(s) included: VENLAFAXINE taken for depression; ARIPIPRAZOLE taken for depression; ZOLPIDEM taken for sleep disorder. Vaccination history included: Covid-19 vaccine (DOSE NUMBER UNKNOWN; , MANUFACTUERER UNKNOWN), for COVID-19 Immunization. The following information was reported: IMMUNISATION (non-serious), outcome "unknown", described as "Booster"; SWELLING (non-serious), AXILLARY MASS (non-serious), PAIN (non-serious) all with onset 07Dec2021, outcome "not recovered" and all described as "I have got a really large swollen area like a big lump under my arm pit and it''s really painful"; HEADACHE (non-serious), outcome "unknown", described as "I am also experiencing headache pretty bad headache"; CONDITION AGGRAVATED (non-serious), outcome "unknown", described as "It seems to be sustaining or worsening". Therapeutic measures were taken as a result of swelling, axillary mass, pain, headache. Additional information: The patient received a Pfizer booster dose (Unspecified Shot) a few days ago and had a large swollen area like a big lump under her arm pit and which was painful. Patient guessed, she started at the night of 7th and really on the 8th of this month Dec. Patient received a shot around 48 hours ago and so may be 12 hours after she received the booster shot, she woke up and she was having lot of she was experiencing a lot of pain in her underarm that was continued she did not notice, when she went to shower, she noticed. The patient did take some Tylenol, so it didn't helped too much yesterday, she was also experiencing headache pretty bad headache but she was not sure if that was related, since the lump was right under the injection site so it was probably from that, she was also experiencing headache so all she was taking was Tylenol. It seemed to be sustaining or worsening. The patient's top of arm felt better like she would be able to, but the thing under her arm was very painful but otherwise the injection site felt like it got better. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Depression; Sleep disorder (I have a sleeping medication Zolpidem)
- Andere Medikamente
- VENLAFAXINE; ARIPIPRAZOLE; ZOLPIDEM
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VT
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 30.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 24.12.2021
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest discomfort
Chest pain
Dyspnoea
Electrocardiogram normal
Hypoaesthesia
Lymphadenopathy
Musculoskeletal disorder
Paraesthesia
Symptomtext
Chest pain (central and left started Dec 24th and still experiencing slight central pain), left arm numbness and tingling on the inside (Dec 25- 26th lasted 2 days), swollen lymph nodes in left armpit, shortness of breath when sharp chest pains (24th-26th). I went to ER on Dec 26th for symptoms. They did an EKG, said everything looked normal and told it was likely a reaction to booster. It was effecting my musculoskeletal system. I was told to take ibuprofen and keep an eye out. Called PCP to follow-up with persistent chest tightness. Scheduled to be seen tomorrow, December 31st, to get a second look.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- EKG and vitals are ER on December 26th, everything looked normal.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Head injury, anxiety
- Andere Medikamente
- Nortriptyline, Junel, Tizanidine, Magnesium, Riboflavin, Women's Multivitamin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 29.12.2021
- Impfdatum
- 29.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dyspnoea
Rash macular
Urticaria
Symptomtext
During 15 minute observation period after vaccine, patient presented to pharmacist on duty with severe dyspnea and all-body erythematous blotches/hives. RPh administered epipen while staff called 911. Breathing improved and patient was taken to local emergency department.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 87,0
- Geschlecht
- M
- Eingang
- 29.12.2021
- Impfdatum
- 14.09.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 105,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Dehydration
Pneumonia
Productive cough
Respiratory tract congestion
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Covid19 breakthrough. 1st vaccine given 8/23/21. Pt presented with c/o productive cough, congestion, PNA, dehydration. Covid+. Treated with IV steroids and Abx.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dehydration
- Hospital-Tage
- -
- Labordaten
- SARS Cov 2 PCR Covid19- Detected 12/28/2021
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Chronic lymphocytic leukemia, HTN, FIB, Cardiac pacemaker, CAD, BPH, AAA, cysto, TURP
- Andere Medikamente
- -
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 89,0
- Geschlecht
- F
- Eingang
- 29.12.2021
- Impfdatum
- 16.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Chest pain
Dyspnoea
Symptomtext
Severe chest pains, difficulty breathing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- AFib
- Andere Medikamente
- Prescribed (daily meds).
- Allergien
- Penicillin and mango.
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 29.12.2021
- Impfdatum
- 27.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Decreased appetite
Hyperhidrosis
Injection site pain
Migraine
Symptomtext
Chills, Sweating profusely, no appetite, migraine on and off for 2 days, burning at injection site 30 minutes after receiving vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Cough
- Andere Medikamente
- Clarvis, Vitamin D, Birth Control
- Allergien
- Nut allergy
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 28.12.2021
- Impfdatum
- -
- Beginn
- 25.10.2021
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Condition aggravated
Hyperaesthesia
Lymphadenopathy
Malaise
Symptomtext
I got my third dose of Pfizer's vaccine and developed lymphadenopathy on the side that I had my shot (left arm). Swollen lymph nodes in my arm pit all the way up to my neck just to underneath the jaw. The swelling made my neck very sensible to touch (even when showering) and felt them when stretching my neck. This also happened after my second dose. Since all doses have not been received at a doctor's office, I didn't know they could be related to the vaccine. It was not until a few days later of the second dose, that while visiting my allergist that the connection of the swollen lymph nodes was made. He asked about my vaccine status and how did I do. While talking I mentioned the sensitivity I had to the touch in my armpit and neck on the left side. He assessed the area and said that I had a strong immune response and thus the swelling of the lymph nodes on the side of the injection. Also, the malaise on this third shot was awful, but was able to still get up from bed and be somehow functional to take care of my elder mom.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Hashimoto's. Goiter, Asthma,
- Vorgeschichte
- -
- Andere Medikamente
- Synthroid, Cytomel, Breo, Multi-vitamin, Vitamin D
- Allergien
- Pollen, grass, mold, cat
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 28.12.2021
- Impfdatum
- 11.12.2021
- Beginn
- 11.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest X-ray normal
Chest discomfort
Chest pain
Dyspnoea exertional
Fatigue
Hypersensitivity
Laboratory test normal
Muscle tightness
Musculoskeletal stiffness
Throat tightness
Symptomtext
Received shot 11:45 am at 7:45 pm felt a tightness start from my left arm and felt like it reach across my chest. It felt like a blanket wrapped to tight around my chest and my throat. The symptoms persisted. I proceeded to the emergency room and was determined not to have a PE and was told to contact my PCP but if it got worse I could come back. Symptoms continued and contacted a cardiologist who got me into his clinic on the 21. At this point my symptoms were chest burning constantly right in the center, neck tightness, fatigue and taking deep breath even when walking in a pool. I am having a cardiology work up at this point.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- In the ER all labs were ok. Lab work was ok at cardiologist, chest x-rays ok both times. Waiting for ultrasound January 14. Physician documented this as an allergy and does not recommend getting any other ever again.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- primal defense, black seed currant oil, congaplex
- Allergien
- adhesive EKG patches, Omnicef, Augmentin, Eldir cream
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 27.12.2021
- Impfdatum
- 22.12.2021
- Beginn
- 23.12.2021
- 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
Symptomtext
chest pain the next morning.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- multivitamins
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 25.12.2021
- Impfdatum
- 24.12.2021
- Beginn
- 25.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Dizziness
Headache
Injection site pain
Mobility decreased
Tremor
Symptomtext
Headache which had started a few hours after shot became pounding headache overnight. Soreness in arm about 3 inches in diameter around injection site. These were same symptoms as in first shot. Second shot side effects were only soreness in arm. Difference is chills this third shot, in middle of night, around 1:00 AM ET. Could not stop shaking for about 5 minutes and body locked in fetal position. Spent all of the day in bed until headache cleared around 4:45 PM ET on 12/25. Drank about 30 oz water within 15 minutes of getting shot; kept drinking water and earl grey caffeinated tea during 12/24 and got up sporadically to drink water when not dizzy with headache. Ate one small banana morning of 12/25 and took reported vitamins.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- None, did not seek medical attention as these side effects were considered normal for booster vaccine.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Vitamin D (4000 IU), iron (45 mg slow release), 600 units calcium
- Allergien
- Lactose sensitivity
- Vorherige Impfungen
- First Pfizer COVID shot, date 5/28/21, already reported on this site. Headache, soreness around injection site area extending en
- Staat
- IN
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 10.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Gait disturbance
Hypoaesthesia
Paraesthesia
Symptomtext
About a week after the vaccine , left arm and leg were numb, tingly . Two weeks after , she can barely walk at all with her left leg. We researched GBS,which she seems to be experiencing all symptoms of this .
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Arthritis
- Andere Medikamente
- Docusate sod 100 mg tablets , diflonac sodium 50 mg tablets , tramadol 50 mg, vitamins c, d and zinc.
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 17.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 5,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Chills
Dizziness
Dyspnoea
Headache
Injection site pain
Symptomtext
Pt received booster on 12/17/21. Called hospital call center c/o HA, injection arm pain and worsening, chills, dizziness, difficulty breathing s/p 5 days pfizer booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 23.12.2021
- Impfdatum
- 19.12.2021
- Beginn
- 19.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest discomfort
Chest pain
Dysphagia
Dyspnoea
Throat tightness
Symptomtext
Systemic: Allergic: Difficulty Breathing-Medium, Systemic: Allergic: Difficulty Swallowing, Throat Tightness-Medium, Systemic: Chest Tightness / Heaviness / Pain-Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 22.12.2021
- Impfdatum
- 11.12.2021
- Beginn
- 19.12.2021
- Tage bis Beginn
- 8,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest discomfort
Chest pain
Chills
Flushing
Headache
Pain
Pyrexia
Tachycardia
Symptomtext
I had a fever, headache, aches and chills the next day post vaccine administration. A felt flushed throughout the next week. A week after my booster shot I became tachycardic in the 160s while standing. I worked out later that day and had to stop - it felt as though I had a cylinder block sitting on my chest. The last few days I have had a dull ache in my chest.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- I was instructed by my primary care to monitor and head to the ER if symptoms worsen. Date seen - 12/22/2021.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma
- Andere Medikamente
- None
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 22.12.2021
- Impfdatum
- 06.12.2021
- Beginn
- 06.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Mobility decreased
Pain in extremity
Symptomtext
arm soreness, with restriction in flexion and abduction and extension, internal rotation
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- shoulder exam
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- MVI , probiotics, vitamins, inflamless supplement
- Allergien
- NKDA, no food allergies
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 22.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Paraesthesia
Symptomtext
Student said this morning that he is experiencing a "pins and needles" type of feeling everywhere his clothing touches after receiving his vaccine yesterday morning at a school vaccine clinic. Further evaluation is ongoing
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 21.12.2021
- Impfdatum
- 17.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal pain
Condition aggravated
Diarrhoea
Dyspepsia
Hypersensitivity
Nausea
Pruritus
Urticaria
Symptomtext
Delayed slow over 1 hour palms, feet, abdomen, chest, groin, armpits hives with itching, Indigestion, nausea, abdominal cramping, diarrhea, face itching. Took Benadryl, Pepcid, singulair. with moderate relief. Hives resolved, itching remains but improved. Previous reaction after 2nd dose had to use Epi x3.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Seasonal allergies. 3 Anaphylactic reactions and multiple allergic reactions since 2nd Covid vaccine.
- Andere Medikamente
- Allegra, Singulair.
- Allergien
- NKDA
- Vorherige Impfungen
- Covid 2nd dose. Anaphylaxis x3 with epi use and ER visits. Continued allergic reactions continued. No reactions the last few mon
- Staat
- NY
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 21.12.2021
- Impfdatum
- 18.12.2021
- Beginn
- 20.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Chest pain
Symptomtext
chest pain, went to Hospital for evaluation, admitted to Ped ICU for treatment
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unk
- Vorgeschichte
- -
- Andere Medikamente
- unk
- Allergien
- amoxicillin, fish, corn
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 20.12.2021
- Impfdatum
- 20.12.2021
- Beginn
- 20.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest discomfort
Dyspnoea
Hyperhidrosis
Palpitations
Symptomtext
Patient complained having palpitation, sweating in both palms, and pressure in chest/some difficulty with breathing. Patient agreed to call 911 and go to the hospital. Paramedics came and transported her to the hospital. Patient stated she had history of palpitation and anxiety
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- History of heart palpitation and anxiety based on patient and patient's daughter's comment
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 18.12.2021
- Impfdatum
- 16.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain upper
Asthenia
Cough
Dyspnoea
Dyspnoea at rest
Dyspnoea exertional
Fatigue
Headache
Heart rate increased
Hyperhidrosis
Inappropriate schedule of product administration
Oxygen saturation decreased
Productive cough
Secretion discharge
Symptomtext
headaches increased shortness of breathe while at rest and or talking heart rate up sweating pillow case and sheet wet from top back up stomach pain weakness and very tired. Decreased O2 level higher need for O2 not on O2 before but since hot covid19 on O2 . increased coughing hard with some mucus
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- vital sign and adjustment of O2 as need increase to 4-5ltrs. to keep O2 level above 90%. O2 adjustment up don't know if more side effects will happen by the local health Dept. giving her dose2 only 9 days after they gave the first dose.
- Aktuelle Erkrankungen
- covid 19 long hauler PHTN, fibrous lungs, shortness of breath, arthritis knees, arms, hands, acid reflux, high blood pressure, sleep apnea, anxiety depression tremors
- Vorgeschichte
- acid reflux arthritis knees shoulders hands sleep apnea high blood pressure
- Andere Medikamente
- Tylenol 500mg, albuterol ipratropium 3mls, allopurinol 300mg, apixaban 5mg, bezonante 100 mg, cholecalciferol 25mch, advair disks, furosemide 20mg, lidocaine 4%, lorazepam .5mg, magnesium oxide 400mg, melatonin 6mg, omeprazole 20mg, senna
- Allergien
- ace inhibitors ramipril shellfish derived products
- Vorherige Impfungen
- sore arm
- Staat
- VA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 18.12.2021
- Impfdatum
- 16.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Heart rate increased
Paraesthesia
Symptomtext
experienced rapid heartbeat and tingling in both arms about 12 hours after receiving vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- not known
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 17.12.2021
- Impfdatum
- 17.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain
Chest pain
Symptomtext
Patient experienced crushing chest/abdominal pain. Felt like "a large man was wrapping me up from behind". Pain subsided within 10-15 minutes. This pain was also experienced when she once received IV contrast dye before a CT scan.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- Parenteral contrast dye
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 17.12.2021
- Impfdatum
- 14.12.2021
- Beginn
- 14.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Chills
Condition aggravated
Fatigue
Headache
Lymphadenitis
Myalgia
Symptomtext
Lymph node inflammation, shaking chills, joints pain, muscular pain, headache, fatigue
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Latex allergy, menopause
- Andere Medikamente
- Simvastatin 10 mg
- Allergien
- Latex
- Vorherige Impfungen
- Shaking chills, muscular pain, fatigue, 50, 4/17/2021, pfizer
- Staat
- CA
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 17.12.2021
- Impfdatum
- 11.12.2021
- Beginn
- 12.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Troponin increased
Symptomtext
Patient has a history of myopericarditis in 11/2018. Pt developed chest pain on 12/12 the day after his booster shot. He was hospitalized on 12/14/21 after being found to have troponin level of 141. He was treated with colchicine and ibuprofen. He was discharged home on the following day (12/15).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Troponin 141 -> 194
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Cyclic vomiting syndrome
- Andere Medikamente
- haloperidol 5 mg daily as needed for nausea 2/2 cyclic vomiting syndrome
- Allergien
- Aspirin
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 17.12.2021
- Impfdatum
- 15.12.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Dry throat
Hypoaesthesia oral
Paraesthesia oral
Pharyngeal swelling
Throat irritation
Symptomtext
10mins post vaccination pt reported swelling & tickling throat. MD at bedside @11:27 Vitals: 11:30 156/113, 104, 22 and pt feels anxiety -- > 1131 157/123, 94, 22, O2 100% -- > 1139 199/142, 120, 22, 100% -- > 11:46 161/123, 102, 20, 100% 1129-Pt wearing 2 masks-one mask removed, Lung sounds normal per MD with no signs of wheezing. 11:37 Pt c/o numb tongue-RN administered 0.3mg of epi. Left outer thigh r/t reaction from Pfizer dose #3. Pt tolerated med admin well. Pt remains alert and oriented. 1138 911 called for transport/eval. 1139 Pt talking and laughing. 1145-Pt remains talking and oriented. States tongue "feels so much better:" Pt shaky. Reassurance to pt this is from epi. 1148-Paramedics arrived. Pt stable.Pt states her throat feels dry, tongue swollen Pt taken to the ED ~12:00 In the ED: 45-year-old female with a history of allergic reaction to tree nuts coming in now by ambulance from her vaccination clinic where she had a scheduled appointment for COVID-19 booster shot. 20 minutes after getting the booster shots she developed sensation of tongue swelling and tingling. However she reports that lips and tongue and mouth did not look swollen. She was immediately given an epi shot and it quickly resolved all of her symptoms. The shot was given at 11:30 AM by her doctor. No other medications were given. She has no symptoms at all at this time. Symptoms were mild nonradiating described as possible anxiety or allergic reaction. She denies any ingestion of substances with tree nuts. Did not have any reaction to any Covid 19 vaccinations in the past. No worsening factors were reported. Symptoms were not associate with any rash, trouble breathing or swallowing or speaking or drooling shortness of breath or cough or wheezing abdominal pain passing out syncope lightheadedness or other complaints at all. Pt observed for several hours and given methylprednisolone 125mg IV x1 and diphenhydramine 50mg IV x1. Pt d/c'd in stable condition with RX for Epi 0.3mg Auto-injector, Famotidine 20mg BID x5days, diphenhydramine 25mg PO Q6hrs PRN Itching, and Prednisone 20mg PO Daily x 4 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia oral
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- PMH: Impaired fasting glucose, Depression, Anxiety, Insomnia
- Andere Medikamente
- Medications: acetaminophen (PHARBETOL) 500 MG tablet Take 2 tablets by mouth 3 (three) times daily as needed for Pain. benzonatate (TESSALON) 100 MG capsule Take 1 capsule by mouth 3 (three) times daily as needed for Cough. cetirizine (ZYRT
- Allergien
- Allergies: Tree Nuts (including walnut)- Anaphylaxis
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 17.12.2021
- Impfdatum
- 17.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Hypoaesthesia oral
Paraesthesia
Symptomtext
Patient complained of numbness in tongue and tingling around the mouth. Vital signs were taken. Patient remained COA X4. Patient was transported to Hospital via Ambulance.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- N/a
- Andere Medikamente
- N/a
- Allergien
- None
- Vorherige Impfungen
- Hives All other information is unknown
- Staat
- CA
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 16.12.2021
- Impfdatum
- 15.12.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Extra dose administered
Paraesthesia oral
Swollen tongue
Throat irritation
Symptomtext
following administration of booster dose. Patient reports tongue senation (swelling and tingling) and tickling back of the throat. patient was assessed by onsite provider at 11:28. Lung sounds normal and no wheezing. Epi given to patient at 11:31. EMS was called 11:38 for patient. Pt stable when paramedics arrive.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia oral
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Tree nuts
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 16.12.2021
- Impfdatum
- 15.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dysstasia
Gait disturbance
Headache
Joint stiffness
Mobility decreased
Myalgia
Vomiting
Symptomtext
Onset sixteen (16) hours after injection: Vomiting, Joint Stiffness, Muscle Pain, severe headache, difficulty standing, walking, and bending at the waist.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- None.
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 16.12.2021
- Impfdatum
- 16.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Hypoaesthesia
Paraesthesia
Paraesthesia oral
Swelling face
Symptomtext
As soon as patient got shot he complained of tingling feeling in cheek and lips. Within a few minutes he said it felt numb. Upon taking his mask off, his cheek looked slightly puffy, but not severely. I asked if patient had any adverse events after the first two vaccines, and he said no. However, he did state he had taken an antihistamine before each of the first two vaccines due to seasonal allergies. He recently moved and said since he hasn't had to take an antihistamine daily, so he didn't this morning. I gave him a bottle of water and offered benadryl. He took 1 25mg tablet of benadryl and stated he felt slightly better within a few minutes. He chose to go home. I told him if he got worse again to go to urgent care or ER immediatly. This all was within approx 15 minutes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- patient states he sometimes gets headaches more than usual since he had COVID, but otherwise no other illnesses
- Vorgeschichte
- HIV
- Andere Medikamente
- Biktarvy
- Allergien
- penicillins, eggs, seasonal allergies
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 16.12.2021
- Impfdatum
- 12.12.2021
- Beginn
- 12.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Dyspnoea
Headache
Hypoaesthesia
Symptomtext
Right after the vaccine patient felt dizziness, later severe headache, numbness to left side of he body and SOB.. Till now patient has a headache, numbness of the left side and intermittent SOB.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- None.
- Allergien
- Latex.
- Vorherige Impfungen
- Gardisol 1/2009, Flu vaccine every year, MMR 8/2017. After MMR developed hives, fever, headache,joint pain. After Gardisol pati
- Staat
- RI
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 15.12.2021
- Impfdatum
- 09.12.2021
- Beginn
- 09.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Chest discomfort
Chest pain
Chills
Fatigue
Insomnia
Lymphadenopathy
Malaise
Musculoskeletal pain
Pain
Pyrexia
SARS-CoV-2 test
SARS-CoV-2 test negative
Symptomtext
1st dose pfizer 5/15/21 2nd dose 6/5/21 Booster 12/9/21. Received Covid booster on Thursday afternoon at 11am within 2 hrs started to feel ill with generalized body aches/fatigue/ That evening had severe weakness and developed temp 103, was unable to sleep and body aches were so severe she couldn't even open a bottle of water. ON Friday felt worse with same symptoms, had to stay in bed, continued with fevers/chills/body aches and fatigue. Did not take mpap or ibuprofen. On Saturday when moved in bed felt sharp pain in chest but did not radiate and had no SOB/n/v, pain came and went. On Sunday felt chest discomfort once or twice but it came and went, was a dull ache. Monday had same problem a couple of times, Tues had a couple of episodes. Today has had no episodes of chest pain but continues with upper back pain and lymph node swelling along with severe fatigue. Last time she had a fever was Sunday. On Sunday noticed swelling under left armpit. Chest pain episodes from SUN/MON/TUEs were more of a dull ache that is on the left side of chest and also has pain between both shoulder blades. Has not had any dyspnea. Temperature: 96.6. Pulse (sitting): 94. Blood Pressure (sitting): 145/82. Respirations: 18
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Covid test rapid done 12/15 negative, PCR test 12/14 results pending
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 15.12.2021
- Impfdatum
- 13.12.2021
- Beginn
- 13.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal discomfort
Arthralgia
Chest pain
Dizziness
Dyspnoea
Hyperhidrosis
Immediate post-injection reaction
Joint stiffness
Neck pain
Pain
Pain in extremity
Pyrexia
Symptomtext
Immediately after the injection, the was a sensation of adrenaline in my head for about 6 hours. Thereafter, more symptoms came on and included - chest pain and shortness of breath, headache, hair follicles ache, joints in fingers and toes were stiff and ached, random sharp pains in extremities, upset stomach, neck and shoulder aches, fever and sweating. Treatment included fluids, acetaminophen and bed rest. About 24 hours after the onset of symptoms, my fever broke and all other symptoms were reduced by 25%. Throughout the night, they continued to reduce to almost nothing by 8:00am.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- None at this time.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension, celiac disease
- Andere Medikamente
- Multivitamin (Centrum Silver), Omeprazole (20mg), Loratidine (10mg)
- Allergien
- Naprosyn, penicillin, gluten
- Vorherige Impfungen
- After dose 2, was bedridden for about 5 hours (Pfizer on 3/9/21) age: 58
- Staat
- CA
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 13.12.2021
- Impfdatum
- 09.12.2021
- Beginn
- 09.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Amenorrhoea
Chest discomfort
Chest pain
Condition aggravated
Pyrexia
Urticaria
Symptomtext
Hives, fever chest tightness and burning, missed period
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- glucoma
- Vorgeschichte
- glucoma
- Andere Medikamente
- combigen
- Allergien
- augmentin, ciprofloxacin, cefuroxime,sulfur, dimethylchloride,calcium carbide, naproxen, ibuprofen
- Vorherige Impfungen
- pfizer COVID vaccine dose 1,hives
- Staat
- ME
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 13.12.2021
- Impfdatum
- 11.12.2021
- Beginn
- 11.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Discomfort
Inflammation
Injection site cellulitis
Injection site infection
Injection site pain
Lymphadenopathy
Musculoskeletal pain
Swelling
Symptomtext
Within an hour, I started experiencing left side chest pain and used my rescue inhaler which seem to alleviate the discomfort. However, I had tenderness at the injection site. I applied OTC hydrocortisone creme yesterday. The swelling and inflammation did not improve. I sought medical treatment at a clinic. The female provider told me that I had developed an infection at the injection site called cellulitis Currently, I have swelling underneath my right armpit and right should blade pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- The urgent care provider did a very quick examine. The interaction was less than five minutes.
- Aktuelle Erkrankungen
- I had an asthma exacerbation and sciatic nerve pain.
- Vorgeschichte
- Asthma, epilepsy, Factor V Leiden, Celiac Disease, Hemochromatosis, Thyroid disorder, Migraines, and PTSD.
- Andere Medikamente
- Keppra - 1000 mg twice per day; Qvar - 80 mcg - two inhalations, twice per day; albuterol inhaler - as needed; Ativan - .5mg twice per day, Tylenol - 500 mg, twice per day; magnesium - 250 mg once per day; women's multivitamin without iron
- Allergien
- Latex, Cipro, Sulpha, Penicillin, Propofol, soy, beef, pork, crab, contrast dye, Topamax, aspirin and all NSAIDs.
- Vorherige Impfungen
- Pfizer - first dose - April 27, 2021 - throat swelling
- Staat
- MA
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 13.12.2021
- Impfdatum
- 08.12.2021
- Beginn
- 09.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Injection site pain
Migraine
Nausea
Rash maculo-papular
Urticaria
Vomiting
Symptomtext
Symptoms started 32 hours after injection. Nausea and vomit for 12 hours, vomit each hour. Temperature 100.8, migraine, facial hives, maculopapular rash on torso, extreme fatique. Muscle soreness at injection site for first 24 hours, but no other onsite reaction or rash to vaccine. Symptoms lasted 52 hours. Previous 2 vaccines produced NO symptoms. All symptoms reported above occured for booster only.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None
- Andere Medikamente
- None.
- Allergien
- Thimerosal Neomycin
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 09.12.2021
- Impfdatum
- 05.12.2021
- Beginn
- 06.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Axillary pain
Chest X-ray normal
Chest pain
Dizziness
Dyspnoea
Electrocardiogram
Pain
Pyrexia
Symptomtext
That evening started feeling aches, fever. Around 4:00am next day woke up felt as if I couldn't breathe, light headed and running fever was really scary. I took Ibuprofen didn't do too much. I continued to run fever of 102 for 48 hours. Then on 12/08/2021 my fever was still fairly high 100, exp chest pains and chest pains got worse upon me standing. I went to local ER had a EKG and my fever has finally went away. As of today still have pain in my left armpit.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- EKG, Chest X-ray(normal)
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Finasteride, Minoxidil
- Allergien
- No
- Vorherige Impfungen
- 2nd dose Pfizer(fever lasted a day)
- Staat
- NH
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 09.12.2021
- Impfdatum
- 09.12.2021
- Beginn
- 09.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Disorientation
Fall
Pallor
Paraesthesia
Symptomtext
Post vaccine patient collapsed out of chair. Disoriented, pale, "tingling sensation". Given 2 benadryl and water- ambulance arrived and took over patient care.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Shot anxiety
- Andere Medikamente
- None on file.
- Allergien
- Lactose intolerance
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 07.12.2021
- Impfdatum
- 07.12.2021
- Beginn
- 07.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoaesthesia
Pain in extremity
Paraesthesia
Symptomtext
Patient has numbing from knee down. Experiencing tingling in feet, and slight pains
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- High blood pressure
- Andere Medikamente
- High blood pressure Allergy meds Vitamins D, ad mulitvitamins
- Allergien
- Penacillin, Codine, Asprin
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 29.12.2023
- Impfdatum
- 30.12.2021
- Beginn
- 26.11.2023
- Tage bis Beginn
- 696,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Alanine aminotransferase increased
Anaemia
Aspartate aminotransferase increased
Asthenia
Blood alkaline phosphatase increased
Blood culture negative
C-reactive protein increased
COVID-19
Cancer pain
Chemotherapy
Chest X-ray normal
Computerised tomogram head normal
Cough
Culture urine negative
Fall
Head injury
Hepatomegaly
Hypertransaminasaemia
Symptomtext
Patient is a 64 y.o. female with a history of metastatic breast cancer on chemo, recent ED visit 11/25/23 for fever, discharged with empiric abx for UTI. She re-presented to Hospital 11/26/2023 with few days of fevers and found to have COVID-19. ID followed. Patient was discharged home with HHC in stable condition 11/29/23. 1. COVID-19 Infection: reported dry cough, congestion on admission. Respiratory PCR 11/27/23 positive for COVID-19. CXR 11/27/23 non-acute. Not on O2 so no indication for Decadron. Paxlovid started 11/27/23 per ID. Hold statin until 3 days post therapy, resume 12/6/23 if repeat LFTs stable. 2. Fever: suspect due to COVID-19, less likely UTI. UA 11/25/23 with 8 WBCs. Admit Tmax 101.6, WBC 7.4, neutrophils 76.2, ESR 98, CRP 101, procal 0.2. Urine cx with no growth, Blood cultures 11/27/23 negative to date. Initiated cefepime on admission. Oncology recommended continuing cefepime until blood cultures negative x 48 hours, discontinued 11/29/23. ID followed. 3. Metastatic Breast Cancer: per history with known mets to bone, recent progression of mets in liver. Follows with Dr. (medical oncology) and Dr. (radiation oncology). S/p bilateral mastectomy in 2014. S/p palliative radiation to bone mets. Disease progressed on hormonal therapy and xeloda, paclitaxel, and most recently Enhertu. Last chemo session ~3 weeks PTA. Plan to start gemcitabine 12/4/23. Hem/Onc followed. 4. Mechanical Fall: Reportedly fell due to generalized weakness. Patient hit head, no LOC. Admit CT head non-acute. Supportive care continued; PT/OT followed. 5. Transaminitis: admit ALP 586, AST 114, ALT 105. Likely due to known metastatic disease to liver. RUQ US 11/27/23 with hepatomegaly, numerous hepatic mets. Stable per trend. Recommend repeat labs with PCP/Oncology in 5-7 days. Has scheduled labs 12/1/23. 6. Chronic Anemia: baseline Hgb ~10-11; stable on admit. Likely secondary to metastatic disease. Monitored. 7. Cancer Related Pain: per history. Continued home gabapentin, Narx reviewed on admit. 8. Obesity: Body mass index is 38.62 kg/m?. Recommended diet/lifestyle modifications. 9. Code status: Full code
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cancer pain
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 24.09.2023
- Impfdatum
- 05.01.2022
- Beginn
- 01.01.2023
- Tage bis Beginn
- 361,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Intermenstrual bleeding
Lymphadenopathy
Pyrexia
Symptomtext
Adverse event: Swollen left lymph node: bigger than golf ball Fever Spotty period Treatment: run warm water on lymph node, lymph nodes would swell before period, not as big reaction after 3 dose of vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- Annual exam 7/18/22
- Aktuelle Erkrankungen
- None that I can think of at the moment
- Vorgeschichte
- Thyroid problem
- Andere Medikamente
- Junel Fe 1/20, chia and flax seeds blended about 1 teaspoon
- Allergien
- Peanut, seasonal allergies
- Vorherige Impfungen
- Fever(2-3 days) sore arm, lights seem brighter, vaccine date 5/11/2021, age 29, lot number EW0165 ,Pfizer
- Staat
- MA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 16.08.2023
- Impfdatum
- 06.12.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Pain
Psoriasis
Rash erythematous
SARS-CoV-2 test
Symptomtext
Psoriasis; red rash; burning stinging; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 63-year-old female patient received BNT162b2 (BNT162B2), on 06Dec2021 as dose 3 (booster), single (Lot number: FD7218) at the age of 63 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Obstuctive Sleep Apnea" (unspecified if ongoing); "Anti-Body Thyroid Disease" (unspecified if ongoing); "Thyroid" (unspecified if ongoing); "severe pain" (unspecified if ongoing), notes: Jan2021 /Feb2021. The patient took concomitant medications which included thyroid medications and a statin. Vaccination history included: BNT162b2 (DOSE 2, SINGLE, lot number: EW0172, vaccine location: Right arm), administration date: 24Apr2021, when the patient was 63-year-old, for COVID-19 Immunization, reaction(s): "patch of discolored skin on right ankle area/left lower leg area"; BNT162b2 (DOSE 1, SINGLE, lot number: ER8737,, vaccine location: Right arm), administration date: 02Apr2021, when the patient was 62-year-old, for COVID-19 Immunization. The following information was reported: PSORIASIS (disability) with onset 2021, outcome "not recovered"; PAIN (disability) with onset 2021, outcome "not recovered", described as "burning stinging"; RASH ERYTHEMATOUS (disability) with onset 2021, outcome "not recovered", described as "red rash". The events "psoriasis", "red rash" and "burning stinging" required physician office visit. The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (06Jun2022) Negative. Therapeutic measures were taken as a result of psoriasis, rash erythematous, pain which included ointments, steroid shots, photo light therapy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220606; Test Name: Nasal Swab; Test Result: Negative
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Pain (Jan2021 /Feb2021); Sleep apnea; Thyroid disorder
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 95,0
- Geschlecht
- M
- Eingang
- 31.05.2023
- Impfdatum
- 19.02.2021
- Beginn
- 17.07.2022
- Tage bis Beginn
- 513,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
COVID-19
Chest X-ray normal
Chills
Confusional state
Cough
Dysstasia
Electrocardiogram normal
Encephalopathy
Fall
Rhinorrhoea
SARS-CoV-2 test positive
Troponin increased
Urine analysis normal
Vaccine breakthrough infection
Symptomtext
BREAKTHROUGH COVID: FULLY VACCINATED AND BOOSTED. 97-year-old male with past medical history of , presenting to ED with worsening weakness. COVID-19 positive w/o signs of severe features. Pt was found by himself alert and oriented x 2. He reports he was brought to the hospital because he fell and had trouble standing up. Spoke over the phone with daughter who provided most of the history. She reports she recently tested positive for COVID-19, until last night where the worsening confusion and weakness were evident. Patient had two unwitnessed falls in the last 24hrs. Has not had fever but has been c/o chills. PT TREATED COVID INFECTION WITH Paxlovid 150 mg-100 mg (300 mg-100 mg Dose) oral tablet. Mild runny nose and dry cough noticed. Denies any other complaint such as headache, chest pain, SOB, abd pain, vomiting or diarrhea. Acute encephalopathy superimposed on baseline dementia, POA, likely releated to COVID infection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- CXR w/o signs of pneumonia. EKG w/o acute changes. Troponin slightly elevated. U/A w/o signs of active infection.
- Aktuelle Erkrankungen
- UNKNONWN
- Vorgeschichte
- dementia, hyperlipidemia, hypothyroidism, hypertension, GERD, BPH
- Andere Medikamente
- UNKNOWN
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 03.05.2023
- Impfdatum
- 04.02.2021
- Beginn
- 01.03.2022
- Tage bis Beginn
- 390,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Abortion spontaneous
Heavy menstrual bleeding
Maternal exposure before pregnancy
Menstruation irregular
Ovarian cyst ruptured
Ovulation disorder
Pelvic pain
Polycystic ovaries
Pregnancy
Ultrasound scan
Symptomtext
3 miscarriages in one year - March 2022 - pregnant when received booster D&C -March 2022 Diagnosed with PCOS May 2023 Rupture ovarian cysts -May 2022 Missed ovulation Irregular period-heavy bleeding Severe pelvic pain No know cysts or reproductive issues/pain prior to vaccine .
