- Staat
- -
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 12.06.2023
- Impfdatum
- 30.12.2021
- Beginn
- 20.04.2023
- Tage bis Beginn
- 476,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cardiac failure congestive
Pulmonary embolism
Symptomtext
I26.99 ACUTE PULMONARY EMBOLISM 4/18/2023 CHF (CONGESTIVE HEART FAILURE), UNSPECIFIED
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary embolism
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 03.01.2023
- Impfdatum
- 30.09.2022
- Beginn
- 04.10.2022
- Tage bis Beginn
- 4,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute myocardial infarction
Acute respiratory failure
Anticoagulant therapy
Aspiration
Blood pressure increased
COVID-19
Chest X-ray abnormal
Culture urine positive
Death
Enterococcus test positive
Fungal test positive
Lung disorder
Lung infiltration
Mental status changes
Metabolic encephalopathy
Pneumonia
Renal impairment
SARS-CoV-2 test positive
Symptomtext
10/4/2022-Presents to ED via EMS, with reports of AMS, only responsive to painful stimuli. Ordered ceftriaxone, UTI. Trop peaked at 0.144 consistent with a Type 2 NSTEMI, recieved asa and on Heparin drip. Covid - test. Recent admission 9/11-9/23/2022 for acute hypoxic resp failure PNA. VSS 02 94% on RA. CXR-bibasilar airspace disease. Admit metabolic encephalopathy in setting of UTI. 10/7/2022-BP elevated 181/66 Hydralazine added. Desat 85% 4L via NC placed. Ceftriaxone changed to Unasyn, to cover for aspiration. 10/10/2022-UC yeast and VRE. restart oxybutin and start linezolid and fluconazole. Now covid +. 10/12/2022- Continue on bumex, isodil and Procardia. On RA VSS. CXR-b/l pulm infiltrates. Reanla dysfunction 10/12/2022- does not permit to use remdesivir or baricitinib. 10/13/2022- O2 increased to 6L nc after desat of 87%. Unasyn changed to Zosyn. Dexamethasone started. 10/14/2022-O2 increased to 8L NC. 10/15/2022- o2 increased to 15 L NRB, made palliative. Time of death 2056.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- 11,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Type 1 DM, HTN, CAD and CKD.
- Andere Medikamente
- -
- Allergien
- Codeine
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 21.12.2022
- Impfdatum
- 24.02.2021
- Beginn
- 29.09.2022
- Tage bis Beginn
- 582,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Acute respiratory failure
Angiogram pulmonary abnormal
Blood gases abnormal
COVID-19
Chronic obstructive pulmonary disease
Condition aggravated
Hypercapnia
Hypoxia
Intensive care
Lung consolidation
Respiratory distress
SARS-CoV-2 test positive
Pleural effusion
Respiratory failure
Symptomtext
85y.o. female presenting with acute on chronic hypoxic respiratory failure. She has history of COPD on home oxygen as well as nocturnal BiPAP. Upon presentation, ABG showed significant CO2 retention. She was begun on broad-spectrum antibiotics. She did require temporary transfer to MICU due to worsening hypoxia. Fortunately, patient did improve and did not require intubation. Further work-up included CTA PE protocol which did not show PE but did show partially loculated effusions as well as near complete consolidation of left lower lobe. Patient was seen by infectious disease as well as pulmonology. Eventually, her oxygenation improved back towards her previous baseline. She completed her courses of antibiotics inpatient. She was also treated with steroid burst due to COPD. She was mobilized with PT/OT and was determined appropriate for home with home care. Following this, she was stable for discharge and was discharged home to complete 1 additional day of her steroid burst. She will follow-up with primary care as well as pulmonology outpatient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- 9/29 SARS-CoV-2 -COVID-19 by NAA, Micro -- detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 24.10.2022
- Impfdatum
- 23.12.2021
- Beginn
- 30.08.2022
- Tage bis Beginn
- 250,0
- Dosis
- 3
- Route/Site
- - / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Alveolar lung disease
COVID-19
Chest X-ray normal
Chills
Death
Dyspnoea
Encephalopathy
Endotracheal intubation
Fibrosis
General physical health deterioration
Headache
Hypoxia
Imaging procedure abnormal
Intensive care
Mechanical ventilation
Pain
Paralysis
Pneumonia
Symptomtext
Admitted 08/30/2022 Deceased 10/08/2022 PRESENTING PROBLEM: Shortness of breath HOSPITAL COURSE: 57 yo M with hx of depression, HTN, hyperlipidemia, tobacco and ETOH abuse who presented to the ED on 8/30 with shortness of breath. Had previously tested positive for COVID 19 on 8/22 and completed a course of steroids. Found to be hypoxic in the ED and thus admitted to the hospitalist team for further care. Started on high dose IV steroids and empiric Abx. Despite this, patient continued to clinically decline from a respiratory standpoint and was ultimately transferred to the ICU and intubated/paralyzed/proned on 9/15. IP placed percutaneuous tracheostomy 9/22. Hospital course was unfortunately complicated by encephalopathy, septic shock with Strep bacteremia, and VAP. Serial imaging of his thorax continued to demonstrate progressing alveolar damage and fibrosis. Ventilator mechanics also continued to worsen with patient requiring high amounts of sedation for compliance with concurrent shock. Following extensive conversations with family regarding poor prognosis, patient was transitioned to comfort care on 10/8. ETT was removed and vasopressors suspended. He passed away peacefully with family at bedside.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- 39,0
- Labordaten
- -
- Aktuelle Erkrankungen
- Urgent Care visit on 8/22/2022: Patient is a 57 y.o. male who presents with SHORTNESS OF BREATH (Along with body ache, chills, headache, symptoms onset 3-4 days ago) Patient reports urgent care today for shortness of breath, body aches, chills, headache for last 5-6 days. He reports he is unsure when his symptoms initially started. Reports he is a current everyday smoker and has had some increased shortness of breath. He reports that he has not been in contact with anybody that has been and he is COVID vaccinated but none receive his boosters. Reports he has been able eat and drink without difficulties. He denies any nausea, vomiting, abdominal pain, dysuria, hematuria, chest pain, sore throat, any other concerns. Patient reports he does have history of abnormal liver enzymes. Rapid COVID was obtained and was positive. Chest x-ray was obtained I interpreted the images as no acute cardiopulmonary disease. Formal review is pending. Since is not sure when his symptoms started exactly and has arranged for to 6 days I do not feel like starting antiviral therapy is appropriate. Patient was given the number for monoclonal antibodies. Encouraged close follow-up PCP later this week for re-evaluation. Instructed him to go directly to emergency department with increased shortness of breath, chest pain, fevers, chills, any other concerns. Patient agreed with the plan and verbalized understanding of instructions. Questions were answered. Patient was discharged in stable condition.
- Vorgeschichte
- Acute hypoxemic respiratory failure due to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) disease (HCC) VAP (ventilator-associated pneumonia) (HCC) Hypertension SVT (supraventricular tachycardia) (HCC) hx of Anal fistula Zinc deficiency Moderate protein-calorie malnutrition (HCC) Opioid dependence (HCC) Psychostimulant dependence (HCC) Delirium Gout Hyperlipidemia Depression Tobacco abuse disorder Streptococcus constellatus bacteremia
- Andere Medikamente
- allopurinol (ZYLOPRIM) 100 MG tablet amLODIPine (NORVASC) 10 MG tablet amphetamine-dextroamphetamine (ADDERALL) 20 MG tablet atenolol-chlorthalidone (TENORETIC) 100-25 MG per tablet atorvastatin (LIPITOR) 40 MG tablet DULoxetine (CYMBALTA)
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 22.10.2022
- Impfdatum
- 11.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 8,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
COVID-19 pneumonia
Death
Intensive care
Respiratory failure
SARS-CoV-2 test positive
Sepsis
Symptomtext
Stable after vaccine administration. 10 days later, presented in extremis to the Emergency Department - sepsis / respiratory failure. Transferred to higher level of care (PICU), where the patient died 4 days later of COVID pneumonia.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- 4,0
- Labordaten
- 1/21/22: COVID+ (nucleic acid amplification)
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Spastic cerebral palsy; scoliosis; asthma.
- Andere Medikamente
- levocarnitine; levetiracetam; baclofen; valproic acid
- Allergien
- none known
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 29.09.2022
- Impfdatum
- 31.03.2022
- Beginn
- 30.08.2022
- Tage bis Beginn
- 152,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Cardiac arrest
Heart rate irregular
Implantable defibrillator insertion
Intensive care
Laboratory test
Loss of consciousness
Symptomtext
I blacked out while driving and my husband took me to the hospital. We went to the ER and I passed out again. My heart stopped. I was admitted to the hospital in ICU for 6 days and hospitalized for a total of 18 days. 2 weeks ago an implanted cardioverter defibrillator installed to regulate an irregular heartbeat and to shock my heart if necessary. I do not know whether I have completely recovered or not. I saw my general practitioner today and had an additional COVID-19 vaccine today.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cardiac arrest
- Hospital-Tage
- 18,0
- Labordaten
- 238 medical test or laboratory test run
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Bronchiectasis
- Andere Medikamente
- Losartan; triamterene; levothyroxine; L-lysine; calcium; multivitamin; vitamin D; flaxseed oil
- Allergien
- Peanut oil
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 08.03.2022
- Impfdatum
- 12.01.2022
- Beginn
- 05.03.2022
- Tage bis Beginn
- 52,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute myocardial infarction
Angiogram
Anticoagulant therapy
Chest X-ray
Chest pain
Dyspnoea
Echocardiogram
Fibrin D dimer
Magnetic resonance imaging
Pulmonary embolism
Troponin increased
Symptomtext
Shortness of breath Dx Chest Pain NSTEMI Increased tropinon Pulmonary Embolism Meds ASA Heparin lorazapam
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- -
- Labordaten
- MRI-CTA-ECHO-CXR D-DIMER
- Aktuelle Erkrankungen
- None Reported
- Vorgeschichte
- See med list
- Andere Medikamente
- Albuterol Fluoxetine Duoneb Estradiol Norco Prilosec
- Allergien
- Gabapentin - Naproxen-Procaine
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 04.03.2022
- Impfdatum
- 19.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Angina pectoris
Cerebrovascular accident
Chest X-ray
Electrocardiogram
Headache
Muscle spasms
Neck pain
Pain
Symptomtext
It started a day after with headache and neck ache. I felt a spasm in my neck area. When I move my head up and down I felt very sharp pain. I took a head ache pill. A week later it started back again. I felt a pain from my head coming towards my heart. I believed I was having a stroke. The next week I went to the ER and they gave me muscle relaxer. On 3/3/2022 I had headache again and today it not really as bad.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- -
- Labordaten
- EKG Chest X-ray
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High Blood Pressure Diabetes Rheumatoid arthritis?
- Andere Medikamente
- Prednisone 10MG Vitamin D
- Allergien
- levofloxacin ibuprofen
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 25.02.2022
- Impfdatum
- 24.01.2022
- Beginn
- 24.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / UN
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Condition aggravated
Death
Hyperlipidaemia
Hypertension
Mass
Pulseless electrical activity
Syncope
Unresponsive to stimuli
Symptomtext
ED reported the natural death of a 61-year-old male. 1/24/22, the decedent received a Pfizer shot (presumed booster) 1000h. Later in the morning, he noticed a growth by his groin. He presented to hospital with general surgery, 1420h, and had vitals taken showing heart rate 122 and blood pressure 138/101. He left his appointment and was later found unresponsive by a medic unit on the campus following an unwitnessed collapse. He was taken to the ED where he presented at 1555h and was pronounced at 1619h. No trauma or suspicious circumstances reported. Death Certificate cause of death= Pulseless electrical activity caused by hypertension and hyperlipidemia.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hypertension, Hyperlipidemia
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 22.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Bedridden
Chills
Cough
Fatigue
Gait disturbance
Hyperhidrosis
Immunisation
Migraine
Myalgia
Nasal congestion
Near death experience
Neck pain
Oropharyngeal pain
Pain in extremity
Pyrexia
Symptomtext
I felt like death; Extreme fatigue; high fever; pain in all my muscles; pain in all my muscles and joints (extreme)/As was pain in my quads, shoulders; could barely walk up the stairs; Chills; sweating; sore throat; congestion; migraines; cough; I couldn't even get out of bed; Pain in right calf was unbearable; As was pain in my quads, shoulders , traps and neck.; As was pain in my quads, shoulders , traps and neck.; Dose number: 3; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 50 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 03Jan2022 10:30 (Lot number: 33036BD) at the age of 50 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0187, Location of injection: Arm Left, Vaccine Administration Time: 10:00 AM), administration date: 15May2021, when the patient was 50 years old, for COVID-19 Immunization, reaction(s): "mild fatigue/run down feeling", "pain in my arm"; Bnt162b2 (Dose Number: 1, Batch/Lot No: EW0176, Location of injection: Arm Left, Vaccine Administration Time: 10:15 AM), administration date: 24Apr2021, when the patient was 50 years old, for COVID-19 Immunization, reaction(s): "mild fatigue/run down feeling", "pain in my arm". The following information was reported: IMMUNISATION (medically significant) with onset 03Jan2022 10:30, outcome "unknown", described as "Dose number: 3"; NEAR DEATH EXPERIENCE (medically significant) with onset 03Jan2022 11:00, outcome "recovered with sequelae" (Jan2022), described as "I felt like death"; FATIGUE (non-serious) with onset 03Jan2022 11:00, outcome "recovered with sequelae" (Jan2022), described as "Extreme fatigue"; PYREXIA (non-serious) with onset 03Jan2022 11:00, outcome "recovered with sequelae" (Jan2022), described as "high fever"; MYALGIA (non-serious) with onset 03Jan2022 11:00, outcome "recovered with sequelae" (Jan2022), described as "pain in all my muscles"; ARTHRALGIA (non-serious) with onset 03Jan2022 11:00, outcome "recovered with sequelae" (Jan2022), described as "pain in all my muscles and joints (extreme)/As was pain in my quads, shoulders"; GAIT DISTURBANCE (non-serious) with onset 03Jan2022 11:00, outcome "recovered with sequelae" (Jan2022), described as "could barely walk up the stairs"; CHILLS (non-serious) with onset 03Jan2022 11:00, outcome "recovered with sequelae" (Jan2022), described as "Chills"; HYPERHIDROSIS (non-serious) with onset 03Jan2022 11:00, outcome "recovered with sequelae" (Jan2022), described as "sweating"; OROPHARYNGEAL PAIN (non-serious) with onset 03Jan2022 11:00, outcome "recovered with sequelae" (Jan2022), described as "sore throat"; NASAL CONGESTION (non-serious) with onset 03Jan2022 11:00, outcome "recovered with sequelae" (Jan2022), described as "congestion"; MIGRAINE (non-serious) with onset 03Jan2022 11:00, outcome "recovered with sequelae" (Jan2022), described as "migraines"; COUGH (non-serious) with onset 03Jan2022 11:00, outcome "recovered with sequelae" (Jan2022), described as "cough"; BEDRIDDEN (non-serious) with onset 03Jan2022 11:00, outcome "recovered with sequelae" (Jan2022), described as "I couldn't even get out of bed"; PAIN IN EXTREMITY (non-serious) with onset 03Jan2022 11:00, outcome "recovered with sequelae" (Jan2022), described as "Pain in right calf was unbearable"; ARTHRALGIA (non-serious), NECK PAIN (non-serious) all with onset 03Jan2022 11:00, outcome "recovered with sequelae" (Jan2022) and all described as "As was pain in my quads, shoulders , traps and neck.". Therapeutic measures were taken as a result of near death experience, fatigue, pyrexia, myalgia, arthralgia, gait disturbance, chills, hyperhidrosis, oropharyngeal pain, nasal congestion, migraine, cough, bedridden, pain in extremity, arthralgia, neck pain. Clinical course: Extreme fatigue, high fever, pain in all my muscles and joints (extreme) I could barely walk up the stairs. Chills, sweating, sore throat, congestion, migraines, cough. I couldn't even get out of bed. The pain I had in my muscles was so severe it was difficult to stay in one position or find relief. I took OTC Tylenol, Sudafed. I never felt like this in my entire life. Pain in right calf was unbearable. As was pain in my quads, shoulders , traps and neck. Words cannot express or describe what I went thru. I felt like death! 1st/2nd doses - mild fatigue , run down feeling . Also pain in my arm, I couldn't lay on that side. Patient has not been vaccinated within 4 weeks of vaccination. Patient had not been tested for COVID-19 test prior to vaccination and post-vaccination. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Near death experience
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other medical history: None Known allergies: None
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 10.08.2023
- Impfdatum
- 06.01.2022
- Beginn
- 19.02.2023
- Tage bis Beginn
- 409,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Ischaemic stroke
Lacunar stroke
Symptomtext
ACUTE LACUNAR STROKE, UNSPECIFIED TYPE AND ARTERY ACUTE STROKE DUE TO ISCHEMIA, UNSPECIFIED TYPE AND ARTERY
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ischaemic stroke
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 17.02.2023
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: ja
ER: ja
Erholt: unbekannt
Anticoagulant therapy
Arterial thrombosis
Asthenia
Cardiac failure
Cardiac pacemaker insertion
Catheterisation cardiac
Computerised tomogram thorax abnormal
Cough
Dark circles under eyes
Device related thrombosis
Echocardiogram abnormal
Ejection fraction decreased
Fluid retention
Magnetic resonance imaging heart
Malaise
Mobility decreased
Peripheral swelling
Skin discolouration
Symptomtext
Became very sick right after vaccination. Could not get out of bed for 6 days. Never regained strength. Eyes had black circles around them, skin was grey, and continuous cough. Called family Dr. but couldn't get in until Feb. 14. On the day of appointment she sent him to the ER at Hospital for tests. ER did a CT scan and it was heart failure. Put on water pill and had Echo on Feb. 15. Then Dr. sent him to Hospital to be admitted. Echo was 11-18% Ejection Fraction. Hospital admitted on Feb. 14. Tests: Echo, heart cath, heart mri. Treatment: removed 22 lbs of water weight. Put on meds. Released Feb. 19. After months of medication and several echo's, Dr. referred to Dr. for pacemaker. Prime candidate and pacemaker was put in on October 25, 2022. Continued meds. On Jan. 12, 2023 another echo was done. Ejection Fraction is only at 27% and they were hoping for over 30% atleast. On January 31, 2023 went to family doctor for swelling in left arm. She sent him to the ER for an ultrasound. There is clotting where the wires are in the artery from the pacemaker. ER at hospital gave Eliquis on Dr.'s recommendation. Next appointment with Dr. is on February 23, 2023 to see what the next steps are. Possible heart transplant candidate.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arterial thrombosis
- Hospital-Tage
- 6,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 17.01.2023
- Impfdatum
- 13.01.2022
- Beginn
- 05.08.2022
- Tage bis Beginn
- 204,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
COVID-19
Disorientation
Guillain-Barre syndrome
Intensive care
Laboratory test
Malaise
Paralysis
SARS-CoV-2 test positive
Symptomtext
On 08/05/2022, started to feel sick and tested positive for COVID-19 with a home test; talked to my Doctor and because of my health issues, I wasn't prescribed anything, but told to take a decongestent, Vitamin C and zinc and rest; I became disoriented on 8/20/2022 and taken to Hospital where they discovered that I had Guillain-Barr? syndrome (GBS); On 08/25/2022, right foot was severly effected by this and the front part of the foot near the toes had to be amputated; After surgery, started to have slight paralysis and was in the ICU for a week; Transferred from hospital to Medical Center; Became almost fully paralyzed for 72 hours; The only places I wasn't paralyzed was in my head, throat and chest area's; Stayed in that hospital for over a month, then was transferred to Hospital; Was there for 3 weeks, receiving Speech Therapy, Physical and Occupational Therapy; Still partially paralyzed but was able to come home and goes to an Outpatient Clinic for Rehabilitation three days a week;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Guillain-Barre syndrome
- Hospital-Tage
- 60,0
- Labordaten
- Participant wasn't able to name them all.
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- Osteomyelitis; Diabetes; High Blood Pressure; Congestive Heart Failure.
- Andere Medikamente
- Plavix; Baby Aspirin; Toprol; Lanoxin; Lexapro; Metformin; Lyrica; Crestor; Lasix; CoQ10; Multivitamin; Vitamin B12; Zinc; Stool Softeners.
- Allergien
- Latex; Codeine.
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 06.04.2022
- Impfdatum
- 20.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Anticoagulant therapy
Carotid artery dissection
Carotid artery thrombosis
Chills
Computerised tomogram neck
Cough
Headache
Hypertension
Impaired work ability
Influenza
Intensive care
Magnetic resonance imaging
Malaise
Pain
Pain in extremity
Pyrexia
Rhinorrhoea
Scan with contrast abnormal
Symptomtext
The day of booster I was fine, the next day I had a sore arm, fever, chills, body aches, headache, all of the flu symptoms besides vomiting. I had the same symptoms with all of the Pfizer vaccinations the following day. The day of booster I was fine, the next day I had all of the flu symptoms and remained home from work. On Feb 15 I went to see my PCP, and was put on anxiety medication (fluoxetine 10mg) I was on that for 2 weeks until my PCP asked I move up to 20MG. On 3/2/22 I had a runny nose & cough. On 3/3/22 I stayed home from work sick, and was throwing up, I also remained home on 3/4, 3/5, and 3/6. 3/7 - 3/11. I was managing with mild headaches that regular over the counter tylenol was helping. On 3/14 I was getting more of a tension headache. On 3/15, I had the same headache but worse than any I had before it was making me throw up. I called my doctor on 3/16 and she recommended I go to the ER as I was also hearing a swishing in my ear. I went to local hospital and there they did a CT Scan. On the CT scan with contras they saw some carotid arteries in my neck, and transferred me to ICU for Treatment & Monitoring since being in the hospital my Blood Pressure was extremely high. I stayed at ICU and did some more testing where they found out my carotid arteries on both sides were Torn also. I have had NO trauma to my neck which would cause these dissections, and we do not have connective tissue disease in my family. I am able to leave ICU on 3/18/22 and they sent me home with some headache medication. I was home on 3/19 & 3/20 by continuously taking blood pressure/blood thinner medication also, and could not take what I was previously. On 3/21 the headaches started again and 3/22 was my follow up with PCP, when I left her office she said my BP was still really high and she didn't like that I couldn't get the headache under control. 3/22 she sends me back to the ER and I go to alternate Hospital, they ran some more testing and they called ICU who said I was released from their care and there was nothing more they could do. Alternate Hospital releases me with Norco, which isn't solving the issue, as I have dissections in my neck and they are also torn/clotted. on 3/23 I am following and taking the Norco every 4-6 hours to help my headaches and they are not subsiding, so I end up going to another hospital, and they re-run all new scans and find a 3rd dissection in the Vertebral artery. I stayed at hospital for 2 days after a bunch of tests were ran, they released me with blood thinners, 2 blood pressure meds, sleeping night meds, and headache medication. I was unable to get answers from most of the doctors as to how this came about as it was very random and nothing that I could think would set this off besides the C-19 Booster. They let me know the medication that I thought was causing this was not and that my BP was so high because of these dissections that was the cause for my headaches. After speaking with all of my doctors it had nothing to do with prior medications and since I have stopped taking those and am only on BP, Blood thinners, headache meds, and not sleeping meds, I still have a lingering headache and it hurts to turn my neck from side to side.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Carotid artery thrombosis
- Hospital-Tage
- -
- Labordaten
- CT Scan with and without contrast, MRI with and without contrast, Echo.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- birth control, wellbutrin
- Allergien
- penacillin
- Vorherige Impfungen
- Had side effects to both C19 vaccinations.
- Staat
- VA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 22.02.2022
- Impfdatum
- 10.02.2022
- Beginn
- 12.02.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cardiac assistance device user
Cardioversion
Fall
Feeling abnormal
Intensive care
Muscle spasms
Resuscitation
Unresponsive to stimuli
Ventricular fibrillation
Symptomtext
Patient pre-treatment BP was 94/54 and pre weight was 56.2. She was initially set for 0.7 removal. Her BP was 68/49, the cuff was resized, rewrapped, and rechecked. Reading 83/53 and she complained of leg cramp her UF was cuff off and 200ml NS given. Patient then went unresponsive 500 ML of NS given and AED was place on the patient as well as 4L of O2. Patient recovered and refused EMS transport. But requested tx be ended. Patient is a poor historian. Patient says she has been feeling bad since receiving booster 02/10/22. Patient reported she "fell out" in the bathroom this morning at home and had to be picked up off the floor by her grandson. Per her daughter this did not occur but she has been feeling out of sort since she received the booster. Patient went non responsive again. She was given a total of 1800ml NS. Pt was A&O x 3. Needles were removed without incident. EMS arrived and transported patient to hospital were (privacy) were notified. Spoke to (privacy) after incident, Daughter reports upon arrival to hospital CPR was performed patient's internal defrib shocked her repeatedly. She was A&O requesting food but will be admitted to ICU for observation and a cardiac work up. On 02/14/2022 Physician reports patient is in-patient ICU with V-fib.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Intensive care
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- Iron deficiency anemia, malnutrition,anorexia,
- Vorgeschichte
- ESRD
- Andere Medikamente
- -
- Allergien
- nitroglycerin
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 19.02.2022
- Impfdatum
- 29.08.2021
- Beginn
- 13.02.2022
- Tage bis Beginn
- 168,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Adverse event
Asthenia
Blood pressure increased
COVID-19
Fatigue
Headache
Intensive care
Myalgia
Pain
Therapy interrupted
Symptomtext
Covid19 Adverse Event. 1st vaccine received on 08/08/2021. 30 y/o with PMHx Lupus, Lupus Nephritis with ESRD on Hemodialysis, HTN, GERD, Pancreatitis, Marijuana use presents to ED with c/o generalized weakness, fatigue, headaches and muscle/body aches since received Covid19 booster vaccine on 02/05/2022. Pt immunocompromised due to monthly Brilinta infusions, steroids and Cellcept. As a result of Covid19 vaccine booster side effects, pt missed two hemodialysis sessions resulting in elevated BP requiring ICU stay for Cardene gtt.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Intensive care
- Hospital-Tage
- -
- Labordaten
- Pt admitted to Hospital on 02/13/2022 where ID MD documented covid19 vaccine booster side effects of headaches and body aches.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Lupus, lupus nephritis, ESRD with Hemodialysis, GERD, Gastric ulcer, HTN, Pancreatitis, marijuana use
- Andere Medikamente
- -
- Allergien
- Droperidol
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 18.02.2022
- Impfdatum
- 31.01.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Eyelid function disorder
Facial paralysis
Laboratory test normal
Magnetic resonance imaging
Motor dysfunction
Neuritis
Vitamin D decreased
Symptomtext
7th facial nerve inflammation. Patient woke up and could not close her eye on the right side of face and had facial paralysis on the right side of face in eye brow, cheek, and tongue and facial drooping and can't laugh or whistle. Doctor gave her hydrocortisone 20mg in the morning and at night and artificial tears and will do physical therapy three times a week.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Facial paralysis
- Hospital-Tage
- -
- Labordaten
- Labs were done and were within normal except vitamin D and patient was given vitamin D supplement. Patient underwent MRI at local hospital.
- Aktuelle Erkrankungen
- no sickness at time of vaccine or 1 month prior
- Vorgeschichte
- no chronic or long standing conditions
- Andere Medikamente
- vitamin D
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 15.02.2022
- Impfdatum
- 09.02.2022
- Beginn
- 10.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Exposure during pregnancy
Headache
Night sweats
Pyrexia
Seizure
Tremor
Ultrasound Doppler
Uterine spasm
Symptomtext
Fever, night sweats, full body convulsions/shaking, headache and UTERINE CRAMPING. I was 15 weeks and 5 days pregnant at the time, this was NOT NORMAL.. I had to see my OB the next day for US/Doppler to ensure baby was okay.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- I had to see my OB the next day for US/Doppler to ensure baby was okay.
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- OTC prenatal vitamin
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 12.02.2022
- Impfdatum
- 07.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cardiac disorder
Chest pain
Myocarditis
Symptomtext
myocarditis; cardiac related problems; chest pain; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 39 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 07Jan2022 20:00 (Lot number: 33036BD) at the age of 39 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Thyroid" (unspecified if ongoing); "Covid-19" (unspecified if ongoing), notes: prior vaccination. Concomitant medication(s) included: PREMARIN; CELEBREX; VYVANSE; NURTEC ODT; SYNTHROID. The following information was reported: MYOCARDITIS (medically significant) with onset 10Jan2022 12:00, outcome "not recovered", described as "myocarditis"; CARDIAC DISORDER (non-serious) with onset 10Jan2022 12:00, outcome "not recovered", described as "cardiac related problems"; CHEST PAIN (non-serious) with onset 10Jan2022 12:00, outcome "not recovered", described as "chest pain". The events "myocarditis", "cardiac related problems" and "chest pain" were evaluated at the physician office visit. The patient did not receive other vaccine in four weeks. The patient was not tested for COVID-19 post vaccination. The patient has no known allergies.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocarditis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19 (prior vaccination); Thyroid disorder
- Andere Medikamente
- PREMARIN; CELEBREX; VYVANSE; NURTEC ODT; SYNTHROID
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 02.02.2022
- Impfdatum
- 02.02.2022
- Beginn
- 02.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fall
Syncope
Symptomtext
Patient fainted 1 minute after receiving vaccine and fell to floor.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NKDA
- Vorgeschichte
- N/A
- Andere Medikamente
- unknown
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 01.02.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Seizure
Symptomtext
Systemic: Seizure-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 27.01.2022
- Impfdatum
- 27.01.2022
- Beginn
- 27.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Immediate post-injection reaction
Syncope
Symptomtext
Patient given vaccination at 4:55 p.m. and had syncopal episode immediately following , patient's feet elevated, RRT called. Patient alert and verbal within seconds of feet being elevated. Patient's mother in attendance. RRT arrived at 4:48 p.m. 5:00 p.m. B/P 125/77 P 72 O2 SATS 100%RA. MD assessed patient, spoke with mother and recommended patient go to ER for evaluation, mother declined, stated they would remain in clinic for further observation. Patient stated she hadn't eaten lunch. Patient given apple juice and offered crackers, had own crackers, consumed apple juice and crackers. 5:11 p.m. B/P 112/66 P 76 O2 SATS 00%RA. Patient with no c/o at that time. 5:22 p.m. B/P 112/57 P 71 O2 SATS 100%RA. Patient states she feels fine at that time. Patient and mother left clinic at 5:23 p.m. and patient had no c/o. Mother and patient educated if any adverse reaction occurs to go to ER, verbalized understanding.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- Denies
- Vorgeschichte
- Denies
- Andere Medikamente
- Denies
- Allergien
- Per patient only metal
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 27.01.2022
- Impfdatum
- 25.01.2022
- Beginn
- 25.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Injection site erythema
Syncope
Unresponsive to stimuli
Symptomtext
Site: Redness at Injection Site-Mild, Systemic: Fainting / Unresponsive-Mild, Additional Details: pt didnt need any epinephrine . she was responsive within couple of minutes and then parametics took over and took her to hospital
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 15,0
- 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: ja
Erholt: ja
Blood test
Chest X-ray
Fall
Head injury
Magnetic resonance imaging head
Syncope
Urine analysis
Symptomtext
SYNCOPE AT 1015AM ON 1/15/22 WHILE MAKING BREAKFAST. FELL AND HIT HER HEAD. WAS SEEN AT medical facility.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- BLOOD WORK, URINALYSIS, MRI HEAD, CHEST X-RAY
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- FLUOXETINE HCI 20MG AT BEDTIME HYDROXYZINE 25MG TAB AT BEDTIME
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 20.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal pain upper
Paralysis
Vomiting
Symptomtext
Patient received first dose of Pfizer Adult vaccine at 4:00 pm. Patient called pharmacy at 8:58pm to report adverse reaction of paralysis, vomiting and stomachache. Patient was still breathing fine and was advised to go to the ER to seek medical attention to decrease risk of health risk.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paralysis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- None
- Andere Medikamente
- N/A
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 20.01.2022
- Impfdatum
- 30.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Angina pectoris
Dizziness
Fatigue
Headache
Immediate post-injection reaction
Malaise
Pain
Paranasal sinus hypersecretion
Productive cough
Syncope
X-ray normal
Symptomtext
IMMEDIATE STABBING PAINS IN MY HEART; SUBSEQUENT COVID SYMPTOMS, SEVERE: PRODUCTIVE COUGH, PRODUCTIVE SINUS DISCHARGE (MASSIVE FOR WEEKS); ACHES; HEADACHE; DIZINESS; EXTREME FATIGUE; EXHAUSTION; COLLAPSING. THIS IS MY BOOSTER.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- DOC ORDERED XRAYS WEEK 3 VIA EMERGENCY ROOM; NORMAL XRAY. TREATED AT ER WITH CODEINE, TWO INHALERS ISSUED VIA SCRIPT.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- AICD EF 48% Prior Viral Cardiomyopathy PAD Abdominal Aneurism Type II Diabetic
- Andere Medikamente
- Plavix 75 mg Toprol ER 25 mg Metorpolol 12.5 mg 2 x's a day Furosemide 20 mg 5 MeQ Potassium Flaxseed Oil 1000 mg Zinc 100 mg D3 One A Day Silver
- Allergien
- Mold June Grass
- Vorherige Impfungen
- Normal cold/flu like symptoms first shot; none second
- Staat
- TX
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 18.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dyspnoea
Heart rate increased
Seizure
Swollen tongue
Throat irritation
Throat tightness
Wheezing
Symptomtext
Patient reported itchy throat and then stated her throat felt like it was closing up. Patient breathing rapidly and tongue look swollen. Then difficulty breathing accompanied by wheezing. Epipen administered and patient starting seizing. Patient is okay now.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- HR 125
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Bipolar, Opioid Usse Discorder
- Andere Medikamente
- trazodone neurontin
- Allergien
- nkda
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 19.01.2022
- Impfdatum
- 18.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Dizziness
Hypotension
Syncope
Unresponsive to stimuli
Visual impairment
Symptomtext
Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Medium, Systemic: Hypotension-Medium, Systemic: Visual Changes/Disturbances-Medium, Additional Details: 10 minutes post vaccination, BP 68/39, HR 50, pulse ox 100%. Visual changes noted. EMS called. 15 minutes post vaccination, BP not improved, pulse ox 68%. EMS arrived and after roughly 15 minutes of EMS monitoring, patient's symptoms had resolved and EMS cleared him for discharge
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 16.01.2022
- Beginn
- 16.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Flushing
Hyperhidrosis
Nausea
Syncope
Vomiting
Symptomtext
Systemic: Dizziness / Lightheadness-Mild, Systemic: fainted immediately awoke-Mild, Systemic: Flushed / Sweating-Mild, Systemic: Nausea-Mild, Systemic: Vomiting-Mild, Additional Details: fainted but immediately awoke, some vomiting, she said she has passed out while getting blood draws.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 19.01.2022
- Impfdatum
- 11.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hypotension
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Fainting/Unresponsive-Severe, Systemic: Hypotension-Medium.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 17.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Electrocardiogram normal
Seizure
Symptomtext
Seizure. lasted 8 seconds. Went to ER> was discharged with normal EKG but told to follow up for EEG with Neuro
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- EKG
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 16.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Brain natriuretic peptide increased
Chest pain
Dyspnoea
Electrocardiogram abnormal
Intensive care
Musculoskeletal pain
Myocarditis
Pain
Pain in extremity
Troponin increased
Ventricular tachycardia
Symptomtext
Pt reports that approx 4 days following administration- he experienced substernal chest pain - radiating to left arm with SOB. Pain also accompanied by Right sided scapula pain. Pt taken to ER for eval. Troponin found to be elevated as well as BNP. Pt transferred to PICU for monitoring and evaluation. Dx- post vaccination myocarditis.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Intensive care
- Hospital-Tage
- 2,0
- Labordaten
- EKG- episode of V-tach 1/15/2022 @1855 BNP initial 1/15/22 668. Repeat 1/16/22 BNP 381 Troponin initial. 15110. 1/15 @ 1153 Troponin 22,480 1/15 @1340 Troponin 17,885. 1/15@ 1628 Troponin 15,054 1/15 @1846 Troponin. 11,941. 1/15 @2033 Troponin 5,188 1/16@0615
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Focalin XR 20mg po BID Focalin 10mg po daily @ 1600 Zoloft 50mg po daily am
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Cyanosis
Dyspnoea
Fall
Heart rate increased
Hypoaesthesia
Loss of consciousness
Palpitations
Paraesthesia
Throat tightness
Tremor
Symptomtext
They gave me the shot and told me to go sit down and wait a half hour. I didn?t even make it to the chairs and sat down on the bench for the pharmacy. I put my purse down, took a drink of liquid Benadryl because I couldn?t breathe, blacked out and keeled over onto my purse. I have no clue how long I was out for/I?m not sure how long it took them to realize I was not OK. I came to when the lady who gave me my shot was yelling ? ma?am, are you ok? I couldn?t talk to I just showed her my I watch with the heart rate app. Which read 165? and I had my epi pen in my hand in my pocket. I heard the pharmacist say I?ve never had to give anyone an epi pen before. A employee said ?all the thousands of shots they giving out they?ve never had anyone have a reaction like this before I couldn?t breath/my throat closed, my heart rate remained high and my blood pressure was 178/147. I felt like I was having a heart attack or a stroke. I started violently shaking, my lips and hand turned blue on my right side (shot side). I looked like a Smurf. Now I can?t feel my fingers and my whole right arm and hand is numb/tingling. My heart rate is still high but not as bad. Just sitting down it?s 125 or higher. After being completely embarrassed and laid out in Walmart they let me go. I refused to go to the hospital and be a Guinea pig. I only got this shot because my work gave me an ultimatum. The rest of the day on Wednesday the 12th I felt like I was having a heart attack. My heart was beating out of my chest, I can?t take a deep breath, my right arm, hand and fingers are still numb and tingling. I can?t hold things in my right hand and I have no strength in that hand. 2 1/2 days later (Friday, January 14th) my symptoms are still the same. If I didn?t drink the liquid Benadryl I would have to have given myself and epi pen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- None. I can?t afford to go to the hospital. I was told by my family doctor to take Benadryl, drink water and go to the hospital to get my 2nd vaccine.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Was hit head on in April 2021 and still receiving treatment and working on a diagnosis
- Andere Medikamente
- Daily vitamin Allerga Allergy pill Fish oil Vitamin E Magnesium
- Allergien
- Aspirin
- Vorherige Impfungen
- I was a child. Unknown /nobody to ask
- Staat
- CA
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- Impfdatum
- 08.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Fall
Head injury
Syncope
Symptomtext
Patient fainted post COVID vaccine while in Observation area. She was seated and fell to the floor, hitting the right side of her head. She was A&O x3 initially. EMS was called, patient assessed and treated while laying on the floor. When she was helped back to a sitting position, she fainted again, and was transported. After the adverse event, the patient reported that she has a history of fainting post-vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- Unknown
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 08.01.2022
- Impfdatum
- 08.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Immediate post-injection reaction
Nausea
Syncope
Symptomtext
syncope immidiately after vaccination - dizzy and nauseated - relieved with ice packs and 12 minutes of waiting.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 08.01.2022
- Impfdatum
- 08.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Seizure
Syncope
Vomiting
Symptomtext
ADMINISTER FIRST DOSE OF PFIZER 0.3ML TO PATIENT'S LEFT ARM. PATIENT WAS FINE FOR THE FIRST COUPLE MINUTES. AFTER A FEW MINUTES PATIENT FAINTED IN THE CHAIR AND WOKE UP. HE HAD A SEZIURE FOR A COUPLE MINUTES AND THEN VOMITTED. WE CALLED 911 RIGHT AWAY AND EMS SHOWED UP. ALL HIS VITALS WERE NORMAL AND EMS SENT HIM HOME.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- ADMINISTER FIRST DOSE OF PFIZER 0.3ML TO PATIENT'S LEFT ARM. PATIENT WAS FINE FOR THE FIRST COUPLE MINUTES. AFTER A FEW MINUTES PATIENT FAINTED IN THE CHAIR AND WOKE UP. HE HAD A SEZIURE FOR A COUPLE MINUTES AND THEN VOMITTED. WE CALLED 91
- Allergien
- NO KNOWN ALLERGIES
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 16,0
- 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: ja
Erholt: unbekannt
Loss of consciousness
Seizure
Symptomtext
Patient experienced multiple seizures and briefly lost consciousness within 30 minutes of vaccine administration.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- Passed out and possible seizure following Moderna vaccine (1st dose)
- Staat
- PA
- Alter
- 20,0
- 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: ja
Confusional state
Flushing
Hyperhidrosis
Interchange of vaccine products
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Confusion-Mild, Systemic: Fainting / Unresponsive-Severe, Systemic: Flushed / Sweating-Mild, Additional Details: Patient came in for her Pfizer Booster vaccination. Patient received the Johnson and Johnson vaccination previously. The patient vaccine screening questions were answered and no adverse reactions from vaccinations was listed in the questionaire and in her profile. Ambulance was called immediately and patient was able to walk out of the store with no issues. Patient also stated she did not eat or drink anything that day and seemed nervous about the vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 02.01.2022
- Impfdatum
- 02.01.2022
- Beginn
- 02.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Confusional state
Dizziness
Flushing
Hyperhidrosis
Syncope
Unresponsive to stimuli
Vomiting
Symptomtext
Systemic: Confusion-Medium, Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Severe, Systemic: Flushed / Sweating-Medium, Systemic: Vomiting-Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 01.01.2022
- Impfdatum
- 31.12.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Fainting / Unresponsive-Mild, Additional Details: pt was sitting in monitoring area for observation after vaccine. tech noticed pt leaning and nurse who gave vaccine immediately responded, layed her down and elevated pt legs. pt had pulse and was breathing but not responding to verbal commands. EMS was called. pt responded and opened her eyes and was alert shortly after laying down. Ambulance arrived, evaluated pt. pt declined to go to hospial. Pt stayed at the pharmacy for another 30 min. pt has history of fainting after lab draws.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 27.12.2021
- Impfdatum
- 27.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Condition aggravated
Dizziness
Immediate post-injection reaction
Interchange of vaccine products
Loss of consciousness
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Fainting / Unresponsive-Medium, Additional Details: Patient announced that she was going to "pass out" prior to losing consciousness immediately after the administration of the Pfizer booster. Her first series was the single Janssen shot, and she was at the pharmacy getting her 2nd dose/Pfizer booster as well as the Flucelvax Flu Shot. The flu shot was administered first on the left arm, followed by the Pfizer COVID vaccine. The patient stated that she has a history of these type of reactions when having blood drawn, but never with a vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 24.12.2021
- Impfdatum
- 24.12.2021
- Beginn
- 24.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Immediate post-injection reaction
Presyncope
Symptomtext
Client stated she has a history passing out after vaccinations. Immediately following vaccination of Pfizer booster to left deltoid, patient had a vasovagal reaction. Patient was placed in a supine position with legs elevated and supportive care was given by Doctor and clinical staff. Patient recovered instantly and was monitored for an additional 30 minutes before she left in stable condition, accompanied by her parents.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- None.
- Allergien
- No known Allergies.
- Vorherige Impfungen
- Patient had a vasovagal reaction following previous vaccinations.
- Staat
- -
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 10.08.2023
- Impfdatum
- 11.01.2022
- Beginn
- 24.02.2023
- Tage bis Beginn
- 409,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Hypotension
Symptom recurrence
Symptomtext
HYPOTENSION 1/21/2023 -- RECURRENCE OF HOSPITALIZATION WITH SAME SYMPTOMS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 09.01.2023
- Impfdatum
- 06.01.2022
- Beginn
- 15.11.2022
- Tage bis Beginn
- 313,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain upper
Arthralgia
Burning sensation
COVID-19
Cough
Dyspnoea
Fatigue
Feeling abnormal
Lethargy
Oropharyngeal pain
Rhinorrhoea
SARS-CoV-2 test positive
Sinus disorder
Symptomtext
I first noticed mental and memory fogginess, significant joint and hip pain. I had a burning in my legs that was significant, sinus problems, fatigue and lethargy. Runny nose, cough. sore throat, minor shortness of breath, I also had right upper abdominal pain. I now become winded easily.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- COVID-19 home test, positive result.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Endometriosis; Asthma; Migraine Headaches
- Andere Medikamente
- None
- Allergien
- Latex; penicillin; ADVIL
- Vorherige Impfungen
- Twelve hours after shot terrible chills, felt feverish, lethargy. Age 43 04/30/2021 Dose 2 COVID-19 Pfizer Lot #EW0171
- Staat
- FL
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 23.09.2022
- Impfdatum
- 29.12.2021
- Beginn
- 02.09.2022
- Tage bis Beginn
- 247,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Dyspnoea
SARS-CoV-2 test positive
Symptomtext
Hospitalization: 9/2/22 - 9/19/22. Presentation to the ED: dyspnea x 1 day. COVID-19 + date: 9/2/22. Treatment: Continue with daily vitamin-C, nebulizer and inhaler treatment p.r.n. Remdesivir and dexamethasone. Discharge to: SNF.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HTN, HLD, AFIB, ESRD, DM, CHRONIC ANEMIA.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 17.09.2022
- Impfdatum
- 16.02.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Feeling abnormal
Inner ear disorder
Palpitations
Peripheral swelling
Tinnitus
Weight
Weight increased
Symptomtext
heart palpitations; clouded ears; ringing in the ears; swollen feet; brain fog; weight gain; This is a spontaneous report received from a contactable reporter(s) (Nurse). The reporter is the patient. A 39-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 16Feb2022 as dose 1, single (Lot number: 33036BD) at the age of 39 years intramuscular, in left arm for covid-19 immunisation. The patient's relevant medical history included: "covid" (unspecified if ongoing). There were no concomitant medications. The following information was reported: FEELING ABNORMAL (non-serious) with onset 17Feb2022, outcome "not recovered", described as "brain fog"; INNER EAR DISORDER (non-serious) with onset 17Feb2022, outcome "not recovered", described as "clouded ears"; PALPITATIONS (non-serious) with onset 17Feb2022, outcome "not recovered", described as "heart palpitations"; TINNITUS (non-serious) with onset 17Feb2022, outcome "not recovered", described as "ringing in the ears"; PERIPHERAL SWELLING (non-serious) with onset 17Feb2022, outcome "not recovered", described as "swollen feet"; WEIGHT INCREASED (non-serious) with onset 17Feb2022, outcome "not recovered", described as "weight gain". The events "heart palpitations", "clouded ears", "ringing in the ears", "swollen feet", "brain fog" and "weight gain" required physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of palpitations, inner ear disorder, tinnitus, peripheral swelling, feeling abnormal, weight increased. Additional information: The patient had no other vaccine in four weeks and no other medications in two weeks. The patient received the first dose on 16Feb2022 and second dose on 16Mar2022 but after both doses she experienced clouded ears, ringing in the ears, heart palpitations, swollen feet, brain fog and weight gain. Still till this day in Sep2022 experiencing clouded ears where its hard for her to hear at times and periodically heart palpitations, brain fog, and increase weight gain. The events required Doctor or other healthcare professional office/clinic visit. The patient had covid prior vaccination. The patient was not covid tested post vaccination. The patient had no/none known allergies and no other medical history. No follow-up attempts are possible. No further information is expected
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220217; Test Name: weight; Result Unstructured Data: Test Result:weight gain
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 02.08.2022
- Impfdatum
- 02.05.2022
- Beginn
- 30.07.2022
- Tage bis Beginn
- 89,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Chest X-ray normal
Chest pain
Cough
Dyspnoea
Dyspnoea exertional
Exposure to SARS-CoV-2
Fatigue
SARS-CoV-2 test positive
Symptomtext
I had shortness of breath, very tired, I had been exposed to someone who had COVID-19. I decided to use my home COVID-19 test that came back positive. Once it came back positive I went to the hospital and they did a chest x-ray that came back clear. They did prescribe me a cough suppressant, MUCINEX, albuterol and PAXLOVID. I started to the medications immediately. I am still feeling tired, I have chest pains when I cough and shortness of breath when I walk around.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Chest x-ray.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Diabetes; High Cholesterol: Hypertension
- Andere Medikamente
- Losartan; CRESTOR; women's multivitamin; JANUMET; FIORICET
- Allergien
- Codeine, VICODIN; morphine
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 18.07.2022
- Impfdatum
- 13.01.2022
- Beginn
- 30.06.2022
- Tage bis Beginn
- 168,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Dyspnoea
Exposure to SARS-CoV-2
Headache
Oropharyngeal pain
Pyrexia
SARS-CoV-2 test negative
Wheezing
Symptomtext
Contracted COVID-19 from my wife who recently returned from an out of state trip. My symptoms began about 3 days after hers. Severe sore throat, some breathing stress and wheezing, headache, low grade fever of about 100.5, and some severe coughing. The fever started on Friday 7/1 and continued until Monday until 7/4. The sore throat continued to be severe until Wednesday 7/6. My labored breathing continued until 7/7, but my sore throat lessened then. I continue to have slight wheezing. The medications that I took were HALLS cough drops, 1000mg of vitamin C for about 10 days starting on 7/1. I also took some cough syrup, aspirin, ADVIL, and TYLENOL at different points to help with headache and fever. I took a home test but came up negative, however was presumed positive. Did email my primary care and they responded to treat with OTC medication based on symptoms, and would only prescribe medication if I had a confirmed lung infection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- At home COVID-19 test
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Obstructive Sleep Apnea; Coronary Arteriosclerosis; Hyperlipidemia; Impaired Glucose Tolerance; Benign Essential Hypertension; Bypass Stint
- Andere Medikamente
- TOPROL; CENTRUM silver multivitamin; coQ10 NATURE MADE; vitamin B3 NATURE MADE; omega 3 fish oil NATURE MADE; lisinopril; PLAVIX; aspirin; REPATHA injection
- Allergien
- Seasonal (primarily mountain cedar; mold)
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 97,0
- Geschlecht
- F
- Eingang
- 15.07.2022
- Impfdatum
- 06.04.2021
- Beginn
- 12.07.2022
- Tage bis Beginn
- 462,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Dyspnoea
SARS-CoV-2 test positive
Vaginal haemorrhage
Symptomtext
07/12/22 presents to ED for "vaginal bleeding and shortness of breath". PMHx of "anemia, right total knee arthroplsaty, pancytopenia, malignant lymphoma, arthritis, cellulitis, obesity, gait instability, MI, myelodysplastic syndrome, and coronary artery disease"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 07/12/22 SARS-CoV-2 (COVID-19) by detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 27.06.2022
- Impfdatum
- 27.06.2022
- Beginn
- 28.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Condition aggravated
Dizziness
Headache
Nausea
Pain
Symptomtext
Headaches, chills, dizziness/lightheadedness, body aches, nausea started around 0530 AM 28JULY22, and began worsening from 0830 AM to 1030 AM, and have continued to worsen (specifically headaches and dizziness/lightheadedness)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- Previous Moderna vaccine, 2nd dose on 03/16/21 where patient experienced a low grade fever and body aches and chilla
- Staat
- TX
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 22.06.2022
- Impfdatum
- 24.03.2021
- Beginn
- 30.04.2021
- Tage bis Beginn
- 37,0
- Dosis
- 3
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Allodynia
Anaemia
Aphasia
Brain injury
Computerised tomogram head
Computerised tomogram spine
Dysphemia
Electrocardiogram
Electroencephalogram
Gait disturbance
Headache
Hepatic encephalopathy
Hepatic steatosis
Herpes zoster
Hyperaesthesia
Laboratory test
Language disorder
Liver disorder
Symptomtext
non intractable headaches, lymphadenopathy, expressive disorder d/t brain damage, liver disease, fatty liver, liver encephalopathy, anemia, aphasia, Alodynia
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- 1,0
- Labordaten
- May 20, 2022 - neurology-psychologist, dementia, Alzheimers, Parkinson?s testing June 25, 21 - shingles July 1, 21 - CT cervical spine, and head, MRI brain, cervical and thoracic spine, ECG July 9, 21 - saw primary MD July 21,21 - saw orthopedic surgeon Aug 6, 21 - saw MD for cervical spondylosis Aug 11, 21 - saw neurology - high sensitivity to touch, tremors, difficulty walking, stammers - labs, EEG Oct 22, 21 - electrophysiology Oct 25, 21 - saw neurology Dec 1, 21 saw MD
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Mixed connective tissue disease, Sjogrens Syndrome, Meniere's disease, Fibromyalgia, Interstitial lung disease, COPD, SLE, Osteoporosis (mild-mod)
- Andere Medikamente
- Aspirin 81mg, Celebrex, Dexilant, Gabapentin, Plaquenil, Flonase, symbicort INH, lasix, hydroduril, singular, benicar, effexor, Vit D, lactulose, Roboxan, Imitrex as needed, Botox injections for migraines
- Allergien
- IV iodine, sulfa, sulfa dyne
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 14.06.2022
- Impfdatum
- 02.06.2022
- Beginn
- 02.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Condition aggravated
Fatigue
Headache
Vaccination site pain
Symptomtext
At 12:00 pm on 03Jun2022 the joint pain was more intense; mild headache; about 11:00 pm on 02Jun2022 I noticed fatigue and joint pain in the back, hips and shoulder; about 11:00 pm on 02Jun2022 I noticed fatigue and joint pain in the back, hips and shoulder; sore arm at the injection site; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 56-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 02Jun2022 at 13:45 as dose 4 (booster), single (Lot number: 33036BD) at the age of 56 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "MDS" (unspecified if ongoing); "bone marrow transplant" (unspecified if ongoing); "GVHD" (unspecified if ongoing); "graves disease" (unspecified if ongoing); "if covid prior vaccination: Yes" (unspecified if ongoing). The patient took concomitant medications. Vaccination history included: BNT162b2 (DOSE 1, SINGLE; Lot No: EL3248), administration date: 03Mar2021, when the patient was 55-year-old, for COVID-19 immunization.BNT162b2 (DOSE 2, SINGLE; Lot nub: EP7534), administration date: 15Apr2021, when the patient was 55-year-old, for COVID-19 immunization; BNT162b2 (DOSE 3, SINGLE; Lot nub: EW0176), administration date: 22Oct2021, when the patient was 55-year-old, for COVID-19 immunization The following information was reported: VACCINATION SITE PAIN (non-serious) with onset 02Jun2022 at 16:00, outcome "recovering", described as "sore arm at the injection site"; FATIGUE (non-serious), ARTHRALGIA (non-serious) all with onset 02Jun2022 at 23:00, outcome "recovering" and all described as "about 11:00 pm on 02Jun2022 I noticed fatigue and joint pain in the back, hips and shoulder"; CONDITION AGGRAVATED (non-serious) with onset 03Jun2022 at 12:00, outcome "recovering", described as "At 12:00 pm on 03Jun2022 the joint pain was more intense"; HEADACHE (non-serious) with onset 03Jun2022 at 12:00, outcome "recovering", described as "mild headache". Therapeutic measures were not taken as a result of vaccination site pain, fatigue, arthralgia, condition aggravated, headache. Additional information: Patient noticed events joint pain was more intense and a mild headache. Follow-up (06Jun2022): This is spontaneous follow-up report received in response to the mail trail sent regarding the confirmation query and the response included:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Bone marrow transplant; COVID-19; Graves' disease; GVHD; MDS
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 10.06.2022
- Impfdatum
- 26.04.2022
- Beginn
- 01.05.2022
- Tage bis Beginn
- 5,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Heart rate increased
Palpitations
Symptomtext
About a week after I received the vaccine I noticed my heart started beating faster than normal. I stopped what I was doing and my heart returned to normal. This comes out of nowhere, I have no way knowing when it will happen. My heart just starts to race, I stop what I am doing then it slows back to normal. I made an appointment with my doctor after four weeks of it happening more frequently. She feels that the second booster may have exacerbated the arrhythmia of my heart.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- No test were done at this time.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Sinus infection that comes and goes
- Andere Medikamente
- Aspirin; multivitamin; loratadine; calcium; glucosamine; vitamin D; dairy relief as needed; TYLENOL with caffeine; ALEVE 12hr
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 10.05.2022
- Impfdatum
- 29.12.2021
- Beginn
- 25.02.2022
- Tage bis Beginn
- 58,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cough
Dyspnoea
Rhinorrhoea
Symptomtext
Shortness of breath, cough, felt like a sinus infection. I had a nasal drip.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Azelastine spray, albuterol, benzonatate.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Multivitamin; Zyrtec; cod liver oil; vitamin C
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 03.05.2022
- Impfdatum
- 27.01.2022
- Beginn
- 29.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- UNK
- Route/Site
- UN / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Back pain
Chest X-ray
Chest pain
Impaired work ability
Injected limb mobility decreased
Needle issue
Pain
Pain in extremity
Wrong technique in product usage process
Symptomtext
loss of use of left arm , emergency room vadnais heights, back pain ,chest pain radiating from back to front and down arm to elbow chest xray in er. followed by series of other dr app. still doing physical therapy unable to work, asm of need roto cuff on right arm which is why i opted to have shot in left arm, when man gave shot needle came out and he popped it back in with a flat hand, just didnt seem right , now i know why . thank you
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- call the doctor
- Aktuelle Erkrankungen
- roto cuff right arm
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 25.04.2022
- Impfdatum
- 22.04.2022
- Beginn
- 23.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Condition aggravated
Hyperaesthesia
Myalgia
Pyrexia
Vaccine positive rechallenge
Symptomtext
Fever (102), chills, myalgia, hyperesthesia gradually resolve over 2 days
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- hypertension, hypothyroidism
- Vorgeschichte
- -
- Andere Medikamente
- levothyroxine, lisinopril, metoprolol, rivaroxaban
- Allergien
- -
- Vorherige Impfungen
- fever, chills, myalgia, hyperesthesia after 1st COVID booster
- Staat
- OH
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 21.04.2022
- Impfdatum
- 18.01.2022
- Beginn
- 07.04.2022
- Tage bis Beginn
- 79,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
COVID-19
Fatigue
Headache
Malaise
Migraine
Productive cough
SARS-CoV-2 test positive
Symptomtext
COVID-19 symptoms started on April 7th or 8th, and a positive COVID-19 test on April 9th. It started with a headache and since I have migraines it's hard to tell but they were more frequent and persistent. I also had back ache, fatigue, and was coughing phlegm, and that's pretty much it. I'm still coughing and have a little fatigue but for the most part I was feeling better by April 13th or 14th. My doctor had me get the Bebtelovimab Infusion injection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- COVID-19 (04/09/22- Positive); Infusion Injection
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Diabetes; HBP; Gout
- Andere Medikamente
- Alopurinol, Losartan, Zonisamide, Farxiga, Trazadone, Verapamil.
- Allergien
- Codeine; Morphine; Hydrocodone
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 18.04.2022
- Impfdatum
- 08.01.2022
- Beginn
- 30.01.2022
- Tage bis Beginn
- 22,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acoustic stimulation tests abnormal
Blood test normal
COVID-19
Computerised tomogram normal
Condition aggravated
Deafness unilateral
Sudden hearing loss
Symptom recurrence
Tinnitus
Vitamin D decreased
Symptomtext
After the first two Pfizer shots, ~6 months later I developed a buzzing in my ear, echo with higher pitched noises & subsequently tested ny hearing after developing these symptoms & found to have a sudden hearing loss, all in my right ear. The symptoms began Nov 23, 2021. I was put on 3 weeks of a high dosage of Prednisone, and this helped to recover most of my hearing in my right ear & the buzzing & echo also lessened. I also had MRI & CT scan done, all negative. On January 8, 2022 once I finished my prednisone & allowed a few weeks for that to leave my system, I got my 3rd Pfizer booster shot. This was after my sudden hearing loss had reversed. About one week later, for a day, my symptoms all went away but then by January 30th, they all returned & worse than ever. I went on a second round of oral prednisone, which slowed the sudden hearing loss, but did not recover much & the tinnitus symptoms never stopped. Then we tried 3 steroid injections in my right ear, beginning March 3, 2022, which helped for a few weeks, but since all symptoms have returned again & especially as I contracted COVID on 4/12/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- - Hearing tests: (1) 12/8/2021 (Right ear- hearing loss drops to ~35 decibels) (2) 12/17/2022 (Right ear-hearing loss back to ~25 decibels) (3) 1/14/2022 (Right ear-hearing loss back to 10-20 decibels, normal range) (4) 2/8/2022 (Right ear- hearing loss drops to ~55 decibels) (5) 2/21/2022 (Right ear- hearing loss stabilizes ~40 decibels) (6) 4/8/2022 (Right ear- hearing loss remain below normal ~35-40 decibels) - MRI: 12/29/2021 - No Abnormalities - CT Scan: 2/8/2022 No abnormalities - Blood Test: 1/17/2022 - Normal, except low Vitamin D
- Aktuelle Erkrankungen
- Tinnitus & hearing loss began in November after 2nd vaccination, got better & returned worse after 3rd booster
- Vorgeschichte
- None
- Andere Medikamente
- triamterene dyazide
- Allergien
- clindamycin
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- F
- Eingang
- 16.04.2022
- Impfdatum
- 16.02.2022
- Beginn
- 24.02.2022
- Tage bis Beginn
- 8,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Feeling hot
Limb discomfort
Pain in extremity
Paraesthesia
Temperature intolerance
Symptomtext
This is a spontaneous report received from a contactable reporter(s) (Nurse). The reporter is the patient. An adult female patient (not pregnant) received BNT162b2 (BNT162B2), on 16Feb2022 as dose 3 (booster), single (Lot number: 33036BD), in left arm for Covid-19 immunisation. The patient's relevant medical history included: "Thalassemia Trait" (unspecified if ongoing), notes: Other medical history: Thalassemia Trait; "Mitral Valve Prolapse" (unspecified if ongoing). There were no concomitant medications. Vaccination history included: BNT162b2 (Dose 1, single, lot number: EL3247, vaccine location: Left arm), administration date: 15Jan2021, for COVID-19 Immunization; BNT162b2 (Dose 2, single , Lot number: EM9810, vaccine location: Left arm), administration date: 07Feb2021, for COVID-19 Immunization, reaction(s): "palpitations", "severe chest pain". The following information was reported: PARAESTHESIA (disability) with onset 24Feb2022, outcome "not recovered", described as "Developed tingling"; LIMB DISCOMFORT (disability) with onset 24Feb2022, outcome "not recovered", described as "Feelings that there were shards of glass being thrown into my lower extremities"; FEELING HOT (disability) with onset 24Feb2022, outcome "not recovered", described as "Hot feeling"; PAIN IN EXTREMITY (disability) with onset 24Feb2022, outcome "not recovered", described as "most severe severe pain in my feet"; TEMPERATURE INTOLERANCE (disability) with onset 24Feb2022, outcome "not recovered", described as "sensations of heat". The events "developed tingling", "sensations of heat", "feelings that there were shards of glass being thrown into my lower extremities", "most severe severe pain in my feet" and "hot feeling" required emergency room visit. Therapeutic measures were taken as a result of paraesthesia, temperature intolerance, limb discomfort, pain in extremity, feeling hot. Clinical course: Developed tingling, hot feeling, and sensations of heat as well as feelings that there were shards of glass being thrown into my lower extremities within a few days of receiving the booster. Also had the most severe pain in my feet and legs and had difficulty walking (felt like patient was walking on my bones and there was no padding/flesh on the sole of my feet). Went to emergency room twice. Now being followed by podiatrist and neurologist. Patient treatment received as Toradol IV. Oxycodone PO. Gabapentin. Patient not had Covid-19 prior vaccination and not tested post vaccination. No known allergies. Sender's Comments: As there is limited information in the case provided, the causal association between the Reported events and the suspect drug cannot be excluded. The case will be reassessed once new information is available. The impact of this report on the benefit/risk profile of the Pfizer drug is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees, and Investigators, as appropriate.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Mitral valve prolapse; Thalassemia trait (Other medical history: Thalassemia Trait).
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 17.03.2022
- Impfdatum
- 16.01.2022
- Beginn
- 16.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Pain in extremity
Tremor
Urticaria
Symptomtext
chills with violent shaking; chills with violent shaking; arm stayed sore; several large welts on my left arm.; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. An adult patient received bnt162b2 (BNT162B2), administered in arm left, administration date 16Jan2022 (Lot number: 33036BD) as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history was not reported. The patient took concomitant medications. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0176, Location of injection: Arm Left), administration date: 16May2021, for COVID-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EW0176, Location of injection: Arm Left), administration date: 25Apr2021, for COVID-19 immunization. The following information was reported: CHILLS (non-serious), TREMOR (non-serious) all with onset 16Jan2022, outcome "recovered" and all described as "chills with violent shaking"; PAIN IN EXTREMITY (non-serious) with onset 16Jan2022, outcome "recovered", described as "arm stayed sore"; URTICARIA (non-serious) with onset 16Jan2022, outcome "recovered", described as "several large welts on my left arm.". Therapeutic measures were not taken as a result of chills, tremor, pain in extremity, urticaria. Additional information: Patient got the booster Sunday morning. By bedtime, had chills with violent shaking. Patient arm stayed sore for several days, and by Wednesday, there were several large welts on my left arm. No other vaccine in four weeks. Other medications in two weeks: multivitamin. No COVID prior vaccination. No COVID tested post vaccination. No known allergies. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 08.03.2022
- Impfdatum
- 22.02.2022
- Beginn
- 08.03.2022
- Tage bis Beginn
- 14,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Chest pain
Fatigue
Feeling abnormal
Lymphadenopathy
Nausea
Pain
Symptomtext
Severe left armpit pain with lymph node swelling. It radiated to left chest causing chest pain and severe nausea. Brain fog, severe fatigue, lasted for a week. It is now 2 weeks and the armpit swelling briefly went down but the pain is still there along with the left chest pain. Nausea, brain fog, and fatigue are also still happening.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- No tests yet. Just Tramadol for pain and nausea medication.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Migraine Headaches
- Andere Medikamente
- Vitamin D
- Allergien
- Venofer
- Vorherige Impfungen
- Covid Vaccine 1 and 2- Migraine Headache and severe fatigue
- Staat
- IL
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 07.03.2022
- Impfdatum
- 08.02.2022
- Beginn
- 12.02.2022
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dyspnoea
General physical health deterioration
Laboratory test
Symptomtext
On 2/12/2022 (4 days after vaccination), patient went to the ER due to difficulty breathing, where he was admitted for health failure. He was admitted for 1 week, then discharged home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 6,0
- Labordaten
- Admitted 2/13-2/17/2022. Multiple labs, tests done while admitted. However, I do not have access to those reports at this time, as they were at an outside facility.
- Aktuelle Erkrankungen
- None known.
- Vorgeschichte
- Hyperlipidemia, intermittent asthma
- Andere Medikamente
- Atorvastatin 20 mg
- Allergien
- Allergy to "meat"
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 01.03.2022
- Impfdatum
- 05.01.2022
- Beginn
- 27.02.2022
- Tage bis Beginn
- 53,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dyspnoea
Symptomtext
case had breathing difficulty and went to hospital
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 3,0
- Labordaten
- unnown
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 27.02.2022
- Impfdatum
- 17.02.2022
- Beginn
- 18.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Amnesia
Arthralgia
Asthenia
Blood test
Fatigue
Axillary pain
Body temperature
Breast pain
Breast swelling
Dizziness
Feeling abnormal
Headache
Hypokinesia
Hypoaesthesia
Limb discomfort
Oedema
Pain
Joint swelling
Symptomtext
All body swollen/ Under the left armpit, left breast pain and swollen; Body aches; Joints pain/ Left shoulder, under the left armpit, left breast pain; Fever 102; Headaches; Left shoulder, under the left armpit, left breast pain and swollen; Under the left armpit, left breast pain; Left breast pain; Left breast pain and swollen; Can not move my left arm; Brain fog; Weakness; Dizziness; This is a spontaneous report from a contactable reporter (nurse). The reporter is the patient. A 54-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in left arm, administration date 17Feb2022 (Lot number: 33036BD) at the age of 54 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "COVID-19" (unspecified if ongoing), notes: Prior to vaccination, was the patient diagnosed with COVID-19:Yes. Concomitant medications were not reported. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE; Lot Number: EL8982; Anatomical location: Left Arm; Route of administration: Intramuscular), administration date: 27Jan2021, when the patient was 53 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE; Lot Number: EL9264; Anatomical location: Left Arm; Route of administration: Intramuscular), administration date: 17Feb2021, when the patient was 53 years old, for COVID-19 immunisation. The following information was reported: SWELLING (non-serious) with onset 18Feb2022, outcome "not recovered", described as "All body swollen/ Under the left armpit, left breast pain and swollen"; PAIN (non-serious) with onset 18Feb2022, outcome "not recovered", described as "Body aches"; ARTHRALGIA (non-serious) with onset 18Feb2022, outcome "not recovered", described as "Joints pain/ Left shoulder, under the left armpit, left breast pain"; PYREXIA (non-serious) with onset 18Feb2022, outcome "not recovered", described as "Fever 102"; HEADACHE (non-serious) with onset 18Feb2022, outcome "not recovered", described as "Headaches"; JOINT SWELLING (non-serious) with onset 18Feb2022, outcome "not recovered", described as "Left shoulder, under the left armpit, left breast pain and swollen"; AXILLARY PAIN (non-serious) with onset 18Feb2022, outcome "not recovered", described as "Under the left armpit, left breast pain"; BREAST PAIN (non-serious) with onset 18Feb2022, outcome "not recovered", described as "Left breast pain"; BREAST SWELLING (non-serious) with onset 18Feb2022, outcome "not recovered", described as "Left breast pain and swollen"; HYPOKINESIA (non-serious) with onset 18Feb2022, outcome "not recovered", described as "Can not move my left arm"; FEELING ABNORMAL (non-serious) with onset 18Feb2022, outcome "not recovered", described as "Brain fog"; ASTHENIA (non-serious) with onset 18Feb2022, outcome "not recovered", described as "Weakness"; DIZZINESS (non-serious) with onset 18Feb2022, outcome "not recovered", described as "Dizziness". The events "All body swollen/ Under the left armpit, left breast pain and swollen", "Body aches", "Joints pain/ Left shoulder, under the left armpit, left breast pain", "Fever 102", "Headaches", "Left shoulder, under the left armpit, left breast pain and swollen", "Under the left armpit, left breast pain", "Left breast pain", "Left breast pain and swollen", "Can not move my left arm", "Brain fog", "Weakness" and "Dizziness" were evaluated at the physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. It was unknown whether therapeutic measures were taken as a result of swelling, pain, arthralgia, pyrexia, headache, joint swelling, axillary pain, breast pain, breast swelling, hypokinesia, feeling abnormal, asthenia and dizziness. Additional Information: The patient did not receive any other vaccines within four weeks prior to COVID vaccine. Prior to vaccination, the patient was diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220218; Test Name: Body temperature; Result Unstructured Data: Test Result:fever 102
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19 (Prior to vaccination, was the patient diagnosed with COVID-19:Yes)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 26.02.2022
- Impfdatum
- 10.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Asthenia
Immediate post-injection reaction
Incorrect route of product administration
Injection site reaction
Mobility decreased
Muscle spasms
Pain
Pain in extremity
Symptomtext
Immediately I had a spasm in the muscle or site she injected into. I had a sharp pain shoot into my top shoulder area. She either injected it into the nerve or shoulder socket. I was unable to lift my arm for 3 days after injection and now 7 weeks later, I have constant pain in my shoulder that has now moved down into my arm. It interferes with my ability to raise my arm above my head and to lift things.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- lisinopril, synthroid, vitamin D
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 23.02.2022
- Impfdatum
- 10.02.2022
- Beginn
- 12.02.2022
- Tage bis Beginn
- 2,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Musculoskeletal chest pain
Paraesthesia
Symptomtext
Pt states that there is tingling in the arm she got the vaccine, along with pain below the rib cage. both started on 2/12/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Musculoskeletal chest pain
- Hospital-Tage
- -
- Labordaten
- na
- Aktuelle Erkrankungen
- None reported
- Vorgeschichte
- none reported
- Andere Medikamente
- None
- Allergien
- None reported
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 23.02.2022
- Impfdatum
- 10.02.2022
- Beginn
- 12.02.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Hypoglycaemia
Hypotension
Lethargy
Malaise
Symptomtext
Patient received COVID-19 Booster shot on 02/10/2022 LOT #33036BD. Upon returning to the clinic on 02/12/2022, The patient was lethargic and not feeling well. He had a hypotensive episode and a hypoglycemic episode as well. Vitals were baseline during the assessment for this patient. He had no complaints post treatment. He returned to the clinic 02/15/2022 and was back at baseline without complaint.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- ESRD- End-Stage Renal Disease
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 22.02.2022
- Impfdatum
- 09.02.2022
- Beginn
- 09.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood pressure measurement
Burning sensation
Dizziness
Hypertension
Symptomtext
severe dizziness; high BP 180/90; legs feeling like on ''fire''; This is a spontaneous report received from contactable reporter(s) (Other HCP). The reporter is the patient. A 51 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 09Feb2022 08:45 (Lot number: 33036BD) at the age of 51 years as dose 2, single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose 1, lot number: EL 1284, administrator route=Intramuscular, Left arm), administration date: 29Dec2020, when the patient was 51 years old, for COVID-19 immunization, reaction(s): "Nausea", "Vomiting", "multiple episodes of diarrhea", "weight dropped from 107 lb to 104lb in 2 days", "could not work the day of vaccine administration". The following information was reported: DIZZINESS (non-serious) with onset 09Feb2022, outcome "unknown", described as "severe dizziness"; HYPERTENSION (non-serious) with onset 09Feb2022, outcome "unknown", described as "high BP 180/90"; BURNING SENSATION (non-serious) with onset 09Feb2022, outcome "unknown", described as "legs feeling like on ''fire''". The events "severe dizziness", "high bp 180/90" and "legs feeling like on ''fire''" 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 dizziness, hypertension, burning sensation. Additional information: Vaccination facility: Doctor's office/urgent care. No other vaccine in four weeks. Patient received treatment for events with Observation. Patient had no covid prior vaccination. patient was not tested for covid post vaccination. had no Known allergies. It was reported patient could not work the day of vaccine administration. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220209; Test Name: BP; Result Unstructured Data: Test Result:180/90; Comments: High
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 20.02.2022
- Impfdatum
- 03.02.2022
- Beginn
- 03.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Aggression
Agitation
Anxiety
Aphasia
Arthralgia
Blood test normal
Computerised tomogram normal
Asthenia
C-reactive protein
Chest X-ray
Computerised tomogram head
Confusional state
Drug screen
Dysphagia
Dysphemia
Electrocardiogram
Fatigue
Hypersomnia
Symptomtext
Feb 3rd evening started to have a fever of 99.7. Next morning woke up achy and I slept most of the day. Saturday feb 5th lost control of my thought processes and became extremely agitated with lots of yelling, kicking, and screaming which i could not control. Finally I calmed somewhat but I could no longer speak and i had great difficulty swallowing. When asked to move my limbs, eyes, etc. I could not but I was still able to walk February 6th I went tp the hospital. Cat-scan, mri and blood work was all negative. Discharged Monday afternoon February 7th. Primary physician prescribed methylprednisolone for 6 days. Today feb 20th I still have a significant stutter and I have difficulty swallowing hard food.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- 2,0
- Labordaten
- Cat-scan February 6th MRI February 7th
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Migraine Hypothyroid Depression
- Andere Medikamente
- Excederin Fioricet Maxalt Cymbalta Lamotrigine Levothyroxine Vitamin C
- Allergien
- Amoxicillin Bactrim Dust mites Grass
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 19.02.2022
- Impfdatum
- 29.12.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Symptomtext
I started to experience chest pain two weeks after receiving booster shot; This is a spontaneous report from a contactable reporter (consumer or other non-HCP). The reporter is the patient. A 54-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in left arm, administration date 29Dec2021 (Lot number: 33036BD) at the age of 54 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "None" (unspecified if ongoing). The patient did not take concomitant medications. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE; Lot number: EP7533, Route of administration: Unspecified, Anatomical site: Left arm), administration date: 17Apr2021, when the patient was 54 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE; Lot number: EW0162, Route of administration: Unspecified, Anatomical site: Right arm), administration date: 08May2021, when the patient was 54 years old, for COVID-19 immunisation. The following information was reported: CHEST PAIN (non-serious) with onset an unknown date in Jan2022, outcome "recovering", described as "I started to experience chest pain two weeks after receiving booster shot". Therapeutic measures were not taken as a result of chest pain. Additional Information: The patient had no known allergies. The patient did not receive any other vaccines within 4 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
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- HI
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 16.02.2022
- Impfdatum
- 03.02.2022
- Beginn
- 05.02.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Laboratory test
Paraesthesia
Symptomtext
I started to feel pins and needle all over my body, the doctor prescribed gabapentin. I am still dealing with the pain currently.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- lab work for 02/16/22- blood count / inflammation markers.
- Aktuelle Erkrankungen
- Positive for COVID-19 12/2021
- Vorgeschichte
- autoimmune arthritis
- Andere Medikamente
- none
- Allergien
- penicillin, Sudafed
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 15.02.2022
- Impfdatum
- 28.01.2022
- Beginn
- 03.02.2022
- Tage bis Beginn
- 6,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest discomfort
Dyspnoea
Electrocardiogram
Palpitations
Symptomtext
Heart palpitation, mild shortness of breath, chest discomfort Palpitation was roughly one week after the shot Symptoms began slightly before one week after the vaccine and have become more mild over 2.5 weeks
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- ECG found a normal heartbeat on02/15/2022
- Aktuelle Erkrankungen
- I had Covid one month prior
- Vorgeschichte
- Mild asthma
- Andere Medikamente
- Doxycyline, multivitamin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 07.02.2022
- Impfdatum
- 13.01.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arteriogram coronary normal
Catheterisation cardiac normal
Condition aggravated
Hypertension
Troponin increased
Symptomtext
HTN, elevated troponin
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- 2,0
- Labordaten
- left heart catheterization which revealed normal coronaries on angiogram
- Aktuelle Erkrankungen
- HTN
- Vorgeschichte
- none
- Andere Medikamente
- Losartan 25mg
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 05.02.2022
- Impfdatum
- 05.02.2022
- Beginn
- 05.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pallor
Tremor
Symptomtext
Patient is here for covid booster consent reviewed, EUA given/offered, and pt monitored for 15 min post vaccine, tolerated well- vaccine card given to guardian. Shortly after receiving the vaccine, patient became pale and shaky. Immediately took the patient vitals. Provider called to the room to assess. Monitored the patient for 1 hour. Vitals repeated 2 more times before letting the patient leave. Patient was given an apple juice and 2 pediapops while being monitored.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Austism, allergic rhinitis, GAD
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 04.02.2022
- Impfdatum
- 11.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 6,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Mobility decreased
Myalgia
Pain in extremity
Sleep disorder
Symptomtext
Left arm hurts and unless I take several ibuprofen I can hardly raise my arm. I haven?t been to a doctor about it because I keep thinking it will stop hurting. It sometimes wakes me in the middle of the night. I honestly didn?t connect my vaccine to it until today when I went to pick up a prescription from my pharmacy where I got the shot. It just clicked. This feels like a muscle pain. I?m not sure if it?s from the shot but I haven?t done anything to hurt my arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Sinus infection
- Vorgeschichte
- Acid reflux, ADD
- Andere Medikamente
- Omeprazole, Prozac, Adderall
- Allergien
- Lactose intolerance
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 03.02.2022
- Impfdatum
- 18.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoaesthesia
Injection site pain
Paraesthesia
Tremor
Symptomtext
Site: Pain at Injection Site-Medium, Systemic: Numbness (specify: facial area, extremities)-Medium, Systemic: Shakiness-Medium, Systemic: Tingling (specify: facial area, extemities)-Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 02.02.2022
- Impfdatum
- 28.01.2022
- Beginn
- 30.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Fatigue
Lethargy
Lymphadenopathy
Mechanical urticaria
Pruritus
Urticaria
Symptomtext
1. Fatigue, Fever, Lethargy (Now Recovered; Dates: 1/29/22 & 1/30/22) 2. Lymph node swelling under right armpit (Now Recovered; Dates: 1/30/22 - 2/2/22) 3. Hives all over body, except face: exacerbated by itching (Persisting: 2/1/22 - present) Side Bar:---i have no hx of dermatographia. last incidence of hives was in the early 1990s,
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Obese, BMI >30 (Height: 5'10"; Weight: 220 lb)
- Andere Medikamente
- Thorne Research Vitamin D: 10,000 IU Nordic Naturals: Algae Omega 3 - 715 mg Thorne Research Basic Vitamin 2-Day: Multi Vitamin
- Allergien
- N/A
- Vorherige Impfungen
- Fatigue & Lethargy; Age 31; Vaccination Date: 5/8/2021; Covid19 MRNA Vaccine; Pfizer-BioNTech
- Staat
- WA
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 01.02.2022
- Impfdatum
- 18.01.2022
- Beginn
- 29.01.2022
- Tage bis Beginn
- 11,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
COVID-19 pneumonia
Inappropriate schedule of product administration
Nausea
SARS-CoV-2 test positive
Vomiting
Symptomtext
Patient received Pfizer COVID vaccine on 4/27/21 (lot # ER8736), 5/24/21 (lot # EW0177), 9/5/21 (lot # 301308A), and 1/18/22 (lot # 33036BD). On 1/24/22 and 1/29/22, patient tested positive for COVID. On 1/29/22, patient admitted to our inpatient facility for COVID19 pneumonia with nausea/vomiting. Patient stayed in the med/surg unit and discharged today (2/1/22).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19 pneumonia
- Hospital-Tage
- 3,0
- Labordaten
- COVID status positive 1/24/22 and 1/29/22.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- follicular lymphoma on maintenance chemotherapy Gazyva q56 days with stable residual mass
- Andere Medikamente
- benzonatate, guaifenecin er, ondansetron, prochlorperazine, Bactrim
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 28.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Asthenia
Condition aggravated
Feeling abnormal
Gait disturbance
Movement disorder
Nausea
Thinking abnormal
Vaccination site pain
Vision blurred
Symptomtext
very weak and is struggling; very weak and is struggling; soreness in right arm; Nausea; Difficulty in walking/left leg and left arm just give out and he is not able to walk very well; Difficulty lifting his arms; Blurred vision; starting to slur words and is having difficulty collecting his thoughts; He got his vaccine injection in his right arm and it still hurts; gotten worse each day; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 49 year-old male patient received bnt162b2 (BNT162B2), administered in arm right, administration date 05Jan2022 13:00 (Lot number: 33036BD) at the age of 49 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Relevant medical history:None" (unspecified if ongoing), notes: Patient history: No. There were no concomitant medications. Vaccination history included: Bnt162b2 (1st dose of covid vaccine, Pfizer Covid 19 Vaccine, 1st dose received in left arm., Lot: EW0172, Expiry: 31Aug2021), administration date: 20Apr2021, when the patient was 48 years old, for COVID-19 Immunization, reaction(s): "States that he had mild reactions after the first two Covid 19 vaccines. He just had some queasiness for a day or 2 from a sore arm, but no major reactions.", "States that he had mild reactions after the first two Covid 19 vaccines. He just had some queasiness for a day or 2 from a sore arm, but no major reactions."; Bnt162b2 (2nd dose of covid vaccine, Pfizer Covid 19 Vaccine, 2nd dose received in left arm. , Lot: EW0182, Expiry: Aug2021), administration date: 10May2021, when the patient was 48 years old, for COVID-19 Immunization, reaction(s): "States that he had mild reactions after the first two Covid 19 vaccines. He just had some queasiness for a day or 2 from a sore arm, but no major reactions.", "States that he had mild reactions after the first two Covid 19 vaccines. He just had some queasiness for a day or 2 from a sore arm, but no major reactions.". The following information was reported: ASTHENIA (non-serious), FEELING ABNORMAL (non-serious) all with onset 06Jan2022, outcome "not recovered" and all described as "very weak and is struggling"; ARTHRALGIA (non-serious) with onset 06Jan2022, outcome "unknown", described as "soreness in right arm"; NAUSEA (non-serious) with onset 06Jan2022, outcome "unknown", described as "Nausea"; GAIT DISTURBANCE (non-serious) with onset 06Jan2022, outcome "unknown", described as "Difficulty in walking/left leg and left arm just give out and he is not able to walk very well"; MOVEMENT DISORDER (non-serious) with onset 06Jan2022, outcome "unknown", described as "Difficulty lifting his arms"; VISION BLURRED (non-serious) with onset 06Jan2022, outcome "unknown", described as "Blurred vision"; THINKING ABNORMAL (non-serious) with onset 06Jan2022, outcome "unknown", described as "starting to slur words and is having difficulty collecting his thoughts"; VACCINATION SITE PAIN (non-serious) with onset 06Jan2022, outcome "not recovered", described as "He got his vaccine injection in his right arm and it still hurts"; CONDITION AGGRAVATED (non-serious) with onset 06Jan2022, outcome "not recovered", described as "gotten worse each day". Additional information: The patient reported that he was very weak right now and was struggling. Stated that he was extremely healthy prior to receiving the booster, but he was struggling now. Patient's side effects have included the normal soreness in his arm, like he had been punched in the arm. But the last 2-3 days he has had severe nausea, overall weakness, and he is having difficulty walking and lifting his arms, particularly the left side which is the opposite of where he got the shot. Clarifies that his left leg and left arm just give out and he is not able to walk very well. He got his vaccine injection in his right arm and it still hurts. He also has blurred vision, and difficulty with forming thoughts and communicating which is different than before. States that he is a teacher and tutor so he speaks for a living but he has noticed that he is starting to slur words and is having difficulty collecting his thoughts. The events began on 06Jan2022 and have progressively gotten worse each day. He could barely get out of bed at this point. At first he thought it may be a coincidence, but wanted to check on it because it is pretty significant at this point. Stated that now he could not straighten out without tipping over and he could not even walk his dog at this point. No investigation assessment. No emergency room visit or physician office visit. The patient did not have any recourse to get medical care. The patient stated that he felt like he was about to fall over so he needed to go and would call later. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: Relevant medical history:None, Comment: Patient history: No
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 28.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Injection site bruising
Injection site erythema
Injection site pain
Injection site pruritus
Injection site swelling
Joint swelling
Loss of personal independence in daily activities
Mobility decreased
Pain in extremity
Peripheral swelling
Pruritus
Symptomtext
Site: Bruising at Injection Site-Mild, Site: Itching at Injection Site-Mild, Site: Pain at Injection Site-Mild, Site: Redness at Injection Site-Mild, Site: Swelling at Injection Site-Mild, Systemic: Allergic: Itch (specify: facial area, extremities)-Medium, Systemic: Pain in her hand. Swelling started with her fingers. The swelling and pain keeps moving up her hand to her wrist. It is affecting her ability to move her hands as before/affecting her daily activities. Severe, Systemic: Joint Pain-Medium.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 27.01.2022
- Impfdatum
- 15.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 5,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest X-ray normal
Chest discomfort
Dyspnoea
Electrocardiogram ST segment elevation
Electrocardiogram abnormal
Right ventricular hypertrophy
Symptomtext
chest tightness and shortness of breath with abnormal EKG, symptoms lasted 24 hours and in the process of further evaluation by cardiologist. Pt reports similar symptoms after the first dose, but did not seek medical attention at the time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Chest x-ray 1/21/2022: results normal EKG 1/21/2022: results showed right ventricular hypertrophy and ST elevation
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- Pfizer 1st dose on 05/29/2021
- Staat
- -
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 26.01.2022
- Impfdatum
- 29.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Cardiac discomfort
Chest pain
Electrocardiogram
Palpitations
Symptomtext
Chest pain on left side, heart palpitations, pressure
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Ekg on 1/5/22 everything was normal
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 24.01.2022
- 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: nein
Chest discomfort
Chest pain
Dyspnoea
Feeling abnormal
Palpitations
Vertigo
Symptomtext
Pt. states that after receiving the 3rd dose of Phizer 01/06/2022, started experiencing symptoms that evening of chest pains, shortness of breath, chest pressure, and vertigo. No noted Primary visit/communications. Vertigo and brain fog continuing, chest pressure and heart palpations have subsided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 20.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Chest pain
Symptomtext
Patient returned to vaccine clinic at 11:47 a.m. and stated she had chest pain, that was 6/10 under right breast. RRT called. VS obtained. B/P 121/71 P 78 R 18 O2SATS 99%RA. RRT arrived and patient was agreeable to got to ER for evaluation. Patient remained alert and verbal. Patient was later discharged from the ER.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- unknown
- Aktuelle Erkrankungen
- denies
- Vorgeschichte
- denies
- Andere Medikamente
- denies
- Allergien
- denies
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 27,0
- 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: ja
Dizziness
Hypotension
Nausea
Symptomtext
Dizziness, Nausea. hypotension.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- -
- Labordaten
- BP 90/56 > 96/63 > 112/72
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Cannabis
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 15.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Dizziness
Dysphagia
Dyspnoea
Throat tightness
Symptomtext
Systemic: Allergic: Difficulty Breathing-Mild, Systemic: Allergic: Difficulty Swallowing, Throat Tightness-Mild, Systemic: Chills-Mild, Systemic: Dizziness / Lightheadness-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 10.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Contusion
Dizziness
Dyspnoea
Injection site pain
Nausea
Pain
Symptomtext
Site: Pain at Injection Site-Medium, Systemic: Body Aches Generalized-Medium, Systemic: Dizziness / Lightheadness-Medium, Systemic: Nausea-Medium, Systemic: Weakness-Medium, Additional Details: Patient also indicates shortness of breath, and bruising of arms and hips since recieving injection of third dose. She reported all these details back to pharmacy in person on 1/15/22, 5 days after injection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 19.01.2022
- 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: ja
Injection site pain
Lymph node pain
Lymphadenopathy
Mobility decreased
Sleep disorder
Symptomtext
Site: Pain at Injection Site-Severe, Systemic: Lymph Node Swelling-Severe, Additional Details: patient described having a large goose egg form under his arm/armpit that was extremely painful and prevent him from puting his arm down and kept him from sleep for 2 nights
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 31.12.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Limb injury
Paraesthesia
Symptomtext
Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 09.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Diarrhoea
Dyspnoea
Epistaxis
Headache
Influenza virus test negative
Lymphoedema
Productive cough
Pyrexia
Rash
Rash vesicular
SARS-CoV-2 test negative
Scab
Throat irritation
Symptomtext
Headache 4 days Fever 4 days Chills 4 days Loose stools 2 days Abdominal blister rash ( post 7 days and it has crusted over and it slowly disappearing) Productive Cough 4 days (started on z-pack on 1/14/22) Raw throat 4 days (started on z-pack on 1/14/22) Slight shortness of breath 3 days Lymphedema 4 days. Nose Bleeds 4 days (right side only)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- COVID test 1/13/22 Negative FLU test 1/13/22 Negative
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension Panic Attacks Seasonal Allergies Pre-Diabetic Pigmented Villonodular Synovitis Chronic Migraines Morbid Obesity
- Andere Medikamente
- Singular 10mg QD Prilosec 20mg QD Losartan 110/25mg QD Estroven Mood Enhancer QD Women's Vitamin 50+ QD Potassium 20meqs twice qwk Propranolol 60mg QD Fluoxetine 15 mg Mon, Wed, Fri, Sat & Sun Fluoxetine 10mg Tues & Thurs\ Biotin 5000mcg Q
- Allergien
- Latex Type 1 (Anaphylaxis reaction) Codeine Morphine Toradol Compazine Vicodin Sulfa Naproxen Lexapro **Multiple foods due to latex allergy
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 17.01.2022
- Impfdatum
- 23.04.2021
- Beginn
- 16.01.2022
- Tage bis Beginn
- 268,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Diarrhoea
Dizziness
Dyspnoea
Headache
Nasal congestion
Oropharyngeal pain
Pain
Sinus congestion
Upper-airway cough syndrome
Symptomtext
headache, sore throat, chills, shortness of breath, body aches, diarrhea, sinus congestion, nasal congestion, post nasal drainage, dizziness. starting 1/16/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- 07/2000 - MVA - pneumothoraces, rib fractures, fx pelvis (Right side fx superior & inferor pubic rami-nondisplaced), 05/2005 - Abnl pap - SIL/mild dysplasia + HPV, 10/2005 - Pyelonephritis, Hx of polysubstance abuse, PTSD, Depression, Anxiety/panic disorder, Dysmenorrhea, chronic low back pain due to MVA (2000).
- Andere Medikamente
- Taking Vitamin C 500 MG Capsule as directed Orally , Taking Ibuprofen 600 MG Tablet 1 tablet with food or milk Orally every 6 hours as needed, Taking Prenatal 28-0.8 MG Tablet 1 tablet Orally Once a day, Taking Vitamin D 50 MCG (2000 UT) Ca
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 16.01.2022
- 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: unbekannt
Erholt: ja
Chills
Pyrexia
Tachycardia
Symptomtext
Tachycardia (120 bpm) for 5 hours within 24 hours of vaccination following chills and fever. Brief episode of tachycardia ( few minutes) the following day. In both cases, heart rate returned to normal without treatment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tachycardia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Metaprolol 25 mg
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest discomfort
Dyspnoea
Erythema
Fatigue
Oropharyngeal pain
Palpitations
Skin warm
Swelling
Symptomtext
Large lump with redness and warm to touch. Sore throat Heart felt heavy and pounding Shortness of breath Very fatigued
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- None yet thinking about going in. Had neighbor draw a circle around the lump to see if it gets larger and redder.
- Aktuelle Erkrankungen
- Depression Osteoporosis Arthritis Kidney Back pain Joint pain
- Vorgeschichte
- Depression Osteoporosis Arthritis Kidney Back pain Joint pain
- Andere Medikamente
- Sertraline Over the counter Tylenol Over the counter Advil Doxepin
- Allergien
- Doxicycaline
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- 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: ja
Arthralgia
Axillary pain
Back pain
Breast pain
Chest pain
Injection site pain
Lymphadenitis
Lymphadenopathy
Mobility decreased
Musculoskeletal pain
Neck pain
Pain
Symptomtext
Pain began migrating away from injection site about 24 hours after injection. Went up shoulder and into my shoulder blade, causing enough pain I couldn't left my arm nor lay down on that side. After 48 hours, the pain was further migrating down the left side of my back, up the left side of my neck, around my shoulder into my armpit, and under my left breast. After 72 hours, the pain had further migrated into the center of my back and chest - basically the entire upper left quadrant of my chest cavity was in severe pain. Urgent Care clinic noted that all lymph nodes on my left side were severely swollen/inflamed. Prescribed a high dose of steroid- Prednisone- and recommended taking ibuprofen to help reduce the swelling, and heating pad to also help alleviate the pain. Some of the pain began to subside within about 8 hours of first dose of prescription. Today is the third day of taking the steroid and my pain, while still present, I would consider mild now.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Women's One a Day Multi-Vitamin Collagen
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 13.01.2022
- Impfdatum
- 14.04.2021
- Beginn
- 04.01.2022
- Tage bis Beginn
- 265,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Dyspnoea
Nasal congestion
Sinus congestion
Symptomtext
cough- shortness of breath- sinus congestion- nasal congestion. starting on 1/4/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Tob abuse. Anxiety/depression. HTN.
- Andere Medikamente
- ?hydroCHLOROthiazide 25 MG Tablet 1 tablet in the morning Orally Once a day ?Metoprolol Succinate ER 100 MG Tablet Extended Release 24 Hour 1 tablet Orally Once a day Not-Taking ?Ibuprofen 200 MG Tablet 1 tablet with food or milk as n
- Allergien
- Augmentin: Allergy
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 11.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arthralgia
Chills
Decreased appetite
Dehydration
Fatigue
Hallucination
Injection site rash
Migraine
Nausea
Pain
Pyrexia
Vomiting
Symptomtext
Nausea, vomiting, rash on site arm, rash, fever, hallucinating, loss of appetite, fatigue, migraines, body aches, chills, dehydrated, and joint pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dehydration
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Chronic Migraines
- Andere Medikamente
- Topamax; Emgality; levocetirizine
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 11.01.2022
- Impfdatum
- 06.12.2021
- Beginn
- 07.01.2022
- Tage bis Beginn
- 32,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest pain
Feeling abnormal
Pain
Symptomtext
Pt reports 3 day hx of Lt sided chest pain that radiates into midsternum. Pt reports pain is constant, feels like a throbbing and sharp pain and that it feels like her heart "is going to burst"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Pt denies any previous history of illness prior to receiving booster. Pt received first Pfizer dose: 5/1/2021, 2nd dose of Pfizer 5/22/21 and booster of Pfizer: 12/6/2021.
- Vorgeschichte
- Pt denies any chronic or long standing health conditions.
- Andere Medikamente
- Pt denies taking any routine meds
- Allergien
- No known drug allergies
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 08.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bacille Calmette-Guerin scar reactivation
COVID-19
Condition aggravated
Fatigue
Injection site erythema
Injection site pain
Injection site warmth
Pain
Pyrexia
SARS-CoV-2 test positive
Tremor
Symptomtext
BCG scar inflammation. Booster given in same arm (dominant arm) and redness, warmth, and pain from same. Positive covid 19 rapid test on 8/1/22. Three days following booster. Severe body aches, fever, shakes, and fatigue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 07.01.2022
- Impfdatum
- 21.04.2021
- Beginn
- 15.07.2021
- Tage bis Beginn
- 85,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Allergy test
Condition aggravated
Full blood count
Urticaria
Symptomtext
July15 2021 the patient had onset of generalized urticaria with profound pruritis which worsened over next several weeks. No hx of prolonged or recurrent urticaria prior to this. No history of dermatitis. No fevers or chills. The urticaria had transient improvement with diphenhydramine and short course of oral steroids. He saw two allergists over the next several months and was started on daily cetirizine with mild improvement and intermittent remission. He received his booster on January 4, 2022 and the urticaria has worsened.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- CBC and other allergy tests(do not have access to them at the moment) but was told all negative
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- sertraline
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 06.01.2022
- Impfdatum
- 04.01.2022
- Beginn
- 04.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Condition aggravated
Pruritus
Symptomtext
Vaccinated: 10:25AM Reaction: 10:35AM 10 minutes after receiving 2nd dose Pfizer, pt reported pruritus across back, left side neck, and sternum. Pt noted "it's not severe" with no hives noted at 10:45AM. Vitals: 115/81, 95, 16 Patient was given 50mg of Benadryl at 10:50AM with patient reporting feeling better at 11:05AM. Patient was released with husband who will drive her home. Advised patient to call ER or go to express care if any further issues.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No known PMH.
- Vorgeschichte
- No known PMH.
- Andere Medikamente
- No known medications.
- Allergien
- Ceftriaxone (pruritus).
- Vorherige Impfungen
- 32 year old patient received 1st dose Pfizer on 12/13/2021 and. Pt c/o of itching, rash in post observation area to PA @1830 (15
- Staat
- NY
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 05.01.2022
- Impfdatum
- 04.01.2022
- Beginn
- 04.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Headache
Pain in extremity
Symptomtext
headache, feet hurting, left arm sore, chest area hurting
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Rapid Heartbeat
- Andere Medikamente
- Metoprolol Succ ER
- Allergien
- -
- Vorherige Impfungen
- 05/27/2021 Pfizer-BioNTech Headache, Feet Hurting 35 years old
- Staat
- -
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 04.01.2022
- Impfdatum
- 27.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Breast pain
Injected limb mobility decreased
Injection site erythema
Injection site swelling
Injection site warmth
Lymph node pain
Lymphadenopathy
Palpitations
Sleep disorder
Swelling of eyelid
Symptomtext
2 days after vaccination, patient reports "heart palpitations and increasing size in my lymph nodes in my armpit, elbow, and left breast. The injection site(left deltoid) is also warm, red, and swollen to the touch. The size in pain in my lymph nodes on the left side have gotten so bad I have limited mobility in that arm. The pain in my left breast wakes me up at night. My heart rate can reach up to 160bpm 6-8 hours following the doses. My vital signs have been within normal limits today and seem to be improving overall". Pt also reported left eye lid swelling after injection and was recommended to go to ED if heart palpitations and swelling persisted. Also educated to use warm compress to help with arm mobility. Patient did not end up going to ED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HTN
- Andere Medikamente
- Medication list: asparin 81mg - 1 tab Qday - Lisinopril 20mg - 1 tab Qday - Hydrocortisone 2.5% cream - apply to affected areas BID
- Allergien
- Allergic to Penicillin G
- Vorherige Impfungen
- After booster shot on 12/27/2021, patient reported "heart palpitations and increasing size in my lymph nodes in my armpit, elbow
- Staat
- -
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 03.01.2022
- Impfdatum
- 29.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Cold sweat
Condition aggravated
Deafness
Dizziness
Pallor
Symptomtext
Vaccinated: 10AM Reaction: 10:01AM Pt experienced dizziness and light headedness after receiving her Pfizer booster. PT noted also to be clammy and pale. PT taken to hospital to lay down and was given juice and crackers. PT later reported she briefly lost her hearing until she sat in wheelchair to be taken to hospital and her hearing came back. Patient noted to have significant history of dizziness with needlesticks. Father says she gets this from him. Vitals: 109/48, 65, 14 -> @10:31: 108/72, 56, 14, O2 100% Pt reported feeling better after laying down and after sitting up and eating crackers and juice. Her adverse symptoms resolved and she left facility ambulating independently with steady gate, accompanied by her parents, and in NAD at 10:34AM. Patient educated to stay well hydrated before and after needlestick injections in future and to have future needlestick injections given at facility where she can receive injection while laying down, i.e. doctor's office, vaccine center.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No Known PMH
- Vorgeschichte
- -
- Andere Medikamente
- No Known Medications
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 03.01.2022
- 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
Arthralgia
Back pain
Mobility decreased
Myositis
Pain
Pain in extremity
Spinal pain
Symptomtext
Severe pain in the shoulder radiating to the spine and down the arm to the elbow more severe during the 2 nights following vaccination. Slight impairment in arm mobility (lifting laterally and over the head) next day, more severe after 48h. Severe lower back pain, persistent. Now (1/3/22) there is very little pain but there is no improvement in arm function. Cannot lift over the head at all. Laterally I can lift it only partially. Back pain persists. On day 2 I asked for advice from a colleague who is a neurologist. She suspects inflammation in the deltoid; demyelination is unlikely. Taken tylenol ~ 30 ml/day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Diabetes, hypertension
- Vorgeschichte
- Diabetes, hypertension
- Andere Medikamente
- Labetalol, Fosinopril, Metformin, Vitamin B12
- Allergien
- Paxil
- Vorherige Impfungen
- COVID 19 immunizations, Pfizer EW0176 (05/8/21) and EW0180 (05/29/21). Difficulty swallowing for 1 month after immunization.
- Staat
- NY
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 29.12.2021
- Impfdatum
- 22.12.2021
- Beginn
- 23.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Chest pain
Symptomtext
Back and chest pain
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 29.12.2021
- Impfdatum
- 29.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Condition aggravated
Erythema
Throat irritation
Symptomtext
Client c/o HX of rash and itchy throat post previous vaccination. Client initially requested to monitor for 30 minutes by MD on site. At 15 minute mark, client's husband approached writer to request assistance for itchy throat. Writer noted redness to clients chest. Writer requested assistance from MD onsite, safety team and immediate supervisor. Client visited EMT and sat in ambulance for monitoring. V/S WNL for client, per client, at B/P 145/81, HR 67, and 98% O2 on RA. MD recommend continue monitoring. Client discharged by MD at 3:35 pm with no further c/o itchy throat or redness to chest.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Unknown but reports allergic reaction to 2nd dose of Covid 19 Pfizer vaccination.
- Vorherige Impfungen
- Client states that she had a reaction with her previous Pfizer vaccination. Client states that she had hives and difficulty brea
- Staat
- CA
- Alter
- 46,0
- 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
Chest pain
Dysphagia
Headache
Symptomtext
Client c/o difficulty swallowing, chest pain and H/A. Client remained conscious throughout the entire event. Initial vital signs noted as B/P 155/87, o2 of 100% on R/A, and HR 96. Writer notified MD and MD authorized administration of 50 mg IM Benadryl. Staff called 911. Client refused service of 911 but agreed to remain in observation an additional 15 minutes. Clients last V/S noted as 146/93, O2 100% on RA, and HR 84. Client left with a continued complaint of slight H/A .
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- IM Bendaryl 50 mg to the left thigh.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Aspirin
- Allergien
- Seasonal only
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 14.06.2023
- Impfdatum
- 05.01.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Vaccination site pain
Symptomtext
hurt after she received; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP), Program ID: (RA). The reporter is the patient. A 63-year-old female patient received BNT162b2 (BNT162B2), on 05Jan2022 as dose 3 (booster), single (Lot number: 33036BD) at the age of 62 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Factor V Leiden bleeding disorder" (unspecified if ongoing), notes: not on blood thinners or statins. The patient's concomitant medications were not reported. Vaccination history included: BNT162b2 (Dose 1, single, Lot: EW0150), administration date: 01Apr2021, when the patient was 61-year-old, for COVID-19 immunisation; BNT162b2 (Dose 2, single, Lot: EW0172), administration date: 23Apr2021, when the patient was 61-year-old, for COVID-19 immunisation, reaction(s): "hurt after she received". The following information was reported: VACCINATION SITE PAIN (non-serious) with onset 2022, outcome "unknown", described as "hurt after she received". Additional information: It was reported that the vaccine was given in left shoulder.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300218053 Same patient/vaccine/event, different dose;US-PFIZER INC-202300218534 Same patient/vaccine/event, different dose;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Haemorrhage (not on blood thinners or statins)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 19.05.2023
- Impfdatum
- 16.06.2022
- Beginn
- 01.08.2022
- Tage bis Beginn
- 46,0
- Dosis
- 3
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Facial pain
Magnetic resonance imaging head normal
Trigeminal neuralgia
Symptomtext
Began experiencing sharp, sporadic, excruciating pain on L side of face, in 08/2022. Saw dentist on 09/09/2022, who ruled out TMJ. Appointment with PCP, at the time, the MD on 09/22/2022. Dr. diagnosed condition as Trigeminal Neuralgia, she prescribed Carbamazepine 200 mg 3 x a day. Referred me to a Dr. Neurologist, appt on 10/03/2022, he concurred with diagnosis and the prescribed medication, he scheduled MRI for 10/17/2022. I experienced an allergic reaction to Cabamazepine, visited Urgent Care on 10/07/2022, for shot and medication, stopped Cabamazepine. Started taking Advil and Extra Strength Tylenol 3 times a day, and mouth guard at night. I saw Dr. on 11/23/2022 for MRI results. No abnormalities on MRI.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Facial pain
- Hospital-Tage
- -
- Labordaten
- MRI on 10/17/2022 of brain, no abnormalities found.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Migraine Headache Herpes
- Andere Medikamente
- ;Hydrochlorothiazide 25mg 1 day; Multi Vitamin
- Allergien
- Motrin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 03.04.2023
- Impfdatum
- 04.01.2022
- Beginn
- 06.12.2022
- Tage bis Beginn
- 336,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
COVID-19
Chills
Cough
Decreased appetite
Dysphonia
Fatigue
Hypersomnia
Oropharyngeal pain
Pain
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Taste disorder
Throat irritation
Symptomtext
On 4 December, in the afternoon I had loss of appetite and a drop of energy with 99degrees which is a low grade fever for me. I slept for a long time which was over 10 hrs. By Monday fever 102.5 which a lot of aches and chills . Then I continued sleeping with zero appetite, very weak and fatigue. Mild congestion. I only drank tea for the 3 days. The food tasted super bland when I ate it. I contacted my doctor on 12/7/22 via telehealth. I had no fever but I took Tylenol. The fatigue and loss appetite lasted till 12/13/2022. After the 12/14/22 I felt normal. It long time till I got back my stamina. I had COVID-19 again Mar2023 where I had a scratchy throat, chills and a drop in energy and low appetite . The next day I woke up coughing and the temperature was 99 and lost of sleeping. I though it was a head cold or a cough. It was not as bad as the last time I had COVID-19. I took Nightquill on Monday night evening Dayquil and Suphedrine PE on Tuesday. On Wednesday, I had lots of congestion with cough and my voice was like laryngitis but no sorethroat until Friday. On Saturday I felt better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- 6Dec2022 - COVID-19 Positive; 9dec2022 Positive, COVID-19- 3/31/23 & 4/3/23 Positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Multivitamins over 50; Bupropion HCL XL
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 07.03.2023
- Impfdatum
- 08.09.2022
- Beginn
- 18.02.2023
- Tage bis Beginn
- 163,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Nausea
SARS-CoV-2 test positive
Vomiting
Symptomtext
02/18/23 presents to ED for "nausea, vomiting" "no significant past medical history"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- 02/18/23 SARS-CoV-2 (COVID-19) by NAA detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 24.02.2023
- Impfdatum
- 17.02.2022
- Beginn
- 21.02.2023
- Tage bis Beginn
- 369,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal pain
Arthralgia
Blood test abnormal
Blood urea increased
COVID-19
Crying
Cyst
Headache
Laboratory test
Lymphadenopathy
Lymphocyte count abnormal
Malaise
Moaning
Monocyte count abnormal
Musculoskeletal discomfort
Nasal congestion
Neck mass
Neutrophil count abnormal
Symptomtext
I noticed a lump on my neck so I went to a clinic, and it was recommended that I go to the ER to have what was believed to be a cyst that needed to be drained. The ER doctor gave me a swab for strep and noted all lymph nodes in my neck were swollen including the lump in my neck at around 1700 hours I felt like the screws in my hip were being pulled out and pain everywhere in my body. I was coughing up mucous and my nose was very clogged. The pain was different in different parts of my body, abdomen was very sharp and pins in my head like someone was driving an axe through my head, hip pain was like someone had opened it up and was stabbing and clawing at it. My throat was like someone was pouring itching powder down my throat and my pain level was a ten out of one through ten. I called the nurse through the insurance provider and asked about the ER again and it was recommended I go to an urgent care, the next day I took a muscle relaxer and it allowed me to sleep more. I was going to the clinic building but to walk six hundred meters it took one and one half hours. The pain was so bad it caused me to cry and went back to the ER I was crying a groaning, tests were ran.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- COVID-19 positive result. BUN 22mg. Blood profile had some abnormal results; Lymphocyte; Monocyte; Neutrophil
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hip dysplasia
- Andere Medikamente
- Amitriptyline
- Allergien
- Penicillin; amoxicillin; tizanidine
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 09.01.2023
- Impfdatum
- 06.01.2022
- Beginn
- 06.10.2022
- Tage bis Beginn
- 273,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Epstein-Barr virus infection
Epstein-Barr virus test positive
Fatigue
Symptomtext
Extreme fatigue. I was advised to rest to stay hydrated and eat well. I was advised this as it was the end of its cycle and had run its course, Epstein Barr virus.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- I tested positive for EBV, Epstein Barr virus.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Obesity; Depression; Asthma; Hypothyroidism
- Andere Medikamente
- Zinc; calcitriol; B12; methyl; folate; iron; SINGULAIR; sertraline; loratadine; levothyroxine; calcium citrate; vitamin C; ibuprofen; PROAIR; albuterol sulfate; AUVI-Q; immunotherapy
- Allergien
- ZYRTEC; CLARITIN; ergocalciferol; cholecalciferol; LEXAPRO; CIPRO; VOLTAREN; clindamycin; penicillin; sulfa; TYLENOL; aspirin; shellfish; seafood; dairy; kiwi; almonds; latex; cherries; sycamore; lawn grass; pollen; mold; dust ; dust mites; chalk
- Vorherige Impfungen
- Severe headache and body aches chills soreness at injection site. Age 45. 02/24/2021 MODERNA COVID-19 & 03/24/2021 MODERNA COVID
- Staat
- TX
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 05.01.2023
- Impfdatum
- 04.01.2022
- Beginn
- 19.12.2022
- Tage bis Beginn
- 349,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Aphonia
COVID-19
Cough
Headache
Paranasal sinus discomfort
Productive cough
Pyrexia
SARS-CoV-2 test positive
Secretion discharge
Surgery
Symptomtext
On Monday the 19th I was having a slight cough. That worsened and I had a lot of mucus the next day. I had been with my mom, and she was having a surgery and took a test for the procedure, and she tested positive. On the 21st I took a test, and it was positive. That day I had a fever 101 which it ranged from that to 103. It would come and go, I had a lot of mucus and I think I could have had a sinus infection at the same time, so I had the sinus pressure and headache. I reached out to a telehealth doctor through my insurance because I was having the fever and wanted PAXLOVID, but they did not end up helping or giving me anything to help. I did not have a fever after the 21st but the productive cough lasted another ten days or so. I am recovered but I had lost my voice due to coughing and that is not back fully so I would say I am recovered about 95%.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- COVID-19 home test
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Asthma
- Andere Medikamente
- ZYRTEC; folic acid
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 08.09.2022
- Impfdatum
- 24.01.2022
- Beginn
- 10.02.2022
- Tage bis Beginn
- 17,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Biopsy skin abnormal
Burning sensation
Musculoskeletal stiffness
Pain in extremity
Pruritus
Skin disorder
Skin lesion
Symptomtext
She had pain in her arm for 3-4 days and a stiff neck. She kept a heating pad on it. In February, she noticed a spot on her feet near her ankle. She would scratch it and it continued to grow. She went to a dermatologist in May when it was small. She had a biopsy. She was not given anything then. She then called last month on 7/29/2022 as it continued to worsen and could not get an appointment due to being so far out. She has an appointment 9/23/2022. The doctor called her in a prescription for metronidazole, which is not working. She is to take them for about 2 weeks, miss a week and then take again until gone. She has been taking them about a month with no effect. She went to a dermatologist, who gave her some medicine for the itching (loratadine 10mg). She continues to have itching. About once a week, she has burning real bad. She has to pat it to get the sensation away. It has spread all over the bottom of her legs, thighs, her hands and her chest. It is also on her stomach. It seems to move from her stomach to her breast, her arms, hands and middle part of her arms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- Biopsy done at dermatologist office.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High blood pressure, high cholesterol, diabetes
- Andere Medikamente
- Metformin 1000mg, Atorvastatin, Atenolol 100mg, Losartan 100mg, Amlodipine 10mg, Glipizide 10mg, Januvia
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- HI
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 26.08.2022
- Impfdatum
- 20.05.2022
- Beginn
- 12.07.2022
- Tage bis Beginn
- 53,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Bronchitis
Chest X-ray normal
Chills
Cough
Headache
Influenza A virus test negative
Influenza B virus test
Lacrimation increased
Oropharyngeal pain
Pain
Pyrexia
Rhinorrhoea
SARS-CoV-2 test negative
Streptococcus test negative
Throat irritation
Urinary tract infection
Urine analysis abnormal
Symptomtext
On 7-12-2022, I started noticing a scratchy throat. The next day, i started noticing a cough and I thought it may have been a seasonal allergy. I took a home COVID-19 test and it was negative. On 7-14, I called my primary care office and we done a telehealth visit. She suggested a COVID-19 PCR test which was done on 7-19 with negative results. The doctor's office stated this was probably viral. On 7-15, I started to have body aches, a headache, runny nose, watery eyes and my sore throat was getting worse. 7-20, I went to an urgent care because I was not feeling any better. They performed a COVID-19 test and FLU A/B, all were negative. They determined it was bronchitis from a viral infection. They ordered me to have albuterol inhaler. On 8-4, I called my primary care doctors office again and had a telehealth visit due to continued symptoms and now a possible eye infection. I spoke with the Nurse Practitioner and she ordered dextromethorphan and trimethoprim. She diagnosed me with bronchitis. On 8-9-2022, I had a chest xray and it was negative. On 8-18, I went to the local ER due to the same symptoms but now chills, fever up to 100.3 and more body aches. They done alot of bloodwork and diagnosed me with a Bronchitis. They gave me a prescription for Cephalexin. It seemed like my cough and sore throat was getting better but last night it came back. I still have the scratchy throat and a persistent cough.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- 7-12-2022 home COVID-19 test - negative results 7-19-2022 COVID-19 PCR test - negative results 7-20-2022 COVID-19 test and FLU A/B, negative results. 8-9-2022 Chest XRAY - negative results 8-18-2022 COVID-19 test and FLU A/B, Strep test- Chest XRAY - all negative results. Other bloodwork and Urinalysis performed in the ER. Urinalysis showed UTI Multiple other PCR/home antigen tests were all negative
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High Blood Pressure
- Andere Medikamente
- Lisinopril; Hydrochlorothiazide; Multivitamin; Calcium supplement; Omega 3
- Allergien
- Naproxen; Ibuprofen; Shrimp
- Vorherige Impfungen
- 2-24-2021 Pfizer dose 2 (age 51) and 11-19-2021 Pfizer dose 3 - (age 52) Heart palpitations with both.
- Staat
- MA
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 23.08.2022
- Impfdatum
- 20.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Myalgia
Pyrexia
Symptomtext
One day after receiving the vaccine, I experienced a day of fever, chills, muscle aches. This is not my typical response to vaccinations I have received in the past. These symptoms lasted for about 48 hours. I slept and took Tylenol for the symptoms. I also drank hot tea for my symptoms. I completely recovered from my symptoms within 48 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Multiple Sclerosis; Long Haul COVID 19; Cervical Cancer Survivor
- Andere Medikamente
- Adderall XR; Lyrica; Cymbalta; Dalfampridine; Zafirlukast; Ocrevus; Vitamin B12; Vitamin D3
- Allergien
- Seafood; Shellfish; Latex; Erythromycin
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 20.07.2022
- Impfdatum
- 07.01.2022
- Beginn
- 20.06.2022
- Tage bis Beginn
- 164,0
- Dosis
- 3
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal discomfort
Body temperature fluctuation
COVID-19
Chills
Cough
Fatigue
Hepatic enzyme increased
Pain
SARS-CoV-2 test positive
Symptomtext
Started on 06/20/2022, I had symptoms. I took an at-home COVID-19 test (06/21/2022) which was positive. I called my doctor the same day and he prescribed me a steroid, an antibiotic to help with secondary infection and told me to take vitamin D and Vitamin C. The symptoms started as pain, chills and temperature swings. Then, I got a cough that lingered for a bit and fatigue that also lingered. The actual symptoms lasted for a few days and the cough lingered but by 10 days later I didn't feel sick anymore. 2 weeks after testing positive the first time, I tested positive again. At day 15, I finally tested negative. I was still having fatigue and some GI issues that my doctor thought was related to the antibiotic use. Then, I started having pain issues again and we just got the labs back that my liver enzymes were significantly out of range. So, we are looking into the cause of that.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- At-home COVID-19 test (06/21/2022): Positive; At-home COVID-19 test (10 days out): Positive; At-home COVID-19 (15 days out): Negative; Blood work: elevated liver enzymes.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma and Hypothyroidism
- Andere Medikamente
- Levothyroxine; Montelukast; Advair Diskus
- Allergien
- Lavender and Fire ants
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 30.06.2022
- Impfdatum
- 27.12.2021
- Beginn
- 15.05.2022
- Tage bis Beginn
- 139,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Headache
Influenza like illness
Malaise
Pain
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
COVID-19 symptoms started on 05/15/22; tested positive on 05/16/22. Symptoms were body aches, headache, flu-like symptoms, runny nose, and congestion. I took vitamin c, d, zinc, and Paxlovid. Symptoms lasted for 2 weeks.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- COVID-19 Positive 05/16/22
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Gout
- Andere Medikamente
- N/A
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 19.06.2022
- Impfdatum
- 18.04.2022
- Beginn
- 18.06.2022
- Tage bis Beginn
- 61,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Malaise
SARS-CoV-2 test positive
Symptomtext
Positive COVID-19 test with symptoms
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- COVID-19 Ag 6/19/2022
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma
- Andere Medikamente
- Advair, proventil, multivitamins, fish oil, magnesium, glucosamine
- Allergien
- Tree nuts, flowers, grasses, trees, animal dander, latex
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 09.05.2022
- Impfdatum
- 06.05.2022
- Beginn
- 07.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood pressure increased
Malaise
Peripheral swelling
Sensory disturbance
Symptomtext
I woke the next day and I wasn't feeling well. When I went to shower, I felt like someone knocked me in the arm with a fist. It was swollen for about 24 hours. I feel fine but not 100%. My BP is good but it slightly elevated on the next morning.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- No
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- *Prefers to not say
- Andere Medikamente
- *Prefers to not say
- Allergien
- Penicillin Ampicillin Pollen
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 06.05.2022
- Impfdatum
- 06.05.2022
- Beginn
- 06.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Eructation
Hypoaesthesia oral
Immediate post-injection reaction
Pruritus
Retching
Vomiting
Symptomtext
Immediate within 5 seconds retching, burping, vomiting, itchiness, numbness sensation on the top of mouth,
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- Vitals done
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Allergies and obesity
- Andere Medikamente
- Benadryl 50 MGS, Zofran 4MGS and Zyrtec 20 MGS.
- Allergien
- Medications Amoxicillin , Codine, Food allergies anaphylaxis) to food allergens: Pepper (black and white), turmeric, all capsicums, bell pepper, pistachios, oregano, rosemary, cayenne pepper, chili pepper, black currant , paprika, coriander, parsley, curry, ginger, chili spice, currant (black & red), hot peppers, arugula, jalape?o, nutmeg, olive oil, vanilla & vinegar. allergies to vaccinations: TB vaccination,& Covid vaccines.
- Vorherige Impfungen
- Covid Vaccines Pfizer April and May 2021, retching, pale, vomitting, hives, high heart rate, tingling on my throat and lips, lig
- Staat
- NY
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 01.05.2022
- Impfdatum
- 13.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Musculoskeletal stiffness
Pain in extremity
Symptomtext
Arm pain stiffness
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 20.04.2022
- Impfdatum
- 23.01.2022
- Beginn
- 23.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site discolouration
Injection site pruritus
Injection site urticaria
Injection site warmth
Myalgia
Pyrexia
Rash macular
Symptomtext
Large hive (~4 inches in diameter) at injection site, heated pink and itchy. Hives down right arm, splotchy. Fever (~101 consistently), muscle aches took benadryl, tylenol, advil and topical anti-itch cream.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site discolouration
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- PCOS, ADHD, Autism spectrum disorder, GERD, gastritis, gastric ulcers, ileitis, hypothyroidism, reynaud's phenomenon
- Andere Medikamente
- Vyvanse 40mg, Lexapro 10mg, Melatonin 10mg, Levothyroxine 50mcg, Mirena IUD
- Allergien
- Cipro, Sulfa, Augmentin, Omnicef, Ceftin, Prevacid, Solodyn, Tetracycline, Aztreonan, Cephlex, Latex, Ferrous metals, Carrots, Sweet potatoes, Apricots, Nectarines, Brazil nuts
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 20.04.2022
- Impfdatum
- 19.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Sleep disorder
Symptomtext
10 hours after receiving vaccines patient awoke with moderate to severe chills and shivering. Over next 6 hours woken several times due to chills , drifting in and out of sleep. At 6:15 patient got out of bed, and dressed for the day. Lingering chills, but shivering has stopped.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- No testing performed
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 19.04.2022
- 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
Arthralgia
Neuralgia
Pain
Pain in extremity
Symptomtext
Patient developed arm pain starting from her shoulder and shooting down her arm shortly after receiving her vaccine. She described it as a nerve pain and is still experiencing symptoms today.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 30.03.2022
- Impfdatum
- 08.01.2022
- Beginn
- 24.01.2022
- Tage bis Beginn
- 16,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Fatigue
Impaired work ability
Nasopharyngitis
SARS-CoV-2 test positive
Throat irritation
Symptomtext
developed a scratchy throat in the afternoon of 1/24/2022, this progressed into a head cold and then to being very tired over the 10 days I was away from work
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- home covid kit tested positive on 1/26/2022 and 1/31/2022
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- tarsal tunnel cervical degenerative disc migraines
- Andere Medikamente
- mvi magnesium/calcium/zinc acetaminophen acidophilus propranolol pregabalin riboflavin tramadol lansoprazole metanx
- Allergien
- codeine amoxicillin sulfa fluorescein dye
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 28.03.2022
- Impfdatum
- 26.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Pain
Symptomtext
I had achiness near my breast and under arm on both sides, Its not severe, Its kind of like when I move I feel it. Its a surprise shot of pain. And a slight headache.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Acid reflux; High blood pressure; Eczema
- Andere Medikamente
- Pantoprazole, Lisinopril, Centrum Women's Silver vitamin, Vitamin D3
- Allergien
- Penicillin metronidazole; raw vegetables ie. cauliflower and broccoli, cucumbers, dried tomatoes
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 24.03.2022
- Impfdatum
- 02.02.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Nausea
Symptomtext
He has been complaining about nausea; Fatigue; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the parent. A 13 year-old male patient received bnt162b2 (BNT162B2), administration date 02Feb2022 (Lot number: 33036bd) at the age of 13 years as dose 1, single for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: IBUPROFEN. The following information was reported: NAUSEA (non-serious) with onset Feb2022, outcome "not recovered", described as "He has been complaining about nausea"; FATIGUE (non-serious) with onset Feb2022, outcome "not recovered", described as "Fatigue". The events "he has been complaining about nausea" and "fatigue" were evaluated at the physician office visit. Therapeutic measures were taken as a result of nausea, fatigue. Additional Information: Pfizer Safety hopes that the child is feeling much better. Thank you for reporting the below information to safety on (SRD) 10Mar2022, with the first Pfizer Awareness Date (PRD) 23Feb2022. Since the information was reporting outside of the 24-hour compliance period for AE reporting we are actioned to follow-up on the delayed AE report. Please provide a reason for the delay in reporting and confirm completion of AE reporting training. Please also confirm understanding reporting responsibilities and the compliance timelines. We file this in the event that the documentation is required during an audit. Response: Something I didn't specifically say in the report is that (Name) is my son. The reason for the delay is distinguishing between expected immune response to the vaccine and an adverse event. So while I listed the date he got the vaccination as the date of the adverse event I did not view it as that on 23Feb. I viewed what was happening as the expected immune response. Defining the date when I first became aware of the event wasn't straight forward so I just picked the day he got the 2nd dose of the vaccine. What triggered me to report it as an adverse event is when he came home on 10Mar and told me about his sharp pain because that seemed to be going the wrong way in recovering. Facility where the most recent COVID-19 vaccine was administered: Doctor's office/urgent care. The patient did not received any other vaccine within 4 weeks prior to the COVID vaccine. List of any other medications the patient received within 2 weeks of vaccination: Ibuprofen. Treatment received for adverse event was prescribed antacid and referral to GI specialist. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. There were no known allergies. No medical history. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- IBUPROFEN.
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 23.03.2022
- Impfdatum
- 31.12.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arthralgia
Impaired driving ability
Loss of personal independence in daily activities
Muscle spasms
Musculoskeletal pain
Axillary mass
Feeling abnormal
Lymphadenopathy
Muscle tightness
Nasal congestion
Neck pain
Pain
Tenderness
X-ray
Symptomtext
stabbing pain; muscle that tightens in his neck; lymphadenopathy/ swollen on left side below clavicle; Feeling of congestion in the front; Left armpit tender; very lumpy down his rib cage; Left side pain from neck to scapula; Felt a little funny; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). A 73 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 31Dec2021 (Batch/Lot number: unknown) at the age of 73 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Spinal fusion surgery", start date: Oct2019 (unspecified if ongoing), notes: Verbatim: Spinal fusion, She later stated it was Oct2019 instead of Nov2019, He had spinal surgery and had neck and vertebrae fused Nov2019.; "Food allergies diagnosed when he was in high school." (unspecified if ongoing), notes: Food allergies diagnosed when he was in high school. There were no concomitant medications. Vaccination history included: Bnt162b2 (DOSE 1, Vaccine Name: , Lot Number / Expiry Date: Unknown/Unknown, Route, Anatomical Location: Injected in left arm, No. of Previous Doses: 0, Date: 05Feb2021), administration date: 05Feb2021, when the patient was 72 years old, for COVID-19 Immunization, reaction(s): "Sore left arm"; Bnt162b2 (DOSE 2, 5. History of all previous immunization with the Pfizer vaccine considered as suspect (or patient age at first and subsequent immunizations if dates of birth or immunizations are not available): , Vaccine Name: Pfizer COVID vaccine, Lot Number / Expiry Date: Unknown/Unknown, Route, Anatomical Location: Injected in left arm, No. of Previous Doses:1, Date: 26Feb2021), administration date: 26Feb2021, when the patient was 72 years old, for COVID-19 immunization, reaction(s): "Sore left arm". The following information was reported: FEELING ABNORMAL (non-serious) with onset 31Dec2021, outcome "not recovered", described as "Felt a little funny"; NECK PAIN (non-serious) with onset 01Jan2022, outcome "not recovered", described as "Left side pain from neck to scapula"; TENDERNESS (non-serious) with onset 03Jan2022, outcome "recovering", described as "Left armpit tender"; AXILLARY MASS (non-serious) with onset 03Jan2022, outcome "recovering", described as "very lumpy down his rib cage"; LYMPHADENOPATHY (non-serious) with onset 04Jan2022, outcome "recovering", described as "lymphadenopathy/ swollen on left side below clavicle"; NASAL CONGESTION (non-serious) with onset 04Jan2022, outcome "unknown", described as "Feeling of congestion in the front"; PAIN (non-serious), outcome "unknown", described as "stabbing pain"; MUSCLE TIGHTNESS (non-serious), outcome "unknown", described as "muscle that tightens in his neck". The events "left side pain from neck to scapula", "left armpit tender", "lymphadenopathy/ swollen on left side below clavicle", "feeling of congestion in the front" and "stabbing pain" were evaluated at the physician office visit. The event "muscle that tightens in his neck" was evaluated at the emergency room visit. Relevant laboratory tests and procedures are available in the appropriate section. Additional information: 31Dec2021 is the day he received booster shot. The day after the booster shot, he began to have pain in left side, which he never had on that side before. It was in his neck and went down to his scapula. Then, his armpit was tender and very lumpy down his rib cage, so she looked it up and there had been reports of lymphadenopathy. On the day received booster shot, they had to drive quite a distance to come back to (State Initials) and knew he struggled the entire way. She first stated it was persisting. She would say it is a tiny bit better, he can find places where he sits or moves where he can stop it, but it is a stabbing pain. It is hard to describe. It is a muscle that tightens in his neck and she can feel it and it goes down the scapula. Then he has a feeling of congestion in the front. He is swollen on left side below clavicle. She did not feel armpit because he got worse after driving. She tried to probe around to try and help relieve him. That was by 03Jan2022. Lumpy rib cage improved quite a bit. She used it as a massage center for him and could not get into a doctor right away. It seemed as though massaging tending to help them release. On 04Jan2022, he said that was bothering him. That was the least of the things. The stabbing pain is in his shoulder and connection where trapezius comes across that spot in his shoulder. It is not painful, just kind of a presence. Vaccination Facility Type as Pharmacy. Physician Office visited, the Orthopedic doctor. He x-rayed him to determine if related to surgery and it was not. He said he could not offer anything other than take Tylenol unless he wanted a heavier medication, which he did not. X-ray neck and where surgery was and cervical and it was ok. No-any other vaccinations within four weeks prior to the first administration received. Felt a little funny was reported as worsened. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected. Follow-up (24Feb2022): This follow-up is being submitted to notify that the lot/batch number is not available despite the follow-up attempts made. Follow-up attempts completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- Test Name: X-ray neck; Result Unstructured Data: Test Result:it was ok; Comments: Relevant Tests: X-ray neck and where surgery was and cervical and it was ok.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Food allergy (Food allergies diagnosed when he was in high school.); Spinal fusion (Verbatim: Spinal fusion.)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 22.03.2022
- Impfdatum
- 26.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Pain in extremity
Poor quality product administered
Product administration error
Product temperature excursion issue
Symptomtext
Right arm soreness; Caller confirmed that the vaccine was given 12 hours passed the 6 hour window after dilution; Caller states a pharmacist gave a dose to a patient that was expired by about 12 hours. vaccine was given 12 hours passed the 6-hour window after dilution//Received vaccine 12 hours after use by date; Caller confirmed that the vaccine was given 12 hours passed the 6 hour window after dilution/Received vaccine 12 hours after use by date; This is a spontaneous report received from a contactable reporter(s) (Pharmacist) from medical information team. A 20 year-old male patient received bnt162b2 (BNT162B2), intramuscular, administered in deltoid right, administration date 26Jan2022 11:00 (Lot number: 33036BD, Expiration Date: Jun2022) at the age of 20 years as dose 3 (booster), 0.3 ml single for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (The first dose was given on 06Apr2021.Lot, expiration and site of administration are unknown.), administration date: 06Apr2021, when the patient was 20 years old, for COVID-19 Immunization; Bnt162b2 (2nd dose was given on 27Apr2021, Lot, expiration and site of administration are unknown), administration date: 27Apr2021, when the patient was 20 years old, for COVID-19 Immunization. The following information was reported: PRODUCT TEMPERATURE EXCURSION ISSUE (non-serious) with onset 26Jan2022 11:00, outcome "unknown", described as "Caller confirmed that the vaccine was given 12 hours passed the 6 hour window after dilution"; PRODUCT ADMINISTRATION ERROR (non-serious) with onset 26Jan2022 11:00, outcome "unknown", described as "Caller states a pharmacist gave a dose to a patient that was expired by about 12 hours. vaccine was given 12 hours passed the 6-hour window after dilution//Received vaccine 12 hours after use by date"; POOR QUALITY PRODUCT ADMINISTERED (non-serious) with onset 26Jan2022 11:00, outcome "unknown", described as "Caller confirmed that the vaccine was given 12 hours passed the 6 hour window after dilution/Received vaccine 12 hours after use by date"; PAIN IN EXTREMITY (non-serious), outcome "unknown", described as "Right arm soreness". Additional information: Caller was a pharmacist calling regarding the adult formulation purple cap Pfizer BioNTech Covid-19 vaccine. Caller states a pharmacist gave a dose to a patient that was expired by about 12 hours. Caller confirmed that the vaccine was given 12 hours passed the 6-hour window after dilution. Caller states the vaccine was diluted, stored in the vial at room temperature. Caller would like to know what he should do and if the dose should be repeated. He did talk to patient this morning, close to 24 hours after administration, and the only adverse effect was soreness in arm that was typical with immunization and there were no others. This was a booster dose. Additional Vaccines Administered on Same Date of the Pfizer Suspect If applicable, list all vaccines administered on same date with the Pfizer vaccine considered as suspect: none. Adverse Event (AE) Details: Provide the time of onset of AE(s): Right arm soreness ? Unknown. Received vaccine 12 hours after use by date-recovered. It was unknown- (when he talked to patient there was no indication of that) whether adverse event resulted in Emergency or physician office visit. Prior Vaccinations (within 4 weeks) If applicable, list any other vaccinations within four weeks prior to the first administration date of the suspect vaccine(s) and AE(s) following prior vaccinations: Unknown. Patient's Medical History (including any illness at time of vaccination): None or Unknown Provide other relevant medical history including but not limited to these conditions: diagnosed allergies, compromised immune status, respiratory illness, genetic/chromosomal abnormalities, endocrine abnormalities (including diabetes) and obesity Illness/AE: Unknown. Family Medical History Relevant to AE(s) and Relevant Tests was reported as unknown. Other products: Unknown. Investigation assessment: No. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 22.03.2022
- Impfdatum
- 26.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Pain in extremity
Poor quality product administered
Product administration error
Product temperature excursion issue
Symptomtext
Right arm soreness; Caller confirmed that the vaccine was given 12 hours passed the 6 hour window after dilution; Caller states a pharmacist gave a dose to a patient that was expired by about 12 hours. vaccine was given 12 hours passed the 6-hour window after dilution//Received vaccine 12 hours after use by date; Caller confirmed that the vaccine was given 12 hours passed the 6 hour window after dilution/Received vaccine 12 hours after use by date; This is a spontaneous report received from a contactable reporter(s) (Pharmacist) from medical information team. A 20 year-old male patient received bnt162b2 (BNT162B2), intramuscular, administered in deltoid right, administration date 26Jan2022 11:00 (Lot number: 33036BD, Expiration Date: Jun2022) at the age of 20 years as dose 3 (booster), 0.3 ml single for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (The first dose was given on 06Apr2021.Lot, expiration and site of administration are unknown.), administration date: 06Apr2021, when the patient was 20 years old, for COVID-19 Immunization; Bnt162b2 (2nd dose was given on 27Apr2021, Lot, expiration and site of administration are unknown), administration date: 27Apr2021, when the patient was 20 years old, for COVID-19 Immunization. The following information was reported: PRODUCT TEMPERATURE EXCURSION ISSUE (non-serious) with onset 26Jan2022 11:00, outcome "unknown", described as "Caller confirmed that the vaccine was given 12 hours passed the 6 hour window after dilution"; PRODUCT ADMINISTRATION ERROR (non-serious) with onset 26Jan2022 11:00, outcome "unknown", described as "Caller states a pharmacist gave a dose to a patient that was expired by about 12 hours. vaccine was given 12 hours passed the 6-hour window after dilution//Received vaccine 12 hours after use by date"; POOR QUALITY PRODUCT ADMINISTERED (non-serious) with onset 26Jan2022 11:00, outcome "unknown", described as "Caller confirmed that the vaccine was given 12 hours passed the 6 hour window after dilution/Received vaccine 12 hours after use by date"; PAIN IN EXTREMITY (non-serious), outcome "unknown", described as "Right arm soreness". Additional information: Caller was a pharmacist calling regarding the adult formulation purple cap Pfizer BioNTech Covid-19 vaccine. Caller states a pharmacist gave a dose to a patient that was expired by about 12 hours. Caller confirmed that the vaccine was given 12 hours passed the 6-hour window after dilution. Caller states the vaccine was diluted, stored in the vial at room temperature. Caller would like to know what he should do and if the dose should be repeated. He did talk to patient this morning, close to 24 hours after administration, and the only adverse effect was soreness in arm that was typical with immunization and there were no others. This was a booster dose. Additional Vaccines Administered on Same Date of the Pfizer Suspect If applicable, list all vaccines administered on same date with the Pfizer vaccine considered as suspect: none. Adverse Event (AE) Details: Provide the time of onset of AE(s): Right arm soreness ? Unknown. Received vaccine 12 hours after use by date-recovered. It was unknown- (when he talked to patient there was no indication of that) whether adverse event resulted in Emergency or physician office visit. Prior Vaccinations (within 4 weeks) If applicable, list any other vaccinations within four weeks prior to the first administration date of the suspect vaccine(s) and AE(s) following prior vaccinations: Unknown. Patient's Medical History (including any illness at time of vaccination): None or Unknown Provide other relevant medical history including but not limited to these conditions: diagnosed allergies, compromised immune status, respiratory illness, genetic/chromosomal abnormalities, endocrine abnormalities (including diabetes) and obesity Illness/AE: Unknown. Family Medical History Relevant to AE(s) and Relevant Tests was reported as unknown. Other products: Unknown. Investigation assessment: No. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 20.03.2022
- Impfdatum
- 08.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Pain in extremity
Symptomtext
Patient complaining of Sore Arm ever since shot was administered
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- Patient reports went to clinic; blood work done. Dr. suggesting MRI
- Aktuelle Erkrankungen
- None reported
- Vorgeschichte
- Not Known
- Andere Medikamente
- Not known
- Allergien
- None reported
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 17.03.2022
- Impfdatum
- 07.01.2022
- Beginn
- 14.03.2022
- Tage bis Beginn
- 66,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Burning sensation
Headache
Muscle contractions involuntary
Symptomtext
muscle fasciculation overall the body, especially on arms and legs. Joint pain. burning pain on hands. mild headache.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- no
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 17.03.2022
- Impfdatum
- 01.02.2022
- Beginn
- 05.02.2022
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Rash
Rash papular
Symptomtext
Small red bumps; skin rash; itchy; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 39 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 01Feb2022 18:30 (Lot number: 33036BD) at the age of 39 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: IBUPROFEN; SUDAFED [PSEUDOEPHEDRINE HYDROCHLORIDE]. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: ER8729, Location of injection: Arm Left, Vaccine Administration Time: 09:00 AM), administration date: 22Apr2021, when the patient was 38 years old, for COVID-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: ER8733, Location of injection: Arm Left, Vaccine Administration Time: 09:00 AM), administration date: 01Apr2021, when the patient was 38 years old, for Covid-19 immunization. The following information was reported: RASH PAPULAR (non-serious) with onset 05Feb2022 10:00, outcome "not recovered", described as "Small red bumps"; RASH (non-serious) with onset 05Feb2022 10:00, outcome "not recovered", described as "skin rash"; PRURITUS (non-serious) with onset 05Feb2022 10:00, outcome "not recovered", described as "itchy". Therapeutic measures were not taken as a result of rash papular, rash, pruritus. Additional information: It was reported that no other vaccine in fourweeks. No treatment for the events. No covid prior vaccination. Patient was not tested covid post vaccination. Patient had No Known allergies. Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- IBUPROFEN; SUDAFED [PSEUDOEPHEDRINE HYDROCHLORIDE]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 17.03.2022
- Impfdatum
- 31.01.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal discomfort
Chills
Hyperhidrosis
Pain
Pyrexia
Symptomtext
24 hours later after injection started feeling achy; upset stomach; felt feverish; sweating; chilled; This is a spontaneous report received from contactable reporter(s) (Other HCP). The reporter is the patient. A 45 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 31Jan2022 18:30 (Lot number: 33036BD) at the age of 45 years as dose 3 (booster) single for covid-19 immunisation. Relevant medical history included: "Thyroid problem" (unspecified if ongoing). The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (prev dose product:COVID 19,, prev dose brand:Pfizer,, prev dose brand unknown:False,, prev dose lot number:Er8731,, prev dose lot unknown:False,, prev dose administration date:22Apr2021, prev dose number:2,, prev dose vaccine location:Right arm), administration date: 22Apr2021, when the patient was 44 years old, for COVID-19 immunization; Bnt162b2 (prev dose product:COVID 19,, prev dose brand:Pfizer,, prev dose brand unknown:False,, prev dose lot number:SR8733, prev dose lot unknown:False,, prev dose administration date:10Apr2021, prev dose number:1, prev dose vaccine location:Left arm), administration date: 10Apr2021, when the patient was 44 years old, for COVID-19 immunization. The following information was reported: PAIN (non-serious) with onset 01Feb2022 10:00, outcome "recovering", described as "24 hours later after injection started feeling achy"; ABDOMINAL DISCOMFORT (non-serious) with onset 01Feb2022 10:00, outcome "recovering", described as "upset stomach"; PYREXIA (non-serious) with onset 01Feb2022 10:00, outcome "recovering", described as "felt feverish"; HYPERHIDROSIS (non-serious) with onset 01Feb2022 10:00, outcome "recovering", described as "sweating"; CHILLS (non-serious) with onset 01Feb2022 10:00, outcome "recovering", described as "chilled". The events "24 hours later after injection started feeling achy", "upset stomach", "felt feverish", "sweating" and "chilled" were evaluated at the physician office visit. It was unknown if therapeutic measures were taken as a result of pain, abdominal discomfort, pyrexia, hyperhidrosis, chills. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202200204856 same patient and drug, different event separated in time
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Thyroid disorder
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 17.03.2022
- Impfdatum
- 25.01.2022
- Beginn
- 25.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Incorrect route of product administration
Lymphadenopathy
Pain
Swelling
Symptomtext
ipsilateral supraclavicular lymphadenopathy after covid 19 vaccination; The pain and swelling was excruciating; The pain and swelling was excruciating; The vaccine was given to high in the deltoid; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 55 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in deltoid right, administration date 25Jan2022 10:30 (Lot number: 33036BD) at the age of 55 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Goji Berries allergy" (unspecified if ongoing); "High Cholesterol" (unspecified if ongoing); "Gerd" (unspecified if ongoing); "Migraines" (unspecified if ongoing). Concomitant medication(s) included: LIPITOR. Past drug history included: Flu vaccine, reaction(s): "Allergy". Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: FC3183, Location of injection: Arm Right, Route of Administration: Intramuscular), administration date: 31Aug2021, when the patient was 55 years old, for COVID-19 immunization; Bnt162b2 (Dose Number: 1, at 12:30 PM, Batch/Lot No: FA7485, Location of injection: Arm Right, Route of Administration: Intramuscular), administration date: 10Aug2021, when the patient was 55 years old, for COVID-19 immunization. The following information was reported: INCORRECT ROUTE OF PRODUCT ADMINISTRATION (non-serious) with onset 25Jan2022 10:30, outcome "not recovered", described as "The vaccine was given to high in the deltoid"; LYMPHADENOPATHY (non-serious) with onset 25Jan2022 20:00, outcome "not recovered", described as "ipsilateral supraclavicular lymphadenopathy after covid 19 vaccination"; SWELLING (non-serious), PAIN (non-serious) all with onset 25Jan2022 20:00, outcome "not recovered" and all described as "The pain and swelling was excruciating". The events "the vaccine was given to high in the deltoid", "ipsilateral supraclavicular lymphadenopathy after covid 19 vaccination", "the pain and swelling was excruciating" and "the pain and swelling was excruciating" were evaluated at the emergency room visit. Therapeutic measures were taken as a result of incorrect route of product administration, lymphadenopathy, swelling, pain. Additional Information: As treatment patient received Toradolim and Muscle Relaxant. Covid was prior vaccination. Covid was not tested post vaccination. No follow-up attempts are possible. No further information is expected. Follow-up (07Feb2022): Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Fruit allergy; GERD; High cholesterol; Migraine
- Andere Medikamente
- LIPITOR
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 12.03.2022
- Impfdatum
- 16.02.2022
- Beginn
- 18.02.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Symptomtext
PATIENT HAD RASH TWO DAYS AFTER VACCINATION OF RIGHT UNDERARM. SHE REPORTS PERSISTENT RASH. PRESENTS INTO CLINIC TODAY WITH HISTORY OF WORSENING RASH. PATIENT EVALUATED AND PROVIDED TOPICAL PRESCRIPTION CORTICOSTEROIDS AND ANTIHISTAMINE, WITH RECOMMENDAITON FOR RE-EVALUATION IN A WEEK WITH DERMATOLOGY/URGENT CARE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 08.03.2022
- Impfdatum
- 30.12.2020
- Beginn
- 30.12.2020
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Decreased appetite
Differential white blood cell count
Fatigue
Full blood count
Hallucination
Immature granulocyte count
Myalgia
Neutrophil count
Pyrexia
White blood cell count increased
Symptomtext
#1- Fever 100.8 x 2 days. Fatigue, hallucinations, anorexia, myalgia #2- No reaction #3- No reaction Lab results 2/9/22 - immature granulocytes noted diff of CBC, absolute neutrophils increased at 7.4 WBC count increased 11.1 K
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- as above
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Anxiety, PTSD, Migraines, Hypothyroidism, Migraines, Obesity, IBS, Vitamin D deficiency, Hyperlipidemia
- Andere Medikamente
- Baclofen, Cymbalta, Klonopin, Linzess, Nurtec, Prazosin, Synthroid, Topamax
- Allergien
- Latex, Sulfa
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 01.03.2022
- Impfdatum
- 17.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Muscular weakness
Myalgia
Symptomtext
Systemic: Legs began to feel weak. Overall muscle pain and weakness-Severe
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 28.02.2022
- Impfdatum
- 11.02.2022
- Beginn
- 11.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Anxiety
Dizziness
Dizziness postural
Gait disturbance
Symptomtext
Patient was given COVID 19 booster at 11 am in left deltoid. At 11:03AM patient felt anxious and lightheaded. Patient was instructed to sit in a chair. Skilled nurse notice patient walking sideways, skilled nurse stopped patient in hallway to sit and rest in chair; patient stated she felt ok about 2 minutes after siting in chair. Patient stated that she was fine and wanted to continue to observation room, upon getting out the chair patient stated she felt Dizzy. Patient was eased to floor to keep her from falling, A RRT was called; no head injury; patient was stable. Patient was transferred to ER via stretcher
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- N/A
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 23.02.2022
- Impfdatum
- 17.02.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pruritus
Rash
Vaccine positive rechallenge
Symptomtext
Patient reported both lower legs itching and left ankle rash-like appeared just before 4 hours post-vaccine. Same event was described by patient after Covid vaccine dose 1 and 2. Patient reported itching subsided after 3 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None stated
- Vorgeschichte
- Agorophobia
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- 09/21/2021 Covid-19 vaccine, Pfizer
- Staat
- NJ
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 22.02.2022
- Impfdatum
- 11.02.2022
- Beginn
- 12.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Fatigue
Lethargy
Nausea
Pain in extremity
Vomiting
Symptomtext
Left arm painful for two days. On February 15th woke with nausea, fatigue, lethargy, dizziness and vomiting.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- IBS, Rheumatoid arthritis, Chronic Idiopathic Uticaria, Insomnia, Osteoporosis
- Andere Medikamente
- Xolair, Inderal, plaquenil, Prolia, Carafate, Protonix, Lunesta, Gabapentin, Vitamin C, Zinc, Calcium, Zyrtec, Multivitamin, Aspirin, Krill oil
- Allergien
- Horse radish
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 22.02.2022
- Impfdatum
- 10.02.2022
- Beginn
- 12.02.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dizziness
Fatigue
Headache
Lethargy
Malaise
Symptomtext
Patient received COVID 19 Booster shot on 02/10/2022 LOT#33036BD. Upon returning to the clinic on 02/12/2022. The patient was lethargic, not feeling well, and complaining of headache. Vitals were baseline for this patient. She complained of dizziness and fatigue post treatment. She returned to the clinic 02/15/2022 and was back at baseline without complaint.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- ESRD
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 21.02.2022
- Impfdatum
- 17.02.2022
- Beginn
- 18.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Diarrhoea
Erythema
Eyelid oedema
Fatigue
Headache
Lacrimation increased
Pain
Pain in extremity
Pyrexia
Swelling of eyelid
Visual impairment
Symptomtext
After receiving the COVID-19 Pfizer booster dose, I developed swelling in my left eyelid. The swelling was unilateral, on my left eyelid, upper lid only. This resulted in blocked vision to where 80-90% of my eye had closed. The swelling was slightly red and edamatous. When pressed, tears would flow from my eye, but otherwise did not itch and was not painful. The swelling started about 20 hours after the dose was administered. It was accompanied by other symptoms more typical of the COVID vaccine - fever/chills, headache/bodyache, fatigue, arm pain and diarrhea that I had experienced with the second dose. All symptoms, including swelling resolved 48-60 hours after the administration.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- None
- Allergien
- N/A
- Vorherige Impfungen
- Pfizer COVID Vaccine (2nd Dose in series): Fever/chills, headache/bodyache, fatigue, arm pain and diarrhea starting approximatel
- Staat
- VA
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 21.02.2022
- Impfdatum
- 10.02.2022
- Beginn
- 12.02.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Fatigue
Lethargy
Malaise
Symptomtext
Patient received COVID 19 Booster shot on 02/10/2022 LOT#33036BD. Upon returning to the clinic on 02/12/2022. The patient was lethargic and not feeling well. Vitals were baseline for this patient. She complained fatigue post treatment. She returned to the clinic 02/15/2022 and was back at baseline without complaint.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- ESRD
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 21.02.2022
- Impfdatum
- 10.02.2022
- Beginn
- 12.02.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dizziness
Fatigue
Lethargy
Malaise
Symptomtext
Patient received COVID 19 Booster shot on 02/10/2022 LOT#33036BD. Upon returning to the clinic on 02/12/2022. The patient was lethargic and not feeling well. Vitals were baseline for this patient. She complained of dizziness and fatigue post treatment. She returned to the clinic 02/15/2022 and was back at baseline without complaint.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 20.02.2022
- Impfdatum
- 11.02.2022
- Beginn
- 11.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Lymph node pain
Lymphadenopathy
Odynophagia
Symptomtext
Swollen, painful lymph nodes to left-side of neck and axilla. Painful swallowing lasted for 4 days post-vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymph node pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Rheumatoid arthritis, HTN
- Andere Medikamente
- Lisinopril
- Allergien
- Penicillin, Plaquenil
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 20.02.2022
- Impfdatum
- 18.02.2022
- Beginn
- 19.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Lymph node pain
Lymphadenopathy
Tenderness
Symptomtext
painful, swollen lymph node in left clavicle with tenderness/pain in left axilla
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- bactrim
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 20.02.2022
- Impfdatum
- 28.12.2021
- Beginn
- 03.01.2022
- Tage bis Beginn
- 6,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Dizziness
Rash
Symptomtext
Severe dizziness, patchy skin rash on my arms, hips, legs and several days later on my neck and face. Skin rash on my neck and face was accompanied with severe burning sensation. I started taking Benadryl, but it did not help. My PCP Dr prescribed me Allegra and famotidine. I also got two shots of KENALOG 40mg each. I am still taking Allegra and famotidine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- M?ni?re's disease
- Andere Medikamente
- meclizine 25mg/day
- Allergien
- Vicodin, ampicillin
- Vorherige Impfungen
- Pfizer ER2613 (second dose) on 7/6/2021 at the age of 68yo. Skin rash on my neck and face that went away itself in one week.
- Staat
- NY
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 18.02.2022
- Impfdatum
- 16.02.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Swelling
Symptomtext
Next day she had a painful lump on the left side under her armpit.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- no
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 17.02.2022
- Impfdatum
- 16.02.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Back pain
Haemorrhage
Headache
Insomnia
Musculoskeletal stiffness
Pain in extremity
Peripheral swelling
Sleep disorder
Symptomtext
Was having a hard time sleeping, kept tossing and turning. Woke up at 2am with sore and swollen left arm. Headache at top of my head and occiput, stiff neck. Within 4 hrs after that, developed joint tenderness and stiffness throughout my whole body. I also have been perimenopausal with no period in over 63 days and started bleeding again. By the afternoon, all of these symptoms remained and I also developed lower back achiness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypothyroid Current Gastric Ulcer
- Andere Medikamente
- Levothyroxine Carafate Omeprozole Flintstone Vitamins Chewable Vitamin C Adderall ER
- Allergien
- Flexeril
- Vorherige Impfungen
- After 2nd Pfizer COVID dose I was run down and felt slightly ill. That was Jan. 11th, 2021
- Staat
- CA
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 16.02.2022
- Impfdatum
- 11.02.2022
- Beginn
- 12.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Burning sensation
Erythema of eyelid
Mouth swelling
Oral discomfort
Oral pruritus
Peripheral swelling
Pruritus
Skin burning sensation
Skin swelling
Swelling of eyelid
Symptomtext
Swelling & redness to right eyelid, swelling, burning & itching to the inside of mouth, scalp & palms of both hands
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oral pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- Hypothyoridism HTN
- Andere Medikamente
- Levothoxyn Lisonopril Effexor
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 16.02.2022
- Impfdatum
- 14.02.2022
- Beginn
- 14.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Chest discomfort
Lymphadenopathy
Pain
Symptomtext
02/14/22, 14:20 tightness in upper chest, 18:17 tightness in upper chest; 02/15 full body aching joints entire day including spine, took Tylenol 325mg every 3 hours, 22:47 right lymph nodes swelling throughout front & underside of armpit - closest to injection site. 2/16 iced armpit and Tylenol 325mg every 3 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None to date
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Daily vitamin, Methylphenidate (Ritalin), vitamin D
- Allergien
- -
- Vorherige Impfungen
- Dose 1-Pfizer 1/28/21, small capillary response, hands turned blue; 43 yo
- Staat
- NY
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 15.02.2022
- 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: unbekannt
Erholt: nein
Breast pain
Breast swelling
Chills
Fatigue
Headache
Lymphadenopathy
Pain
Symptomtext
Severe headache, body aches, chills, fatigue. Left axillary and left lateral breast swelling and pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Breast pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypothyroidism
- Andere Medikamente
- Levothyroxine
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 12.02.2022
- 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
Chest discomfort
Urticaria
Symptomtext
Chest tightness developing within 4 hours of administration, resolved overnight. Widespread urticaria that lasted about 1.5 weeks, resolving with oral prednisone.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Osteonecrosis of the femoral heads bilaterally
- Vorgeschichte
- Osteonecrosis of the femoral heads bilaterally
- Andere Medikamente
- Emgality
- Allergien
- Emgality
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 12.02.2022
- Impfdatum
- 02.02.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain upper
Fatigue
Headache
Illness
Overdose
Pain
Pain in extremity
Peripheral swelling
Product administration error
Pyrexia
Symptomtext
Arm was sore and swollen; fever; body ache; stomach ache; Arm was sore; headache; fatigue; My children were given an unknown concentrated dose of Covid-19 Vaccine/Second dose vaccine administered improperly; received over 2ml of the vaccine, not 0.3ml or 0.2ml as necessary; sick; 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 parent. A 14 year-old male patient received bnt162b2 (BNT162B2), administered in deltoid right, administration date 02Feb2022 (Lot number: 33036BD) at the age of 14 years as dose 2, single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (DOSE 1, Batch/lot number: 33036BD, Route of administration: Deltoid, doesn't know which arm), administration date: 12Jan2022, when the patient was 14 years old, for Covid-19 immunization. The following information was reported: PRODUCT ADMINISTRATION ERROR (non-serious) with onset 02Feb2022, outcome "unknown", described as "My children were given an unknown concentrated dose of Covid-19 Vaccine/Second dose vaccine administered improperly"; OVERDOSE (non-serious) with onset 02Feb2022, outcome "unknown", described as "received over 2ml of the vaccine, not 0.3ml or 0.2ml as necessary"; ILLNESS (non-serious) with onset Feb2022, outcome "unknown", described as "sick"; PERIPHERAL SWELLING (non-serious) with onset 03Feb2022, outcome "recovered" (Feb2022), described as "Arm was sore and swollen"; PYREXIA (non-serious) with onset 03Feb2022, outcome "recovered" (Feb2022), described as "fever"; PAIN (non-serious) with onset 03Feb2022, outcome "recovered" (Feb2022), described as "body ache"; ABDOMINAL PAIN UPPER (non-serious) with onset 03Feb2022, outcome "recovered" (Feb2022), described as "stomach ache"; PAIN IN EXTREMITY (non-serious) with onset 03Feb2022, outcome "recovered" (Feb2022), described as "Arm was sore"; HEADACHE (non-serious) with onset 03Feb2022, outcome "recovered" (Feb2022), described as "headache"; FATIGUE (non-serious) with onset 03Feb2022, outcome "recovered" (Feb2022), described as "fatigue". Additional information: The reporter is the parent of the 3 patients, kids who are 14, 11 and 8 to received unknown concentrated second dose Pfizer COVID 19 Vaccine on 02Feb2022. The second dose Pfizer COVID 19 Vaccine was administered improperly over 2ml of the vaccine, not 0.3ml or 0.2ml as necessary, but a lot. The kids were okay a week later but were sick. The patient Arm was sore later the evening of 03Feb2022. The patient's arm was sore and swollen. The patient's arm did not hurt anymore or felt fine. Then on 03Feb2022, the patient had fever, body ache, stomach ache and headache. The patient was very fatigued. The fatigue lasted the longest. The reporter Can't pinpoint the day the fatigue resolved. The morning of 03Feb2022 when the patient woke up for school and didn't' go to school is when the fatigue began. The reporter stated that everything resolved yesterday, 07Feb2022 or the day before 06Feb2022. Reporter clarifies by everything resolving, the caller means, fever, body ache, stomach ache, headache, sore arm and fatigue resolved yesterday 07Feb2022 or the day before, 06Feb2022. The reporter stated the patient recovered completely from fever, body ache, stomach ache, headache, arm being sore and fatigue. Reporter seriousness for The next morning, 03FEB2022 when woke up to go to school had a fever was Unspecified. The reporter stated height of the patient was 5' 9.5, then clarifies between 5'9 and 5'10 and weight as 125 or 130.Sender's Comments: Linked Report(s) : US-PFIZER INC-202200229780 Same reporter/drug/AE, different patient;US-PFIZER INC-202200229781 Same reporter/drug/AE, different patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 12.02.2022
- Impfdatum
- 10.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Rash
Symptomtext
her face is very red; rash all over her face; This is a spontaneous report received from contactable reporter(s) (Pharmacist) from medical information team. The reporter is the parent. A 12-year-old female patient received bnt162b2 (COMIRNATY), administered in arm left, administration date 10Jan2022 15:45 (Lot number: 33036BD) at the age of 12 years as dose 1, 0.3 ml single for covid-19 immunisation. Relevant medical history included: "Asthma" (ongoing). There were no concomitant medications. The following information was reported: RASH (non-serious) with onset 10Jan2022 21:15, outcome "not recovered", described as "rash all over her face"; ERYTHEMA (non-serious) with onset 12Jan2022, outcome "unknown", described as "her face is very red". Therapeutic measures were taken as a result of rash, erythema. Additional information: The reporter who was a pharmacist stated that she gave her daughter the first dose of the Comirnaty vaccine in left arm on Monday 10Jan2022 and that the rash started on same day and by Tuesday 11Jan2022 her daughter's entire face was covered, and today 12Jan2022 her face was very red. She said that she treated her daughter's rash with Benadryl gel and said that the rash keeps changing and that was what concerning to her. It was really red and almost like it was white heads all over her face now. She said that she has never seen this reaction before. The reporting parent asked about any information on reports of children 12 years and older that developed a rash on the face following administration of COMIRNATY and what was the percentage. Dates for Comirnaty: (10Jan2022). NDC number of Comirnaty: 59267100002 and confirmed this was the adult dose of the Comirnaty vaccine. Vaccination Facility Type: Pharmacy. No history of all previous immunization with the Pfizer vaccine considered as suspect (or patient age at first and subsequent immunizations if dates of birth or immunizations are not available). No additional Vaccines Administered on Same Date of the Pfizer Suspect. The start time of the event was unknown but noticed it when she got home from work at about 2115 10Jan2022. The events did not require a visit to Emergency Room or Physician Office. Prior Vaccinations (within 4 weeks) was none. AE(s) following prior vaccinations was none. Family Medical History Relevant to AE(s) was none. Relevant Tests were none, she has just been monitoring her daughter herself.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Asthma
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 12.02.2022
- Impfdatum
- 21.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inflammation
Interchange of vaccine products
Oropharyngeal pain
Pharyngitis
Symptomtext
inflammation; sort throat; 1st, dose J&j 2nd Pfizer; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 46 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 21Jan2022 16:00 (Lot number: 330368D) at the age of 46 years as dose 2 (initial pfizer dose), single for covid-19 immunisation. Relevant medical history included: "Period disorder low iron" (unspecified if ongoing), notes: Period disorder low iron; "Period disorder" (unspecified if ongoing), notes: Period disorder low iron, known_allergies: No. Concomitant medication(s) included: VITAMIN C; IRON. Vaccination history included: J &j (Dose: 01), for Covid-19 immunization. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (non-serious) with onset 21Jan2022 16:00, outcome "unknown", described as "1st, dose J&j 2nd Pfizer"; INFLAMMATION (non-serious) with onset 23Jan2022 07:00, outcome "not recovered", described as "inflammation"; OROPHARYNGEAL PAIN (non-serious) with onset 23Jan2022 07:00, outcome "not recovered", described as "sort throat". Therapeutic measures were taken as a result of inflammation, oropharyngeal pain. Additional information: The patient had no other vaccine in four weeks. The patient received Tylenol as treatment for the adverse events. The patient had no known allergies. The patient had no covid prior to vaccination nor was tested post vaccination. The patient was vaccinated in doctor's office. Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Iron low (Period disorder low iron); Menstrual disorder (Period disorder low iron known_allergies: No)
- Andere Medikamente
- VITAMIN C; IRON
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 11.02.2022
- Impfdatum
- 10.02.2022
- Beginn
- 10.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Back pain
Fatigue
Injection site urticaria
Symptomtext
Significant hives and urticaria at injection site (up and down the same side) on left arm. Noticeable joint and back pain began 6 hours post injection. Noticeable fatigue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Multivitamin
- Allergien
- Penicillin
- Vorherige Impfungen
- Same effects.
- Staat
- MN
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 10.02.2022
- Impfdatum
- 18.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Symptomtext
a headache pounding currently taking 1000 mg of tylenol every 6 hours
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- morphine
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 09.02.2022
- Impfdatum
- 02.02.2022
- Beginn
- 02.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain
Headache
Incorrect dose administered
Injection site erythema
Injection site pain
Injection site swelling
Pain
Pyrexia
Symptomtext
Site: Pain at Injection Site-Severe, Site: Redness at Injection Site-Severe, Site: Swelling at Injection Site-Severe, Systemic: Abdominal Pain-Medium, Systemic: Body Aches Generalized-Medium, Systemic: Fever-Medium, Systemic: Headache-Medium, Error: Wrong Dose of Vaccine - Too High-, Additional Details: parent gave ibuprofen night of vaccination
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 08.02.2022
- Impfdatum
- 05.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 5,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Gingival pain
Interchange of vaccine products
Symptomtext
Around 01/10/2022- pain in my gum, on the lower left side at the very back, where I used to have my wisdom tooth. 01/13/2022- I went to see my dentist, he could not see anything, He said there maybe something under the gum and he asked me to use salt water to rinse. After a week after I saw the dentist it resolved. On 01/22/2022- I had the pain in my gum again, this time on the right side lower gum, at the very back. I treated it by rinsing it with salt water and it resolve after 5 to 7 days. Around that time, I started thinking, could it be related to the vaccine. So when I received the prompt from the smartphone based tool I entered it into the system.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Gingival pain
- Hospital-Tage
- -
- Labordaten
- No
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Multivitamin; high dose prescription of omega 3; ZYRTEC -generic version
- Allergien
- No
- Vorherige Impfungen
- Moderna dose 1 and 2, 04/2021 and 05/2021, fever, headache, chills sweating, nauseous and I just felt tired. After the Moderna,
- Staat
- GA
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 08.02.2022
- Impfdatum
- 02.02.2022
- Beginn
- 03.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Oropharyngeal pain
Pain
Product preparation issue
Pyrexia
Symptomtext
Headaches, body aches, low grade fever, sore throat the day following vaccine administration. Vaccine dose was most likely correct but an excess volume of diluent was also administer. Parent gave age appropriate dose of Motrin the evening of vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 07.02.2022
- Impfdatum
- 10.01.2022
- Beginn
- 30.01.2022
- Tage bis Beginn
- 20,0
- Dosis
- 1
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Rash
Urticaria
Symptomtext
My 13 year old daughter had her 1st dose of the Pfizer vaccine on 1/10/22. She started randomly experiencing whelps/hives that itch significantly on 1/30/22. Treatment: prednisone, benadryl, loratadine, and cetirizine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- Rash was observed by her doctor at the office.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Epilepsy and Asthma
- Andere Medikamente
- Zonisamide 50mg Zonisamide 25mg Taken twice a day for epilepsy
- Allergien
- No allergies to medication or food just seasonal allergies, pollen, dust, rugs, dog, cats, etc.
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 06.02.2022
- Impfdatum
- 10.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Blood thyroid stimulating hormone
Cough
Dizziness
Fatigue
Headache
Muscle spasms
Pain in extremity
Symptomtext
The night of the vaccine my arm started hurting and I had a bad headache and dizziness. The next day headache, pain in joints, severe cramps in feet, Bad cough, exhausting tiredness, extreme dizziness. This was severe for 3 weeks and the end of the third week slowly started improving. This is the 4th week and still have cough and tiredness. I had covid twice and this was much worse
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None. I had blood test taken after for tsh after this.
- Aktuelle Erkrankungen
- Complete thyroidectomy 12/31/2021. Started medication a week later.
- Vorgeschichte
- Rhuematoid arthritis. I was on hydroxychloroquin 6 mo earlier for 2years. Methotrexate a year earlier for 2years.
- Andere Medikamente
- Estratest, Omeprazole, thyroxazine, famotadine, beta sisterole, calcium, krill oil, college, vit D, claritin
- Allergien
- Sulfa
- Vorherige Impfungen
- Shingrix in 2020. Sore arm, severe tiredness and shoulder pain for 3months. Went to Dr and put me on high doses of steroids
- Staat
- NH
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 05.02.2022
- Impfdatum
- 13.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Immunisation
Pain
Pyrexia
Symptomtext
Chills; fever; body ache; booster dose; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A 15 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 13Jan2022 16:00 (Lot number: 33036BD) at the age of 15 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "No" (unspecified if ongoing). There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0217, Location of injection: Arm Left, Vaccine Administration Time: 12:00 PM, Route of Administration: Intramuscular), administration date: 05Jun2021, when the patient was 15 years old, for Covid-19 Immunization, reaction(s): "Body aches", "Fever", "Dizziness", "pain(arm)", "soreness at site of injection"; Bnt162b2 (Dose Number: 1, Batch/Lot No: EW0182, Location of injection: Arm Left, Vaccine Administration Time: 12:00 PM, Route of Administration: Intramuscular), for Covid-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 13Jan2022 16:00, outcome "unknown", described as "booster dose"; CHILLS (non-serious) with onset 14Jan2022 02:00, outcome "recovering", described as "Chills"; PYREXIA (non-serious) with onset 14Jan2022 02:00, outcome "recovering", described as "fever"; PAIN (non-serious) with onset 14Jan2022 02:00, outcome "recovering", described as "body ache". Therapeutic measures were taken as a result of chills, pyrexia, pain. Follow-Up (21Jan2022): Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: No
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 05.02.2022
- Impfdatum
- 21.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal discomfort
Fatigue
Headache
Movement disorder
Pain
Pyrexia
Symptomtext
Headache, stomach upset, fever, all over body aches, sever fatigue. Unable to get out of bed for3 days/
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- lung cancer
- Vorgeschichte
- lung cancer
- Andere Medikamente
- Losartan amlodipiene zolpedium keytruda
- Allergien
- none
- Vorherige Impfungen
- soreness at injection sight, severe fatigue, aches,and pains
- Staat
- GA
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 04.02.2022
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain upper
Bradykinesia
Dizziness
Feeling cold
Feeling hot
Heart rate increased
Hyperhidrosis
Nausea
Pallor
Symptomtext
Patient came to receive her covid vaccine at 11:00. This was her first dose in the series. She received the Pfizer vaccine. She has no known allergies. I gave paitent her injection at 11:10. I told her to wait 15 minutes in the waiting room in case of an adverse reaction. At 11:20 she reported feeling cold and dizzy. I brought her back to our injection room and had her sit down. She was pale, sweating, and moving very slow. She reported feeling very dizzy, nauseous, and reported having stomach cramps. When she sat down she said she was hot, so I helped her remove her jacket. I checked her vitals at 11:25 - HR was 107, BP 116/75, O2 saturation 100%. I continued to sit with her and her symptoms persisted. Her vitals at 11:33 - BP 112/75, HR 87, 02 100% on room air. At 11:40 she said the dizziness was easing off, but the cramping was remaining. She was not sweating anymore but was still a little pale. Her vitals were BP 109/98, HR 99, O2 99%. At 12:00 I had NP-C come assess and talk to patient. Patient was still cramping and felt dizzy when she stood and her heart rate did increase to 110 when she stood, but it came back down to the 80s within a short time. Patient reported feeling her heart rate increase in her chest, but did not feel faint. She sat back down and I checked her vitals again. HR 80 and O2 100%. At 12:30 she stood again and did not feel dizzy. Her skin tone was back to normal and not pale. We stood together for a little while to assess how she was feeling. NP-C said that she approved for her to go home now, and instructed her not to go back to work, but to go home and rest. NP-C told patient that if she had chest pain or tightness later to go to the emergency room. I walked with down the stairs, out the door, and to her car. She left at 12:40. Patient text me at 1:08 and let me know that she had made it home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- n/a
- Allergien
- No Known Allergies
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 04.02.2022
- Impfdatum
- 27.12.2021
- Beginn
- 17.01.2022
- Tage bis Beginn
- 21,0
- Dosis
- UNK
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Herpes zoster
Intervertebral disc operation
Rash
Sensitive skin
Symptomtext
Developed shingles along T10 dermatome with classic presentation - 5 or 6 rash patches. Started famciclovir within two days. Uncomfortable, but not horribly painful. Accompanied by headaches. 2.5 weeks later, the rashes are fading and the sensitivity receding, but still not gone.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Fluoxetine
- Allergien
- Ibuprofen; mango
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 02.02.2022
- Impfdatum
- 07.01.2022
- Beginn
- 29.01.2022
- Tage bis Beginn
- 22,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Henoch-Schonlein purpura
Rash
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- HSP (Henoch Schonlein purpura)
- Vorgeschichte
- HSP (Henoch Schonlein purpura) GERD
- Andere Medikamente
- famotidine 10mg
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 31.01.2022
- Impfdatum
- 17.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Body temperature increased
Chills
Headache
Hyperhidrosis
Symptomtext
Body Temperature 100.2F, Headache, Chills, Sweat - Continued for 2.5 days
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 29.01.2022
- Impfdatum
- 27.01.2022
- Beginn
- 29.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Peripheral swelling
Skin warm
Urticaria
Symptomtext
Hives, painful lump under left arm, redness and warm to touch
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hypothyroidism
- Andere Medikamente
- Zrtec
- Allergien
- Lidocaine
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 29.01.2022
- Impfdatum
- 24.01.2022
- Beginn
- 24.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Dizziness
Headache
Nausea
Pain
Pyrexia
Vomiting
Symptomtext
Chills with shivering; Body pain all over; Nausea; Vomiting; Fever; Headache; Dizziness; This is a spontaneous report from a non-contactable reporter (consumer or other non HCP). The reporter is the patient. A 28-year-old male patient received bnt162b2 (BNT162B2), administration date 24Jan2022 at 09:15 (Lot number: 33036BD) at the age of 28 years as dose 2, single for COVID-19 immunisation. The patient's relevant medical history was not reported. Concomitant medications included: BUSPIRON and CITALOPRAM. Vaccination history included: Covid-19 vaccine (DOSE 1; MANUFACTURER UNKNOWN, Lot Number: 330368D, Route of administration: unspecified), for COVID-19 immunisation. The following information was reported: CHILLS (non-serious) with onset 24Jan2022 at 10:00, outcome "not recovered", described as "Chills with shivering"; PAIN (non-serious) with onset 24Jan2022 at 10:00, outcome "not recovered", described as "Body pain all over"; NAUSEA (non-serious) with onset 24Jan2022 at 10:00, outcome "not recovered", described as "Nausea"; VOMITING (non-serious) with onset 24Jan2022 at 10:00, outcome "not recovered", described as "Vomiting"; PYREXIA (non-serious) with onset 24Jan2022 at 10:00, outcome "not recovered", described as "Fever"; HEADACHE (non-serious) with onset 24Jan2022 at 10:00, outcome "not recovered", described as "Headache"; DIZZINESS (non-serious) with onset 24Jan2022 at 10:00, outcome "not recovered", described as "Dizziness". Therapeutic measures were not taken as a result of chills, pain, nausea, vomiting, pyrexia, headache and dizziness. Additional Information: The patient had known allergies to Bo. The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The events did not result in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- BUSPIRON [BUSPIRONE HYDROCHLORIDE]; CITALOPRAM
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 29.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain upper
Chromaturia
Faeces discoloured
Off label use
Product use issue
Symptomtext
Urine turned red; mild stomach pain; stool turned red; Booster shot and flu shot together; Booster shot and flu shot together; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 37 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 07Jan2022 19:00 (Lot number: 33036BD) at the age of 37 years as dose 3 (booster), single for covid-19 immunisation; influenza vaccine (FLU VACCINE VII), administration date 07Jan2022 (Batch/Lot number: unknown) as unk unk, single for immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose Number: 2, Lot No: EW0180), administration date: 26Jun2021, when the patient was 36 years old, for COVID-19 immunization; Bnt162b2 (Dose Number: 1, Lot No: EW0217), administration date: 05Jun2021, when the patient was 36 years old, for COVID-19 immunization. The following information was reported: OFF LABEL USE (non-serious), PRODUCT USE ISSUE (non-serious) all with onset 07Jan2022 17:00, outcome "unknown" and all described as "Booster shot and flu shot together"; CHROMATURIA (non-serious) with onset 08Jan2022, outcome "not recovered", described as "Urine turned red"; ABDOMINAL PAIN UPPER (non-serious) with onset 08Jan2022, outcome "not recovered", described as "mild stomach pain"; FAECES DISCOLOURED (non-serious) with onset 08Jan2022, outcome "not recovered", described as "stool turned red". Therapeutic measures were not taken as a result of chromaturia, abdominal pain upper, faeces discoloured. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 29.01.2022
- Impfdatum
- 10.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Joint stiffness
Joint swelling
Symptomtext
swelling, pain and stiffness in joints in hands and wrist.; swelling, pain and stiffness in joints in hands and wrist.; swelling, pain and stiffness in joints in hands and wrist.; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 45-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 10Jan2022 14:45 (Lot number: 33036BD) at the age of 45 years as dose 3 (booster dose), single for covid-19 immunisation. Relevant medical history included: "Known allergies: MAngo" (unspecified if ongoing). Family history included: "Autoimmune disease" (unspecified if ongoing), notes: Other medical history: Autoimmune disease in family. Concomitant medication(s) included: MULTIVITAMIN [VITAMINS NOS]. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0153, Location of injection: Arm Left), administration date: 14Apr2021, when the patient was 44 years old, for COVID-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EP7534, Location of injection: Arm Left), administration date: 24Mar2021, when the patient was 44 years old, for COVID-19 immunization. The following information was reported: JOINT SWELLING (non-serious), ARTHRALGIA (non-serious), JOINT STIFFNESS (non-serious) all with onset 11Jan2022 17:00, outcome "not recovered" and all described as "swelling, pain and stiffness in joints in hands and wrist.". Therapeutic measures were not taken as a result of joint swelling, arthralgia, joint stiffness. Additional information: Patient did not receive any other vaccines within 4 weeks. Other medications in two weeks were daily multivitamin. Patient was not received treatment for AE. Prior to vaccination, the patient was not diagnosed with COVID. Post vaccination patient was not tested for COVID. Device date was 12Jan2022. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Autoimmune disorder (Other medical history: Autoimmune disease in family); Fruit allergy
- Andere Medikamente
- MULTIVITAMIN [VITAMINS NOS]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- HI
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 28.01.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dizziness
Hypoaesthesia
Nausea
Symptomtext
Nausea, dizziness and numbness from neck to waist area. Patient provided liquids and snacks initially. After approximately 15 minutes of observation, he was transferred to the emergency room for further observation and care.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- Unknown at the time of this report.
- Aktuelle Erkrankungen
- Not disclosed
- Vorgeschichte
- Not disclosed
- Andere Medikamente
- Not known
- Allergien
- Shellfish
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 27.01.2022
- Impfdatum
- 10.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Rash
Urticaria
Symptomtext
Soon after vaccine rash on face , next day entire face covered in rash and red certain spots looks like mini hives but not itchy; Soon after vaccine rash on face , next day entire face covered in rash and red certain spots looks like mini hives but not itchy; Soon after vaccine rash on face , next day entire face covered in rash and red certain spots looks like mini hives but not itchy; This is a spontaneous report received from a contactable reporter(s) (Pharmacist). The reporter is the parent. A 12 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 10Jan2022 15:45 (Lot number: 33036bd) at the age of 12 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Asthma" (unspecified if ongoing). There were no concomitant medications. The following information was reported: RASH (non-serious) with onset 10Jan2022, outcome "not recovered", ERYTHEMA (non-serious), URTICARIA (non-serious) all with onset 11Jan2022, outcome "not recovered" and all described as "Soon after vaccine rash on face , next day entire face covered in rash and red certain spots looks like mini hives but not itchy". Therapeutic measures were taken as a result of rash, erythema, urticaria. Additional information: No covid prior vaccination. No known allergy. No other vaccine in four weeks, no other medications in two weeks. Ae treatment: Applied Benadryl day 1 and hydrocortisone cream day 2. No covid tested post vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Asthma.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 26.01.2022
- Impfdatum
- 27.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Fatigue
Loss of personal independence in daily activities
Myalgia
Symptomtext
Severe muscle and joint pain throughout body making walking and doing daily activities extremely difficult or impossible that lasted for 36 hours approximately. Severe fatigue that made walking and doing daily activities extremely difficult or impossible that lasted for 36 hours approximately. Adverse event began at about 26 hours after receiving the Pfizer booster shot #1.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 26.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Discomfort
Rash erythematous
Rash pruritic
Symptomtext
Approximately 15 hours after, patient began seeing little bumps on body (stomach, thighs, neck) The bumps continued to spread, get bigger(welts), turn red and very itchy. This continued, he could not attend school, he did not participate nor engage in usual activities or behavior...very bothered and uncomfortable. After a couple days, I saw the rash was not going away and made an appointment with his Primary DR. The doc was surprised and agreed it was a reaction and he should refrain from taking 2nd dose. She prescribed Prednisone on 1/18 twice a day...that helped tremendously but now that he is off of it...it seems like its coming back.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash erythematous
- Hospital-Tage
- -
- Labordaten
- Observation-visual 1/18/2022
- Aktuelle Erkrankungen
- Tested positive for COVID 12/05/2021 Symptoms 12/04/2021
- Vorgeschichte
- none
- Andere Medikamente
- Quercetin, Vitamin C, Vitamin D + K2
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 25.01.2022
- Impfdatum
- 11.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymph node pain
Lymphadenopathy
Symptomtext
Patient received a Covid Booster on 1/11/22 at a healthcare facility . The next morning he woke up with a large swollen and tender lymph node under the arm where he got the shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymph node pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Allergic rhinitis Ephelis Melanocytic nevus of trunk ADD Insomnia
- Andere Medikamente
- Adderall XR 20mg capsules
- Allergien
- None
- Vorherige Impfungen
- Patient had a similar, but less severe reaction to second Covid vaccine. Second Covid vaccine was also Pfizer, lot # EW0191,. P
- Staat
- CA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 23.01.2022
- Impfdatum
- 27.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test normal
Chest X-ray normal
Headache
Neck pain
Pyrexia
Urethritis
Urine analysis
Symptomtext
The next day 12/28/2021 after the third dose of vaccine, had fever around 101-103F for 2 days and half, took Tylenol to reduce the fever. But I keep had low fever around 99F every night, neck pain and headache for about 2 weeks, then I went to see urgent care on 1/14/2021, did blood test, and it was normal, and will do another ultrasound next week. After the urgent visit, I started having higher fever again around 100-101F since noon, not evening anymore, same neck pain and headache, I went to medical center emergency on 1/18/2021, did another blood test, chest xray and urinalysis, and the doctor diagnosed I had urethritis which I didn't agree with because I have no related symptom, and prescribed me "Cefalexin" which I have been taking for almost one week with no cure, and I still having fever every day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Blood test-normal on 1/14/2021 Blood test-normal on 1/18/2021 Chest Xray-normal on 1/18/2021 Urinalysis
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- No
- Vorherige Impfungen
- Had fever for only few days from the first and second dose of Pfizer Covid vaccine
- Staat
- NY
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 22.01.2022
- Impfdatum
- 22.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Nausea
Symptomtext
At 3:15 p.m. patient's mother reported to nurse patient was feeling nauseas. Nurse assessed patient, VS obtained B/P 87/39 P 57 RR 18 O2 SATS 99%RA. RRT called. Patient given 8oz of water, patient drank. Patient remained alert and verbal. Patient placed on stretcher. At 3 :17 p.m. VS retaken B/P 99/64 P 68 RR 18 O2 SATS 100%. RRT arrived at 3:18 p.m.. Patient taken to ER at 3:19 p.m. for evaluation. Patient remained alert and verbal, stated she was feeling better. Mother accompanied patient to ER.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- unknown
- Aktuelle Erkrankungen
- denies
- Vorgeschichte
- denies
- Andere Medikamente
- denies
- Allergien
- denies
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 21.01.2022
- Impfdatum
- 17.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Myalgia
Symptomtext
Full body muscle aches. Treated with rest and drinking extra fluids. Symptoms dissipated in 24 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Chronic Hematuria, Depression/Anxiety
- Andere Medikamente
- Lexapro- 10 mg
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Fatigue
Headache
Symptomtext
Chills, headache, fatigue
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Multi-vitamin Vitamin D Calcium
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 20.01.2022
- Impfdatum
- 17.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Muscle spasms
Pyrexia
Symptomtext
Fever of 101.8, extreme muscle cramping, joint pain (hips, fingers, shin)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- None.
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 10.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Injection site pain
Joint range of motion decreased
Symptomtext
Site: Pain at Injection Site-Severe, Systemic: Joint Pain-Medium, Additional Details: just pain in shoulder with limited range of motion
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 27.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blepharospasm
Headache
Malaise
Symptomtext
The next day after vaccine had a very bad pounding headache, which made her right eye start to twitch. She became very ill.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- No.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- Sulfa drugs and Ibuprofen
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 03.03.2021
- Beginn
- 16.01.2022
- Tage bis Beginn
- 319,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Duodenal ulcer
Eye pruritus
Lymphadenopathy
Nasal congestion
Oesophagogastroduodenoscopy normal
Sneezing
Upper gastrointestinal haemorrhage
Urosepsis
Symptomtext
nonproductive cough, nasal congestion, swollen glands, sneezing, itchy eyes. starting 1/16/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Eye pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Hypertension. Diabetes: Type 2. Dyslipidemia. Atypical chest pain 11/05, evaluated with negative Cardiolite.3/12 stress echo moderate tricuspid regurg. mild elevation in pulm. pressure. Positive PPD, TX'd TB as a child. Paroxysmal Afib with CP in 2009 -Negative stress cardiolite and normal ECHO with EF at 55% unable to assess for RWMA. No LA abnl. ECHO 9/20: nml. CEM 9/20 nml CHA2DS2-VASc 3.2%. pt declines anticoagulation therapy other than ASA. Microhematuria: referred to urology.. PROTEINURIA: KSM consult 10/19. Atypical CP: 3/12 (DOE) referred to CARDS. Normal Stress ECHO with EF at . OSTEOPOROSIS: lumbar spine on bone density scan 8/16: Started alendronate 8/17 but inconsistent dosing. Resumed 5/18. CORONARY CALCIUM SCORE: 9.2 LOW RISK. ECHO 2020 : NML EF 60-65%. Mild TR. Nml pulm pressure. Nml atria. ANEMIA OF CHRONIC DISEASE. UROSEPSIS (9/21). DUODENAL ULCER with UGI BLEED 9/21. EGD 11/21: ulcers healed.
- Andere Medikamente
- ?metFORMIN HCl 1000 MG Tablet 0.5 tablet Orally two times a day ?Losartan Potassium 25 mg Tablet 1 tablet Orally Once a day ?Metoprolol Succinate ER 25 MG Tablet Extended Release 24 Hour take 1/2 tablet by mouth once daily Orally
- Allergien
- Lipitor: myalgia - Side Effects
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pruritus
Rash
Symptomtext
Systemic: Allergic: Itch Generalized-Mild, Systemic: Allergic: Rash Generalized-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect route of product administration
Injection site bruising
Injection site erythema
Injection site pain
Injection site swelling
Symptomtext
Site: Bruising at Injection Site-Mild, Site: Pain at Injection Site-Mild, Site: Redness at Injection Site-Mild, Site: Swelling at Injection Site-Mild, Error: Wrong Route (SC, IM, etc.).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site swelling
Symptomtext
Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Additional Details: Swelling and redness at injection site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 04.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Fatigue
Injection site erythema
Injection site nodule
Injection site pain
Lethargy
Pain
Pyrexia
Symptomtext
Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Systemic: Body Aches Generalized-Medium, Systemic: Chills-Medium, Systemic: Exhaustion / Lethargy-Medium, Systemic: Fever-Medium, Additional Details: Patient reported a knot under her arm near her arm pit
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Rash
Symptomtext
Sever rash, itching and spreading all over body.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- No test done, just a visual look. 1/17/2022.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- 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: ja
Pruritus
Urticaria
Symptomtext
After receiving Pfizer booster, Pt felt itching on both arms, upon assessment hives were noted on chest and both arms. BP 143/72 HR 107 RR 18 O2 sat 99-100% RA Temp 97.9 F. Per Dr., Zyrtec 1 tab given. Pt felt better after taking Zyrtec and ice pack application. Pt left with her husband without itching or hives.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- HASHIMOTO THYROIDITIS MIGRAINE GERD (GASTROESOPHAGEAL REFLUX DISEASE) ASTHMA, UNSPECIFIED SEAFOOD ANAPHYLAXIS VITAMIN D DEFICIENCY ALLERGIC RHINITIS FLEXIBLE SIGMOIDOSCOPY LUMBAR DISC HERNIATION VITAMIN B12 DEFICIENCY ADULT OBSTRUCTIVE SLEEP APNEA, MILD SINUS TACHYCARDIA BMI 27-27.9 ADULT HX OF TOTAL HYSTERECTOMY PERIPHERAL VENOUS INSUFFICIENCY
- Vorgeschichte
- HASHIMOTO THYROIDITIS MIGRAINE GERD (GASTROESOPHAGEAL REFLUX DISEASE) ASTHMA, UNSPECIFIED SEAFOOD ANAPHYLAXIS VITAMIN D DEFICIENCY ALLERGIC RHINITIS FLEXIBLE SIGMOIDOSCOPY LUMBAR DISC HERNIATION VITAMIN B12 DEFICIENCY ADULT OBSTRUCTIVE SLEEP APNEA, MILD SINUS TACHYCARDIA BMI 27-27.9 ADULT HX OF TOTAL HYSTERECTOMY PERIPHERAL VENOUS INSUFFICIENCY
- Andere Medikamente
- Metoprolol Succinate (TOPROL XL) 25 mg Oral 24hr SR Tab Meloxicam (MOBIC) 15 mg Oral Tab Cyanocobalamin (VITAMIN B-12) 1,000 mcg/mL Inj Soln Cyanocobalamin (VITAMIN B-12) 1,000 mcg/mL Inj Soln Syringe with Needle, Disp, (MONOJECT 3CC SYR 25
- Allergien
- Betadine [Povidone Iodine]- Anaphylaxis Omnipaque [Iohexol- ]Anaphylaxis Plastic Ciprofloxacin -Rash Penicillins Class Shellfish Derived Products Covid-19 Vaccine, Mrna, Bnt162b2, Lnp-s (Pfizer)- Hives
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 15.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Myalgia
Pyrexia
Symptomtext
High fever peaking at 103.4. 2 hours after shot started to get muscle aches and mild fever. Fever got far worse into evening with extreme body chills. Fever in the evening was 102.2. Was 101.5 in middle of night and morning. Fever in middle of day 1/15/21 briefly spiked to 103.4. Was about to go to hospital since >103 degrees but fever reduced to 102.4 quickly. Took Tylenol, fluids and consulted with Doctor over phone.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Tretinoin gel USP. .025%
- Allergien
- N/A
- Vorherige Impfungen
- 23, milder fevers and chills from previous 2 Pfizer Covid 19 shots. Patient was also 23
- Staat
- VA
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Skin discolouration
Symptomtext
Color drained from patient's face/skin and she became dizzy. Did not lose consciousness. Gave her support, moved her to floor, ice pack, and water until her color returned and she felt well enough to get up and move around.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
Fatigue
Immunisation
Pain
Pyrexia
Symptomtext
Fever 99.3; Body aches; Fatigues; Dose received: 3; This is a spontaneous report from a contactable reporter (consumer or other non-HCP). The reporter is the patient. A 56-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 07Jan2022 at 15:00 (Lot number: 33036BD) at the age of 56 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "Hypertension" (unspecified if ongoing), notes: HTN; "Asthma" (unspecified if ongoing); "Obesity" (unspecified if ongoing); "Postmenopause" (unspecified if ongoing); "Hay fever" (unspecified if ongoing); "Pre-diabetic" (unspecified if ongoing) and "Sulfonamide allergy" (unspecified if ongoing), notes: Known allergies: Sulfa. Concomitant medications included: CHLORTHALIDONE, COREG, ALLEGRA, POTAS and unspecified multivitamin. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE; Lot number: EK5730; Route of administration: unspecified), administration date: 23Dec2020, when the patient was 55 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE; Lot number: EK4176; Route of administration: unspecified), administration date: 13Jan2021, when the patient was 55 years old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 07Jan2022 at 15:00, outcome "unknown", described as "Dose received: 3"; PYREXIA (non-serious) with onset 08Jan2022, outcome "recovering", described as "Fever 99.3"; PAIN (non-serious) with onset 08Jan2022, outcome "recovering", described as "Body aches"; FATIGUE (non-serious) with onset 08Jan2022, outcome "recovering", described as "Fatigues". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of pyrexia, pain and fatigue. Additional information: Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the COVID-19 vaccine. The events did not result in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care. Since the vaccination, the patient had not been tested for COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220108; Test Name: Body temperature; Result Unstructured Data: Test Result:99.3
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Asthma; Hay fever; Hypertension (HTN); Obesity; Postmenopause; Pre-diabetic; Sulfonamide allergy (Known allergies: Sulfa)
- Andere Medikamente
- CHLORTHALIDONE; COREG; ALLEGRA; POTAS
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Headache
Herpes simplex
Hypersensitivity
Immunisation
Nausea
Oral herpes
Symptomtext
Agressive cold sore; herpes simplex; Covid arm; Chills; Nausea; Headache; Dose received: 3; This is a spontaneous report received from contactable reporter (Consumer or other non-HCP). The reporter is the patient. A 49 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in right arm, administration date 05Jan2022 at 17:45 (Lot number: 33036BD)at the age of 49 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "Cold sores" (unspecified if ongoing), notes: History of cold dore (last one 1 year ago). There were no concomitant medications. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE, Lot Number:EN6201, Anatomical Location: Right arm, Administration Time: 13:00, Route of Administration: Unspecified), administration date: 19Mar2021, when the patient was 48 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE, Lot Number: ER8734, Anatomical Location: Right arm, Administration Time: 14:00, Route of Administration: Unspecified), administration date: 09Apr2021, when the patient was 48 years old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 05Jan2022 at 17:45, outcome "unknown", described as "Dose received: 3"; ORAL HERPES (non-serious) with onset 07Jan2022, outcome "not recovered", described as "Agressive cold sore"; HERPES SIMPLEX (non-serious) with onset 07Jan2022 , outcome "not recovered", described as "herpes simplex"; HYPERSENSITIVITY (non-serious) with onset 07Jan2022, outcome "not recovered", described as "Covid arm"; CHILLS (non-serious) with onset 07Jan2022, outcome "not recovered", described as "Chills"; NAUSEA (non-serious) with onset 07Jan2022, outcome "not recovered", described as "Nausea"; HEADACHE (non-serious) with onset 07Jan2022, outcome "not recovered", described as "Headache". Therapeutic measures were taken as a result of oral herpes, herpes simplex, hypersensitivity, chills, nausea and headache. Additional Information: The patient had no known allergies. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the COVID-19 vaccine. The patient received Valacyclovir as the treatment for the reported events. Since the vaccination, the patient had not been tested for COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Cold sores (History of cold dor? ( last one 1 year ago))
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 15.07.2021
- Beginn
- 21.07.2021
- Tage bis Beginn
- 6,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Confusional state
Dissociation
Electroencephalogram normal
Emotional disorder
Fatigue
Feeling abnormal
Memory impairment
Vision blurred
Symptomtext
Symptoms begin suddenly. I experience extreme brain fog, disassociation, unable to focus my vision, spacing out, forgetfulness, fatigue, and absolute emotional numbness. The first time I have ever experienced this feeling was on July 21-22, 2021, which was 6 or 7 days after I received my first COVID19 Pfizer shot. The feeling lasted only half an hour and went away. Throughout the following months it came back once a month. However, in late December 2021, the feeling returned suddenly and would not go away for one week. It was the most intense brain fog and emotional/psychological shutdown I have ever experienced. Usually I am a happy and energetic person with no history of anxiety, depression, or other mental disorders. I also do not do any drugs. But when this feeling came I had no motivation (physical or psychological) to do anything, even to speak or to stand up. I felt confused, removed from reality, and very fatigued. I slept for 10-12 hours per day and woke up with the same dreadful feeling of disassociation and fatigue. It is a difficult feeling to describe in words. It feels terrifying, as though you have permanently gone crazy and cannot bring your sanity back, or like you are trapped in a state of extreme depression. Lastly, it feels like the brain has completely shut off your emotions, energy, and ability to communicate normally.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- EEG: January 11, 2022 -- normal results Referral to psychiatrist: January 2022 -- unknown results Referral to psychologist: January 25, 2022 -- unknown results
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Anemia
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 13.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymph node pain
Lymphadenopathy
Symptomtext
Tender lymphadenopathy in the left axilla
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymph node pain
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 13.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 6,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Peripheral swelling
Rash
Symptomtext
Patient states that he woke up with a rash all over his body and swelling in the legs. I strongly advised the patient to call his physician. (Provider's office closed at this time)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 13.01.2022
- Impfdatum
- 10.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Feeling abnormal
Testicular pain
Symptomtext
Mid morning the next day started feeling pain in my left testical. Not a constant pain but enough to know it?s not normal.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Testicular pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 11.01.2022
- Impfdatum
- 11.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Exposure during pregnancy
Feeling hot
Hyperhidrosis
Nausea
Symptomtext
Patient received Pfizer vaccine (dose 2) at 11:55am, started to feel hot/sweaty/nauseated at 12:05pm. Gave patient ice pack at 12:06pm, checked BP at 12:10pm 134/96 Pulse 80. Checked BP again at 12:23pm 106/74 Pulse 84. Patient is pregnant. Did not have any issues after 1st dose. Patient felt okay to go home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 11.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 5,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Rash macular
Urticaria
Symptomtext
Full body hives started on 1/9/21. (About 80% coverage) Started taking Benedryl and Zyrtec before going to Urgent Care. I was prescribed Prednisone and to continue taking Benadryl and Zyrtec on 1/10/21. By the evening of 1/10/21 about 80% of the hives were gone with just red blotches left. I took another benedryl that evening. Woke up 1/12/21 and immediately started being covered in hives again about 80% of my body. Took Zyrtec and Prednisone.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash macular
- Hospital-Tage
- -
- Labordaten
- No tests or lab results yet.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Psoriasis
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- Impfdatum
- 08.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Gait disturbance
Tinnitus
Vertigo
Symptomtext
Patient has been very dizzy/vertiginous today. unsteady gait. ringing in her ears.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anxiety
Chills
Headache
Nausea
SARS-CoV-2 test negative
Symptomtext
anxiety, chills, naseau, headache
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- covid test-negative
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- tessalon
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 09.01.2022
- Impfdatum
- 08.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Urticaria
Symptomtext
Within 30 minutes of booster, she developed hives. They first appeared on her arms and then on her legs. She was treated with Benadryl and then examined by urgent care. Her oxygen levels remained near 100 the entire time. She continues to experience hives and must continuously take Benadryl 24 hours later.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- Urgent care just monitored her heart rate and oxygen, which were within normal ranges.
- Aktuelle Erkrankungen
- Slight cold (COVID-19 test negative)
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- No known allergies. Earlier allergy testing indicated an allergy to coconut and cinnamon, however these are eaten regularly with no adverse reaction, but were not eaten within several weeks of vaccination.
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 09.01.2022
- 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
Injection site erythema
Urticaria
Symptomtext
red sized area around injection and now has spread to left shoulder, spread to large area/welt
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 08.01.2022
- Impfdatum
- 08.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Symptomtext
Pt received her Pfizer booster and 5 minutes later complained of lightheadedness and dizziness. Abruptly had pt in supine position and administered 8 oz of water x2, cold compress applied to forehead, and open windows for ventilation. Observed pt throughout , performed vital check every 15 minutes, and performed safety check. Pt at bedside with mother, nurse, and supervisor. Reports improvement in symptoms 45 minutes later and was escorted by mom out of facility.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- N/A
- Allergien
- No allergies
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 07.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood pressure increased
Dizziness
Nausea
Symptomtext
Patient received Pfizer vaccine at 1426. Shortly after, patient began complaining of dizziness and nausea. Patient observed and vital signs were monitored. O2 remained 100% RA. BP and HR as follows--BP 196/97 HR 84; BP 202/106 HR 84; BP 235/113 HR 89. Patient denies rash, hives, tongue or facial swelling, difficulty breathing or shortness of breath. Patient denies history of hypertension. Patient taken to ED for further evaluation of BP.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- DM 2, DM 2 W DYSLIPIDEMIA, HIGH DENSITY LIPOPROTEIN DEFICIENCY, HYPERTENSION ONYCHOMYCOSIS, OPIOID MEDICATION AGREEMENT LETTER, OSTEOARTHRITIS OF RIGHT KNEE, POSTMENOPAUSAL BLEEDING, VACCINATION FOR STREP PNEUMONIA W PNEUMOVAX SEBORRHEIC KERATOSIS, SOAPP SCORE LESS THAN 4, SCREENER OPIOID ASSESSMENT PATIENTS W PAIN 5 QUESTIONS, NONTOXIC MULTINODULAR THYROID GOITER
- Andere Medikamente
- glipiZIDE (GLUCOTROL) 5 mg Oral Tab, Simvastatin (ZOCOR) 20 mg Oral Tab, Doxycycline Monohydrate (AVIDOXY) 100 mg Oral Tab, morphine (MSIR) 15 mg Oral Tab, Gabapentin (NEURONTIN) 100 mg Oral Cap, Lidocaine (LIDODERM) 5 % Top PTMD Patch
- Allergien
- Aspirin, Tylenol, Penicillin
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 06.01.2022
- Impfdatum
- 04.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pain
Injection site pruritus
Injection site swelling
Symptomtext
Redness, swelling, itching, stinging burn-like rash at injection site and a similar, not painful red spot underneath injection site. Applied Neosporin Blood spots thru bandaid(s) -two Planning on taking a Benadryl when home
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Vitiligo
- Andere Medikamente
- -
- Allergien
- Anti-seizure medications
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 04.01.2022
- Impfdatum
- 31.12.2021
- Beginn
- 02.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Breast pain
Lymph node pain
Lymphadenopathy
Mammogram normal
Pain
Symptomtext
Sunday afternoon discovered painful swollen lymph node in left armpit with pain radiating to left breast. Had mammogram in December and results were negative for breast cancer, but it was scary to feel the sensation in my breast.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Breast pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hypothyroidism aka Hashimoto Thyroiditis
- Andere Medikamente
- Synthroid
- Allergien
- Sulfa, bactrim
- Vorherige Impfungen
- Age 55, Second Pfizer COVID-19 vaccine, Lot ER8736, on 5/5/21, gave me horribly loud tinnitus which I already suffer from due to
- Staat
- NY
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 04.01.2022
- Impfdatum
- 02.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymph node pain
Lymphadenopathy
Symptomtext
Swollen Painful Lymphnodes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymph node pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- -
- Allergien
- Pencillin.
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 04.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anxiety
Dizziness
Symptomtext
Systemic: Dizziness / Lightheadness-Mild, Additional Details: Patient felt anxious after recieving pfizer vaccine booster, paramedics were called, paramedics siad patient was not having an allergic reaction, patient decided to go home
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 8,0
- Geschlecht
- M
- Eingang
- 04.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Eye swelling
Incorrect dose administered
Incorrect product formulation administered
Mouth swelling
Rash
Swelling face
Swollen tongue
Vomiting
Symptomtext
Systemic: Allergic: Rash (specify: facial area, extremeties)-Mild, Systemic: Allergic: Swelling of Face / Eyes / Mouth / Tongue-Mild, Systemic: Vomiting-Medium, Error: Wrong Vaccine Formulation (ex. different manufact. initial and booster)-, Additional Details: Pt was inadvertently given 2/3(0.2ml) of a 12+ pfizer dose when should have had 5-11 y/o dose, incorrect vial placed in pediatric vaccine bin, pt mother said took pt to ermergency room and was given benadryl for swelling of face by Dr., given 1x 25mg benedryl and sent home, said pt also vomitted 4 times prior to ER and mild facial rash.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 03.01.2022
- Impfdatum
- 29.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dizziness
Symptomtext
Primary Series: Janssen Booster dose: Pfizer Vaccinated: 16:59 Reaction: 17:15 Pt reports feeling "a little dizzy" 16 minutes after vaccination, reported being nervous before getting booster Vitals: @1720: 147/84, 58, 20, O2 100% -> @1732: 140/84, 63, 20, O2 99% Pt was taken to clinic via ambulation and laid down for several minutes and reported feeling better. He was also given orange juice, water, and graham crackers. Pt reported feeling back to normal with dizziness resolved and no other adverse side effects reported or observed. Pt also reported he had not eaten or drank anything since 9:30 today and was also nervous about receiving the booster vaccine. Pt was educated to stay well hydrated day of any needlestick injection and for future vaccinations to be given laying down. Pt was able to ambulate independently with steady gait, out of facility at 17:34.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No known PMH
- Vorgeschichte
- -
- Andere Medikamente
- No Known Medications
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 03.01.2022
- 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: unbekannt
Dizziness
Headache
Nausea
Symptomtext
Vaccinated: 11:54AM Reaction: 12:10PM Pt reported slight headache and dizziness 16 minutes after vaccination 12:30: patient complains of nausea, no vomiting; remains lying down; observation continues 12:45: BP 108/63, 74, 18, O2 100%; resting quietly 12:50: patient complains of headache, ice applied to forehead and no further complaint of nausea at this time 12:55: patient asleep, vital signs remain stable 13:05: to bathroom via wheelchair, voided, stable 13:10: returned to observation room, stated "I feel much better now, requested to sit at edge of bed" 13:24: patient stated "I'm feeling good now and can go home" 13:30: patient is stable, educated on s/sx of vaccine, encouraged to drink more water and if still not feeling good, should follow up with her MD Vitals: 122/178, 85, 19, O2 100% Pt states she did not eat or drink before the vaccine and was given orange juice and crackers; patient stable and released from vaccination site at 13:30
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No Known PMH
- Vorgeschichte
- -
- Andere Medikamente
- No Known Medications
- Allergien
- No Known Allergies
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 03.01.2022
- Impfdatum
- 02.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Headache
Pain
Pyrexia
Symptomtext
Headache, low fever, joint ache, body ache and moderate headache. Drank water and coffee; short nap; relaxed and light stretching. May have to take ibuprofen for headache but I don't want to.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Daily vitamin, Echinacea, Elderberry, Garlic, Oil of Oregano
- Allergien
- No
- Vorherige Impfungen
- Headache, body aches and low fever.
- Staat
- NY
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 02.01.2022
- Impfdatum
- 31.12.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Fatigue
Headache
Lymph node pain
Lymphadenopathy
Night sweats
Symptomtext
Severe swollen lymph node in left arm pit with severe pain- size of a plum Severe headache - 2days Extreme tiredness - 2days Chills - 2 days Night sweats x 2 days
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- A-fib CREST syndrome
- Andere Medikamente
- Eliquis Metetoprol Vitamin D
- Allergien
- Bactrum Penicillin
- Vorherige Impfungen
- 49, 4/3/21, 2nd vaccine COVID 19 Pfizer, similar side effects
- Staat
- VA
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 02.01.2022
- 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
Rash
Symptomtext
Systemic: Allergic: Rash Generalized-Severe
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 31.12.2021
- Impfdatum
- 29.12.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inflammation
Lymph node pain
Lymphadenitis
Symptomtext
Woke up Friday morning with inflamed left armpit - lymph nodes are inflamed on left side slightly painful. I did not find this as a side effect on the CDC listing of Pfizer booster side effects. Concerning as this did not happen after my 1st or 2nd dose. Suggests to me that the 6 month post 2nd dose recommendation may be too soon for younger healthier individuals. Maybe needs to be revised to 12 months. My wife also is experiencing same symptom but much worse (like armpit is on fire).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymph node pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 30.12.2021
- Impfdatum
- 22.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dizziness
Immediate post-injection reaction
Symptomtext
Immediately after vaccination pt reported dizziness. Vitals: 152/56, 76, 20 Pt states she took Oxycontin 20mg 1 her ago and she did not eat all day. A&O x4 Pt responds appropriately to verbal stimuli. No c/o pain or discomfort. No further dizziness. Assisted to car in w/c. Pt stable and released from the vaccination site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- PMH: HLD, HCV, chronic headaches, chronic neck pain with nicotine dependence
- Andere Medikamente
- Medications: diazepam 5mg daily PRN Oxycontin 20mg BID
- Allergien
- Allergies: Barbiturates (abdominal disorder), Hyantoins (anaphylaxis), Iron Complex/c/b12 (anaphylaxis), PCNs(Anaphylaxis), Cephalosporins (hives), Erythromycin Base(N/V), Iron (neurological disorder), Macrolide ABX (abdominal disorder)
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 18,0
- Geschlecht
- M
- 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: ja
Dizziness
Symptomtext
01:55 PM: client feel light headed, has history of fainting with needle stick, client lay down on the floor. Legs elevated. 01:57 PM: Dr, EMS, site director present, pls at 54/min, sat at 99%, BP at 96/52. 02:02PM: client feel better, . 02:05PM: 106/46, pls at 52/min, SAT at 98%. 02:07 PM: client seat upwright, eat snack, feel better. 02:10PM: 113/60, pls at 63/min, SAT at 97%. client seating in chair. 02:12 PM: client stand up but feel dizzy, lay down again. 02: 15 PM: 133/62, pls at 50/min, SAT at98%. 02:18 PM : seat upwright and eat snack. 02:20PM: 114/58,pls at 58/min and SAT at100%. 02: 22 PM: stand up < 127/87,pls at 70/min and SAT at 100%. client feel good and discharge by Dr.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- history of fainting with needle stick
- Andere Medikamente
- anti depressor
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 27.12.2021
- Impfdatum
- 23.12.2021
- Beginn
- 24.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pain
Injection site swelling
Symptomtext
Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 26.12.2021
- Impfdatum
- 26.12.2021
- Beginn
- 26.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Nausea
Vomiting
Symptomtext
11:46: client in observation, feel lightheaded and nauseous,lay down flat with legs elevated, EMS, site director present, called. 11:48 AM: 160/110, pls at 68/min and SAT at 95%. 11:50AM: client feel Nausous, client seat upright with emesis coup. doctor notified about client status. 11:57 AM: 157/97, pls at 71/min and SAT at 97%, client feel better. 12:01 PM: client drink Gaterade, feel good, no more nausous. 12:07 PM: 143/92, pls at 81/min and SAT at94%. 12:16 PM: client stand up, feel good, 145/94, pls at 67/min and SAT at 97%. client feel good, doctor on the phone and update about the client, client discharge home after advice to go see his physician tomorrow and advice to call 911 if get sign and symptoms of hearth attack or stroke.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/a
- Andere Medikamente
- baby aspirine
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 11.08.2023
- Impfdatum
- 29.12.2021
- Beginn
- 19.02.2023
- Tage bis Beginn
- 417,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Neuropathy peripheral
Symptomtext
PERIPHERAL NEUROPATHY
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Neuropathy peripheral
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 18.07.2023
- Impfdatum
- 30.07.2021
- Beginn
- 10.05.2022
- Tage bis Beginn
- 284,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood thyroid stimulating hormone increased
Weight increased
Symptomtext
Dose 1 received 07/30/2021. Dose 2 received 08/20/2021. Dose 3 (booster) received 05/11/2022. ? Prior to my first dose, my thyroid (TSH) was slightly elevated at 7.84. After Dose 1 and 2, at my next test a few months later, my TSH had nearly tripled to 20 ? never been that high. Nothing else had changed in my diet or routines. My appetite was the same, but I gained 4 lbs (138 to 142). The further I've gotten from my booster, by late 2022, my weight returned to 138, and my TSH has been dropping back toward acceptable range. At the very minimum, if the Pfizer vax did not cause the TSH spike, it at least magnified what might have been a small spike from something else.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood thyroid stimulating hormone increased
- Hospital-Tage
- -
- Labordaten
- (age40) 9/18/12 2.999 TSH. (42) 10/23/13 2.192. (45) 10/2/17 3.85. (49) 5/19/21 7.84. (50) 5/10/22 20. (50) 6/3/22 19.9. (50) 8/1/22 12.9. (51) 11/28/22 6.87.
- Aktuelle Erkrankungen
- (none)
- Vorgeschichte
- Allergy - pollen, dust, raw banana, raw avocado
- Andere Medikamente
- Rx eyedrop,nasalspray. VitmnCode mv,iron. Nordic Omg3. Allegra
- Allergien
- Raw banana, raw avocado
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 09.05.2023
- Impfdatum
- 30.12.2021
- Beginn
- 07.06.2022
- Tage bis Beginn
- 159,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Symptomtext
PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 89,0
- Geschlecht
- F
- Eingang
- 02.05.2023
- Impfdatum
- 16.01.2022
- Beginn
- 03.02.2022
- Tage bis Beginn
- 18,0
- 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 3/29/21 Lot# ER8734; PFizer 4/19/21 Lot# ER8735; Pfizer 1/16/22 Lot# 33036BD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 26.04.2023
- Impfdatum
- 04.01.2022
- Beginn
- 01.03.2022
- Tage bis Beginn
- 56,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Acoustic stimulation tests abnormal
Deafness neurosensory
Tinnitus
Tympanometry
Symptomtext
In March 2022 after receiving the Pfizer booster in Jan 2022 I noticed intermittent tinnitus symptoms. By August the tinnitus was constant. I still have tinnitus today. I have seen two ENTs. The first diagnosed the follow codes Sensorineural hearing loss and Tinnitus. The second said I have little to no hearing loss and saw no signs of autoimmune inflammation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acoustic stimulation tests abnormal
- Hospital-Tage
- -
- Labordaten
- 12/7/2022 Comprehensive hearing test, Tympanometry & Reflex Threshold, and Ear Microscopy Exam. 2/28/2023 the second ENT performed an exam and a comprehensive hearing test with normal results other than a small decrease in high frequency.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hashimoto's autoimmune thyroiditis, eosinophilic esophagus, Sjogren's
- Andere Medikamente
- pantoprazole 40mg, synthroid 75 mcg, cytomel 75 mcg
- Allergien
- penicillin, vicodin, codeine, metronydazole; sensitivity to gluten and soy
- Vorherige Impfungen
- Shingles March 2013 after Jan 2013 TDAP, Shingles in Nov 2021 possibly after March and April 2021 Pfizer Covid doses a and 2
- Staat
- FL
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 21.04.2023
- Impfdatum
- 19.04.2022
- Beginn
- 01.08.2022
- Tage bis Beginn
- 104,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Exposure to SARS-CoV-2
Patient isolation
SARS-CoV-2 test positive
Symptomtext
I did not have an adverse reaction to the vaccine. I was exposed to COVID-19 while moving my son in 08/2022. I tested positive for COVID-19 in 08/2022. I isolated, rested, stayed hydrated and ate light meals. As of today, I do not have any lingering symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- AUG2022 COVID-19 test positive
- Aktuelle Erkrankungen
- Head cold
- Vorgeschichte
- N/A
- Andere Medikamente
- Simvastatin
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 21.02.2023
- Impfdatum
- 30.12.2021
- Beginn
- 22.06.2022
- Tage bis Beginn
- 174,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 3 vaccines Pfizer 4/15/21 Lot# Ew0150; Pfizer 5/6/21 Lot# Ew0164; Pfizer 12/30/21 Lot# 33036BD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 20.01.2023
- Impfdatum
- 11.02.2022
- Beginn
- 26.12.2022
- Tage bis Beginn
- 318,0
- Dosis
- 3
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Symptomtext
Hospitalization for COVID-19 on dates 12/26/2022-12/29/2022. 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
- COVID-19
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 18.01.2023
- Impfdatum
- 04.01.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 52-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 02Apr2021 as dose 1, single (Lot number: Er87376031), in right arm, on 23Apr2021 as dose 2, single (Lot number: H2ew0171), in right arm and on 04Jan2022 at 10:45 as dose 3 (booster), single (Lot number: 33036BD) at the age of 51 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Endometriosis" (unspecified if ongoing); "Known allergies: Flaxseed" (unspecified if ongoing), notes: Known allergies: Flaxseed. There were no concomitant medications. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 2022, outcome "unknown" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (2022) Positive, notes: Treatment of COVID-19. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: The patient was not pregnant at the time of vaccination. No other medications reported in 2 weeks. It was reported that, about 4 days after finished Paxlovid, the patient got feverish again and got all COVID symptoms again and was even sicker the second time. Therapeutic measures included Anti-viral details, Product: COVID 19 Treatment, Brand: Paxlovid, Treatment started on 12Nov2022 and stopped on 17Nov2022, Indication: Treatment of COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 2022; Test Name: COVID-19 test; Test Result: Positive ; Comments: Treatment of COVID-19
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Endometriosis; Food allergy (Known allergies: Flaxseed)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 08.12.2022
- Impfdatum
- 11.03.2021
- Beginn
- 09.09.2022
- Tage bis Beginn
- 547,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19 immunisation
Suspected COVID-19
Symptomtext
SUSPECTED COVID-19 INFECTION; REVACCINATION WITH DIFFERENT COVID-19 VACCINE; This spontaneous report received from a patient via other manufacturer (Pfizer) concerned a 32 year old, female. The patient's height, and weight were not reported. The patient's concurrent conditions included: nasal allergies, and vocal cord dysfunction and the patient was not pregnant at time of vaccination. The patient received covid-19 vaccine ad26.cov2.s (dose number in series 1) (suspension for injection, route of admin, batch number and expiry date were not reported) dose was not reported, 1 total administered on 11-MAR-2021 for covid-19 prophylaxis. The batch number was not reported and has been requested. Age at time of vaccination 30 years old. Concomitant medications included bupropion, Zyrtec (cetirizine hydrochloride), Vit d3 (colecalciferol), Sprintec (ethinylestradiol/norgestimate), Lamictal (lamotrigine), and Singulair (montelukast sodium). It was unknown whether patient had any adverse events following vaccination with covid-19 vaccine ad26.cov2.s (dose number in series 1). The patient additionally received non-company suspect vaccine Pfizer (tozinameran) (dose number in series 2) (form of admin and route of admin were not reported, batch number: 33036BD, expiry date: UNKNOWN) dose and frequency were not reported, administered on 27-DEC-2021 for covid-19 prophylaxis. It was unknown whether patient had any adverse event following vaccination with Pfizer (tozinameran) (dose number in series 2). The patient additionally received non-company suspect vaccine Moderna (elasomeran) (dose number in series 3) (form of admin, route of admin, batch number and expiry date were not reported) dose and frequency were not reported, administered in left arm on 09-SEP-2022 for covid-19 prophylaxis. The patient was revaccinated with different covid-19 vaccine (dose number in series 3). On an unspecified date, the patient experienced suspected covid-19 infection (dose number in series 3). The patient received non-company suspect drug included: Paxlovid (form of admin, route of admin, and batch number were not reported, expiry: unknown) dose was not reported, administered from 16-NOV-2022 to 21-NOV-2022 for treatment of Covid-19. On 23-NOV-2022, the patient experienced rebound covid-19 infection after taking Paxlovid, symptoms started 2 days after last dose of Paxlovid (dose number in series 3). The action taken with covid-19 vaccine ad26.cov2.s, tozinameran, and elasomeran was not applicable and with Paxlovid was drug discontinued. The patient was recovering from suspected covid-19 infection, and the outcome of revaccination with different covid-19 vaccine was not reported. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19 immunisation
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Nasal allergy; Vocal cord dysfunction
- Vorgeschichte
- Comments: Patient was not pregnant at time of vaccination.
- Andere Medikamente
- ZYRTEC [CETIRIZINE HYDROCHLORIDE]; SINGULAIR; VIT D3; SPRINTEC; BUPROPION; LAMICTAL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 30.11.2022
- Impfdatum
- 27.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Interchange of vaccine products
SARS-CoV-2 test
Symptomtext
Treatment of COVID-19; Treatment of COVID-19; Janssen Dose Number: 1, Pfizer / BioNTech Dose Number: 2, Moderna Dose Number: 3; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 31-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 27Dec2021 as dose 2 (booster), single (Lot number: 33036BD) at the age of 31 years for covid-19 immunisation; coviD-19 vaccine nrvv ad26 (jnj 78436735) (JANSSEN COVID-19 VACCINE), on 11Mar2021 as dose 1, single (Batch/Lot number: unknown) for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 09Sep2022 as dose 3 (booster), single (Batch/Lot number: unknown), in left arm for covid-19 immunisation. The patient's relevant medical history included: "Known allergies : Nasal Allergies" (unspecified if ongoing); "vocal chord dysfunction" (unspecified if ongoing). Concomitant medication(s) included: BUPROPION; LAMICTAL; SINGULAIR; SPRINTEC; VIT D3; ZYRTEC [CETIRIZINE HYDROCHLORIDE]. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 27Dec2021, outcome "unknown", described as "Janssen Dose Number: 1, Pfizer / BioNTech Dose Number: 2, Moderna Dose Number: 3"; DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 2022, outcome "unknown" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (2022) Positive, notes: COVID 19 Treatment; (2022) Positive, notes: Covid rebound. Paxlovid was taken as therapeutic measures for drug ineffective, covid-19 from 16Nov2022 to 21Nov2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 2022; Test Name: Covid-19 test; Test Result: Positive ; Comments: COVID 19 Treatment; Test Date: 2022; Test Name: Covid-19 test; Test Result: Positive ; Comments: Covid rebound
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Nasal allergy; Vocal cord dysfunction
- Andere Medikamente
- BUPROPION; LAMICTAL; SINGULAIR; SPRINTEC; VIT D3; ZYRTEC [CETIRIZINE HYDROCHLORIDE]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 12.11.2022
- Impfdatum
- 03.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Parosmia
Taste disorder
Symptomtext
an altered sense of taste and smell for many foods; an altered sense of taste and smell for many foods; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 63-year-old female patient received BNT162b2 (BNT162B2), on 03Jan2022 as dose number unknown (booster), 0.3 ml single (Lot number: 33036BD) at the age of 63 years, in left arm for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: LEVOTHYROXINE taken for thyroid disorder. Vaccination history included: BNT162b2 (DOSE 1, SINGLE, 1st dose Pfizer COVID-19 Vaccine: , Route of Administration: Intramuscular , Batch/Lot number: ER8735), administration date: 30Mar2021, when the patient was 62-year-old, for COVID-19 immunization; BNT162b2 (DOSE 2, SINGLE, 2nd dose Pfizer COVID-19 Vaccine:, Route of Administration: Intramuscular , Lot number: ER8731), administration date: 20Apr2021, when the patient was 62-year-old, for COVID-19 Immunization; Flu shot (She got the flu shot but doesnt know if last year or year before but thinks 2021), administration date: 2021, when the patient was 62 years old, for immunization. The following information was reported: TASTE DISORDER (non-serious), PAROSMIA (non-serious) all with onset Jan2022, outcome "not recovered" and all described as "an altered sense of taste and smell for many foods". Additional information: Patient took Over the counter vitamin supplements as concomitant.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Parosmia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other Conditions: No
- Andere Medikamente
- LEVOTHYROXINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 01.11.2022
- Impfdatum
- 12.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Burning mouth syndrome
Laboratory test
Restless legs syndrome
Symptomtext
Subsequently diagnosed with primary burning mouth syndrome and restless leg syndrome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Burning mouth syndrome
- Hospital-Tage
- -
- Labordaten
- Rule out labs of multiple types spanning a 10 month time frame
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Migraines Anxiety
- Andere Medikamente
- Propranolol for migraine Pristiq for anxiety Zyrtec
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 21.10.2022
- Impfdatum
- 11.01.2022
- Beginn
- 31.01.2022
- Tage bis Beginn
- 20,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acne
Biopsy
Blood pressure increased
Dry skin
Lip disorder
Lip lesion excision
Lip swelling
Neoplasm malignant
Pathology test
Squamous cell carcinoma
Symptomtext
1/31/2022 BP sky rocketed from 120 to 166 (systolic) and because of that I was put on a blood pressure medication. I believe I first noticed my lip lesion was in May of 2022 I notice my lower lip had a oval , 1 cm, rough to the touch, 2nd one that developed shortly after was small like a raised pimple and it started turning while also and rough to the touch. On 8/25/2022 the first lesion was removed and sent to pathology with a positive result of deruquis cancer then the 2nd one was removed on 9/15/2022 and sent to pathology with a squamous cell cancer result. The last time I went to see the ENT 10/12/2022 for follow up and now he wants me to come in once a month due the aggressiveness of this type of cancer cell. If it does return the removal will be more radical. Last time I checked my blood pressure was 9/29/2022 137/68 taking losartan for blood pressure control.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acne
- Hospital-Tage
- -
- Labordaten
- Pathology specimen test on 8/15/2022 and 9/25/2022
- Aktuelle Erkrankungen
- NO
- Vorgeschichte
- ARITITIES IN THE RIGHT SHOULDER, LACKING CARTIGE.
- Andere Medikamente
- FENISTRIDE, VIT, MULTI, ARGENINE, GLUCOSOMINE, OMEGA 3, GREENTEA EXTRACT, DHA, HYLORANIC ACID, MSM, REFBERATROL, CURCUMIN, D3, KRILL, NAD, N-ACETYL-L-SYSTINE, CAFFINE, COLOGAN PEPTIDE.
- Allergien
- NO ONLY AS A KID PENICILLIAN, VYCOMYCINE, SYNERGEN
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 19.10.2022
- Impfdatum
- 03.06.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable reporter(s) (Consumer or other non-HCP). The reporter is the patient. A 70-year-old male patient received BNT162b2 (BNT162B2), on 03Jun2022 as dose 4 (booster), single (Lot number: 33036BD) at the age of 70 years, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 3 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Coronary artery calcification" (unspecified if ongoing); "Known allergies: Carba Mix and Thioram Mix (2 rubber chemicals)" (unspecified if ongoing), notes: Known allergies: Carba Mix and Thioram Mix (2 rubber chemicals); "Known allergies: Sulfa" (unspecified if ongoing), notes: Known allergies: sulfa; "OSA" (unspecified if ongoing), notes: OSA. The patient took concomitant medications. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 2022, outcome "unknown" and all described as "COVID 19 Treatment". Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical Course: It was reported that rebound. Patient began Paxlovid on the second day of COVID symptom onset. COVID symptoms improved rapidly. But COVID symptoms returned 2 days after completing the five-day course of Paxlovid treatment. Patient had fatigue and still have cough, nasal congestion, copious mucus, burning of nasal mucosa. Information on the lot/batch number has been requested.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Coronary artery calcification; Obstructive sleep apnoea syndrome (OSA); Rubber sensitivity (Known allergies: Carba Mix and Thioram Mix (2 rubber chemicals)); Sulfonamide allergy (Known allergies: sulfa)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 06.10.2022
- Impfdatum
- 03.10.2022
- Beginn
- 03.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
PT WAS GIVEN EXPIRED COVID VACCINE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- HI
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 05.10.2022
- Impfdatum
- 19.07.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 62-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 29Jan2021 as dose 1, single (Lot number: EL9261), in left arm, on 19Feb2021 as dose 2, single (Lot number: EN6200), in right arm, on 13Nov2021 as dose 3 (booster), singe (Lot number: 30135BA), in left arm and on 19Jul2022 as dose 4 (booster), single (Lot number: 33036BD) at the age of 62 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "diabetes" (unspecified if ongoing); "lung issue" (unspecified if ongoing). The patient took concomitant medications. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 2022, outcome "unknown" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: COVID 19 Treatment. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: The patient received other medication in two weeks. The patient had no know allergies. The patient took Paxlovid for covid-19 treatment from 24Sep2022 to 29Sep2022 with lot number NDC0069-0345-30. No follow up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID-19 test; Test Result: Positive ; Comments: COVID 19 Treatment
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Diabetes; Lung disorder
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- M
- Eingang
- 17.09.2022
- Impfdatum
- 05.01.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 50-year-old male patient received BNT162b2 (BNT162B2), on 27Apr2021 as dose 1, single (Lot number: ew0171), in left arm, on 18May2021 as dose 2, single (Lot number: ew0173), in left arm and on 05Jan2022 as dose 3 (booster), single (Lot number: 33036BD), in left arm for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Negative, notes: Tested on day 4 night, negative; Positive, notes: Tested on day 6 night, positive; Positive, notes: COVID 19 Treatment. Therapeutic measures were taken as a result of vaccination failure, covid-19. Patient received Paxlovid from 05Sep2022 to 10Sep2022. Patient did not receive other medication in 2 weeks. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: Covid-19 test; Test Result: Negative ; Comments: Tested on day 4 night, negative.; Test Name: Covid-19 test; Test Result: Positive ; Comments: Tested on day 6 night, positive.; Test Name: Covid-19 test; Test Result: Positive ; Comments: COVID 19 Treatment
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 29.08.2022
- Impfdatum
- 28.01.2022
- Beginn
- 18.08.2022
- Tage bis Beginn
- 202,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asymptomatic COVID-19
SARS-CoV-2 test positive
Symptomtext
Tested positive for COVID-19 (routine test) for placement at inpatient rehab 8/18/2022 PCR (asymptomatic).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asymptomatic COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID-19 test positive.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Gait instability due to spinal issues.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 17.08.2022
- Impfdatum
- 13.12.2021
- Beginn
- 03.01.2022
- Tage bis Beginn
- 21,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Alopecia
Symptomtext
After taking last booster shot on 12/23/21 about month later I started to notice 2 bald spots on my head. After a few months they grew back but 2 more large patches emerged.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Alopecia
- Hospital-Tage
- -
- Labordaten
- Haven?t seen a specialist yet. Waiting on doctor referral
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Not applicable
- Andere Medikamente
- Not applicable
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 12.08.2022
- Impfdatum
- 10.02.2022
- Beginn
- 25.03.2022
- Tage bis Beginn
- 43,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acoustic stimulation tests abnormal
Deafness bilateral
Tinnitus
Symptomtext
Ringing in my ears started on March 25, 2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acoustic stimulation tests abnormal
- Hospital-Tage
- -
- Labordaten
- On June 23, 2022 I had a hearing test at an ENT office. The report noted I have a degree of hearing lost in both of my ears. I never had ringing in my ears prior to receiving the vaccine.
- Aktuelle Erkrankungen
- No illnesses at the time of vaccination or up to one month prior.
- Vorgeschichte
- I am very healthy. I do no have any health conditions. The only health issues I have now is the ringing in my ears that started approximately one month after my second vaccination.
- Andere Medikamente
- I do not take any medications. I did not take any vitamins on the day of vaccination.
- Allergien
- I am allergic to all fresh fruit except, citrus fruit, bananas and grapes. I am allergic to all shellfish and all large nuts, (walnuts, pecans, almonds).
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 11.08.2022
- Impfdatum
- 31.01.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
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), on 19Mar2021 as dose 1, single (Lot number: EP6955), in left arm, on 09Apr2021 as dose 2, single (Lot number: EW0153), in left arm, on 15Aug2021 as dose 3 (booster), single (Lot number: FA7485), in left arm and on 31Jan2022 as dose 4 (booster), single (Lot number: 33036BD) at the age of 43 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Common Variable Immune Deficiency (CVID)" (unspecified if ongoing); "hypothyroid" (unspecified if ongoing); "migraines" (unspecified if ongoing); "trigeminal neuralgia" (unspecified if ongoing); "B-12 deficiency" (unspecified if ongoing); "high blood pressure" (unspecified if ongoing), notes: high blood pressure (well-controlled with medication). The patient took concomitant medications. Past drug history included: Fioricet, reaction(s): "Known allergies: Fioricet"; Keflex, reaction(s): "Known allergies: Keflex". The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Negative, notes: antigen tests (her mom has ALS so patient didn't want to take chance of her getting it) for 6 days and had negative results and no symptoms; Positive, notes: daily antigen test it came back positive; Positive, notes: at-home "PCR-like" test and it was also positive; Positive; Negative, notes: Patient completed the entire regimen and tested negative and had no symptoms. Therapeutic measures were taken as a result of vaccination failure, covid-19. Additional information: On 26Jul2022 (the day symptoms started), started a 5-day Rx of Paxlovid, taking the first dose in and evening. Completed the entire regimen and tested negative and had no symptoms. After symptoms resolved, continued to use antigen tests (her mom has ALS so patient didn't want to take chance of her getting it) for 6 days and had negative results and no symptoms. On 06Aug2022, she woke up with an asthma attack, a cough and scratchy throat, and when she did the daily antigen test it came back positive. To be sure, she used the more sensitive, at-home "PCR-like" test and it was also positive. So, despite 5-day Paxlovid treatment, she tested positive again 6 days later and have worse symptoms than she originally had. Other medication in 2weeks was unknown.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: antigen tests; Test Result: Negative; Comments: antigen tests (her mom has ALS so patient didn't want to take chance of her getting it) for 6 days and had negative results and no symptoms; Test Name: antigen tests; Test Result: Positive; Comments: daily antigen test it came back positive; Test Name: at-home PCR-like; Test Result: Positive; Comments: at-home "PCR-like" test and it was also positive; Test Name: COVID-19 test; Test Result: Positive; Test Name: COVID-19 test; Test Result: Negative; Comments: Patient completed the entire regimen and tested negative and had no symptoms.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Blood pressure high (high blood pressure (well-controlled with medication)); Common variable immunodeficiency; Hypothyroidism; Migraine; Trigeminal neuralgia; Vitamin B12 deficiency
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 05.08.2022
- Impfdatum
- 27.12.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 53-year-old male patient received BNT162b2 (BNT162B2), on 27Dec2021 as dose 3, (booster) single (Lot number: 33036bd) at the age of 52 years, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 2, single (Batch/Lot number: unknown) and as dose 1, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Iga nephropathy" (unspecified if ongoing); "essential thrombocytopenia" (unspecified if ongoing); "Gout" (unspecified if ongoing); "hypertension" (unspecified if ongoing). Concomitant medication(s) included: METOPROLOL SUCCINATE, start date: 04Oct2021; ALLOPURINOL; ECOTRIN; VITAMIN D3; GUAIFENESIN. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: COVID-19: (unspecified date) positive, notes: Treatment of COVID-19; (27Jul2022) positive, notes: Verified Covid positive with test 2 days later. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: If vaccine received: Yes. Other medication in 2 weeks: Yes. Patient received Paxlovid from 20Jul2022 to 25Jul2022 for Covid 19 treatment. Patient received her medication in 2weeks product: Farxiga (lot no Pa0051) from 01Mar2022. On 04Oct2021 Metoprolol succ er 25 mg tab, Allopurinol 300 mg tablet, Asprin 325mg, Ecotrin, Vitamin D3 50 mcg, Guaifenesin 400 mg. Acetaminophen 500mg, on 22Jul2022, started Diphenhydramine HCL 25mg, 22Jul2022, Pseudoephedrine HCL 30mg. Covid symptoms returned 3 days after last dose of Paxlovid. Verified Covid positive with test 2 days later. Eevnt onset is 28Jul2022 at 03:00 PM and no treatment and no known allergy reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: covid-19; Test Result: Positive ; Comments: Treatment of COVID-19; Test Date: 20220727; Test Name: covid-19; Test Result: Positive ; Comments: Verified Covid positive with test 2 days later.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Gout; Hypertension; IgA nephropathy; Thrombocytopenia
- Andere Medikamente
- METOPROLOL SUCCINATE; ALLOPURINOL; ECOTRIN; VITAMIN D3; GUAIFENESIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 19.07.2022
- Impfdatum
- 26.04.2021
- Beginn
- 26.04.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Amenorrhoea
Hypomenorrhoea
Menstruation irregular
Symptomtext
After my first vaccine I didn?t get my period. My cycle was regular since I was taking birth control. I don?t remember the exact timeline but I went from having very heavy regular periods to having mild spotting after a few months of no period. I think it took a couple months for my period to come back, I don?t exactly remember. After my booster shot I again stopped having my period. I stopped taking birth control in august I think? Since then I have only had my period twice and it?s been almost a year. My main concern is that my periods were very regular and the symptoms were always the same up until I started getting vaccinated for COVID. I know birth control can affect your cycle when you stop taking it, but I have gotten it a few times and this irregularly started after my vaccines.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Amenorrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- I was taking a hormonal birth control, nuvaring
- Allergien
- Ibuprofen, hazelnuts, latex
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 15.07.2022
- Impfdatum
- 09.01.2022
- Beginn
- 14.07.2022
- Tage bis Beginn
- 186,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Symptomtext
patient hospitalized
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- 1,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- M
- Eingang
- 14.07.2022
- Impfdatum
- 21.01.1963
- Beginn
- 14.07.2022
- Tage bis Beginn
- 21.724,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Symptomtext
Patient did not experience any adverse reactions at time of vaccine administration.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Finasteride
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 14.07.2022
- Impfdatum
- 05.01.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- 177,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test abnormal
Symptomtext
At time of 16 yr old physical, June 30, 2022, blood work was drawn that indicates possible thyroid condition. Will be retested in one month.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood test abnormal
- Hospital-Tage
- -
- Labordaten
- Blood Panel, partial abnormal
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Pro Biotic; Zyrtec; Nasal Spray
- Allergien
- Plants; Grass; Wasp
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 13.07.2022
- Impfdatum
- 10.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Disturbance in attention
Feeling abnormal
Immunisation reaction
Impaired work ability
Symptomtext
About a week after vaccine, I could not focus for very long. I can not focus properly like I use to. I seems to have caused a brain fog. I talked to my doctor during my yearly annual and my doctor did not have any suggestion other than an adverse event. This is still continuing to this day. It does affect my job with not being able to focus. This has stopped me from getting the 4th dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Disturbance in attention
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 08.07.2022
- Impfdatum
- 11.01.2022
- Beginn
- 01.06.2022
- Tage bis Beginn
- 141,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 50-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 11Jan2022 at 13:00 as dose 3 (booster), single (Lot number: 33036BD) at the age of 49 years, in right arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown) and as dose 2, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "known allergies: Penicillin" (unspecified if ongoing), notes: known allergies: Penicillin. The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Jun2022, outcome "unknown" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical Information:Patient took Paxlovid for COVID 19 treatment from 21Jun2022 to 26Jun2022. Patient was not taking any other medications/products within 2 weeks of starting COVID-19 treatment. Previously patient had received a COVID-19 Vaccine. COVID rebound 3 days after final dose of Paxlovid. Cough, congestion, severe headache, fatigue. Relatedness of drug to reaction(s)/event(s): COVID-19, SARS-CoV-2 PCR test positive: Source of assessment: RA Result of Assessment: D. Unclassifiable.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: SARS-CoV-2 PCR test positive; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Penicillin allergy (known allergies: Penicillin)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- F
- Eingang
- 08.07.2022
- Impfdatum
- 28.12.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Symptomtext
Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 47-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 28Dec2021 as dose 3 (booster), single (Lot number: 33036BD), in right arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown) and as dose 2, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Migraine headaches" (unspecified if ongoing). There were no concomitant medications. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "Treatment of COVID-19". Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: The patient has no known allergies. The patient has experienced Awful taste in mouth Severe lower abdominal pain (start date: 28Jun2021) and was not recovered. The patient has taken Paxlovid for the treatment of covid-19 (treatment start date=25Jun2022, Treatment stop date=29Jun2022, Lot number=GC6416).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Migraine headache
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 06.07.2022
- Impfdatum
- 30.12.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Muscular weakness
Symptomtext
WEAKNESS OF LOWER EXTREMITIES
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Muscular weakness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- PREDIABETES, HYPERTENSION, HYPOTHYROIDISM
- Andere Medikamente
- IRBESARTAN 150MG DAILY, METFORMIN 500 MG DAILY, ATORVASTATIN 10MG DAILY AND LEVOTHYROXINE 50 MCGDAILY,
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 21.06.2022
- Impfdatum
- 03.01.2022
- Beginn
- 01.03.2022
- Tage bis Beginn
- 57,0
- Dosis
- 3
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dysmenorrhoea
Heavy menstrual bleeding
Ultrasound uterus abnormal
Uterine leiomyoma
Uterine mass
Uterine polyp
Symptomtext
Extremely painful and prolonged menses beginning 3/2022 and continuing through 6/2022. Former length of menses was 1-2 days; current length is 4 days. Crippling cramping every day of menses; cramping does not taper off, but rather gets stronger throughout menses. Length of cycle previously was 27 days with very small variation; since 3/2022, cycle length has varied from 26 days to 30 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dysmenorrhoea
- Hospital-Tage
- -
- Labordaten
- 5/31/2022 ultrasound shows 1cm mass in uterus. Polyp or fibroid. Hysteroscopy planned.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 10,0
- Geschlecht
- M
- Eingang
- 21.06.2022
- Impfdatum
- 21.06.2022
- Beginn
- 21.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product preparation issue
Symptomtext
Adult > 12 years old was reconstituted with 1.3 sterile saline and 0.2 mL was administered IM Patient observed for 30 minutes post vaccination, no adverse reaction noted
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product preparation issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 20.06.2022
- Impfdatum
- 20.06.2022
- Beginn
- 20.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
PHARMACIST GAVE EXPIRED COVID VACCINE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 09.06.2022
- Impfdatum
- 05.05.2022
- Beginn
- 12.05.2022
- Tage bis Beginn
- 7,0
- Dosis
- 4
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from contactable reporter(s) (Nurse) from product quality group. The reporter is the patient. A 61-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 05May2022 at 13:00 as dose 4 (booster), single (Lot number: 33036BD) at the age of 61 years, in right arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 3 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "hypertension" (unspecified if ongoing); "T2DM" (unspecified if ongoing); "gerd" (unspecified if ongoing); "known allergies: Penicillin" (unspecified if ongoing). Concomitant medication(s) included: NEXIUM [ESOMEPRAZOLE MAGNESIUM]; LEXAPRO; LISINOPRIL; XYZAL; METFORMIN; PRAVACHOL. Past drug history included: Cephalosporins, reaction(s): "known allergies: Cephalosporins"; Cipro, reaction(s): "known allergies: Cipro"; Neosporin oint, reaction(s): "known allergies: Neosporin oint". The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 12May2022, outcome "not recovered" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (12May2022) Positive, notes: First positive test 12May. Metallic taste in mouth during treatment; (19May2022) Negative, notes: Tested negative 19May; (24May2022) Positive, notes: returned to work 23May, 24May started sneezing with nasal discharge, tested positive; (28May2022) Positive, notes: 28May, still testing positive. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: Pfizer Paxlovid; Treatment start date: 12May2022; Treatment stop date: 17May2022; Indication: Treatment of COVID-19. Other medication in 2 weeks product: Nexium, Lexapro, Lisinopril, Zyxal, Metformin, Pravachol. First positive test 12May. Metallic taste in mouth during treatment. Tested negative 19May, returned to work 23May, 24May started sneezing with nasal discharge, tested positive. 28May, still testing positive. This is a notification generated from the system. As part of the LOE simplification process, the following Complaint Records were classified as Product Use Attributes // Lack of Effect and have been moved to Closed (No Investigation) state referencing a previously completed investigation for the same product and lot as per the One and Done business process according to in PQSQ1215 and/or Q1252. Refer to the below table for details: Conclusion of Previously Completed Investigation: The complaint for a Lack of effect of the pfizer-biontech covid-19 vaccine lot 33036BD was investigated. The investigation included reviewing incoming quality and manufacturing batch records, deviation investigations, an analysis of the complaint history for the reported lot and product type and final release assay testing. This product was received as preformulated bulk and was manufactured, labeled and packaged by Pfizer (name-withheld). The final scope was determined to be lot 33036BD. No quality issues were identified during the investigation. There was no impact on 6705425 6705085 product quality. An NTM was not issued for the complaint. No regulatory notification were held as a result of this complaint. The complaint condition of lack of effect was not confirmed, therefore the root cause cannot be attributed to manufacture or vendor processes. The root cause was not determined to be manufacture or vendor related as incoming quality component testing and the results of all analytical tests performed at the time of lot release confirmed that the batch met potency specifications. No corrective or preventative actions are required as the complaint condition was not determined to be manufacture or vendor related and there are quality systems in place to detect defects prior any lot being released to the market. No further investigation required.; Sender's Comments: The efficacy of a drug varies from patient to patient and can be affected by different factors; however, a contributory role of the suspect product bnt162b2 to the reported Drug ineffective/ COVID-19 cannot be ruled out
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220512; Test Name: Covid-19; Test Result: Positive ; Comments: First positive test 12May. Metallic taste in mouth during treatment.; Test Date: 20220519; Test Name: Covid-19; Test Result: Negative ; Comments: Tested negative 19May; Test Date: 20220524; Test Name: Covid-19; Test Result: Positive ; Comments: returned to work 23May, 24May started sneezing with nasal discharge, tested positive.; Test Date: 20220528; Test Name: Covid-19; Test Result: Positive ; Comments: 28May, still testing positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: GERD; Hypertension; Penicillin allergy; Type 2 diabetes mellitus
- Andere Medikamente
- NEXIUM [ESOMEPRAZOLE MAGNESIUM]; LEXAPRO; LISINOPRIL; XYZAL; METFORMIN; PRAVACHOL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 03.06.2022
- Impfdatum
- 24.01.2022
- Beginn
- 01.05.2022
- Tage bis Beginn
- 97,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
COVID; COVID; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 60-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 31Dec2020 as dose 1, single (Lot number: EL1284), in left arm, on 21Jan2021 as dose 2, single (Lot number: EK9231), in left arm, on 04Sep2021 as dose 3 (booster), single (Lot number: FC3182), in left arm and on 24Jan2022 as dose 4 (booster), single (Lot number: 33036BD) at the age of 59 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "high blood pressure" (unspecified if ongoing), notes: high blood pressure; "Type 2 Diabetes" (unspecified if ongoing). Concomitant medication(s) included: METFORMIN [METFORMIN HYDROCHLORIDE], start date: Mar2017; LISINOPRIL, start date: Mar2008. Past drug history included: Amoxicillin, reaction(s): "Known allergies: amoxicillin", notes: Known allergies: amoxicillin; Iodine for Known allergies: Iodine, notes: Known allergies: Iodine. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset May2022, outcome "unknown" and all described as "COVID". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (May2022) Negative, notes: I have a positive COVID test after six days with negative results; (May2022) Positive, notes: I have a positive COVID test after six days with negative results. Therapeutic measures were taken as a result of vaccination failure, covid-19.Product:COVID 19 Treatment, Brand: Paxlovid, Treatment start date:20May2022,Treatment stop date:24May2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 202205; Test Name: COVID Test; Test Result: Negative ; Comments: I have a positive COVID test after six days with negative results.; Test Date: 202205; Test Name: COVID Test; Test Result: Positive ; Comments: I have a positive COVID test after six days with negative results.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Blood pressure high (high blood pressure); Type 2 diabetes mellitus
- Andere Medikamente
- METFORMIN [METFORMIN HYDROCHLORIDE]; LISINOPRIL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 02.06.2022
- Impfdatum
- 10.01.2022
- Beginn
- 01.05.2022
- Tage bis Beginn
- 111,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 60-year-old male patient received BNT162b2 (BNT162B2), on 19Mar2021 as dose 1, single (Lot number: EP7534), on 09Apr2021 as dose 2, single (Lot number: EW0153), on 16Aug2021 as dose 3 (booster), single (Lot number: FA3120) and on 10Jan2022 as dose 4 (booster), single (Lot number: 33036BD) at the age of 60 years for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: ATORVASTATIN, start date: 01Jul2014, stop date: 20May2022; RAMIPRIL AUROBINDO, start date: 01Oct2019, stop date: 20May2022. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset May2022, outcome "not recovered" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (May2022) negative, notes: I tested negative after treatment; (30May2022) positive, notes: Intested positive again on 30May2022. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical Course: Paxlovid was taken for covid-19 and After finishing the Paxlovid treatment on 25May2022, I had a relapse with all symptoms except fever. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 202205; Test Name: tested; Test Result: Negative ; Comments: I tested negative after treatment; Test Date: 20220530; Test Name: tested; Test Result: Positive ; Comments: Intested positive again on 30May2022.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- ATORVASTATIN; RAMIPRIL AUROBINDO
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 18.05.2022
- Impfdatum
- 09.01.2022
- Beginn
- 15.05.2022
- Tage bis Beginn
- 126,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Symptomtext
patient hospitalized
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 7,0
- Geschlecht
- M
- Eingang
- 09.05.2022
- Impfdatum
- 06.05.2022
- Beginn
- 06.05.2022
- 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
Product administered to patient of inappropriate age
Symptomtext
Noted after vaccination for COVID-19 that client was vaccinated with Pfizer- (purple cap - 12 years and older).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none known
- Vorgeschichte
- none known
- Andere Medikamente
- none known
- Allergien
- none known
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 05.05.2022
- Impfdatum
- 05.05.2022
- Beginn
- 05.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product preparation error
Symptomtext
Patient elected to receive the first dose of Pfizer COVID19 vaccine. While medic was prepping the vaccine for administration she did not realize the vaccine had to be diluted with saline. A full vial of Pfizer vaccine (6 doses) was drawn up and administered to the patient. The patient was advised of the incident and will be monitored over the next 72 hours to check for any adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product preparation error
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Gabepentin
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 05.05.2022
- Impfdatum
- 17.01.2022
- Beginn
- 01.05.2022
- Tage bis Beginn
- 104,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
Tested positive for COVID-19; Tested positive for COVID-19; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from product quality group. A 15-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 18Jun2021 as dose 1, single (Lot number: EW0180), on 09Jul2021 as dose 2, single (Lot number: EW0196) and on 17Jan2022 as dose 3 (booster), single (Lot number: 33036BD) at the age of 14 years for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: VACCINATION FAILURE (medically significant) with onset 01May2022, outcome "unknown", COVID-19 (medically significant) with onset 01May2022, outcome "recovering" and all described as "Tested positive for COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (01May2022) Positive, notes: Nasal Swab. Therapeutic measures were not taken as a result of vaccination failure, covid-19. Clinical course included no other vaccines in four weeks and No other medications in two weeks. No known allergies.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220501; Test Name: COVID-19; Test Result: Positive ; Comments: Nasal Swab
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 25.04.2022
- Impfdatum
- 05.01.2022
- Beginn
- 25.03.2022
- Tage bis Beginn
- 79,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Human papilloma virus test positive
Symptomtext
Possible reactivation of latent HPV. Pt say she was positive for HPV 20 years ago but then it cleared and she has only had normal paps since until 3/25/22 when her pap came back positive again for HPV.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Human papilloma virus test positive
- Hospital-Tage
- -
- Labordaten
- 3/25/22 PAP INTERPRETATION: EPITHELIAL CELL ABNORMALITY, SQUAMOUS. Atypical squamous cells of undetermined significance. MOLECULAR RESULTS POSITIVE for High Risk HPV.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- None
- Allergien
- Codeine
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 15.04.2022
- Impfdatum
- 05.01.2022
- Beginn
- 02.02.2022
- Tage bis Beginn
- 28,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest X-ray
Cough
Delivery
Exposure during pregnancy
Fluid retention
Peripheral swelling
Premature rupture of membranes
Urine analysis normal
Symptomtext
Coughing on and off for several weeks. At 38 weeks my water broke, legs very swollen, urine test for preeclampsia was negative. 38 weeks and delivered on March 3, 2022. Had so much fluid accumulated that I almost had preeclampsia.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest X-ray
- Hospital-Tage
- 7,0
- Labordaten
- Chest x-ray - premature cardiac activity
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Prenatal vitamins, Tylenol or Fioricet migraine headache
- Allergien
- Walnuts and Pecans
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- -
- Geschlecht
- F
- Eingang
- 18.03.2022
- Impfdatum
- 12.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Heart rate
Heart rate irregular
Symptomtext
Irregular heartbeat; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 61 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 12Jan2022 02:45 (Lot number: 33036BD) as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history was not reported. The patient took concomitant medications. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EP7533, Location of injection: Arm Left, Route of Administration: Intramuscular), administration date: 11Apr2021, for COVID-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EN6204, Location of injection: Arm Left, Route of Administration: Intramuscular), administration date: 21Mar2021, for COVID-19 immunization. The following information was reported: HEART RATE IRREGULAR (non-serious) with onset 13Jan2022 08:00, outcome "recovered", described as "Irregular heartbeat". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of heart rate irregular. Additional information: The patient had not received any other vaccines within 4 weeks prior to the COVID vaccine. The patient received other medications within 2 weeks of vaccination include hydrothiachlorizide. The patient didn't have covid prior vaccination, no known allergies and not tested for covid post vaccination. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Heart rate
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220113; Test Name: Irregular heartbeat; Result Unstructured Data: Test Result:irregular
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 11.03.2022
- Impfdatum
- 28.12.2021
- Beginn
- 03.01.2022
- Tage bis Beginn
- 6,0
- Dosis
- 2
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ear discomfort
Vertigo
Symptomtext
Intermittent episodes of vertigo started about a week after the vaccine. Episodes occur with bending down, looking up, rolling over in bed etc. Feels like there is fluid in the left ear.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ear discomfort
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 10.03.2022
- Impfdatum
- 24.02.2022
- Beginn
- 24.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (temperature)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 10.03.2022
- Impfdatum
- 19.02.2022
- Beginn
- 19.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (temperature)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 10.03.2022
- Impfdatum
- 22.02.2022
- Beginn
- 22.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (temperature)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 10.03.2022
- Impfdatum
- 24.02.2022
- Beginn
- 24.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (temperature)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 10.03.2022
- Impfdatum
- 24.02.2022
- Beginn
- 24.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (temperature)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 10.03.2022
- Impfdatum
- 21.02.2022
- Beginn
- 21.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (temperature)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 10.03.2022
- Impfdatum
- 20.02.2022
- Beginn
- 20.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (temperature)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 10.03.2022
- Impfdatum
- 21.02.2022
- Beginn
- 21.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (temperature)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 10.03.2022
- Impfdatum
- 25.02.2022
- Beginn
- 25.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (temperature)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 10.03.2022
- Impfdatum
- 24.02.2022
- Beginn
- 24.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (temperature)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 10.03.2022
- Impfdatum
- 21.02.2022
- Beginn
- 21.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (temperature)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 10.03.2022
- Impfdatum
- 21.02.2022
- Beginn
- 21.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (temperature)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 10.03.2022
- Impfdatum
- 19.02.2022
- Beginn
- 19.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (temperature)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 10.03.2022
- Impfdatum
- 21.02.2022
- Beginn
- 21.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (temperature)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 10.03.2022
- Impfdatum
- 21.02.2022
- Beginn
- 21.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (temperature)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 10.03.2022
- Impfdatum
- 23.02.2022
- Beginn
- 23.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (temperature)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 10.03.2022
- Impfdatum
- 23.02.2022
- Beginn
- 23.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (temperature)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 10.03.2022
- Impfdatum
- 20.02.2022
- Beginn
- 20.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (temperature)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 10.03.2022
- Impfdatum
- 19.02.2022
- Beginn
- 19.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (temperature)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 10.03.2022
- Impfdatum
- 19.02.2022
- Beginn
- 19.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (temperature)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 10.03.2022
- Impfdatum
- 20.02.2022
- Beginn
- 20.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (temperature)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 10.03.2022
- Impfdatum
- 24.02.2022
- Beginn
- 24.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (temperature)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 10.03.2022
- Impfdatum
- 20.02.2022
- Beginn
- 20.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (temperature)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 10.03.2022
- Impfdatum
- 23.02.2022
- Beginn
- 23.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (temperature)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 10.03.2022
- 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 storage error
Symptomtext
Error: Improper Storage (temperature)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 10.03.2022
- Impfdatum
- 23.02.2022
- Beginn
- 23.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (temperature)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 10.03.2022
- Impfdatum
- 22.02.2022
- Beginn
- 22.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (temperature)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 10.03.2022
- Impfdatum
- 23.02.2022
- Beginn
- 23.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (temperature)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 10.03.2022
- Impfdatum
- 23.02.2022
- Beginn
- 23.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (temperature)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 10.03.2022
- Impfdatum
- 24.02.2022
- Beginn
- 24.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (temperature)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 10.03.2022
- Impfdatum
- 20.02.2022
- Beginn
- 20.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (temperature)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 8,0
- Geschlecht
- M
- Eingang
- 28.02.2022
- 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
Incorrect dose administered
Symptomtext
Adult dose given instead of pediatric
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 22.02.2022
- Impfdatum
- 21.01.2022
- Beginn
- 24.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Magnetic resonance imaging
Magnetic resonance imaging head
Optic neuritis
Venogram
Visual impairment
Symptomtext
On the day after the booster vaccination 01/22/2022 I had a temperature of 102F. I then felt ok the following day 01/23/2022. On Monday, 01/24/2022, around mid day I started to notice a degradation in my eye sight and chalked it up to the possible need for new glasses. By the weekend of 01/29-30/2022, the degradation was bothering me enough to try my own test where I covered one eye and then the other. At that time I determined that I was having a very difficult time seeing out of my left eye. On 02/02/2022, I contact my Optometrist who referred me to an Opthalmologist. The Opthalmologist advised me that I had extreme inflammation of the Optic Nerve in my left eye and that I should go directly to the ER at Eye Institute which I did. I was diagnosed with Optic Neuritis in my left eye and was treated with Intravenous Steroids on 02/03/2022, 02/04/2022, and 02/05/2022. I then went on a course of Prednisone tablets for 16 days ending yesterday, 02/21/2022. I have a follow up appointment with Dr. this coming Friday, 02/25/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood test
- Hospital-Tage
- -
- Labordaten
- 02/02/2022 - MRI Brain, MRI Orbits, MRI Venogram;02/03/2022, 02/04/2022, 02/05/2022 - 1000Mg of IV Steroids; 02/06/2022 - 02/21-2022 - Prednisone; Many blood tests on 02/04/2022 and a few more by Rheumatologist on 02/15/2022.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Aneurysm of right common Iliac artery; Prostate Cancer; GERD.
- Andere Medikamente
- Bystolic; Lipitor; Prilosec; Xanax; Remeron; Ambien; Uroxatral; Cialis; Alive for Men 50+ (Multi-Vitamin); Vitamin C.
- Allergien
- Intravenous Iodine.
- Vorherige Impfungen
- Fever of 101F, 06/20/21-06/22/21, COVID-19 VAC1, Fever of 101F, 07/11/21 - 07/13/21, COVID-19 VAC2, Age 59 for both vaccines.
- Staat
- NJ
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 18.02.2022
- Impfdatum
- 17.02.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
No adverse event
Symptomtext
Patient returned to health on Thursday February 17th to request her Covid 19 booster injection as a result of the mandate deadline for all hospital workers to have their booster vaccine by February 21st of 2022. Patient was given the third dose three weeks and five days too soon as per miscalculations by Nurse . Patient spoke with NP to reassure that it would be reported . Patient tolerated vaccine well with no adverse reactions noted at that time nor at the 15 minute observation period after.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 18.02.2022
- Impfdatum
- 14.02.2022
- Beginn
- 15.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary mass
Symptomtext
Axillary lump noted in left arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary mass
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 15.02.2022
- Impfdatum
- 14.02.2022
- Beginn
- 14.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
Error: Booster 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
- AZ
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 13.02.2022
- Impfdatum
- 12.02.2022
- Beginn
- 12.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
Symptomtext
Patient was inadvertently given the second dose of Pfizer earlier than the recommended interval. Dose #1 was given 1/30/22 and dose #2 was given 2/12/22. Per the CDCs Administration Errors Revaccination Guidance, patient should be re-vaccinated with dose #2 on 2/20/22; patient was informed via phone call.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- HI
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 10.02.2022
- Impfdatum
- 07.02.2022
- Beginn
- 07.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
No adverse event
Symptomtext
Client recieved booster shot on 2/7/22. Information was taken from his vaccination card, Upon looking in system it was discovered that he had a booster shot previous to this one on 12/9/21 at another facility. Contacted client on 2/10/22 @ 2:00 pm by telephone. He reported that he didn't know he had been given a booster at the other facility. He denied adverse effects at the time and presently.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 10.02.2022
- Impfdatum
- 10.02.2022
- Beginn
- 10.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product preparation issue
Symptomtext
Incorrect # of doses noted to vial after administration of dose #1 & #2. Pt who received dose #1 reports no s/s of adverse reaction.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Squid Oil (hives, itching, dyspnea), Shrimp (hives)
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 10.02.2022
- Impfdatum
- 10.02.2022
- Beginn
- 10.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product preparation issue
Symptomtext
Incorrect # of doses in vial after reconstitution after administration to patient. Pt denies s/s of adverse reaction.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 10,0
- Geschlecht
- F
- Eingang
- 10.02.2022
- Impfdatum
- 11.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
Error: Patient Too Young for Vaccine Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 9,0
- Geschlecht
- F
- Eingang
- 08.02.2022
- Impfdatum
- 17.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
Error: Patient Too Young for Vaccine Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 08.02.2022
- Impfdatum
- 19.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
No adverse event
Symptomtext
Patient requested Pfizer COVID vaccine on 1/19/22 at clinic. He reported that he initially got his first dose about a year prior. He was advised to contact the clinic where he got his first dose for their records. He then came back to the clinic and stated that they did not have record of him receiving his COVID vaccine and isn't sure if he maybe received a flu vaccine instead. He then reported he needed 2 doses of the COVID vaccine to start work. His first dose was given on 1/19/22. His 2nd dose was given on 2/5/22. Patient received 2nd dose 4 days early. Patient was immediately notified he received his dose too early and was advised to closely monitor for symptoms. Dose is considered valid since within 4 days of first dose. Patient did not experience any adverse effects. Error was noted when RN went to hand the patient his vaccine card and thought the dates seemed off.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 08.02.2022
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine administered on 02/04/2022, expired on 02/03/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 08.02.2022
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Vaccine administered on 02/04/2022, expired on 02/03/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 08.02.2022
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Vaccine administered on 02/04/2022 was expired on 02/03/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 07.02.2022
- 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 storage error
Symptomtext
Vaccine administered on 02/04/2022 was expired on 02/03/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 07.02.2022
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Vaccine administered on 02/04/2022 was expired on 02/03/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 07.02.2022
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine administered on 02/04/2022, expired on 02/03/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 06.02.2022
- Impfdatum
- 15.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Symptomtext
Error: Patient Too Young for Vaccine Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 05.02.2022
- Impfdatum
- 28.12.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
SARS-CoV-2 test
Tic
Symptomtext
Developed serious tics out of the blue about 3 or 4 days later and never has a history before.; This is a spontaneous report received from a contactable reporter (Consumer or other non HCP). The reporter is the patient. A 45 year-old male patient received bnt162b2 (COMIRNATY), administered in arm left, administration date 28Dec2021 16:45 (Lot number: 33036BD) at the age of 45 years as dose 1, single for covid-19 immunisation. The patient had no relevant medical history. The patient had no known allergies. The patient had no covid prior vaccination. There were no concomitant medications. There were no other vaccine in four weeks, no other medications in two weeks. The following information was reported: TIC (disability) with onset 31Dec2021, outcome "not recovered", described as "developed serious tics out of the blue about 3 or 4 days later and never has a history before.". The event "developed serious tics out of the blue about 3 or 4 days later and never has a history before." was resulted in doctor or other healthcare professional office/clinic visit, disability or permanent damage. The patient underwent the following laboratory tests and procedures: sars-cov-2 test: (04Jan2022) negative, notes: Rapid at pediatrician; Nasal Swab. Therapeutic measures were taken as a result of tic included so far, treatment with magnesium and B6. Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- SARS-CoV-2 test
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220104; Test Name: Rapid; Test Result: Negative ; Comments: Rapid at pediatrician Nasal Swab
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 05.02.2022
- Impfdatum
- 18.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
Error: Booster 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
- CA
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 03.02.2022
- Impfdatum
- 06.01.2022
- Beginn
- 23.01.2022
- Tage bis Beginn
- 17,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Dysphagia
Gastroenteritis viral
Impaired work ability
Pharyngeal inflammation
SARS-CoV-2 test negative
SARS-CoV-2 test positive
Throat tightness
Symptomtext
stomatch bug on 01/20/2022, that lasted 24hrs. then she felt well for two days and she did a COVID swab since she was at work she was sent for testing and it was negative then on 01/23/2022 throut felt felt tight and she thought it was allergies and she took an allegy pill the later in early moring of 01/24/2022 could not swallow and through was inflammed and she did a home COVID tested Avid was the brand of test and she received a positive test. Other at work was covid positive and fluids and isolation and called doctor a few days later because she thought that she had stempt throught. Another associate with COVID gave her zpac that she received and she took it and a few days later her throught felt better. 60% better and tested again at day 6 and still tested positive for COVID so she had to stay off work. Televisit and talk with Dr. at hospital that she works for, also gave directive of the zpac.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID had verbal obsevation by provider who gave directives of fluid and issolation not script was called in .
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Allergies and sinus issues mild sinus head aches
- Andere Medikamente
- Airborne gummies, Hair and Nail health gummies
- Allergien
- No seasional allergies
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 02.02.2022
- Impfdatum
- 01.02.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Interchange of vaccine products
Symptomtext
Error: Wrong Vaccine Formulation (ex. different manufact. initial and booster)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 31.01.2022
- Impfdatum
- 13.04.2021
- Beginn
- 29.01.2022
- Tage bis Beginn
- 291,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Interchange of vaccine products
Symptomtext
patient hospitalized
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 31.01.2022
- Impfdatum
- 17.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest discomfort
Dysphonia
Laryngitis
Pharyngeal swelling
Symptomtext
couple hours after the shot, my throat felt swollen and chest felt tight, and sudden laryngitis and some hoarse voice. Till today still feels swollen and hoarse.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest discomfort
- Hospital-Tage
- -
- Labordaten
- none just took benadryl
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- asthma, gluten enteropathy,
- Andere Medikamente
- none
- Allergien
- omeprazole, tramadol hydrochloride, vicodin ,Percocet, norco, amoxicillin, penecillin, clavulanate potassium, gabpentin, cephalexin, zithromax, bactrim,
- Vorherige Impfungen
- flu shots-sick for 3 months, 38, 39
- Staat
- HI
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 31.01.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Product preparation issue
Symptomtext
Patient was administered the whole vial without dilution.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- UNK
- Andere Medikamente
- UNK
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 11,0
- Geschlecht
- F
- Eingang
- 29.01.2022
- 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
Product administered to patient of inappropriate age
Symptomtext
Error: Patient Too Young for Vaccine Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 9,0
- Geschlecht
- M
- Eingang
- 28.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Symptomtext
Error: Patient Too Young for Vaccine Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 26.01.2022
- Impfdatum
- 22.01.2022
- Beginn
- 23.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bacterial test
Herpes simplex test
Vaccine positive rechallenge
Vulval ulceration
Symptomtext
Patient has now had sores on vulva after 2 of her COVID vaccines. Dose number two and dose number 3. The COVID vaccine 2nd dose was given on 6/11/21 and she developed the sores on 6/15/21. The vaccine was Pfizer lot EW0183 and given IM in left arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bacterial test
- Hospital-Tage
- -
- Labordaten
- Today 1/26/22 I am doing a herpes culture and herpes blood test and a bacterial culture.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- No
- Allergien
- No
- Vorherige Impfungen
- see above
- Staat
- CA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 25.01.2022
- Impfdatum
- 17.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Fear
Feeling abnormal
Impaired driving ability
Inflammation
Joint swelling
Lacrimation increased
Visual impairment
Symptomtext
Within about an hour receiving the booster my right wrist swelled up. The injection caused an inflammatory response. By about 3:00 p.m. my vision became challenging. I don't know the best way to describe it other than "off." My eyes became watery and I didn't want to drive a car because I could tell my vision was "off." I seemed to feel ok while laying down. By that evening around 6 p.m. felt like I had a hangover without the nausea. I can only describe the feeling as "wonky." It was an effort to move around. I didn't do anything that I didn't have to do. These symptoms continued daily. On Tuesday I noticed that my brain became affected. It was scary. My son came home from school. He was petting our 4 year old dog and I petting our 8 year old cat and I said "don't we have the best puppies?" I mean nothing that crazy has ever come out of my mouth. Then I walked with my daughter. We crossed a street and I was looking to my right to look for cars and I said to her "always look left at this intersection." and she's like mom that is right. It continues with these examples...one night I made tater tots and I called them hash browns 3 times even after my family corrected me. These are not things that happen. Never have I ever made so many brain disconnection mistakes. By Thursday I made an appointment to see my primary care physician. I saw him today and he asked me to report these symptoms on this website. My brain as of yesterday January 24th seems much improved. I feel 80% less wonky but my vision still feels affected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood test
- Hospital-Tage
- -
- Labordaten
- My doctor ordered some lab tests. He can't test for a stroke but he thought I may have had a small blood clot. He thinks that I might have had covid in December. I had the blood drawn today.
- Aktuelle Erkrankungen
- I had cold symptoms that started on the holiday: sore throat, shortness of breath, chest pain mild, dry cough, exhaustion and lower back pain. I did an at home test kit on December 27th that said negative for covid. I couldn't get an appointment for another test.
- Vorgeschichte
- I have Rheumatoid Arthritis. I've taken Enbrel for over 20 years. I went off Enbrel on December 21st because I wanted my body to be able to work better. I have not done my Enbrel shot since then as of today (January 25th). I have Hashimoto's disease and Sjogren's syndrome.
- Andere Medikamente
- Garden of Life collagen, Mega Foods women over 40 daily vitamin, Vitamin D3, L-Thyroxine 125 mg.
- Allergien
- Sensitivity to: Gluten, nuts all nuts including peanuts, and some cheeses. Allergic to Penicillin, Erythromycin, Keflex/Cephalexin, Clindamycin,, Tetracycline and Ciprofloxacin
- Vorherige Impfungen
- Pfizer
- Staat
- MN
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 25.01.2022
- Impfdatum
- 15.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 5,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Vaccine stored in freezer temperature for too long. We recommended to the patient to get revaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 25.01.2022
- Impfdatum
- 15.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 5,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Vaccine stored in freezer temperature for too long. We recommended to the patient to get revaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 25.01.2022
- Impfdatum
- 15.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 5,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Vaccine stored in freezer temperature for too long. We recommended to the patient to get revaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 22.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Immunisation
SARS-CoV-2 test
Vaccination failure
Symptomtext
COVID-19 / covid test result=Positive; COVID-19 / covid test result=Positive; 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 31 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 03Jan2022 10:00 (Lot number: 33036BD) at the age of 31 years as dose 3 (booster), single, administered in arm left, administration date 23Apr2021 (Lot number: EW0175) as dose 2, single and administered in arm left, administration date 02Apr2021 (Lot number: EW0151) 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: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 09Jan2022, outcome "not recovered" and all described as "COVID-19 / covid test result=Positive"; IMMUNISATION (medically significant) with onset 03Jan2022 10:00, outcome "unknown", described as "dose received: 3". The patient underwent the following laboratory tests and procedures: sars-cov-2 test: (09Jan2022) positive, notes: Nasal Swab. Therapeutic measures were not taken as a result of vaccination failure, covid-19. Patient did not take other vaccine in four weeks and no covid prior vaccination. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220109; Test Name: Rapid home test; Test Result: Positive ; Comments: Nasal Swab
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 21.01.2022
- Impfdatum
- 28.12.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Excessive eye blinking
Grimacing
Tic
Symptomtext
3 days after the shot patient developed uncontrollable facial tics, blinking, grimacing and shrugging that he?s never had prior.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Excessive eye blinking
- Hospital-Tage
- -
- Labordaten
- Pediatrician visit
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- HI
- Alter
- 10,0
- Geschlecht
- M
- Eingang
- 20.01.2022
- Impfdatum
- 20.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
No adverse event
Symptomtext
Patient was given 30 micrograms dose of Pfizer who was suppose to receive 10 micrograms dose of Pfizer. Patient waited 15 minutes with no adverse effects noted. Patient family was called and notified who was okay with the dose; "Okay. Thanks for letting me know."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No/Unknown
- Vorgeschichte
- No/Unknown
- Andere Medikamente
- No/Unknown
- Allergien
- No/Unknown
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- 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: nein
Incorrect dose administered
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- 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: ja
Underdose
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 18.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
Symptomtext
Patient received her 2nd dose of the Pfizer COVID-19 vaccine on 9/7/2021 and was due for a 3rd booster dose on 2/7/2022. Patient's booster dose was administered early on 1/18/2022 by pharmacist because it was not identified that it was too soon for her booster dose until after administration. Spoke with CDC representative and booster is considered valid. Patient notification completed and patient was advised of side effects to monitor for. Patient reported feeling fine on 1/19/2022 at 5pm and had not experienced any side effects from the vaccine. Patient will follow up with the pharmacy and primary care doctor with any concerns or adverse effects if they occur.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Error: Wrong Vaccine Formulation (ex. different manufact. initial and booster)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 19.01.2022
- Impfdatum
- 10.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
Error: Wrong Dose of Vaccine - Too High-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Error: Booster 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
- GA
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Underdose
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Underdose
Symptomtext
Error: Wrong dose of vaccine - too low.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Underdose
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- 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: ja
Confusional state
Symptomtext
Systemic: Confusion-Mild, Additional Details: pt did not go with the paramedics, but 911 was called. held pt from 12:45pm (injection time) to 1:36pm (after additional monitoring)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Confusional state
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 9,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 09.01.2022
- Beginn
- 09.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Symptomtext
Error: Wrong Dose of Vaccine - Too High-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 16.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Vulval ulceration
Symptomtext
within 48hours of third dose of Pfizer covid vaccine developed Lipschutz ulcers on her vulva. no fever
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vulval ulceration
- Hospital-Tage
- -
- Labordaten
- exam
- Aktuelle Erkrankungen
- none other than mild asthma, not requiring inhaled steroid or oral prednisone
- Vorgeschichte
- Asthma GERD
- Andere Medikamente
- prilosec
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 10,0
- Geschlecht
- F
- Eingang
- 17.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Symptomtext
Error: Patient Too Young for Vaccine Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 17.01.2022
- Impfdatum
- 17.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Peripheral swelling
Symptomtext
Patient had slight swelling on his left arm within the medial epicondyle area. The patient was vaccinated at 11am, and symptoms appeared at 11:35am. Patient was advised to take ibuprofen, and monitor for any worsening symptoms. Patient was advised to go to the emergency room immediately if symptoms worsen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Peripheral swelling
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 17.01.2022
- Impfdatum
- 17.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
No adverse event
Symptomtext
PATIENT RECEIVED A DOUBLE BOOSTER OF PFIZER VACCINE. NO ADVERSE REACTIONS HAVE BEEN REPORTED. I WILL REVIEW POLICY AND PROCEDURE .
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 16.01.2022
- Impfdatum
- 16.01.2022
- Beginn
- 16.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
No adverse event
Symptomtext
11 year old male received 0.3ml of an adult Pfizer. Father informed and verbalized understanding of the error. Patient escorted to observation with no reactions noted. Advised father to follow up with the pediatrician if any severe symptoms occur. Patient discharged with his father.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- DENIES
- Vorgeschichte
- DENIES
- Andere Medikamente
- DENIES
- Allergien
- DENIES
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 7,0
- Geschlecht
- F
- Eingang
- 15.01.2022
- Impfdatum
- 15.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
No adverse event
Symptomtext
PT receive Pfizer 12+ 0.3 mL dose and should have received Pfizer 5-11 0.2mL dose No adverse reactions noted PT stayed in facility greater than 30 min
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- none required
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 14.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
No adverse event
Symptomtext
Pt arrived for first dose vaccine. Guardian advised Pt was 11 years old. Registration and vaccinator confirmed birthday but missed that the Pt just turned 12 years old. Pt was given Pediatric pfizer by mistake instead of adult pfizer. Guardian made aware. Pt had no complications and left stable.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 5,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Vertigo
Symptomtext
vertigo after post vaccination after day 5
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vertigo
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Pepcid
- Allergien
- Amoxicillin
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 11,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
The patient was mistakenly given a dose of Pfizer vaccine intended for a person 12 years or older when she should have been given a pediatric dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- HI
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 13.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
Symptomtext
Booster dose given within 5 months.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 12.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
No adverse event
Symptomtext
PT DOES NOT SHOW ANY ADVERSE REACTION AS OF NOW. PT WAS GIVEN A BOOSTER SHOT 2 MONTHS AFTER THE SECOND VACCINATIONS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- N/A
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 12.01.2022
- Impfdatum
- 08.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Epistaxis
Nasal discomfort
Scab
Symptomtext
On late Monday night around 11 pm, Patient laid down to go to sleep after taking her regular spray of Fluticasone in each nostril shortly before, and immediately when she laid down, she felt blood going down the back of her throat and sat up and her right nostril was bleeding. It was a constant flow and so we had her lean slightly forward and applied pressure to her nose for about an hour, every 10 minutes releasing pressure to see if it had stopped. It wouldn't stop so I placed a call to the doctor's office after hours service and a nurse walked me through other tactics we could try to get it to stop. We tried repositioning the pressure on the nose and also tried a piece of gauze with a couple drops of water on it to place it in the nostril to put pressure on it once again and eventually, after 2 and a half hours, the bleeding stopped. The next morning, Tuesday 1/11/2022, I made an appointment for Patient to be checked out at her pediatrician's office with Dr. She checked Patient's nose and saw it looked raw inside and also a scab over a capillary (I think that is what you call it) which is where the bleeding was coming from. Dr. recommended an ENT referral for further treatment but also recommended Patient not use Fluticasone right now until the nose heals and also to use just a saline nose spray to humidify the nose, use a q-tip to apply vasoline to inside of nose 2 times a day, and also to use a humidifier in bedroom at night. We have been able to manage to keep Patient's nose moist so that the nosebleed has not reoccurred. She has been weak since the nosebleed and has gradually gotten strength back but her nose is very irritated and when wearing a mask at school today, she could not breathe well due to her nose irritation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asthenia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- Reactive airway disease, innocent heart murmur, History of seasonal allergies
- Andere Medikamente
- Fluticasone, Zyrtec, Claritin, children's multivitamins
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 12.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood pressure increased
Peripheral coldness
Vertigo
Symptomtext
elevated blood pressure, cold hands and feet, vertigo
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood pressure increased
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- hypertension
- Andere Medikamente
- Flexeril 10mg, Tramadol, Cozaar, Tizanidine, ondanstron, medrol dospak
- Allergien
- Quinolones, NSAID
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 08.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
No adverse event
Symptomtext
0.2ML OF PURPLE CAP PFIZER ADMINISTERED INSTEAD OF ORANGE CAP. NO REPORTABLE ADVERSE EFFECT BY THE EVENING BY MOTHER
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 9,0
- Geschlecht
- F
- Eingang
- 08.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
No adverse event
Symptomtext
PT RECEIVED 0.2ML OF THE PURPLE CAP FORMULATION INSTEAD OF ORANGE CAP. NO REPORTABLE SIDE EFFECTS BY MOTHER IN EVENING
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 5,0
- Geschlecht
- F
- Eingang
- 08.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
No adverse event
Symptomtext
PT RECEIVED 0.2ML OF ADULT PURPLE CAP FORMULATION. SHOULD HAVE RECCEIVED 0.2ML OF ORANGE CAP. BY EVENING, NO NOTICABLE ADVERSE REACTIONS BY MOTHER
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 07.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
Patient received 4th covid shot when not currently approved. Patient made appointment as 3rd shot. Patient said she was immunocompromised.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 07.01.2022
- Impfdatum
- 30.12.2021
- Beginn
- 02.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Tinnitus
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tinnitus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Vitamin D vitamin B, calcium
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 07.01.2022
- Impfdatum
- 31.12.2020
- Beginn
- 08.02.2021
- Tage bis Beginn
- 39,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Haemoglobin decreased
Heavy menstrual bleeding
Menstrual disorder
Symptomtext
After the second dose of moderna I started having an unusual and excessive menstrual flow. Went to the OBGYN for a check up and nothing seems to be wrong and it all started after the second dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Haemoglobin decreased
- Hospital-Tage
- -
- Labordaten
- Low hemoglobin, went from 14 to 10 in a few months after the second dose.
- Aktuelle Erkrankungen
- NO
- Vorgeschichte
- NO
- Andere Medikamente
- NO
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 06.01.2022
- Impfdatum
- 30.12.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Tinnitus
Symptomtext
I had my shot on a Thursday morning , Dec. 30, at 10:00 AM. On Friday, Dec. 31, I noticed both ears started ringing in the morning. It has not gone away and it's been one week.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tinnitus
- Hospital-Tage
- -
- Labordaten
- I haven't had any tests yet.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Synthroid 50MCG Liothyronine 5MCG (2 tablets in the morning) Bupropion 100MG SR 1 time per day Progesterone 200MG Vitamin D and K Glucosomine Bio-identical hormone replacement (pellets)
- Allergien
- Latex
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 06.01.2022
- Impfdatum
- 28.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
The individual is 14 years old and was given Pfizer Booster dose. The booster dose was only approved for 16+ as of the date it was administered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 06.01.2022
- Impfdatum
- 04.01.2022
- Beginn
- 04.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Hypoaesthesia
Symptomtext
Vaccinated: 10:51AM Reaction: 11:14AM 23 minutes after receiving 1st dose Pfizer, pt reported feeling like she was going numb. Vitals: 143/92, 72, 16, 100% O2 Patient was given crackers, rested, and felt better. Patient was stable and released from vaccination site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypoaesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- PMH: hypothyroidism, adrenal insufficiency, type 2 polyglandular autoimmune syndrome
- Andere Medikamente
- Medication list: Premarin 1.25mg - 1 tab daily, fludrocortisone 0.1mg tab - 1 tab BID, hydrocortisone 10mg - 1 tab QAM and 0.5 tab in afternoon, levothyroxine 88mcg - 1 tab QAM
- Allergien
- Allergies: Promethazine
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 06.01.2022
- 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: nein
Dysmenorrhoea
Heavy menstrual bleeding
Menstruation irregular
Symptomtext
Woke in middle of night 16 hours post booster vaccine with intense menstrual cramps and heavy bleeding. Past month's menses was on time and normal and ended 1 week prior to receiving the booster vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dysmenorrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- vaso-vagal syndrome w/prolonged QT wave
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 04.01.2022
- Impfdatum
- 30.12.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Somnolence
Symptomtext
Could not wake up day after vaccine. Hard time walking after woke up. Out of it until Sunday. Felt almost normal on Sunday.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Somnolence
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 8,0
- Geschlecht
- F
- Eingang
- 04.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Error: Wrong Vaccine Formulation (ex. different manufact. initial and booster)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 03.01.2022
- Impfdatum
- 30.12.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymphadenopathy
Symptomtext
Swollen lymph node / arm pit on left arm - same side as injection site
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymphadenopathy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 03.01.2022
- Impfdatum
- 03.01.2021
- Beginn
- 03.01.2021
- 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
Error: Booster 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
- CA
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 31.12.2021
- 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
Inappropriate schedule of product administration
Symptomtext
Error: Booster 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
- -
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 30.12.2021
- Impfdatum
- 22.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Hypoaesthesia
Symptomtext
5mins post vaccination pt c/o slight numbness to feft fingertips for a few seconds. Numbness subsided. Injection in L deltoid. No redness or swelling noted Vitals: 87/58, 66, 24, 91% -- > 91/57, 87, 22, 100% -- > 89/56, 87, 22 -- > 19:25 89/59, 85, 20, 100% Pt c/o thirst. Pt given orange juice and pt reports feeling better. 19:25 Instructed pt to contact MD if not feeling well. Do not hesitate to seek ER assistance if needed. Pt verbalized understanding. Pty stable and released from vaccination site in no distress.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypoaesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- PMH: Major depressive disorder with single episode, remission status unspecified, Generalized anxiety disorder
- Andere Medikamente
- Medications: citalopram (CeleXA) 20 mg tablet take 1 Tab (20 mg total) by mouth daily buPROPion (WELLBUTRIN-XL) 300 mg extended release tablet take 1 Tab (300 mg total) by mouth every morning
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 29.12.2021
- Impfdatum
- 28.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Haemorrhage
Symptomtext
Systemic: BLEEDING AFTER INJECTION WAS GIVEN-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Haemorrhage
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 29.12.2021
- 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
Incorrect dose administered
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ME
- 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
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
Family of three individuals, a father and two daughters, approached vaccination table and placed all three forms on table. Vaccinator took the top paper and verified paperwork with individual seated in chair. Individual confirmed identity as a 17-year-old, and vaccination was administered. When the second child sat down, her identity was confirmed on the second sheet of paper presented, of which she stated that that was her sister who had just been vaccinated. The second individual then confirmed that she was the 17- year- old.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- No test needed.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Unknown
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 23,0
- 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: ja
Inappropriate schedule of product administration
Symptomtext
Patient received booster 3 months early
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -