- Staat
- -
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 15.08.2023
- Impfdatum
- 16.12.2021
- Beginn
- 15.08.2022
- Tage bis Beginn
- 242,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Pulmonary embolism
Reversible ischaemic neurological deficit
Symptomtext
REVERSIBLE ISCHEMIC NEUROLOGIC DEFICIT SYNDROME ACUTE PULMONARY EMBOLISM
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary embolism
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 31.01.2023
- Impfdatum
- 28.12.2021
- Beginn
- 03.03.2022
- Tage bis Beginn
- 65,0
- Dosis
- 1
- Route/Site
- IM / AR
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Amyotrophic lateral sclerosis
Blood test
Computerised tomogram
Death
Dysarthria
Dysphagia
Fall
Magnetic resonance imaging
Symptomtext
One month after the second vaccine she developed slurred speech, difficulty swallowing and frequent falls. She was a healthy, active lady before these events. After much testing, and hospitaliztions, a neurologist at local Hospital diagnosed her with Bulbar ALS. her symptoms progressed quickly, and she passed away on November 7th, 2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- CT scans MRI blood tests
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Kidney stones
- Andere Medikamente
- Metropolol
- Allergien
- PCN
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 09.12.2022
- Impfdatum
- 27.12.2021
- Beginn
- 28.11.2022
- Tage bis Beginn
- 336,0
- Dosis
- 2
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Acute respiratory failure
COVID-19
Symptomtext
Hospitalization for Acute Repiratory Failure due to COVID-19 on dates 11/28/2022- 12/5/2022. Treated with dexamethasone, baricitinib, Remdesivir, vitamin C 1,000 mg PO daily, vitamin D 25 mcg PO daily, zinc 50 mg PO daily.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 8,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- morphine (anaphylaxis), heparin (itching), NSAIDs (to protect her one kidney)
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 23.11.2022
- Impfdatum
- 11.01.2022
- Beginn
- 20.10.2022
- Tage bis Beginn
- 282,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Asthenia
Atelectasis
C-reactive protein increased
COVID-19
Chest X-ray abnormal
Cough
Obesity
Pulmonary fibrosis
Pyrexia
Red blood cell sedimentation rate increased
SARS-CoV-2 test positive
Systemic inflammatory response syndrome
Viral sepsis
Symptomtext
Patient is a 79 y.o. male patient of MD with history of pulmonary embolism, stroke, traumatic brain injury, aspiration risk presented with COVID-19 infection Acute hypoxic respiratory failure Viral sepsis due to Covid-19 Virus infection Date of onset of symptoms: 10/18/2022 Symptoms present on admission: Fever, cough, weakness Date of covid positive test: 10/20/2022 Vaccination status: vaccinated. Patient is unsure if had booster Imaging: Chest x-ray shows left basilar atelectasis/scarring Oxygen requirements on admission: 2 L Current oxygen requirements: room air Medical therapy: Remdesivir and Steroids (10 days total of therapy) Consultants following: None Anticipated special isolation end date: 10/28/22 CRP 40, ESR 18 SIRS (+) Albuterol, Tessalon Perles, Robitussin PRN IS Home O2 eval today. Does not qualify for home oxygen Discharge on Decadron x7 more days, and Tessalon Perles PRN History of pulmonary embolism Continue Apixaban Traumatic brain injury At baseline able to walk with help of walker Continue Baclofen 10mg TID PRN, Donepezil 5mg, Lexapro 20mg, Remeron 7.5mg HS Continue aspiration precautions PT/OT/CM consulted. 2-3 days per week of therapy. HHC at discharge Obesity BMI 30.9 Recommend lifestyle changes
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 82,0
- Geschlecht
- M
- Eingang
- 23.11.2022
- Impfdatum
- 04.02.2022
- Beginn
- 18.11.2022
- Tage bis Beginn
- 287,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain
Acute respiratory failure
Aspiration
Barium swallow
Blood lactic acid increased
Angiogram pulmonary abnormal
Atelectasis
Bacterial disease carrier
Blood culture positive
Blood lactic acid
Brain natriuretic peptide increased
COVID-19
COVID-19 pneumonia
Chemotherapy
Blood pH decreased
Chest X-ray abnormal
Dysphagia
Dyspnoea
Symptomtext
PRESENTING PROBLEM: Acute on chronic respiratory failure with hypoxia and hypercapnia (HCC) HOSPITAL COURSE: Patient is an 83 y.o. male with history of oxygen-dependent COPD (on 2 L oxygen at baseline), stage IV adenocarcinoma of the left lung on chemotherapy, chronic pain, paroxysmal atrial fibrillation, and recent hospitalization for COVID-19 who presented with increased shortness of breath and nausea with vomiting. Symptoms started about 1-2 hours after eating chili and fries at a restaurant. Had frequent vomiting, was eventually placed on BIPAP per EMS then weaned to nasal cannula. Work-up did reveal elevated lactic acid, respiratory acidosis (pH 7.21, pCO2 69), WBC count 27.7, hsTnT 25-33. Chest x-ray suggested patchy infiltrate in left lung base suggestive of pneumonia and small layering left pleural effusion (present previously). He was started on IV Cefepime and IV Vancomycin and improved clinically with a 5-day course. He did have abdominal pain that improved with Maalox. He was evaluated by SLP who performed a videofluroscopy swallow study which showed mild-moderate pharyngeal dysphagia and aspiration with thin liquids. He was recommended general solids, thin liquids, liquids by cup, no straws, meds in appelsauce and strategies for safe oral intake including chin tuck, upright for all intake, repeat swallow, small bites and small sips. Patient had no further abdominal pain. He was clinically improved and discharged in stable condition.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- *** PREVIOUS VAERS SUBMITTED ON 10/26/2022*** Respiratory Adenocarcinoma of lung, left (HCC) Pneumonia due to COVID-19 virus Circulatory Cardiomyopathy, unspecified type (HCC) Paroxysmal atrial fibrillation (HCC) Digestive Dysphagia Alternating constipation and diarrhea Nervous Cancer related pain Other Age-related osteoporosis without current pathological fracture Secondary malignant neoplasm of bone (HCC) Opiate analgesic use agreement exists Poor appetite
- Andere Medikamente
- albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler apixaban (ELIQUIS) 2.5 MG tablet bisacodyl (DULCOLAX) 5 MG enteric coated tablet carboxymethylcellulose (REFRESH PLUS) 0.5 % SOLN digoxin (LANOXIN) 125 MC
- Allergien
- wellbutrin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 31.10.2022
- Impfdatum
- 05.03.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- 118,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Anticoagulant therapy
Cardio-respiratory arrest
Cerebrovascular accident
Chest discomfort
Computerised tomogram head abnormal
Dyspnoea
Feeling abnormal
Hypertension
Infection
Myocardial infarction
Thrombosis
Vision blurred
Symptomtext
The first of July, I was having difficulty breathing and chest tightness. I went to an urgent care for an infection in my ankle. They prescribed antibiotics for my ankle. I needed a second round of antibiotics. They told me my blood pressure was high at that time. The chest tightness and difficulty breathing were still present, but they didn?t seem concerned about it. A week later, I started feeling bad and had my son call the ambulance. I threw a clot. I coded in the ambulance. When I woke up, I had been out for a while. I found out I had a heart attack. I received blood pressure medication from the nurse. As I was telling her I felt weird, my vision blurred. I had a stroke in the left occipital lobe. They did a CT scan to see I had a stroke. After about a week in the hospital, they gave my blood thinners and oxygen and sent me home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cardio-respiratory arrest
- Hospital-Tage
- 9,0
- Labordaten
- 08/23/2022 CT Scan - Stroke Occipital Lobe
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Type 2 Diabetes; Hypertension
- Andere Medikamente
- Turmeric; Folic Acid; Aspirin; Niacin; Vitamin B Complex
- Allergien
- Perfume; Seasonal; Sulpha Drugs
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 04.03.2022
- Impfdatum
- 31.12.2021
- Beginn
- 05.01.2022
- Tage bis Beginn
- 5,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Angiogram pulmonary abnormal
Anticoagulant therapy
Atelectasis
Blood pressure systolic
Chest X-ray abnormal
Computerised tomogram head normal
Diabetes mellitus
Disorientation
Dizziness
Dyspnoea
Electrocardiogram abnormal
Electrocardiogram normal
Fibrin D dimer increased
Hypoxia
Mitral valve calcification
Myocardial infarction
Oxygen saturation decreased
Pulmonary arterial hypertension
Symptomtext
On January 5, 2022, I woke up feeling dizzy, light headed, disoriented and had trouble breathing. My blood pressure was 90 systolic and my oxygen level/O2 saturation was at 85%, both taken at home. Since both were low, I was taken to the local ER. I was admitted to the hospital. Principal diagnosis was right pulmonary embolus, associated diagnosis was hypoxia, elevated troponin, and diabetes melititus. I was discharged on January 8, 2022 after being given Eliquis to dissolve the blood clots and will remain on this medication until further notice from PCP.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocardial infarction
- Hospital-Tage
- 4,0
- Labordaten
- Medical tests on 01/05/2022 include: CT angiography chest - Numerous segmental and subsegmental filling detfects in the right upper, middle and lower lobe, consistent with acute pulmonary embolism. No findings of right heart strain. Coarse mitral annular calcifications Pulmonary artery is dilated to 4 cm diameter which may suggest pulmonary arterial hypertension. CT Heah Scan W/O Contrast - No acute intracranial abnormality. Xray chest - The heart size and mediastinum are unremarkable. There unchanged mild areas of atelectasis or scarring at the left lung base. The lungs are otherwise well aerated without inflirated or effusion. ECG - EKG shows heart rate of 70, no ST-T changes, no ectopy, normal intervals. ECG - Septal Myocardial Infarction of indeterminate age Doppler ultrasound on lower extremities - unremarkable for DVT. D-Dimer - 20.00 Troponin - 186 and 144 (high)
- Aktuelle Erkrankungen
- High Blood Pressure, Hligh Cholesterol, Pre-diabetes, Osteoarthritis, Osteopenia, Obesity
- Vorgeschichte
- High Blood presure, high cholesterol, pre-diabetes, Osteoarthritis, Osteopenia, Obesity
- Andere Medikamente
- Telmisartan, Atorvastatin, Vitamin D2 ERGO, Zinc, Ketorolac Tromethamine ophthalmic and prednisoLONE acetate 1% opthlamic right eye only
- Allergien
- Codeine and Chlorohydrothiazide,
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 84,0
- Geschlecht
- M
- Eingang
- 27.02.2022
- Impfdatum
- 29.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Death
Dizziness
Fall
Symptomtext
Day after vaccine, family reported that patient dizzy and frequently falling. They were monitoring blood pressure and temperature which were within normal range. Admitted to hospital on 1/2/22. Died 1/23/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- 21,0
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- -
- Geschlecht
- M
- Eingang
- 14.01.2022
- Impfdatum
- 01.11.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Balance disorder
Cerebrovascular accident
Illness
Immunisation
Nausea
Sleep disorder
White blood cell count
White blood cell count abnormal
Symptomtext
booster shot; its kind of ?stroke'; nauseous; lack of balance; I went to bed for 12 hours before I could even get up and function; I am speeding up a clear substance looks like white blood cell or something ''flams'' it comes up all the times; I got terrible adverse effect; I got definitely ill on both of the shot, terribly ill; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. An 80 year-old male patient received bnt162b2 (BNT162B2), administration date Nov2021 (Lot number: 330258D) as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Enlarged prostate" (unspecified if ongoing). Concomitant medication(s) included: TAMSULOSINE HCL taken for prostatomegaly. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE.), administration date: 06Mar2021, when the patient was 79 years old, for COVID-19 immunization, reaction(s): "no adverse event from this first shot"; Bnt162b2 (DOSE 2, SINGLE.), administration date: 2021, for COVID-19 immunization, reaction(s): "Nauseous"; Bnt162b2 (DOSE 2, SINGLE., Verbatim: I had the same reaction to Pfizer 2 shot, I have lack of balance), administration date: 2021, for COVID-19 immunization, reaction(s): "lack of balance"; Bnt162b2 (DOSE 2, SINGLE., Verbatim: I had the same reaction to Pfizer 2 shot, I have essentially I went to bed for 12 hours before I can even get up and function), administration date: 2021, for COVID-19 immunization, reaction(s): "I went to bed for 12 hours before I can even get up and function"; Bnt162b2 (DOSE 2, SINGLE., Verbatim: I had the same reaction to Pfizer 2 shot, I have its kind of 'stroke'), administration date: 2021, for COVID-19 immunization, reaction(s): "its kind of ?stroke"; Bnt162b2 (DOSE 2, SINGLE., Verbatim: number 2 Pfizer I am speeding up a clear substance looks like white blood cell or something 'flams' it comes up all the times), administration date: 2021, for COVID-19 immunization, reaction(s): "I am speeding up a clear substance looks like white blood cell or something ''flams'' it comes up all the times". The following information was reported: IMMUNISATION (medically significant) with onset Nov2021, outcome "unknown", described as "booster shot"; CEREBROVASCULAR ACCIDENT (medically significant) with onset 2021, outcome "unknown", described as "its kind of ?stroke'"; NAUSEA (non-serious) with onset 2021, outcome "unknown", described as "nauseous"; BALANCE DISORDER (non-serious) with onset 2021, outcome "unknown", described as "lack of balance"; SLEEP DISORDER (non-serious) with onset 2021, outcome "unknown", described as "I went to bed for 12 hours before I could even get up and function"; WHITE BLOOD CELL COUNT ABNORMAL (non-serious) with onset 2021, outcome "unknown", described as "I am speeding up a clear substance looks like white blood cell or something ''flams'' it comes up all the times"; ILLNESS (non-serious) with onset 2021, outcome "unknown", described as "I got terrible adverse effect; I got definitely ill on both of the shot, terribly ill". The patient underwent the following laboratory tests and procedures: white blood cell count: (2021) abnormal, notes: White blood cell count Abnormal. Therapeutic measures were not taken as a result of cerebrovascular accident, nausea, balance disorder, white blood cell count abnormal, illness. Therapeutic measures were taken as a result of sleep disorder. The consumer want to report an adverse effect from your Pfizer booster shot and actually your Pfizer number 2, I got definitely ill on both of the shot, terribly ill. While confirming the product as Pfizer COVID-19 Vaccine, Consumer stated, "Yeah the booster shot which I had last month I got terrible adverse effect from it and I had the same reaction to Pfizer 2 shot, I have nauseous, lack of balance, essentially I went to bed for 12 hours before I can even get up and function, its kind of 'stroke' (Not Clarified)." Concomitant medication: Consumer stated, no unless you wanna consider Flomax medication. Its for enlarged prostate there is a technical name for it I can read it off here, Tamsulosin HCL. Treatment for adverse event: Consumer stated, no I didn't take any treatment for that except sleep. Consumer stated, no but I have one question I don't know if you can answer or not. Is the side effect from this drug, this shot booster and number 2 Pfizer I am speeding up a clear substance looks like white blood cell or something 'flams' it comes up all the times. I have 2 friends that are having the same condition and we are wondering if this related to this COVID shot. It seems kind of funny that all of us are having the same issue. Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- -
- Labordaten
- Test Date: 2021; Test Name: White blood cell count; Result Unstructured Data: Test Result:Abnormal; Comments: White blood cell count Abnormal
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Enlarged prostate
- Andere Medikamente
- TAMSULOSINE HCL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- -
- Geschlecht
- M
- Eingang
- 14.01.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Balance disorder
Cerebrovascular accident
Feeling abnormal
Illness
Nausea
Sleep disorder
Symptomtext
I went to bed for 12 hours before I could even get up and function, its kind of ?stroke'; nauseous; lack of balance; I went to bed for 12 hours before I could even get up and function; I am speeding up a clear substance looks like white blood cell or something ''flams'' it comes up all the times; I got terrible adverse effect; I got definitely ill on both of the shot, terribly ill; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 80 year-old male patient received bnt162b2 (BNT162B2), administration date 2021 (Lot number: 330258D) as dose 2, single for covid-19 immunisation. Relevant medical history included: "Enlarged prostate" (unspecified if ongoing), notes: Verbatim: Enlarged prostate. Concomitant medication(s) included: TAMSULOSIN HYDROCHLORIDE taken for prostatomegaly. Vaccination history included: Bnt162b2 (1st dose of covid vaccine), administration date: 06Mar2021, when the patient was 79 years old, for COVID-19 Immunization, reaction(s): "I had no adverse event from this first shot.". The following information was reported: CEREBROVASCULAR ACCIDENT (medically significant) with onset 2021, outcome "unknown", described as "I went to bed for 12 hours before I could even get up and function, its kind of ?stroke'"; NAUSEA (non-serious) with onset 2021, outcome "unknown", described as "nauseous"; BALANCE DISORDER (non-serious) with onset 2021, outcome "unknown", described as "lack of balance"; SLEEP DISORDER (non-serious) with onset 2021, outcome "unknown", described as "I went to bed for 12 hours before I could even get up and function"; FEELING ABNORMAL (non-serious) with onset 2021, outcome "unknown", described as "I am speeding up a clear substance looks like white blood cell or something ''flams'' it comes up all the times"; ILLNESS (non-serious) with onset 2021, outcome "unknown", described as "I got terrible adverse effect; I got definitely ill on both of the shot, terribly ill". Therapeutic measures were not taken as a result of cerebrovascular accident, nausea, balance disorder, feeling abnormal, illness. Therapeutic measures were taken as a result of sleep disorder. NDC and UPC number of COVID-19 Vaccine were unknown. Treatment for Adverse Event: Consumer stated, "No I didn't take any treatment for that except sleep." No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Enlarged prostate (Verbatim: Enlarged prostate)
- Andere Medikamente
- TAMSULOSIN HYDROCHLORIDE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 04.01.2022
- Impfdatum
- 23.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 6,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
COVID-19
COVID-19 pneumonia
Immunodeficiency
SARS-CoV-2 test positive
Symptomtext
Patient received Pfizer COVID vaccine first 2 doses (3/2/21 lot # EN6200 and 3/31/21 lot # ER8737). While in state, patient received the third Pfizer COVID vaccine dose on 12/23/21. On 12/29/21, patient admitted to our inpatient facility with acute respiratory failure with hypoxia due to COVID pneumonia. Patient most likely got COVID during her immunocompromised state while on 18-day prednisone taper started on 12/10/21 for atopic dermatitis. As of today (1/4/22), patient is still admitted in our med/surg unit.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 6,0
- Labordaten
- COVID status positive on 12/29/21.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- hypertension, asthma, hyperlipidemia and atopic dermatitis on steroid taper for the past 2 weeks (as of 12/29/21)
- Andere Medikamente
- amlodipine, atorvastatin, betamethasone augmented oint, cetrizine, diphenhydramine, fluticasone/salmeterol 250/50 diskus inh, hydrochlorothiazide, prednisone
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 28.12.2022
- Impfdatum
- 01.12.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Amnesia
Aphasia
Computerised tomogram head
Condition aggravated
Disorientation
Drug level
Drug screen
Seizure
Unresponsive to stimuli
Symptomtext
My initial two (Moderna) vaccines in March 2021 made me very ill (103/104 degree fever), but it lasted less than 24 hours. I had my booster vaccine on December 27, 2021. A few hours later I had a seizure. I had at least three more over the next 12 hours. Due to my disorientation and inability to speak or follow instructions, I was admitted to the hospital overnight. I had significant memory loss from before my vaccination until about a week later. I have had seizures in the past but it had been over 15 years since my last one, I was taking medication, and none of my known risk factors were present. I also had never had multiple seizures or memory loss. I had another seizure in August 2022 for no apparent reason and with no other health changes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- 1,0
- Labordaten
- Head CT, Lamictal level, drug panel
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Lamictal (prescription, 300mg/day)
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 14.02.2022
- Impfdatum
- 08.01.2022
- Beginn
- 25.01.2022
- Tage bis Beginn
- 17,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: ja
ER: unbekannt
Erholt: nein
Cardiac index decreased
Dyspnoea
Ejection fraction decreased
Loss of personal independence in daily activities
Lung assist device therapy
Myocarditis
Supraventricular tachycardia
Symptomtext
Pt presented 1/25 with symptoms of shortness of breath x 1 day. Found to be in SVT with EF 15% CI 1.3 myocarditis of unclear etiology: possibly tachycarrhythmia-mediated vs fulminant viral myocarditis vs sequelae of connective tissue disorder. Patient was previously working and active 1/23. Pt now requiring ecmo plan to transition to LVAD/ RVAD.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocarditis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- BMI 26
- Andere Medikamente
- none
- Allergien
- nkda
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 10.02.2022
- Impfdatum
- 09.02.2022
- Beginn
- 10.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Dizziness
Electrocardiogram
Pallor
Syncope
Symptomtext
We had a 14 year old female who had a Vasovagal syncope episode in the outpatient pharmacy after a booster dose of Pfizer was administered to her. We called a rapid response team after assessing the child when the parent reported that the patient was feeling dizzy and upon examination had also turned very pale. We provided a snack, water, and Pedialyte to the patient before she was taken to the ER. Patient was discharge from the ER later in the afternoon. BP 101/68, Pulse 64, Temp 36.8 C, Resp 18, SpO2 99%. ED discharge diagnoses was Vasovagal episode after vaccination and dehydration.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- ECG 12 Lead performed in ER.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 25.01.2022
- Impfdatum
- 15.12.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Back pain
Balance disorder
Chest pain
Gait inability
Immobile
Muscle contractions involuntary
Muscle twitching
Pain in extremity
Paralysis
Symptomtext
This statement is solely contingent on the symptoms that i have developed and or aquired after the pfizer booster shot i received on 12/15/2021. I started developing symptoms of imbalance 2 days after (12/19/2021) teh booster was administered. I was experiencing pains in my back, left arm, and under neath my breast. I developed severe twitching and involuntary muscle contractions. By the date of 12/20/2021 i was unable to walk. i have become completely immobile from the waist down. i am somewhat paralyzed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paralysis
- Hospital-Tage
- -
- Labordaten
- 12/28/2021 local Health clinic and emergency room
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- High blood pressure
- Andere Medikamente
- Losortan 100mg cut in half taken twice daily, vitamin c, vitamin d, irish seamoss, asprin
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 13.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 4,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Electrocardiogram
Magnetic resonance imaging
Seizure
Symptomtext
Patient experienced a seizure 4 days after 2 dose of pfizer vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 13.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 4,0
- Dosis
- 2
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Electrocardiogram
Magnetic resonance imaging
Seizure
Symptomtext
Patient experienced a seizure 4 days after 2 dose of pfizer vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 05.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood glucose normal
Dizziness
Electrocardiogram normal
Loss of consciousness
Unresponsive to stimuli
Symptomtext
Patient reported feeling light headed after receiving second vaccine (Fluarix) and quickly loss consciousness. The technician called for the pharmacist to assist and 911 was called. Patient was unresponsive for approx. 1min. At which time a pulse was found and normal breath sounds were present. She was seated on the bench where the vaccine was administered. Her head was supported and began to respond. She reported being able to hear, but not respond. EMS checked glucose and did an EKG . No issues found. Patient reported that these episodes occurred frequently as a child. but had been without an episode in many years. She decided not to go to the hospital and her parents arrived to take her home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- EKG and glucose test both were negative
- Aktuelle Erkrankungen
- None reported
- Vorgeschichte
- Patient has history of syncope after vaccinations/blood draws, but has not had episode in many years
- Andere Medikamente
- NK
- Allergien
- NKA
- Vorherige Impfungen
- routine childhood vaccines
- Staat
- IL
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 26.12.2021
- Impfdatum
- 26.12.2021
- Beginn
- 26.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Eye movement disorder
Muscle rigidity
Syncope
Symptomtext
Mother stated her daughter's body became rigid, her eyes rolled back, and she briefly fainted. Paramedics were called and she was taken to hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- unknown
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 16.12.2021
- 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: nein
Chest discomfort
Chest pain
Discomfort
Dyspnoea
Myocarditis
Symptomtext
I received a COVID19 booster shot and a seasonal Flu shot in my left and right arms respectively at around 11:30 AM on 12/14/21. I waited for 20 minutes in their auditorium before leaving. I felt no major effects until the following morning at maybe around 10 AM on 12/15. I think it could be myocarditis because my chest, specifically around my heart feels tight and even slightly painful at times. I researched other symptoms of myocarditis, but I don't think I'm experiencing shortness of breath or abnormal rhythms. It almost feels like I over-worked my left pectoral muscles... but the feeling is deeper in my chest, so it's probably my heart... which is a new and uncomfortable sensation to say the least. FYI, I received my second dose of the initial Pfizer vaccine on 4/28/21 and had no major side effects. I have not yet seen a doctor about this, and likely won't as I'm currently uninsured. But, I thought I ought to report my symptoms for the record. I hope the symptoms subside soon.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocarditis
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- occasional antihistamines for seasonal allergies
- Allergien
- peanuts, pistachios, potentially other nuts?
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 90,0
- Geschlecht
- M
- Eingang
- 07.11.2023
- Impfdatum
- 10.01.2022
- Beginn
- 24.10.2023
- Tage bis Beginn
- 652,0
- Dosis
- 3
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Cardiac failure congestive
Condition aggravated
Pleural effusion
SARS-CoV-2 test positive
Troponin increased
Symptomtext
Hospitalization for acute CHF exacerbation and bilateral pleural effusions, elevated troponins, tested covid positive on admission day, 10/24/2023 on dates 10/24/2023- 10/27/2023. Treated with vitamin C 1,000 mg PO daily, zinc 50 mg PO daily.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 21.08.2023
- Impfdatum
- 28.12.2021
- Beginn
- 09.08.2023
- Tage bis Beginn
- 589,0
- Dosis
- 3
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Accelerated hypertension
COVID-19
Chest pain
Hypomagnesaemia
Troponin increased
Symptomtext
Hospitalization for chest pain, accelerated hypertension, elevated troponin level, hypomagnesemia, and COVID-19 on dates 8/9/2023-8/12/2023. Treated with dexamethasone, Remdesivir, vitamin C 1,000 mg PO daily, vitamin D 25 mcg PO daily, zinc 50 mg PO daily.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Accelerated hypertension
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- hydrocodone, zolpidem
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 88,0
- Geschlecht
- F
- Eingang
- 09.06.2023
- Impfdatum
- 01.02.2022
- Beginn
- 06.06.2023
- Tage bis Beginn
- 490,0
- Dosis
- 2
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Alanine aminotransferase normal
Anion gap
Aspartate aminotransferase increased
Asthenia
Atelectasis
Basophil count decreased
Basophil percentage decreased
Blood albumin normal
Blood alkaline phosphatase normal
Blood bilirubin normal
Blood calcium decreased
Blood chloride decreased
Blood creatinine increased
Blood glucose normal
Blood potassium decreased
Blood sodium normal
Blood urea increased
Carbon dioxide increased
Symptomtext
Document Type: ED Physician Progress Note Document Subject: ED Progress Note Performed By: on June 06, 2023 20:58 EDT Verified By: MD on June 09, 2023 00:57 EDT Encounter Info: Hospital, Observation, 06/06/23 - * Final Report * Basic Information Time Seen: MD / 06/06/2023 20:46 Chief Complaint SOA History of Present Illness Patient Seen: 06/06/23 20:57:06 89 year old female presents to the ED via private vehicle complaining of hypotension. Pt lives at an assisted living facility and called her family friend earlier this evening regarding her shortness of breath, weakness, and low BP for the past several days. Her friend, who accompanies her in ED, states pt's O2 reading at the facility was 88. Endorses ankle swelling and cough x3 days. Denies fever, chills, or chest pain. She uses a walker to ambulate and reports increased difficulty over the past few days since onset of symptoms. Review of Systems Refer to HPI for pertinent positives and negatives noted on review of systems. Physical Exam/Objective Vitals & Measurements most recent T: 37 ?C (Oral) BP: 93/58 HR: 104 (Monitored) RR: 20 SpO2: 99% Oxygen Therapy: Nasal Cannula Oxygen Flow Rate: 2 (L/min) WT: 49.67 kg (Ideal Body Weight Calculated) WT: 68.2 kg WT: 49.665 kg (Ideal Body Weight Calculated) HT: 157 cm General: alert, no acute distress Skin: warm, dry , pink, no pallor, no rash Head: normocephalic Eye: PERRLA, EOMI, normal conjunctiva ENT: oral mucosa moist , no pharyngeal erythema or exudate Neck: supple Cardiovascular: tachycardic rate and regular rhythm , no murmur, no edema Respiratory: expiratory wheezes, bibasilar crackles Chest Wall: no deformity, no tenderness Back: normal ROM Gastrointestinal: soft, non tender , non distended , normal BS,, no organomegaly Extremities: no tenderness , normal ROM, normal strength, no swelling Neurological: no focal neuro deficits , A&O x4, CN II - XII intact, normal sensory, normal motor, normal speech Psych: cooperative , appropriate mood and affect Medical Decision Making DDx includes but is not limited to: pneumonia, sepsis, CHF exacerbation, hypovolemia, COPD exacerbation, other SOB, PE, other generalized weakness Documentation Review: PCP note (2/20/23), Nursing Notes I have ordered the following tests: basic labs, D dimer, lactate, urine, troponin, EKG, CXR Symptomatic Management provided: IVF_ Pain Control_Antibiotics _Other: Breathing Tx LabsReviewed ImagingReviewed EKGReviewed EKG Interpretation: Date: 6/6/23 Time: 20:15 Rhythm: atrial-sensed ventricular-paced rhythm Rate: 106 bpm PR interval: 162 ms QRS duration: 118 ms QT/QTc: 398/528 ms P-R-T axes: 48 92 23 Comments: no significant changes compared to prior tracing on 12/6/22 Additional Orders: None Results Discussion: CBC is mostly WNL, Creatinine is 1.5, which is improved from prior. CXR shows bilateral opacifications at bases, per my review. Consults: Hospitalist Social Determinants of Health: Polypharmacy; lives at ECF 06/07/23 00:20:10 Chose not to give patient IV fluids, given her history of heart failure. Her BP and HR have improved without medicine or fluids. Suspect polypharmacy has been contributing to her low BP. She has been asking for her home Norco and Xanax pills, but I have not given them, as she is hypotensive. 06/07/23 00:30:36 Pt's CXR shows new bilateral lower infiltrates. Her troponin and repeat troponin were both elevated at 15 and 17, respectively. Her D-dimer was elevated but CTA chest can not be obtained at this time as her creatine clearance is low. Will seek admission for the patient. Disposition: Admit to Dr. here at hospital Condition Stable Assessment/Plan Chronic heart failure with preserved ejection fraction (HFpEF) I50.32 Chronic, continuous use of opioids F11.90 COPD with emphysema J43.9 Hypotension I95.9 Pneumonia J18.9 Orders: Blood CX Blood CX Follow Up No qualifying data available Chronic Problem List Anxiety and depression Aortic stenosis Chronic heart failure with preserved ejection fraction (HFpEF) Chronic kidney disease stage 3 (disorder) Chronic kidney disease stage 4 (disorder) Chronic pain syndrome Chronic, continuous use of opioids COPD with emphysema Elevated troponin Encounter for long-term current use of medication Fatigue History of colon polyps HTN (hypertension) Hyperlipidemia Hypertension Hypothyroidism Hypoxia Iron deficiency anemia Long term use of drug Low back pain Lupus Medication management Nonrheumatic aortic valve stenosis with insufficiency Obstructive hypertrophic cardiomyopathy Pacemaker Peripheral edema Pulmonary emphysema (disorder) S/P TAVR (transcatheter aortic valve replacement) Systemic lupus erythematosus (disorder) Tachycardia Thoracic back pain UTI (urinary tract infection) Procedure/Surgical History ?cardiac cath (04/15/2019) ?bunionectomy (11/13/2018) ?Colonoscopy (03/11/2016) ?Mammogram - screening (05/14/2012) ?bunionectomy (1960) ?Appendectomy ?LEEP ?Tonsillectomy ?Vocal cord nodule Surgical History Internal 11/07/2019 Transcatheter Aortic Valve Replacement MD 11/13/2018 Hammertoe Repair (Left) DPM 03/11/2016 Colonscpy Diagnostic/Screen MD Medications Home Medications (15) Active atorvastatin 40 mg oral tablet 40 mg = 1 Tablet, Orally, At Bedtime clopidogrel 75 mg oral tablet 75 mg = 1 Tablet, Orally, Daily ferrous sulfate 325 mg (65 mg elemental iron) oral delayed release tablet 325 mg = 1 Tablet, Orally, Daily hydroCODONE-acetaminophen 10 mg-325 mg oral tablet 1 Tablet, PRN, Orally, TID hydroCODONE-acetaminophen 10 mg-325 mg oral tablet 1 Tablet, PRN, Orally, TID levothyroxine 88 mCg (0.088 mg) oral tablet 88 mCg = 1 Tablet, Orally, Daily metoPROLOL tartrate 50 mg oral tablet 50 mg = 1 Tablet, Orally, BID MiraLax oral powder for reconstitution 17 GM, Orally, Daily, dissolve in water before taking Mirapex 0.5 mg oral tablet 0.5 mg = 1 Tablet, Orally, At Bedtime multivitamin with minerals oral tablet 1 Tablet, Orally, Daily olanzapine 5 mg oral tablet 5 mg = 1 Tablet, Orally, TID Plaquenil 200 mg oral tablet 200 mg = 1 Tablet, Orally, Daily potassium chloride 99 mg oral tablet 99 mg = 1 Tablet, Orally, Daily predniSONE 10 mg oral tablet See Instructions, 4 tab x 3 days, then 3 tab x 3 days, then 2 tab x 3 days, then 1 tab x 3 days Xanax 0.5 mg oral tablet 0.5 mg = 1 Tablet, PRN, Orally, TID Medication Administration Given albuterol 2.5 mg/0.5mL (0.5%) inhalation solution, 5 mg, Neb Inhal ipratropium 0.5 mg/2.5 mL (0.02%) inhalation solution, 0.5 mg, Neb Inhal Allergies sulfa drugs (Unknown) Social History Alcohol Denies Electronic Cigarette/Vaping E-Cigarette Use 26-50 inhales/day. Employment/School Retired Home/Environment Lives with Alone. Substance Abuse Denies Tobacco Tobacco Use: Former smoker, quit more than 30 days ago. Family History Heart attack..: Father. Stroke: Mother. Lab Results Hemogram-Platelets-WBC Differential FS LATEST RESULTS HISTORICAL RESULTS WBC 06/08/23 03:41 9.5 02/09/23 11.3 High RBC 06/08/23 03:41 4.05 02/09/23 4.39 Hgb 06/08/23 03:41 11.8 Low 02/09/23 12.6 Hct 06/08/23 03:41 35.0 02/09/23 39.0 MCV 06/08/23 03:41 87 02/09/23 89 MCH 06/08/23 03:41 29.3 02/09/23 28.7 MCHC 06/08/23 03:41 33.8 02/09/23 32.4 RDW 06/08/23 03:41 14.6 High 02/09/23 14.9 High Platelet 06/08/23 03:41 200 02/09/23 262 MPV 06/08/23 03:41 10.2 02/09/23 9.1 Neutrophils % 06/08/23 03:41 76 02/09/23 74 Lymphocytes % 06/08/23 03:41 16 02/09/23 14 Monocytes % 06/08/23 03:41 8 02/09/23 10 Eosinophils % 06/08/23 03:41 0 02/09/23 2 Basophils % 06/08/23 03:41 0 02/09/23 1 Absolute Neutrophil 06/08/23 03:41 7.2 02/09/23 8.4 High Absolute Lymphocyte 06/08/23 03:41 1.6 02/09/23 1.6 Absolute Monocyte 06/08/23 03:41 0.7 02/09/23 1.1 Absolute Eosinophil 06/08/23 03:41 0.0 02/09/23 0.2 Absolute Basophil 06/08/23 03:41 0.0 02/09/23 0.1 Routine Chemistry Tests FS LATEST RESULTS HISTORICAL RESULTS Sodium SerPl QN 06/08/23 03:41 137 02/09/23 142 Potassium SerPl QN 06/08/23 03:41 4.5 02/09/23 3.4 Low Chloride SerPl QN 06/08/23 03:41 100 02/09/23 97 Low Carbon Dioxide SerPl QN 06/08/23 03:41 28 02/09/23 35 High Anion Gap 06/08/23 03:41 9 02/09/23 10 BUN SerPl QN 06/08/23 03:41 30 High 02/09/23 43 High Creatinine SerPl QN 06/08/23 03:41 1.50 High 02/09/23 1.87 High Estimated GFR (CKD-EPI, no race) 06/08/23 03:41 33 Low 02/09/23 25 Low Estimated CRCL (CG) 06/08/23 03:41 23 Low 12/06/22 13 Low Glucose SerPl QN 06/08/23 03:41 104 High 02/09/23 83 Calcium Total SerPl QN 06/08/23 03:41 8.3 Low 02/09/23 9.6 Alkaline Phos SerPl QN 06/07/23 12:16 67 12/06/22 72 ALT SerPl QN 06/07/23 12:16 6 Low 12/06/22 35 AST SerPl QN 06/07/23 12:16 13 12/06/22 91 High Bilirubin Total SerPl QN 06/07/23 12:16 0.7 12/06/22 0.8 Total Protein SerPl QN 06/07/23 12:16 6.6 12/06/22 7.8 Albumin SerPl QN 06/07/23 12:16 3.6 12/06/22 4.4 Serology Tests LATEST RESULTS HISTORICAL RESULTS Procalcitonin 06/08/23 03:41 0.11 10/03/22 0.06 Molecular Diagnostic Tests LATEST RESULTS MRSA PCR 06/07/23 12:16 Negative Staph aureus PCR 06/07/23 12:16 Negative Diagnostic Results XR Chest PA or AP Portable 06/06/23 23:36:12 IMPRESSION: 1. Shallow inspiration with new mild bibasilar atelectasis and/or pneumonia. 2. Otherwise stable chronic changes, as described. Thank you for consulting our team of subspecialty radiologists at Radiology. Electronically Signed by: Signed By: MD Signature Line Electronically Signed on 06/07/23 01:59 EDT ________________________________________________________ Electronically Signed on 06/09/23 00:57 EDT ________________________________________________________ MD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 47,0
- Geschlecht
- M
- Eingang
- 10.05.2023
- Impfdatum
- 02.01.2022
- Beginn
- 11.07.2022
- Tage bis Beginn
- 190,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Hypotension
Symptom recurrence
Symptomtext
PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE CHRONIC HYPOTENSION 8/2/2022 & 8/22/2022 -- RECURRENCE OF SAME SYMPTOMS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 26.12.2022
- Impfdatum
- 22.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 5,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: ja
ER: unbekannt
Erholt: nein
Anaemia
Blindness
Blood test
Central venous catheter removal
Central venous catheterisation
Diabetic ketoacidosis
Pancreatitis
Renal failure
Diabetes mellitus
Dialysis
Electrolyte imbalance
Hypertension
Magnetic resonance imaging
Pneumonia
Unresponsive to stimuli
Symptomtext
found unresponsive. pancreatitis, diabetic ketoacidosis, kidney failure, legally blind, electrolyte imbalance, anemia. needed dialysis for 3 months, pneumonia, hypertension. resulting diabetes, permanent legal blindness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- 21,0
- Labordaten
- MRI 12/27/2021 bloodwork 12/27/2021 through 1/16/2022 central line insertion 1/1/2022 tunnel catheter insertion 1/15/2022 dialysis 1/1/2022 through 3/10/2022 tunnel catheter removal 3/2022
- Aktuelle Erkrankungen
- none known
- Vorgeschichte
- none known
- Andere Medikamente
- Sprintec birth control
- Allergien
- none known
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 02.11.2022
- Impfdatum
- 09.01.2022
- Beginn
- 30.08.2022
- Tage bis Beginn
- 233,0
- Dosis
- 3
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19 pneumonia
Symptomtext
Hospitalization for COVID-19 Pneumonia on dates 8/30/22-9/2/22. Treated with vitamin C 1,000 mg PO daily, vitamin D 25 mcg PO daily, zinc 50 mg PO daily.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19 pneumonia
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- penicillin, tramadol
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 08.09.2022
- Impfdatum
- 19.03.2021
- Beginn
- 15.08.2022
- Tage bis Beginn
- 514,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Catheterisation cardiac normal
Chest pain
Coronary artery disease
Diarrhoea
Dizziness
Echocardiogram abnormal
Malaise
Palpitations
SARS-CoV-2 test positive
Sinusitis
Visual impairment
Symptomtext
52-year-old female presents with chest pain and episodes of palpitations feeling lightheaded which she describes as dizzy and feeling visual spots. Patient has been lightheaded with standing more recently. She was working here in the food service area when she began to feel the symptoms and came to the emergency department for evaluation. Patient has been seen in urgent care last week and placed on Augmentin for sinus infection. She has had diarrhea since being placed on the Augmentin recently. She had an echo with some wall motion abnormalities, albeit smaller are, in the septum. Due to this and risk factors, she was advised to have an ischemic eval - due to COVID precautions and inability to get her HR to a target for a CTA, she had a cardiac cath with essentially normal coronaries (one report did mention "nonobstructive CAD" but the cath report does not mention lesions or stenosis). She will follow with cardiology.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- 7,0
- Labordaten
- 8/15 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC --detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 03.08.2022
- Impfdatum
- 02.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 8,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Bradycardia
Cytokine test
Dizziness
Fatigue
Feeling abnormal
Gene mutation identification test
Headache
Immunosuppression
Orthostatic hypotension
Sensory processing disorder
Tachycardia
Temperature intolerance
Tinnitus
Vascular endothelial growth factor assay
Vasodilatation
Vision blurred
Symptomtext
chronic 10/10 head pain, dizziness, blurriness, orthostatic hypotension, bradycardia, tachycardia, overstimulation, vasodilatation, brain fog, exhaustion, pooling, hot/cold sensitivity, tinnitus.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Orthostatic hypotension
- Hospital-Tage
- 5,0
- Labordaten
- Cytokine 14 panel. positive high VEGF and CCL5 high, 6/30/22 Shows low immune suppression of T8.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 01.07.2022
- Impfdatum
- 30.06.2022
- Beginn
- 30.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Dyspnoea
Hypoaesthesia oral
Interchange of vaccine products
Symptomtext
Pt was stable upon arrival. Denies any current discomfort or illness. Denies adverse reactions with prior vaccines. States he needs booster dose to leave the country soon. Received moderna for primary series but desired Pfizer for a booster dose. Vaccine administered intramuscularly without complications; tolerated well by patient. Patient was observed in an auditorium by staff. Approximately 30-45min later, staff notified me of patient having difficulty breathing. I immediately instructed them to call EMS and rapidly presented to patient with epilepsy-pen. Staff was already administering the patients own epi pen. Patient able to talk and breath and this point. Dr. immediately presented to the scene to evaluate patient. Patient was sent to ER for further evaluation. Contacted patient today to follow up with patient. Patient reports feeling fine with some lip numbness today but knows to carry his own epic-pen due to allergy of wasps/bees.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Assessment per Dr.
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- has own episodes pen for bee/wasp allergy
- Allergien
- bees/wasps
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 16.05.2022
- Impfdatum
- 21.01.2022
- Beginn
- 05.05.2022
- Tage bis Beginn
- 104,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal cavity drainage
Adult failure to thrive
Ammonia increased
Anaemia
Ascites
Asthenia
Bicytopenia
Blood bilirubin increased
COVID-19
Condition aggravated
Culture urine positive
Dehydration
Enterococcus test positive
Haemoglobin decreased
Hepatic cirrhosis
Hepatic failure
Hypokalaemia
Hypomagnesaemia
Symptomtext
Discharge Provider: MD Primary Care Provider: PA Admission Date: 5/5/2022 Discharge Date: May 10, 2022 PRESENTING PROBLEM: Dehydration [E86.0] Failure to thrive in adult [R62.7] Bicytopenia [D75.89] Hepatic cirrhosis, unspecified hepatic cirrhosis type, unspecified whether ascites present [K74.60] COVID-19 [U07.1] HOSPITAL COURSE: This is a 55-year-old male with a history of chronic alcohol abuse who presented to the emergency room with a 5 day history of weakness and malaise. He was found to have COVID-19 without respiratory component, liver failure with a bilirubin of 5.9, hypo magnesemia, hypokalemia, anemia with a hemoglobin of 7.9 right lower lobe pneumonia, urinary tract infection with findings of Enterococcus in the on urine culture, and an elevated ammonia level of 57. Abdominal imaging demonstrated large volume ascites and he had an ultrasound-guided paracentesis prior to discharge of 1.9 L. he did not demonstrate alcohol withdrawal throughout his hospitalization but was monitored for that possibility. He was substantially improved by discharge was felt to be stable to discharge to home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- 5,0
- Labordaten
- -
- Aktuelle Erkrankungen
- 1/2/2022 ED Visit to Hospital 1. Idiopathic acute pancreatitis, unspecified complication status 2. Jaundice due to hepatitis 3. Thrombocytopenia 4. Chronic anemia 5. Elevated bilirubin Discharge Provider: MD Primary Care Provider at Discharge: DO Admission Date: 12/24/2021 Discharge Date: 12/29/2021 DIAGNOSIS at time of disposition: 1. Acute pancreatitis, unspecified complication status, unspecified pancreatitis type 2. Thrombocytopenia 3. Chronic liver disease and cirrhosis 4. Hypocalcemia Discharge Provider: MD Primary Care Provider at Discharge: DO Admission Date: 12/17/2021 Discharge Date: 12/21/2021 PRESENTING PROBLEM: GI bleed [K92.2] 1. Acute liver failure without hepatic coma 2. Thrombocytopenia 3. Gingival bleeding 4. Acute blood loss anemia 5. Esophageal varices in alcoholic cirrhosis 6. Acute upper GI bleed
- Vorgeschichte
- Portal hypertension HTN (hypertension) Hyperlipidemia LDL goal < 130 Fatty liver History of prostate cancer Cervical disc displacement Hearing loss, unspecified hearing loss type, unspecified laterality Anemia, unspecified type GERD (gastroesophageal reflux disease) OSA (obstructive sleep apnea), severe Erectile dysfunction due to diseases classified elsewhere Prostate cancer Congenital contracture of left gastrocnemius muscle Congenital contracture of right gastrocnemius muscle Plantar fasciitis of left foot Plantar fasciitis of right foot Alcohol use disorder, moderate, dependence Closed right hip fracture, initial encounter Bicytopenia Acute blood loss anemia Cirrhosis of liver with ascites Moderate protein-calorie malnutrition Psoriasis
- Andere Medikamente
- adalimumab CF (HUMIRA) 40 MG/0.4ML prefilled pen amoxicillin (AMOXIL) 875 MG tablet (Expired) atenolol (TENORMIN) 100 MG tablet desvenlafaxine (PRISTIQ) 100 MG 24 hr tablet furosemide (LASIX) 40 MG tablet lactulose (CONSTULOSE) 20 GM/3
- Allergien
- Lisinopril-Angioedema
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 05.03.2022
- Impfdatum
- 06.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Blood pressure measurement
Echocardiogram
Hypertension
Ultrasound scan
Symptomtext
uncommonly high blood pressure that she never had before/blood pressure was 276/199; 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 female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 06Jan2022 13:00 (Lot number: 330258D) at the age of 55 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "MS" (ongoing), notes: Diagnosed prior to Pfizer Covid vaccine; caller states she has had MS for 8 years.; "low blood pressure" (unspecified if ongoing), notes: always had low blood pressure. There were no concomitant medications. Vaccination history included: Bnt162b2 (1st dose of the Pfizer Covid vaccine, lot EP7534), administration date: 18Mar2021, when the patient was 54 years old, for COVID-19 Immunization; Bnt162b2 (2nd dose of the Pfizer Covid vaccine , lot EW0153), administration date: 08Apr2021, when the patient was 55 years old, for COVID-19 Immunization. The following information was reported: HYPERTENSION (hospitalization, medically significant) with onset Jan2022, outcome "not recovered", described as "uncommonly high blood pressure that she never had before/blood pressure was 276/199". The patient was hospitalized for hypertension (start date: 09Feb2022, discharge date: 11Feb2022, hospitalization duration: 2 day(s)). The event "uncommonly high blood pressure that she never had before/blood pressure was 276/199" was evaluated at the emergency room visit. The patient underwent the following laboratory tests and procedures: blood pressure measurement: (Jan2022) 276/199; echocardiogram: (Feb2022) cardiac workup came out fine; ultrasound scan: (Feb2022) cardiac workup came out fine. Therapeutic measures were taken as a result of hypertension with Valsartan 80mg tablets and Carvedilol 6.25mg. Clinical course: The patient was calling about the Pfizer covid vaccine and stated that she wanted to report that she got both the Pfizer covid vaccines and the booster also and had MS. Caller stated that as soon as she got the booster vaccine, she was in the emergency room with uncommonly high blood pressure that she never had before and always had low blood pressure and it got to the point where she was at stroke level and when she got to the emergency room, her blood pressure was 276/199. Her blood pressure began to rise it seemed like towards the end of Jan2022 which was after her booster dose of the Pfizer Covid vaccine and it was the first time she had that and always had low blood pressure and has a blood pressure machine at home; stated she knew she was experiencing a horrible worse than a migraine and took her blood pressure at home and it was in the 200s when she went to the emergency room and she got to the emergency room and they took her blood pressure and treated her like a stroke victim. The patient's high blood pressure was still ongoing and she was still having that problem and when she was in the hospital, the cardiologist did a complete workup of her heart and it came out ok and they could not give her any answers of why that was happening and she was still dealing with the issue. She was prescribed two different blood pressure medications and they were the only two that worked for her and she then took her blood pressure three times per day and even with that was having to call the on call doctor and the blood pressure was going really high and they were having her double up on the medications to get it down; states she had no lot numbers or names of the medications that did not work for her but the two she was taking were Valsartan 80mg tablets and was supposed to take it once per day and it was an orange pharmacy bottle and did not have the lot, expiry date or NDC as it was a pharmacy bottle; states the second medication was Carvedilol 6.25mg and she was supposed to take it once every 12 hours and it was also an orange pharmacy bottle and does not have the lot, expiry date or NDC as it was a pharmacy bottle. The vaccination was given in the afternoon around 1:00pm. Anatomical location of administration of Pfizer vaccine considered as suspect was provided as upper left arm. The vaccination administered at pharmacy and it was not a Military facility. No additional vaccines administered on same date of the Pfizer suspect and was not treated with any medication prior vaccinations (within 4 weeks). MS diagnosed 8 years ago and family medical history relevant to AE(s) was provided as none. The patient had MS and was not allowed to get vaccines but got this because of covid regarding the Pfizer Covid vaccines. Caller stated that for testing they basically did a complete cardiac workup on her while she was in the hospital and they did an echo and an ultrasound and wanted to make sure her heart was ok and basically the cardiologist said those came out fine. Caller stated that she noticed when they did clinical trials that nobody in the clinical trials had MS or lupus or anything and there was no way to follow up to see how they were doing; stated she was just concerned also about other people that have MS or lupus and how they were doing for those kinds of concerns. Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- 2,0
- Labordaten
- Test Date: 202201; Test Name: blood pressure; Result Unstructured Data: Test Result:276/199; Test Date: 202202; Test Name: echo; Result Unstructured Data: Test Result:cardiac workup came out fine; Test Date: 202202; Test Name: ultrasound; Result Unstructured Data: Test Result:cardiac workup came out fine
- Aktuelle Erkrankungen
- MS (Diagnosed prior to Pfizer Covid vaccine; caller states she has had MS for 8 years.)
- Vorgeschichte
- Medical History/Concurrent Conditions: Low blood pressure (always had low blood pressure)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 26.01.2022
- Impfdatum
- 18.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dyspnoea exertional
Fatigue
Headache
Malaise
Myalgia
Nasal congestion
Nasopharyngitis
Oropharyngeal pain
Pain
Pain in extremity
Rhinorrhoea
SARS-CoV-2 test negative
Secretion discharge
Vomiting
Symptomtext
She had a sore throat, a runny nose, felt stuffy, tired, achy, headache, muscle aches, fatigue, and pain in arm. She didn't have a fever. Her headache, fatigue, and muscle aches were moderate. She ended up leaving school early that day because she wasn't feeling well. Her arm stopped hurting on 1/20/2022. She still had a headache, muscle aches, fatigue, and a sore throat. Then she started throwing up mucus drainage. She said she was getting out of breath when walking up the stairs, but she had no tightness in her chest. Sunday she started to feel better. She just had a sore throat, headache, mucus, and runny nose. Friday we took her to get a covid test which came back as negative. She had a mild headache on Sunday. Since we found out that she does not have covid we think its just a cold she caught in coincidental timing of getting the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea exertional
- Hospital-Tage
- -
- Labordaten
- Covid Test- negative (1/21/2022)
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 26.01.2022
- Impfdatum
- 24.01.2022
- Beginn
- 24.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Chills
Condition aggravated
Dehydration
Headache
Musculoskeletal stiffness
Nausea
Neck pain
Oropharyngeal pain
Pain
Pain in extremity
Pyrexia
Urticaria
Symptomtext
Fever, chills, headache, sore and stiff in upper torso and neck and injection arm, sore wrist joints, dehydration, nausea, hives
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- covid 1 month prior
- Vorgeschichte
- Chronic Urticaria which had cleared up January 1st, 2022
- Andere Medikamente
- Vitamin C, Vitamin D3, Magnesium/calcium, Iron, Folic Acid
- Allergien
- none
- Vorherige Impfungen
- 2nd pfizer bioNTech ER8737 vaccube given on 04/05/2021, age 55, Same results as the booster, high fever, severe soreness and hea
- Staat
- IL
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 15.01.2022
- Impfdatum
- 15.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Dyspnoea
Paraesthesia
Symptomtext
After 30 minutes after vaccination, patient started to feel faint, fingers started to tingle and SOB reported by patient in the front of the store as he was going home. Patient was sat in chair and pharmacy was contacted of the emergency. Pharmacist rushed to front with epi-pen but patient stated that his symptoms had left and that he was ok. Patient denied tongue swelling, SOB, throat swelling, loss of feeling in limbs. Patient reported feeling fine and needed to sit down. 911 was immediately called for further evaluation. They arrived quickly and left with patient to evaluate him.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- NONE REPORTED
- Vorgeschichte
- NONE REPORTED
- Andere Medikamente
- NONE REPORTED
- Allergien
- NONE REPORTED
- Vorherige Impfungen
- Dad described he had a reaction like this many years ago a vaccine but couldn't remember which vaccine.
- Staat
- TX
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 15.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Dizziness
Dysstasia
Mobility decreased
Muscular weakness
Nausea
Symptomtext
I got up at midnight to give my son more medication for his congestion and started to feel extremely weak in my legs and arms. I could barely stand and needed support and could not lift my arms. I felt extremely nauseous and light headed as well with chills. This lasted for about 5 minutes total from start to finish.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Prilosec, vitamin C, vitamin d, magnesium, vitamin b, Zyrtec
- Allergien
- Wheat
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 10.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 09.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Chest pain
Echocardiogram normal
Electrocardiogram normal
Pain
Painful respiration
Prohormone brain natriuretic peptide increased
Troponin increased
Symptomtext
Patient was admitted to the hospital with complains of chest pain that was non-positional. He states it was a dull ache that was exacerbated by taking deep breath. Pro-BNP and troponin are elevated.. Echocardiogram and EKG was normal for his age.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 09.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest pain
Troponin increased
Symptomtext
Elevated troponin levels, chest pain, admitted to hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- NO
- Andere Medikamente
- Multivitamin
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 07.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoaesthesia
Immediate post-injection reaction
Paraesthesia
Symptomtext
pt got the pfizer vaccine dose 3 . she immediately experienced tingling and numbness in her left foot. i called her 48 hours later and she was still experiencing the tingling/numbness
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 02.01.2022
- Impfdatum
- 27.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
Blood test normal
Chest X-ray normal
Electrocardiogram normal
Exercise tolerance decreased
Fibrin D dimer normal
Headache
Heart rate increased
Liver function test normal
Loss of personal independence in daily activities
Nausea
Renal function test normal
Tremor
Symptomtext
By Tuesday evening, I was experiencing an elevated heart rate. Laying in bed, my heart rate could be anywhere from 90-120 whereas it would typically be around 65-70. Walking slowly up the stairs to my second story would cause my heart rate to shoot up past 160. I was nauseous, weak and had a headache. I was worried that I was having a heart complication so I called nurse advice for hospital and they advised me to go to the ER and not to drive myself. I went to the ER of the Hospital in the early hours of the morning on December 29th. They proceeded to check me for causes of this and tried to determine if my heart was in any immediate danger. They were able to verify that I did not appear to be in immediate danger and they advised me to follow up with my doctor within 1-2 days. No treatment was given, only testing. I am still unable to resume daily normal activities or any type of exercise, my heart rate continues to be elevated and I am shaky and weak.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- At the Hospital ER I was given the following tests, all on the morning on December 29th, 2021. - EKG (results normal) - X-ray of Heart (appeared normal) - Blood tests including those to check on my liver and kidney function, identify anemia, all appeared normal. - Blood test (D-Dimer) to check for signs of blood clots, which appeared normal as well.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None Known
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 01.01.2022
- Impfdatum
- 31.12.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoaesthesia
Pain in extremity
Paraesthesia
Symptomtext
Numbness, tingling, and light pain in right leg. Vaccine about midday and symptoms can about 10 hours later.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Men's Multivitamin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 29.12.2021
- 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: ja
Erholt: ja
Chest pain
Chills
Fibrin D dimer normal
Influenza virus test negative
Myalgia
Pleuritic pain
Pyrexia
SARS-CoV-2 test negative
Symptomtext
Pleuritic L sided chest pain onset about 2 hours after vaccination, along with chills, myalgias and fever to 104. Fever and chills resolved overnight, chest pain persisted for 3 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Negative DDIMER Negative Covid and influenza pcr tests
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hyperlipidemia
- Andere Medikamente
- Prilosec OTC 20 mg daily Nexletol 180mg daily
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 29.12.2021
- Impfdatum
- 07.04.2021
- Beginn
- 21.04.2021
- Tage bis Beginn
- 14,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cardiac stress test
Electrocardiogram
Electrocardiogram ambulatory
Fatigue
Heart rate irregular
Palpitations
Ultrasound kidney
Ultrasound liver
Symptomtext
Al started post shot 2 in mid-April 2021. Heart palpitations, felt like AFIB but wasn't. Bad fatigue for months. Wound up at a Cardiologist, Nephrologist and my primary Doctor. Had to wear a heart monitor for a few days. My heart beats feel different several times during the day and still do.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- Stress test Heart monitor Ultrasound of the liver and kidneys Electrocardiogram EKG
- Aktuelle Erkrankungen
- Perfectly fine
- Vorgeschichte
- high blood pressure, high cholesterol, Type 2 all under control
- Andere Medikamente
- Metformin, Allopurinol, Lipitor, Naproxen, Atorvastatin
- Allergien
- None known
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 26.12.2021
- Impfdatum
- 26.12.2021
- Beginn
- 26.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest discomfort
Dyspnoea
Flushing
Symptomtext
Patient started having difficulty breathing, feeling pressure on her chest, and flushing a couple of minutes after getting the vaccine. Symptoms resolved after 10 mins. Patient was prescribed an Epipen by her prescriber to use in case of anaphylaxis. I made a caring call an hour after, she reports being fine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 21.03.2023
- Impfdatum
- 25.01.2022
- Beginn
- 12.12.2022
- Tage bis Beginn
- 321,0
- Dosis
- 3
- Route/Site
- UN / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Blood sodium decreased
COVID-19
Hyponatraemia
Inappropriate antidiuretic hormone secretion
Laboratory test abnormal
Nausea
Pain
SARS-CoV-2 test positive
Symptomtext
Patient took a home COVID test on 12/6/22 which resulted positive. On 12/12/22, she was seen in urgent care, where she was found to have abnormal labs (sodium level was 114). Patient was told to be evaluated in the ED due to her abnormal labs. Ultimately, she was admitted 12/12/22 - 12/18/22 for severe hyponatremia; intractable nausea, suspect due to COVID infection; and severe body aches, suspect due to COVID infection. Per discharge summary, provider notes "Sodium was 114 on presentation, likely due to SIADH related to COVID-related symptoms of severe nausea and body aches...as the patient's body aches and nausea has further improved, the patient has not required additional salt tablets or hypertonic saline." She has received the primary COVID vaccine series and one booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 04.01.2023
- 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: ja
Back pain
Chills
Fatigue
Influenza like illness
Lethargy
Pain
Pyrexia
Skin sensitisation
Symptomtext
Within one hour of receiving vaccine, I begin to feel flu like symptoms. Low-grade fever, chills, every hair was sore on my body, very tired / lethargic , and my body ached on every bone. My lower back was so sore and achy. Then it started feeling painful. All of my symptoms ended within a few days with the exception of very tired and lower back pain. The lower back pain lasted for 6 months !
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- I never sought tests
- Aktuelle Erkrankungen
- Hyperthyroidism
- Vorgeschichte
- -
- Andere Medikamente
- Vit D
- Allergien
- Jelly fish stings
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 08.09.2022
- Impfdatum
- 21.07.2021
- Beginn
- 10.08.2022
- Tage bis Beginn
- 385,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain
Abdominal pain upper
Autism spectrum disorder
Biopsy
COVID-19
Cough
Duodenitis
Headache
Hypoglycaemia
Laboratory test
Lipase abnormal
Oesophagogastroduodenoscopy abnormal
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
Hospital Course: 1. Acute, recurrent abdominal pain. Lipase was just under twice the upper limit of normal. He was having epigastric area pain, which was worse with eating. Ordered for IV fluids, anti-emetics, and pain control. GI service consulted and acute pancreatitis was considered doubtful. Pain resolved on follow-up today. Underwent EGD which noted duodenitis signs. Biopsies were taken. He is stable for discharge home with outpatient GI follow-up regarding biopsy results and further care plan. 2. Acute hypoglycemia. Resolved. Monitored labs. Encouraged PO intake. 3. Recent covid-19 infection. Had headache on 7-31 followed by runny nose and cough. These symptoms resolved. He tested positive at home on 8-1.Discussed with epidemiology and released from covid isolation. No specific treatment is currently needed. 4. Autistic spectrum disorder. He is to have outpatient follow-up. 5. DVT prophylaxis. He is low risk and ambulatory. Disposition: He is stable for discharge home with outpatient follow-up. Discussed management plan with patient at bedside and mother earlier today.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- 2,0
- Labordaten
- 8/11 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC -- detected
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 84,0
- Geschlecht
- M
- Eingang
- 09.08.2022
- Impfdatum
- 26.02.2022
- Beginn
- 11.06.2022
- Tage bis Beginn
- 105,0
- Dosis
- 4
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Malaise
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
I just got back from a cruise and when I got home I started feeling like I had a cold. After a couple of days I still didn't feel well, so I took a home COVID-19 test and it was positive. I went to the clinic inside of a local store and was prescribed PAXLOVID. Said it was a very mild breakthrough, he really didn't think it was COVID at first.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- Home COVID-19 test - positive. Home COVID-19 test - positive.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Blood Pressure
- Andere Medikamente
- Lisinopril; pantoprazole; indomethacin; vitamin D3; probiotics; magnesium; krill oil.
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 11.07.2022
- Impfdatum
- 06.01.2022
- Beginn
- 03.07.2022
- Tage bis Beginn
- 178,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Oropharyngeal pain
Pain
Respiratory tract congestion
SARS-CoV-2 test positive
Sinus congestion
Throat irritation
Symptomtext
I tested positive for COVID-19 on 7/8/22. I developed a scratchy throat on 7/3/22 and developed sore throat on 7/6/22. Started experiencing congestion and sinuses w/ a few body aches. I spoke to doctor on 7/9/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 03.01.2022
- Beginn
- 07.02.2022
- Tage bis Beginn
- 35,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Feeling abnormal
Nausea
Pruritus
Sensitive skin
Urticaria
Weight decreased
Symptomtext
hives; sensitive skin; itchy; nauseous; Some brain fog; Weight loss; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 69-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 03Jan2022 as dose 3 (booster), single (Lot number: 330258D) at the age of 69 years, in right arm for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: CLARITIN [CLARITHROMYCIN]; BENADRYL [DIPHENHYDRAMINE HYDROCHLORIDE]; VITAMIN D [COLECALCIFEROL]. Vaccination history included: BNT162b2 (dose number 2, Prev dose product - COVID 19, Prev dose brand - Pfizer Bio Tech, Prev dose lot number - EN6202, vaccine location - Left leg,), administration date: 11Mar2021, when the patient was 68-year-old, for COVID-19 immunization; BNT162b2 (dose number 1, Prev dose product - COVID 19, Prev dose brand - Pfizer Bio Tech, Prev dose lot number - EN6201, vaccine location - Left arm), administration date: 18Feb2021, when the patient was 68-year-old, for COVID-19 Immunization. The following information was reported: FEELING ABNORMAL (non-serious) with onset 07Feb2022, outcome "unknown", described as "Some brain fog"; WEIGHT DECREASED (non-serious) with onset 07Feb2022, outcome "unknown", described as "Weight loss"; URTICARIA (non-serious) with onset 07Feb2022, outcome "unknown", described as "hives"; PRURITUS (non-serious) with onset 07Feb2022, outcome "unknown", described as "itchy"; NAUSEA (non-serious) with onset 07Feb2022, outcome "unknown", described as "nauseous"; SENSITIVE SKIN (non-serious) with onset 07Feb2022, outcome "unknown". Therapeutic measures were taken as a result of urticaria, sensitive skin, pruritus, nausea, feeling abnormal, weight decreased. Adverse event: With recent vaccine, a month after consumer began having hives after eating. She have been tested for the foods and don't have an allergy. She also began having very sensitive skin, very itchy. Sometimes feel nauseous. Some brain fog. Weight loss due to the unknown problem with food. Ae treatment: Have seen many doctors, on Claritin Pepcid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- CLARITIN [CLARITHROMYCIN]; BENADRYL [DIPHENHYDRAMINE HYDROCHLORIDE]; VITAMIN D [COLECALCIFEROL]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 28.06.2022
- Impfdatum
- 27.12.2021
- Beginn
- 25.06.2022
- Tage bis Beginn
- 180,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Cough
Fatigue
Feeling abnormal
Headache
Oropharyngeal pain
Pain
Pyrexia
SARS-CoV-2 test positive
Sinus operation
Symptomtext
I started getting symptoms of headache, nasal drainage, fever, and sore throat. Then my fever progressed to 101-102 and a cough. I took an at home COVID-19 test and took a PCR COVID-19 test which were positive. I received Paxlovid which I had an allergic reaction to and experienced a rash and hives all over my body. I called my PCP and was told to go to an urgent care. While at urgent care I was given Benadryl and was told not to take Paxlovid. I still have lingering effects of cough, sore throat, headache, tiredness, brain fog, and body aches.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 test - positive
- Aktuelle Erkrankungen
- Stomach Flu - 2 - 3 weeks prior
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 02.06.2022
- Impfdatum
- 14.01.2022
- Beginn
- 28.05.2022
- Tage bis Beginn
- 134,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Blood magnesium normal
Blood pressure increased
COVID-19
Chest X-ray normal
Confusional state
Electrolyte imbalance
Haemoglobin decreased
Pyrexia
Respiratory tract infection
SARS-CoV-2 test positive
Symptomtext
Discharge Provider: MD Primary Care Provider: MD Admission Date: 5/28/2022 Discharge Date: May 31, 2022 PRESENTING PROBLEM: Confusion [R41.0] Weakness [R53.1] Respiratory tract infection due to COVID-19 virus [U07.1, J98.8] COVID-19 [U07.1] HOSPITAL COURSE: 77 y.o. male with Hx of DM type II, HTN, RA, and OSA who presented with confusion and generalized weakness. In the emergency department the patient was febrile to 39? C. BP was elevated while in the emergency department. Mg 1.4. Hgb 10.4. COVID PCR was positive. CXR without an acute process. 1 L of IV fluids was given as well as 2 g of IV magnesium sulfate. Patient stayed in hospital for approximately 3 days. Patient had remained stable throughout hospital stay. His electrolyte imbalances were all corrected after the 1st 24 hours of stay. Patient's confusion also had resolved. Dr. assess him initially and recommended skilled nursing facility. On subsequent days he has strength significantly improved that with reassessment recommendations had changed to home with home health. And with patient stable he was then discharged home on 5/31/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Rheumatoid arthritis (HCC) Type 2 diabetes mellitus without complication (HCC) Pure hypercholesterolemia BPH (benign prostatic hyperplasia) Environmental allergies OSA on CPAP Multiple thyroid nodules Non-toxic multinodular goiter Pancreatitis Hot flashes Hypogonadism male HTN (hypertension) Ankylosing spondylitis (HCC) Cognitive impairment, mild, so stated Encounter for long-term (current) use of high-risk medication Generalized osteoarthritis Osteoarthrosis Other long term (current) drug therapy Spondylosis without myelopathy Undifferentiated spondyloarthropathy COVID-19 Generalized Weakness
- Andere Medikamente
- adalimumab CF (HUMIRA) 40 MG/0.4ML prefilled pen atorvastatin (LIPITOR) 40 MG tablet citalopram (CELEXA) 20 MG tablet donepezil (ARICEPT) 10 MG tablet glipiZIDE CR (GLUCOTROL) 10 MG 24 hr tablet lisinopril (PRINIVIL,ZESTRIL) 20 MG tabl
- Allergien
- Amoxicillin-Shortness of Breath
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 05.05.2022
- Impfdatum
- 25.02.2021
- Beginn
- 30.04.2022
- Tage bis Beginn
- 429,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Fatigue
SARS-CoV-2 test positive
Vomiting
Symptomtext
Case went to hospital with ongoing vomiting and fatigue. Tested positive upon admission. No other COVID symptoms were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- unknown
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- None reported
- Andere Medikamente
- unknown
- Allergien
- No Known Allergies
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 06.04.2022
- Impfdatum
- 22.02.2022
- Beginn
- 01.03.2022
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lip swelling
Malaise
Nasal oedema
Pain
Rash erythematous
Rash
Urticaria
SARS-CoV-2 test
Swelling face
Swelling of eyelid
Symptomtext
red raised rash/ on my sons face, down his back on his legs/ than spread to his whole body; nickel sized hives/ on chest, tummy, arms, hives around his arm pits on his hands; Swollen face; Swollen face, eyelids; Swollen face, eyelids, and nose; Swollen face, eyelids, and nose, lips; pain; feeling sick; This is a spontaneous report received from contactable reporter (Consumer or other non HCP). The reporter is the parent. A 17-year-old male patient received bnt162b2 (BNT162B2), administered in arm right, administration date 22Feb2022 14:30 (Lot number: 330258D) at the age of 17 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "Autism" (unspecified if ongoing); "intellectual disability" (unspecified if ongoing); "mood disorder" (unspecified if ongoing). The patient had COVID-19 prior vaccination. Concomitant medications included: CLONIDINE; PEPCID; ZYRTEC; TEGRETOL; FLUXAMINE. Past drug history included: Codeine, reaction(s): "vomiting"; Claritin, reaction: "hallucinations"; Risperdal, reaction: "acute torticollis". Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: Ew0171, Location of injection: Arm Right), administration date: 30Apr2021, when the patient was 16 years old, for COVID-19 Immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: ER8732, Location of injection: Arm Right), administration date: 01Apr2021, when the patient was 16 years old, for COVID-19 Immunization. The following information was reported: RASH ERYTHEMATOUS (non-serious) with onset 01Mar2022 07:00, outcome "not recovered", described as "red raised rash/ on my sons face, down his back on his legs/ than spread to his whole body"; URTICARIA (non-serious) with onset 01Mar2022 07:00, outcome "not recovered", described as "nickel sized hives/ on chest, tummy, arms, hives around his arm pits on his hands"; SWELLING FACE (non-serious) with onset 01Mar2022 07:00, outcome "not recovered", described as "Swollen face"; SWELLING OF EYELID (non-serious) with onset 01Mar2022 07:00, outcome "not recovered", described as "Swollen face, eyelids"; NASAL OEDEMA (non-serious) with onset 01Mar2022 07:00, outcome "not recovered", described as "Swollen face, eyelids, and nose"; LIP SWELLING (non-serious) with onset 01Mar2022 07:00, outcome "not recovered", described as "Swollen face, eyelids, and nose, lips"; PAIN (non-serious) with onset 01Mar2022 07:00, outcome "not recovered", described as "pain"; MALAISE (non-serious) with onset 01Mar2022 07:00, outcome "not recovered", described as "feeling sick". The events "red raised rash/ on my sons face, down his back on his legs", "nickel sized hives/ on chest, tummy, arms, hives around his arm pits on his hands", "swollen face", "swollen face, eyelids", "swollen face, eyelids, and nose", "swollen face, eyelids, and nose, lips", "pain" and "feeling sick" 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 rash erythematous, urticaria, swelling face, swelling of eyelid, nasal oedema, lip swelling, pain, malaise, and included prednisone 5 days, antibiotics, prednisone 10 days. Additional information: on 01Mar2022 red raised rash and nickel sized hives all over. The red raised rash was on reporter's son face, down his back on his legs, nickel sized hives on chest, tummy, arms, hives around his arm pits on his hands, the red raised rash had than spread to his whole body. Swollen face, eyelids, and nose, lips, hives and rash hurt reporter's son he was autistic and he was feeling sick and in pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220316; Test Name: Binaxx; Test Result: Negative ; Comments: Covid test type post vaccination: Nasal Swab
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Autism; Intellectual disability; Mood disorder
- Andere Medikamente
- CLONIDINE; PEPCID; ZYRTEC; TEGRETOL; FLUXAMINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 06.04.2022
- Impfdatum
- 22.02.2022
- Beginn
- 01.03.2022
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lip swelling
Malaise
Nasal oedema
Pain
Rash erythematous
Rash
Urticaria
SARS-CoV-2 test
Swelling face
Swelling of eyelid
Symptomtext
red raised rash/ on my sons face, down his back on his legs/ than spread to his whole body; nickel sized hives/ on chest, tummy, arms, hives around his arm pits on his hands; Swollen face; Swollen face, eyelids; Swollen face, eyelids, and nose; Swollen face, eyelids, and nose, lips; pain; feeling sick; This is a spontaneous report received from contactable reporter (Consumer or other non HCP). The reporter is the parent. A 17-year-old male patient received bnt162b2 (BNT162B2), administered in arm right, administration date 22Feb2022 14:30 (Lot number: 330258D) at the age of 17 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "Autism" (unspecified if ongoing); "intellectual disability" (unspecified if ongoing); "mood disorder" (unspecified if ongoing). The patient had COVID-19 prior vaccination. Concomitant medications included: CLONIDINE; PEPCID; ZYRTEC; TEGRETOL; FLUXAMINE. Past drug history included: Codeine, reaction(s): "vomiting"; Claritin, reaction: "hallucinations"; Risperdal, reaction: "acute torticollis". Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: Ew0171, Location of injection: Arm Right), administration date: 30Apr2021, when the patient was 16 years old, for COVID-19 Immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: ER8732, Location of injection: Arm Right), administration date: 01Apr2021, when the patient was 16 years old, for COVID-19 Immunization. The following information was reported: RASH ERYTHEMATOUS (non-serious) with onset 01Mar2022 07:00, outcome "not recovered", described as "red raised rash/ on my sons face, down his back on his legs/ than spread to his whole body"; URTICARIA (non-serious) with onset 01Mar2022 07:00, outcome "not recovered", described as "nickel sized hives/ on chest, tummy, arms, hives around his arm pits on his hands"; SWELLING FACE (non-serious) with onset 01Mar2022 07:00, outcome "not recovered", described as "Swollen face"; SWELLING OF EYELID (non-serious) with onset 01Mar2022 07:00, outcome "not recovered", described as "Swollen face, eyelids"; NASAL OEDEMA (non-serious) with onset 01Mar2022 07:00, outcome "not recovered", described as "Swollen face, eyelids, and nose"; LIP SWELLING (non-serious) with onset 01Mar2022 07:00, outcome "not recovered", described as "Swollen face, eyelids, and nose, lips"; PAIN (non-serious) with onset 01Mar2022 07:00, outcome "not recovered", described as "pain"; MALAISE (non-serious) with onset 01Mar2022 07:00, outcome "not recovered", described as "feeling sick". The events "red raised rash/ on my sons face, down his back on his legs", "nickel sized hives/ on chest, tummy, arms, hives around his arm pits on his hands", "swollen face", "swollen face, eyelids", "swollen face, eyelids, and nose", "swollen face, eyelids, and nose, lips", "pain" and "feeling sick" 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 rash erythematous, urticaria, swelling face, swelling of eyelid, nasal oedema, lip swelling, pain, malaise, and included prednisone 5 days, antibiotics, prednisone 10 days. Additional information: on 01Mar2022 red raised rash and nickel sized hives all over. The red raised rash was on reporter's son face, down his back on his legs, nickel sized hives on chest, tummy, arms, hives around his arm pits on his hands, the red raised rash had than spread to his whole body. Swollen face, eyelids, and nose, lips, hives and rash hurt reporter's son he was autistic and he was feeling sick and in pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220316; Test Name: Binaxx; Test Result: Negative ; Comments: Covid test type post vaccination: Nasal Swab
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Autism; Intellectual disability; Mood disorder
- Andere Medikamente
- CLONIDINE; PEPCID; ZYRTEC; TEGRETOL; FLUXAMINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 04.04.2022
- Impfdatum
- 01.04.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Headache
Rash
Sinus congestion
Symptomtext
EMPLOYEE COMPLAINED OF HEADACHE, CHILLS, SINUS CONGESTION AND GENERALIZED SKIN RASH THE DAY AFTER RECEIVING THE COVID VACCINE WITH SYMPTOMS STILL PRESENT ON 4/4/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- PCN
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 18.03.2022
- Impfdatum
- 17.03.2022
- Beginn
- 18.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Headache
Symptomtext
COMPLAINT OF SEVERE HEADACHE, CHILLS STARTED 3/18/2022 MORNING AFTER 2ND DOSE COVID VACCINE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 22.02.2022
- Impfdatum
- 03.02.2022
- Beginn
- 09.02.2022
- Tage bis Beginn
- 6,0
- Dosis
- 2
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Burning sensation
Hypersensitivity
Pain
Rash macular
Symptomtext
allergic reaction; Raised painful , burny , sore blotches in several places after my 2nd vaccine.; Raised painful , burny , sore blotches in several places after my 2nd vaccine.; Raised painful , burny , sore blotches in several places after my 2nd vaccine.; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 33 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 03Feb2022 11:30 (Lot number: 330258D) at the age of 33 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Sulfa drugs" (unspecified if ongoing); "Nickel" (unspecified if ongoing). The patient took concomitant medications. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: 330258D, Location of injection: Arm Left, Vaccine Administration Time: 12:00 PM), administration date: 13Jan2022, when the patient was 33 years old, for COVID-19 immunization. The following information was reported: HYPERSENSITIVITY (non-serious) with onset 09Feb2022 14:00, outcome "recovering", described as "allergic reaction"; PAIN (non-serious), BURNING SENSATION (non-serious), RASH MACULAR (non-serious) all with onset 09Feb2022 14:00, outcome "recovering" and all described as "Raised painful , burny , sore blotches in several places after my 2nd vaccine.". The events "allergic reaction", "raised painful , burny , sore blotches in several places after my 2nd vaccine.", "raised painful , burny , sore blotches in several places after my 2nd vaccine." and "raised painful , burny , sore blotches in several places after my 2nd vaccine." were evaluated at the emergency room visit. Therapeutic measures were taken as a result of hypersensitivity, pain, burning sensation, rash macular. Additional information: Raised painful, burny, sore blotches in several places after my 2nd vaccine. Went to urgent care clinic and was prescribed meds for an allergic reaction, steroids and hydroxyzine. No other vaccine in four weeks. Patient received Other Medication in two weeks: Multivitamin/ birth control. Patient did not have covid prior vaccination. Since the vaccination, the patient had not been tested for COVID-19. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Nickel sensitivity; Sulfonamide allergy
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 20.02.2022
- Impfdatum
- 06.02.2022
- Beginn
- 07.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Nodule
Pain in extremity
Symptomtext
Sore arm, knott like, that is very sore since after vaccination
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- none
- Andere Medikamente
- unknown
- Allergien
- penicillin, shellfish, shrimp
- Vorherige Impfungen
- pt sts Flu vaccination makes sick x 1wk after
- Staat
- WA
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 17.02.2022
- Impfdatum
- 22.01.2022
- Beginn
- 02.02.2022
- Tage bis Beginn
- 11,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Malaise
Pyrexia
Urticaria
Vomiting
Symptomtext
Received booster on 1/21/22, followed by malaise, mild fever and three instances of vomiting from 1/22/22 through 1/24/22. Appeared normal until hives presented throughout upper legs to neck area on the afternoon of 2/2. Treated with OTC Benadryl, to no effect, with hives worsening each day and becoming much denser. Treated at urgent care on 2/10, with a prescription antihistamine and OTC lotion. Hives resolved on 2/16/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- N/A Treated at urgent care by visual inspection.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Autism. Low muscle tone. Cognitive delays.
- Andere Medikamente
- Daily vitamin c tablet, and child multi-vitamin
- Allergien
- None known. Possible grass allergies.
- Vorherige Impfungen
- Fever and vomiting the two days following Shots 1 and 2 of Pfizer Covid received on 7/1/21 an d7/21/21.
- Staat
- TX
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 16.02.2022
- Impfdatum
- 06.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Headache
Pyrexia
Malaise
Meningitis viral
Symptomtext
2 day after taking the vaccine he had chills, headache and fever. It lasted 5 days and he went to the doctor. He was given an antibiotic and after taking them he still didnt get better. He went back and was admitted to the hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- 30,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- high blood pressure
- Andere Medikamente
- tamsulosin, amlodipine, flonase
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 16.02.2022
- Impfdatum
- 06.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Headache
Pyrexia
Malaise
Meningitis viral
Symptomtext
2 day after taking the vaccine he had chills, headache and fever. It lasted 5 days and he went to the doctor. He was given an antibiotic and after taking them he still didnt get better. He went back and was admitted to the hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- 30,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- high blood pressure
- Andere Medikamente
- tamsulosin, amlodipine, flonase
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 14.02.2022
- Impfdatum
- 05.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Myalgia
Ventricular extrasystoles
Symptomtext
Frequent premature ventricular contractions first noticed about 20 hours after the vaccine injection . These persisted for about 48 hours from the time I first noticed them . The frequency varied from one every 4 beats to one every 15 beats during this time. There were no associated symptoms of chest pain, shortness of breath, or dizziness. I did have some fatigue and mild muscle aches. I am a physician . I used my spouse's watch to periodically check the type of rhythm. I did not seek medical attention.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- GERD
- Andere Medikamente
- Famotidine
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 11.02.2022
- Impfdatum
- 01.02.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Axillary pain
Breast pain
Burning sensation
Hypersensitivity
Lymphadenopathy
Myalgia
Oropharyngeal pain
Pruritus
Rash macular
Rhinorrhoea
Symptomtext
1st Shot - swollen lymph nodes , achy muscles, edema/ fluid in joints, sore muscles , sore arm pits and sore breasts for 5 days. 2nd Shot- same symptoms as above for a day. 5 days after shot, got itchy, burning, sore blotches all over the body (legs, chest, neck and armpits) also had runny nose with clear discharge and a sore throat. Went to an urgent care center because wouldn?t get into physician soon enough. Doctor prescribed hydroxyzine and prednisone and told me it was allergic reaction.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Birth Control/ Multivitamin
- Allergien
- Sulfa drugs, Nickel
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 09.02.2022
- Impfdatum
- 21.01.2022
- Beginn
- 03.02.2022
- Tage bis Beginn
- 13,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Activated partial thromboplastin time normal
Blood lactate dehydrogenase increased
C-reactive protein normal
Epistaxis
Gingival bleeding
C-reactive protein
Differential white blood cell count
Full blood count
Immune thrombocytopenia
International normalised ratio
Haematochezia
Haemorrhage
Immunoglobulin therapy
International normalised ratio normal
Malaise
Mucosal haemorrhage
Petechiae
Platelet count decreased
Symptomtext
On 2/4/2022, presented to ER with parents for concerns of nosebleeds, bleeding gums, and petechial rash for one day. Patient reports his gums started bleeding earlier today; this also occurred two days ago but stopped on it's own and they attributed it to his braces so didn't think much of it. He started to have a nosebleed around 1500 today; he has since had four more nosebleeds. His mother also noticed some blood in his underwear today; patient states he has not seen any blood in the toilet or in his stool. Mom reports the patient does not have any significant medical problems. He's never had something like this happen before. No daily medications. UTD on vaccines per parent. Did recently receive his COVID booster on 1/21 per patient, and did feel ill for a few days after. No family history of bleeding disorders. Patient was then admitted to the Pediatric Hematology-Oncology Service for further evaluation and management of Immune thrombocytopenia . 2/5/2022: Although platelets did not significantly increase after one dose of IVIG, mucosal bleeding has stopped and petechiae are regressing, he has no new sites. He still endorses blood in his stools.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- 2,0
- Labordaten
- In the ED 2/4/2022, vitals were significant for BP 123/85 and HR up to 110. Labs significant for platelets 0, LDH 328, UA with trace blood and 11-25 RBCs. PT, PTT, INR, CRP, Ferritin unremarkable. After first IVIG infusion, platelet count improved to 2. Due to this, he was given repeat IVIG. Oral tylenol on 2/5 resulted in bloody emesis, attributed to a recent nosebleed. Platelets improved to 24 after second IVIG. Patient was then given a dose of IV decadron prior to discharge and a repeat platelet level was obtained which was 34.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 09.02.2022
- Impfdatum
- 21.01.2022
- Beginn
- 03.02.2022
- Tage bis Beginn
- 13,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Activated partial thromboplastin time normal
Blood lactate dehydrogenase increased
C-reactive protein normal
Epistaxis
Gingival bleeding
C-reactive protein
Differential white blood cell count
Full blood count
Immune thrombocytopenia
International normalised ratio
Haematochezia
Haemorrhage
Immunoglobulin therapy
International normalised ratio normal
Malaise
Mucosal haemorrhage
Petechiae
Platelet count decreased
Symptomtext
On 2/4/2022, presented to ER with parents for concerns of nosebleeds, bleeding gums, and petechial rash for one day. Patient reports his gums started bleeding earlier today; this also occurred two days ago but stopped on it's own and they attributed it to his braces so didn't think much of it. He started to have a nosebleed around 1500 today; he has since had four more nosebleeds. His mother also noticed some blood in his underwear today; patient states he has not seen any blood in the toilet or in his stool. Mom reports the patient does not have any significant medical problems. He's never had something like this happen before. No daily medications. UTD on vaccines per parent. Did recently receive his COVID booster on 1/21 per patient, and did feel ill for a few days after. No family history of bleeding disorders. Patient was then admitted to the Pediatric Hematology-Oncology Service for further evaluation and management of Immune thrombocytopenia . 2/5/2022: Although platelets did not significantly increase after one dose of IVIG, mucosal bleeding has stopped and petechiae are regressing, he has no new sites. He still endorses blood in his stools.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- 2,0
- Labordaten
- In the ED 2/4/2022, vitals were significant for BP 123/85 and HR up to 110. Labs significant for platelets 0, LDH 328, UA with trace blood and 11-25 RBCs. PT, PTT, INR, CRP, Ferritin unremarkable. After first IVIG infusion, platelet count improved to 2. Due to this, he was given repeat IVIG. Oral tylenol on 2/5 resulted in bloody emesis, attributed to a recent nosebleed. Platelets improved to 24 after second IVIG. Patient was then given a dose of IV decadron prior to discharge and a repeat platelet level was obtained which was 34.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 08.02.2022
- Impfdatum
- 07.01.2022
- Beginn
- 08.02.2022
- Tage bis Beginn
- 32,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Computerised tomogram normal
Headache
SARS-CoV-2 test negative
Symptomtext
After I had the vaccine, I woke up with a very bad headache. I waited for a few days, but the headache never went away at all. Tylenol and nothing worked. I made an appointment with my doctor to see if I can get a prescription for the pain. I went to walk in clinic they prescribed 50 mg of Imitrex (1/21) daily. No relief after I took the pills. On 1/24 I went to the ER. They gave me an infusion and that help with the headache. I left the hospital. And I am planning to see my doctor, this time with a Neurologist. Appointment is March 17, 2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- COVID test - Negative. CT - Normal.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Blackcohosh, (heb), daily . Chytoestrogen, daily.
- Allergien
- Demerol
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 07.02.2022
- Impfdatum
- 09.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Angina pectoris
Malaise
Symptomtext
First shot was ok no major side affects, second shot not feeling well for the first week, did not feel normal until 3 weeks. the 3 rd shot, did not feel well at all the first week, started to develop heart pain on the 3rd day. After 4 weeks it was time to go to the doctor and find out what is wrong.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- Going in for a Lexiscan nuclear test and blood work in the next 4 weeks
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 05.02.2022
- Impfdatum
- 14.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 4,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Rash
Symptomtext
Patient reported that rashes developed on his left trunk 4 days after the administration of the first dose of Pfizer COVID vaccine. Rashes resolved one day without self-treatment. No difficulty breathing or other serious allergic reactions were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 05.02.2022
- Impfdatum
- 10.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Incorrect dose administered
Wrong product administered
Symptomtext
headache; went to receive the flu shot/ they gave him another Pfizer COVID-19 vaccine; went to receive the flu shot/ they gave him another Pfizer COVID-19 vaccine; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team for a Pfizer sponsored program (005570). The reporter is the patient. A 59 year-old male patient received bnt162b2 (BNT162B2), administration date 10Jan2022 (Lot number: 330258D, Expiration Date: 28Feb2022) at the age of 59 years as dose 4 (booster), single for covid-19 immunisation; influenza vaccine (FLU) (Batch/Lot number: unknown). The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Bnt162b2 (First dose of the Pfizer COVID-19 vaccine was 02Mar2021 with LOT: EN6198, with no EXP provided on his printout for that dose., first dose injected in his arm), administration date: 02Mar2021, when the patient was 58 years old, for COVID-19 immunization; Bnt162b2 (Second dose was on 23Mar2021 and was LOT: EN6207, with the EXP not provided on vaccine card printout.), administration date: 23Mar2021, when the patient was 58 years old, for COVID-19 immunization; Bnt162b2 (Third dose was given 09Nov2021 of LOT: EW0183, with EXP not provided on vaccine card printout.), administration date: 09Nov2021, when the patient was 59 years old, for COVID-19 immunization. The following information was reported: INCORRECT DOSE ADMINISTERED (non-serious), WRONG PRODUCT ADMINISTERED (non-serious) all with onset 10Jan2022, outcome "unknown" and all described as "went to receive the flu shot/ they gave him another Pfizer COVID-19 vaccine"; HEADACHE (non-serious), outcome "recovering", described as "headache". Therapeutic measures were taken as a result of headache. Additional information: Caller reported that everything was fine until the day before yesterday, he went into the (pharmacy name withheld) for a flu shot and was accidentally given a Pfizer Covid-19 vaccine, making this the fourth dose he has received. Caller was asking if there was anything to be worried about? Caller asked what the recommended time frame was for the immunocomprise to receive each dose. This report was not related to a study or programme. RA number of Unspecified flu shot was not Provided Investigation Assessment: No. Caller confirmed above details and clarifies that it was 10Jan, when the fourth dose of the Pfizer COVID-19 vaccine was given. Caller said he had printouts and they only handwrote the dates of the vaccinations on them, the rest was printed on the vaccination record card, CDC version. Caller said that 10Jan2022 he received his fourth dose which he was not trying to get or supposed to get. He said that the idiot so called pharmacist gave him Pfizer, when he was supposed to be getting a flu shot. RA number for fourth dose of Pfizer vaccine was 59267-1000-03. Initially he said that the LOT could be ending with a zero but then he said it doesn't have the slash like the other zero so he thought it look more like a D. Caller said that the flu shot was what he registered for, which somehow didn't transmit to the pharmacist, who admitted he didn't read the top line of the paperwork when they gave it to him. The patient had been consuming a lot of water anyway, so he continued to drink a lot. He said he had a headache after a couple days and yesterday he took some extra strength Tylenol, of which he took two tablets by mouth, since it was a pretty bad headache. He said he didn't know the exact dose of the extra strength Tylenol he took. He said he also took two Excedrin last night on the 11th. He said it was in the morning around 09:00AM give or take when he took the Tylenol, then he took the Extra Strength Excedrin, which were 250mg each, and he took two of those last night around 2300 hours. He said his headache was better. Caller said that he would like to provide information for which pharmacy it was, which was the (pharmacy name) location off of (withheld) in (withheld). Caller provided (Pharmacy name) Address: (withheld). He said the pharmacist's name was (name withheld), which was all he knew about him. He said he wanted to report it and make sure Pfizer had this information in case this was more of a problem or there were other issues than there are now in the future.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- 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
- FL
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 01.02.2022
- Impfdatum
- 13.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blister
Chills
Erythema
Fatigue
Hyperhidrosis
Pruritus
Pyrexia
Skin warm
Sluggishness
Swelling
Urticaria
Symptomtext
She got her vaccine, didn't bother her that day. She noticed itching that night. Then the following morning she woke up sluggish, but went to PT for her knee anyway. She continued to feel tired. She noticed itching on her arm continued, and then looked at it and it was red with a welt. She measured it and it was 3 1/2" wide by 2 1/2" in length. By Saturday it was 6" wide and 4" in length. It was warm to touch and itchy. During Saturday and Sunday she had chills, slight fever, took Tylenol, stayed covered up. She broke her fever occasionally and started to sweat. She had a doctors APT on Tuesday 1/18/22, it was still red and not as elevated. She then started to get little bubbles/blisters in it. She was advised to let it take it's course. It has now all gone away.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Chronic kidney disease stage III, parathyroid removed (4) nodes had tumor growing on the thyroid, depression, bipolar.
- Andere Medikamente
- Rosuvastatin 40 mg, Levothyroxine 0.75 mcg, Lorazepam 1 mg,, Oxycodone 10 mg, Zinc 50 mg, B complex with folic acid and vitamin C.
- Allergien
- Erythromycin (hives), Aleve (hives), Zantac (turns body fluid black like tar). Celexa, Zoloft, Plavix, depression medications (rash).
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 29.01.2022
- Impfdatum
- 24.01.2022
- Beginn
- 25.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Oedema peripheral
Symptomtext
Patient developed swelling under the arm (armpit) and pain in the arm. No redness or swelling around the site and movement in the arm was okay.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 28.01.2022
- Impfdatum
- 28.12.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anxiety
Back pain
Headache
Pyrexia
Symptomtext
Severe Back pain; Fever; Severe Headaches; Anxiety was worse; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 37 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 28Dec2021 (Lot number: 330258D, Expiration Date: Feb2022) at the age of 37 years as dose 2, single for covid-19 immunisation; influenza vaccine (FLU), administered in arm right, administration date 28Dec2021 (Batch/Lot number: unknown) as dose number unknown, single. Relevant medical history included: "obese", start date: 2020 (unspecified if ongoing), notes: starting 2 years ago; "Hashimoto's disease", start date: 2018 (unspecified if ongoing), notes: Diagnosed 4 years.; "Anxiety" (unspecified if ongoing); "underlying back problems" (unspecified if ongoing); "detoxing off of alcohol" (unspecified if ongoing); "rehab", start date: 19Dec2021, stop date: 24Dec2021, notes: alcohol detox center. Family history included: "high blood pressure" (unspecified if ongoing), notes: before the vaccine., Family Medical History Relevant to AE(s): High blood pressure. The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (DOSE 1, 1st dose Lot FH8027, Expiration is Feb2022, Injected in right arm.), administration date: 04Dec2021, when the patient was 37 years old, for COVID-19 immunization, reaction(s): "no side effect". The following information was reported: HEADACHE (non-serious) with onset 29Dec2021, outcome "recovering", described as "Severe Headaches"; BACK PAIN (non-serious), outcome "not recovered", described as "Severe Back pain"; PYREXIA (non-serious) with onset 29Dec2021, outcome "recovering", described as "Fever"; ANXIETY (non-serious) with onset Dec2021, outcome "not recovered", described as "Anxiety was worse". Therapeutic measures were taken as a result of anxiety. Additional information: She received first dose 04Dec2021 and had no side effects. She received her 2nd vaccine on 28Dec2021. The next morning, she had severe headaches and had been lingering around since, but gotten better now. She also had back pain, which was very severe. She had a doctor's appointment on Tuesday. She had underlying back problems and it got worse since she got the vaccine. It was years ago and she was a professional dancer. Her back problems got better and after the vaccine got a lot worse. The back pain happened a few days after 2nd dose, and had gotten progressively worse. She called a nurse help line and was said to call Pfizer to report. Her mom was bugging her to get it. Everyone was getting COVID and she wanted to protect herself. She did mention to the nurse that she was taking more anxiety medication than usual. She doesn't think it has to do with the vaccine. Her anxiety is worse than usual and she is needing to take more. She noticed it was worse around 22Dec2021 or 23Dec2021, when she began Buspar. She was also detoxing off of alcohol. She was not necessarily detoxing, but she was there for cravings and the hospital gave her Buspar and started giving it to her there. She said she went to the hospital before this 2nd dose. She has not had to go to the hospital since the 2nd vaccine. She had been in and out of the hospital since Oct2021. She said it was a rehab or clinic, not a hospital. It was a nursing home that they turned to a rehab. She was admitted on 19 of Dec 2021 and stayed until 24Dec2021. She stayed for 6 days. This was in an alcohol detox center. She was not detoxing bad at all and she took a little Buspar while she was there. Since the vaccine she has been taking more. She needed it every 2-3 hours. Her husband also had a headache and fever. The next morning, they felt like poo poo. They felt really bad, more so her. His symptoms went away, but hers did not. She just had underlying back pain. She had high blood pressure, which was before the vaccine. She wanted to know if she should get booster dose or not. The severe headaches started in the morning as soon as she woke up; severe back pain started in the morning; anxiety was worse in the morning and afternoon it got worse toward 11:00-12:00; fever started in the morning. The events did not require visits to Emergency Room or Physician Office.; Sender's Comments: The event anxiety is assessed as an intercurrent condition that is unrelated to the administration of BNT162B2 vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Alcohol detoxification; Anxiety; Back disorder; Blood pressure high (before the vaccine. Family Medical History Relevant to AE(s): High blood pressure); Hashimoto's disease (Diagnosed 4 years.); Obesity (starting 2 years ago); Rehabilitation therapy (alcohol detox center)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 27.01.2022
- Impfdatum
- 25.01.2022
- Beginn
- 25.01.2022
- 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 erythema
Injection site warmth
Symptomtext
Erythema and warmth at injection site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma
- Andere Medikamente
- None
- Allergien
- Environmental
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 21.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Feeding disorder
Impaired work ability
Pyrexia
Symptomtext
Severe weakness, unable to eat, prolonged high temp 103 for almost 2 days. Had to take days off from work. Returned after 6 days still very weak. Better today (day 8).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- No
- Andere Medikamente
- None other than serovital powder antioxidant - have taken for years
- Allergien
- Bee sting!!
- Vorherige Impfungen
- Pfizer second shot 1/18/2021 lot #EL1283
- Staat
- -
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 20.01.2022
- Impfdatum
- 22.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Fatigue
Immunisation
Lymphadenopathy
Myalgia
Symptomtext
Dose Number: 3; Fatigue; Chills; muscle soreness (entire body); swollen lymph node under left arm; This is a spontaneous report received from a non-contactable reporter(s) (Other HCP). The reporter is the patient. A 38-years-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 22Dec2021 (Lot number: 330258D) at the age of 38 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "known_allergies:Sulfa Drugs" (unspecified if ongoing); "known_allergies:Dill" (unspecified if ongoing). Concomitant medication(s) included: LEXAPRO. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0151, Location of injection: Arm Left), administration date: 15Apr2021, when the patient was 37 years old, for COVID-19 Immunization, reaction(s): "No AEs occurred with previous two Doses"; Bnt162b2 (Dose Number: 1, Batch/Lot No: ER8730, Location of injection: Arm Left), administration date: 24Mar2021, when the patient was 37 years old, for COVID-19 Immunization, reaction(s): "No AEs occurred with previous two Doses". The following information was reported: IMMUNISATION (non-serious) with onset 22Dec2021, outcome "not recovered", described as "Dose Number: 3"; FATIGUE (non-serious) with onset 22Dec2021, outcome "not recovered", described as "Fatigue"; CHILLS (non-serious) with onset 22Dec2021, outcome "not recovered", described as "Chills"; MYALGIA (non-serious) with onset 22Dec2021, outcome "not recovered", described as "muscle soreness (entire body)"; LYMPHADENOPATHY (non-serious) with onset 22Dec2021, outcome "not recovered", described as "swollen lymph node under left arm". Therapeutic measures were not taken as a result of immunisation, fatigue, chills, myalgia, lymphadenopathy. Additional Information: The patient had fatigue, chills, muscle soreness (entire body), swollen lymph node under left arm within first 24 hours. No adverse events occurred with previous two doses. The patient had known allergies: SULFA Drugs, DILL. The patient had no other medical history. The patient had no other vaccine in four weeks. Other medications in two weeks: LEXAPRO. No treatment received for adverse events. The patient did not have COVID-19 prior to vaccination and was not tested for COVID-19 since vaccination. 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 to plants; Sulfonamide allergy
- Andere Medikamente
- LEXAPRO
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 17.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Impaired work ability
Injection site pain
Tenderness
Symptomtext
Arm pain at site if injection 12-24 hours after injection, then improved. Axillary tenderness and pain 24-48 hours after injection, not yet improved causing difficulty with physical responsibilities at work.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Lactose intolerant, gluten intolerance
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- 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: nein
Ageusia
Anosmia
Fatigue
Menstruation delayed
Pharyngeal swelling
Sinusitis
Symptomtext
Two days after the 3rd shot I started with swollen throat, swollen sinuses, extreme fatigue , taste and smell has reduced 90% and my period hasn?t started and was due the day after my shot. I still am having the same symptoms almost two weeks later
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Injection site pain
Product preparation issue
Symptomtext
Patient was accidently given 0.3 ml of the undiluted vaccine. Patient has been monitored since then for any adverse effects. Patient complains of soreness at injection site and 'feeling tired'. No other symptoms. Encouraged oral fluids. Vital signs stable
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Lactose, penicillin, dairy
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 13.01.2022
- Impfdatum
- 04.01.2022
- Beginn
- 04.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Injection site erythema
Injection site pain
Peripheral swelling
Swelling
Symptomtext
"37 year old female usually healthy and without significant medical history presents for pain and swelling after covid booster. She received her vaccine booster 01/04/2022 and experienced some pain with redness to the local area of her left deltoid that evening. She does not like taking medications and so did not take any OTC analgesics. The next day she awoke with increased pain and noted palpable swelling to her upper arm/shoulder area extending to her left anterior and lateral neck. No dysphagia, no hoarseness, no difficulty swallowing, no shortness of breath. No overlying redness. No fever. The pain continues 01/06/2022 worse with even light palpation over the area as well as rotation of her head and neck." "Left upper extremity deltoid area contiguous with the top of her shoulder and supraclavicular region indurated without overlying erythema, no fluctuance, tender to palpation. No axillary lymphadenopathy" "This is likely a noninfectious inflammation secondary to her Covid vaccine..."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- No labs done at ER visit
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- none documented in ER visit
- Andere Medikamente
- none known
- Allergien
- sulfa antibiotics
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 13.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Headache
Symptomtext
Developed headache
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 12.01.2022
- Impfdatum
- 04.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain in extremity
Vaccination site erythema
Vaccination site swelling
Vaccination site warmth
Symptomtext
The injection site is swelling; The injection site is swelling, redness; Arm pain; No fever other than at the injection site; This is a spontaneous report from a contactable reporter (consumer or other non-HCP). The reporter is the patient. A 57-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in left arm, administration date 04Jan2022 at 12:15 (Lot number: 330258D) at the age of 57 years as dose 1, single for COVID-19 immunisation. The patient did not have any relevant medical history. There were no concomitant medications. The following information was reported: VACCINATION SITE SWELLING (non-serious) with onset 05Jan2022 at 13:00, outcome "unknown", described as "The injection site is swelling"; VACCINATION SITE ERYTHEMA (non-serious) with onset 05Jan2022 at 13:00, outcome "unknown", described as "The injection site is swelling, redness"; PAIN IN EXTREMITY (non-serious) with onset 05Jan2022 at 13:00, outcome "unknown", described as "Arm pain"; VACCINATION SITE WARMTH (non-serious) with onset 05Jan2022 at 13:00, outcome "unknown", described as "No fever other than at the injection site". It was unknown whether therapeutic measures were taken as a result of events. Additional information: The patient had no known allergies. The patient did not receive any other vaccines within four weeks prior to the COVID 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. 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
- Pain in extremity
- 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
- CA
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 11.01.2022
- Impfdatum
- 10.12.2021
- Beginn
- 23.12.2021
- Tage bis Beginn
- 13,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Angiogram
Computerised tomogram
Dysuria
Echocardiogram
Gene mutation identification test negative
Malaise
Pain
Renal infarct
Symptomtext
13 days after the booster my husband began to feel ill in the afternoon he assumed it was food poisoning he was unable to vomit or use the restroom the pain became more intense to the point he needed to be taken to the ER put on morphine and was discovered to have had a renal infarction
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- 6,0
- Labordaten
- CT scan, angiogram, echocardiogram, bubble test, DNA gene blood testing With all these test run and completed nothing was determined to have caused the renal infarction that is why we are filing this report he had no heart problem no problem problem no family history completely healthy male adult doesn?t drink doesn?t smoke works out every day so this was shocking to say the least
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Singular, Q-Var
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- Impfdatum
- 09.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Back pain
Chills
Pyrexia
Symptomtext
lower back and hips are extremely sore and painful, 102 fever, chills
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- zoloft, vitamin d,
- Allergien
- amoxicillin,
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Injection site pain
Joint swelling
Lymphadenopathy
Pain
Pain in extremity
Rash
Urticaria
Symptomtext
Day after shot, shooting pain from injection site to my fingertips. Then pain started across left shoulder. Rash/Hives on both forearms, lymph nodes swelling under left arm and left knee swelling. Shooting pain has gone and rash/hives are slowly disappearing, but swelling of lymph nodes and knee are still present 3 days after shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- N/A - Unable to get an appointment at the VA.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Levothyroxine; Simvastatin; Lisinopril; Omeprazole; Vitamin D; Zinc; Multi Vitamin; Zyrtec.
- Allergien
- Penicillin; Erythromycin; Bactrim; Tramadol; Tamiflu; Aspirin; Acetaminophen; Naprosyn; Ibuprofen.
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 09.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Diarrhoea
Fatigue
Pain
Pain in extremity
Pyrexia
Symptomtext
Severe body aches, fever, fatigue, and arm pain, much worse than after 2nd shot. Diarrhea began 1/8/2022 and is ongoing. Today is Day 3 of symptoms; I was sick for only 1 day after the 2nd shot. Treating with Tylenol and Immodium. I have had no (zero) contact with other people since I got the booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Multivitamin, alphalipoic acid
- Allergien
- Codeine, sulfa
- Vorherige Impfungen
- Pfizer Covid-19 vaccine, 2nd dose, flu-like symptoms for 24 hours
- Staat
- -
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 08.01.2022
- Impfdatum
- 22.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Headache
Immunisation
Lymphadenopathy
Pain in extremity
Symptomtext
Extreme Fatigue; headache; Sore Arm; swollen lymph nodes in the arm pit where she received the injection; Booster; 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), administered in arm right, administration date 22Dec2021 18:45 (Lot number: 330258D) at the age of 39 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, Lot: ER8734, her glands under her chin were swollen on one side after one of the first or second vaccines), administration date: 21Apr2021, when the patient was 38 years old, for COVID-19 vaccination, reaction(s): "glands under her chin were swollen on one side after"; Bnt162b2 (Second Dose, Lot: EW0170), administration date: 12May2021, when the patient was 38 years old, for COVID-19 vaccination, reaction(s): "glands under her chin were swollen on one side after". The following information was reported: IMMUNISATION (non-serious) with onset 22Dec2021 18:45, outcome "unknown", described as "Booster"; FATIGUE (non-serious) with onset 23Dec2021 08:00, outcome "recovered" (27Dec2021), described as "Extreme Fatigue"; HEADACHE (non-serious) with onset 23Dec2021 08:00, outcome "recovered" (26Dec2021), described as "headache"; PAIN IN EXTREMITY (non-serious) with onset 23Dec2021 08:00, outcome "recovered" (25Dec2021), described as "Sore Arm"; LYMPHADENOPATHY (non-serious) with onset 23Dec2021 08:00, outcome "recovered" (26Dec2021), described as "swollen lymph nodes in the arm pit where she received the injection". Therapeutic measures were taken as a result of fatigue, headache, pain in extremity, lymphadenopathy. Additional information: The patient stated that she wanted to report the side effects she experienced with the Booster Dose. The patient stated that most were standard symptoms and they lasted a solid 4 days after booster, some 4.5 to 5 days. The patient stated that they were extreme fatigue, headache, swollen lymph nodes in the arm pit where she received the injection, and sore arm. The patient stated that she received the Booster Dose on Wednesday evening at 6:45 p.m. and she started having the side effect when she woke up the next morning at 8:00 a.m. on Thursday 23Dec2021. The patient stated that she had to call off work and take multiple naps each day. The patient stated that she took Acetaminophen and when that didn't start to help she also took Aspirin and at different points she took Tylenol and Ibuprofen. Acetaminophen 1000mg; 2 500mg. The patient stated that it did help but the Tylenol and Ibuprofen were working better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- 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
- 33,0
- Geschlecht
- F
- Eingang
- 06.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Arthralgia
Symptomtext
Pt c/o moderate-severe left shoulder pain, recommended otc pain meds, f/u with pcp if symptoms worsen or do not improve
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 06.01.2022
- 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: unbekannt
Erholt: nein
Pain in extremity
Symptomtext
Patient's daughter, reported her arm is still significantly sore today after more than a week since vaccination. Recommend patient sees a doctor.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 05.01.2022
- 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: nein
Asthenopia
Chills
Eye pain
Fatigue
Pain in extremity
Symptomtext
Patient describes that she had a sore arm the night of. The next day she reported feeling "super super tired" with sore arm, chills, and her eyes were hurting. When asked to describe the pain, she said she just felt like her eyes were tired and hurt. Couldn't describe eye pain well. Recommended that patient follow up with a doctor about eye pain especially if it gets worse/does not go away.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 05.01.2022
- Impfdatum
- 31.12.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Cough
Headache
Influenza like illness
Joint stiffness
Lymphadenopathy
Malaise
Nasopharyngitis
Sinus congestion
Symptomtext
Swollen lymph node- right armpit. No treatment Cold/flu like symptoms(headache, joint pain/tightness, malaise, sinus congestion, cough). Treat at home/rest.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Vitamin D, Vitamin B-12, fish oil, Fexofenadine, eye supplement (Vitamin A, Vitamin E, lucopene, Lutein, Zeaxanthin, Astaxanthin Algae Extract), Curcumin.
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 03.01.2022
- Impfdatum
- 20.12.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 12,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Rash
Urticaria
Symptomtext
11 days after Pfizer booster shot (first two were Moderna) skin started breaking out in extremely itchy hives all over body. At this time it has been 3 days with little to no improvement. Antihistamines such as Zyrtec have helped with itching, but adverse effects are still present. Have never had any allergies to any other foods/medicines.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 30.12.2021
- Impfdatum
- 27.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Decreased appetite
Diarrhoea
Dizziness
Exposure during pregnancy
Injection site induration
Injection site mass
Injection site pain
Somnolence
Symptomtext
14 weeks pregnant Estimated due date is June 2022. Uncontrollable diarrhoea. Drowsiness. Lack of appetite. Dizziness arm tenderness at injection site. Hard limp at injection site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 30.12.2021
- Impfdatum
- 29.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dizziness
Pharyngeal swelling
Swollen tongue
Symptomtext
Dizziness, enlarged throat, swollen tongue
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Vitamin C Zinc Vitamin D
- Allergien
- Cantaloupe Honeydew Raw Almonds Bananas Avocado Propolis
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 29.12.2021
- 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: unbekannt
Erholt: unbekannt
Asthenia
Chills
Headache
Injection site pain
Pain
Pyrexia
Symptomtext
Mild headache, fever, chills, body ache, lack of energy. I still have a very strong pain in my left arm where I received the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 29.12.2021
- Impfdatum
- 24.12.2021
- Beginn
- 25.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Gait disturbance
Headache
Loss of personal independence in daily activities
Pain
Symptomtext
Elevated temperatures 99.8 every day since injection. Extreme body aches and exhaustion. I am only able to walk very slow because of the body pain. I have not been able to leave my house due to the excutating pain. Extreme headaches, level 7. I do suffer from migraines, my migraines are by my right occipital nerve. The headaches I am currently having are an all over brain ache, pulsating pain. Advil and tylenol are providing no relief. The CDC page said side effects only last a day or 2, I am now on day 5 of side effects and I am not seeing any relief.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- IBS, migraines, alopecia
- Andere Medikamente
- Amitriptyline, librax, botox for migraines, magnesium, multivitamin, Pravastatin, singular, tizanidine, atenolol, alprazolam
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 29.12.2021
- Impfdatum
- 28.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Myalgia
Symptomtext
Mild pain in injection site-left arm, mild body/muscle aches
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Chronic cervical spinal stenosis/nerve pain
- Andere Medikamente
- Tylenol
- Allergien
- Imitrex
- Vorherige Impfungen
- 44
- Staat
- OH
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 27.12.2021
- Impfdatum
- 27.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
Lethargy
Malaise
Nausea
Pain in extremity
Symptomtext
Her husband came to the pharmacy stating that his wife was waiting in the parking lot ,after her second covid vaccine, and wasn't feeling well. I went to the parking lot and she was sitting in the car. She was lethargic, complaining of left arm pain, nausea, and weak. She was awake and able to communicate. I asked if she wanted me to call the ambulance and she said yes. I placed the call and they were here in about 10 minutes. The emt determined she should be taken to the hospital. At this point, she was feeling better. She stated she didn't want to go l, but in her best interest it was determined she should be assessed at the hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No other illnesses listed.
- Vorgeschichte
- No health conditions listed.
- Andere Medikamente
- Patient did not list medications on VAR and no medications are filled at this chain pharmacy.
- Allergien
- Patient stated no allergies on VAR form and none listed in her profile in the pharmacy. Later during reaction, husband stated she is allergic to sulfa.
- Vorherige Impfungen
- Patient was lethargic after her first Covid (pfizer) vaccine. Generally not feeling well for a couple days.
- Staat
- GA
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 21.12.2021
- Impfdatum
- 17.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Haemorrhage
Injection site swelling
Symptomtext
IMMEDIATE SWELLING AT INJECTION SITE. SOME BLEEDING BUT CONTAINED. PATIENT DID NOT COMPLAIN OF PAIN OR PRESSURE FROM SWELLING.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site swelling
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 21.12.2021
- Impfdatum
- 19.12.2021
- Beginn
- 19.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Breast swelling
Chills
Dizziness
Fatigue
Feeling abnormal
Hypoaesthesia
Illness
Pain
Pain in extremity
Peripheral swelling
Pyrexia
Sensitive skin
Symptomtext
dizzy, severe arm pain, swollen arm, swollen under breast/underarm, skin ultra sensitive, arm numbness, ear ringing, 99F to 100F fever over 24 hour period, extreme fatigue, extreme chills. I felt so terrible and in pain, I wished someone would just take me out, unbearable sickness, fatigue, pains, and chills for 3 days. Despite I moved my arm around lots after the shot, drinking lots of fluids including Gatorade, and ate good meals. This was merely my COVID Booster (3rd shot), as I thought it would be a smaller dose; and this is my worst reaction of the 3 shots I've received. I'm still recovering from this shot on my 3rd day, hopefully all will be well, but this was beyond painful.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- all NSAIDs
- Vorherige Impfungen
- every Flu shot and both previous COVID shots, but less severe than this one
- Staat
- NM
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 21.12.2021
- Impfdatum
- 19.12.2021
- Beginn
- 19.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Dysstasia
Neck pain
Pain in extremity
Symptomtext
shortly after injection the patient felt a sharp pain through arm and neck, felt very dizzy and could not stand
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- EMS was activated per the patients request, and the paramedics could not find any abnormal lab values
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- bipolar disorder
- Andere Medikamente
- -
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 14.12.2021
- Impfdatum
- 14.12.2021
- Beginn
- 14.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Erythema
Formication
Nausea
Pruritus
Symptomtext
The client received the vaccine at 1459 and started feeling nauseous at 1415. She was given water and advised to stay additional 15 minutes for detailed observation. At 12:30, she c/o of itching and "bugs crawling under her skin." Bright red erythema spots were noted on the chest, back, and hands. BP was measured to be 126/62. No wheezing or SOB. Called EMS. EMS instructed to activate EMS, and administer epinephrine. Epi-pen was administered along with 50 mg of diphenhydramine at 1440. BP measured post Epi administration 140/60, O2 99% HR 90. No SOB or wheezing. Patient reported itching has stopped as evidenced by a decrease in erythema on patient's chest, back, and hands. BP at 1500 was measured. 110/60, HR90, O2 99%. Paramedics arrived at 1506 and took the patient at 1508. No vitals were checked on the spot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 26.06.2023
- Impfdatum
- 02.01.2022
- Beginn
- 16.03.2023
- Tage bis Beginn
- 438,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthma
Respiratory failure
Tracheal stenosis
Symptomtext
J96.90 RESPIRATORY FAILURE, UNSPECIFIED ACUITY 3/30/2023 SEVERE PERSISTENT ASTHMA W ACUTE EXACERBATION J96.90 RESPIRATORY FAILURE, UNSPECIFIED ACUITY 3/30/2023 ASTHMA, UNSPECIFIED J96.90 RESPIRATORY FAILURE, UNSPECIFIED ACUITY 3/30/2023 TRACHEAL STENOSIS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asthma
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 22.06.2023
- Impfdatum
- 27.12.2021
- Beginn
- 17.05.2022
- Tage bis Beginn
- 141,0
- 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 4/21/21 lot# Ew0171; Pfizer 5/12/21 lot# Ew0177; Pfizer 12/27/21 lot# 330258D
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 01.05.2023
- Impfdatum
- 30.12.2021
- Beginn
- 24.04.2023
- Tage bis Beginn
- 480,0
- 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 2/8/21 Lot# EL9267; Pfizer 3/11/21 Lot# EN6199; Pfizer 12/30/21 Lot# 330258D;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 05.04.2023
- Impfdatum
- 28.12.2021
- Beginn
- 09.03.2023
- Tage bis Beginn
- 436,0
- 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 5/27/21 Lot# EW0187; Pfizer 6/17/21 Lot# Ew0196; Pfizer 12/28/21 Lot# 330258D
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 14.02.2023
- Impfdatum
- 26.12.2021
- Beginn
- 17.08.2022
- Tage bis Beginn
- 234,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
Covid positive; Covid positive; This is a spontaneous report received from a contactable reporter(s) (Nurse). The reporter is the patient. A 55-year-old female patient received BNT162b2 (BNT162B2), on 06Jan2021 at 11:00 as dose 1, single (Lot number: ER9231), in left deltoid, on 27Jan2021 at 11:00 as dose 2, single (Lot number: EL9261), in right deltoid and on 26Dec2021 at 10:00 as dose 3 (booster), single (Lot number: 330258D) at the age of 55 years, in left deltoid, all intramuscular for covid-19 immunisation. The patient's relevant medical history included: "Grief", start date: 2020 (ongoing); "Allergies" (unspecified if ongoing); "Joint health" (unspecified if ongoing); "Bone health" (unspecified if ongoing); "Knee surgery" (ongoing); "Depression", start date: 2020 (ongoing). Concomitant medication(s) included: VENLAFAXINE oral taken for depression, start date: 2020 (ongoing); CETRIZINE oral taken for multiple allergies, start date: 2007 (ongoing); OSTEO BI-FLEX [CHONDROITIN SULFATE;GLUCOSAMINE HYDROCHLORIDE] oral taken for arthropathy, start date: 2015 (ongoing); CALCITRATE oral taken for bone disorder, start date: 2018 (ongoing). The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 17Aug2022, outcome "recovered" (22Aug2022) and all described as "Covid positive". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (14Aug2022) Positive; (17Aug2022) Positive. Clinical course: Complete if a 3rd or Subsequent dose was administered. Check one option: Booster dose due to high risk of frequent institutional or occupational exposure to coronavirus (and at risk of serious COVID-19 complications): Checked, Healthcare. worker. Drug Name: Multivitamin, route: oral. Farmly Covid positive on 14Aug2022. Patient tested positive on 17Aug, only symptoms are sinus drip daily plus low-grade fever 100.5 on day 0. fever free next 5 days. Family Medical History Relevant to Adverse Events (AEs): Her husband contracted COVID early in the pandemic and dead due to the illness in May2020. She had initial exposure, but never had symptoms, therefore never tested but did have a neg antibody test months later. Specific Relevant Test for thromboembolic events with thrombocytopenia was none reported.; Sender's Comments: Based on the information currently available, The casual association between the reported eventS and suspected drug cannot be completely excluded.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220814; Test Name: COVID-19 test; Test Result: Positive ; Test Date: 20220817; Test Name: COVID-19 test; Test Result: Positive
- Aktuelle Erkrankungen
- Depression; Grief reaction; Knee operation
- Vorgeschichte
- Medical History/Concurrent Conditions: Allergy multiple; Bone disorder; Joint disorder
- Andere Medikamente
- VENLAFAXINE; CETRIZINE; OSTEO BI-FLEX [CHONDROITIN SULFATE;GLUCOSAMINE HYDROCHLORIDE]; CALCITRATE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 23.01.2023
- Impfdatum
- 09.04.2021
- Beginn
- 01.06.2021
- Tage bis Beginn
- 53,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acoustic stimulation tests
Tinnitus
Symptomtext
Severe tinnitus in both ears.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acoustic stimulation tests
- Hospital-Tage
- -
- Labordaten
- Hearing tests, series of prescriptions including SSRIs, Amitriptyline and Gabapentin.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Losartan 100 mg Levothyroxine 50mcg Atorvastatin 10 mg
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 09.08.2022
- Impfdatum
- 07.01.2022
- Beginn
- 08.08.2022
- Tage bis Beginn
- 213,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Inappropriate schedule of product administration
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after three vaccines Pfizer 3/13/21 Lot# EN6200; Pfizer 4/5/21 Lot# ER2613; Pfizer 1/7/22 Lot# 33025
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 22.06.2022
- Impfdatum
- 29.12.2021
- Beginn
- 21.06.2022
- Tage bis Beginn
- 174,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Delivery
Exposure during pregnancy
SARS-CoV-2 test positive
Symptomtext
positive covid test in fully vaccinated and boostered pt; G1P0 40wks4days on 06/21/22, no birth weight avail
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 06.04.2022
- Impfdatum
- 12.02.2021
- Beginn
- 09.10.2021
- Tage bis Beginn
- 239,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Cough
COVID-19
Chest X-ray abnormal
Hypoxia
Pneumonitis
Scar
Symptomtext
reports his cough is been ongoing since Saturday
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 28.03.2022
- Impfdatum
- 28.03.2022
- Beginn
- 28.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
No adverse event
Symptomtext
No adverse event noted. Patient was due for third vaccine. Administered vaccine 1/13/2022. Wife brought card into clinic on 3/28/22 and noted pt received a previous booster in 12/2021 from a different facility.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Sulfa antibiotics
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 18.03.2022
- Impfdatum
- 10.02.2022
- Beginn
- 10.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
Vaccine Administration Error. The Pfizer vaccine given was outside of the usage date range and was administered to five patients on 2/10/2022. The vaccine was received into inventory on 12/15/2021 and was placed in the refrigerator. Pfizer was contacted and stated that the vaccine wasn't harmful but its efficacy/ potency may be in question and all patients who received it should be contacted and offered to be revaccinated. This was done and all patients declined to be revaccinated and stated that they felt fine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 18.03.2022
- Impfdatum
- 10.02.2022
- Beginn
- 10.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine Administration Error. The Pfizer vaccine given was outside of the usage date range and was administered to five patients on 2/10/2022. The vaccine was received into inventory on 12/15/2021 and was placed in the refrigerator. Pfizer was contacted and stated that the vaccine wasn't harmful but its efficacy/ potency may be in question and all patients who received it should be contacted and offered to be revaccinated. This was done and all patients declined to be revaccinated and stated that they felt fine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 18.03.2022
- Impfdatum
- 10.02.2022
- Beginn
- 10.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product storage error
Symptomtext
Vaccine Administration Error. The Pfizer vaccine given was outside of the usage date range and was administered to five patients on 2/10/2022. The vaccine was received into inventory on 12/15/2021 and was placed in the refrigerator. Pfizer was contacted and stated that the vaccine wasn't harmful but its efficacy/ potency may be in question and all patients who received it should be contacted and offered to be revaccinated. This was done and all patients declined to be revaccinated and stated that they felt fine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 18.03.2022
- Impfdatum
- 10.02.2022
- Beginn
- 10.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
Vaccine Administration Error. The Pfizer vaccine given was outside of the usage date range and was administered to five patients on 2/10/2022. The vaccine was received into inventory on 12/15/2021 and was placed in the refrigerator. Pfizer was contacted and stated that the vaccine wasn't harmful but its efficacy/ potency may be in question and all patients who received it should be contacted and offered to be revaccinated. This was done and all patients declined to be revaccinated and stated that they felt fine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 18.03.2022
- Impfdatum
- 10.02.2022
- Beginn
- 10.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine Administration Error. The Pfizer vaccine given was outside of the usage date range and was administered to five patients on 2/10/2022. The vaccine was received into inventory on 12/15/2021 and was placed in the refrigerator. Pfizer was contacted and stated that the vaccine wasn't harmful but its efficacy/ potency may be in question and all patients who received it should be contacted and offered to be revaccinated. This was done and all patients declined to be revaccinated and stated that they felt fine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 18.03.2022
- Impfdatum
- 17.02.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cough
Product administration error
Product storage error
Secretion discharge
Symptomtext
ADMINISTRATION ERROR: The vial had the expiration date for ultra cold storage on the vial and was used as the expiration date for the medication. The vial was stored in the refrigerator and was due to expire before the date given. Patient reported no ill effects from the vaccine other than coughing and some mucous later that day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cough
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- none reported.
- Vorgeschichte
- Heart condition.
- Andere Medikamente
- Furosemide, Atorvastatin, Potassium, Carvedilol.
- Allergien
- None reported.
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 18.03.2022
- Impfdatum
- 18.08.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Symptomtext
got COVID; got COVID; 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 left, administration date 06Feb2022 17:30 (Batch/Lot number: unknown) at the age of 55 years as dose 2, single and administration date 18Aug2021 (Lot number: 330258D) 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: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "got COVID". Clinical course: Patient stated she lost card but luckily took a picture of it. She thought they do not put that on there. That was the problem why did they not put that on. Patient stated yes for Prior vaccination (within 4 weeks) and when probed to confirm if vaccination was four weeks ago then stated, that was basically six month prior to this one and did not have any sore arm or anything (further not clarified). Just immediately got COVID so, that was bad. The lot number for bnt162b2 was not provided and will be requested during follow up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 28.02.2022
- Impfdatum
- 24.12.2021
- Beginn
- 23.02.2022
- Tage bis Beginn
- 61,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Dysphagia
SARS-CoV-2 test positive
Symptomtext
Presents to the hospital with dysphagia and borderline blood pressures. Referred per primary care physician. During the course of admission patient was found to have (+) COVID-19. Patient did not have any hypoxia, did not require supplementation throughout the admission. Did not require inpatient management for COVID-19. Admitted 2/23/22-2/26/22 Pfizer 3/1/21, 3/23/21 & 12/24/21
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 3,0
- Labordaten
- COVID 19 + 2/23/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Parkinson's disease, seizure disorder
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 24.02.2022
- 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
Unevaluable event
Symptomtext
none reported
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- n/a
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 19.02.2022
- 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
Abortion spontaneous
Maternal exposure during pregnancy
SARS-CoV-2 test
Symptomtext
miscarriage; booster vaccine at 27Dec2021, 2 days after I was conceived; 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 (pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 27Dec2021 19:00 (Lot number: 330258D) at the age of 31 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. Date of last menstrual period: 14Dec2021. The patient was 2 days pregnant at the time of exposure to bnt162b2. The patient was 2 weeks pregnant at the event onset. The patient was expected to deliver a baby(s) on 20Sep2022. Concomitant medication(s) included: PRENATAL VITAMINS [ASCORBIC ACID;BETACAROTENE;CALCIUM SULFATE;COLECALCIFEROL;CYANOCOBALAMIN;FERROUS FUMARATE;FOLIC ACID;NICOTINAMIDE;PYRIDOXINE HYDROCHLORIDE;RETINOL ACETATE;RIBOFLAVIN;THIAMINE MONONITRATE;TOCOPHERYL ACETATE;ZINC OXIDE]. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0162, Location of injection: Arm Left, Vaccine Administration Time: 09:00 AM), administration date: 18Apr2021, when the patient was 31 years old, for COVID-19 Immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: ER8730, Location of injection: Arm Right, Vaccine Administration Time: 11:00 AM), administration date: 27Mar2021, when the patient was 31 years old, for COVID-19 Immunization. The patient had not received any other vaccines in 4 weeks and was not diagnosed with COVID prior to vaccination and had no known allergies. The following information was reported: MATERNAL EXPOSURE DURING PREGNANCY (medically significant) with onset 27Dec2021, outcome "recovering", described as "booster vaccine at 27Dec2021, 2 days after I was conceived"; ABORTION SPONTANEOUS (medically significant) with onset 29Jan2022 12:30, outcome "recovering", described as "miscarriage". The event "miscarriage" were evaluated at the physician office visit. The patient underwent the following laboratory tests and procedures: sars-cov-2 test: (06Jan2022) positive, notes: Nasal Swab. Therapeutic measures were not taken as a result of abortion spontaneous. The patient reported she received the booster vaccine at 27Dec2021, "2 days after I was conceived." After one week of booster shot, she was lab tested positive for COVID; almost the same time, she was confirmed pregnant. Until 29Jan2021, she experienced the extreme pain in lower "ab" and bleeding. Later on, she was confirmed miscarriage by her provider. The events did not require hospitalization.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abortion spontaneous
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220106; Test Name: PCR; Test Result: Positive ; Comments: Nasal Swab
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other medical history: no
- Andere Medikamente
- PRENATAL VITAMINS [ASCORBIC ACID;BETACAROTENE;CALCIUM SULFATE;COLECALCIFEROL;CYANOCOBALAMIN;FERROUS
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 19.02.2022
- 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
COVID-19
Maternal exposure before pregnancy
SARS-CoV-2 test
Vaccination failure
Symptomtext
After one week of booster shot, I was lab tested positive for covid.; After one week of booster shot, I was lab tested positive for covid.; After one week of booster shot, I was lab tested positive for covid. Almost the same time, I was confirmed pregnant; 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 received bnt162b2 (BNT162B2), administered in arm left, administration date 27Dec2021 19:00 (Lot number: 330258D) at the age of 31 years as dose 3 (booster), single, administered in arm left, administration date 18Apr2021 09:00 (Lot number: EW0162) as dose 2, single and administered in arm right, administration date 27Mar2021 11:00 (Lot number: ER8730) as dose 1, single for covid-19 immunisation. The patient had no relevant medical history. The patient took concomitant medications. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 06Jan2022, outcome "unknown" and all described as "After one week of booster shot, I was lab tested positive for covid."; MATERNAL EXPOSURE BEFORE PREGNANCY (non-serious) with onset 27Dec2021, outcome "unknown", described as "After one week of booster shot, I was lab tested positive for covid. Almost the same time, I was confirmed pregnant". The patient underwent the following laboratory tests and procedures: sars-cov-2 test: (06Jan2022) positive, notes: Nasal Swab. Clinical course: Patient stated, I received the booster vaccine at 27Dec2021, 2 days after I was conceived. After one week of booster shot, I was lab tested positive for covid. Almost the same time, I was confirmed pregnant. Until 29Jan21, I experienced the extreme pain in lower ab and bleeding. Later on, I was confirmed miscarriage by my provider. The patient had no known allergies. No other vaccine in four weeks. Patient took prenatal vitamin medications in two weeks. No covid prior vaccination. Post vaccination patient was COVID tested. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220106; Test Name: PCR; Test Result: Positive ; Comments: Nasal Swab
- 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
- AZ
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 11.02.2022
- Impfdatum
- 05.02.2022
- Beginn
- 05.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Patient received booster dose early (4 months) instead of at least 5 months between
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 09.02.2022
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product preparation issue
Symptomtext
Patient given Pfizer booster that was mixed with sterile diluent.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product preparation issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 09.02.2022
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product preparation issue
Symptomtext
Patient given a Pfizer booster mixed with sterile diluent
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product preparation issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 09.02.2022
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product preparation issue
Symptomtext
Patient received Pfizer booster mixed with sterile diluent
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product preparation issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 82,0
- Geschlecht
- M
- Eingang
- 09.02.2022
- Impfdatum
- 08.02.2022
- Beginn
- 08.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Product preparation error
Symptomtext
resident was given 0.3 ml of pfizer vaccine without being diluted with normal saline, resident received a concentrated dose of vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product preparation error
- Hospital-Tage
- -
- Labordaten
- increased monitoring
- Aktuelle Erkrankungen
- positive for covid on 1/19/22
- Vorgeschichte
- dementia, GERD, gout, parkinsons disease
- Andere Medikamente
- tylenol, aspirn, sinemet, colace, lasix, metoprolol, omperozole, miralax, potassium, senna, flomax, aricept
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 27.01.2022
- Impfdatum
- 10.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 10,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Depression
SARS-CoV-2 test positive
Suicidal ideation
Symptomtext
1/20/22 Pt is a 17 yr/o female who presents with complaints of depression. Office called and therapist recommendation was to be seen in ER due to suicidal thoughts. Admitted to hospital for depression/suicidal thoughts. COVID positive test was incidental *CONST : no fever. Normal appetite *NEURO : no headache. No dizziness *MUSC/SKLT : No extremity pain/ swelling noted. *EYES : No eye discharge seen. No redness appreciated. *HENT : No sore throat. No ear pain. *RESPIR : No respiratory difficulty. No significant cough *CARDIAC: No fast heart rate noted. No chest pain noted. *GI : No abdominal pain. Normal stools. *GU : No change in urine output noted. No dysuria *INTEGM : No rash or wounds. *HEME / LYMPH : No easy bruising/bleeding
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Depression
- Hospital-Tage
- -
- Labordaten
- 1/20/22 COVID-19 Result Detected Abnormal
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asthma, concussion, PFO (patent foramen ovale), Seasonal allergies, frequent UTI's
- Andere Medikamente
- albuterol HFA 108 (90 Base) MCG/ACT inhaler Inhale 2 puffs o bacitracin ointment Apply topically 2 (two) times daily to affected area(s).. o docusate sodium (COLACE) 100 MG capsule Take 1 capsule by mouth 2 (two) times daily. o flutica
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 27.01.2022
- Impfdatum
- 27.01.2022
- Beginn
- 27.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Feeling abnormal
Throat irritation
Throat tightness
Symptomtext
Itchy throat, feeling uneasy, slight tightness in throat @ 1135 Emergency zertec given @ 1140 Patient reports feeling better @ 1150 Patient observation time extended from 30 minutes to 1 hour with constant monitoring Patient leaves @ 1234 and states he feels better
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Feeling abnormal
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- covid 1 month prior to vaccine
- Vorgeschichte
- seizures
- Andere Medikamente
- lamictal, panto prozole
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 25.01.2022
- Impfdatum
- 22.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Immunisation
SARS-CoV-2 test
Vaccination failure
Symptomtext
Tested positive for Covid-19; Tested positive for Covid-19; Dose received:3; 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 44 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm right, administration date 22Dec2021 (Lot number: 330258D) at the age of 44 years as dose 3 (booster), single, intramuscular, administered in arm right, administration date 24Mar2021 (Lot number: EK5730) as dose 2, single and intramuscular, administered in arm right, administration date 03Mar2021 (Lot number: EJ1685) as dose 1, single for covid-19 immunisation; influenza vaccine (FLU), administered in arm right, administration date 22Dec2021 (Batch/Lot number: unknown) as dose number unknown, single for immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: IMMUNISATION (medically significant) with onset 22Dec2021, outcome "unknown", described as "Dose received:3"; VACCINATION FAILURE (medically significant) with onset 12Jan2022, outcome "unknown", COVID-19 (medically significant) with onset 12Jan2022, outcome "recovering" and all described as "Tested positive for Covid-19". The event "tested positive for covid-19" was evaluated at the physician office visit. The patient underwent the following laboratory tests and procedures: sars-cov-2 test: (12Jan2022) positive. Therapeutic measures were not taken as a result of covid-19. Clinical course: covid prior vaccination was reported as no. No follow-up attempts are needed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220112; Test Name: Nasal Swab; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 11,0
- Geschlecht
- F
- Eingang
- 22.01.2022
- Impfdatum
- 22.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
Patient's age and DOB were falsified so patient could receive Adult dose of Pfizer covid shot
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 21.01.2022
- Impfdatum
- 20.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
NONE, PATIENT RECIEVED VACCINE THAT WAS BEYOND USE DATE IN FRIDGE. DAY 34 INSTEAD OF DAY 31
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 21.01.2022
- Impfdatum
- 20.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
NONE, PATIENT RECIEVED VACCINES THAT WAS BEYOND USE DATE IN FRIDGE. DAY 34 INSTEAD OF DAY 31
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 21.01.2022
- Impfdatum
- 20.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
NONE, PT RECIEVED VACCINE THAT WAS BEYOND USE DATE. ON DAY 34 IN FRIDGE INSTEAD OF RECOMMENDED DAY 31
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 91,0
- Geschlecht
- F
- Eingang
- 21.01.2022
- Impfdatum
- 20.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
none, patient recieved pfizer booster shot that was in fridge after beyond use date by 3 days
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 20.01.2022
- Impfdatum
- 04.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymphadenopathy
Swelling
Symptomtext
Enlargement of the supraclavicular right lymph node by the collar bone. Enlargement/swelling persists 15 days later.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymphadenopathy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Vitamin D 2000IU 1x day
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
2nd dose given 8-30-2021 - 3rd dose given too early
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- 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
Inappropriate schedule of product administration
Symptomtext
Gave booster too early. Second dose Pfizer on 11/10/21. Given booster 1/19/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- nONE
- Vorgeschichte
- None
- Andere Medikamente
- nO
- Allergien
- nO
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 29.12.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fall
Muscle spasms
Muscle disorder
Symptomtext
2 days after patient received the vaccine she started having spasms which started in her hands. Since then she has continued to have spasm randomly throughout her body. She has not had spasm everyday but has had severe ones that have caused her to fall as part of them.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Muscle disorder
- Hospital-Tage
- -
- Labordaten
- Patient contacted PCP but has not been evaluated physically yet, PCP recommended holding off on second shot for now.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 16.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Lip swelling
Symptomtext
Red dot appeared between nose and top lip, next morning my top lip was fully swollen and unable to close completely
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Chronic regional pain syndrome
- Andere Medikamente
- Melatonin 10mg
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product preparation issue
Symptomtext
The nurse accidently injected undiluted 0.3mL of the vaccine to the patient. The patient was closely monitored. She reported no adverse reactions at this time. Vital signs stable. Encouraged plenty of fluids. Patient is still being monitored.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product preparation issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 13.01.2022
- Impfdatum
- 09.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Tinnitus
Symptomtext
Patient complained of tinnitus in both ears starting the morning after vaccination. Persisted for 48 hours at time vaccinating facility was contacted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tinnitus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- None known
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 10,0
- Geschlecht
- F
- Eingang
- 12.01.2022
- Impfdatum
- 11.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Symptomtext
DAD AND 2 CHILDREN CAME INTO THE ROOM FOR COVID-19..A LOT OF NOICE WITH THE KIDS AND TALKING WITH DAD ..SO I LOOK AT THE BIRTH DATE OF SISTER AND NOT THE PATIENT ..SHOW 12 YEAR OLD AND GAVE THE ADULT DOSE..AFTER GOING BACK TO THE PHARMACY NOTICE THAT THAT THE BIRTHDATE I LOOK AT WAS THE SISTER AND NOT THE PATIENT..CALL MOM AND DISCUSS THE PROBLEM..MOM WAS VERY UNDERSTANDING AND THANKUS FOR CALLING HER,,SHE REPEATED THAT SHE WAS SORRY ..TOO BUSY AND THE KIDS WERE ONLY BEING KIDS..
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- 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: unbekannt
Product storage error
Symptomtext
Patient given booster of Pfizer covid vaccine on 01/07/2022. Vaccine was removed from freezer and thawed and given to patient. The vaccine should have been moved to fridge on 12/31/2021, excursion of 7 days. Notified patient and Pfizer manufacturer same day. No issues reported by patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 10.01.2022
- Impfdatum
- 10.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Product preparation issue
Symptomtext
Patient received 0.3 ml of undiluted vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- NONE
- Andere Medikamente
- unknown
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 06.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood pressure increased
Heart rate increased
Symptomtext
About 10 minutes after receiving vaccine, patient states she feels like her heart is beating fast. I took her blood pressure and was high 187/114, then took two more times and went down almost immediately. Last reading was 128/79 about 15 minutes after first reading. She was feeling good when she left. Observed the patient for a total of 40 minutes after vaccine administed. Her pulse was slightly high 110, 103. Slight headache, but had this before receiving vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood pressure increased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 05.01.2022
- Impfdatum
- 30.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product administered to patient of inappropriate age
Symptomtext
no know adverse affects, shot given outside of the approved booster age range
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 05.01.2022
- 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
Expired product administered
Product expiration date issue
Symptomtext
Adverse Event: Prepared vaccination vial prepared 01/04/2022 , however labeled with 01/05/2022. Dose given today from the vial labeled as 1/5/2022 , however expiration time alerted RN the vial had Expired. Upon discovery of the expiration , this patient was present with physician and explained the situation to both PCP and patient. Patient agreed to receiving another dose with a VIABLE vaccination ;prepared and labeled correctly.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- at that time patient was in heart failure and being examined by her PCP, discussing her need for immediate hospitalization . Bipolar, Chronic bronchitis, morbid obesity, anxiety, permanent Atrial Fib, , moderate aortic stenosis, polypharmacy, OSA, CHF
- Vorgeschichte
- see above
- Andere Medikamente
- Last Taken albuterol sulfate 90 mcg/actuation inhaler albuterol sulfate HFA 90 mcg/actuation aerosol inhaler allopurinoL (ZYLOPRIM) 100 mg tablet allopurinol 100 mg tablet take 1 tablet by mouth twice a day ARIPiprazole (ABILIFY) 15 m
- Allergien
- Adhesive Tape Adhesive TapeRashMediumNot Verified4/5/2018Deletion Reason: Sulfa (Sulfonamide Antibiotics) Sulfa (Sulfonamide Antibiotics)RashMediumNot Verified4/5/2018Deletion Reason: Codeine
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 05.01.2022
- Impfdatum
- 04.01.2022
- Beginn
- 04.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Symptomtext
FDA only cleared booster for this age group and CDC had not signed off on order. Provider gave vaccine under impression booster was approved.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 10,0
- Geschlecht
- M
- Eingang
- 03.01.2022
- Impfdatum
- 30.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Symptomtext
Administration error, Patient received pfizer 12 years plus formulation. Patient is 10 years old. This occurred at a Pop Up clinic. Parent contacted. Per mom's request, patient's pediatrician was contacted as well to report. Mother reports patient is doing well, with no ADRs.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- unknown to reporter
- Aktuelle Erkrankungen
- unknown to reporter,
- Vorgeschichte
- Parent reports patient being in remission and receiving a bone marrow transplant at 6 months of age. The patient's pediatrician was contacted to report the error with Mom's approval. Mom reports patient is not considered immunocompromised at this point and is not taking medications related to transplant.
- Andere Medikamente
- Per mom ,medications for ADHD
- Allergien
- None noted on consent form
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 30.12.2021
- Impfdatum
- 30.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product storage error
Symptomtext
Patient received vaccine outside of 6 hour storage window following reconstitution. Pfizer was contacted and reported that the vaccine dose was still viable. Patient was contacted and informed of the error. No adverse reactions were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 30.12.2021
- Impfdatum
- 30.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
Patient received vaccine outside of 6 hour storage window following reconstitution. Pfizer was contacted and reported that the vaccine dose was still viable. Patient was contacted and informed of the error. No adverse reactions were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 30.12.2021
- Impfdatum
- 28.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Patient was 14 at time of booster shot and has no side effect
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 30.12.2021
- Impfdatum
- 29.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Swollen tongue
Throat irritation
Symptomtext
Itchy above throat and swelling of tongue, I called pharmacist she advised to take Benadryl. 16 hours later still feel itchy waiting for doctor to return my call.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Swollen tongue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- IBS
- Andere Medikamente
- Daily , Liberax , ( for IBS) Crestor, vitamin D with calcium And Zinc.
- Allergien
- I have had bad allergies to generic Liberax in the pass I ended in hospital. No doctor was able to tell what ingredient affected me .
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 28.12.2021
- Impfdatum
- 28.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Pt had no adverse event but was given a booster shot at the age of 15 instead of 16
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 28.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
No adverse event
Product administered to patient of inappropriate age
Symptomtext
IT IS NOT AN ADVERSE EFFECT, THE PATIENT WAS ADMINISTERED A THIRD DOSE AND IS ONLY 12 YEARS OLD. THE PATIENT IS IN WELL HEALTH AND I DID NOT PRESENT ANY EFFECT. I AM REPORTING AN ERROR MADE BY THE PERSONNEL THAT MANAGED IT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NO DISEASES.
- Vorgeschichte
- DOES NOT APPLY
- Andere Medikamente
- Patient does not take medication.
- Allergien
- DOES NOT HAVE ALLERGIES.
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 28.12.2021
- Impfdatum
- 20.12.2021
- Beginn
- 20.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Raynaud's phenomenon
Symptomtext
Patient described adverse event as "activation of Raynaud's" in bilateral hands. Symptoms began within about 15 minutes of vaccination and began to resolve in about 30 additional minutes. Patient left facility without additional incident.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Raynaud's phenomenon
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 15,0
- Geschlecht
- M
- 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
Product administered to patient of inappropriate age
Symptomtext
pt is only 15 years old and got a Pfizer booster
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- no
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 7,0
- Geschlecht
- M
- Eingang
- 22.12.2021
- Impfdatum
- 22.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
No adverse event
Symptomtext
Adult dose vaccine was accidentally given to the pediatric patient. Patient does not have any adverse reaction as of right now.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 21.12.2021
- Impfdatum
- 17.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Pfizer vaccine booster was administered to a 13-year-old child. Per Pfizer guidelines, boosters should be administered to patients 16-17 years of age and older. No adverse effects were reported. We followed up 2 days later and still no adverse effects. The patient reported good health per the parent's admission
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 15,0
- 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
Product administered to patient of inappropriate age
Symptomtext
PATIENT WAS GIVEN PFIZER BOOSTER SHOT AT 15 YEARS AND 10 MONTHS OLD. 2 MONTHS SHY OF 16 YEAR OLD FOR BOOSTER IN ERROR. NO OTHER ADVERSE EVENT NOTED/REPORTED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 7,0
- Geschlecht
- F
- Eingang
- 16.12.2021
- Impfdatum
- 15.12.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Symptomtext
Patient received the incorrect Pfizer vaccine concentration. Patient received 12+ rather than 5-11. No untoward events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- Non
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- N/A
- Allergien
- None
- Vorherige Impfungen
- -