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pelvic pain
- Hospital-Tage
- -
- Labordaten
- Internal ultrasound -May 2022 & May 2023
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Venlafaxine - 75mg
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 07.03.2023
- Impfdatum
- 16.08.2022
- Beginn
- 18.02.2023
- Tage bis Beginn
- 186,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Diarrhoea
Dizziness
Nausea
SARS-CoV-2 test positive
Symptomtext
02/18/23 presents to ED for "dizziness, nausea and diarrhea". PMHx of "right eye blindness, partial vision loss of left eye, CHI, CKD stage 2, T2DM, GERD, HTN, HLD, CAD, PVD, OSA, Pulmonary hypertension, anemia of chronic disease"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- 02/18/23 SARS-CoV-2 (COVID-19) by NAA detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 25.01.2023
- Impfdatum
- 05.01.2022
- Beginn
- 15.06.2022
- Tage bis Beginn
- 161,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Headache
Magnetic resonance imaging
Symptomtext
Constant headaches since June got worse after dose 4 in October.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Blood work, MRI
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Depression; Anxiety
- Andere Medikamente
- None
- Allergien
- Coconut; mango
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 30.12.2021
- Beginn
- 20.12.2022
- Tage bis Beginn
- 355,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Chills
Cough
Dysgeusia
Eye irritation
Feeling abnormal
Headache
Nasal congestion
Pain
Pyrexia
SARS-CoV-2 test positive
Sneezing
Symptomtext
I tested positive for COVID-19 12/22/2022 with a home test. I had a cough, headache, chills for a day, low grade fever, stuffy nose, sneezing, a little bit of body aches. I did feel miserable. My doctor prescribed Paxlovid but I did not finish it. I only took a day and a half worth of the medication. I took one pack then the next day I only took the morning dose then stopped. The medication had a metallic taste that lasted all day and had tasted like acid reflux. Drinking and eating had not gotten rid of the taste. I also experienced some irritation with my eyes during this course. After that, I just started taking generic Mucinex to help with the symptoms. Currently, I do still have a cough.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- 22DEC2022 At Home COVID-19 Test - Positive; 31DEC2022 At Home COVID-19 Test - Negative
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Arthritis; Depression
- Andere Medikamente
- Levothyroxine; Hydrochlorothiazide; Meloxicam; Omeprazole
- Allergien
- Oxycodone
- Vorherige Impfungen
- 1st COVID-19 Pfizer vaccine 11FEB2021 - Felt very sick after vaccine, body aches; 2nd COVID-19 Pfizer vaccine 04MAR2021 - Swolle
- Staat
- MI
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 10.01.2023
- Impfdatum
- 04.01.2022
- Beginn
- 25.11.2022
- Tage bis Beginn
- 325,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Pyrexia
Renal transplant
Symptomtext
11/25/22 presents to ED for "fever". PMHx of "ESRD secondary to FSGS s/p kidney transplant 6 months ago"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 06.01.2023
- Impfdatum
- 19.01.2021
- Beginn
- 18.06.2021
- Tage bis Beginn
- 150,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Arthralgia
Blood test
Bone disorder
Contusion
Magnetic resonance imaging
Pain in extremity
X-ray
Symptomtext
1st Pfizer dose 2/28/21 EL9266 , 2nd dose 3/16/21 EN6206 both at site for Hospital. On 6/18/21 me and my family noticed circle bruises all over both of my arms and they were hurting me so I went to Hospital Emergency Room. I have those records in Chart . The Dr's couldn't understand why I was bruising in perfect circles and they watched bruising appear on my arms. July 12, 2021 I was referred to a specialist but by that time they was gone. On 1/19/22 I had my 3rd dose FD7218 @ nursing home. I went to the Dr on 4/2022 with wrist pain, 6/2022 with wrist pain and in August 2022 they defray and found Keinbocks disease of my right wrist. No Blood flow to lunate bone.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- hospital have all x rays! Blood work, and MRI taken.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Asthma, High Blood Pressure, Arthritis of hip
- Andere Medikamente
- Ibuprofen, Amlodipine , propanolol, naproxen
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 27.12.2022
- Impfdatum
- 12.01.2022
- Beginn
- 26.10.2022
- Tage bis Beginn
- 287,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Confusional state
Cough
Diarrhoea
Hypophagia
Influenza virus test positive
Lethargy
Malaise
Mental status changes
Nausea
Pyrexia
Respiratory syncytial virus test positive
SARS-CoV-2 test positive
Vomiting
Symptomtext
10/26- presents with Covid sx- fever, malaise, cough, decreased intake, nausea vomiting diarrhea, more lethargic with altered mental status and increased confusion from baseline and tested positive for COVID-19, 3 days ago (10/23, sx started 10/21).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- 10/26 Covid-19, Flu, RSV by NAA, Detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 12.12.2022
- Impfdatum
- 10.12.2021
- Beginn
- 16.11.2022
- Tage bis Beginn
- 341,0
- Dosis
- 3
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Headache
Middle insomnia
Nasal congestion
Paranasal sinus discomfort
Rash
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
11/16/22 I woke up in the middle of the night with a headache, sinus pressure and nasal congestion. I got up, blew my nose and went back to sleep. I tested myself the next morning with a home COVID test and it was positive. I took TYLENOL and alerted everyone that I was positive. For three of four days I continued to have sinus pressure, headache and nasal congestion. I continued to take TYLENOL every 4-6 hours. On Day 4 or 5, I developed a rash on both sides of my neck. I contacted my doctor. She told me it would be unusual it would be related to COVID being on both sides of my neck but wanted to keep an eye on it. The next day, the rash went away. 2 days later, 11/26/2022, it came back on 1 side of my neck and I went to urgent care to see if it was Shingles. They said it looked like some type of contact dermatitis. I was told to use an over-the-counter cream for the rash. It did not get any better, so I took a picture on 11/28/22 and sent it to my doctor. She gave me a prescription for fluocinonide. I used that for several days and it went away. Things are great and I feel good now.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- At home COVID test, positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypothyroidism; High Blood Pressure
- Andere Medikamente
- 11/16/22 I woke up in the middle of the night with a headache, sinus pressure and nasal congestion; I got up, blew my nose and went back to sleep; I tested myself the next morning with a home COVID test and it was positive; I took TYLENOL a
- Allergien
- Betadine; amoxicillin; latex
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 08.12.2022
- Impfdatum
- 06.12.2021
- Beginn
- 20.10.2022
- Tage bis Beginn
- 318,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
COVID-19
Cough
Fatigue
Feeling abnormal
Malaise
Oropharyngeal pain
Pyrexia
SARS-CoV-2 test positive
Sinusitis
Symptomtext
I felt fatigue and weak. The next morning went I woke up my throat hurt. My wife made me take a COVID-19 test when I got a 102 fever, and it was positive. The next day I felt like crap, I had a cough and the other symptoms as well. I ended up getting a sinus infection. Six days later I tested negative. I still have a cough. The fever lasted for 2-3 days. I talked to my doctor and he gave me a cough syrup but I never took it.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 10/21/2022, COVID-19 test, positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Aspirin
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 07.11.2022
- Impfdatum
- 15.01.2021
- Beginn
- 09.09.2022
- Tage bis Beginn
- 602,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Rash
SARS-CoV-2 test positive
Symptomtext
09/09/22 presents to EC ED for "rash". PMHx of "paroxysmal afib on Xarelto and aspirin and hypothyroidism"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- 09/10/22 SARS-CoV-2 (COVID-19) by regulatory authority detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 24.08.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Symptomtext
patient complains of injection site pain for the past 7 months.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 16.08.2022
- Impfdatum
- 13.12.2021
- Beginn
- 06.08.2022
- Tage bis Beginn
- 236,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anaemia
Anticoagulant therapy
Breast feeding
COVID-19
Caesarean section
Exposure during pregnancy
Headache
Nasal congestion
Pain
Pyrexia
SARS-CoV-2 test positive
Symptomtext
Patient received Pfizer vaccine on 5/26/21, 6/16/21 and 12/13/21. Presented to ER on 8/5/22 to give birth at 39 weeks gestation. Found to be COVID positive. Patient was admitted for repeat cesarean section. Please see operative note for full details. On POD#1 she was advance and reports pain is well controlled with oral medications and denies heavy bleeding. She was ambulating, tolerating regular diet, and voiding without difficulty. She was noted to have anemia and was started on iron supplementation. She was having a fever with temp 101 F, nasal congestion and headache and was noted to be COVID +. On POD#2 she was meeting all of her postoperative and postpartum milestones and was passing flatus. She was feeling better and was afebrile for > 24 hours. She is breast & bottle feeding without difficulty. Fundus is firm and below umbilicus, no LE edema. She is felt stable for discharge home. She was given standard postoperative precautions and restrictions. She was given COVID 19 precautions and restrictions. She was discharged home on Lovenox 40 mg QD and was given DVT/PE precautions on 8/7/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- 2,0
- Labordaten
- 8/6/22 COVID19: positive.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- docusate sodium 100 MG Caps Take 100 mg by mouth daily. HYDROcodone-acetaminophen 5-325 MG Tabs Commonly known as: NORCO Take 1-2 Tablets by mouth every 6 hours as needed for Moderate or more severe pain. ibuprofen 600 MG Tabs Commonly
- Allergien
- penicillins
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 29.07.2022
- Impfdatum
- 07.12.2021
- Beginn
- 18.07.2022
- Tage bis Beginn
- 223,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood sodium decreased
COVID-19
Cough
Fatigue
Hyponatraemia
Hypophagia
Inappropriate antidiuretic hormone secretion
Laboratory test
SARS-CoV-2 test positive
Symptomtext
Patient with 3 Pfizer COVID vaccinations who admitted to hospital with COVID detected test. Provider D/C note below: "71-year-old male with a past medical history of ulcerative colitis and BPH. He presented to the emergency department on 07/18/2022 with a chief complaint of fatigue. He was diagnosed with COVID but did not require any oxygen supplementation and had minimal symptoms except for dry cough. He was admitted to the hospital due to notable hyponatremia at 118. The patient does have a history of chronic hyponatremia of unclear etiology. He was originally given fluids due to some poor oral intake at home but sodium actually decreased so further workup was performed. Workup revealed SIADH so patient was placed on a fluid restriction and sodium tablets. Nephrology was also consulted for further recommendations. Labs were not revealing of an etiology of the SIADH, but COVID could have been a contributing factor. Patient was also on Wellbutrin at home which was held due to the possibility that this could be contributing, states he has been on this for years but does not think it is helping him anymore so we discussed stopping and discussing with his PCP alternative treatment. His sodium was very slow to improve, on day of discharge was 132 which is close to his baseline. He was discharged home with instructions per Nephrology for continued fluid restriction given his chronic hyponatremia. Labs are ordered for later this week to recheck. He will follow-up with his PCP. All questions were answered at time of discharge and patient was given strict return precautions to which he verbalized understanding."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- 9,0
- Labordaten
- COVID detected PCR on 07/18/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Depression, major, recurrent, mild Unknown Solar lentigo Unknown FATIGUE IMPAIRED FASTING GLUCOSE HX, PERSONAL, EXPOSURE TO ASBESTOS Elevated blood-pressure reading without diagnosis of hypertension 3/23/2021 BPH (benign prostatic hyperplasia)
- Andere Medikamente
- -
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 21.07.2022
- Impfdatum
- 09.12.2021
- Beginn
- 09.07.2022
- Tage bis Beginn
- 212,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Clostridium difficile colitis
Diarrhoea
Frequent bowel movements
SARS-CoV-2 test positive
Symptomtext
Patient received pfizer vaccine on 5/6/21, 5/27/21 and 12/9/21. Presented to ER on 7/9/22 and found to be COVID positive. presented with diarrhea. He has been having more than 10 bowel movements. Recently in the hospital treated for C diff colitis. Not reporting any fevers chills nausea or vomiting. No abdominal pain. Found to be COVID positive in the ED. does not seem to have active COVID infection. Admitted for C. diff. Discharged on 7/18/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- 9,0
- Labordaten
- 7/9/22 COVID19: positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Aphasia, Bowel disease, BPH (benign prostatic hyperplasia), Diverticular disease, Eczema, Gait disturbance, Glucose intolerance (impaired glucose tolerance), Hearing loss, Hyperlipidemia, MCI (mild cognitive impairment), and Vitamin D deficiency.
- Andere Medikamente
- Cholecalciferol 2,000 Units Oral DAILY Glucosamine-Chondroitin 500-400 MG 1 Capsule Oral DAILY Loperamide HCl 2 mg Oral 4 TIMES DAILY PRN Multiple Vitamins-Minerals 1 Tablet Oral EVERY 12 HOURS Rosuvastatin Calcium 10 mg Oral NIGHTLY
- Allergien
- caritin D
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 27.06.2022
- Impfdatum
- 21.12.2021
- Beginn
- 10.05.2022
- Tage bis Beginn
- 140,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Cough
Exposure to SARS-CoV-2
Myalgia
Nasal congestion
Oropharyngeal discomfort
Oropharyngeal pain
Rhinorrhoea
SARS-CoV-2 test positive
Upper-airway cough syndrome
Symptomtext
One in our group had tested positive, I had a tickle in my throat but was testing negative. As the day progressed the tickle became a sore throat and I got a post nasal drip I went to the drive through testing sight and my PCR COVID test was positive. By this time I had a runny and stuffy nose, muscle aches, the testing sight advised me to isolate. Thursday May 12, 2022 I did a telehealth visit and was prescribed Paxlovid because of my genetic blood clotting factor. I felt fine May 16, 2022 but had a residual cough.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- PCR COVID Test.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Children Multivitamins
- Allergien
- No
- Vorherige Impfungen
- Second COVID 19 shot rash around vaccine site.
- Staat
- CA
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 22.06.2022
- Impfdatum
- 23.12.2021
- Beginn
- 10.06.2022
- Tage bis Beginn
- 169,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Cough
Headache
Laboratory test abnormal
Laryngitis
Nasopharyngitis
Sneezing
Symptomtext
I had cold symptoms, cough sneezing laryngitis and headache. I waited five days to test and was positive. i was treating a lot of the joint pain with Ibprophen. I was positive for 11 days. I still have cold like symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Osteoarthritis and Osteopenia
- Andere Medikamente
- Hydroxychloroquine, Cetiprine, Vitamin D, Probiotic, Krill oil, Turmeric and B12 injections
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 22.06.2022
- Impfdatum
- 23.12.2021
- Beginn
- 23.03.2022
- Tage bis Beginn
- 90,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Ageusia
Anosmia
COVID-19
Fatigue
Headache
Influenza like illness
Pain
Pyrexia
SARS-CoV-2 test positive
Symptomtext
On 12/23/2021, I received my first Pfizer booster for COVID-19. On 3/23/2022, I had mild flu-like symptoms that included fatigue, headaches, body aches, and fever. I also lost my senses of taste and smell for a few days, but they returned to normal after a short time. I did an at-home test for COVID that day, and the result was positive. I called my doctor's office on 3/24/2022, and he prescribed me Paxlovid. I also took Tylenol for my headaches. I would say that both the Paxlovid and Tylenol were effective, because the symptoms were gone after about 3 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Hemangioma pericytoma (in remission for 22 years).
- Andere Medikamente
- Keppra, Lexapro, vitamin B6, Emgality.
- Allergien
- Dilantin.
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 21.06.2022
- Impfdatum
- 20.12.2021
- Beginn
- 28.05.2022
- Tage bis Beginn
- 159,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Mammogram normal
Rash
Rash erythematous
Rash pruritic
Ultrasound breast normal
Symptomtext
On 5-28-2022, I started having a itchy, red rash on my right breast. I had a physical already scheduled for 6-1-2022 so I told my PCP about the rash. He looked at it and stated this was not a normal occurrence with the breast. I have had breast cancer in the left breast but none in my right. He told me to schedule an appointment with my oncologist. I had my oncology visit with the APRN on 6-7-2022 and she did not think that it looked or felt like cancer. On that same day, they had me scheduled a diagnostic mammogram. An ultrasound was also done right after the mammogram at a local hospital. Neither test showed any cancer or reason for the symptom. The APRN ordered hydrocortisone cream, told me to keep an eye on the rash and to notify her if there was a significant change. The rash is still present but looks a little lighter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- 6-7-2022 Diagnostic Mammogram at a local hospital- negative results. 6-7-2022 Ultrasound of R Breast at the local hospital- negative results.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Bipolar 2; Conversion Disorder; Psychogenic Seizures; Seasonal Allergies; Anxiety; Insomnia; R sided weakness; Hypothyroid
- Andere Medikamente
- Multivitamin; vit D3; gabapentin; oxcarbazepine; lithium carbonate er; clonazepam; vit D2; levothyroxine; topiramate; bupropion; desmopressin acetate; lamotrigine
- Allergien
- Latex; PHENERGAN; erythromycin; Seasonal Allergies; cats
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 21.06.2022
- Impfdatum
- 14.12.2021
- Beginn
- 14.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Symptomtext
With her first booster shot, had mild lightheadedness.; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. An 82-year-old female patient received BNT162b2 (BNT162B2), on 14Dec2021 as dose 3 (booster), single (Lot number: FD7218) at the age of 82 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "cholesterol" (ongoing), notes: cholesterol problems Diagnosed years ago; "High blood pressure" (ongoing), notes: high blood pressure Diagnosed years ago. Was told her blood pressure was very good.; "COVID" (unspecified if ongoing), notes: a very mild case of it. Confirmed this was prior to caller receiving any of her COVID-19 Vaccines.; "ton of allergies" (unspecified if ongoing), notes: States she has a ton of allergies.; "urinary tract infection" (unspecified if ongoing), notes: Had a urinary tract infection about a month ago. The patient's concomitant medications were not reported. Vaccination history included: BNT162b2 (COVID-19 Vaccine: Dose 1, Single, Manufacturer: Pfizer, Date: 25Feb2021, LOT: EN6202, Left arm), administration date: 25Feb2021, when the patient was 81-year-old, for COVID-19 immunization; BNT162b2 (COVID-19 Vaccine: Dose 2, Single, Manufacturer: Pfizer, Date: 18Mar2021, LOT: EN6204, Left arm), administration date: 18Mar2021, when the patient was 81-year-old, for COVID-19 immunization; Pneumonia shot (pneumonia shot), administration date: 2022, for Immunisation. The following information was reported: DIZZINESS (non-serious) with onset 14Dec2021, outcome "recovered", described as "With her first booster shot, had mild lightheadedness.". The action taken for BNT162b2 was unknown. Additional information: She was at hospital receiving the vaccine, stayed there for a while and then went home. Was at the hospital for an hour when everyone else left after 20-25min. It stopped on the same day. She is calling about her second booster shot: She was there at the hospital and was lightheaded She stayed for a while, it seemed to be getting better She went home Her arm where she got the booster shot was her left arm, was extremely painful. When she went to sleep, couldn't sleep on left side Couldn't press anything on that left arm Had tiredness, headache, muscle pain, muscle pain in the left arm, left arm was splotchy red, had joint pain. Something seemed wrong with muscles and joints. She lives in assisted living. When she came back was told she had a slight fever, she took Tylenol, stating this was in morning. In the afternoon, she took another Tylenol, and the slight fever went away. Then something happened that night. Went to sleep, in middle of night, her eyes opened, and she was shaking all over. Her arms instead of being flat on bed, from the elbows to fingertips were elevated and shaking badly. Whole body was shaking. She was scared and terrified. This was not a side effect on the chart. Didn't know what was happening. Thought she was dying. She blanked out. She didn't know anything until 6am the following morning and couldn't believe she was alive. Spent the rest of the day in bed, didn't want to move Was so scared of what was going on. The patient received treatment for Tylenol for slight fever, no other treatment was received. After this experience, hopes she doesn't have to get a third booster. No follow-up attempts are needed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Blood pressure high (high blood pressure Diagnosed years ago. Was told her blood pressure was very good.); Cholesterol (cholesterol problems Diagnosed years ago)
- Vorgeschichte
- Medical History/Concurrent Conditions: Allergy (States she has a ton of allergies.); COVID-19 (a very mild case of it. Confirmed this was prior to caller receiving any of her COVID-19 Vaccines.); Urinary tract infection (Had a urinary tract infection about a month ago)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 15.06.2022
- Impfdatum
- 14.12.2021
- Beginn
- 02.05.2022
- Tage bis Beginn
- 139,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Fatigue
Oropharyngeal pain
Pain
Productive cough
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Throat irritation
Symptomtext
I tested positive for COVID-19 4/19/22. On 4/16/22, I had some fatigue, runny nose, slight fever, a raw sore throat, mucus, coughing, and body aches. This lasted for about a week and a half before I started to feel better. I still have some remanence of mucus and a runny nose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 Test- 4/16/22- Negative COVID-19 Test- 4/19/22- Positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Azithromycin
- Vorherige Impfungen
- About 5 years ago my arm swelled up pretty bad after a tetanus shot.
- Staat
- MA
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 14.06.2022
- Impfdatum
- 13.12.2021
- Beginn
- 05.05.2022
- Tage bis Beginn
- 143,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Headache
Nasal congestion
Pain
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
On 5-5-2022, I started having a stuffy nose, cough, headache and body aches. I took a home Covid test on this day and it was negative. My symptoms increased in severity. I took a second home Covid test on 5-8 and it was negative as well. I took another home test on 5-11 and it was positive. I called my doctors office and had a telehealth visit on that same day. They prescribed Cetirizine, Flonase and a pain medication due to headaches. On 5-12, I took a drive thru Covid test and it was positive as well. I am doing very well today and all symptoms have resolved. I am reporting a breakthru case of Covid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- 3 home Covid tests 1 Covid test at Drive Thru, positive result
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Depression
- Andere Medikamente
- Cyclobenzaprine, Duloxetine, Fluconazole, Multivitamin, Citracal, Hair/skin/nails vitamin,
- Allergien
- Seasonal allergies
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 25.05.2022
- Impfdatum
- 28.12.2021
- Beginn
- 11.05.2022
- Tage bis Beginn
- 134,0
- Dosis
- 3
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Pain
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
I was coughing, I had congestion and I ached all over. The coughing was pretty intense and I ached all over and it hurt to move. The worst of it lasted 24 hours and I started getting better the following day. I still was coughing but the 1st day was the worst. Each day it got better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- At home Covid test- positive; today was the first day it was negative- 5/25/2022.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Cholesterol; slight blood pressure
- Andere Medikamente
- Atorvastatin, Calcium 20mg, Triamterene, Hydrochlorothiazide
- Allergien
- Amoxicillin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 25.05.2022
- Impfdatum
- 29.12.2021
- Beginn
- 07.02.2022
- Tage bis Beginn
- 40,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blister
Pain
Rash
Symptomtext
complains of burning pain with rash medial to right shoulder blade x 2-3 days. Cluster of vesicles over one dermatome near scapula, no drainage or erythema.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- F
- Eingang
- 17.05.2022
- Impfdatum
- 15.12.2021
- Beginn
- 09.05.2022
- Tage bis Beginn
- 145,0
- Dosis
- 3
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Pain
Pyrexia
Rhinorrhoea
SARS-CoV-2 test
Vaccination failure
Symptomtext
Tested positive for Covid 19 on 09May2022; Tested positive for Covid 19 on 09May2022; Fever; Body ache; Runny nose; Cough; This is a spontaneous report received from a contactable reporter(s) (Pharmacist). An adult female patient (not pregnant) received BNT162b2 (BNT162B2), on 10Mar2021 as dose 1, single (Lot number: EL3248), in left arm, on 31Mar2021 as dose 2, single (Lot number: 3248), in left arm and on 15Dec2021 as dose 3 (booster), single (Lot number: FD7218), in right arm, all intramuscular for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: PAIN (non-serious) with onset 09May2022, outcome "not recovered", described as "Body ache"; COUGH (non-serious) with onset 09May2022, outcome "not recovered"; PYREXIA (non-serious) with onset 09May2022, outcome "not recovered", described as "Fever"; RHINORRHOEA (non-serious) with onset 09May2022, outcome "not recovered", described as "Runny nose"; VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 09May2022, outcome "not recovered" and all described as "Tested positive for Covid 19 on 09May2022". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (09May2022) Positive. Therapeutic measures were taken as a result of vaccination failure, covid-19, pyrexia, pain, rhinorrhoea, cough. Clinical information:No other vaccine in four weeks.No other medications in two weeks. AE were treated with acetaminophen. No covid prior vaccination and no known allergies.; Sender's Comments: Based on known drug safety profile, there is reasonable possibility of causal association between the events and the suspect drug BNT162B2.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220509; Test Name: Nasal Swab; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: other medical history: none
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 11.05.2022
- Impfdatum
- 28.01.2021
- Beginn
- 24.02.2022
- Tage bis Beginn
- 392,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Diplopia
Headache
SARS-CoV-2 test positive
Symptomtext
02/25/22 presents to ED for "headache and double vision". PMHx of "HTN, Diabetes".
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- 02/25/22 SARS-CoV-2 (COVID-19) by NAA detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 05.05.2022
- Impfdatum
- 02.02.2022
- Beginn
- 07.02.2022
- Tage bis Beginn
- 5,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Amnesia
Blepharospasm
Bone pain
Cardiac disorder
Cognitive disorder
Educational problem
Fatigue
Feeling abnormal
Hypoaesthesia
Impaired work ability
Laboratory test
Metabolic disorder
Muscle twitching
Nausea
Pain
Retching
Speech disorder
Symptomtext
My cognitive function started to get foggy and I couldn't remember information that was given to me and reiterate information that was given to me. I had a hard saying certain words, nausea, dry heaving, my heart and metabolism started to go out of control, full body pain down to bone pain. Normally I walk to school or ride bike and was unable to do that because of muscle twitching and pain. I had to quit my job because I was unable to type because my eyes would twitch, had to take leave from school because of the fatigue of just walking to class. New symptoms of left side facial numbness that goes into the palate of my mouth.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bone pain
- Hospital-Tage
- -
- Labordaten
- currently undergoing testing.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- aspirin, cipro
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 02.05.2022
- Impfdatum
- 29.01.2022
- Beginn
- 26.03.2022
- Tage bis Beginn
- 56,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal pain lower
Computerised tomogram abdomen abnormal
Laboratory test abnormal
Ovarian calcification
Ovarian mass
Phlebolith
Surgery
Symptomtext
I had lower abdominal pain and went to the hospital for a CT scan; they found a lump next to my ovaries. I had an emergency surgery appointment to get the lump removed. Upon testing the tissue from the lump, they diagnosed it as calcium buildup/phleboliths in the pelvic area. I was discharged the same day and still in recovery since the procedure.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain lower
- Hospital-Tage
- -
- Labordaten
- Tissue testing: 04/20/2022.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Tylenol; Multivitamin Supplement
- Allergien
- Sulfa Antibiotics; Nickel
- Vorherige Impfungen
- 24, 03/01/2021, COVID-19, Pfizer-BioNTech.
- Staat
- UT
- Alter
- 47,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 18.12.2021
- Beginn
- 20.02.2022
- Tage bis Beginn
- 64,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Rash
Skin exfoliation
Symptomtext
Approximately 2 months after my booster shot (dose 3) I experienced the following symptoms: Twenty-five cent piece-sized rash (it was flaky and scaly), itchiness. I saw my doctor about it and was prescribed with cortisone cream but I haven't gone to get one as of now yet.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Seasonal Allergies.
- Andere Medikamente
- Zyrtec.
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 27.04.2022
- Impfdatum
- 14.12.2021
- Beginn
- 21.03.2022
- Tage bis Beginn
- 97,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Cough
Glossodynia
Hypophagia
Oropharyngeal pain
Quarantine
Respiratory tract congestion
SARS-CoV-2 test positive
Speech disorder
Symptomtext
Starting 03/20/2022, I developed a sore throat and a bit of congestion. I woke up the next morning feeling the same and I took an at home test which was positive. I cancelled travel plans and quarantined for 5 days. I didn't develop too severe of symptoms but I had severe congestion, minor cough and the worse symptom was a sore on my tongue that lasted for about 10 days. It made it hard to talk or eat. After about 5 days, all the symptoms but the sore on the tongue were pretty much resolved.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- COVID-19 at home test (03/21/2022): Positive; urgent care test on 03/20/2022: negative and a PCR test (03/22/2022-03/23/2022): Positive.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 26.04.2022
- Impfdatum
- 13.12.2021
- Beginn
- 26.12.2021
- Tage bis Beginn
- 13,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Biopsy skin abnormal
Lymphocytic infiltration
Rash
Rash pruritic
Skin test positive
Symptomtext
Began noticing a rash on hips around 12/26/2021. Rash was extremely itchy. Over the following week, rash spread over entire torso and on arms, legs and scalp. Visited dermatologist on 01/11/2022. She prescribed prednisone (pills), hydroxyzine hydrochloride (pills), and triamcinolone acetonide (topical cream). Rash mostly dissipated within two weeks with medication but fully returned -- on torso, arms, legs, scalp -- around 02/13/2022. Dermatologist re-prescribed medications on 02/24/2022. Rash dissipated with medication and has not returned since.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- Biopsy conducted on right forearm on 02/24/2022. Biopsy showed "a superficial to mid-dermal perivascular lymphocytic infiltrate with eosinophils." Skin patch test administered on 03/15/2022. Test confirmed an allergy to methylisothiazolinone and methylchloroisothiazolinone. (Note: I found this chemical present only in my spouse's shampoo and in our dish soap. It is unknown why rash was as extensive as it was.)
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Methylisothiazolinone, methylchloroisothiazolinone
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 21.04.2022
- Impfdatum
- 22.12.2021
- Beginn
- 24.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Loss of personal independence in daily activities
Musculoskeletal stiffness
Neck pain
New daily persistent headache
Pain in extremity
Symptomtext
Starting a few days after receiving the vaccine, I experienced massive headaches. I suffer from migraines from Meniere's disease but these were much worse and they were every day. They were so intense I had to take a lot of painkillers (more than usual) to treat them but they seemed to persist no matter what I did. These lasted for several months. I developed neck problems (stiff neck and sore more so on the right side from neck through shoulder to arm). The pain in the shoulder/neck is still persisting but its getting better. The headaches have calmed down for the most part and I'm back to my normal routine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypothyroidism; Meniere's Disease
- Andere Medikamente
- Levothyroxine, Lipitor, Omeprazole, Multivitamin, Vitamin C and Vitamin D
- Allergien
- Crestor; Latex (Deathly)
- Vorherige Impfungen
- Shingles shot made me feel down for the week. After the 2nd dose of Pfizer, I was extremely fatigued for a day. Typically flu sh
- Staat
- GA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 13.04.2022
- Impfdatum
- 10.12.2021
- Beginn
- 20.12.2021
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Fatigue
Feeling abnormal
Gait disturbance
Headache
Impaired work ability
Nasopharyngitis
Oropharyngeal pain
SARS-CoV-2 test negative
Sneezing
Vertigo
Symptomtext
About 10 days after receiving the Pfizer booster (3rd shot) I started getting a sore throat 12/20/21. The next day 12/21/21 I couldn't stop sneezing although my sinuses were not clogged & it felt different from a regular cold. I felt like I had a slight cold & stayed home from work on Wednesday 12/22/21. I tested negative for covid using an at home test on 12/22/21. The symptoms seemed to go away except for the sore throat from 12/23/21 - 12/29/21. On Thursday 12/30/21 I had piercing pain in my head, was really tired, dizzy & had vertigo. My body kept pulling to the left, had to walk holding the wall. It felt like the left side of my body wouldn't move. Sneezing rapidly, non stop. Tested positive for covid-19 using an at-home test on 12/30/21. Isolated at home for 10 days. After the second day had no symptoms at all. Long term symptoms are tiredness at times, brain fog. Antigen test was negative on 1/9/22, took at pharmacy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- High blood pressure High cholesterol
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 06.04.2022
- Impfdatum
- 03.03.2021
- Beginn
- 09.02.2022
- Tage bis Beginn
- 343,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Activated partial thromboplastin time normal
Angiogram normal
Aphasia
Blood folate normal
Blood thyroid stimulating hormone normal
Computerised tomogram normal
Confusional state
Dizziness
Echocardiogram normal
Electrocardiogram normal
Full blood count normal
Glycosylated haemoglobin normal
Hemiplegia
Lipids normal
Magnetic resonance imaging normal
Metabolic function test normal
Prothrombin time normal
SARS-CoV-2 test negative
Symptomtext
On 2/9/22 at approximately 7p, I suddenly developed severe dizziness followed by whole right side paralysis, aphasia, & confusion. The symptoms lasted about 5 mins. EMT arrived at my home and transported me to the ER. While in route to the hospital via ambo, the dizziness, paralysis, aphasia, and confusion started again. This was all observed my medics. I was hospitalized from 2/9/22 - 2/11/22. I had an extensive work-up done which was all negative. I continue to feel dizzy after my hospitalization. The dizziness increased to several times a week to several times a day. I went back to the ER on 3/16 for the dizziness ( all diagnostic test and labs were negative). I have since started vestibular physical therapy and is awaiting to see an ENT specialist scheduled later in April 2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- 3,0
- Labordaten
- 2/9/22- CTA, MRI, EKG, ECHO, CMP, BMP, UA, Covid-19 test, PT, APTT, TSH, A1C, Vit B12, Folate, Lipid Panel (all results normal) 3/16/22 - CT, EKG, CBC, CMP (all results normal) 3/24/22- MRI (normal)
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Migraines Acne OAB Allergies
- Andere Medikamente
- Ajovy, Excedrin, Aldactone, Hydroxyzine, Flonase, Vit C
- Allergien
- Seasonal allergies
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 06.04.2022
- Impfdatum
- 18.12.2021
- Beginn
- 16.03.2022
- Tage bis Beginn
- 88,0
- Dosis
- 2
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Diarrhoea
Dry throat
Inappropriate schedule of product administration
Interchange of vaccine products
Off label use
Vomiting
Symptomtext
off-label use; Inappropriate schedule of drug administered; Inappropriate schedule of drug administered; dry throat; diarrhoea; vomiting; This is a spontaneous report received from non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 38 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 18Dec2021 (Lot number: FD7218) at the age of 38 years as dose 2, single for covid-19 immunisation; janssen covid-19 vaccine (JANSSEN COVID-19 VACCINE), administered in arm left, administration date 07Apr2021 (Batch/Lot number: unknown) as dose 1, single for immunisation. Relevant medical history included: "Aspirin allergy" (unspecified if ongoing); "Interchange of vaccine product" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: OFF LABEL USE (non-serious), outcome "unknown", described as "off-label use"; INTERCHANGE OF VACCINE PRODUCTS (non-serious), INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (non-serious), outcome "unknown" and all described as "Inappropriate schedule of drug administered"; DRY THROAT (non-serious), outcome "recovering", described as "dry throat"; DIARRHOEA (non-serious) with onset 16Mar2022, outcome "recovering", described as "diarrhoea"; VOMITING (non-serious) with onset 16Mar2022, outcome "recovering", described as "vomiting". Additional information: The reporter's assessment of the causal relationship of the events with the suspect product was reported as Possible at the time of this report. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Drug allergy; Interchange of vaccine products.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 05.04.2022
- Impfdatum
- 14.12.2021
- Beginn
- 25.12.2021
- Tage bis Beginn
- 11,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Angioedema
Chronic spontaneous urticaria
Symptomtext
Angeo Adema, chronic idiopathic uticaria (both still active as of today, 4/4/22)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chronic spontaneous urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Ulcerative colitis
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 04.04.2022
- Impfdatum
- 30.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Headache
Myalgia
Nausea
Pyrexia
Symptomtext
I had severe headaches, and a fever 101-103.8 degrees. I also had nausea and muscles aches. My symptoms lasted for 4 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High Blood Pressure, Asthma
- Andere Medikamente
- Lisinopril Levothyroxine Singulair Topiramate
- Allergien
- Sulfa Antibiotics
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 30.03.2022
- Impfdatum
- 28.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arthralgia
Back pain
Blood test
Gait disturbance
Intervertebral disc protrusion
Joint swelling
Pain in extremity
Swelling
Symptomtext
On the 30th, my knee started swollen and hurting. I could barely walk about 2 weeks it moved to my back. I ended with a hernia disc. Soreness in my joints in my hand, knees, fingers, and back. Like traveling Joint pain and swollen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- Blood work
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Thyroid, high blood pressure
- Andere Medikamente
- Atenolol, Dilantin, Eliquis, Folbee, Levothyroxine, Montelukast, Pantoprazole, Triamterene, Vitamin D2
- Allergien
- Sulfa drugs, Shellfish, Bees, Dust mice, Feathers, Mold, Mildew, seasonal allergies, NSAIDS
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 29.03.2022
- Impfdatum
- 23.03.2021
- Beginn
- 19.01.2022
- Tage bis Beginn
- 302,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Chills
Pyrexia
SARS-CoV-2 test positive
Symptomtext
01/19/22 presents to ED for "Covid +; fever; chills". PMHx of "kidney L and liver tx in 2011"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 29.03.2022
- Impfdatum
- 08.03.2021
- Beginn
- 18.01.2022
- Tage bis Beginn
- 316,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asthenia
Back pain
COVID-19
Chills
SARS-CoV-2 test positive
Symptomtext
01/18/22 presents to ED for "weakness, chills, and back pain". PMHx of "ESRD on hemodialysis, T2DM, D-CHF, and recent AV fistula repair"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- 01/18/22 SARS-CoV-2 (COVID-19) by NAA detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 28.03.2022
- Impfdatum
- 07.12.2021
- Beginn
- 12.12.2021
- Tage bis Beginn
- 5,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pain in extremity
Ultrasound scan
Symptomtext
pain below left knee
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- ultrasound
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- omeprazole, centrum silver, glucosamine, tylenol
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 26.03.2022
- Impfdatum
- 19.01.2022
- Beginn
- 05.02.2022
- Tage bis Beginn
- 17,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Gait disturbance
Headache
Insomnia
Symptomtext
This is a spontaneous report received from contactable pharmacist, consumer or other non-HCP. A 56-year-old female patient received the 1st dose of BNT162B2 (Pfizer-BioNTech COVID-19 vaccine, batch/lot# FD7218, expiration date: Feb 28, 2022), at the age of 56, in left arm, on Jan 19, 2022, single dose, for COVID-19 immunisation. Medical history included migraines (unspecified if ongoing), notes: patient usually suffers from migraines before the vaccine. Concomitant medications not reported. The patient had gait disturbance (needed a cane to walk for more than 2 weeks), arthralgia (arthritis pain, worse after the vaccine/knee pain), onset 2022, outcome of unknown; headache (bad headache; couldn't fall asleep until 4 am) and insomnia, onset Feb 5, 2022, with outcome of recovered (Feb 5, 2022). No follow-up attempts possible. No further information expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Migraine (patient usually suffers from migraines before the vaccine).
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 25.03.2022
- Impfdatum
- 08.04.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Pain in extremity
Symptomtext
had the 1st 2 shots in Apr2021 and May2021; arm soreness; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 56 year-old female patient received bnt162b2 (BNT162B2), administered in arm right, administration date 08Apr2021 (Batch/Lot number: unknown) at the age of 55 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Diverticulitis", start date: Jan2021 (ongoing), notes: Verbatim: Diverticulitis; "Retinitis pigmentosa" (ongoing), notes: Verbatim: Retinitis pigmentosa. The patient's concomitant medications were not reported. The following information was reported: INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (non-serious), outcome "unknown", described as "had the 1st 2 shots in Apr2021 and May2021"; PAIN IN EXTREMITY (non-serious), outcome "unknown", described as "arm soreness". Additional information: She was first told about her diverticulitis in Jan2021 and she had an issue in her sigmoid area, she had a micro perforation and a small abbess that they had to drain. She had an inflammation that was visible on a CT scan that they did on her pelvis. Arm Soreness: She says that the only symptoms that she had seemed to be that she was tired for so many hours after the 1st COVID vaccines and then she had a little arm soreness afterwards but nothing else. She confirms these were side effects were felt after her 1st and 2nd dose of the Pfizer COVID vaccine. She got those doses in her right arm and for some reason the pharmacist suggested that she have the booster dose in her left arm, which is a different arm. 1st dose ( 08Apr2021) Lot Number: She thinks the lot number is either EN6201 or EIV6201, the handwriting is hard to read. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Diverticulitis (Verbatim: Diverticulitis); Retinitis pigmentosa (Verbatim: Retinitis pigmentosa)
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- -
- Geschlecht
- M
- Eingang
- 24.03.2022
- Impfdatum
- 23.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Swelling
Tenderness
Symptomtext
Developed swelling, soreness, and tenderness in the left arm pit area.; Developed swelling, soreness, and tenderness in the left arm pit area.; Developed swelling, soreness, and tenderness in the left arm pit area.; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 50 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 23Dec2021 (Lot number: FD7218) as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: LISINOPRIL. Vaccination history included: Bnt162b2 (Dose: 1, Lot No: ER8733, Location: Arm Left), administration date: 24Mar2021, when the patient was 49 years old, for COVID-19 immunization; Bnt162b2 (Dose: 2, Lot No: EW0164, Location: Arm Left), administration date: 14Apr2021, when the patient was 49 years old, for COVID-19 immunization. The following information was reported: AXILLARY PAIN (non-serious), SWELLING (non-serious), TENDERNESS (non-serious) all with onset 30Dec2021, outcome "not recovered" and all described as "Developed swelling, soreness, and tenderness in the left arm pit area.". The event "developed swelling, soreness, and tenderness in the left arm pit area.", "developed swelling, soreness, and tenderness in the left arm pit area." and "developed swelling, soreness, and tenderness in the left arm pit area." was evaluated at the physician office visit. It was unknown if therapeutic measures were taken as a result of axillary pain, swelling, tenderness. Additional Information: Prior to vaccination, patient was not diagnosed with Covid-19. Since the vaccination, patient has not been tested for Covid-19. Patient did not receive any other vaccines within 4 weeks prior to the Covid vaccine. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: allergies: No medical history: No
- Andere Medikamente
- LISINOPRIL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 22.03.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain in extremity
Symptomtext
Soreness in the arm; 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) (Lot number: FD7218) 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: PAIN IN EXTREMITY (non-serious), outcome "unknown", described as "Soreness in the arm". Additional Information: Consumer stated that, about two weeks ago, I received COVID-19 vaccine. Well, the first dose, I had no problems, I just had soreness in the arm. When clarified the concern, consumer stated that first I would like to get some medical information. I do not know if it was an allergic reaction, or I do not know what to do. QR Comment: Reporter type was not clarified over the call. Hence captured as consumer or other non-health professional by default. 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
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 22.03.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain in extremity
Symptomtext
Pain across my right foot, my instep; 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 2022 (Lot number: FD7218) as dose 2, single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose 1), administration date: 2022, for Covid-19 Immunization, reaction(s): "soreness in the arm". The following information was reported: PAIN IN EXTREMITY (non-serious) with onset 2022, outcome "unknown", described as "Pain across my right foot, my instep". 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
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 19.03.2022
- Impfdatum
- 07.04.2021
- Beginn
- 16.03.2022
- Tage bis Beginn
- 343,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Diarrhoea
Dry throat
Vomiting
Symptomtext
DRY THROAT; DIARRHOEA; VOMITING; This spontaneous report received from a patient concerned a 38 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included: aspirin allergy. The patient received covid-19 vaccine ad26.cov2.s (dose number in series 1) (suspension for injection, route of admin not reported, batch number: 1808609, expiry: unknown) dose was not reported, 1 total administered on 07-APR-2021 on left arm for prophylactic vaccination. It was unknown if patient experienced any adverse events following vaccination with covid-19 vaccine ad26.cov2.s (dose number in series 1). The patient later received non-company suspect vaccine tozinameran (Pfizer) (dose number in series 2) (form of admin, route of admin were not reported, batch number: FD7218 expiry: unknown) dose was not reported, administered on 18-DEC-2021 on left arm for prophylactic vaccination. No concomitant medications were reported. On 16-MAR-2022, the patient experienced symptoms like diarrhoea and vomiting (dose number in series 2). On an unspecified date, patient experienced dry throat (dose number in series 2). The patient did not undergo any Covid-19 test. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient was recovering from diarrhoea, dry throat and vomiting. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Drug allergy
- Vorgeschichte
- Comments: Unknown
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 17.03.2022
- Impfdatum
- 27.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Symptomtext
Complaining of headache since receiving last vaccine.; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 16 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 27Dec2021 13:00 (Lot number: FD7218) at the age of 16 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Penicillin" (unspecified if ongoing), notes: known allergies: Penicillin; "Ache" (unspecified if ongoing). Concomitant medication(s) included: MINOCYCLINE taken for acne, start date: Sep2021 (ongoing). Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0181), administration date: 15Jun2021, when the patient was 15 years old, for Covid-19 Immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EW1080), administration date: 21May2021, when the patient was 15 years old, for Covid-19 Immunization. The following information was reported: HEADACHE (non-serious) with onset 27Dec2021, outcome "not recovered", described as "Complaining of headache since receiving last vaccine.". Therapeutic measures were taken as a result of headache. Additional information:The patient received treatment with Tylenol and Advil.The patient did not receive any other vaccines within 4 weeks prior to the COVID-19 vaccine. The patient had not been diagnosed with COVID-19 prior to vaccination and had not been tested since the vaccination. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Ache; Penicillin allergy (known allergies: Penicillin)
- Andere Medikamente
- MINOCYCLINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 16.03.2022
- Impfdatum
- 13.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Chills
Feeling abnormal
Illness
Nausea
Tinnitus
Vision blurred
Symptomtext
Nauseated; Chills; Joint pain; Ears ringing; I feel awful/feel so bad; My vision is blurred; I am so sick; 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 13Jan2022 (Lot number: FD7218) as dose number unknown (booster), single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Primary Immunization series complete; unknown manufacturer), for COVID-19 immunization. The following information was reported: NAUSEA (non-serious) with onset Jan2022, outcome "unknown", described as "Nauseated"; CHILLS (non-serious) with onset Jan2022, outcome "unknown", described as "Chills"; ARTHRALGIA (non-serious) with onset Jan2022, outcome "unknown", described as "Joint pain"; TINNITUS (non-serious) with onset Jan2022, outcome "unknown", described as "Ears ringing"; FEELING ABNORMAL (non-serious) with onset Jan2022, outcome "unknown", described as "I feel awful/feel so bad"; VISION BLURRED (non-serious) with onset Jan2022, outcome "unknown", described as "My vision is blurred"; ILLNESS (non-serious) with onset Jan2022, outcome "unknown", described as "I am so sick". Additional information: When patient was asked about lot number, they reported Pfizer FD7218 or 51 and don't know. Follow-up attempts completed. No further information expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 16.03.2022
- Impfdatum
- 12.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Nausea
Pyrexia
Symptomtext
Fever; Nausea; This is a spontaneous report received from a non-contactable reporter(s) (Other HCP). A 28 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administration date 12Jan2022 (Lot number: FD7218) at the age of 28 years as dose 2, single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: Unknown. Not available/provided to reporter at the time of report completion), for Covid-19 Immunization. The following information was reported: PYREXIA (non-serious) with onset Jan2022, outcome "unknown", described as "Fever"; NAUSEA (non-serious) with onset Jan2022, outcome "unknown", described as "Nausea". Additional information: Device Date: 14Jan2022 No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 16.03.2022
- Impfdatum
- 04.01.2022
- Beginn
- 04.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
Chills
Lymph node pain
Lymphadenopathy
Pain
Pyrexia
Symptomtext
lymph glands in my left arm pit are very enlarged and very painful to touch; lymph glands in my left arm pit are very enlarged and very painful to touch.; running a fever of 100.1 to 101 for the past three days; extreme body aches/ left area is terribly sore; chills; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 58 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 04Jan2022 13:45 (Lot number: FD7218) at the age of 58 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Ulcerative colitis" (unspecified if ongoing); "HTN" (unspecified if ongoing). Concomitant medication(s) included: LISINOPRIL; SULFASALAZINE. The following information was reported: LYMPHADENOPATHY (non-serious) with onset 04Jan2022 21:30, outcome "unknown", described as "lymph glands in my left arm pit are very enlarged and very painful to touch"; LYMPH NODE PAIN (non-serious) with onset 04Jan2022 21:30, outcome "unknown", described as "lymph glands in my left arm pit are very enlarged and very painful to touch."; PYREXIA (non-serious) with onset 04Jan2022 21:30, outcome "unknown", described as "running a fever of 100.1 to 101 for the past three days"; PAIN (non-serious) with onset 04Jan2022 21:30, outcome "unknown", described as "extreme body aches/ left area is terribly sore"; CHILLS (non-serious) with onset 04Jan2022 21:30, outcome "unknown", described as "chills". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of lymphadenopathy, lymph node pain, pyrexia, pain, chills. Additional Information: No other vaccine was taken in four weeks. No covid prior vaccination. No covid tested post vaccination. Patient's left area was terribly sore but what was most concerning was that the lymph glands in her left arm pit were very enlarged and very painful to touch. She had been running a fever of 100.1 to 101 for the past three days. She had extreme body aches and chills. Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220104; Test Name: Body temprature; Result Unstructured Data: Test Result:100.1-101; Comments: Running a fever of 100.1 to 101 for the past three days.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Hypertension; Ulcerative colitis
- Andere Medikamente
- LISINOPRIL; SULFASALAZINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 15.03.2022
- Impfdatum
- 25.02.2022
- Beginn
- 25.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Malaise
Product storage error
Symptomtext
The vaccine was administered outside of the expiration date range. The patient did have an immune response to the vaccine in that she "felt sick".
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 15.03.2022
- Impfdatum
- 23.12.2021
- Beginn
- 23.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Accidental exposure to product
Eye irritation
Eye pain
Ocular hyperaemia
Underdose
Symptomtext
solution got on her eye.; solution got on her eye. It was irritated/patient's eye was irritated; patient's eye was irritated and stinging; solution got on her eye. It was irritated, "not super red" and stinging pain; Adult Dose; Not a full dose--some sprayed into eye; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. A 23 year-old female patient received bnt162b2 (COMIRNATY), administration date 23Dec2021 (Lot number: FD7218, Expiration Date: 28Feb2022) at the age of 23 years as dose number unknown, single for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. The following information was reported: ACCIDENTAL EXPOSURE TO PRODUCT (non-serious) with onset 23Dec2021, outcome "unknown", described as "solution got on her eye."; EYE IRRITATION (non-serious) with onset 23Dec2021, outcome "unknown", described as "solution got on her eye. It was irritated/patient's eye was irritated"; EYE PAIN (non-serious) with onset 23Dec2021, outcome "unknown", described as "patient's eye was irritated and stinging"; OCULAR HYPERAEMIA (non-serious) with onset 23Dec2021, outcome "unknown", described as "solution got on her eye. It was irritated, "not super red" and stinging pain"; UNDERDOSE (non-serious) with onset 23Dec2021, outcome "unknown", described as "Adult Dose; Not a full dose--some sprayed into eye". Therapeutic measures were taken as a result of eye irritation, eye pain, ocular hyperaemia. Additional information: Caller asked about the Pfizer COVID-19 Vaccine Purple Cap presentation. No other products. No investigation assessment. Caller stated that she is calling about the Pfizer Covid 19 Vaccine Adult Dose. Caller stated that one of the pharmacy interns was drawing up a dose from the vial and the air pressure must have been too high because when she pulled the syringe out, the product sprayed, and it got in her eye. Caller stated that the patient's eye was irritated, "not super red" and stinging pain. Caller stated they rinsed it out in the sink and with eye wash. She washed it with saline. Eye contact: Rinsed thoroughly with plenty of water for at least 15 minutes, lifting lower and upper eyelids. Consulted a physician. Caller wanted to know if there are any further instructions for this. Caller was asking is there anything else they should do or any procedures to follow. Treatment received was eye rinse. Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Eye pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 14.03.2022
- Impfdatum
- 07.12.2021
- Beginn
- 23.01.2022
- Tage bis Beginn
- 47,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Diarrhoea
Stool analysis
Symptomtext
Sudden onset of chronic diarrhea 6 weeks after shot. No previous history of GI issues. Conditions still currently persist.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- Blood and stool samples
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- High Blood pressure, high Cholesterol, high triglicerides, stage 3 kidney disease
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 10.03.2022
- Impfdatum
- 20.12.2021
- Beginn
- 20.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Symptomtext
Patient said her symptoms started not too long after her vaccine. She is having pain in her shoulder. She says the pain has gotten worse instead of better. Patient will be having an appointment with an orthopedic doctor soon.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Not known
- Vorgeschichte
- Not known
- Andere Medikamente
- Not known
- Allergien
- Amoxicillin, Demerol, Penicillin
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 04.03.2022
- Impfdatum
- 19.12.2021
- Beginn
- 19.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Inflammation
Injection site pain
Periarthritis
X-ray limb abnormal
Symptomtext
Per patient; Pain in left arm right where she got the shot, went to the doctor...waited a little while thinking it would pass, finally saw the doctor on Feb 16, about two months after the vaccine, and he told her she has capsulitis (inflammation in her shoulder) and the treatment is oral steroids and physical therapy which she started and if that doesnt help then she has to get US guided cortisone injection and then surgery if that doesn't work. MD was Dr. (Privacy) at Clinic.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- X-ray 2/16 indicated capsulitis. Currently doing physical therapy for one month to see if that helps. Goes back to MD at the beginning of April to get injection because PT does not seem to be helping. Has had PT eval and one session so far.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 04.03.2022
- Impfdatum
- 03.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Asthenia
Blood pressure increased
Electrocardiogram
Fatigue
Influenza like illness
Symptomtext
I had flu like symptoms around 8:00PM and I had a blood pressure spike where it went up to 205. I went to the emergency room and it took a few hours but they were able to get it down with medication. I was observed for about 2 hours and released. I still had symptoms of feeling weak and tired. I still felt flu like symptoms the next day. I was nauseous for at least another 24 hours. It took about 3 days to fully recover.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- EKG, pulse OX test
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Lisinopril, Atenolol, Allopurinol, Lipitor
- Allergien
- Shellfish
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 03.03.2022
- Impfdatum
- 29.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Bacterial test
Blister
Burning sensation
Erythema
Headache
Lip blister
Myalgia
Rash
Scar
Sensory disturbance
Viral infection
Viral test positive
Symptomtext
Headache. Muscle aches. Face red and rashy. No fever. Herpes Zoster-type symptoms. Blister on left side of face around eye. Blisters in nose and lips. Burning sensation. Felt like needles. Still have scarring. May be a coincidence. PT suspected it was shingles. Sx presented the day after the Covid Shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Bacterial and Viral test confirmed to be viral.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Olmesa Medox 20mg, Omeprazole 20mg
- Allergien
- A
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 02.03.2022
- Impfdatum
- 07.02.2022
- Beginn
- 08.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain
Back pain
Headache
Pain
Tinnitus
Symptomtext
Constant Headache, ringing in ear, Body Aches, and Pain in abdomen and lower back.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- Sonogram - 02/28/2022 - Endometrial, Fibroid, ending urine lab results.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Gastritis, hiatal hernia, lactose intolerance, Acid sensitivity.
- Andere Medikamente
- Tylenol, Mylanta, Pepto-Bismol, Nature Made Folic Acid
- Allergien
- Urticaria, idiopathic L50.1; Drug allergy Z88.9; Allergic rhinitis due to pollen J30.1; Allergic rhinitis due to American house dust mite J30.89 and Allergic rhinitis due to animal (cat) (dog) hair and dander J30.81
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 28.02.2022
- Impfdatum
- 14.12.2021
- Beginn
- 14.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal discomfort
Colonoscopy
Computerised tomogram
Flatulence
Headache
Bone pain
Haemorrhage
Inflammation
Hypoaesthesia
Laboratory test
Magnetic resonance imaging
Nausea
Rectal haemorrhage
Investigation
Pain in jaw
SARS-CoV-2 test
Thermal burn
Weight
Symptomtext
Rectal bleeding, pain on temple, gas, pressure in stomach, numbness in leg and foot, and nausea.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bone pain
- Hospital-Tage
- -
- Labordaten
- colonoscopy, MRI, CT scan, lab work.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 28.02.2022
- Impfdatum
- 14.12.2021
- Beginn
- 14.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal discomfort
Colonoscopy
Computerised tomogram
Flatulence
Headache
Bone pain
Haemorrhage
Inflammation
Hypoaesthesia
Laboratory test
Magnetic resonance imaging
Nausea
Rectal haemorrhage
Investigation
Pain in jaw
SARS-CoV-2 test
Thermal burn
Weight
Symptomtext
Rectal bleeding, pain on temple, gas, pressure in stomach, numbness in leg and foot, and nausea.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bone pain
- Hospital-Tage
- -
- Labordaten
- colonoscopy, MRI, CT scan, lab work.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 20.02.2022
- Impfdatum
- 16.02.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cellulitis
Injection site erythema
Injection site pain
Injection site warmth
Mental status changes
Rash
Symptomtext
Less than 24 hours after injection, pt started having pain to site of injection. Pt then developed altered mental status and was admitted to the hospital. Pts arm 2 days later had large area of erythema, pain and warmth. The site has been monitored the past 2 days and the area of erythema continues to spread, pt now prescribed Clindamycin for 5 days. MD believes it is a rash/cellulitis.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypothyroid, GERD, IBS, fibromyalgia, migraine, asthma
- Andere Medikamente
- Depakote, omeprazole, meclizine, linaclotide, Synthroid,
- Allergien
- aspartame, clarithromycin, clonidine, latex, miralax, penicillin, perfume, sulfa, sumatriptan, topamax, barium sulfate, atenolol, alendronate, capsaicin, cephradine, cyclobenzaprine
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 20.02.2022
- Impfdatum
- 18.02.2022
- Beginn
- 19.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymphadenopathy
Oropharyngeal pain
Pain
Pyrexia
Swelling
Tenderness
Symptomtext
Body aches 2:00am for approx 24 hrs. Sore throat 2:00am for approx 24 hrs. Low grade fever 2:00am for approx 24 hrs. Motrin taken at 9:30 am Swollen under left arm approx. 12:30 am Sunday took hot shower at 8:00 am swelling down, but still a little swelling and tenderness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Sinusitus Hypertension
- Andere Medikamente
- D3 - 2000 IU Bistolic- 20mg Hydroclorothorizide - 25mg Claritin 10mg Amlopidine 5mg Olmesa Medox 20mg Levothyroxine 100-5 and 75-2
- Allergien
- Penicillin Sulfa Dairy
- Vorherige Impfungen
- Fever, aches, cough, headache, 51, 2/15/2021 and 3/22/2021, covid 19, Moderna
- Staat
- SC
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 15.02.2022
- Impfdatum
- 11.02.2022
- Beginn
- 12.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Injection site erythema
Injection site swelling
Injection site warmth
Lymphadenopathy
Nipple pain
Pain
Symptomtext
Body aches and fatigue. Swelling, redness and heat at injection site. Swollen lymph nodes under left arm and alongside of left breast. Painful nipples on both breasts.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Sinus infection
- Vorgeschichte
- Arthritis, degenerative disc disease, fibromyalgia
- Andere Medikamente
- Pantoprazole, Diclofenac, Estradiol, Cyanocobalamin, Gabapentin, Hydrocodone, Vitamin D3
- Allergien
- Codeine, Cymbalta
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 12.02.2022
- Impfdatum
- 08.12.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Arthritis
Computerised tomogram
Feeling abnormal
Inflammation
Magnetic resonance imaging
Nausea
Oropharyngeal pain
Pain
Pain assessment
Pelvic inflammatory disease
White blood cell count
Wrong technique in product usage process
Symptomtext
extensive severe inflammation throughout her pelvis; vaccine has magnified the inflammation; odd administration of the vaccine/ so painful. Didn't feel it went straight into her arm and it really hurt.; arthritis; weirdness; sore throat; waves of pain would make her nauseous with her jaw; excruciating pain in left shoulder, left arm, left side of her neck and her head; 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 56 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 08Dec2021 (Lot number: FD7218) at the age of 56 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "diverticulitis", start date: Jan2021 (ongoing), notes: inflammation in her pelvic area could be related to her history of diverticulitis, Verbatim: Diverticulitis; "Retinitis pigmentosa" (ongoing), notes: Verbatim: Retinitis pigmentosa. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: EN6201 or EIV6201, the handwriting is hard to read.), administration date: 08Apr2021, when the patient was 55 years old, for COVID-19 immunization, reaction(s): "arm soreness"; Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0171), administration date: 11May2021, when the patient was 55 years old, for COVID-19 immunization, reaction(s): "arm soreness".The following information was reported: PELVIC INFLAMMATORY DISEASE (hospitalization), outcome "unknown", described as "extensive severe inflammation throughout her pelvis"; INFLAMMATION (hospitalization), outcome "unknown", described as "vaccine has magnified the inflammation"; WRONG TECHNIQUE IN PRODUCT USAGE PROCESS (non-serious), outcome "unknown", described as "odd administration of the vaccine/ so painful. Didn't feel it went straight into her arm and it really hurt."; PAIN (non-serious) with onset Dec2021, outcome "recovering", described as "excruciating pain in left shoulder, left arm, left side of her neck and her head./ pain all the way down her arm, in her shoulder, in her neck into her head and the waves of pain would make her nauseous with her jaw"; ARTHRITIS (non-serious), outcome "unknown", described as "arthritis"; FEELING ABNORMAL (non-serious), outcome "recovering", described as "weirdness"; OROPHARYNGEAL PAIN (non-serious) with onset Dec2021, outcome "recovering", described as "sore throat"; NAUSEA (non-serious) with onset Dec2021, outcome "recovering", described as "waves of pain would make her nauseous with her jaw". The patient was hospitalized for pelvic inflammatory disease, inflammation (start date: 22Dec2021, discharge date: 24Dec2021, hospitalization duration: 2 day(s)). The events "extensive severe inflammation throughout her pelvis", "excruciating pain in left shoulder, left arm, left side of her neck and her head./ pain all the way down her arm, in her shoulder, in her neck into her head and the waves of pain would make her nauseous with her jaw" and "sore throat" were evaluated at the emergency room visit. The patient underwent the following laboratory tests and procedures: computerised tomogram: inflammation; magnetic resonance imaging: increase, notes: increase in pelvic inflammation/tiny, tiny arthritis in the left part of her neck; pain assessment: 8 to 10; white blood cell count: normal. Therapeutic measures were taken as a result of pelvic inflammatory disease, pain, feeling abnormal. Clinical course: Patient did have an MRI done and it showed a "tiny bit" of arthritis on the left side of the neck, but it was noted that it should not cause "this level of pain." The NP correlated if she already have a little bit of inflammation in an area, through their experience, the vaccine has magnified the inflammation 10 times over. Due to the "tiny bit of arthritis" noted in the left side of her neck, the NP advised that getting the vaccine high on the left arm with the odd administration of the vaccine, it could have taken the tiny inflammation and magnified it in her case. Patient notes her "weird aching and discomfort" being "nominal" and last night it was more so located in her jaw. She does also note that it seems to be slowly resolving and hoping that the "weirdness will completely go away in the not too distant future" and she "hopes she dont get these for forever." Patient was taking PT through the (Name Withheld) as well in hopes to help relieve her symptoms. When she was in the ER in Dec, she stated she had imaging done and it did show increase in pelvic inflammation, however she also noted that she was diagnosed with diverticulosis Jan of last year. She went to the ER for discomfort in her colon/pelvic area as well as the significant pain in her neck, shoulder, and head area. They evaluated all of her concerns and deemed that the inflammation in her pelvic area could be related to her history of diverticulitis and be more of coincidental finding after having the booster. Patient was most concerned about the inflammation in her pelvic area vs the neck "stuff" because she now has the recommendation from a surgeon to remove her sigmoid colon due to 2 hospitalizations in one year, one being a complicated hospital stay and the other not. She was looking into a 2nd opinion at this time and was interested in the relevance of the vaccine to the pelvic inflammation because that can certainly affect the bigger picture for her and the decisions she had to make regarding surgery. Patient stated she had contacted (Name Withheld) regarding this as well but notes that "it was a very odd injection." She stated it was "so painful. Didn't feel it went straight into her arm and it really hurt." She told the pharmacist who administered the product "her other 2 did not hurt that bad" because she "yelled out a little bit." She asked him if it would still work and did it go in right and he advised that it would still work although she felt that he noted something was "off" but again, advised that the vaccine would still be effective. The NP that the patient saw afterwards, at the (Name Withheld), advised her that due to this experience, she should in the future get further COVID vaccinations in the thigh and have it done at the provider's office. She stated he may have missed the muscle and went into "fluid or hit a nerve" and each of those "can be very problematic." Patient asked at what point does Pfizer start seeing a pattern of reported adverse events that people are having, specifically significant inflammation, before making it known to the public. The Patient noted that these findings should be important to Pfizer and the scientists who are studying and working with the product. Patient said that she had her Pfizer COVID vaccine booster on 08Dec2021, she had the 1st 2 shots in Apr2021 and May2021 without any real issues she just had arm soreness. For this third dose she went to a (Name withheld) location and it was a very strange shot. Her first 2 doses were little pricks but for this one the pharmacist was kind of higher on her left arm than normal and it went in at a funny angle but it was extremely painful to where she even said oh my gosh that hurt, her other two didn't hurt like that. He made some comment about missing something but she didn't think much about it other than asking him if it was still going to work to which the pharmacist said yes. She doesn't remember the exact timing but a day or 2 later she started to get excruciating pain in her neck. She had already gone to the chiropractor and gotten an adjustment because if she slept on her neck or her back funny she needed an adjustment, that pain was almost gone but it was still there a tiny bit prior to having her booster dose. She should have never told the pharmacist that it was okay to give the booster dose in her left arm. So she already had that tiny bit of pain that sent her to the chiropractor 10 days before but after the booster dose the pain went though the roof. She had pain all the way down her arm, in her shoulder, in her neck into her head and the waves of pain would make her nauseous with her jaw. She was taking Ibuprofen and Tylenol around the clock. Probably around 22Dec2022 she was still dealing with all of this pain in her neck and her shoulder and then she started to have pain in her colon. Baseline she has diverticulitis, she had an acute complication in Jan2021 and she had no problems with it until 22Dec2021 so she went to the hospital for 2 things the excruciating pain in her neck, shoulder and her jaw into her head and then what felt like the beginning of a diverticulitis flare. The hospital focused on the diverticulitis flare but they did do an MRI of her spine and said they saw no reason for the pain, she did have a tiny area of arthritis in her neck but that wouldn't cause the level of pain that she was experiencing. She was then hospitalized on 22Dec2021 because her pelvis was fully inflamed, they didn't see any abscess or perforation, her white blood cell count was normal but they were concerned with the level of inflammation in her pelvis. She then spent the next 2 nights in the hospital. After 1 day of IV antibiotics, or whatever they had going in, her abdomen got better but she kept asking for pain medications because of her neck and shoulder hurting so bad. After the antibiotics she was released and sent home but then she ended up back in the emergency room 2 days later because she woke up and the pain was so bad in her neck, shoulder and arm that even the oxycodone that she was prescribed for the diverticulitis wasn't cutting it. She went back to the emergency room thinking that she was dying and that was actually when they did the MRI of her spine. They did it this 2nd time, not on the first emergency room visit that she had mentioned previously. Due to all of this she has been researching the heck out of this. One doctor said that she now needed to get her sigmoid colon removed because she 2 flares within a year but she was trying to get a 2nd opinion. She also went to the (Name Withheld) because she was referred there for physical therapy and to see an orthopedist because they couldn't figure out why she was having all this pain going on. (Name Withheld) also did an MRI of her spine, neck and shoulder and said that they couldn't find anything. She was telling the orthopedic nurse practitioner there that this all started a day or 2 days after she had her COVID vaccine booster and the nurse practitioner said that she thought that's the cause of the pain. The nurse practitioner has seen a number of cases like this and maybe the Patient the issue was either that maybe the pharmacist didn't give the vaccine in the muscle or with the Patient having that tiny inflammation, the tiny arthritis and already having to see the chiropractor sometimes, then maybe that affected it. She was just there getting physical therapy from them but she needed to if this was documented within Pfizer's resources. She did see that the vagal nerve runs from the neck down into part of the colon. All of this that she has been experienced has happened on her left side and she just needs to know about this from Pfizer. She did report this to the pharmacy and she was waiting to hear back from Walgreens on if they have anything to say regarding this. She wanted to know if there was any chance that the COVID vaccine caused something with her nerves on that side and then continued to aggravate her pelvis causing the inflammation because she needed to know. There was a surgeon who wanted to remove her colon because she has had a 2nd hospitalization within the last year that he was attributing to her diverticulitis. She had no issues with her first 2 doses and she doesn't know why the booster was like this for her, maybe it was how it was administered but she still believed that. Last night she was still getting weird sensations in her neck, jaw and her swallowing was a little weird. She also has been getting a slight sore throat. She has been tested for COVID and she doesn't have that. She just wanted Pfizer to know that, she is not at a level that would send her to the emergency room so she thought that it was getting better but the weird symptoms in her jaw, neck and throat are not 100% gone. She will go to the cupboard and get some Tylenol, she doesn't take Ibuprofen anymore, and the Tylenol helped her. If all of this had gone away she wouldn't have called about it but with it going on this long it was wigging her out about the discomfort. Not at this time, maybe some time down the road she will. When she has mentioned to probably 2 doctors that she thought the COVID vaccine may be part of all of her issues they look at her like she has horns and they just say that there is no empirical evidence for that but she knows that this was all new stuff. She has seen an orthopedic doctor, a surgeon, her family doctor and she has talked to a gastroenterologist on an online consult through the (clinic name). She has circled her bases in talking to medical professionals. Event Details: Inquired for when the pain began and she clarified and confirmed what was previously stated by saying that she was thinking that it began within 24 hours. She knew that she felt good at first because she has a son who became a marine and he was coming home so she was excited because her neck issue was pretty much gone and she wanted to get the booster to ensure that she didn't get sick and she didn't wanted to get him sick and him not be able to go back. So she remembered that because she felt so much better and then 24 hours later or so the pain just went through the roof, it was not just in her neck anymore it was the whole area. It was pretty much right on the heels of being within 24 hours or so of that booster. She said it had improved a lot so that gave her hope that whatever was causing it, the booster or something else, was not permanent. The orthopedic nurse practitioner said that she didn't think that there would be permanent damage. She was told to get it in the thigh because the muscle there was bigger. So if she got the courage to get another booster then she will get it but she will definitely not get it in her arm again. The pain was at an 8 to 10 when she went to the emergency room and then what was weird was that it would come in different parts of her left side in waves. It was just a weird thing. Then she would have a wave of nausea and now it's just creeping up at a lower level, maybe a 2 or a 3, at most. She has been trying to relax. She has the weirdness in her jaw, a little bit in her ear, and her throat has felt funny and was kind of annoying her last night. It was weird and was just probably at like a 2 or a 2 1/2 last night and she took 2 Tylenol. She felt a little weirdness this morning in the same area and took 2 more Tylenol. It was not nearly as severe as it was. Inquired for when the issues with her throat area began and she said that was the weird part. She thought that she may have had a minor sore throat. Again, it could all be unrelated. She went to an urgent care before she ever went to the emergency room around 20Dec2021 because of the pain she was having all around her neck. She was trying to remember if the sore throat started initially, she thought it did. She remembered that the doctor at the urgent care looked at her throat and saw some redness there and she was prescribed with something that they ended up changing at the hospital because they didn't feel like it was the right antibiotic for it. To make the long answer shorter it does seem like all of that started at the same time. She was trying to now think if she had any sore throat before she had the COVID booster but she can't remember for sure. She thought the sore throat developed after the COVID booster but it was the first thing that started and then the pain went deeper and was moving in all areas and that started shortly afterwards. Diverticulitis Flare: On her hospital release report they have that she had extensive severe inflammation throughout her pelvis area, this was what the emergency room doctor and the surgeon that treated her last Jan2021 had said. She was first told about her diverticulitis in Jan2021 and she had an issue in her sigmoid area, she had a micro perforation and a small abbess that they had to drain. At that time, Jan2021, she had a fever, a high white blood cell count and pain that was much, much greater. Honestly, if she wouldn't have had the neck and shoulder pain she may have ignored the Discomfort in her pelvic area at this time because it felt so minor, But that was what they called it but she did not have the elevated white blood cells and it didn't seem to be like the infection she had in Jan2021, it was just inflammation that was visible on a CT scan that they did on her pelvis. She was admitted to the hospital on 22Dec2021 and stayed on 22Dec2021 and 23Dec2021 and then they let her go home late on 24Dec2021. She thought that they would have kept her longer but other than her neck and shoulder still bugging her, they did another CT scan for that, she had no more concerns for her colon so they let her go home with a bunch of antibiotics. Arm Soreness: She said that the only symptoms that she had seemed to be that she was tired for so many hours after the 1st COVID vaccines and then she had a little arm soreness afterwards but nothing else. She confirmed these were side effects were felt after her 1st and 2nd dose of the Pfizer COVID vaccine. She got those doses in her right arm and for some reason the pharmacist suggested that she have the booster dose in her left arm, which is a different arm. Therapy start date populated as the date for the Patient's first COVID vaccine and the therapy stop date populated as the date for the Patient's booster COVID vaccine. 1st dose- 08Apr2021 Lot Number: She thought the lot number is either EN6201 or EIV6201, the handwriting was hard to read. 2nd dose- 11May2021 Lot Number: EW0171 booster dose- 08Dec2021 Lot Number: FD7218. History/ Investigations: So like she said the 2nd time that she went back to the emergency room, after they released her, because her neck, shoulder, arm and head pain was horrible they did an MRI of her spine and neck she guesses they were looking to see if there was any cancer and there said that they did not see any concerns other than the tiny, tiny arthritis in the left part of her neck that should never cause this level of pain. So she had no issues in her spine and neck. And like she said, the diverticulitis was a new diagnosis. She also has an eye condition that doesn't cause pain but it has caused her to lose her peripheral vision, this has been going on her whole life, she had good central vision but the diagnosis is retinitis pigmentosa. So that was another diagnosis but there was no treatment for it at this point in time other than to take care of herself. She doesn't think that there was anything else that was relevant. She will be going to (Name Withheld) for more neck exercises next Monday and for another therapy session. She might do dry needling in her neck area, they thought that might could help. Oxycodone: She said she only took a couple. She was dispensed 10 and there are 7 left, so she only ended up taking 3 when she got home from the hospital. She was hoping that it would help her neck and stuff but it didn't and after she took the 3rd she went to the emergency room. She realized Tylenol worked better for this and then she never took anymore of the Oxycodone. Inquired for NDC, lot number and expiry date and Patient declined to provide since those are not on the orange pharmacy bottle from (Name Withheld) that she has. She says the medication specifically is Oxycodone HCl 5 mg tablets. They gave her another pain killer in the emergency room through her IV but she doesn't remember what that was. Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- 2,0
- Labordaten
- Test Name: CT scan; Result Unstructured Data: Test Result:inflammation; Test Name: MRI; Result Unstructured Data: Test Result:Increase; Comments: increase in pelvic inflammation/ tiny, tiny arthritis in the left part of her neck; Test Name: pain; Result Unstructured Data: Test Result:8 to 10; Test Name: white blood cell count; Result Unstructured Data: Test Result:normal
- Aktuelle Erkrankungen
- Diverticulitis (inflammation in her pelvic area could be related to diverticulitis Verbatim: Diverticulitis); Retinitis pigmentosa (Verbatim: Retinitis pigmentosa)
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 12.02.2022
- Impfdatum
- 12.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Nausea
Pyrexia
Symptomtext
This is a spontaneous report received from a noncontactable reporter other HCP. A 54-year-old female patient received the 1st dose of BNT162B2 (Pfizer-BioNTech COVID-19 vaccine, batch/lot# FD7218), at the age of 54, on Jan 12, 2022, single dose, for COVID-19 immunisation. The patient's medical history and concomitant medications not reported. The patient developed pyrexia/fever, and nausea, onset Jan 2022, with outcome of unknown. Additional information: The case received via the regulatory authority reported as non-serious: no results in death, not life-threatening, no caused/prolonged hospitalization, not disabling/incapacitating and no congenital anomaly/birth defect. No follow-up attempts possible. No further information expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 12.02.2022
- Impfdatum
- 14.12.2021
- Beginn
- 14.01.2022
- Tage bis Beginn
- 31,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Feeling abnormal
Frustration tolerance decreased
Lymph node pain
Mental disorder
Disorientation
Tension headache
Visual impairment
Vision blurred
Symptomtext
sore lymph nodes; tension headache; brain fog; vision issues; frustrating and debilitating; frustrating and debilitating; trouble focusing; feeling mentally clouded; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 31 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 14Dec2021 16:00 (Lot number: FD7218) at the age of 30 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Known allergies: penicillin" (unspecified if ongoing). There were no concomitant medications. Vaccination history included: Bnt162b2 (lot number=ER8732, administration date=28Mar2021, administration time=12:00PM, dose number=2, vaccine location=Left arm), administration date: 28Mar2021, when the patient was 30 years old, for Covid-19 immunization, reaction(s): "tension headache", "brain fog", "visual field disorientation", "tunnel vision", "elt like things in my periphery were harder to process", "felt mentally a beat behind"; Bnt162b2 (lot number=EN6206, administration date=07Mar2021 , administration time=12:00 PM , dose number=1, location=Left arm), administration date: 07Mar2021, when the patient was 30 years old, for Covid-19 immunization, reaction(s): "sore arm". The following information was reported: LYMPH NODE PAIN (non-serious) with onset 14Jan2022 15:00, outcome "not recovered", described as "sore lymph nodes"; TENSION HEADACHE (non-serious) with onset 14Jan2022 15:00, outcome "not recovered", described as "tension headache"; FEELING ABNORMAL (non-serious) with onset 14Jan2022 15:00, outcome "not recovered", described as "brain fog"; VISUAL IMPAIRMENT (non-serious) with onset 14Jan2022 15:00, outcome "not recovered", described as "vision issues"; FRUSTRATION TOLERANCE DECREASED (non-serious), ASTHENIA (non-serious) all with onset 14Jan2022 15:00, outcome "not recovered" and all described as "frustrating and debilitating"; VISION BLURRED (non-serious) with onset 14Jan2022 15:00, outcome "not recovered", described as "trouble focusing"; MENTAL DISORDER (non-serious) with onset 14Jan2022 15:00, outcome "not recovered", described as "feeling mentally clouded". The events "sore lymph nodes", "tension headache", "brain fog", "vision issues", "frustrating and debilitating", "frustrating and debilitating", "trouble focusing" and "feeling mentally clouded" were evaluated at the physician office visit. Therapeutic measures were not taken as a result of lymph node pain, tension headache, feeling abnormal, visual impairment, frustration tolerance decreased, asthenia, vision blurred, mental disorder. Clinical course reported as Initially, only sore lymph nodes. However, a month after the shot, out of seemingly nowhere the tension headache and brain fog returned, with vision issues. This has lasted about a week now, and has been more consistent than before, but a bit more mild- however still frustrating and debilitating. I am having trouble focusing and this is also preventing me from Cycling (my passion), as I feel it's risky when feeling mentally clouded. I've never experienced any of these symptoms/sensations in my life prior to vaccination- which leads me to correlate my symptoms to the shot. The patient did not have covid prior vaccination and not tested for covid post vaccination. No other vaccine in four weeks. No other medications in two weeks Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymph node pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Penicillin allergy
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 12.02.2022
- Impfdatum
- 14.12.2021
- Beginn
- 14.01.2022
- Tage bis Beginn
- 31,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Feeling abnormal
Frustration tolerance decreased
Lymph node pain
Mental disorder
Disorientation
Tension headache
Visual impairment
Vision blurred
Symptomtext
sore lymph nodes; tension headache; brain fog; vision issues; frustrating and debilitating; frustrating and debilitating; trouble focusing; feeling mentally clouded; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 31 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 14Dec2021 16:00 (Lot number: FD7218) at the age of 30 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Known allergies: penicillin" (unspecified if ongoing). There were no concomitant medications. Vaccination history included: Bnt162b2 (lot number=ER8732, administration date=28Mar2021, administration time=12:00PM, dose number=2, vaccine location=Left arm), administration date: 28Mar2021, when the patient was 30 years old, for Covid-19 immunization, reaction(s): "tension headache", "brain fog", "visual field disorientation", "tunnel vision", "elt like things in my periphery were harder to process", "felt mentally a beat behind"; Bnt162b2 (lot number=EN6206, administration date=07Mar2021 , administration time=12:00 PM , dose number=1, location=Left arm), administration date: 07Mar2021, when the patient was 30 years old, for Covid-19 immunization, reaction(s): "sore arm". The following information was reported: LYMPH NODE PAIN (non-serious) with onset 14Jan2022 15:00, outcome "not recovered", described as "sore lymph nodes"; TENSION HEADACHE (non-serious) with onset 14Jan2022 15:00, outcome "not recovered", described as "tension headache"; FEELING ABNORMAL (non-serious) with onset 14Jan2022 15:00, outcome "not recovered", described as "brain fog"; VISUAL IMPAIRMENT (non-serious) with onset 14Jan2022 15:00, outcome "not recovered", described as "vision issues"; FRUSTRATION TOLERANCE DECREASED (non-serious), ASTHENIA (non-serious) all with onset 14Jan2022 15:00, outcome "not recovered" and all described as "frustrating and debilitating"; VISION BLURRED (non-serious) with onset 14Jan2022 15:00, outcome "not recovered", described as "trouble focusing"; MENTAL DISORDER (non-serious) with onset 14Jan2022 15:00, outcome "not recovered", described as "feeling mentally clouded". The events "sore lymph nodes", "tension headache", "brain fog", "vision issues", "frustrating and debilitating", "frustrating and debilitating", "trouble focusing" and "feeling mentally clouded" were evaluated at the physician office visit. Therapeutic measures were not taken as a result of lymph node pain, tension headache, feeling abnormal, visual impairment, frustration tolerance decreased, asthenia, vision blurred, mental disorder. Clinical course reported as Initially, only sore lymph nodes. However, a month after the shot, out of seemingly nowhere the tension headache and brain fog returned, with vision issues. This has lasted about a week now, and has been more consistent than before, but a bit more mild- however still frustrating and debilitating. I am having trouble focusing and this is also preventing me from Cycling (my passion), as I feel it's risky when feeling mentally clouded. I've never experienced any of these symptoms/sensations in my life prior to vaccination- which leads me to correlate my symptoms to the shot. The patient did not have covid prior vaccination and not tested for covid post vaccination. No other vaccine in four weeks. No other medications in two weeks Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymph node pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Penicillin allergy
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 11.02.2022
- Impfdatum
- 13.12.2021
- Beginn
- 14.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal pain upper
Blood test
Chest X-ray
Dyspepsia
Electrocardiogram
Endoscopy
Nausea
Ultrasound abdomen
Vomiting
Symptomtext
Vaccine caused nausea and vomitting, which gave way to extreme persistent heartburn. Patient visited ER to diagnose and treat heartburn, Pepcid administered. 7 weeks later, patient is still experiencing heartburn and stomach pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- EKG , chest X-ray, bloodwork to rule out other causes (12/14/21) Endoscopy (2/2/22) and Abdominal ultrasound (2/8/22) to assess potential causes of heartburn
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Zyrtec Multi-vitamin Vitamin D
- Allergien
- Sucralose
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 09.02.2022
- Impfdatum
- 27.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Myalgia
Pain in extremity
Symptomtext
Patient describes pain in the arm over a month after receiving the vaccine. Described as muscular pain that runs up and down the arm. Started about 24 hours after receiving booster dose and has not subsided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 07.02.2022
- Impfdatum
- 07.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 21,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Hypoxia
Malaise
Pain
Rib fracture
SARS-CoV-2 test positive
Symptomtext
01/28/2022 - Most likely hypoxia in setting of rib fractures and possible obstructive process. Pt had minimal sx of COVID, and is fully vaccinated. However, given his new oxygen requirement, history of heavy drinking, and unclear support at home, will plan to admit for the hospital for multimodal pain contol and obs. 01/28/2022 - Report called to RN,. All questions answered and care transferred. Patient going to room. 01/31/2022 - Patient discharged following pain control, Covid+
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 05.02.2022
- Impfdatum
- 05.02.2022
- Beginn
- 05.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inflammation
Rash erythematous
Rash pruritic
Symptomtext
Around 10 minutes after getting the vaccine, the patient broke out in a red, itchy rash with inflammation all over her entire body from her face down to her feet. Patient stated the she had taken diphenhydramine 50 mgs approximately 15 minutes prior to getting the Covid vaccine due to a past experience where hives occured from a flu vaccine (which she believed to have occured due to her egg allergy).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash erythematous
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- Hashimoto Borderline Diabetic Asthma
- Andere Medikamente
- Prilosec Vitamin E, D, C B-complex
- Allergien
- Egg Latex Penicillin Keflex Erythromycin
- Vorherige Impfungen
- Patient stated that she broke out in itchy hives all over her entire body after her flu vaccine, which she received in September
- Staat
- NY
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 05.02.2022
- Impfdatum
- 22.12.2021
- Beginn
- 25.12.2021
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Asthenia
Polymyalgia rheumatica
Symptomtext
Patient up until this day was healthy and active until dec25 /2021 patient woke in the morning In severe pai in his shoulders and hip and extremely weak ! Was diagnosed with poly myalgia rumetica
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Peptic ulcer
- Vorgeschichte
- None
- Andere Medikamente
- Pepcid
- Allergien
- Compazine Codiene
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 05.02.2022
- Impfdatum
- 15.12.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Fatigue
Immunisation
Pain
Pruritus
Symptomtext
dose number: 3; achy; fatigued; red itchy spots on the top of my right thigh and left side of my chest/ many more red itchy spots on my lower back and bottom; red itchy spots on the top of my right thigh and left side of my chest/ many more red itchy spots on my lower back and bottom; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 56 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 15Dec2021 12:00 (Lot number: FD7218) at the age of 56 years as dose 3 (booster), single for covid-19 immunization. Relevant medical history included: "tree nuts" (unspecified if ongoing). Concomitant medication(s) included: PRILOSEC [OMEPRAZOLE]; TOPROL XL. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: ER8727, Location of injection: Arm Right, Vaccine Administration Time: 10:00 AM), administration date: 23Mar2021, when the patient was 55 years old, for COVID-19 immunization, reaction(s): "low grade fever", "body aches", "Chills", "Fatigue", "tiny red itchy spots on my abdomen", "tiny red itchy spots on my abdomen"; Bnt162b2 (Dose Number: 1, Batch/Lot No: EN6203, Location of injection: Arm Right), administration date: 02Mar2021, when the patient was 55 years old, for COVID-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 15Dec2021 12:00, outcome "unknown", described as "dose number: 3"; PAIN (non-serious) with onset Dec2021, outcome "not recovered", described as "achy"; FATIGUE (non-serious) with onset Dec2021, outcome "not recovered", described as "fatigued"; ERYTHEMA (non-serious), PRURITUS (non-serious) all with onset Dec2021, outcome "not recovered" and all described as "red itchy spots on the top of my right thigh and left side of my chest/ many more red itchy spots on my lower back and bottom". Therapeutic measures were taken as a result of pain, fatigue, erythema, pruritus. Additional information: Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. 1 week later developed a few tiny red itchy spots on my abdomen. These spots continued to develop and cause discomfort for 4 months all over my body. My primary care physician prescribed steroid creams. Did not help much, but spots kept appearing on my body. Finally saw my dermatologist who prescribed a stronger cream. Not sure if the cream did the trick or not but the spots finally turned brown and stopped itching. Third shot booster felt achy, fatigued and that same evening developed some red itchy spots on the top of my right thigh and left side of my chest. These spots are slightly bigger than last time. A month later 15Jan developed many more red itchy spots on my lower back and bottom. They are currently active and again everyday new ones appear, causing discomfort and concern. 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: Allergy to nuts
- Andere Medikamente
- PRILOSEC [OMEPRAZOLE]; TOPROL XL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 05.02.2022
- Impfdatum
- 12.01.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Nausea
Pyrexia
Symptomtext
Fever; Nausea; This is a spontaneous report received from a non-contactable reporter(s) (Pharmacist). A 54 year-old female patient (unknown if pregnant) received bnt162b2 (BNT162B2), administration date 12Jan2022 (Lot number: FD7218) at the age of 54 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: Covid-19 vaccine (dose number=2, Prev dose product=COVID 19, Prev dose brand unknown= true, Prev dose brand name unknown = Covid 19 vaccine, Prev dose lot unknown= true, Prev dose lot unknown reason = not available/provided to reporter at the time of report completion.), for COVID-19 immunization; Covid-19 vaccine (dose number= 1, Prev dose product=COVID 19, Prev dose brand unknown= True, Prev dose lot number unknown, prev dose brand name unknown= Covid 19 vaccine, Prev dose lot unknown= true, Prev dose lot unknown reason = not available/provided to reporter at the time of report completion), for COVID-19 immunization. The following information was reported: PYREXIA (non-serious), outcome "unknown", described as "Fever"; NAUSEA (non-serious), outcome "unknown", described as "Nausea". No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 05.02.2022
- 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: nein
Nausea
Pyrexia
Symptomtext
Fever; Nausea; This is a spontaneous report received from a non-contactable reporter(s) (Other HCP). A 57 year-old female patient (unknown if pregnant) received bnt162b2 (BNT162B2), administration date 12Jan2022 (Lot number: FD7218) at the age of 57 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: Covid19 vaccine (Prev dose product: COVID-19, Prev dose lot unknown: True, prev dose brand name unknown: COVID19 Vaccine, Prev dose dose number: 1), for COVID-19 Immunization; Covid19 vaccine (Prev dose product: COVID-19, Prev dose lot unknown: True, prev dose brand name unknown: COVID19 Vaccine, Prev dose dose number: 2), for COVID-19 Immunization. The following information was reported: PYREXIA (non-serious) with onset Jan2022, outcome "unknown", described as "Fever"; NAUSEA (non-serious) with onset Jan2022, outcome "unknown", described as "Nausea". No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 05.02.2022
- 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: nein
Nausea
Pyrexia
Symptomtext
This is a spontaneous report received from a noncontactable other healthcare professional. A 25-year-old female patient (unknown if pregnant) received the 3rd (booster) dose of BNT162B2 (Pfizer-BioNTech COVID-19 vaccine, batch/lot# FD7218), at the age of 25, on Jan 12, 2022, single dose, for COVID-19 immunisation. The patient's medical history and concomitant medications not reported. Vaccination history included the 1st and 2nd dose of BNT162B2 (Pfizer-BioNTech COVID-19 vaccine, batch/lot# unknown/not available/not provided to at the time of report), for COVID-19 immunization. The patient had pyrexia/fever and nausea, onset Jan 2022, with outcome of unknown. No follow-up attempts possible. No further information expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 05.02.2022
- 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: nein
Nausea
Pyrexia
Symptomtext
Fever; Nausea; This is a spontaneous report received from a non-contactable reporter(s) (Other HCP). A 40-year-old female patient (unknown if pregnant) received bnt162b2 (BNT162B2), administration date 12Jan2022 (Lot number: FD7218) at the age of 40 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: Covid-19 vaccine (Dose Number: 1, manufacturer unknown), for Covid-19 Immunization; Covid-19 vaccine (Dose Number: 2, manufacturer unknown), for Covid-19 Immunization. The following information was reported: PYREXIA (non-serious) with onset Jan2022, outcome "unknown", described as "Fever"; NAUSEA (non-serious) with onset Jan2022, outcome "unknown", described as "Nausea". Additional information: The report was assessed as non-serious. The events did not result into death, Life threatening, Caused/prolonged hospitalization, Disabling/Incapacitating and Congenital anomaly/birth defect. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 05.02.2022
- 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: nein
Nausea
Pyrexia
Symptomtext
Fever; Nausea; This is a spontaneous report received from a non-contactable reporter(s) (Other HCP). A 47 year-old female patient (unknown if pregnant) received bnt162b2 (BNT162B2), administration date 12Jan2022 (Lot number: FD7218) at the age of 47 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_number=1), for Covid-19 immunization; Bnt162b2 (dose_number=2), for Covid-19 immunization. The following information was reported: PYREXIA (non-serious) with onset Jan2022, outcome "unknown", described as "Fever"; NAUSEA (non-serious) with onset Jan2022, outcome "unknown", described as "Nausea". No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 05.02.2022
- 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: nein
Nausea
Pyrexia
Symptomtext
Fever; Nausea; This is a spontaneous report received from a non-contactable reporter(s) (Other HCP). A 48 year-old female patient (unknown if pregnant) received bnt162b2 (BNT162B2), administration date 12Jan2022 (Lot number: FD7218) at the age of 48 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: Covid 19 vaccine (Dose 1, Single, Manufacturer Unknown, Lot number- UNKNOWN), for COVID-19 Immunization; Covid 19 vaccine (Dose 2, Single, Manufacturer Unknown, Lot number- UNKNOWN), for COVID-19 Immunization. The following information was reported: PYREXIA (non-serious) with onset Jan2022, outcome "unknown", described as "Fever"; NAUSEA (non-serious) with onset Jan2022, outcome "unknown", described as "Nausea". Additional information: Device Date was reported as 14Jan2022. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 05.02.2022
- 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: nein
Nausea
Pyrexia
Symptomtext
Fever; Nausea; This is a spontaneous report received from a non-contactable reporter(s) (Other HCP). A 51 year-old female patient (unknown if pregnant) received bnt162b2 (BNT162B2), administration date 12Jan2022 (Lot number: FD7218) at the age of 51 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 Number: 2, Batch/Lot No: Unknown. Not available/provided to reporter at the time of report completion), for COVID-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: Unknown. Not available/provided to reporter at the time of report completion), for COVID-19 immunization. The following information was reported: PYREXIA (non-serious) with onset Jan2022, outcome "unknown", described as "Fever"; NAUSEA (non-serious) with onset Jan2022, outcome "unknown", described as "Nausea". No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 05.02.2022
- 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: nein
Nausea
Pyrexia
Symptomtext
Fever; Nausea; This is a spontaneous report received from a non-contactable reporter(s) (Other HCP). A 45 year-old female patient received bnt162b2 (BNT162B2), administration date 12Jan2022 (Lot number: FD7218) at the age of 45 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: Covid-19 vaccine (Prev dose Product: COVID 19, Prev dose Dose number: 1, MANUFACTURER UNKNOWN), for COVID-19 Immunization; Covid-19 vaccine (Prev dose Product: COVID 19, Prev dose Dose number: 2, MANUFACTURER UNKNOWN), for COVID-19 Immunization. The following information was reported: PYREXIA (non-serious) with onset Jan2022, outcome "unknown", described as "Fever"; NAUSEA (non-serious) with onset Jan2022, outcome "unknown", described as "Nausea". No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 05.02.2022
- 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: nein
Immunisation
Nausea
Pyrexia
Symptomtext
dose number: 3; Fever; Nausea; This is a spontaneous report received from a non-contactable reporter(s) (Other HCP). A 43 year-old female patient (unknown if pregnant) received bnt162b2 (BNT162B2), administration date 12Jan2022 (Lot number: FD7218) at the age of 43 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: Moderna (Dose Number: 2), for Covid-19 Immunization; Moderna (Dose Number: 1), for Covid-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 12Jan2022, outcome "unknown", described as "dose number: 3"; PYREXIA (non-serious) with onset Jan2022, outcome "unknown", described as "Fever"; NAUSEA (non-serious) with onset Jan2022, outcome "unknown", described as "Nausea". No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 03.02.2022
- Impfdatum
- 22.12.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pruritus
Rash
Symptomtext
patient developed rash and itching (mild/moderate) over legs and arms
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 02.02.2022
- Impfdatum
- 26.01.2022
- Beginn
- 27.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Fatigue
Feeling abnormal
Headache
Injection site rash
Malaise
Nausea
Pain
Pain in extremity
Symptomtext
After I received the vaccine, I didn't have a problem until about 12 hours later. The next morning, I didn't feel like myself; I felt achy, tired, nauseous, my arm was sore, had a headache, I just felt weak and sick and tired. I didn't have any symptoms from the previous 2 doses. I took two Tylenol extra strength to try to help fight off the symptoms. I developed a rash in the area of the injection site a couple of days after the vaccination. I went to the doctor last Friday, 01/28/2022. I got an IV in my arm and felt a bit better; the nausea and fatigue went away, but my headache didn't go away.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Allegra allergy medicine; Vitamin C; Vitamin D; Vitamin B12 Supplements; Montelukast; Cyclospora; Probiotic supplement
- Allergien
- Codeine; Gluten
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 29.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Nausea
Pyrexia
Symptomtext
This is a spontaneous report received from a noncontactable reporter (other HCP). A 64-year-old female patient received the 3rd (booster) dose of BNT162B2 (Comirnaty, batch/lot# FD7218), at the age of 64, on Jan 13, 2022, single dose, for COVID-19 immunisation. The patient's medical history and concomitant medications not reported. Vaccination history included the 1st and 2nd dose of the COVID-19 vaccine (batch/lot# unknown/not available/provided), for COVID-19 immunisation. The patient developed pyrexia/fever, and nausea, onset Jan 2022, with outcome of unknown. No follow-up attempts possible. No further information expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 29.01.2022
- 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: nein
Nausea
Pyrexia
Symptomtext
This is a spontaneous report received from a noncontactable reporter (other HCP). A 58-year-old female patient received the 3rd (booster) dose of BNT162B2 (Comirnaty, batch/lot# FD7218), at the age of 58, on Jan 12, 2022, single dose, for COVID-19 immunisation. The patient's medical history and concomitant medications not reported. Vaccination history included the 1st and 2nd dose of the COVID-19 vaccine (manufacturer unknown), for COVID-19 immunisation. The patient had pyrexia/fever and nausea, onset Jan 2022, with outcome of unknown. No follow-up attempts possible. No further information expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 29.01.2022
- Impfdatum
- 14.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Fatigue
Feeling abnormal
Influenza like illness
Neck mass
Nodule
Pain
Pyrexia
Symptomtext
Body aches; slight fever; brain fog; chills; felt like the flu; tired; getting a lump in my neck near my collarbone and one in my a pit area near my boob; both lumps sore both on the same side as the injection; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 42 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 14Dec2021 13:30 (Lot number: FD 7218) at the age of 41 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Hernia" (unspecified if ongoing); "uterine fibroids" (unspecified if ongoing); "allergies: penicillin" (unspecified if ongoing). Concomitant medication(s) included: FISH OIL; GLYCOPYRROLATE. Past drug history included: Pecans, reaction(s): "allergies"; Nickel, reaction(s): "allergies". Vaccination history included: Bnt162b2 (Dose Number: 2, Lot No: FW0161, vaccine location: Left arm), administration date: 14May2021, when the patient was 41 years old, for COVID-19 Immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EW0161, vaccine location: Right arm), administration date: 23Apr2021, when the patient was 41 years old, for COVID-19 Immunization. The following information was reported: PAIN (non-serious) with onset 16Dec2021, outcome "recovering", described as "Body aches"; PYREXIA (non-serious) with onset 16Dec2021, outcome "recovering", described as "slight fever"; FEELING ABNORMAL (non-serious) with onset 16Dec2021, outcome "recovering", described as "brain fog"; CHILLS (non-serious) with onset 16Dec2021, outcome "recovering", described as "chills"; INFLUENZA LIKE ILLNESS (non-serious) with onset 16Dec2021, outcome "recovering", described as "felt like the flu"; FATIGUE (non-serious) with onset 16Dec2021, outcome "recovering", described as "tired"; NECK MASS (non-serious) with onset 16Dec2021, outcome "recovering", described as "getting a lump in my neck near my collarbone and one in my a pit area near my boob"; NODULE (non-serious) with onset 16Dec2021, outcome "recovering", described as "both lumps sore both on the same side as the injection". Therapeutic measures were not taken as a result of pain, pyrexia, feeling abnormal, chills, influenza like illness, fatigue, neck mass, nodule. Additional information: Patient did not tested for covid post and prior vaccination. Concomitant medication included multivitamins. No follow-up attempts are possible. No further information is expected. Follow-Up (04Jan2022):Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Hernia; Penicillin allergy; Uterine fibroids
- Andere Medikamente
- FISH OIL; GLYCOPYRROLATE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 27.01.2022
- Impfdatum
- 27.01.2022
- Beginn
- 27.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Rash
Swelling face
Symptomtext
a skin rash appear on the face in 10 minutes after getting the vaccine, epipen been used,also the face begin to look buffy
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- no
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 27.01.2022
- Impfdatum
- 22.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
Chills
Immunisation
Lymphadenopathy
Neuralgia
Pain in extremity
Pyrexia
Symptomtext
Severe pain and lymph node swelling in right arm; Lymph node swelling in right arm; Nerve pain in right arm and left leg; High fever; Chills; Dose received: 3; This is a spontaneous report from a contactable reporter (consumer or other non HCP). The reporter is the patient. A 34-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in right arm, administration date 22Jan2022 at 10:00 (Lot number: FD7218) at the age of 34 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "Proteinuria" (unspecified if ongoing); "Blood pressure high" (unspecified if ongoing), notes: High blood pressure and "Nickel sensitivity" (unspecified if ongoing), notes: Known allergies: Nickel. Concomitant medication included: LISINOPRIL. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE, Lot Number: EP6955, Anatomical location: Left arm, Administration time: 15:30), administration date: 31Mar2021, when the patient was 33 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE, Lot Number: ER8736, Anatomical location: Right arm, Administration time: 15:00), administration date: 23Apr2021, when the patient was 33 years old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 22Jan2022 at 10:00, outcome "unknown", described as "Dose received: 3"; PAIN IN EXTREMITY (non-serious) with onset 22Jan2022 at 13:00, outcome "not recovered", described as "Severe pain and lymph node swelling in right arm"; LYMPHADENOPATHY (non-serious) with onset 22Jan2022 at 13:00, outcome "not recovered", described as "Lymph node swelling in right arm"; NEURALGIA (non-serious) with onset 22Jan2022 at 13:00, outcome "not recovered", described as "Nerve pain in right arm and left leg"; PYREXIA (non-serious) with onset 22Jan2022 at 13:00, outcome "not recovered", described as "High fever"; CHILLS (non-serious) with onset 22Jan2022 at 13:00, outcome "not recovered", described as "Chills". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of pain in extremity, lymphadenopathy, neuralgia, pyrexia and chills. 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 not been tested for COVID-19. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220122; Test Name: Body temperature; Result Unstructured Data: Test Result:High fever; Comments: at 13:00
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Blood pressure high (High blood pressure); Nickel sensitivity (Known allergies: Nickel); Proteinuria
- Andere Medikamente
- LISINOPRIL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 27.01.2022
- Impfdatum
- 17.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Immunisation
Pruritus
Rash
Urticaria
Symptomtext
Patient c/o itchy feet within 24 hours of receiving his booster.; He developed a rash; Hives all over his body; Dose number: 3; This is a spontaneous report from a contactable reporter (nurse). A 13-year-old male patient received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 17Jan2022 (Lot number: FD7218) at the age of 13 Years as dose 3 (booster), single for COVID-19 immunisation. The patient's relevant medical history was reported as none. It was unknown whether the patient had received any concomitant medications. Past drug history included: Amoxicillin, reaction: "Drug allergy", notes: known allergies: Amoxicillin. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE; Lot Number: Unknown; Route of Administration: Unspecified), administration date: 14May2021, when the patient was 12 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE; Lot Number: Unknown; Route of Administration: Unspecified), administration date: 04Jun2021, when the patient was 12 years old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 17Jan2022, outcome "unknown", described as "Dose number: 3"; PRURITUS (non-serious) with onset 18Jan2022, outcome "not recovered", described as "Patient c/o itchy feet within 24 hours of receiving his booster"; RASH (non-serious) with onset 18Jan2022, outcome "not recovered", described as "He developed a rash"; URTICARIA (non-serious) with onset 18Jan2022, outcome "not recovered", described as "Hives all over his body". The events "Patient c/o itchy feet within 24 hours of receiving his booster.", "He developed a rash" and "Hives all over his body" were evaluated at the physician office visit. Therapeutic measures were taken as a result of pruritus, rash and urticaria. Additional information: Prior to the 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. Since the vaccination, the patient had not been tested for COVID-19. Treatment included oral steroid and topical steroid for pruritus, urticaria and rash.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- F
- Eingang
- 27.01.2022
- Impfdatum
- 22.12.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Back pain
Fatigue
Feeling abnormal
Gait inability
Gait disturbance
Illness
Hyperhidrosis
Nausea
Night sweats
Nightmare
Pain
Screaming
Vomiting
Symptomtext
Cannot walk/ I cannot like stand up and walk; She has been having nightmares/ every time I sleep I have horror sick nightmares; This is making her very very sick; I just felt really bad like cloudiness in my head; Severe back pain, I can not like stand up and walk; Very Tired; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). A female patient received bnt162b2 (BNT162B2), administration date 22Dec2021 (Lot number: FD7218) as dose 2, single for covid-19 immunisation. Relevant medical history included: "COVID", start date: 2020 (unspecified if ongoing), notes: She already had COVID a year ago and she has the antibodies. The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose 01, she got sick for two days), administration date: Dec2021, for COVID-19 immunization, reaction(s): "she got sick"; Bnt162b2 (Dose 01), administration date: Dec2021, for COVID-19 immunization, reaction(s): "felt really bad like she had the flu", "felt really bad". The following information was reported: GAIT DISTURBANCE (non-serious) with onset Dec2021, outcome "unknown", described as "Cannot walk/ I cannot like stand up and walk"; NIGHTMARE (non-serious) with onset Dec2021, outcome "unknown", described as "She has been having nightmares/ every time I sleep I have horror sick nightmares"; ILLNESS (non-serious) with onset Dec2021, outcome "unknown", described as "This is making her very very sick"; FEELING ABNORMAL (non-serious) with onset Dec2021, outcome "unknown", described as "I just felt really bad like cloudiness in my head"; BACK PAIN (non-serious) with onset Dec2021, outcome "unknown", described as "Severe back pain, I can not like stand up and walk"; FATIGUE (non-serious) with onset Dec2021, outcome "unknown", described as "Very Tired". Additional Information: Reporter stated, the concern patient was his wife. She had one shot on couple weeks ago, she went back to work, she was out of work because of injured (Further clarification unknown) and she has to get a shot to get back in and she got a shot somewhere prior to 16Dec at withheld (Further clarification unknown). So, she made the appointment, she got the shot, she got sick for two days, felt really bad like she had the flu and sometimes it does suppose me give you that. She already had COVID a year ago and she has the antibodies but here is the problem. she went and got the second shot on Wednesday. she cannot walk, she has been having nightmares, this is making her very very sick and she is going to work tonight. Reporter also stated, she has shot on little prior to 16Dec as she went back to work think that may be within a week or it is on the card and then she had to get the second shot which was schedule on Wednesday which has past this past Wednesday and now she was not only sick she cannot walk. The patient reported that just felt really bad like cloudiness in head, severe back pain, cannot like stand up and walk and very tired every time she sleep have horror sick nightmares and do not what to do about side effects. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19 (She already had COVID a year ago and she has the antibodies.)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 26.01.2022
- Impfdatum
- 11.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Feeling abnormal
Headache
Herpes virus infection
Laryngitis
Lymphadenopathy
Pain
Pyrexia
Symptomtext
A headache started morning after shot. Then started chills and fever up to 102.5 and major aches about 2-3 in the afternoon. The lymph nodes in my armpits became swollen (prior to noticed fever) and the left side was so bad that I couldn't lay on that side of my body for a week. The fever, headache, and aches lasted about 24 hours. The headache was so bad that i struggled breathing and walking. After a week of swollen lymph nodes, i had a breakout of a dormant virus for a week herpes). After healing from this i got laryngitis with no other symptoms besides swollen lymph nodes. I believe that all these swollen nodes are from handling this booster shot and I've been miserable. I hope it stops.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None taken
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None, unless you count overweight
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 25.01.2022
- Impfdatum
- 27.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Headache
Joint stiffness
Pain
Pyrexia
SARS-CoV-2 test negative
Symptomtext
Initial reaction was similar to reaction of second dose: low fever, body aches, headache and exhaustion. New reaction: joint stiffness and pain. This lasted from 28 hours post-injection to 72 hours post-injection, but the joint stiffness, some body aches and exhaustion remained. Over the next three weeks, joint stiffness has mostly resolved, but exhaustion and some body aches remain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- SARS CoV-2 PCR test 01/16/2022, negative.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Major depression
- Andere Medikamente
- Loestrin, Zyrtec, Celexa 40mg
- Allergien
- Dust mite and pollen allergy
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 22.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
Immunisation
Insomnia
Interchange of vaccine products
Pain in extremity
Pyrexia
Restlessness
Vaccination site erythema
Vaccination site mass
Vaccination site pain
Vaccination site pruritus
Symptomtext
By Saturday, the red area was about 6-inches wide, itchy, and painful.; By Saturday, the red area was about 6-inches wide, itchy, and painful.; "I" also maintained a fever hovering around 100 all day; On Friday "I" noticed there was a red bump like a bee sting at the injection site. By Saturday, the red area was about 6- inches wide, itchy, and painful.; On Friday "I" noticed there was a red bump like a bee sting at the injection site. By Saturday, the red area was about 6-inches wide, itchy, and painful.; Nothing happened for about 12 hours, but then "my" arm started throbbing and "my" whole body became restless.; Nothing happened for about 12 hours, but then "my" arm started throbbing and "my" whole body becamerestless.; Primary immunisation: MODERNA; Booster: COMIRNATY; dose number=3; "I" was unable to sleep Thursday night.; This is a spontaneous report from a contactable reporter (consumer or other non-HCP). The reporter is the patient. A 49-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 13Jan2022 at 08:30 (Lot number: FD7218)at the age of 49 Year(s) as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "Breast cancer" start date: an unknown date in 2006 (unspecified if ongoing) and "Breast cancer" start date: an unknown date in 2012 (unspecified if ongoing). There were no concomitant medications. Vaccination history included: Moderna covid-19 vaccine (DOSE 1, SINGLE; Lot Number: unknown; Route of administration: unspecified), for COVID-19 immunisation, reaction(s): "No adverse reaction" and Moderna covid-19 vaccine (DOSE 2, SINGLE; Lot Number: unknown; Route of administration: unspecified), for COVID-19 immunisation, reaction(s): "No adverse reaction". The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (non-serious) with onset 13Jan2022 at 08:30, outcome "unknown", described as "Primary immunisation: MODERNA; Booster: COMIRNATY"; IMMUNISATION (non-serious) with onset 13Jan2022 at 08:30, outcome "unknown", described as "dose number=3"; PAIN IN EXTREMITY (non-serious) with onset 13Jan2022 at 20:30, outcome "not recovered", described as "Nothing happened for about 12 hours, but then "my" arm started throbbing and "my" whole body became restless"; RESTLESSNESS (non-serious) with onset 13Jan2022 at 20:30, outcome "not recovered", described as "Nothing happened for about 12 hours, but then "my" arm started throbbing and "my" whole body became restless"; INSOMNIA (non-serious) with onset 13Jan2022, outcome "not recovered", described as ""I" was unable to sleep Thursday night"; VACCINATION SITE ERYTHEMA (non-serious) with onset 14Jan2022, outcome "not recovered", described as "On Friday "I" noticed there was a red bump like a bee sting at the injection site. By Saturday, the red area was about 6- inches wide, itchy, and painful"; VACCINATION SITE MASS (non-serious) with onset 14Jan2022, outcome "not recovered", described as "On Friday "I" noticed there was a red bump like a bee sting at the injection site. By Saturday, the red area was about 6-inches wide, itchy, and painful"; VACCINATION SITE PRURITUS (non-serious), VACCINATION SITE PAIN (non-serious), PYREXIA (non-serious) all with onset 15Jan2022, outcome "not recovered", and all described as "By Saturday, the red area was about 6-inches wide, itchy, and painful". The events "Nothing happened for about 12 hours, but then "my" arm started throbbing and "my" whole body became restless.", "Nothing happened for about 12 hours, but then "my" arm started throbbing and "my" whole body became restless.", ""I" was unable to sleep Thursday night.", "On Friday "I" noticed there was a red bump like a bee sting at the injection site. By Saturday, the red area was about 6- inches wide, itchy, and painful.", "On Friday "I" noticed there was a red bump like a bee sting at the injection site. By Saturday, the red area was about 6-inches wide, itchy, and painful.", "By Saturday, the red area was about 6-inches wide, itchy, and painful." and ""I" also maintained a fever hovering around 100 all day" were evaluated at the physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of pain in extremity, vaccination site erythema, vaccination site mass, vaccination site pruritus, vaccination site pain and pyrexia. Additional Information: The patient reported that "I had my booster on Thursday, 1/13. My vaccinations were both Moderna, and I did not have any adverse reactions". The patient had no known allergies. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. The events pain in extremity, vaccination site erythema, vaccination site mass, vaccination site pruritus, vaccination site pain and pyrexia, the treatment included Aleve and patient was advised to add cold compresses, use calamine lotion. Since the vaccination, the patient had not been tested for COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220115; Test Name: Body temperature; Result Unstructured Data: Test Result:100; Comments: fever hovering around 100 all day
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Breast cancer
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 22.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Immunisation
Interchange of vaccine products
Nausea
Off label use
Pyrexia
Symptomtext
Primary immunisation: Janssen covid-19 vaccine; Booster: Pfizer covid-19 vaccine; Primary immunisation: Janssen covid-19 vaccine; Booster: Pfizer covid-19 vaccine; Primary immunisation: Janssen covid-19 vaccine; Booster: Pfizer covid-19 vaccine; Fever; Nausea; This is a spontaneous report received from a non-contactable reporter (Other healthcare professional). A 51-year-old female patient (unknown if pregnant) received bnt162b2 (BNT162B2), administration date 12Jan2022 (Lot number: FD7218) at the age of 51 years as dose 2 (booster), single for COVID-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Janssen covid-19 vaccine (johnson & johnson) (DOSE 1, SINGLE, Lot number: UNKNOWN, Route of administration: Unspecified), for COVID-19 immunisation. The following information was reported: OFF LABEL USE (non-serious), INTERCHANGE OF VACCINE PRODUCTS (non-serious), IMMUNISATION (non-serious) all with onset 12Jan2022, outcome "unknown", and all described as "Primary immunisation: Janssen covid-19 vaccine; Booster: Pfizer covid-19 vaccine"; PYREXIA (non-serious) with onset an unknown date in Jan2022, outcome "unknown", described as "Fever"; NAUSEA (non-serious) with onset an unknown date in Jan2022, outcome "unknown", described as "Nausea". No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 22.01.2022
- 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: nein
Immunisation
Nausea
Pyrexia
Symptomtext
Dose received: 3; Fever; Nausea; This is a spontaneous report from a non-contactable reporter (healthcare professional). A 53-year-old female patient (unknown if pregnant) received bnt162b2 (BNT162B2), administration date 12Jan2022 (Lot number: FD7218) at the age of 53 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: Covid-19 vaccine manufacture unknown (DOSE 1; MANUFACTURER UNKNOWN, Lot Number: UNKNOWN), for COVID-19 immunisation and Covid-19 vaccine manufacture unknown (DOSE 2; MANUFACTURER UNKNOWN, Lot Number: UNKNOWN), for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 12Jan2022, outcome "unknown", described as "Dose received: 3"; PYREXIA (non-serious) with onset an unknown date in Jan2022, outcome "unknown", described as "Fever"; NAUSEA (non-serious) with onset an unknown date in Jan2022, outcome "unknown", described as "Nausea". No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 22.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Nausea
Pyrexia
Symptomtext
fever; nausea; This is a spontaneous report from a non-contactable reporter (healthcare professional). A 51-year-old female patient (unknown if pregnant) received bnt162b2 (BNT162B2), administration date 12Jan2022 (Lot number: FD7218) at the age of 51 year(s) as dose 2, single for COVID-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (DOSE 1; MANUFACTURER UNKNOWN; Lot number: Unknown; Route of administration: Unspecified.), for COVID-19 immunisation. The following information was reported: PYREXIA (non-serious) with onset an unknown date in Jan2022, outcome "unknown", described as "fever"; NAUSEA (non-serious) with onset an unknown date in Jan2022, outcome "unknown", described as "nausea". No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- F
- Eingang
- 22.01.2022
- 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: nein
Immunisation
Nausea
Pyrexia
Symptomtext
Dose number 3; Fever; Nausea; This is a spontaneous report from a non-contactable reporter (other healthcare professional). A 55-year-old female patient (unknown if pregnant) received bnt162b2 (BNT162B2), administration date 12Jan2022 (Lot number: FD7218) as dose 3 (booster), single for COVID-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Covid 19 vaccine (DOSE 1, MANUFACTURER UNKNOWN, Lot Number: Unknown, Route of Administration: unspecified), for COVID-19 immunisation and Covid 19 vaccine (DOSE 2, MANUFACTURER UNKNOWN, Lot Number: Unknown, Route of Administration: unspecified), for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 12Jan2022, outcome "unknown", described as "Dose number: 3"; PYREXIA (non-serious) with onset an unknown date in Jan2022, outcome "unknown", described as "Fever"; NAUSEA (non-serious) with onset an unknown date in Jan2022, outcome "unknown", described as "Nausea". No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 22.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Nausea
Pyrexia
Symptomtext
Fever; Nausea; This is a spontaneous report from a non-contactable reporter (other healthcare professional). A 38-year-old female patient (unknown if pregnant) received bnt162b2 (BNT162B2), administration date 12Jan2022 (Lot number: FD7218) at the age of 38 years as dose 2, single for COVID-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Covid19 vaccine (DOSE 1, MANUFACTURER UNKNOWN, Lot Number: Unknown, Route of administration: Unspecified), for COVID-19 immunisation. The following information was reported: PYREXIA (non-serious) with onset an unknown date in Jan2022, outcome "unknown", described as "Fever"; NAUSEA (non-serious) with onset an unknown date in Jan2022, outcome "unknown", described as "Nausea". No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 22.01.2022
- 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: nein
Immunisation
Nausea
Pyrexia
Symptomtext
Dose received: 3; Fever; Nausea; This is a spontaneous report from a non-contactable reporter (other healthcare professional). A 24-year-old female patient (unknown if pregnant) received bnt162b2 (BNT162B2), administration date 12Jan2022 (Lot number: FD7218) at the age of 24 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: Covid-19 vaccine (DOSE 1; MANUFACTURER UNKNOWN; Lot number: unknown; Route of administration: unspecified), for COVID-19 immunisation and Covid-19 vaccine (DOSE 2; MANUFACTURER UNKNOWN; Lot number: unknown; Route of administration: unspecified), for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 12Jan2022, outcome "unknown", described as "Dose received: 3"; PYREXIA (non-serious) with onset an unknown date in Jan2022, outcome "unknown", described as "Fever"; NAUSEA (non-serious) with onset an unknown date in Jan2022, outcome "unknown", described as "Nausea". No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 22.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Nausea
Pyrexia
Symptomtext
Fever; Nausea; This is a spontaneous report from a non-contactable reporter (healthcare professional). A 26-year-old female patient (unknown if pregnant) received bnt162b2 (BNT162B2), administration date 12Jan2022 (Lot number: FD7218) at the age of 26 years as dose 2, single for COVID-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (DOSE 1, MANUFACTURER UNKNOWN, Lot Number: unknown, Route of administration: unspecified.), for COVID-19 immunisation. The following information was reported: PYREXIA (non-serious) with onset an unknown date in Jan2022, outcome "unknown", described as "Fever"; NAUSEA (non-serious) with onset an unknown date in Jan2022, outcome "unknown", described as "Nausea". No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 22.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Nausea
Pyrexia
Symptomtext
Fever; Nausea; This is a spontaneous report from a non-contactable reporter (other healthcare professional). A 51-year-old female patient (unknown if pregnant) received bnt162b2 (BNT162B2), administration date 12Jan2022 (Lot number: FD7218) at the age of 51 years 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: PYREXIA (non-serious) with onset an unknown date in Jan2022, outcome "unknown", described as "Fever"; NAUSEA (non-serious) with onset an unknown date in Jan2022, outcome "unknown", described as "Nausea". No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 22.01.2022
- 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: nein
Immunisation
Nausea
Pyrexia
Symptomtext
Dose number: 3; Fever; Nausea; This is a spontaneous report received from a non-contactable reporter (other healthcare professional). A 40-year-old female patient (unknown if pregnant) received bnt162b2 (BNT162B2), administration date 12Jan2022 (Lot number: FD7218) at the age of 40 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: Covid-19 vaccine (DOSE 1, MANUFACTURER UNKNOWN, Lot number: UNKNOWN, Route of administration: unspecified), for COVID-19 immunisation and Covid-19 vaccine (DOSE 2, MANUFCATURER UNKNOWN, Lot number: UNKNOWN, Route of administration: unspecified), for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 12Jan2022, outcome "unknown", described as "Dose number: 3"; PYREXIA (non-serious) with onset an unknown date in Jan2022, outcome "unknown", described as "Fever"; NAUSEA (non-serious) with onset an unknown date in Jan2022, outcome "unknown", described as "Nausea". No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 22.01.2022
- 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: nein
Immunisation
Nausea
Pyrexia
Symptomtext
Dose received: 3; Fever; Nausea; This is a spontaneous report from a non-contactable reporter (healthcare professional). A 45-year-old female patient (unknown if pregnant) received bnt162b2 (BNT162B2), administration date 12Jan2022 (Lot number: FD7218) at the age of 45 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: Covid-19 vaccine manufacture unknown (DOSE 1; MANUFACTURER UNKNOWN, Lot Number: UNKNOWN), for COVID-19 immunisation and Covid-19 vaccine manufacture unknown (DOSE 2; MANUFACTURER UNKNOWN, Lot Number: UNKNOWN), for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 12Jan2022, outcome "unknown", described as "Dose received: 3"; PYREXIA (non-serious) with onset an unknown date in Jan2022, outcome "unknown", described as "Fever"; NAUSEA (non-serious) with onset an unknown date in Jan2022, outcome "unknown", described as "Nausea". No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 22.01.2022
- Impfdatum
- 17.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Adnexa uteri pain
Angina pectoris
Cardiac discomfort
Immunisation
Menstruation delayed
Muscle tightness
Ultrasound scan
Symptomtext
Heart started to squeeze/I was awoken from my sleep with chest pains - it felt like a tight squeeze that radiated to the neck and right shoulder; Heart started to squeeze/I was awoken from my sleep with chest pains - it felt like a tight squeeze that radiated to the neck and right shoulder; Ovary pain on the left side; Delayed period by about 6 days; Heart started to squeeze/I was awoken from my sleep with chest pains - it felt like a tight squeeze that radiated to the neck and right shoulder; Dose 3; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 31 year-old female patient (not pregnant) received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), administered in arm left, administration date 17Dec2021 20:00 (Lot number: FD7218) at the age of 31 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Migraine" (unspecified if ongoing). Concomitant medication(s) included: ZINC; VIT C. The patient also concomitantly used vit b, prenatal, et (as reported). Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0221, Location of injection: Arm Left), administration date: 07Jun2021, when the patient was 31 years old, for COVID-19 immunization, reaction(s): "I also experienced ovary pain", "inconsistent cycle", "endometrioma", "I attributed that to stress and maybe a normal reaction to the vaccine"; Bnt162b2 (Dose Number: 1, Batch/Lot No: EY4825, Location of injection: Arm Left), administration date: 29Apr2021, when the patient was 31 years old, for COVID-19 immunization, reaction(s): "I also experienced ovary pain", "inconsistent cycle", "I attributed that to stress and maybe a normal reaction to the vaccine", "endometrioma". The following information was reported: ANGINA PECTORIS (medically significant), MUSCLE TIGHTNESS (medically significant) all with onset 20Dec2021 05:00, outcome "recovered" (Dec2021) and all described as "Heart started to squeeze/I was awoken from my sleep with chest pains - it felt like a tight squeeze that radiated to the neck and right shoulder"; IMMUNISATION (medically significant) with onset 17Dec2021 20:00, outcome "recovered", described as "Dose 3"; CARDIAC DISCOMFORT (medically significant) with onset 19Dec2021, outcome "recovered" (Dec2021), described as Heart started to squeeze/I was awoken from my sleep with chest pains - it felt like a tight squeeze that radiated to the neck and right shoulder"; ADNEXA UTERI PAIN (medically significant) with onset 19Dec2021, outcome "recovered" (Dec2021) described as "Ovary pain on the left side"; MENSTRUATION DELAYED (medically significant) with onset 19Dec2021, outcome "recovered" (Dec2021), described as "Delayed period by about 6 days". The patient underwent the following laboratory tests and procedures: ultrasound scan: (2021) discovered an endometrioma; (2021) endometrioma was no longer there. Therapeutic measures were not taken as a result of angina pectoris, immunisation, cardiac discomfort, muscle tightness, adnexa uteri pain, menstruation delayed. Clinical course: The patient reported that: "my heart started to squeeze a day and half after the 3rd shot (so throughout the 19). At 5am on 20Dec2021, I was awoken from my sleep with chest pains - it felt like a tight squeeze that radiated to the neck and right shoulder. After a few minutes, it released and I don't believe I experienced any further chest pains" and "ovary pain on the left side and a delayed period by about 6 days. After the first 2 shots, I also experienced ovary pain and an inconsistent cycle. I attributed that to stress and maybe a normal reaction to the vaccine at first, but after 2 or so months, the pain and inconsistent cycles persisted so my doctor gave me an ultrasound where they discovered an endometrioma. I took some supplements (serrapeptase, DIM, NAC) and did acupuncture and 3 months later, the follow up ultrasound showed that the endometrioma was no longer there. This was end of Oct2021. I didn't feel anymore discomfort and had a regular cycle in Nov and Dec until the booster." The patient reported the events as serious (reported as Serious: Yes). The patient did not received any other vaccines within 4 weeks prior to the COVID vaccine. The patient had no known allergies, not diagnosed with COVID-19 prior to vaccination and not been tested for COVID-19 since the vaccination. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202200030735 same patient, same vaccine but different doses with different AEs
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Adnexa uteri pain
- Hospital-Tage
- -
- Labordaten
- Test Date: 2021; Test Name: Ultrasound; Result Unstructured Data: Test Result:discovered an endometrioma; Test Date: 2021; Test Name: Ultrasound; Result Unstructured Data: Test Result:endometrioma was no longer there
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Migraine
- Andere Medikamente
- ZINC; VIT C
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 21.01.2022
- Impfdatum
- 19.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Diarrhoea
Dizziness
Nausea
Pyrexia
Symptomtext
dizzines, naseau, fever, diarrhea
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- lexipro,
- Allergien
- prednisone
- Vorherige Impfungen
- er8735 4/15/2021 Pfizer
- Staat
- MA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 21.01.2022
- Impfdatum
- 17.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dysgeusia
Exposure to SARS-CoV-2
Lymphadenopathy
Oropharyngeal pain
SARS-CoV-2 test negative
Throat irritation
Symptomtext
When I got my vaccine, I waited the 15 minutes before leaving, and as soon as I walked out the building I could taste this metal taste in my mouth. That symptom lasted for almost a month. I went about my day and I kind of noticed that as the day went on my throat was scratchy so I started taking Emergen-C because I thought I was getting a cold. I took a Covid home test because I thought I could be getting Covid, but it was negative. My glands were swollen and my throat was sore but I had no fever and it was lingering for a day or two and then it was fine and then it would just come back. I was exposed to Covid on New Years Eve and I took another covid test and it was negative. The sore throat subsided last week. This is the most reaction I've had with all three of my vaccines. I'm getting a physical in 2 weeks and she will see if my glands are still swollen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- Multiple Covid Home Tests
- Aktuelle Erkrankungen
- I just had a radiofrequency lesioning the day before shot which I had to be under local anesthesia.
- Vorgeschichte
- mild asthma, acid reflux, chronic neck issue (being treated for bulging disc in neck).
- Andere Medikamente
- water pill for blood pressure, Valtrex every day, Prilosec, potassium, magnesium, b12, folate, vitamin c, d3, zinc.
- Allergien
- Seasonal allergies
- Vorherige Impfungen
- Flu- 10 Years ago- Scratchy throat and swelling
- Staat
- IL
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 20.01.2022
- Impfdatum
- 19.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Immediate post-injection reaction
Nausea
Pallor
Symptomtext
Pt c/o light headedness and nausea almost immediately after the injection. Pallor noted. Pt moved from chair to floor mat, and legs elevated on chair. BP 102/60, HR 76, RR 18, Pulse oxygen 96. Color pinked up. Pt stated he felt better. Tolerated sitting up well. Recheck BP 96/60. After a couple minutes, tolerated standing without distress. Left with parent and sibling In good condition.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None known
- Vorgeschichte
- None
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 15.12.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Blood chloride decreased
Blood pressure measurement
Blood sodium decreased
Chest X-ray
Differential white blood cell count
Fatigue
Full blood count
Gait inability
Haemoglobin decreased
Interchange of vaccine products
Mean cell haemoglobin decreased
Metabolic function test
Nausea
Pain
Pyrexia
Sitting disability
Speech disorder
Vertigo
Symptomtext
Dose 1 Moderna within 15 minutes of dose: Vertigo, high blood pressure (>200/90), fatigue. subsequent 2 days, fever, nausea, body aches, fatigue. Treated at home with fluids and rest. Dose 2 Moderna within 15 minutes of dose: Vertigo, high blood pressure. Treated by paramedics at scene with fluids. Subsequent 3 days, fever nausea, body aches, fatigue. Recovered at home. Dose 3 Pfizer within 15 minutes of dose: Vertigo, high blood pressure, extreme fatigue, difficulty speaking. Could not sit up or walk. Treated at scene by paramedics and transported to ER. Given fluids and oxygen, released after 3 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- CBC-W differential: slightly low hemoglobin, slightly low MCHC Comp Metabolic Panel: slightly low sodium, slightly low chloride Chest X-ray: small convexity along left lung ape
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- -
- Andere Medikamente
- Daily: Duloxetine, 60 mg; valacyclovir 500 mg; Losartan 25 mg
- Allergien
- allergic to sulfa drugs
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 27.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Diarrhoea
Fatigue
Immunisation
Pain
Pyrexia
Symptomtext
Diarrhea; chills; low grade fever; body aches; fatigue; Dose number = 3; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 42 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 27Dec2021 11:45 (Lot number: FD7218) at the age of 42 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Eczema" (unspecified if ongoing); "Migraines" (unspecified if ongoing); "Known allergies: Sugar" (unspecified if ongoing); "Known allergies: wheat, corn" (unspecified if ongoing); "Known allergies: dairy" (unspecified if ongoing); "Known allergies: soy" (unspecified if ongoing). Concomitant medication(s) included: CALCIUM; SUMATRIPTAN. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0158, Location of injection: Arm Left), administration date: 12Apr2021, when the patient was 41 years old, for COVID-19 Immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EP7534, Location of injection: Arm Left), administration date: 22Mar2021, when the patient was 41 years old, for COVID-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 27Dec2021 11:45, outcome "unknown", described as "Dose number = 3"; DIARRHOEA (non-serious) with onset 27Dec2021 17:45, outcome "recovering", described as "Diarrhea"; CHILLS (non-serious) with onset 27Dec2021 17:45, outcome "recovering", described as "chills"; PYREXIA (non-serious) with onset 27Dec2021 17:45, outcome "recovering", described as "low grade fever"; PAIN (non-serious) with onset 27Dec2021 17:45, outcome "recovering", described as "body aches"; FATIGUE (non-serious) with onset 27Dec2021 17:45, outcome "recovering", described as "fatigue". Therapeutic measures were not taken as a result of diarrhoea, chills, pyrexia, pain, fatigue. Additional Information : Prior to vaccination and since the vaccination the patient had not diagnosed with COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient received multivitamin within 2 weeks of vaccination. Facility where the most recent COVID-19 vaccine was administered: Pharmacy or Drug Store. 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: Allergy; Allergy to grains; Dairy intolerance; Eczema; Food allergy; Migraine
- Andere Medikamente
- CALCIUM; SUMATRIPTAN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 20.01.2022
- Impfdatum
- 27.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ear pain
Immunisation
Tinnitus
Symptomtext
I have a terrible ringing in my ear and a bad pain in my ear; I have a terrible ringing in my ear and a bad pain in my ear; booster; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 23 year-old male patient received bnt162b2 (BNT162B2), administration date 27Dec2021 (Lot number: FD7218) at the age of 23 years as dose number unknown (booster), single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Covid-19 vaccine (Manufacturer: Unknown), for COVID-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 27Dec2021, outcome "unknown", described as "booster"; EAR PAIN (non-serious), TINNITUS (non-serious) all with onset 28Dec2021, outcome "unknown" and all described as "I have a terrible ringing in my ear and a bad pain in my ear". Therapeutic measures were taken as a result of ear pain, tinnitus. Additional information: Consumer stated, "he like to report an adverse side effect from, have the question about it, he got booster shot yesterday and now he had a terrible ringing in his ear and a bad pain in his ear and he didn't know that was the common, he couldn't find anything online about that being a side effect so he wanted to see if that side effect was reported before or it was anything known about that." Consumer stated that he wanted to know if that's a common side effect, if not he would like to report it.The patient took Ibuprofen, like over a counter pain medication. Consumer didn't see the expiration date on vaccine card. Consumer stated he had no underline conditions and I take no medications." Further probing was not done. Hence, limited information was available over the call. Patient had no family history. Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ear pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Patient History: No
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 20.01.2022
- Impfdatum
- 29.12.2021
- Beginn
- 02.01.2022
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Back pain
Blood creatine phosphokinase
Blood lactate dehydrogenase
Fatigue
Full blood count
Glomerular filtration rate
Injection site pain
Laboratory test
Metabolic function test
Muscular weakness
Musculoskeletal pain
Pain
Pain in extremity
Red blood cell sedimentation rate normal
Sleep disorder
Symptomtext
Day of injection-Mild soreness in left arm Day 2-Moderate-Severe pain at site of injection that continued for 5 plus days Day 5- Leg weakness/fatigue to present day ( fatigued, deep aching pain like to the bone, pain in multiple locations including front and back of thighs in each leg, pain in calves, sharp stabbing, shooting, and pinching pains in legs. Legs hurt all day even affecting sleep, hurts if sitting or walking but walking/ exercising appears to fatigue them exponentially. Severe pain in upper middle part of back behind heart past 2 weeks. Also having bilateral shoulder pain and arm fatigue bilaterally as well. Hip/Buttock pain since day 5.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- CMP, CBC, ADOLASE, ESR, LDH, GFR, CK-ALL WITHIN NORMAL RANGE. Scheduled to see a rheumatologist.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- GERD,anxiety,umbilical hernia
- Andere Medikamente
- Prevacid, vit d3, Vitamin C, magnesium
- Allergien
- peanuts, codeine, phenergan
- Vorherige Impfungen
- Similar incident in 2002 after Flu shot vaccine-This adverse reaction is worse
- Staat
- IL
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 20.01.2022
- Impfdatum
- 27.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Cough
Dizziness
Illness
Immunisation
Confusional state
Epistaxis
Headache
Nasal congestion
Oropharyngeal pain
Pain
Pyrexia
Respiratory tract congestion
Symptomtext
booster; booster: fever; booster: hurting all over; booster: chills; booster: nose stopped up; booster: sore throat; booster: coughing up brown mucus; booster: head became light (dizzy); sick; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 66 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 27Dec2021 (Lot number: FD7218) at the age of 66 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "COVID-19", start date: 27Mar2020, stop date: 20Apr2020. The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose 1, Lot number: EL3249), administration date: 15Feb2021, when the patient was 65 years old, for COVID-19 Immunization, reaction(s): "felt like they had stuck Covid in him", "head pain", "pain all over body", "diarrhea", "nose stopped up", "nose running", "sore throat", "sick"; Bnt162b2 (Dose 2, Lot number: EM9809), administration date: 08Mar2021, when the patient was 65 years old, for COVID-19 Immunization, reaction(s): "real bad headache", "fever", "chills", "real bad body aches". The following information was reported: IMMUNISATION (non-serious) with onset 27Dec2021, outcome "unknown", described as "booster"; PYREXIA (non-serious) with onset 27Dec2021, outcome "not recovered", described as "booster: fever"; PAIN (non-serious) with onset 27Dec2021, outcome "not recovered", described as "booster: hurting all over"; CHILLS (non-serious) with onset 27Dec2021, outcome "not recovered", described as "booster: chills"; NASAL CONGESTION (non-serious) with onset 27Dec2021, outcome "not recovered", described as "booster: nose stopped up"; OROPHARYNGEAL PAIN (non-serious) with onset 27Dec2021, outcome "not recovered", described as "booster: sore throat"; COUGH (non-serious) with onset 27Dec2021, outcome "not recovered", described as "booster: coughing up brown mucus"; DIZZINESS (non-serious) with onset 27Dec2021, outcome "not recovered", described as "booster: head became light (dizzy)"; ILLNESS (non-serious) with onset 27Dec2021, outcome "unknown", described as "sick". Additional information: Stated that he had the first shot on 15Feb and it felt like they had Covid stuck in him and went back to hospital on 16Feb and they started pumping antibiotics in him to reduce his symptoms and head pain. Stated that he had pain diarrhea, sore throat, nose stopped up and running. Stated that he had the second shot and it lasted 2.5-3 days. Stated that he had real bad headache, chills, fever and real bad body aches. Clarified that he had been in the hospital for Covid prior to the first dose. Wanted to know how get through this (pain). Stated that he has watch service on Friday. Stated that it took 4 days to recover, and he got back to his old self. Stated that he recovered in 6-7 days from his head pain completely. Later clarified that he was not admitted to the hospital but in the emergency room on 16 Feb for 6 hours. Stated that he received antibiotics. Stated that he recovered from that pain all over his body from the first dose 5 days later completely. Stated that he recovered completely from diarrhea from first dose in 3-4 days. Stated that he recovered completely from nose stopped up from first dose in four days. Stated that his nose running from the first dose took about four days to recover completely. Stated that he recovered completely from real bad headache from the second dose in about three days. Stated that the fever from the second dose lasted for about two days and he recovered completely. Stated that he took Aleve for the fever. Stated that it took about two days to recover completely from chills from second dose. Stated that he recovered completely from real bad body aches on third day. 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: COVID-19
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 20.01.2022
- Impfdatum
- 27.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Cough
Dizziness
Illness
Immunisation
Confusional state
Epistaxis
Headache
Nasal congestion
Oropharyngeal pain
Pain
Pyrexia
Respiratory tract congestion
Symptomtext
booster; booster: fever; booster: hurting all over; booster: chills; booster: nose stopped up; booster: sore throat; booster: coughing up brown mucus; booster: head became light (dizzy); sick; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 66 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 27Dec2021 (Lot number: FD7218) at the age of 66 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "COVID-19", start date: 27Mar2020, stop date: 20Apr2020. The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose 1, Lot number: EL3249), administration date: 15Feb2021, when the patient was 65 years old, for COVID-19 Immunization, reaction(s): "felt like they had stuck Covid in him", "head pain", "pain all over body", "diarrhea", "nose stopped up", "nose running", "sore throat", "sick"; Bnt162b2 (Dose 2, Lot number: EM9809), administration date: 08Mar2021, when the patient was 65 years old, for COVID-19 Immunization, reaction(s): "real bad headache", "fever", "chills", "real bad body aches". The following information was reported: IMMUNISATION (non-serious) with onset 27Dec2021, outcome "unknown", described as "booster"; PYREXIA (non-serious) with onset 27Dec2021, outcome "not recovered", described as "booster: fever"; PAIN (non-serious) with onset 27Dec2021, outcome "not recovered", described as "booster: hurting all over"; CHILLS (non-serious) with onset 27Dec2021, outcome "not recovered", described as "booster: chills"; NASAL CONGESTION (non-serious) with onset 27Dec2021, outcome "not recovered", described as "booster: nose stopped up"; OROPHARYNGEAL PAIN (non-serious) with onset 27Dec2021, outcome "not recovered", described as "booster: sore throat"; COUGH (non-serious) with onset 27Dec2021, outcome "not recovered", described as "booster: coughing up brown mucus"; DIZZINESS (non-serious) with onset 27Dec2021, outcome "not recovered", described as "booster: head became light (dizzy)"; ILLNESS (non-serious) with onset 27Dec2021, outcome "unknown", described as "sick". Additional information: Stated that he had the first shot on 15Feb and it felt like they had Covid stuck in him and went back to hospital on 16Feb and they started pumping antibiotics in him to reduce his symptoms and head pain. Stated that he had pain diarrhea, sore throat, nose stopped up and running. Stated that he had the second shot and it lasted 2.5-3 days. Stated that he had real bad headache, chills, fever and real bad body aches. Clarified that he had been in the hospital for Covid prior to the first dose. Wanted to know how get through this (pain). Stated that he has watch service on Friday. Stated that it took 4 days to recover, and he got back to his old self. Stated that he recovered in 6-7 days from his head pain completely. Later clarified that he was not admitted to the hospital but in the emergency room on 16 Feb for 6 hours. Stated that he received antibiotics. Stated that he recovered from that pain all over his body from the first dose 5 days later completely. Stated that he recovered completely from diarrhea from first dose in 3-4 days. Stated that he recovered completely from nose stopped up from first dose in four days. Stated that his nose running from the first dose took about four days to recover completely. Stated that he recovered completely from real bad headache from the second dose in about three days. Stated that the fever from the second dose lasted for about two days and he recovered completely. Stated that he took Aleve for the fever. Stated that it took about two days to recover completely from chills from second dose. Stated that he recovered completely from real bad body aches on third day. 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: COVID-19
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 21.12.2021
- Beginn
- 18.01.2022
- Tage bis Beginn
- 28,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain
Arthralgia
Blood thyroid stimulating hormone
Constipation
Diarrhoea
Fatigue
Feeling cold
Full blood count
Metabolic function test
Nausea
Pain
Pain in extremity
Pyrexia
Symptomtext
<12 hours after receiving the vaccine patient experienced nausea, chills fever to 101., fatigue 1 week after the vaccine started having abdominal pain, alternating constipation and diarrhea. She persists in having a sore shoulder radiating down her left arm from 12/21-1/18
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- 1/18/2022 TSH, cBC, CMP ordered
- Aktuelle Erkrankungen
- No known illnesses prior
- Vorgeschichte
- legally blind, asthma, HSV-2 +, Grave's disease
- Andere Medikamente
- estradiol 10mcg tabs, fluticasone 50mcg nasal spray, levothyroxine 100mcg daily, montelukast 10mg tab, valtrex 500mg tab
- Allergien
- flagyl caused nausea, vomiting, palpitations. Naproxen causes nausea, vomiting
- Vorherige Impfungen
- at age 59 when she recieved first covid-19 pfizer vaccine 2/2021, patient had very similar symptoms to those experienced after h
- Staat
- NY
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 19.12.2021
- Beginn
- 25.12.2021
- Tage bis Beginn
- 6,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pruritus
Urticaria
Symptomtext
Received my second dose of Pfizer vaccine on 4/5/21. Six days after injection I developed a small patch of hives on my neck. They lasted for approximately two weeks then cleared up. Received my Pfizer booster on 12/19/21. On 12/25/21 I woke up with hives behind my knees, in my groin area, and a large patch on the left side of my stomach. Hives also appeared on my wrists and in front of my elbows. Antihistamines did not help. Finally went to the doctor on 1/7/22 and was given a cortisone shot and took a 7 day course of prednisone. As of today hives have cleared up and itching has stopped.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- Had no medical or lab tests at this time.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension and high cholesterol Osteoarthritis in hands
- Andere Medikamente
- Amlodipine-Benaz 5/10 mg daily Atorvastatin 10 mg daily
- Allergien
- Penicillin and Ceclor
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
Burning sensation
Fatigue
Immunisation
Pain
Pyrexia
SARS-CoV-2 test
Vulval ulceration
Symptomtext
This is a spontaneous report from a contactable reporter (consumer or other non-HCP). The reporter is the patient.A 12-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 07Jan2022 at 15:15 (Lot number: FD7218) at the age of 12 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "None", notes: Other medical history: none; Known allergies: no. There were no concomitant medications. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE; Lot number: EW0185; Administration time: 16:15; Anatomical site: left arm; Route of administration: unspecified), administration date: 13May2021, when the patient was 12 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE; Lot number: EW0191; Administration time: 16:00; Anatomical site: left arm; Route of administration: unspecified), administration date: 03Jun2021, when the patient was 12 years old, for COVID-19 immunisation.The following information was reported: IMMUNISATION (non-serious) with onset 07Jan2022 at 15:15, outcome "unknown", described as "Dose received: 3"; PYREXIA (non-serious) with onset 08Jan2022 at 04:15, outcome "recovered" (09Jan2022 at 04:15), described as "Fever (101.5)"; FATIGUE (non-serious) with onset 08Jan2022 at 04:15, outcome "recovered" (09Jan2022 at 04:15), described as "Fatigue"; VULVAL ULCERATION (non-serious) with onset 09Jan2022 at 20:00, outcome "recovering", described as "48 hours post vaccination, developed painful vulvar ulcer"; BURNING SENSATION (non-serious), PAIN (non-serious) all with onset 09Jan2022 at 20:00, outcome "recovering", and all described as "Burning/stinging sensation". The events "Fever (101.5)", "Fatigue", "48 hours post vaccination, developed painful vulvar ulcer" and "Burning/stinging sensation" were evaluated at the physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of vulval ulceration, burning sensation and pain.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 patient was not sexually active. Treatment included topical ointment (Lidocaine and Triamcinolone acet) for vulval ulceration, burning sensation and pain. Since the vaccination, the patient had been tested for COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220108; Test Name: Body temperature; Result Unstructured Data: Test Result:101.5; Comments: at 04:15; Test Date: 20220113; Test Name: Bionax; Test Result: Negative; Comments: Nasal Swab.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History:Patient Other Relevant History 1: None, Comment: Other medical history: none; Known allergies: no.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- 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: nein
Immunisation
Nausea
Pyrexia
Symptomtext
Dose number: 3; Fever; Nausea; This is a spontaneous report received from a non-contactable reporter (Pharmacist). A 46-year-old female patient (unknown if pregnant) received bnt162b2 (BNT162B2), administration date 12Jan2022 (Lot number: FD7218) at the age of 46 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: Covid19 vaccine (DOSE 1, MANUFACTURER UNKNOWN, Lot Number: UNKNOWN, Route of administration: Unspecified), for COVID-19 immunisation and Covid19 vaccine (DOSE 2, MANUFACTURER UNKNOWN, Lot Number: UNKNOWN, Route of administration: Unspecified), for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 12Jan2022, outcome "unknown", described as "Dose number: 3"; PYREXIA (non-serious) with onset an unknown date in Jan2022, outcome "unknown", described as "Fever"; NAUSEA (non-serious) with onset an unknown date in Jan2022, outcome "unknown", described as "Nausea". No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 17.01.2022
- Impfdatum
- 02.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Pruritus
Urticaria
Symptomtext
Pt developed generalized urticaria 1 day after vaccination. pt has had intermittent urticaria and generalized pruritis intermittently since onset 1/3/22. OTC medication recommended to manage pruritis after clinic visit 1/17/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 15.01.2022
- Impfdatum
- 09.12.2021
- Beginn
- 10.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Hypoaesthesia
Muscle fatigue
Symptomtext
Right arm fatigue & numbness since booster shot. Right leg fatigue & numbness since booster shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Muscle fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Cleft palate, anemia
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 13.01.2022
- Impfdatum
- 11.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Urticaria
Symptomtext
Urticarial rash covering the trunk, thighs, and arms beginning about 48 hours after injection worsened with time. Some resolution with benedryl.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Amethyst
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- Impfdatum
- 04.01.2022
- Beginn
- 04.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Symptomtext
Rash underarms, advised to take Benadryl and Advil.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- Recommended Allergy Test
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Thyroid; Asthma
- Andere Medikamente
- Levothyroxine; Albuterol
- Allergien
- Seasonal Allergies; Shellfish
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 11,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Headache
Incorrect dose administered
Loss of personal independence in daily activities
Rash
Symptomtext
Child was given Pfizer for 12yrs +, 30mcg, instead of Pfizer for 5-11 year olds (10mcg) . Parents notified. Mother reports child had a headache and a light rash to torso which has resolved. Did not seek medical attention, did miss school.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 09.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Breast swelling
Lymphadenopathy
Pyrexia
Symptomtext
Severe lymphatic swelling under arm and breast tissue swelling on the same side with fever
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Focal seizures
- Andere Medikamente
- Vimpat Progesterone Estrogen Singular Zoloft Ursodiol Protonix
- Allergien
- Plaquenil Aspirin Erythromycin Penicillin
- Vorherige Impfungen
- 52
- Staat
- SC
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- Impfdatum
- 07.12.2021
- Beginn
- 09.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Pruritus
Urticaria
Symptomtext
Hives(welts) on both legs appeared after the first and second covid shot. Hives were a dime size to pea size around, red and raised. Itched but not out of control itching. First time lasted 2 days. After the second shot they lasted 4 days. Controlled with Benadryl and Epstein salt baths.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Melatonin 3mg
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 09.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Lymph node pain
Lymphadenopathy
Symptomtext
Tender and swollen lymph node under left armpit.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymph node pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Amphetamine Salts
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Fatigue
Feeling abnormal
Headache
Nausea
Pain
Pain in extremity
Symptomtext
I have a previous VAERS Report. VAERS ID: 1939748/ E-Report Number: 741016. My right arm began throbbing around 7:00 p.m. Thurs., Jan. 6, and I began feeling queasy. I went to bed and woke up around 1:00 a.m. with a headache, shivering, rigors, nausea, body aches, that just increased as the night wore on. I wasn't able to sleep again until the early morning of Sat., Jan. 8. I slept 4 or 5 hours and awoke to more of the same. I felt better yesterday, Sunday, Jan. 9, and was able to sleep through the night. I'm very tired now. I didn't get the ice-pick headache, but I still had a bad headache. I have a dull headache today, Mon., Jan 10. This time, I made sure to drink a lot of water and take Motrin, but the same thing happened as with shot #2. I guess I'm hypersensitive to the shot, but it was hell. I don't usually moan when I'm sick, but I was moaning out loud with shots #2 & 3. If it had just been a very sore arm, I could have cared less, but it was all the other symptoms and the sore arm that made me report my incident to VAERS. Thank you.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- I used to struggle with asthma, but no longer, except when I exercise. I don't use an inhaler when I go for walks, but I do if I'm doing aerobics.
- Andere Medikamente
- 75 mg / daily / Venlafaxine capsule
- Allergien
- Bactrim gives me extreme headaches. Cipro makes me extremely nauseous and tired. Allergies to dust, dander, pollen, and perfume. Allergic to strawberries and cherries, but not enough to stop eating them.
- Vorherige Impfungen
- Covid Shot #2, Pfizer, Lot# ER8735, April 29, 2021, Same medical group.
- Staat
- IA
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 09.01.2022
- Impfdatum
- 12.12.2021
- Beginn
- 14.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood test normal
Impaired work ability
Pain
Skin lesion
Wound
Symptomtext
developed painful lesion 2 days after receiving her third vaccine. Similarly, she developed multiple vaginal sores after her second dose. Symptoms began with general soreness of the area that developed into open wounds which were very painful. was unable to work or attend school for 7 days due to the pain. Steroids eventually contributed to healing of the area and reduction of the pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- has never been sexually active. However, to be safe and thorough, STDs and Herpes were ruled out by her physician. Blood work was conducted to rule out other infections or illnesses.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Pimtrea Miralax Multivitamin Probiotic
- Allergien
- None
- Vorherige Impfungen
- Similar adverse event 2 days after second dose at 17 years of age
- Staat
- PA
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 09.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ageusia
Chills
Dizziness
Headache
Nausea
Pain
Pyrexia
Symptomtext
Nausea, body aches, fever, lightheadedness, loss of taste, headache and chills. Chills started about 16 hrs after shot. Rest of the symptoms happened about 24 hrs later from initial injection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- HBP, menopause, arthritis
- Andere Medikamente
- Multi vitamin, collagen, Norvavc
- Allergien
- None
- Vorherige Impfungen
- Flu-like symptoms, 55, 4/20/21, 2nd COVID shot/PFIZER - EM9809. Symptoms not as bad as severe as booster shot.
- Staat
- IL
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 08.01.2022
- Impfdatum
- 08.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Nausea
Tinnitus
Vision blurred
Visual impairment
Symptomtext
Patient received pfizer booster left arm after administering patient was been observed began to feel dizzy, blurry and white vision, nausea, Ringing of right ear. Patient was lowered to the ground patient received crackers, water. Patient states this has happened before when getting blood drawn and denies eating or drinking anything prior to vaccination. Patient and guardian denied when offered emt services. Patient was sitting back up in chair with in 5 mins of vaccination. Patient and guardian states they will call HCP if needed for additional are.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- None
- Andere Medikamente
- N/a
- Allergien
- N/a
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 08.01.2022
- Impfdatum
- 29.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Body temperature
Chills
Headache
Immunisation
Pyrexia
Symptomtext
Slight headache; Chills; 101.6 degree fever; Dose number 3; This is a spontaneous report from a non-contactable reporter (consumer or other non-HCP). The reporter is the patient. A 59-year-old male patient received bnt162b2 (BNT162B2), administered in right arm, administration date 29Dec2021 at 12:30 (Lot number: FD7218) at the age of 59 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "None", notes: Other medical history: None; Known allergies: No. There were no concomitant medications. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE; Lot Number: EP7534; Administration location: Right arm), administration date: 01Apr2021, when the patient was 58 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE; Lot Number: ER8734; Administration location: Right arm), administration date: 22Apr2021, when the patient was 58 years old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 29Dec2021 at 12:30, outcome "unknown", described as "Dose number 3"; HEADACHE (non-serious) with onset 30Dec2021 at 00:15, outcome "recovered" (30Dec2021 at 08:15), described as "Slight headache"; CHILLS (non-serious) with onset 30Dec2021 at 00:15, outcome "recovered" (an unknown date in Dec2021), described as "Chills"; PYREXIA (non-serious) with onset 30Dec2021 at 00:15, outcome "recovered" (an unknown date in Dec2021), described as "101.6 degree fever". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of headache, chills and pyrexia. 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 vaccine. Commencing approximately 12 hours after receiving dose began having chills and slight headache and then within an hour had a 101.6-degree fever, the fever and chills lasted several hours and started to wane. The headache lasted 8 hours. Since the vaccination, the patient had not been tested for COVID-19. The events did not result in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Test Date: 20211230; Test Name: Body temperature; Result Unstructured Data: Test Result:101.6 degree
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other medical history: None; Known allergies: No
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 08.01.2022
- Impfdatum
- 19.12.2021
- Beginn
- 19.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Breast pain
Breast tenderness
Immunisation
Interchange of vaccine products
Myalgia
Symptomtext
Both Breast sore and tender; Both Breast sore and tender; Pfizer Booster; Pfizer Booster/initial COVID vaccine was J&J; muscle was sore in the arm she got injection in; 202101844781 -This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 67 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 19Dec2021 14:00 (Lot number: FD7218) at the age of 67 years as dose number unknown (booster), single for covid-19 immunisation. Relevant medical history included: "Lumpectomy", start date: 2021 (unspecified if ongoing), notes: Lumpectomy was a month after the J&J COVID vaccine and the radiation was completed Jul2021. There were no concomitant medications. Vaccination history included: J&j vaccine (initial COVID vaccine was J&J., Batch/lot number: 206A21A, Unknown Dose. Injected in the left upper arm in the muscle.), administration date: 12Apr2021, when the patient was 66 years old, for Prevention, reaction(s): "muscle soreness in left arm". The following information was reported: IMMUNISATION (non-serious) with onset 19Dec2021 14:00, outcome "unknown", described as "Pfizer Booster"; INTERCHANGE OF VACCINE PRODUCTS (non-serious) with onset 19Dec2021 14:00, outcome "unknown", described as "Pfizer Booster/initial COVID vaccine was J&J"; BREAST PAIN (non-serious), BREAST TENDERNESS (non-serious) all with onset 20Dec2021, outcome "recovering" and all described as "Both Breast sore and tender"; MYALGIA (non-serious) with onset 19Dec2021, outcome "recovering", described as "muscle was sore in the arm she got injection in". Additional information: She said both breast were sore and tender, but the one that she had the lumpectomy and radiation in this past spring/summer was more sore. That was prior to getting the Pfizer vaccine. Her initial COVID vaccine was J&J. The surgery and radiation was a couple of months after the J&J vaccine. She had Pfizer COVID booster shot on Sunday, 19Dec2021, so Monday, 20Dec2021, is when the breast tenderness and soreness began. On Monday and Tuesday, it was quite uncomfortable, but today is still tender when she took shower, but a little improved. Her muscle was sore in the arm she got injection in, but she thought everyone got that. Muscle soreness has improved at injection site, but it is still a little sore. She wants to be fully protected. They put a prescription number of withheld, on the J&J card. It says RX number. She then found the lot number. The only reaction was muscle soreness to left arm after that one. She is not on any other medications. The Lumpectomy was a month after the J&J COVID vaccine and the radiation was completed Jul2021. Both breast sore and tender morning and Left arm muscle soreness at injection site right after driving home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Breast pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Lumpectomy (Lumpectomy was a month after the J&J COVID vaccine and the radiation was completed Jul2021)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 08.01.2022
- Impfdatum
- 19.12.2021
- Beginn
- 19.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Immunisation
Peripheral swelling
Vaccination site pain
Symptomtext
Booster; Pain and swelling in armpit.; Pain and swelling in armpit; Injection site pain; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). A 19 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 19Dec2021 (Lot number: FD7218) at the age of 19 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose Number: 2, brand=Pfizer , Batch/Lot No: EW0167, Location of injection: Arm Left, Route of Administration: Intramuscular), administration date: 03May2021, when the patient was 18 years old, for Covid-19 immunization; Bnt162b2 (Dose Number: 1, brand=Pfizer, Batch/Lot No: EW0153, Location of injection: Arm Left, Route of Administration: Intramuscular), administration date: 06Apr2021, when the patient was 18 years old, for Covid-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 19Dec2021, outcome "unknown", described as "Booster"; AXILLARY PAIN (non-serious) with onset 19Dec2021, outcome "recovering", described as "Pain and swelling in armpit."; PERIPHERAL SWELLING (non-serious) with onset 19Dec2021, outcome "recovering", described as "Pain and swelling in armpit"; VACCINATION SITE PAIN (non-serious) with onset 19Dec2021, outcome "recovering", described as "Injection site pain". Therapeutic measures were not taken as a result of axillary pain, peripheral swelling, vaccination site pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: other medical history: None
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 08.01.2022
- Impfdatum
- 18.12.2021
- Beginn
- 18.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Breast injury
Fall
Immunisation
Malaise
Peripheral swelling
Symptomtext
breast hurts a little; left arm swollen; Booster; fell; doesn't feel that good; The initial case was missing the following minimum criteria: Other-Info not qualifying for AE reporting. Upon receipt of follow-up information on (20Dec2021), this case now contains all required information to be considered valid. This is a spontaneous report received from a contactable consumer from medical information team. The reporter is the patient. A 71-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), administered in arm left, administration date 18Dec2021 11:30 (Lot number: FD7218) at the age of 71 years as DOSE 3 (BOOSTER), SINGLE for COVID-19 immunisation. Relevant medical history included: "High blood pressure" (ongoing), notes: had it for a long time, took medication and is ok, has been under control for years; "thyroid" (ongoing), notes: had this condition for over 20 years, took medication; "Little overweight" (ongoing). There were no concomitant medications. : Hasn't taken any new mediations in a long time. Vaccination history included: BNT162B2 (dose 1), administration date: 2020, for COVID-19 immunization, reaction(s): "didn't feel any reaction"; BNT162B2 (dose 2), administration date: 2020, for COVID-19 immunization, reaction(s): "didn't feel any reaction". The following information was reported: IMMUNISATION (medically significant) with onset 18Dec2021 11:30, outcome "unknown", described as "Booster"; FALL (medically significant) with onset 18Dec2021, outcome "unknown", described as "fell"; BREAST INJURY (medically significant), outcome "unknown", described as "breast hurts a little"; PERIPHERAL SWELLING (medically significant), outcome "unknown", described as "left arm swollen"; MALAISE (non-serious) with onset 18Dec2021, outcome "unknown", described as "doesn't feel that good". The patient stated that she thought she got the booster dose, however, when looking at the papers, it says to come back for a second shot, she didn't think there was a second shot for the booster. She was already given the two vaccines last year, already had the first two doses of the COVID-19 Vaccine. She went to the pharmacy at the grocery store, asked for the booster and was given a shot she already had, received it on 18Dec2021. She fell Saturday, 18Dec2021, evening when she went home and was going up the stairs, fell, hit her knee, and the breast, and shoulder, was in bed all day Saturday night and Sunday. Her left arm was now swollen, and her breast hurt a little. Had not gone to the doctor. Her left arm was swollen after the fall. She got the Pfizer COVID-19 Vaccine, came home, fell, hit her left arm, and right knee. She didn't feel that good from Saturday. Couldn't believe it. She took two of the COVID-19 Vaccines last year and didn't feel any reaction. She was given this extra dose. She asked for the booster and was given the wrong one. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Blood pressure high (had it for a long time, took medication and is ok, has been under control for years); Overweight; Thyroid disorder (had this condition for over 20 years, took medication)
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 08.01.2022
- Impfdatum
- 19.12.2021
- Beginn
- 12.04.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Breast mass
Breast pain
Breast tenderness
Injection site pain
Myalgia
Symptomtext
BREAST LUMP; BOTH BREASTS TENDER; BOTH BREASTS SORE; LEFT ARM MUSCLE SORENESS AT INJECTION SITE; MUSCLE SORENESS IN LEFT ARM; This spontaneous report received from a patient concerned a 66 year old female. The patient's weight was 55.79 kilograms, and height was 155 centimeters. The patient was not ill at the time of vaccination. The patient did not have any vaccination within four weeks prior to the first administration date of the suspect vaccine. The patient was not on any other medications. The patient received covid-19 vaccine ad26.cov2.s (Janssen, Dose number in series 1) (suspension for injection, intramuscular, batch number: 206A21A, and expiry: UNKNOWN) dose was not reported, 1 total, administered on 12-APR-2021 on left upper arm in the muscle for prophylactic vaccination. No concomitant medications were reported. In the afternoon of 12-APR-2021, the patient experienced muscle soreness in left arm. On an unspecified date, patient experienced a breast lump. In MAY-2021 (a month after the J and J COVID vaccine), the patient had the lumpectomy. On an unspecified date in 2021 (last spring/summer), the patient had radiation therapy which completed in JUL-2021 (Dose number in series 1). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from breast lump and recovering from muscle soreness in left arm. On 19-DEC-2021 14:00, the patient received additional non-company suspect vaccine bnt 162 (Dose number in series 2) (form of admin not reported, intramuscular, batch number: FD7218) dose was not reported, administered on left upper arm in the muscle for prophylactic vaccination. On 19-DEC-2021, right after driving home, the patient experienced muscle was sore in the arm she got injection in. Muscle soreness has improved at injection site, but it was still a little sore (left arm muscle soreness at injection site). On the morning of 20-DEC-2021, the patient experienced an unusual side effect described as, breasts got sore like a PMS (Premenstrual syndrome symptom) even though she had been through menopause for quite some time. She said both breasts were sore and tender, but the one that she had the lumpectomy and radiation in this past spring/summer was more sore. The patient also had breast tenderness. On 20-DEC-2021 and 21-DEC-2021, it was quite uncomfortable, but on 22-DEC-2021, it was still tender when patient took shower, but a little improved (Dose number in series 2). The patient was recovering from both breasts tender, both breasts sore and left arm muscle soreness at injection site. This report was serious (Other Medically Important Condition).; Sender's Comments: V0: 20211261375-covid-19 vaccine ad26.cov2.s-Breast lump. This event(s) is considered unassessable. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Breast pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: The patient was not ill at the time of vaccination. The patient did not have any vaccination within four weeks prior to the first administration date of the suspect vaccine. The patient was not on any other medications.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 07.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Confusional state
Disturbance in attention
Dizziness
Fatigue
Impaired work ability
Symptomtext
Fatigued Light-headed Confusion Trouble focusing on tasks These symptoms have been sporadic since receiving the Pfizer booster shot on 1/3/22. I have had to call off of work twice because they were so bad. My original vaccine was the J&J version administered on 3/11/21
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Obese
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 07.01.2022
- Impfdatum
- 26.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Eye pain
Fatigue
Feeling abnormal
Pain
Symptomtext
Along with severe fatigue that started the day after the vaccine and lasted one full day, I also experienced SEVERE EYE PAIN in both left and right eyes that lasted 5 days. My eyeballs hurt! The first three days were torture when moving eyes left to right or up and down. It was better to just keep them closed. The fourth day was still painful, but the left eye was less painful than the right and by the fifth day, there was little to no pain toward the end of the day. There were no redness, itching, draining, or swelling just severe eye pain- I was very concerned that I would to end up with vision problems, or worse, blindness. It was just a miserable 5 days of eye pain- kind of like what eye pain you experience when you have the flu but intensified making you worry because it's just so painful. On a scale of 1-10 with 10 being the worst, I would rate the pain over the first 2 days at a 9, the third day at a 7, the fourth day at a 5, and the fifth day started at a 3 or 4 and then went away at some point by the next morning.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Eye pain
- Hospital-Tage
- -
- Labordaten
- I did not seek medical care - I just assumed it would eventually go away, and if it didn't I would see my doctor.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Diabetes (controlling by diet, prescribed metformin 500 mg - wasn't taking at the time of vaccination) Mild atrial valve regurgitation
- Andere Medikamente
- None
- Allergien
- Penicillin, peanuts, Zithromax
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 07.01.2022
- Impfdatum
- 18.12.2021
- Beginn
- 19.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Eye movement disorder
Headache
Movement disorder
Pyrexia
Speech disorder
Symptomtext
When I woke up I could not move or speak, my eyes could not even move, my wife tried to speak to me and see what is wrong with me, and I could not respond, slowly my eyes started to open a little bit, and then my mouth opened a little bit but I still could not speak, then my finger moved a little bit, but still could not move very much, had to use the bathroom but could not move myself to go to the bathroom. My wife thought I was playing and put water on me, but I could not move, a little while later I was able to move my arm and my wife helped me to the bathroom, and then sat me on the couch however I still could not move. After about two hours, I started to began to walk and move slowly on my ow. I also had a headache and a low fever the whole day, but by the next day everything was back to normal and I am fine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- 2nd Shot of Vaccine, Got a rash all over my face
- Staat
- WI
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 06.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Immediate post-injection reaction
Injection site bruising
Injection site mass
Pain in extremity
Symptomtext
Immediately after administration the patient had a lump that formed at injection site. At 15 minutes the lump was still palpable and had not reduced in size. Patient called at 1630 reporting that the lump was still there and the same size. Patient was advised to take a pain reliver and use a warm compress and call back if not improved. The patient did not call back by end of day 1/5/22. Follow-up call was made 1/6/22 in AM. Patient reported that there was no visible lump put the injection site was had a large bruise and hard lump that was below the surface. Also, she reported that her left arm was very sore. Patient was advised to call and check-in with her PCP and call the pharmacy to inform of her progress.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- not known
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 06.01.2022
- Impfdatum
- 31.12.2021
- Beginn
- 03.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Contusion
Inflammation
Pain in extremity
Symptomtext
Pt. states that after receiving the 3rd dose of Phizer 12/31/2021, started experiencing symptoms 01/03/2022 of pain in the palm of the hand (inflamed vessel) with bruising and right Middle Finger slight bruising with pain. Primary appt. scheduled for 01/07/2021. Previous Covid + 09/2021 with Monoclonal Treatment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Psoriasis
- Andere Medikamente
- Melatonin
- Allergien
- Latex
- Vorherige Impfungen
- High-Dose Influenza 11/2021 (raised swelling of the temple Left side); Influenza (Seasonal) (Fluzone High-Dose Quadrivalent) Sa
- Staat
- FL
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 06.01.2022
- Impfdatum
- 04.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Injection site erythema
Injection site swelling
Oedema peripheral
Tenderness
Symptomtext
Injection was in left arm and left armpit is very sore, painful, swollen and tender. Injection site is also red and swollen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Citalopram, Nexplanon, Metoprolol, Montelukast
- Allergien
- Corn
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 05.01.2022
- Impfdatum
- 04.01.2022
- Beginn
- 04.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Pallor
Symptomtext
patient became pale and white. He got dizzy and sat down.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 05.01.2022
- Impfdatum
- 04.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Pyrexia
Symptomtext
Incorrect Pfizer product was administered to an 11 year old male. Client should have received 5-11 year old product and received >12 year old product. Child was vaccinated on 1/4/22 and Mom emailed Health Officer on 1/5/22 that child woke up with a fever.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 05.01.2022
- Impfdatum
- 02.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Injection site erythema
Injection site pruritus
Injection site swelling
Injection site warmth
Symptomtext
Injection site was warm and swelling to about 2 inches . Itching and red
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Vitamins
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 04.01.2022
- Impfdatum
- 18.12.2021
- Beginn
- 18.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Dizziness
Headache
Lymphadenopathy
Pain
Pyrexia
Symptomtext
Fever over 101 degrees F., chills, dizziness, headache, sweats, body aches, and swollen glands lasting for 24 hours. Headache and swollen glands persisted for 7 days. Continue to have headaches and swollen glands come and go daily.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hashimoto's Thyroiditis
- Andere Medikamente
- NP Thyroid, Progesterone, CMPD Testosterone, Montelukast
- Allergien
- Penicillin, Eggs, Dairy
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 03.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Fatigue
Symptomtext
Patient felt tired and dizzy a few minutes after vaccine (didn't completely faint). I asked her to lay down on her back and elevate her legs on the chair. she started to feel a lot better. She decided to sit up and I gave her some water. I monitored her until she regained full energy and felt back to 100% normal
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 03.01.2022
- Impfdatum
- 01.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 28,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Myalgia
Pyrexia
Symptomtext
Muscle and joint pain with mild fever (99 to 100 degrees) lasting approximately 24 hours
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma
- Andere Medikamente
- None
- Allergien
- Sulpha
- Vorherige Impfungen
- 19 year old, 1996, yellow fever
- Staat
- FL
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 03.01.2022
- Impfdatum
- 20.12.2021
- Beginn
- 24.12.2021
- Tage bis Beginn
- 4,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Vertigo
Symptomtext
I have been affected by Dizziness and Vertigo since 4 days after my second dose of the COVID 19 vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 02.01.2022
- Impfdatum
- 30.12.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Rash erythematous
Symptomtext
Red dot rash around the posterior and anterior abdomen
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- Patient is going to contact PCP to get evaluation
- Aktuelle Erkrankungen
- Recently recovered from COVID
- Vorgeschichte
- -
- Andere Medikamente
- Unknown
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 01.01.2022
- Impfdatum
- 30.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site pain
Nausea
Pain
Symptomtext
Injection site pain, body aches , nausea
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High blood pressure
- Andere Medikamente
- Aleve
- Allergien
- N/A
- Vorherige Impfungen
- other Covid shot
- Staat
- ME
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 31.12.2021
- Impfdatum
- 07.12.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 24,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site pruritus
Injection site pustule
Injection site scar
Symptomtext
on 12/07 patient received Fluad vaccine on left deltoid and 3rd dose of Covid Pfizer vaccine on right deltoid. 12/29 peitnt came to [pharmacy to report that 3 days after his vaccine, his right deltoid was itching then a pus came out and resulting of a scar that appear like a eating flesh scar. I clean the area with alcohol wipes and highly recommended an urgent followed up with primary care provider or medical facility.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 31.12.2021
- Impfdatum
- 14.12.2021
- Beginn
- 14.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Immunisation
Loss of personal independence in daily activities
Vaccination site erythema
Vaccination site mass
Vaccination site pruritus
Vaccination site reaction
Vaccination site swelling
Vaccination site warmth
Symptomtext
I've experienced a localized reaction at the injection site, it's hot and itchy, is red with a lump sized like a walnut; I've experienced a localized reaction at the injection site, it's hot and itchy, is red with a lump sized like a walnut; I've experienced a localized reaction at the injection site, it's hot and itchy, is red with a lump sized like a walnut; I've experienced a localized reaction at the injection site, it's hot and itchy, is red with a lump sized like a walnut/It is interfering with my daily life; I've experienced a localized reaction at the injection site, it's hot and itchy, is red with a lump sized like a walnut; I've experienced a localized reaction at the injection site, it's hot and itchy, is red with a lump sized like a walnut; I've experienced a localized reaction at the injection site, it's hot and itchy, is red with a lump sized like a walnut; received my booster dose of the Pfizer BioNTech COVID-19 vaccine adult formulation (purple cap); 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 54 year-old female patient received bnt162b2 (BNT162B2), administered in arm right, administration date 14Dec2021 17:30 (Lot number: FD7218) at the age of 54 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Lots of allergies" (unspecified if ongoing); "GERD" (unspecified if ongoing). Concomitant medication(s) included: PANTOPRAZOLE taken for gastrooesophageal reflux disease (ongoing). Vaccination history included: Bnt162b2 (Dose:1, Lot: EW0164, Expiry: Unknown, Pfizer Covid 19 Vaccine), administration date: 16Apr2021, when the patient was 54 years old, for COVID-19 Immunization; Bnt162b2 (Dose:2, Lot: ER8736, Expiry: Unknown, Pfizer Covid 19 Vaccine), administration date: 07May2021, when the patient was 54 years old, for COVID-19 Immunization; Flu (Flu Vaccine, received before the holidays); Shingles vaccine (received before the holidays). The following information was reported: VACCINATION SITE REACTION (non-serious), VACCINATION SITE WARMTH (non-serious), VACCINATION SITE PRURITUS (non-serious) all with onset 15Dec2021, outcome "not recovered" and all described as "I've experienced a localized reaction at the injection site, it's hot and itchy, is red with a lump sized like a walnut"; IMMUNISATION (non-serious) with onset 14Dec2021 17:30, outcome "unknown", described as "received my booster dose of the Pfizer BioNTech COVID-19 vaccine adult formulation (purple cap)"; VACCINATION SITE SWELLING (non-serious), VACCINATION SITE ERYTHEMA (non-serious), VACCINATION SITE MASS (non-serious) all with onset 16Dec2021, outcome "not recovered" and all described as "I've experienced a localized reaction at the injection site, it's hot and itchy, is red with a lump sized like a walnut"; LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (non-serious) with onset 15Dec2021, outcome "unknown", described as "I've experienced a localized reaction at the injection site, it's hot and itchy, is red with a lump sized like a walnut/It is interfering with my daily life". Therapeutic measures were taken as a result of vaccination site reaction, vaccination site warmth, vaccination site pruritus, vaccination site swelling, vaccination site erythema, vaccination site mass, loss of personal independence in daily activities. Additional information : The consumer stated that she received her booster dose of the Pfizer BioNTech COVID-19 vaccine adult formulation (purple cap) on Tuesday 14Dec2021 and she had experienced a localized reaction at the injection site, it's hot and itchy, was red with a lump sized like a walnut. It was interfering with her daily life. States that she had a localized reaction to it, similar to a reaction to an allergy shot. States that she has had a lot of allergy shots in her life. She needs to know how long this might last, and if there is anything she needs to do for it? States that she has taken Benadryl twice, but it's getting bigger and it's not diminishing the itching sensation. She got the injection on Tuesday, 14Dec2021 at 5:30pm. She thought, by today, that it would have gone away. She does not have the complete contact information for her physician. States that she noticed the reaction at the injection site on Wednesday afternoon while she was at work, it felt hot and itchy. She took a Benadryl Wednesday night, and Thursday morning it was worse; it was red, itchy, and there was a lump like a walnut. She took another Benadryl on Thursday night; states that she could only take Benadryl at night because they knock her out. Today the circumference of the reaction was a little bit bigger, and it was still red, itchy and hot. She Clarified that she actually took withheld Pharmacy generic, Wal-dryl, not Benadryl. At first she stated that she could not read the fine print, but she was able to find the Expiration date: Jun2020. Caller states that she did not realize she was taking an outdated product and maybe that was the reason it did not work. States that she could not find anything on the bottle that says Lot or Batch. States that her adult son got his dose at the same time, at the same location, and has had no reaction. The patient received Flu vaccine and Shingles vaccine within four weeks prior to the first administration date of the suspect vaccine The patient does not know the exact dates received or have the Lot/NDC/Expiry to provide. The patient was lots of allergies. Family Medical History Relevant to AE reported as none.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Allergy; GERD
- Andere Medikamente
- PANTOPRAZOLE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 31.12.2021
- Impfdatum
- 11.12.2021
- Beginn
- 11.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary mass
Immunisation
Peripheral swelling
Vaccination site pruritus
Vaccination site rash
Vaccination site reaction
Vaccination site swelling
Symptomtext
medium size soft bulge (about the size of a ball of ping-pong) in my right arm pit-swollen ganglion; medium size soft bulge (about the size of a ball of ping-pong) in my right arm pit-swollen ganglion; rash on my right deltoid at about 2 cm below the exact spot where the shot was applied; The area is swollen and it itches; The area is swollen and it itches; The area is swollen and it itches; Booster; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 35 year-old male patient received bnt162b2 (BNT162B2), administered in arm right, administration date 11Dec2021 16:15 (Lot number: Fd7218) at the age of 35 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Mild eczema" (unspecified if ongoing); "mild asthma" (unspecified if ongoing), notes: recovering; "sinusitis" (unspecified if ongoing), notes: recovered. Concomitant medication(s) included: CICLESONIDE; ALBUTEROL HFA; CETIRIZINE HYDROCHLORIDE. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: Ew0170, Location of injection: Arm Left), administration date: 22Apr2021, when the patient was 35 years old, for COVID-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: Er8737, Location of injection: Arm Left), administration date: 31Mar2021, when the patient was 35 years old, for COVID-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 11Dec2021 05:00, outcome "not recovered", described as "Booster"; AXILLARY MASS (non-serious), PERIPHERAL SWELLING (non-serious) all with onset 13Dec2021 05:00, outcome "not recovered" and all described as "medium size soft bulge (about the size of a ball of ping-pong) in my right arm pit-swollen ganglion"; VACCINATION SITE RASH (non-serious) with onset 13Dec2021 05:00, outcome "not recovered", described as "rash on my right deltoid at about 2 cm below the exact spot where the shot was applied"; VACCINATION SITE SWELLING (non-serious), VACCINATION SITE REACTION (non-serious), VACCINATION SITE PRURITUS (non-serious) all with onset 13Dec2021 05:00, outcome "not recovered" and all described as "The area is swollen and it itches". Therapeutic measures were not taken as a result of immunisation, axillary mass, peripheral swelling, vaccination site rash, vaccination site swelling, vaccination site reaction, vaccination site pruritus. Additional information: it was reported that patient did not had covid prior vaccination nor tested covid post vaccination. Patient did not took other vaccine in four weeks. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Asthma (recovering); Eczema; Sinusitis (recovered)
- Andere Medikamente
- CICLESONIDE; ALBUTEROL HFA; CETIRIZINE HYDROCHLORIDE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 31.12.2021
- Impfdatum
- 27.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Lymphadenopathy
Swelling
Symptomtext
Swollen lymph nodes under arms. Pain and swelling began under left arm and moved to both mid-day 12/30/2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 30.12.2021
- Impfdatum
- 27.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Blindness
Eye pain
Fatigue
Gait disturbance
Headache
Hyperhidrosis
Urinary incontinence
Symptomtext
Approximately 15 hours after injection, patient woke sweating. Went to get glass of water to kitchen and upon return he states he was unable to see and was walking into the walls. He knew he had to urinate but does not remember going. Called Mom who came into bedroom to find patient sitting on the side of bed and incontinent with a puddle of urine in doorway. He was able to tell her exact sequence of events. Had HA behind eyes but was able to see, aching in all joints-especially knees. Temperature was 99.0. Mom gave Tylenol 500mg at 5am. Patient had headache and fatigue for approx 36 hours post vaccine. 12/30/2021-Mom states all symptoms have resolved and son is his normal self.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Melatonin 5-10mg oral @ HS
- Allergien
- None Known
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 30.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Heart rate increased
Influenza like illness
Pyrexia
Symptomtext
12/22/2021 01:00 am, I had flu like symptoms, but what was concerning was a very rapid resting. Heart was in the 90s normally 65 to 67. Fever and chills for 24 hours. Rapid heart rate for 48 to 54 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- I have an appointment on January 4th I have a visit with my doctor
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Omeprazole (took on 12/20/2021)
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 29.12.2021
- Impfdatum
- 16.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Lymph node pain
Pain in extremity
Symptomtext
Sore lymph nodes/ on armpit of injected arm; ongoing Injected arm is sore; less than 24 hours
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymph node pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 29.12.2021
- Impfdatum
- 17.12.2021
- Beginn
- 18.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Pain in extremity
Symptomtext
Pain in the back of the knees, Dr scheduled ultrasound to check for blood clots.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- -
- Andere Medikamente
- Vitamin D
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 29.12.2021
- Impfdatum
- 17.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Chills
Lymphadenopathy
Pyrexia
Symptomtext
Fever; lasted 2 days Chills; lasted 2 days Swelling in lymph nodes/ armpit region; ongoing
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 5,0
- Geschlecht
- F
- Eingang
- 29.12.2021
- Impfdatum
- 26.12.2021
- Beginn
- 26.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Fatigue
Incorrect dose administered
Pain
Pain in extremity
Pyrexia
Symptomtext
Patient was given an adult dose instead of a pediatric dose. Side effects: sore arm, chills, fever, achyness, tired, fatigue
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Claritin, children's vitamin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 26.12.2021
- Impfdatum
- 23.12.2021
- Beginn
- 24.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Breast swelling
Swelling
Symptomtext
Swelling and pain in left arm pit. Swelling left rib area Swelling below left breast
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 25.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 23.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Feeling abnormal
Head discomfort
Loss of personal independence in daily activities
Muscle spasms
Pain in extremity
Symptomtext
I had the booster on Tuesday Dec 21. Starting Thursday and still today my kegs and shoulder are spasmodic. My head feels full to the point I have to lie down. I can't do normal activities. After a few minutes I have to lie down. Pain from knee down. Braun fog.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- Not yet.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 25.12.2021
- Impfdatum
- 12.12.2021
- Beginn
- 12.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Immunisation
Vaccination site pain
Symptomtext
Soreness at injection site; Some fatigue (3rd dose); 3rd dose; This is a spontaneous report received from a contactable reporter (Other HCP). The reporter is the patient. A 22 year-old male patient received bnt162b2 (Pfizer-BioNTech COVID-19), administered in arm left, administration date 12Dec2021 09:45 (Lot number: FD7218) at the age of 22 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "covid prior vaccination" (unspecified if ongoing), notes: Covid prior vaccination: Yes; "Appendectomy", start date: 2004, stop date: 2004; "Oral herpes" (unspecified if ongoing); "Seasonal allergies" (unspecified if ongoing). Concomitant medication(s) included: MG [MAGNESIUM]; ZINC; ASHWAGANDHA ROOT; VITAMIN C [ASCORBIC ACID]. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0173, Location of injection: Arm Left, Vaccine Administration Time: 05:00 PM, Soreness at injection site (left arm) (all 3 doses): recovered from first two, injections), administration date: 03May2021, when the patient was 21 years old, for COVID-19 immunization, reaction(s): "Soreness at injection site"; Bnt162b2 (Dose Number: 1, Batch/Lot No: EW0158, Location of injection: Arm Left, Vaccine Administration Time: 05:00 PM, Soreness at injection site (left arm) (all 3 doses): recovered from first two, injections), administration date: 12Apr2021, when the patient was 21 years old, for Covid-19 immunization, reaction(s): "Soreness at injection site". The following information was reported: IMMUNISATION (non-serious) with onset 12Dec2021 09:45, outcome "unknown", described as "3rd dose"; VACCINATION SITE PAIN (non-serious) with onset 12Dec2021 16:00, outcome "unknown", described as "Soreness at injection site"; FATIGUE (non-serious) with onset 12Dec2021 16:00, outcome "unknown", described as "Some fatigue (3rd dose)". Therapeutic measures were not taken as a result of vaccination site pain, fatigue. Additional information: patient was not tested for COVID after the vaccination, None of the known allergies. patient has not received other vaccine in four weeks. other medications in two weeks also include Multi-vitamin. No follow-up attempts are possible. No further information is expected. Follow-Up (21Dec2021):Follow-up attempts are completed. No further information is expected
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Appendectomy; COVID-19 (Covid prior vaccination: Yes); Hay fever; Oral herpes
- Andere Medikamente
- MG [MAGNESIUM]; ZINC; ASHWAGANDHA ROOT; VITAMIN C [ASCORBIC ACID]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 17.12.2021
- Beginn
- 18.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Herpes zoster
Lymphadenopathy
Rash
Rash erythematous
Rash papular
Rash vesicular
Symptomtext
Developed clustered, painful blistered papules down right arm the morning after my covid booster. The next day even more developed in a line cluster down my arm. With swollen lymph nodes in my armpit. Sunday evening a rash began on my right scapula towards my spine. Began taking Advil/Tylenol as the area was very red and painful and used cortisone on the papules without relief. Attempted to be seen my employhealth at work Monday but was unable. The papules continues to swell and create significant pain. Finally was able to see employee health on Wednesday and was diagnosed with shingles.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- Dx with shingles based on appearance on 12/22
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- N/a
- Andere Medikamente
- na
- Allergien
- Neomycin
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 11,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 22.12.2021
- Beginn
- 23.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Injection site pain
Symptomtext
Patient received adult formulation of Pfizer vaccine rather than pediatric formulation. No adverse effects noted. F/U call ot patient's mom on 12/23/2021. Mom reports only complaint of pain to injection site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- NOne
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None reported
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 19.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Rash
Symptomtext
COVID arm. Red mark/rash on arm ~3"x4"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Pain
Pain in extremity
Symptomtext
ALL DAY: Sore arm; body aches; fatigue; OFF & ON ALL DAY: 100.3 to 100.8 fever TREATMENT: Tylenol
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Food poisoning December 9
- Vorgeschichte
- Asthma
- Andere Medikamente
- Prenatal; vitamins D, C, & K; magnesium chloride; Zyrtec; iron
- Allergien
- Penicillin; blue cheese
- Vorherige Impfungen
- 103 Fever, fatigue, body aches; missed fertility cycle
- Staat
- TN
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 14.12.2021
- Beginn
- 14.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Body temperature
Chills
Immunisation
Malaise
Nausea
Pain
Pyrexia
Symptomtext
Low grade fever; Chills; Nausea; Body aches; Malaise for about 6 hours; Dose received: 3; This is a spontaneous report from a contactable reporter (consumer or other non HCP). The reporter is the patient. A 40-year-old female patient (not pregnant) received bnt162b2 (COMIRNATY), intramuscular, administered in left arm, administration date 14Dec2021 at 16:30 (Lot number: FD7218) at the age of 40 years as dose 3 (booster), single for COVID-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Comirnaty (DOSE 2, SINGLE, Lot number: EP6955, Anatomical location: Left arm, Route of administration: Intramuscular), administration date: 26Mar2021, when the patient was 39 years old, and Comirnaty (DOSE 1, SINGLE, Lot number: EL3248, Anatomical location: Left arm, Route of administration: Intramuscular), administration date: 05Mar2021, when the patient was 39 years old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 14Dec2021 at 16:30, outcome "unknown", described as "Dose received: 3"; PYREXIA (non-serious) with onset 15Dec2021 at 13:00, outcome "recovered" (15Dec2021), described as "Low grade fever"; CHILLS (non-serious) with onset 15Dec2021 at 13:00, outcome "recovered" (15Dec2021), described as "Chills"; NAUSEA (non-serious) with onset 15Dec2021 at 13:00, outcome "recovered" (15Dec2021), described as "Nausea"; PAIN (non-serious) with onset 15Dec2021 at 13:00, outcome "recovered" (15Dec2021), described as "Body aches"; MALAISE (non-serious) with onset 15Dec2021 at 13:00, outcome "recovered" (15Dec2021), described as "Malaise for about 6 hours". Relevant laboratory tests and procedures are available in the appropriate section. Additional Information: The patient had no known allergies. The patient did not receive any other vaccines within four weeks prior to the COVID-19 vaccine. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. Duration of the event of Malaise was reported as 6 hours. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Test Date: 20211215; Test Name: Body temperature; Result Unstructured Data: Test Result:low grade fever
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 22.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dizziness
Headache
Pain in extremity
Pyrexia
Symptomtext
severe headache, dizzy, fever, harm pain
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Allergy, diarrhea
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Cashew nuts
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 22.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Symptomtext
Patient became lightheaeded shortly after receiving the vaccine and then approached the MA letting her know that he felt like he was going to faint. We elevated his legs up on another chair and lowered him slowly to the ground so he could lie flat on a yoga mat, applied cool compresses to the back of his neck and took his vitals.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- BP was 130/70, P 72 and RR 18 at 1127am. 2nd set of vitals taken were 130/72, P68, and RR 15. Pt. was alert and oriented x 3, speech was clear and logical. Checked pupils ;were equal and reactive to light. Patient drank some water and reported that he felt better 10 minutes later.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma
- Andere Medikamente
- Singulair, one tablet daily. Reports Asthma as his medical history
- Allergien
- N/A
- Vorherige Impfungen
- On April 7, 2021 he received Janssen , one dose and reports he had a high fever that same night.
- Staat
- VA
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 22.12.2021
- Impfdatum
- 20.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Dyspepsia
Myalgia
Symptomtext
Heartburn, more than mild but less than severe muscle pain throughout the body, inclusive of joint pain. The muscle pain lasted a full day and was more pronounced than the typical muscle pain you would feel with the flu. I wonder if the spike protein can mimic other proteins in the body and the immune system targeted those proteins in the muscle tissue.
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
- ME
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 22.12.2021
- Impfdatum
- 22.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Clonus
Cold sweat
Dizziness
Hyperventilation
Hypotonia
Posture abnormal
Symptomtext
Client received Pfizer booster of 0.3ml (Lot # FD7218)) on 12/21 around 9:50am. Previous doses were given by other organization on 4/20/21 and 5/11/21. At approximately 9:55am, client was sitting in monitoring area next to her father. Her father reports client was talking to him, when she slumped over, dropped her phone, and couldn?t hold her head up. She then proceeded to bring curled hands to her chest, and exhibited clonic type movements for approximately 10 seconds. She then began hyperventilating and slowly ?came to.? Client?s father shared client had no history of seizures, nor any known allergies. Client is not on any medications. EMS was alerted at 10:03am. Vital signs at 10:03am were: BP 116/82; HR 76; RR 20. Client oriented to person, place, time, and event. At 10:11 vital signs were BP 90/60; HR 68; RR 24. EMS arrived at 10:12am. Client continued to be alert and oriented. Shared her hands were ?clammy,? and prior to event felt ?light headed.? Client ambulated with assistance to EMS stretcher with planned transport to hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- none reported
- Allergien
- no known allergies
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 21.12.2021
- Impfdatum
- 14.12.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Headache
Hypobarism
Symptomtext
Patient frequently recreates in the mountains. Patient received booster vaccination Tuesday morning, and then drove Wednesday afternoon to a mountain cabin at about 10,300 ft amsl. Began having symptoms of fatigue and headache around 8 p.m. Wednesday and then full-blown altitude sickness symptoms through Thursday at about 1 p.m. Patient has history of altitude sickness at much higher elevations (ascending mountains at 13,000 to 14,000 ft amsl) but has never had a full-blown case of altitude sickness at such a low elevation before, and considers it possible that the booster shot exacerbated or caused the altitude sickness episode.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None known
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 21.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site swelling
Symptomtext
After injection swelling started at injection site, possible hematoma formation under the skin, up to golf ball size at largest, ice applied and medical director also examined patient, swelling started to go down after 10-15 minutes, advised to continue with ice for 24 hours then can switch to heat and will also do 24 hour phone call check in, vital signs were normal
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site swelling
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 20.12.2021
- Impfdatum
- 17.12.2021
- Beginn
- 20.12.2021
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Urticaria
Symptomtext
Hives entire body
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma
- Andere Medikamente
- Olmesartan 40 mg, fenofibrate 160 mg daily, rosuvastatin 20 mg daily, Centrum Silver, Magnesium/Postassium daily, compounded estradiol, progesterone, thyroid, DHEA, Omega 3 capsule 2 daily, Protonix 40 mg daily. Ventolin inhaler prn
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 20.12.2021
- Impfdatum
- 08.12.2021
- Beginn
- 09.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Symptomtext
Headache since shot (12 days)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- NOne
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Estrodiol Patch .025 mg Ambien 10 mg @ night Xanax 25 mg @ night
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 20.12.2021
- Impfdatum
- 15.12.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dizziness
Symptomtext
15 mins post vaccination pt reported dizziness. Vitals: 11:00 169/110, 104, 18, 100% -- > 11:30 180/110, 18, 100% Pt made comfortable and drank 2 bottles of water. Patient states that she does have episode of high BP after getting Ist dose of Covid vaccine. Patient states that she does have h/o high BP at home but do not want to take any medication for high BP. Denies blurred vision. Denies chest pain. Denies radiating pain to upper extremities. Patient has PMH of Preeclampsia. Advised the patient to go to the ER at facility but patient refused. Patient left AMA but dizziness better by the time she left the facility. Patient was given the number of valley connections to schedule an appointment to see her PCP for Hypertension. Pt left AMA at 11:30. Pt reports dizziness is better and refuses to go to the ER. AMA forms signed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- PMH: Preeclampsia, HTN, Gestational Diabetes
- Andere Medikamente
- None
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 20.12.2021
- Impfdatum
- 16.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Headache
Pain
Pain in extremity
Symptomtext
Quick onset of major chills at 1:30 am. Achy body throughout night and day. Headache started around 10 am morning and throughout day all day that went away about 11 pm. Left arm where shot given was sore for 2 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- Dose 1 and 2 similar reactions.
- Staat
- AZ
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 19.12.2021
- Impfdatum
- 16.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Lymph node pain
Lymphadenopathy
Nausea
Pain in extremity
Symptomtext
My left arm grew increasingly sore and painful. My left lymph nodes in my arm pit grew increasingly swollen 24 hours after my shot. My left lymph nodes in my arm pit were visibly large and swollen and extremely painful the night of the seventeenth, around 32 hours after my shot. I have a high pain tolerance and I considered going to urgent care that night if the pain continued. When I woke up the morning of the 18th the pain had reduced but was still noticeable, swelling had subsided. The night of the 19th, 48 hours after symptoms started, swelling has gone away but left arm pit lymph nodes are still painful to touch. I would say right under arm lymph nodes were slightly swollen the night of the 17th, but not painful. Occasional nausea up to 48 hours after shot. I took no pain medication or anti-inflammatories.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymph node pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/a
- Vorgeschichte
- N/a
- Andere Medikamente
- Lo loestrin fe (birth control)
- Allergien
- N/a
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 19.12.2021
- Impfdatum
- 19.12.2021
- Beginn
- 19.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dysphonia
Electrocardiogram normal
Nausea
Symptomtext
4:12 PM Patient c/o N/V 92/53 92 Paramedics responded. Mother with patient. 4:15 PM 120/76 93 O2 sat 100% room air 4:31 PM Patient stated better. 122/78 91 Room air 100% EKG within Normal limt per paramedics. Patient waited 30 mins. escorted out by EMT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- Per mother, patient has mental disability
- Vorgeschichte
- None per mother
- Andere Medikamente
- None per mother
- Allergien
- None per mother
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 7,0
- Geschlecht
- F
- Eingang
- 19.12.2021
- Impfdatum
- 18.12.2021
- Beginn
- 18.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Pain in extremity
Symptomtext
Pateint was given 12 and up Pfizer in error 0.3ml dose, she was observed in store then instructed parent to continue to watch patient over the next couple of days. Watch for side effects, anything heart related call md or go to er. pediatrician would be contacted. Vaerrs would be filled out. Contacted parent at 630pm 12/18 (evening of vaccine dose) he reported sore arm. Contacted parent on 12/19, nothing new, continued sore arm .
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- tree nuts, peanuts
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 19.12.2021
- Impfdatum
- 16.12.2021
- Beginn
- 18.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hyperhidrosis
Pain
Pyrexia
Stomatitis
Symptomtext
fever, sweating, pain, nausea, mouth sores
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- -
- Andere Medikamente
- letrazole, valacyclovir, venlafaxine
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 19.12.2021
- Impfdatum
- 10.12.2021
- Beginn
- 12.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Symptomtext
developed a diffuse body rash that worsened over time. Includes the face. Covers her chest, stomach, back, arms, legs. Not itchy. Not painful. No other symptoms. Looks similar to other rashes reported after vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 19.12.2021
- Impfdatum
- 16.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature increased
Lymph node pain
Lymphadenopathy
Symptomtext
Temperature of 100.9. Began 36 hours after shot. Lasted for 24 hours. Very sore and swollen lymph nodes in left armpit.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymph node pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Psoriatic Arthritis
- Andere Medikamente
- -
- Allergien
- Sulfa drugs, crab
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 18.12.2021
- Impfdatum
- 15.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Musculoskeletal stiffness
Myalgia
Nail pigmentation
Pyrexia
Symptomtext
Little reaction to the first dose lot # EW0172. Headache and muscle pain 12 hours after the second dose but only last 1 day. More headache, fever and severe muscle stiffness near the right arm injection side about 12 hours after the injection and whole body muscle pain on the second day of the injection. Longitudinal Melanonychia on right toe was noticed around second injection lot # EW0178 and confirmed by podiatrist. More melanocytic black spots on the same right toe is noticed 3 days after the third injection lot # FD7218 on 12/18/2021. Otherwise, patient feel normal 0n 12/18/2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Nail clipping was done and tested to have Melanonychia in Nov. 2021.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HIGH LDL from Lipid tests in the past two years
- Andere Medikamente
- none
- Allergien
- don't know
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 10,0
- Geschlecht
- M
- Eingang
- 17.12.2021
- Impfdatum
- 14.12.2021
- Beginn
- 14.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Pyrexia
Symptomtext
Patient was given 0.2mL of the Regular 12+ year pediatric vaccine. Patient's mother states the child had a fever for 2 days, but is now currently feeling well. Patient's mother states the child was not hospitalized nor had other complications.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 17.12.2021
- Impfdatum
- 10.12.2021
- Beginn
- 12.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Blood blister
Eye haemorrhage
Eye pain
Injection site pain
Malaise
Pyrexia
Symptomtext
Right eye bleed. Blood spots over my torso/trunk. Happened after the first dose but I thought it was random. Same thing right eye bleed with pain. Bloody spots over my torso/trunk. Both developed over 48 hours after the dose. Saturday I developed a high fever, severe malaise and arm pain at the injection site. I most most concerned about my eye and the bloody spots over my trunk. Patient received first Pfizer dose on 11/19/21 lot # FE3590.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Eye pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Fluoxetine - hives NSAIDs - Steven Johnson Syndrome PCN - Rash, anaphylaxis Shellfish - anaphylaxis Latex - Rash
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 17.12.2021
- Impfdatum
- 14.12.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Inflammation
Pain
Pruritus
Skin warm
Symptomtext
red inflammed, about 4 to 5 inches diameter. pt states hot to the touch and itchy. was painful first 2 days post-injection, now not painful just itch
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 17.12.2021
- Impfdatum
- 13.12.2021
- Beginn
- 13.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Pruritus
Symptomtext
Patient received 1st dose Pfizer. Pt c/o of itching in post observation area to PA @1830 (15mins post vaccination). Pt escorted to triage area. Charge RN and on-site provider PA notified. Assessed by PA and RN. @1830 V/S: BP 114/79 HR 95 RR 16 SpO2 98% AOx4. Pt denies SOB, chest pain, headache, N/V. PA recommended Benadryl. PA administered 25mg Benadryl PO @1840. Extended observation for 15 minutes. @1855 V/S: BP 118/82 HR 88 SpO2 99% VSS AOx4. Pt denies SOB, chest pain, headache, N/V. Pt continue c/o of generalized itching. Per PA assessment, lungs and airway clear to auscultation, no wheezing. PA recommended Benadryl. PA administered 25mg Benadryl PO @1856. Per PA, no immediate signs of anaphylaxis observed. PA d/c patient with family to home at approx @1900. Patient educated to continue monitoring symptoms and to call 911/ER for symptoms of SOB, wheezing, chest pain, worsening itching. Pt verbalized understanding.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Allergies: Ceftriaxone (Pruritus)
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 17.12.2021
- Impfdatum
- 15.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Lymph node pain
Lymphadenopathy
Myalgia
Pyrexia
Symptomtext
Fever, chills, achey muscles, swollen lymph node under left arm. Lymph node still swollen and painful, all other side effects dissipated after 4 hours
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- PCOS Diverticulosis
- Andere Medikamente
- Influenza (Seasonal) Afluria Quadrivalent
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 10,0
- Geschlecht
- M
- Eingang
- 17.12.2021
- Impfdatum
- 16.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain in extremity
Symptomtext
MOM STATED PT GOT A SORE ARM UNTIL LATER THAT NIGHT OF THE DAY OF VACCINE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- ASTHMA
- Andere Medikamente
- CETIRIZINE, MONTELUKAST, HYDROXYZINE
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- -
- Geschlecht
- F
- Eingang
- 17.12.2021
- Impfdatum
- 10.12.2021
- Beginn
- 10.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
Fatigue
Illness
Immunisation
Impaired work ability
Influenza like illness
Movement disorder
Myalgia
Pain in extremity
Pyrexia
Symptomtext
booster; Arm was sore; Developed high fever, it has got up to 103, I just can''t seem to get it down without medicine/ I am still experiencing it, about 30 minutes ago I took my temperature and it was 102.6; Muscle ache; Fatigue, I am just super tired; I feel like I have flu; This one has knocked me bad like I feel sick; I just can''t do the work; Bone talking like I can't move it forward like it's bad; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 39 year-old female patient received bnt162b2 (BNT162B2), administration date 10Dec2021 (Lot number: FD7218) as dose 3 (booster), 0.3 ml single for covid-19 immunisation. Relevant medical history included: "Verbatim: Hashimoto's Hypothyroidism" (unspecified if ongoing), notes: Verbatim: Hashimoto''s Hypothyroidism. Concomitant medication(s) included: LEVOTHYROXINE taken for autoimmune thyroiditis. Vaccination history included: Covid-19 vaccine (1st dose , manufacturer: Unknown), for COVID-19 Immunization; Covid-19 vaccine (2nd dose, manufacturer: unknown), for COVID-19 Immunization, reaction(s): "my second was like I didn't felt great". The following information was reported: IMMUNISATION (non-serious) with onset 10Dec2021, outcome "not recovered", described as "booster"; PAIN IN EXTREMITY (non-serious) with onset 10Dec2021, outcome "not recovered", described as "Arm was sore"; PYREXIA (non-serious) with onset 10Dec2021, outcome "not recovered", described as "Developed high fever, it has got up to 103, I just can''t seem to get it down without medicine/ I am still experiencing it, about 30 minutes ago I took my temperature and it was 102.6"; MYALGIA (non-serious) with onset 10Dec2021, outcome "not recovered", described as "Muscle ache"; FATIGUE (non-serious) with onset 10Dec2021, outcome "not recovered", described as "Fatigue"; INFLUENZA LIKE ILLNESS (non-serious) with onset 10Dec2021, outcome "not recovered", described as "I feel like I have flu"; ILLNESS (non-serious) with onset 10Dec2021, outcome "not recovered", described as "This one has knocked me bad like I feel sick"; IMPAIRED WORK ABILITY (non-serious) with onset 10Dec2021, outcome "not recovered", described as "I just can''t do the work"; MOVEMENT DISORDER (non-serious) with onset 10Dec2021, outcome "not recovered", described as "Bone talking like I can't move it forward like it's bad". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of immunisation, pain in extremity, pyrexia, myalgia, fatigue, influenza like illness, illness, impaired work ability. Additional information: Reporter seriousness for Developed high fever, it has got up to 103, the patient just can't seem to get it down without medicine; the patient was still experiencing it, about 30 minutes ago, the patient took temperature and it was 102.6: Unspecified. Reporter seriousness for Developed high fever, it has got up to 103, I just can't seem to get it down without medicine; I am still experiencing it, about 30 minutes ago I took my temperature and it was 102.6: Unspecified. Concomitant Products Levothyroxine: Consumer stated, "Just once daily in the PM.". So, the patient received third vaccine yesterday around would 4-4:30 and then about an hour and half arm was sore, bone talking like could'nt move it forward like it's bad, but was like okay, but then by that evening the patient developed high fever that having to keep Advil on board in order to keep it down because it has got up to 103. Just muscle ache, fatigue, feel like I have flu. But the fever is just (voice not clear), I just can't seem to get it down without medicine." Consumer stated, "Yes and was still experiencing it, about 30 minutes ago I took my temperature and it was 102.6 and the patient was on Advil, has been administered about 5 hours before." Concomitant medicine: Consumer stated, "No I take like supplements like magnesium and biotin." Treatment: Consumer stated, "Last night the patient took 2 capsules around 2 am and then when it 'wore off', the patient tried to use one, tried to take a lower dose and it didn't last very long, so the patient had to take another 2 capsules of Advil, it was the liquid gels (Suspect captured conservatively and PC Filed Conservatively)." No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Test Date: 20211210; Test Name: body temperature; Result Unstructured Data: Test Result:103; Test Date: 20211211; Test Name: body temperature; Result Unstructured Data: Test Result:102.6
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Hashimoto's thyroiditis (Verbatim: Hashimoto''s Hypothyroidism)
- Andere Medikamente
- LEVOTHYROXINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 17.12.2021
- Impfdatum
- 09.12.2021
- Beginn
- 09.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Immunisation
Pain in extremity
Swelling
Vaccination site swelling
Symptomtext
Swelling at injection site; Swollen and pain in armpit in days following vaccine; Swollen and pain in armpit in days following vaccine; Pain down arm and stops atelbow; Dose number: 3; This is a spontaneous report from a contactable reporter (consumer or non HCP). The reporter is the patient. A 55 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in left arm, administration date 09Dec2021 at 16:45 (Lot number: FD7218) at the age of 55 years as dose 3 (booster), single for COVID-19 immunisation. The patient had no relevant medical history and concomitant medications was prescribed but not taken. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE; Lot Number: EP6955; Administration Time: 16:45; vaccine location: Left Arm), administration date: 18Mar2021, when the patient was 54 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE; Lot Number: ER8729; Administration Time: 16:45; vaccine location: Left Arm), administration date: 08Apr2021, when the patient was 54 years old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 09Dec2021 at 16:45, outcome "unknown", described as "Dose number: 3"; VACCINATION SITE SWELLING (non-serious) with onset 10Dec2021 at 00:00, outcome was "not recovered", described as "Swelling at injection site"; AXILLARY PAIN (non-serious), SWELLING (non-serious), PAIN IN EXTREMITY (non-serious) both with onset 10Dec2021 at 00:00, outcome "not recovered", and both described as "Swollen and pain in armpit in days following vaccine". Therapeutic measures were not taken as a result of vaccination site swelling, axillary pain, swelling and pain in extremity. Additional information: The patient had no known allergies. 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 prior to the COVID-19 vaccine. It was reported that injection itself was painless with no bleeding afterwards. Since the vaccination, the patient had not been tested for COVID-19. The events did not result in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 16.12.2021
- Impfdatum
- 08.12.2021
- Beginn
- 13.12.2021
- Tage bis Beginn
- 5,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site rash
Pruritus
Symptomtext
Patient states she had a small rash around injection site on 12/8 which has went away. Now she is claiming since 12/13 she is itching underneath her skin up and down her arms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 16.12.2021
- Impfdatum
- 14.12.2021
- Beginn
- 14.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Headache
Pain
Pyrexia
Symptomtext
felt like i had covid again. fever 101.9 very sever body aches and headache and fatigue. lasted about 36 to 38 hours. currently no fever but still have body aches and fatigue
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- RA
- Andere Medikamente
- hydrochlorothiazide
- Allergien
- no
- Vorherige Impfungen
- 2 other covid vaccines
- Staat
- MI
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 15.12.2021
- Impfdatum
- 13.12.2021
- Beginn
- 14.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Balance disorder
Dizziness
Vertigo
Symptomtext
VERTIGO ONSET ABOUT 7PM. ROOM WAS SPINNING AND I LOST MY BALANCE WHEN WALKING. SYMPTOMS WORSENED WHEN LYING ON MY BACK OR RIGHT SIDE. TOOK A BENEDRYL 10MG AND WENT TO BED. SYMPTOMS LASTED THROUGHOUT THE NIGHT WHENEVER I MOVED AROUND. A LITTLE BETTER IN THE MORING BUT STILL SPINNING SO TOOK DRAMAMINE. SYMPTOMS IMPROVED THROUGHOUT THE DAY WITH JUST A LITTLE DIZZINESS BY 8:30 PM
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NOVEMBER 16 2021 SEVERE HEADACHE WITH NASEAU AND BODY ACHES DURATION 8 HOURS.
- Vorgeschichte
- -
- Andere Medikamente
- NEXXIUM DAILY, L-ARGININE, B SUPPLEMENT
- Allergien
- -
- Vorherige Impfungen
- MUSCLE ACHES AND TIREDNESS AFTER 2ND COVID DOSE, LASTED ONE DAY
- Staat
- IL
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 14.12.2021
- Impfdatum
- 12.12.2021
- Beginn
- 12.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Pain
Pyrexia
Sensitive skin
Tenderness
Symptomtext
Fatigue started about 12 hours after the injection. My body ached and was painful to the touch. I had a fever for about 6 hours (hours 12-18 post injection). The fatigue and body sensitivity lasted 24 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Psoriasis
- Andere Medikamente
- Otzela, wellbutrin, Larin FE
- Allergien
- Sulfa drugs, nickel
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 14.12.2021
- Impfdatum
- 09.12.2021
- Beginn
- 10.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Lymph node pain
Lymphadenopathy
Symptomtext
Day one: swelling of lymph nodes underarm , sensitive to touch underarm; fatigue; Day two: swelling of lymph nodes underarm & collar bone, sensitive to touch collar bone Day three: swelling reduced underarm & collar bone; sensitive to touch collar bone Day four: swelling further reduced underarm; swelling collar bone same; no sensitivity to touch
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 14.12.2021
- Impfdatum
- 11.12.2021
- Beginn
- 13.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Extra dose administered
Headache
Lymph node pain
Pain
Pain in extremity
Symptomtext
All three: chills, ache, sore arm, headache Booster: same as above but under armpit soreness in lymph nodes
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- HTN; Hypothyroid
- Andere Medikamente
- Losartan; clonidine; gabapentin; levothyroxine; Cymbalta
- Allergien
- Vicodin; Percocet
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 13.12.2021
- Impfdatum
- 09.12.2021
- Beginn
- 10.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Lymphadenopathy
Mass
Muscle spasms
Pyrexia
Symptomtext
Fever and chills starting approx. 30 hrs after booster that lasted approx 8 hrs Cramps/Charlie horses in both feet and left leg 30 hrs after booster randomly for approx. 8-16 hours Swollen lymph node under left armpit after approx. 48 hrs after booster Lump on chest/neck area possibly Supraclavicular lymph node (left side) after approx. 72 hrs after booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Pepcid AC
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 13.12.2021
- Impfdatum
- 08.12.2021
- Beginn
- 12.12.2021
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chills
Neck pain
Pyrexia
Swelling
Symptomtext
Pt. states that after receiving the 3rd dose of Phizer 12/08/2021, started experiencing symptoms 12/12/2021 of fever, chills, and swelling around the neck. Neck pain associated with swelling, visit 12/13/2021 recommendation for Ultrasound follow-up with Primary. Pt. still experiencing symptoms, no noted Primary visit/communications.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 13.12.2021
- Impfdatum
- 10.12.2021
- Beginn
- 10.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Diarrhoea
Fatigue
Headache
Injection site pain
Nausea
Pain
Peripheral swelling
Pyrexia
Symptomtext
dibilitating pain, headache, nausea, injection site pain/head, arm swollen, diarrhea, chills, fatigue, fever
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- psoriasis, psoriatic arthritis, reflex sympathetic dystrophy
- Andere Medikamente
- -
- Allergien
- penicillin percocet
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 12.12.2021
- Impfdatum
- 09.12.2021
- Beginn
- 10.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Nausea
Symptomtext
Extreme nausea for 60 hours
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- Pfizer Dose 2 (Age 17 April 22, 2021) Chills, nausea, vomiting. Ended 24 hours after vaccine administration.
- Staat
- NC
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 12.12.2021
- Impfdatum
- 10.12.2021
- Beginn
- 11.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Lymph node pain
Lymphadenopathy
Myalgia
Symptomtext
Aching body joints and muscles starting about 12-15 hours after injection. 2nd day following injection presented swelling and tenderness of lymph node in left armpit (vaccinated arm.)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Duloxetine Doxepin
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 11.12.2021
- Impfdatum
- 01.12.2021
- Beginn
- 11.12.2021
- Tage bis Beginn
- 10,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Vomiting
Symptomtext
Vomited 3 times: 3 am, 8 am and 12:30 pm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vomiting
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- No
- Andere Medikamente
- Culterelle probiotic and multivitamin
- Allergien
- No
- Vorherige Impfungen
- Vomited once after a flu shot.
- Staat
- OR
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 10.12.2021
- Impfdatum
- 10.12.2021
- Beginn
- 10.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Urticaria
Symptomtext
Hives on face appearing appropriately three hours after injection. New hives continued appearing over the next few hours up to the size of a half-dollar coin.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Rash on arm
- Vorgeschichte
- Hypothyroid
- Andere Medikamente
- Levothyroxine, PreviDent (RX toothpaste accompanying aligner braces)
- Allergien
- Rash after certain medical adhesive tapes (such as was used with an epidural. Entire back turned into a rash from where the adhesive was used, some band-aid adhesives also cause rash)
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 10.12.2021
- Impfdatum
- 07.12.2021
- Beginn
- 09.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Injection site rash
Injection site warmth
Pain
Paranasal sinus discomfort
Vomiting
Symptomtext
Had the body aches and really bad heachache / sinus pressure. Threw up a couple times Thursday. Now there is a rash at the site and heat (12/10)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Nasal infection - was on zpak 11/8
- Vorgeschichte
- Psoriatic arthritis and hyperlipidemia
- Andere Medikamente
- Humaira Rosuvastatin Magnesium , B12, D - multivitamin Arthritis pain med
- Allergien
- Tetracycline PCN Septra Indomethacin Oxycodone Enbrel Bee sting Cayenne pepper
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 09.12.2021
- Impfdatum
- 08.12.2021
- Beginn
- 08.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Headache
Pain
Symptomtext
The patient had a severe headache and lot's of pain after receiving 2 Covid boosters at the same time. The patient visited her doctor the next day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- not sure
- Vorgeschichte
- not sure
- Andere Medikamente
- not sure
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 09.12.2021
- Impfdatum
- 08.12.2021
- Beginn
- 08.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Headache
Pain
Symptomtext
The patient had a severe headache and lot's of pain after receiving 2 Covid boosters at the same time. The patient visited her doctor the next day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- not sure
- Vorgeschichte
- not sure
- Andere Medikamente
- not sure
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 09.12.2021
- Impfdatum
- 08.12.2021
- Beginn
- 08.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Constipation
Discomfort
Dizziness
Hyperhidrosis
Influenza like illness
Insomnia
Nausea
Pain
Pyrexia
Vomiting
Symptomtext
Third Pfizer COVID vaccine shot. The first one produced exaggerated flu like symptoms, second one mild, the third one has placed me in bed for 24 hours. Symptoms: 102.1 fever for more than 6 hours, severe chills, severe body aches, extreme body sweating, nausea, dizziness, vomiting, constipation, overall prolonged body discomfort, insomnia. Mild symptoms began within 20 minutes of does administration and slowly progressed with symptoms hype about 4 hours after shot. Extreme flu like symptoms not normally felt even before pandemic.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None, other than bursitis pain due to exercise injury
- Vorgeschichte
- None
- Andere Medikamente
- Nature's Trove, SAMe, 400mg Motrin IB 200mg (for bursitis shoulder pain)
- Allergien
- IODINE, all forms.
- Vorherige Impfungen
- Pfizer COVID vaccine first shot, Lot ER2613, administered 5 April 2021
- Staat
- DE
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 08.12.2021
- Impfdatum
- 06.12.2021
- Beginn
- 07.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Fall
Muscular weakness
Vomiting
Symptomtext
Pt experienced chills the night of his vaccination. The next morning upon waking around 8 am, tried to stand and legs gave way (pt fell onto floor). Says he experienced weakness in the legs, no dizziness, headache, or nausea reported. Even up till today (12/8) pt reports weakness in legs when tries to stand, still experiencing chills. Pt also reports vomiting on 12/7 as well.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Diabetes, hypertension
- Andere Medikamente
- allopurinol, aspirin, atorvastatin, bumetanide, carvedilol, ezetimibe, felodipine ER, gabapentin, Humalog, hydralazine, metformin, metolazone, potassium
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 86,0
- Geschlecht
- F
- Eingang
- 15.12.2023
- Impfdatum
- 06.12.2021
- Beginn
- 07.12.2023
- Tage bis Beginn
- 731,0
- Dosis
- 3
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Blood creatine phosphokinase increased
COVID-19
Electrocardiogram normal
Gait disturbance
Myocardial ischaemia
Rhabdomyolysis
SARS-CoV-2 test positive
Troponin increased
Symptomtext
Admit date: 12/7/2023 Discharge date: 12/09/2023 Admitting Physician: MD Attending Physician at the Time of Discharge: MD Primary Care Physician: MD Reason for Admission: unsteady gait Brief Summary of Hospital Stay: (Include Significant Findings and Invasive Procedures) 88 YO year old female with a history of heart failure preserved EF, pulmonary hypertension, recurrent falls, gait instability, hypertension who presented to the ED on 12/7/2023 after being found lying on the floor at her AFC. She was diagnosed with rhabdomyolysis with CPK elevated in the 1500s, treated with IV fluids and CPK downtrended accordingly. She was also found to be COVID positive on admission. She was not hypoxic however. No indication for Decadron or remdesivir at this time. Initially, there were concerns for ACS given elevated troponin; however, troponin downtrended and EKG was unremarkable for acute ST changes. Troponin likely elevated due to demand ischemia. Patient denies any chest pain or shortness for breath at this time. Patient continues to improve and breathing well on room air. Currently, patient is medically stable for discharge back home to AFC.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood creatine phosphokinase increased
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 05.10.2023
- Impfdatum
- 20.12.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 53-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), on 20Dec2021 at 13:00 as dose 3 (booster), single (Lot number: FD7218) at the age of 51 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's relevant medical history included: "High cholesterol" (unspecified if ongoing); "Overweight" (unspecified if ongoing). The patient's concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Primary immunization series complete; manufacturer unknown), for COVID-19 immunization. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID 19 Treatment". Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: Reporter is the patient. No known allergies. Patient received anti viral treatment with Paxlovid from 15Sep2023 to 19Sep2023.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: High cholesterol; Overweight
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 18.08.2023
- Impfdatum
- 11.12.2021
- Beginn
- 14.11.2022
- Tage bis Beginn
- 338,0
- Dosis
- 3
- Route/Site
- - / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Breakthrough COVID-19
Symptomtext
Covid 19 Breakthrough Infection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Breakthrough COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- 2nd degree heart block with syncope
- Andere Medikamente
- No active home medication
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 08.08.2023
- Impfdatum
- 11.12.2021
- Beginn
- 07.12.2022
- Tage bis Beginn
- 361,0
- Dosis
- 3
- Route/Site
- - / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Breakthrough COVID-19
Symptomtext
Breakthrough Covid-19 infection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Breakthrough COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- HTN, CAD, HLD, DM Type II
- Andere Medikamente
- Multivitamin, Glipizide, Labetalol, Metformin, Rosuvastatin
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 07.08.2023
- Impfdatum
- 07.01.2022
- Beginn
- 08.01.2023
- Tage bis Beginn
- 366,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Breakthrough COVID-19
SARS-CoV-2 test positive
Symptomtext
Breakthrough case admission after 3 vaccines Pfizer 3/3/21 lot# EN6198; Pfizer 3/24/21 lot# EN6208; Pfizer 1/7/22 lot# FD7218
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Breakthrough COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 25.07.2023
- Impfdatum
- 21.12.2021
- Beginn
- 01.10.2022
- Tage bis Beginn
- 284,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 3 vaccines Pfizer 5/18/21 lot# Ew0183; Pfizer 6/8/21 lot# Ew0178; Pfizer 12/21/21 lot# FD7218
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 29.06.2023
- Impfdatum
- 13.12.2021
- Beginn
- 02.11.2022
- Tage bis Beginn
- 324,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case after 3 vaccines Pfizer 4/9/21 lot# Ew0158; Pfizer 4/30/21 lot# EW0179; Pfizer 12/13/21 Lot# FD7218
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 13.06.2023
- Impfdatum
- 28.12.2021
- Beginn
- 01.04.2022
- Tage bis Beginn
- 94,0
- Dosis
- 2
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Eye disorder
Impaired driving ability
Laboratory test abnormal
Visual impairment
Symptomtext
I went to a local eye care office, then another, then the local hospital where I was diagnosed with a childhood disease in my right eye. It is off, I can see 2 different things at the same time. It was not double vision, It is 2 separate images. I can't read. If I reach for something I have to close one eye so I don't knock stuff over. I have to drive with one eye closed. It is my dominant eye (right) that is messed up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Eye disorder
- Hospital-Tage
- -
- Labordaten
- yes, diagnosed with childhood eye disease.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- COPD, Sporadic arthritis
- Andere Medikamente
- metformin, omeprazole, pregabalin, metoprolol tartrate, levothyroxine, atorvastatin, folic acid, dychlosenace, enapril malonate, dalirest, methotrexate, Montelukast, ropinirole, theophylline, loratadine, baclocine, primidone. Symbicort, S
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 05.06.2023
- Impfdatum
- 13.04.2022
- Beginn
- 16.10.2022
- Tage bis Beginn
- 186,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Hypoxia
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypoxia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 09.05.2023
- Impfdatum
- 14.01.2022
- Beginn
- 16.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Tinnitus
Symptomtext
Constant Bilateral Tinnitus that is considered to be bothersome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tinnitus
- Hospital-Tage
- -
- Labordaten
- Audiological Evaluation
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Macular Degeneration
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 24.04.2023
- Impfdatum
- 09.12.2021
- Beginn
- 01.03.2022
- Tage bis Beginn
- 82,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Tinnitus
Symptomtext
constant ringing in both ears
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tinnitus
- Hospital-Tage
- -
- Labordaten
- doctor scoped ears, all looks ok
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- mild hypertension (treated)
- Andere Medikamente
- Amolodipine
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- F
- Eingang
- 08.03.2023
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Alanine aminotransferase
Hepatic enzyme increased
Laboratory test
Symptomtext
elevated liver enzymes/ALT 42; This is a spontaneous report received from contactable reporter (Consumer or other non HCP). The reporter is the patient. A 59-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), as dose 3 (booster), single (batch/lot number: FD7218), in right arm for covid-19 immunization. The patient's relevant medical history was not reported. There were no concomitant medications. Past drug history included: Exparel, reaction: "known allergies possibly". Vaccination history included: Bnt162b2 (dose 2, batch/lot EL9269, vaccine location right arm), for COVID-19 immunization, reaction: "broken ankle", "has been quite doozy", "headaches", "highly elevated liver enzymes", "nausea", "high fever", "vomiting"; Bnt162b2 (dose 1, batch/lot EL9262, vaccine location right arm), for COVID-19 immunization, reaction: "felt little poorly for 24 hours", "slight fever". The following information was reported: HEPATIC ENZYME INCREASED (hospitalization), outcome "recovering", described as "elevated liver enzymes/ALT 42". The patient was hospitalized for hepatic enzyme increased (hospitalization duration: 4 day). The event "elevated liver enzymes/alt 42" required emergency room visit. The patient underwent the following laboratory tests and procedures: ALT: 42; liver enzymes: elevated. Clinical course: The reporter informed that facility type vaccine was at doctor's office/urgent care. The patient had no covid prior vaccination. The reporter informed that the patient experienced elevated liver enzymes after each Covid vaccine and after 3 dose, ALT was 42. The reporter informed that the AE resulted in emergency room/department or urgent care and treatment was 4-day hospital stay. The patient was not covid tested post vaccination.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300090366 same patient/product, different dose/events;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Alanine aminotransferase
- Hospital-Tage
- 4,0
- Labordaten
- Test Name: ALT; Result Unstructured Data: Test Result:42; Test Name: liver enzymes; Result Unstructured Data: Test Result:elevated
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 86,0
- Geschlecht
- M
- Eingang
- 07.03.2023
- Impfdatum
- 17.12.2021
- Beginn
- 01.11.2022
- Tage bis Beginn
- 319,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after three vaccines Pfizer 1/18/21 Lot# EK4176; Pfizer 2/8/21 Lot# EL9264; Pfizer 12/17/21 Lot# FD7218
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 14.12.2021
- Beginn
- 21.02.2023
- Tage bis Beginn
- 434,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Symptomtext
patient hospitalized
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 22.02.2023
- Impfdatum
- 10.12.2021
- Beginn
- 30.01.2023
- Tage bis Beginn
- 416,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 37-year-old male patient received BNT162b2 (BNT162B2), on 24Mar2021 as dose 1, single (Lot number: ER8732), in left arm, on 14Apr2021 as dose 2, single (Lot number: EW0162), in left arm and on 10Dec2021 as dose 3 (booster), single (Lot number: FD7218) at the age of 36 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Known allergies: Yes - several foods" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 30Jan2023, outcome "recovered" (09Feb2023) and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (30Jan2023) Positive; (09Feb2023) negative; (14Feb2023) negative. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: Patient had Paxlovid rebound COVID symptoms. Tested positive for COVID 30Jan2023. Took Paxlovid 31Jan2023 to 04Feb2023. Felt better, then got sick again 07Feb2023 with COVID symptoms. Re-tested negative for COVID 09Feb2023 and 14Feb2023. Still sick as of 16Feb2023. Patient had other medication (Digestive Probiotic, Expectorant, DayQuil/Nyquil, Pseudoephedrine) within 2 weeks of Paxlovid therapy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20230130; Test Name: COVID-19 Test; Test Result: Positive ; Test Date: 20230209; Test Name: COVID-19 Test; Test Result: Negative ; Test Date: 20230214; Test Name: COVID-19 Test; Test Result: Negative
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Food allergy
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 86,0
- Geschlecht
- F
- Eingang
- 14.02.2023
- Impfdatum
- 22.12.2021
- Beginn
- 15.01.2023
- Tage bis Beginn
- 389,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Mental status changes
SARS-CoV-2 test positive
Sepsis
Symptomtext
Hospitalization: 1/15/2023 - 1/20/2023 (5 days) Presentation to the ED: sepsis, change in mental status. Coming from Health and Rehabilitation Center. COVID + date: 1/15/2023 Treatment: No indication for steroid or remdsivir. Discharge to: SNF FJ1611 11/30/2021 FD7218 FD7218
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- dementia, DM
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 07.02.2023
- Impfdatum
- 08.12.2021
- Beginn
- 01.01.2023
- Tage bis Beginn
- 389,0
- Dosis
- UNK
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Symptomtext
Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 58-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 06May2021 as dose number unknown, single (Lot number: EW0167), in left arm and on 08Dec2021 as dose number unknown, single (Lot number: FD7218) at the age of 58 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Breast cancer" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Jan2023, outcome "unknown" and all described as "Treatment of COVID-19". Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: On 28Jan2023 the patient took Paxlovid for the treatment of event. The patient had no known allergy. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Breast cancer
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 02.02.2023
- Impfdatum
- 22.12.2021
- Beginn
- 10.01.2022
- Tage bis Beginn
- 19,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case after 3 vaccines
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 31.01.2023
- Impfdatum
- 18.12.2021
- Beginn
- 12.01.2023
- Tage bis Beginn
- 390,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
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 45-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 21Mar2021 as dose 1, single (Lot number: ER8727), in left arm, on 10Apr2021 as dose 2, single (Lot number: EP7533), in left arm and on 18Dec2021 as dose 3 (booster), single (Lot number: FD7218) at the age of 44 years, in left arm for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 12Jan2023, outcome "unknown" and all described as "COVID 19 Treatment". Therapeutic measures were taken as a result of drug ineffective, covid-19. The patient started with sore throat and chills on Thursday, 12Jan2023. On Friday, 13Jan2023 at 8:00 am, the patient started throwing up. The patient went to (Clinic Name) on Saturday, 14Jan2023. The patient was still throwing up. From 14Jan2023 to 19Jan2023, the patient received nirmatrelvir; ritonavir (PAXLOVID) for COVID-19 treatment. The patient had no known allergies. The patient had no other medical history.
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: known allergies: No other medical history: No
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 26.01.2023
- Impfdatum
- 29.12.2021
- Beginn
- 22.01.2023
- Tage bis Beginn
- 389,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
COVID Positive test; COVID Positive test; 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 40-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 02Apr2021 as dose 1, single (Lot number: ER8730), in left arm, on 24Apr2021 as dose 2, single (Lot number: EW0171), in left arm and on 29Dec2021 as dose 3 (booster), single (Lot number: FD7218) at the age of 39 years, in left arm, all intramuscular for covid-19 immunisation. The patient's relevant medical history included: "Asthma" (unspecified if ongoing); "Food: Shellfish Allergy" (unspecified if ongoing). There were no concomitant medications. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 22Jan2023, outcome "unknown" and all described as "COVID Positive test". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (22Jan2023) Positive, notes: Nasal Swab. Therapeutic measures were not taken as a result of drug ineffective, covid-19. Clinical course: Facility where the most recent COVID-19 vaccine was administered was pharmacy or drug store. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient did not receive any other medications within 2 weeks of vaccination. Prior to vaccination the patient was not diagnosed with COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20230122; Test Name; Test Result: Positive ; Comments: Nasal Swab
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Asthma; Shellfish allergy
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 22.01.2023
- Impfdatum
- 28.12.2021
- Beginn
- 19.01.2023
- Tage bis Beginn
- 387,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- unknown
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- Parkinson's Disease, heart disease, chronic kidney disease, dementia
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 88,0
- Geschlecht
- M
- Eingang
- 14.12.2022
- Impfdatum
- 21.12.2021
- Beginn
- 07.12.2022
- Tage bis Beginn
- 351,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Symptomtext
**unable to interview case due to hospitalization**
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- unknown
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 29.10.2022
- Impfdatum
- 15.12.2021
- Beginn
- 01.10.2022
- Tage bis Beginn
- 290,0
- 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
Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from 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 15Dec2021 as dose 3 (booster), single (Lot number: FD7218) at the age of 50 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's relevant medical history included: "Known allergies: shrimp" (unspecified if ongoing); "Known allergies: mildly strawberry/pineapple" (unspecified if ongoing). The patient's concomitant medications were not reported. Past drug history included: Amoxicillin, reaction(s): "Known allergies: Amoxicillin". The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Oct2022, outcome "not recovered" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: Rebound COVID. Therapeutic measures were taken as a result of drug ineffective, covid-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID-19; Test Result: Positive ; Comments: Rebound COVID
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Fruit allergy; Seafood allergy
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 27.10.2022
- Impfdatum
- 17.10.2021
- Beginn
- -
- Tage bis Beginn
- -
- 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 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 32-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 01Apr2021 as dose 1, single (Lot number: EN6207), on 22Apr2021 as dose 2, single (Lot number: EW1071) and on 17Oct2021 as dose 3 (booster), single (Lot number: FD7218) at the age of 31 years for covid-19 immunisation. The patient's relevant medical history included: "Overweight" (unspecified if ongoing); "Depression" (unspecified if ongoing), notes: General depression/anxiety; "Anxiety" (unspecified if ongoing), notes: General depression/anxiety; "ADHD" (unspecified if ongoing), notes: ADHD. Concomitant medication(s) included: PROZAC, start date: Aug2014; ADDERALL, start date: May2016. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (08Oct2022) Positive, notes: Tested positive for Covid on Saturday 8Oct2022; (16Oct2022) Negative, notes: Tested negative for Covid on Sunday 16Oct; (21Oct2022) Positive, notes: Tested strongly positive for Covid Friday 21Oct; (24Oct2022) Negative, notes: Tested negative by Monday 24Oct. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical Course: It was reported that Patient took Other medication in 2weeks. Patient received Paxlovid for treatment of covid-19, Treatment start date was 08Oct2022,Treatment stop date was 13Oct2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20221008; Test Name: COVID-19 test; Test Result: Positive ; Comments: Tested positive for Covid on Saturday 8Oct2022; Test Date: 20221016; Test Name: COVID-19 test; Test Result: Negative ; Comments: Tested negative for Covid on Sunday 16Oct.; Test Date: 20221021; Test Name: COVID-19 test; Test Result: Positive ; Comments: Tested strongly positive for Covid Friday 21Oct.; Test Date: 20221024; Test Name: COVID-19 test; Test Result: Negative ; Comments: Tested negative by Monday 24Oct.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: ADHD; Anxiety (General depression/anxiety); Depression (General depression/anxiety); Overweight
- Andere Medikamente
- PROZAC; ADDERALL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 17.10.2022
- 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: nein
Feeling abnormal
Heart rate decreased
Hyperhidrosis
Mydriasis
Nervousness
Respiration abnormal
Symptomtext
Described not feeling 'right.'Breathing off. Sats remained 99-100%. Pulse 76-88 then approximately 20 minutes after vaccine administered stated feeling shaky. Noted to be diaphoretic with diluted pupils, pulse dropped to 38-46 range. Never lost consciousness. Responding appropriately. 911 called. Refused transport to hospital multiple times. After monitoring for about 1 hour and drinking a bottle of water, stated felt better but still not right. Drove self home. Stated had appointment already scheduled with PCP next morning for a physical. Stated someone would be at home that could check on him. Refused anything to eat.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Feeling abnormal
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- unknown
- Staat
- MI
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 10.10.2022
- Impfdatum
- 02.01.2022
- Beginn
- 04.10.2022
- Tage bis Beginn
- 275,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Caesarean section
Maternal exposure before pregnancy
Symptomtext
Admission Date: 10/4/2022 Discharge Date: 10/6/2022 HOSPITAL COURSE: Patient is a 30 y.o. female G3P1021 underwent an uncomplicated cesarean delivery and was discharged home in stable condition. Delivery complicated by COVID Edinburgh Edinburgh Postnatal Depression Scale Total: 0 ESTIMATED DUE DATE: Estimated Date of Delivery: 10/10/22 GESTATIONAL AGE AT DELIVERY: 39w1d G3P1021 FINDINGS: NEWBORN STATUS: Living NEWBORN SEX: boy Delivery Date/Time: 7:36 AM WEIGHT: 3.27 kg APGAR: 1 minutes 5 minutes 10 minutes 1 4 7
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Vasomotor rhinitis Allergy to dogs Allergy to cats Allergic rhinitis due to mold Allergy to pollen Obesity in pregnancy Palpitations S/P cesarean section COVID-19 virus infection
- Andere Medikamente
- Acetaminophen (TYLENOL PO) albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler benzonatate (TESSALON) 200 MG capsule CALCIUM PO enoxaparin Sodium (LOVENOX) 40 MG/0.4ML injection ibuprofen (MOTRIN) 600 MG ta
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 04.10.2022
- Impfdatum
- 23.02.2021
- Beginn
- 30.09.2022
- Tage bis Beginn
- 584,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Symptomtext
patient hospitalized
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 30.09.2022
- Impfdatum
- 11.12.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / LA
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) (Consumer or other non HCP). The reporter is the patient. A 59-year-old male patient received BNT162b2 (BNT162B2), on 17Mar2021 as dose 1, single (Lot number: EN6206), in left arm, on 07Apr2021 as dose 2, single (Lot number: EN6204), in left arm and on 11Dec2021 as dose 3 (booster), single (Lot number: FD7218) at the age of 58 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Prostate cancer" (unspecified if ongoing). Patient had no known allergies. 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 "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Positive, notes: Indication: Treatment of COVID-19; (23Sep2022) Negative; (26Sep2022) Positive, notes: Tested positive for COVID on 26Sep2022. Therapeutic measures were taken as a result of vaccination failure, covid-19 (Paxlovid).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID-19 Test; Test Result: Positive ; Comments: Indication: Treatment of COVID-19; Test Date: 20220923; Test Name: COVID-19 Test; Test Result: Negative ; Test Date: 20220926; Test Name: COVID-19 Test; Test Result: Positive ; Comments: Tested positive for COVID on 26Sep2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Prostate cancer
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 29.09.2022
- Impfdatum
- 20.12.2021
- Beginn
- 20.09.2022
- Tage bis Beginn
- 274,0
- Dosis
- 3
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Cough
Respiratory tract congestion
Symptomtext
congestion, cough
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cough
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 10.09.2022
- Impfdatum
- 30.12.2021
- Beginn
- 16.08.2022
- Tage bis Beginn
- 229,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Disease recurrence
SARS-CoV-2 test
Vaccination failure
Symptomtext
Two days later (02Sep) I rebounded and tested positive for covid even after having completed my Paxlovid meds (20Aug).; 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 41-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 09Apr2021 as dose 1, single (Lot number: EN8730), in left arm, on 01May2021 as dose 2, single (Lot number: EW0176), in left arm and on 30Dec2021 as dose 3 (booster), single (Lot number: FD7218) at the age of 40 years, in left arm for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Past drug history included: Bactrim, reaction(s): "Known allergies: Bactrim". The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 16Aug2022, outcome "not recovered" and all described as "COVID 19 Treatment"; DISEASE RECURRENCE (medically significant) with onset 02Sep2022, outcome "not recovered", described as "Two days later (02Sep) I rebounded and tested positive for covid even after having completed my Paxlovid meds (20Aug).". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Unknown results, notes: I rebounded; (16Aug2022) Positive; (02Sep2022) Positive, notes: tested positive for covid even after having completed my Paxlovid meds. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: Patient received Paxlovid (Antiviral, Lot number: unknown) from 16Aug2022 to 21Aug2022 for COVID-19 treatment. Patient received other medication in 2 weeks was Coldeeze (Mylan consumer healthcare) from 14Aug2022 to 15Aug2022, Vitamin C from 11Aug2022 to 15Aug2022 and Vitamin D from 11Aug2022 to 15Aug2022. Patient had a lingering cough since testing positive initially on 16Aug2022. Patient was started getting intermittent headaches again on 30Aug2022 after almost two weeks of being okay. Two days later (02Sep2022) patient rebounded and tested positive for covid even after having completed my Paxlovid meds (20Aug2022).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID-19 Test; Result Unstructured Data: Test Result:Unknown results; Comments: I rebounded; Test Date: 20220816; Test Name: COVID-19 Test; Test Result: Positive ; Test Date: 20220902; Test Name: COVID-19 Test; Test Result: Positive ; Comments: tested positive for covid even after having completed my Paxlovid meds
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 08.09.2022
- Impfdatum
- 18.03.2021
- Beginn
- 14.08.2022
- Tage bis Beginn
- 514,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chest X-ray abnormal
Hypoxia
SARS-CoV-2 test positive
Symptomtext
62y.o. female with a history of CAD, COPD/asthma, and cardiac arrest 3/2022 c/b anoxic brain injury (nonverbal at baseline) and chronic respiratory failure s/p tracheostomy (3L trach collar at home) who presented from ECF 3/14 with hypoxia. She was found to be COVID positive. She was admitted to the medical floor on trach collar but than had increased oxygen requirements requiring transfer to higher level of care. A CXR was obtained that demonstrated concern for left bronchial mucus plug. The patient is known to have a #6 uncuffed Shiley. Overall long term prognosis is poor. Have been seen by palliative care and hospice in the past, however, family had desired in the past to continue with full code.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- 8/14 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC-- detected
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 06.09.2022
- Impfdatum
- 21.02.2021
- Beginn
- 20.06.2022
- Tage bis Beginn
- 484,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Biopsy site unspecified normal
Postmenopausal haemorrhage
Urinary tract infection
Vitreous floaters
Symptomtext
Post menopausal spotting. so far twice resulting in a biopsy - negative 6/22, Urinary Tract Infection (in which I haven't had one in several years), 8/22 Nitrofurantoin prescribed on the 5th day still having symptoms. Floaters in right eye, onset 8/27/22, still ongoing - haven't seen eye doctor.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Biopsy site unspecified normal
- Hospital-Tage
- -
- Labordaten
- See above
- Aktuelle Erkrankungen
- lupus, HBP, diabetic
- Vorgeschichte
- Lupus
- Andere Medikamente
- Valsartan 160 mg/12.5 mg 1x, Jentadueto 2.5 mg/1000 2x, Hydroxychloroquine 200 mg 1x (lupus), Vitamin D2 1.23 mg (50,000) 1x a week, aspirin 81 mg 1x, Raw Probiotics 85 billion 1x
- Allergien
- Sulfur
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 27.08.2022
- Impfdatum
- 15.12.2021
- Beginn
- 21.08.2022
- Tage bis Beginn
- 249,0
- 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
Covid19 infection with mild, cold-like symptoms; Covid19 infection with mild, cold-like symptoms; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from product quality group. A 28-year-old male patient received BNT162b2 (BNT162B2), on 14Mar2021 as dose 1, single (Lot number: EN6199), on 05Apr2021 as dose 2, single (Lot number: EP7533) and on 15Dec2021 as dose 3 (booster), single (Lot number: FD7218) at the age of 28 years for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 21Aug2022 at 17:30, outcome "recovering" and all described as "Covid19 infection with mild, cold-like symptoms". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Unknown results, notes: Covid19 infection with mild cold-like symptoms. Therapeutic measures were not taken as a result of vaccination failure, covid-19. Clinical course: Other vaccine in four weeks and other medications in two weeks was unknown. Covid prior vaccination and covid tested post vaccination was unknown
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: Covid 19; Result Unstructured Data: Test Result:Unknown results; Comments: Covid19 infection with mild cold-like symptoms
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 83,0
- Geschlecht
- F
- Eingang
- 26.08.2022
- Impfdatum
- 07.12.2021
- Beginn
- 18.08.2022
- Tage bis Beginn
- 254,0
- Dosis
- 3
- 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
- MA
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 25.08.2022
- Impfdatum
- 04.05.2022
- Beginn
- 22.08.2022
- Tage bis Beginn
- 110,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hyperlipidemia Mild Congntive Impairment Hypthyroidsim Chronic Obstructive Pulmonary Disease ALzheimer's Disease Type 2 Diabetes Mellitus Without Complications Age-Related Osetoporosis Major Depressive Disorder Low Back PainPaxysmal Atrial Fibrillation
- Andere Medikamente
- Acetaminophen 500 mg tabs PRN, three times a day Citalopram Hydrobromide 20 mcg Digoxin 125 mcg Docu Soft 100 mg caps Fluticasone-Sameteri 250-50mg Levtryoxine Sodium 25mcg Lidocaine 5% Patch daily Memenatine 5 mg Tabs Muxienc 600 mg Olanz
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 86,0
- Geschlecht
- M
- Eingang
- 19.08.2022
- Impfdatum
- 22.12.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Biopsy
Insulinoma
Symptomtext
In Mar2022 he had surgery for an insulinoma; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). An 87-year-old male patient received BNT162b2 (BNT162B2), on 22Dec2021 as dose 3 (booster), single (Lot number: FD7218) at the age of 86 years for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: SIMVASTATIN. Vaccination history included: BNT162b2 (Dose: 01, LOT: EN6198), administration date: 26Feb2021, when the patient was 85-year-old, for COVID-19 immunization; BNT162b2 (Dose: 02, LOT: EP7534), administration date: 19Mar2021, when the patient was 85-year-old, for COVID-19 immunization. The following information was reported: INSULINOMA (medically significant), outcome "unknown", described as "In Mar2022 he had surgery for an insulinoma". The patient underwent the following laboratory tests and procedures: Biopsy: Everything was clear and the biopsy was good., notes: Everything was clear and the biopsy was good. Therapeutic measures were taken as a result of insulinoma. Follow up information has been requested.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Biopsy
- Hospital-Tage
- -
- Labordaten
- Test Name: Biopsy; Result Unstructured Data: Test Result:Everything was clear and the biopsy was good.; Comments: Everything was clear and the biopsy was good.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- SIMVASTATIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 17.08.2022
- Impfdatum
- 07.12.2021
- 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
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 42-year-old male patient received BNT162b2 (BNT162B2), on 06Apr2021 as dose 1, single (Lot number: 8737), in right arm, on 28Apr2021 as dose 2, single (Lot number: EW0170), in right arm and on 07Dec2021 as dose 3 (booster), single (Lot number: FD7218) at the age of 41 years, in right arm for covid-19 immunisation. The patient had no relevant medical history. No known allergies. There were no concomitant medications. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: by day 11 solid positive on rapid antigen test; Positive, notes: COVID 19 Treatment; Negative, notes: Tested negative on Day 10, by day 11 solid positive on rapid antigen test. Therapeutic measures were taken as a result of vaccination failure, covid-19 included Paxlovid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: Covid-19 Rapid Antigen test; Test Result: Positive ; Comments: by day 11 solid positive on rapid antigen test; Test Name: Covid-19 test; Test Result: Positive ; Comments: COVID 19 Treatment; Test Name: Covid-19 test; Test Result: Negative ; Comments: Tested negative on Day 10, by day 11 solid positive on rapid antigen test
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Known allergies: No Other medical history: None
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 86,0
- Geschlecht
- M
- Eingang
- 13.08.2022
- Impfdatum
- 22.12.2021
- Beginn
- 01.03.2022
- Tage bis Beginn
- 69,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Biopsy
Blood glucose
COVID-19
Hypoglycaemia
Insulinoma
SARS-CoV-2 test
Vaccination failure
Symptomtext
hypoglycemia / blood sugar dropped; Husband tested positive /took Paxlovid; Husband tested positive /took Paxlovid; insulinoma; This is a spontaneous report received from contactable consumer (patient's wife). An 86-year-old male patient received BNT162b2 (BNT162B2), on 26Feb2021 as dose 1, single (Lot number: EN6198), on 19Mar2021 as dose 2, single (Lot number: EP7534) and on 22Dec2021 as dose 3 (booster), single (Lot number: FD7218) at the age of 86 years for covid-19 immunisation; coviD-19 vaccine mrna (mrna 1273) (MODERNA COVID-19 VACCINE), on 11May2022 as dose 4 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication included: SIMVASTATIN. Patient's wife reported that in Mar2022 patient had surgery for an insulinoma which is a begin tumor on the pancreas that causes the pancreas to secrete too much insulin. Took that off and didn't take much of the pancreas. Everything was clear and the biopsy was good. Has been getting along fine since then. Currently, it's August and he had Covid last week (in Aug2022), took Paxlovid from 30Jul2022 to 03Aug2022, and yesterday (09Aug2022) his blood sugar dropped to 29 and had to be taken to the hospital. Timing seems rather interesting that the Covid, Paxlovid, and then blood sugar drop when there hadn't been any problems with his blood sugar since March until now. Patient's wife is wondering about the possibility of hypoglycemia as a result of the Covid or Paxlovid. She has read where it is a possible side effect of both Covid and Paxlovid. Patient tested positive and was given Paxlovid. Finished Paxlovid a week ago today, 03Aug2022 and his blood sugar dropped yesterday (09Aug2022) and he is in the hospital. Patient's wife is wondering if this is a valid situation. She knew that not a whole lot is known about covid. patient got the Pfizer vaccines. Patient's wife did as well. She has not had covid. Wondering about the timing of this blood sugar drop though. She also reported patient's blood sugar was better as of 10Aug2022. Still hospitalized while the doctors try to figure out why this happened. On an IV that was stabilizing his blood sugar. He's not diabetic. The patient underwent the following laboratory tests and procedures: Biopsy: (Mar2022) Everything was clear and the biopsy was good; Blood glucose: (09Aug2022) 29, notes: Unit Not Provided; (Aug2022) better; SARS-CoV-2 test: (Aug2022) positive. Therapeutic measures were taken as a result of vaccination failure, covid-19, hypoglycaemia, insulinoma. Outcome of hypoglycemia and insulinoma was recovering, outcome of other events was unknown.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Biopsy
- Hospital-Tage
- -
- Labordaten
- Test Date: 202203; Test Name: Biopsy; Result Unstructured Data: Test Result:Everything was clear and the biopsy was good; Test Date: 20220809; Test Name: Blood glucose; Result Unstructured Data: Test Result:29; Comments: Unit Not Provided; Test Date: 202208; Test Name: Blood glucose; Result Unstructured Data: Test Result:better; Test Date: 202208; Test Name: Covid-19 test; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- SIMVASTATIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- M
- Eingang
- 01.08.2022
- Impfdatum
- 04.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 01.08.2022
- Impfdatum
- 22.12.2021
- Beginn
- 27.07.2022
- Tage bis Beginn
- 217,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Unevaluable event
Symptomtext
patient hospitalized
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 30.07.2022
- Impfdatum
- 17.12.2021
- 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
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 58-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 10Feb2021 at 17:30 as dose 1, single (Lot number: EM9810), in right arm, on 03Mar2021 at 15:00 as dose 2, single (Lot number: EN6202), in right arm and on 17Dec2021 at 15:00 as dose 3 (booster), single (Lot number: FD7218) at the age of 57 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "known allergies Yes" (unspecified if ongoing), notes: known allergies Yes. Concomitant medication(s) included: AMLODIPINE BESYLATE; ARMOUR THYROID; VITAMIN C [ASCORBIC ACID]; METHENAMINE HIPPURATE; GLYCOPYRROLATE; VENLAFAXINE. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: COVID 19 Treatment. Therapeutic measures were taken as a result of vaccination failure, covid-19. Paxlovid Treatment start date=25Jul2022,Lot number= 1917017A. No follow-up attempts are needed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: Covid-19 test; Test Result: Positive ; Comments: COVID 19 Treatment
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Allergy NOS (known allergies Yes)
- Andere Medikamente
- AMLODIPINE BESYLATE; ARMOUR THYROID; VITAMIN C [ASCORBIC ACID]; METHENAMINE HIPPURATE; GLYCOPYRROLATE; VENLAFAXINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 27.07.2022
- Impfdatum
- 17.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
Product administered to patient of inappropriate age
Symptomtext
Incorrect dose given to patient. Patient's age was under 12 at the time of vaccine administration and should have received the pediatric dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 22.07.2022
- Impfdatum
- 06.03.2021
- Beginn
- 23.06.2022
- Tage bis Beginn
- 474,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
COVID-19
Fall
SARS-CoV-2 test positive
Symptomtext
WEAKNESS / FALLS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asthenia
- Hospital-Tage
- 9,0
- Labordaten
- POSITIVE COVID TEST 6/23/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- ARF (acute renal failure) CHF (congestive heart failure) right mid back painj Cholecystitis with cholelithiasis Chronic pain Diabetes mellitus Type 2 Esophageal reflux Heartburn HTN (hypertension) NSTEMI (non-ST elevated myocardial infarction) Coronary artery disease involving native coronary artery of native heart Hyperlipidemia GERD (gastroesophageal reflux disease) IBS (irritable bowel syndrome) History of colonic polyps UGIB (upper gastrointestinal bleed) Renal insufficiency Weakness
- Andere Medikamente
- aspirin 81 mg oral enteric coated tablet blood sugar diagnostic (TRUE METRIX GLUCOSE TEST STRIP) Strip testing strips clopidogrel (PLAVIX) 75 mg oral tablet ginger root-pyridoxine HCl,B6, 325-25 mg oral Cap glim
- Allergien
- Metformin Simvastatin
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 19.07.2022
- Impfdatum
- 17.01.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 15,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Menstruation delayed
Oral discomfort
Ovarian cyst
Polymenorrhoea
Ultrasound scan vagina abnormal
Symptomtext
Starting 02/2022, my menstrual cycle was late by 5 days and it lasted for about a week. Then, after a few days of no period, it started again. Since then, I have had 2 periods every month to this day. My periods have normally been regular and I'm still having the burning mouth as well.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Menstruation delayed
- Hospital-Tage
- -
- Labordaten
- Vaginal Ultrasound: Cyst of one ovary.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- IBS; Interstitial Cystitis
- Andere Medikamente
- Multivitamin; elderberry; fish oil; norethindrone; gabapentin; buspirone
- Allergien
- Pertussis vaccine; CEFZIL
- Vorherige Impfungen
- Pertussis vaccine: Bad fever and was very sick and unable to finish series.
- Staat
- -
- Alter
- 87,0
- Geschlecht
- M
- Eingang
- 15.07.2022
- Impfdatum
- 21.12.2021
- Beginn
- 13.07.2022
- Tage bis Beginn
- 204,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Vaccine breakthrough infection
Symptomtext
Fully vaccinated with one booster. COVID breakthrough infection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 08.07.2022
- Impfdatum
- 06.12.2021
- Beginn
- 01.06.2022
- Tage bis Beginn
- 177,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 59-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 06Dec2021 at 15:00 as dose 3 (booster), single (Lot number: FD7218) at the age of 58 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's relevant medical history included: "Low thyroid" (unspecified if ongoing); "known allergies: Penicillin" (unspecified if ongoing), notes: known allergies: Penicillin. The patient's concomitant medications were not reported. Past drug history included: Amoxicillin, reaction(s): "known allergies: amoxicillin", notes: known allergies: amoxicillin. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Jun2022, outcome "unknown" and all described as "COVID 19 Treatment". Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: Therapeutic measures were taken as a result of events with Paxlovid. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Penicillin allergy (known allergies: Penicillin); Thyroid activity decreased
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 27.06.2022
- Impfdatum
- 14.12.2021
- Beginn
- 15.05.2022
- Tage bis Beginn
- 152,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Exercise tolerance decreased
Heart rate increased
Thyroid hormones increased
Ultrasound scan normal
Symptomtext
I started to notice that my runs were getting harder. I run for exercise and enjoyment. What used to be achieved at one pace would now be achievable at a slower pace. I have an smart watch and saw my resting heartbeat was up 20 beats per minute. I went to the doctor and got blood work done. They found that my thyroid levels were high. The initial testing indicated that it was not permanent and may note the side effect of a virus. I did a round of prednisone that was finished last week. Also, on a beta blocker to reduce heart rate. I have more tests coming up in the next few weeks to make sure that the levels continue to reduce and normalize. And just to confirm that it's not permanent. Maybe in relation to a recent virus but not entirely sure. No in the mean time of recovery, but in the process.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood test
- Hospital-Tage
- -
- Labordaten
- Blood work - higher thyroid levels, Ultrasound - nothing physical indicated, Upcoming tests in the future.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Multivitamin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 23.06.2022
- Impfdatum
- 09.12.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Symptomtext
Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 33-year-old female patient (pregnant) received BNT162b2 (BNT162B2), on 09Dec2021 as dose 3 (booster), single (Lot number: FD7218) at the age of 33 years for covid-19 immunisation; coviD-19 vaccine mrna (mrna 1273) (MODERNA COVID-19 VACCINE), on 22Apr2021 as dose 1, single (Lot number: 044b21a) and on 20May2021 as dose 2, single (Lot number: 022b21a) for covid-19 immunisation. The patient's relevant medical history included: "Intolerance to corn/soy" (unspecified if ongoing); "Intolerance to corn/soy" (unspecified if ongoing). Date of last menstrual period: 11Apr2022. The patient was 9 pregnant at the event onset. The patient is expected to deliver a baby(s) on 18Jan2023. Concomitant medication(s) included: ZOFRAN MELT; UNISOM 2; VITAMIN B6. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "Treatment of COVID-19". Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical Course: COVID rebound. Symptom free and very light antigen line by completion of paxlovid course. Symptoms returned (cough and congestion) and strong line on antigen test on day 9.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Food allergy; Soy allergy
- Andere Medikamente
- ZOFRAN MELT; UNISOM 2; VITAMIN B6
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 22.06.2022
- Impfdatum
- 25.12.2021
- Beginn
- 06.06.2022
- Tage bis Beginn
- 163,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
Tested positive 06Jun2022; Tested positive 06Jun2022; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 50-year-old male patient received BNT162b2 (BNT162B2), on 16Mar2021 at 10:00 as dose 1, single (Lot number: Ep7534), in left arm, on 06Apr2021 as dose 2, single (Lot number: ER8743), in left arm and on 25Dec2021 as dose 3 (booster), single (Lot number: FD7218) at the age of 49 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Smoke" (unspecified if ongoing). There were no concomitant medications. Patient did not had allergies. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 01Jun2022, outcome "unknown" and all described as "Tested positive 01Jun2022". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (01Jun2022) positive; (07Jun2022) Negative; (14Jun2022) positive, notes: worse symptoms; (19Jun2022) positive, notes: still. Therapeutic measures were taken as a result of vaccination failure, covid-19. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220601; Test Name: COVID-19; Test Result: Positive ; Test Date: 20220607; Test Name: COVID-19; Test Result: Negative ; Test Date: 20220614; Test Name: COVID-19; Test Result: Positive ; Comments: worse symptoms; Test Date: 20220619; Test Name: COVID-19; Test Result: Positive ; Comments: still
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Smoker
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 16.06.2022
- Impfdatum
- 16.12.2021
- Beginn
- 06.06.2022
- Tage bis Beginn
- 172,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 32-year-old male patient received BNT162b2 (BNT162B2), on 16Dec2021 as dose 3 (booster), single (Lot number: FD7218) at the age of 31 years, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 2, single (Batch/Lot number: unknown) and as dose 1, 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 06Jun2022, outcome "not recovered" and all described as "COVID 19 Treatment". Therapeutic measures were taken as a result of drug ineffective, covid-19. This report was about COVID-19 treatment. Patient did receive the vaccine. Patient received other medications in 2 weeks. Patient received treatment for COVID-19 as Paxlovid from 27May2022 to 31May2022 No follow up attempts are possible. No further information is expected.
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
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 16.06.2022
- Impfdatum
- 18.12.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- 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 contactable reporter(s) (Consumer or other non HCP) from product quality. The reporter is the patient. A 31-year-old male patient received BNT162b2 (BNT162B2), on 18Dec2021 as dose 3 (booster), single (Lot number: FD7218) at the age of 30 years for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown) for 1 day and as dose 2, single (Batch/Lot number: unknown) for 1 day for covid-19 immunisation. The patient's relevant medical history included: "Known allergies: Alpha-gal syndrome" (unspecified if ongoing), notes: Alpha-gal syndrome. The patient's concomitant medications were not reported. 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, covid-19. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Alpha-gal allergy (Alpha-gal syndrome)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 08.06.2022
- Impfdatum
- 14.12.2021
- Beginn
- -
- Tage bis Beginn
- -
- 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
Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a contactable reporter(s) (Physician) from product quality group. A 55-year-old male patient received BNT162b2 (BNT162B2), on 14Dec2021 as dose 3 (booster), single (Lot number: FD7218) at the age of 55 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's relevant medical history included: "Known allergies: penicillin" (unspecified if ongoing); "DM" (unspecified if ongoing); "HTN" (unspecified if ongoing); "hyperlipidemia" (unspecified if ongoing); "depression" (unspecified if ongoing); "fatty liver" (unspecified if ongoing); "vit D deficiency" (unspecified if ongoing), notes: other medical history: vit D deficiency. Concomitant medication(s) included in 2weeks: AMLODIPINE; GLUCOPHAGE; PRAVACHOL; SERTRALINE; VASOTEC [ENALAPRILAT]. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Unknown results, notes: Treatment of COVID-19; (21May2022) Negative, notes: testing negative 21May and 22May; (22May2022) Negative, notes: testing negative 21May and 22May; (23May2022) Positive, notes: 23May and COVID test positive. Therapeutic measures were taken as a result of drug ineffective, covid-19. Anti viral details: product=COVID 19 Treatment, brand=paxlovid, treatment start date=17May2022, treatment stop date=21May2022, indication=Treatment of COVID-19 and administrator route=Oral. Adverse event: Paxlovid rebound. Finished medication 21May testing negative 21May and 22May. Symptoms recurred with malaise and fever 23May and COVID test positive. Adverse event start date: 23May2022. This is a notification generated from the gQTS system. As part of the LOE simplification process, the following Complaint Records were classified as Product Use Attributes // Lack of Effect and have been moved to Closed (No Investigation) state referencing a previously completed investigation for the same product and lot as per the 'One and Done' business process according to in PQS Q1215 and/or Q1252. Refer to the below table for details. Product-description (CR): COMPOUND BNT 162 COVID-19 VACCINE SUSPENSION FOR INTRAMUSCULAR 2ML MULTIPLE DOSE VIAL X 1 Lot-# (CR): FD7218. Conclusion of Previously Completed Investigation (FCI/SI/OffCI)*: The complaint for lack of effect of the PFIZER BIONTECH COVID-19 VACCINE lot FD7218 was investigated. The investigation included a review of manufacturing and packaging batch records, deviation investigations, and an analysis of complaint history for the reported lot. The final scope included the reported finished goods lot FD7218, fill lot FD7213, and the formulated drug product lot FE5063. A complaint sample was not returned. No related quality issues were identified during the investigation. There is no impact to product quality. No root cause or corrective/preventative actions were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. When more than one investigation is found in the family, the Conclusion field could result in repeating rows for the CR in the table. If the Conclusion is blank in the table above, then the investigation record is likely an Offline Contractor Investigation and the conclusion must be obtained directly from the child investigation record(s) of the linked Complaint Record.; Sender's Comments: Based on the available information and the known product safety profile a causal relationship between the reported events, COVID 19, Drug Ineffective and BNT162B2 is considered possible.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID 19; Result Unstructured Data: Test Result:Unknown results; Comments: Treatment of COVID-19; Test Date: 20220521; Test Name: COVID 19; Test Result: Negative ; Comments: testing negative 21May and 22May; Test Date: 20220522; Test Name: COVID 19; Test Result: Negative ; Comments: testing negative 21May and 22May; Test Date: 20220523; Test Name: COVID 19; Test Result: Positive ; Comments: 23May and COVID test positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Depression; Diabetes mellitus; Fatty liver; Hyperlipidemia; Hypertension; Penicillin allergy; Vitamin D deficiency (other medical history: vit D deficiency)
- Andere Medikamente
- AMLODIPINE; GLUCOPHAGE; PRAVACHOL; SERTRALINE; VASOTEC [ENALAPRILAT]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 02.06.2022
- Impfdatum
- 29.10.2021
- Beginn
- 02.06.2022
- Tage bis Beginn
- 216,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
COVID vaccine breakthrough case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID positive test 6/1/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- M
- Eingang
- 28.05.2022
- Impfdatum
- 22.12.2021
- Beginn
- -
- Tage bis Beginn
- -
- 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 55-year-old male patient received BNT162b2 (BNT162B2), on 22Dec2021 at 10:00 as dose 3 (booster), single (Lot number: FD7218), in left arm for covid-19 immunisation; tamsulosin (TAMSULOSIN), from 01Mar2022 (Batch/Lot number: unknown) to 09May2022. The patient's relevant medical history included: "Enlarged prostate" (unspecified if ongoing). The patient's concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Primary Immunization series complete; unknown manufacturer), for COVID-19 Immunization. The following information was reported: DRUG INEFFECTIVE (medically significant), outcome "unknown", COVID-19 (medically significant), outcome "recovering" and all described as "Covid-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Positive, notes: Tested positive for covid and started Paxlovid May 10; (17May2022) Positive, notes: Re-tested positive for covid on May 17 and again May 20; (20May2022) Positive, notes: Re-tested positive for covid on May 17 and again May 20. Clinical Course: Tested positive for COVID and started Paxlovid 10May2022, extremely mild symptoms throughout the 5 days of treatment (stopped taking on 15May2022). Re-tested positive for COVID on 17May2022 and again 20May2022. Cold symptoms (headache, sinus congestion, coughing got worse starting 18May2022. Today, on 22May2022, the patient was still coughing and congested: unwell enough to cause me to stay home from work for at least the next 5 days. The patient plan to retest for COVID on 25May2022 to confirm if he still showing positive or not. Antiviral details: Product: COVID 19 Treatment, Paxlovid treatment started on 10May2022 to 14May2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: Covid test; Test Result: Positive ; Comments: Tested positive for covid and started Paxlovid May 10; Test Date: 20220517; Test Name: Covid test; Test Result: Positive ; Comments: Re-tested positive for covid on May 17 and again May 20; Test Date: 20220520; Test Name: Covid test; Test Result: Positive ; Comments: Re-tested positive for covid on May 17 and again May 20
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Enlarged prostate
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 27.05.2022
- Impfdatum
- 15.01.2022
- Beginn
- 26.05.2022
- Tage bis Beginn
- 131,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
COVID vaccine breakthrough case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID positive test 5/23/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 26.05.2022
- Impfdatum
- 15.12.2021
- 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
SARS-CoV-2 test
Symptomtext
indication=Treatment of COVID-19; indication=Treatment of COVID-19; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 31-year-old male patient received BNT162b2 (BNT162B2), on 30Apr2021 as dose number unknown, single (Lot number: EW0167), in left arm, on 31Jul2021 as dose number unknown, single (Lot number: EW0158), in left arm and on 15Dec2021 as dose number unknown, single (Lot number: FD7218) at the age of 30 years, in left arm for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "indication=Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (May2022) positive. Therapeutic measures were taken as a result of drug ineffective, covid-19.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202200749574 Same patient and drug, different event separated in time
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 202205; Test Name: COVID; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 86,0
- Geschlecht
- M
- Eingang
- 16.05.2022
- Impfdatum
- 12.12.2021
- Beginn
- 13.05.2022
- Tage bis Beginn
- 152,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Symptomtext
hospitalization for Covid 19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 5,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 11.05.2022
- Impfdatum
- 27.01.2021
- Beginn
- 10.02.2022
- Tage bis Beginn
- 379,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Mental status changes
SARS-CoV-2 test positive
Symptomtext
02/10/22 presents to ED for "Altered Mental Status". PMHx of "hypertension, obesity, previous uterine cancer"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- 02/11/22 SARS-CoV-2 (COVID-19) by NAA detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 29.04.2022
- Impfdatum
- 17.01.2022
- Beginn
- 28.04.2022
- Tage bis Beginn
- 101,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Exposure during pregnancy
Induced labour
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
covid vaccine breakthrough case dose 1 Pfizer 12/23/20 EK5730 dose 2 Pfizer 1/13/21 EL0142 admitted for induction of labor at 40.2
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- tested covid+ around 4/28/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 28.04.2022
- Impfdatum
- 13.12.2021
- Beginn
- 21.04.2022
- Tage bis Beginn
- 129,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
A break-through covid inflection. Tested positive on 21Apr2022; A break-through covid inflection. Tested positive on 21Apr2022; 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 13Dec2021 as dose number unknown (booster), single (Lot number: FD7218, Expiration Date: Feb2022) for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose number unknown, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 21Apr2022, outcome "unknown" and all described as "A break-through covid inflection. Tested positive on 21Apr2022". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (21Apr2022) Positive, notes: Tested positive on 21Apr2022. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220421; Test Name: Covid-19 Test; Test Result: Positive ; Comments: Tested positive on 21Apr2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 26.04.2022
- Impfdatum
- 13.12.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 19,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Menstruation irregular
Pemphigoid
SARS-CoV-2 test
Visual impairment
Symptomtext
This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 45-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 13Dec2021 as dose 3 (booster), single (Lot number: FD7218) at the age of 45 years, in left arm 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: EW0173, Location of injection: Arm Left), administration date: 30Apr2021, when the patient was 44-year-old, for Covid-19 Immunization; Pfizer (Dose Number: 1, Batch/Lot No: FW0158, Location of injection: Arm Left), administration date: 09Apr2021, when the patient was 44-year-old, for Covid-19 Immunization. The following information was reported: PEMPHIGOID (medically significant) with onset 01Jan2022, outcome "not recovered", described as "Bullous pemphigoid"; MENSTRUATION IRREGULAR (non-serious) with onset 01Jan2022, outcome "not recovered", described as "Very first month after 3shot - my period changed"; VISUAL IMPAIRMENT (non-serious) with onset 01Jan2022, outcome "not recovered", described as "eye sight changed". The events "bullous pemphigoid", "very first month after 3shot - my period changed" and "eye sight changed" required physician office visit. The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Unknown results. Therapeutic measures were taken as a result of pemphigoid, menstruation irregular, visual impairment. Additional information: The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient did not receive any other medications within 2 weeks of vaccination. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has been tested for COVID-19. Reported Event: Very first month after 3shot - my period changed and eye sight changed. Now my doctor diagnosed Bullous pemphigoid. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Menstruation irregular
- Hospital-Tage
- -
- Labordaten
- Test Name: Nasal Swab; Result Unstructured Data: Test Result: Unknown results.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 24.04.2022
- Impfdatum
- 01.01.2022
- Beginn
- 11.04.2022
- Tage bis Beginn
- 100,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Computerised tomogram
Echocardiogram
Electrocardiogram
Pericardial effusion
Symptomtext
Pericardial effusion
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Computerised tomogram
- Hospital-Tage
- -
- Labordaten
- EKG 04/14/2022 Echo-Cardiogram 04/14/2022 CT Scam 04/13/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Short Gut Syndrome
- Andere Medikamente
- Levothyroxine
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 16.04.2022
- Impfdatum
- 22.12.2021
- Beginn
- 25.12.2021
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Erythema
Eye swelling
Lip swelling
SARS-CoV-2 test
Swelling face
Symptomtext
swelling involving the forehead cheeks eyelids and lips/ facial swelling; swelling involving the forehead cheeks eyelids and lips; swelling involving the forehead cheeks eyelids and lips; Erythema; This is a spontaneous report received from a contactable reporter(s) (Pharmacist). A 44-year-old male patient received BNT162b2 (BNT162B2), on 22Dec2021 as dose 3 (booster), single (Lot number: FD7218) at the age of 44 years for covid-19 immunisation. The patient's relevant medical history included: "multiple myeloma" (unspecified if ongoing), notes: multiple myeloma with amyloidosis earlier this year, who is undergoing treatment with XRT, chemo,; "amyloidosis" (unspecified if ongoing), notes: multiple myeloma with amyloidosis earlier this year, who is undergoing treatment with XRT, chemo,; "XRT" (unspecified if ongoing), notes: multiple myeloma with amyloidosis earlier this year, who is undergoing treatment with XRT, chemo,; "chemo" (unspecified if ongoing), notes: multiple myeloma with amyloidosis earlier this year, who is undergoing treatment with XRT, chemo,. The patient's concomitant medications were not reported. Vaccination history included: BNT162b2 (Dose Number: 2, Batch/Lot No: EP7533, Manufacture: Pfizer), administration date: 24Apr2021, when the patient was 43-year-old, for Covid-19 immunization; BNT162b2 (Dose Number: 1, Batch/Lot No: EP6955, Manufacture: Pfizer), administration date: 03Apr2021, when the patient was 43-year-old, for Covid-19 immunization. The following information was reported: ERYTHEMA (hospitalization) with onset 25Dec2021, outcome "recovered"; EYE SWELLING (hospitalization), LIP SWELLING (hospitalization) all with onset 25Dec2021, outcome "recovered" and all described as "swelling involving the forehead cheeks eyelids and lips"; SWELLING FACE (hospitalization) with onset 25Dec2021, outcome "recovered", described as "swelling involving the forehead cheeks eyelids and lips/ facial swelling". The patient was hospitalized for swelling face, eye swelling, lip swelling, erythema (hospitalization duration: 3 day(s)). The events "swelling involving the forehead cheeks eyelids and lips/ facial swelling", "swelling involving the forehead cheeks eyelids and lips" and "erythema" required physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (14Mar2022) Negative, notes: Nasal Swab. Therapeutic measures were taken as a result of swelling face, eye swelling, lip swelling, erythema. Ae resulted in Doctor or other healthcare professional office/clinic visit, Emergency room/department or urgent care, Hospitalization, treatment ae was IV Steroids. COVID tested post vaccination was yes. COVID test post vaccination: COVID test type post vaccination-Nasal Swab. COVID test name post vaccination-Cepheid Expert Xpress Assay COVID test date-14Mar2022, COVID test result-Negative. Known allergies was no. Other medical history: multiple myeloma with amyloidosis earlier this year, who is undergoing treatment with XRT, chemo. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Based on available information and the drug temporal relationship, the causality between the event s - swelling face, eye swelling, lip swelling, erythema, and the suspect drug "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
- Erythema
- Hospital-Tage
- 3,0
- Labordaten
- Test Date: 20220314; Test Name: Cepheid Xpert Xpress Assay; Test Result: Negative ; Comments: Nasal Swab
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Amyloidosis (multiple myeloma with amyloidosis earlier this year, who is undergoing treatment with XRT, chemo,); Chemotherapy (multiple myeloma with amyloidosis earlier this year, who is undergoing treatment with XRT, chemo,); Multiple myeloma (multiple myeloma with amyloidosis earlier this year, who is undergoing treatment with XRT, chemo,); Radiation therapy (multiple myeloma with amyloidosis earlier this year, who is undergoing treatment with XRT, chemo,)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 05.04.2022
- Impfdatum
- 21.12.2021
- Beginn
- 07.01.2022
- Tage bis Beginn
- 17,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Delivery
Exposure during pregnancy
Normal labour
Symptomtext
Normal labor and delivery on 1/7/2022. Hospital admission within 6 weeks of receiving the COVID vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Delivery
- Hospital-Tage
- 1,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -