- Staat
- MI
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 20.12.2023
- Impfdatum
- 20.01.2023
- Beginn
- 06.12.2023
- Tage bis Beginn
- 320,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Acute respiratory failure
COVID-19
Chest X-ray abnormal
Condition aggravated
Cough
Dyspnoea
Feeding tube user
Intensive care
Lung opacity
Mechanical ventilation
Pneumonia
Positive airway pressure therapy
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Superinfection
Symptomtext
Discharge Provider: MD Primary Care Physician at Discharge: MD Admission Date: 12/6/2023 Discharge Date: 12/14/2023 DETAILS OF HOSPITAL STAY: COVID [U07.1] Acute hypoxic respiratory failure (HCC) [J96.01] COVID-19 [U07.1] HOSPITAL COURSE: Patient is a 3 y.o. female with PMHx HIE, CLD, CP w/ GDD, dysphagia w/ gtube dependence, focal epilepsy, and sialorrhea who was admitted for acute hypoxic respiratory failure 2/2 COVID and superimposed pneumonia. Patient initially started symptoms of cough and congestion on 12/3. She had elevated fevers of 102-103 F. She then progressed to having increased work of breathing on 12/5 which prompted her to be evaluated in the ED. Upon arrive, the patient was placed on high flow nasal cannula. Viral studies were conducted and found to be positive for COVID. An x ray was performed which showed a right upper lobe opacity concerning for pneumonia. She received breathing treatments without benefit. She was admitted to the PICU for further care. She was advanced from HFNC to BiPAP. She was weaned to NIPPV on 12/7 and then to CPAP on 12/8. She was receiving scheduled breathing treatments. She completed 5 days of remdesivir and 5 days of antibiotics for pneumonia. She did receive steroid treatment. She was given g tube feedings at a continuous rate initially due to her respiratory status. She was slowly tapered to room air and returned to her normal feeds. Pulmonology was consulted to evaluate her for a vest for airway clearance, which was ordered. A CXR was ordered which was improved. On 12/14, she was deemed stable for discharge and will follow up with her PCP and necessary specialists (pulmonology, neurology). She will complete her 5 day orapred burst at home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 8,0
- Labordaten
- -
- Aktuelle Erkrankungen
- 1/19/2023 - 1/20/2023 (41 hours) Hospital Acute respiratory distress [R06.03]
- Vorgeschichte
- Hypoxic ischemic encephalopathy Anemia Cortical visual impairment Nystagmus Mixed cerebral palsy (HCC) Global developmental delay Infantile spasms (HCC) Gastrostomy tube dependent (HCC) Sialorrhea Hypertonia Thalassemia minor CLD (chronic lung disease) CP (cerebral palsy), dystonic rigid (HCC) Tight heel cords, acquired, bilateral Sleep difficulties Dysphagia, oropharyngeal phase Acute hypoxic respiratory failure (HCC) Focal epilepsy (HCC)
- Andere Medikamente
- acetaminophen (TYLENOL) 32 MG/ML suspension albuterol (PROVENTIL) (2.5 mg/3 mL) 0.083 % nebulization albuterol HFA (ALBUTEROL) 108 (90 Base) MCG/ACT inhaler albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT in
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 25.07.2023
- Impfdatum
- 19.09.2022
- Beginn
- 07.03.2023
- Tage bis Beginn
- 169,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Hypoxia
Symptomtext
ACUTE RESPIRATORY FAILURE ACUTE HYPOXEMIC RESPIRATORY FAILURE HYPOXIA
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 0,5
- Geschlecht
- M
- Eingang
- 15.10.2022
- Impfdatum
- 16.09.2022
- Beginn
- 26.09.2022
- Tage bis Beginn
- 10,0
- Dosis
- 1
- Route/Site
- SYR / RL
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Death
Pulse absent
Symptomtext
Unexpected death- taking a nap in the afternoon and found pulseless in crib.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- otitis media
- Vorgeschichte
- gastroesophageal reflux
- Andere Medikamente
- famotidine, omeprazole
- Allergien
- None known
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 14.09.2022
- Impfdatum
- 27.08.2022
- Beginn
- 30.08.2022
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Angiogram cerebral abnormal
Aphasia
Arteriogram carotid abnormal
Barium swallow
Cerebral infarction
Cerebrovascular accident
Clumsiness
Echocardiogram normal
Facial paralysis
Fall
Laboratory test
Magnetic resonance imaging head abnormal
Symptomtext
Hospitalized 8/30 - 9/2 after onset R sided facial droop, not talking and clumsy falling towards her R side - admitted and found to have a L CVA - evaluated by neurology, genetics, hematology - started on 1/2 81 mg aspirin - receiving ST and OT due to persistent speech deficits, motor deficits resolved
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- 2,0
- Labordaten
- Brain MRI without contrast 8/30 - Hyperacute infarct (< 6 hrs) at the left striatum. Patent intracranial arteries with no abrupt cut-off, dissection, focal stenosis or aneurysm Brain MRI and MRA head without contrast 8/30 - Hyperacute infarct (< 6 hrs) at the left striatum. Patent intracranial arteries with no abrupt cut-off, dissection, focal stenosis or aneurysm. repeat MRI Brain with/without contrast 8/31 - Expected evolution of an evolving acute infarct within the left striatum. No evidence of hemorrhagic conversion. No evidence of high-grade flow-limiting stenosis, abrupt vessel cut off, dissection, or aneurysm of the cervical vasculature. MRA neck with/without contrast 8/31 - expected evolution of an evolving acute infarct within the left striatum. No evidence of hemorrhagic conversion. No evidence of high-grade flow-limiting stenosis, abrupt vessel cut off, dissection, or aneurysm of the cervical vasculature. Echo 9/1 - normal intracardiac anatomy with normal biventricular size and systolic function modified barium swallow with speech 9/1 - coordinated suck/swallow - no reguritation/aspiration Extensive lab workup 8/30 through 9/2 - awaiting extended gene workup
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none noted
- Andere Medikamente
- none
- Allergien
- no known allergies
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 16.10.2023
- Impfdatum
- 03.08.2022
- Beginn
- 12.08.2022
- Tage bis Beginn
- 9,0
- Dosis
- 1
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Asthenia
Confusional state
Electrocardiogram normal
Electroencephalogram normal
Fall
Loss of consciousness
Musculoskeletal stiffness
Pallor
Symptomtext
Patient was at daycare, experiencing a typical day, sitting and eating a snack, when she made a sqeak/squeal and her arms first curled and then went straight up overhead. The daycare staff stated patient's entire body when stiff which caused her to push away from the table. She fell back off of chair and landed on left side. Patient had loss of consciousness after the accident for about 30 seconds before becoming alert again. When she was alert, she was confused of what happened, pale, and a little weak feeling. Patient correctly answered all cognitive questions immediately after the incident. Staff also stated patient was afebrile after accident. This incidence prompted her parents to bring her to the ED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- Physical exam and Lab/SPO2 Interpretation was normal 08/12/2022. Electroencephalogram 08/17/2022 10:33 am. Result of Activation Procedures: Hyperventilation: Produced no abnormalities. Photic Stimulation: Produced no abnormalities. EKG Description: The EKG tracing was independently reviewed from the EEG waves and was Normal. Normal electroencephalogram, awake, drowsy, asleep and for age with activation procedures. There are no focal lateralizing or epileptiform features.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Children's Zyrtec, Miralax
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- ND
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 15.03.2023
- Impfdatum
- 03.03.2023
- Beginn
- 06.03.2023
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
CSF protein increased
Guillain-Barre syndrome
Magnetic resonance imaging
Symptomtext
Weakness , elevated CSF protein -guillian barre
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Guillain-Barre syndrome
- Hospital-Tage
- 3,0
- Labordaten
- Elevated CSF protein Nl MRI
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Language delay
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 26.12.2022
- Impfdatum
- 06.12.2022
- Beginn
- 06.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Abdominal distension
Acute haemorrhagic oedema of infancy
Ecchymosis
Erythema multiforme
Full blood count abnormal
Generalised tonic-clonic seizure
Joint swelling
Laboratory test
Metabolic function test normal
Microcytic anaemia
Normocytic anaemia
Occult blood positive
Oedema
Peripheral swelling
Postictal state
Rash
Rash erythematous
Rash macular
Symptomtext
One hour after vaccine, patient had a generalized tonic clonic seizure. Forehead temperature prior to seizure was 100.3F. Patient had received acetaminophen 15 mins prior to seizure and has a history of one previous febrile seizure. Post-ictal for 15 mins and returned to baseline. Patient given ibuprofen and acetaminophen around the clock for 24 hours and was on amoxicillin for otitis media. On 12/8/2022, PCP re-evaluated and said otitis improving, no other source of infection. That evening, patient developed nonspecific rash. On 12/9/2022, patient had developed diffuse papular and macular erythematous rash and evaluated in ED. Given steroids and started Zytrec. Amoxicillin discontinued. Rash progressed to edema and swelling of legs/knees, worsening rash and lesions. Saturday 12/10/2022 rash progressed to ecchymotic abdominal lesions and abdominal distention. Returned to ED and admitted 12/10/2022. Diagnosed with erythema multiforme minor. Given hydroxyzine and topical steroids. Discharged 12/11. Swelling progressed to hands on 12/12/2022. Dermatology follow up on 12/13/2022 concern for acute hemorrhagic edema of infancy. Labs and UA performed; occult stool ordered 12/14/2022 due to anemia. Rash improving and resolving, returning to baseline. Occult stool positive 12/16/2022. Dermatology follow up 12/16/2022 with tentative final diagnosis of acute hemorrhagic edema of infancy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Generalised tonic-clonic seizure
- Hospital-Tage
- 1,0
- Labordaten
- CBC: normocytic to microcytic anemia CMP: grossly normal Urinalysis: normal Occult stool: positive
- Aktuelle Erkrankungen
- Otitis media at time of vaccination (day 5) Otitis media (1 month prior) Viral URI (2 weeks prior)
- Vorgeschichte
- One febrile seizure Stills murmur
- Andere Medikamente
- Amoxicillin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 09.12.2022
- Impfdatum
- 12.10.2022
- Beginn
- 14.10.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Electroencephalogram normal
Seizure
Symptomtext
Afebrile isolated seizure within 36 hrs after vaccine. Normal medical w/u for other etiology at ER and nml f/u EEG
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- cow's milk
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 19.11.2022
- Impfdatum
- 12.11.2022
- Beginn
- 12.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Immediate post-injection reaction
Loss of consciousness
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Fainting / Unresponsive-Mild, Additional Details: Pt reported to clinic for 18m - 4y COVID vaccine. Vaccine was within expiration and BUD. This is pt's second dose. Pt was given injection by LPN and within 30 seconds patient became unconscious. Pt was unconscious for less than 30 seconds. EMS activated immediately. Pt placed on bed and sat up. Pt awake at time of provider entry into room. Vital signs assessed and pt sitting on exam table while EMS is arriving. Pt was awake and alert when EMS arrived. EMS recommended f/u at local emergency room.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 1,3
- Geschlecht
- M
- Eingang
- 07.11.2022
- Impfdatum
- 09.08.2022
- Beginn
- 10.08.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Pyrexia
Restlessness
Seizure
Somnolence
Vomiting
Symptomtext
restlessness, vomiting, fever, seizure subsequently taken to ER by ambulance and appeared sleepy after event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- None in ER
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 2,0
- Geschlecht
- M
- Eingang
- 04.11.2022
- Impfdatum
- 28.10.2022
- Beginn
- 29.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Febrile convulsion
Symptomtext
24 hours later, febrile seizure occurred. Patient has never seized, nor had any reaction with Covid-19 vaccines #1 or #2.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Febrile convulsion
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 1,5
- Geschlecht
- M
- Eingang
- 03.11.2022
- Impfdatum
- 09.08.2022
- Beginn
- 10.08.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Generalised tonic-clonic seizure
Symptomtext
About 26 hours after vaccination, patient had a generalized tonic clonic seizure which spontaneously resolved. He was subsequently taken to the emergency room, treated with normal saline and acetaminophen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Generalised tonic-clonic seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 0,5
- Geschlecht
- F
- Eingang
- 31.10.2022
- Impfdatum
- 30.09.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 7,0
- Dosis
- UNK
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Electroencephalogram abnormal
Infantile spasms
Magnetic resonance imaging head abnormal
Thalamic stroke
Symptomtext
1 week after vaccines, patient presented to office with infantile spasms. In ER and admission, Infantile spasms were confirmed on EEG and MRI demonstrated thalamic stroke
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Thalamic stroke
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 06.10.2022
- Impfdatum
- 08.08.2022
- Beginn
- 09.08.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood glucose normal
Cyanosis
Dizziness
Febrile convulsion
Hypotonia
Influenza A virus test negative
Influenza virus test negative
Musculoskeletal stiffness
Respiratory syncytial virus test negative
SARS-CoV-2 test negative
Symptomtext
On 8/9/22 was outside playing. Came in from outside and feel backwards. Initially limp 1-2 minutes, then became stiff and tightened whole body for about 2-3 minutes noted body appeared purplish blue. After five minutes started moving arms and hands and by 10 minutes was normal. EMS was called and transported child to local ER. Discharge diagnosis was febrile seizure. Follow up patient has no further events or illnesses.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Febrile convulsion
- Hospital-Tage
- -
- Labordaten
- 8/9/2022 glucose 165, influenza a/b, rsv, covid all negative
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 01.10.2022
- Impfdatum
- 23.09.2022
- Beginn
- 23.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Dyskinesia
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Fainting / Unresponsive-Severe, Additional Details: On 09/23/2022 at around 1805, the emergency medical button on the wall was pushed and 911 was contacted for an emergency in the clinic. The patient received her first dose of the Covid-19 vaccination. Immediately after the vaccination, the patient started violently jerking and was unconscious. The patient was diaphoretic also. This is the second episode of the FNP being alone and activating the emergency button and no one coming.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 06.09.2022
- Impfdatum
- 02.09.2022
- Beginn
- 03.09.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Febrile convulsion
Gaze palsy
Pyrexia
Tremor
Unresponsive to stimuli
Symptomtext
Had febrile seizure the day following vaccination at 5pm. Woke up with low grade fever from nap that afternoon, parents gave Tylenol. About an hour after that, became unresponsive, then arms shaking, eyes rolled back, Dad picked her up, couldn't keep her alert. Entire event lasted about a minute. Dad blew in her face and that started to make her more responsive. Called EMS, who did vital signs that were normal. Parents took her to ER where diagnosis of febrile seizure was made (temp was 103-104) and pt. is back to baseline.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Febrile convulsion
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- Acute otitis media 8/3/22
- Vorgeschichte
- history of PE tubes
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 06.09.2022
- Impfdatum
- 26.08.2022
- Beginn
- 27.08.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bell's palsy
CSF test
Facial paralysis
Full blood count
Guillain-Barre syndrome
Immunoglobulin therapy
Laboratory test
Lumbar puncture
Magnetic resonance imaging head
Magnetic resonance imaging spinal
Metabolic function test
Respiratory viral panel
Symptomtext
Bell's Palsy-left side of face, slowly progressing paralysis of right side- diagnosed with Guillain-Barre Syndrome. Symptoms developed within 24 hours of second vaccine. Requiring IVIG treatment for the next 5 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bell's palsy
- Hospital-Tage
- -
- Labordaten
- Lumbar Puncture with CSF testing, MRIs of spine and head, CBC, CMP, Respiratory Panel, SARS testing
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Developmental Delay
- Andere Medikamente
- None
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 19.08.2022
- Impfdatum
- 17.08.2022
- Beginn
- 19.08.2022
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Crying
Febrile convulsion
Irritability
Partial seizures
Staring
Symptomtext
Patient arrived to ED with CC of Focal/Febrile Seizure. Parents stated that pt was at home and began to become fussy and crying inconsolably and then began to stare off into space. Pt then proceeded to make a gagging sound and she started to then fall asleep. Upon arrival, pt is now mildly fussy but eating and acting normal.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Febrile convulsion
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Melanocytic nevus of scalp, speech delay, strawberry hemangioma of skin
- Andere Medikamente
- None
- Allergien
- NKDA, no reported food allergies
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 18.08.2022
- Impfdatum
- 11.08.2022
- Beginn
- 14.08.2022
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Asthma
Respiratory distress
Respiratory symptom
Symptomtext
Pt. received COVID vaccine on 8/11/22. Pt developed URI symptoms with severe asthma/resp. distress 4 days later.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Respiratory distress
- Hospital-Tage
- 1,0
- Labordaten
- N/A
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 17.08.2022
- Impfdatum
- 21.07.2022
- Beginn
- 30.07.2022
- Tage bis Beginn
- 9,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Arnold-Chiari malformation
Clumsiness
Electroencephalogram abnormal
Eye movement disorder
Headache
Laboratory test normal
Magnetic resonance imaging head abnormal
Moaning
Psychomotor hyperactivity
Seizure like phenomena
Unresponsive to stimuli
Vomiting
Symptomtext
Patient experienced seizure like activity a little over a week after his second dose. He has no prior hx of seizures. He woke up from a nap groaning and then vomited. He became unresponsive with his eyes open and deviating to the right. He vomited several more times and remained unresponsive. He had no response to painful stimuli. An ambulance was called and after about 20 mins from the onset he closed his eyes and appeared to be sleeping. Upon arrival in the ED he woke up. He was slow to respond, complained of a headache and vomited 2 more times. He was admitted overnight for observation and did not experience any further episodes. Over the next 5 days he appeared hyperactive and clumsy and has since returned to his normal self.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure like phenomena
- Hospital-Tage
- 1,0
- Labordaten
- Lab results were within normal limits EEG showed continuous focal seizure activity in the right occipital lobe and occasionally the left temporal and occipital lobes. MRI of brain showed a Chiari malfunction type 1 but nothing related to his episode.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Kids multivitamin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 1,0
- Geschlecht
- F
- Eingang
- 05.08.2022
- Impfdatum
- 14.07.2022
- Beginn
- 15.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Computerised tomogram normal
Laboratory test
Seizure
Symptomtext
"Patient is a 13-month-old otherwise healthy female child, immunizations up-to-date, who had 2 episodes of seizures, one at daycare and 1 in the ED, improved with IV Ativan 0.5 mg, CT scan negative for bleed or obvious mass, screening labs unrevealing, no trauma and no fever, did have a viral syndrome a week ago but recovered completely. Did have a COVID immunization yesterday. Pediatric hospitalist recommends transfer for pediatric neurology evaluation, emergency consulted and will accept the patient in transfer. Neuro consulted and will assume care of the patient. Patient will be admitted for further treatment and diagnostic testing as felt indicated. Admitting physician aware of reported history, exam findings, and ED results."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- 5,0
- Labordaten
- CT Scan 7/15/22
- Aktuelle Erkrankungen
- Patient had a viral syndrome/febrile illness a week prior with fever and balance issues that resolved by the weekend.
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 05.08.2022
- Impfdatum
- 03.08.2022
- Beginn
- 03.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dizziness
Syncope
Symptomtext
Pt had a syncopal event w/ associated dizziness. Vitals: 95/69, 84, 18, 99.0F, 100% O2 Pt given 2L O2 Pt stable and released from the vaccination site. Recommended pt F/U w/ PCP.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- PMH: Alopecia Areata
- Andere Medikamente
- Medications: Ketoconazole shampoo Fluocinonide 0.05%
- Allergien
- Allergies: None
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 28.07.2022
- Impfdatum
- 24.07.2022
- Beginn
- 24.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fall
Presyncope
Visual impairment
Symptomtext
Systemic: Vasovagal reaction-Mild, Additional Details: ~5 minutes following vaccination pt told his father he started seeing "black spots" and fell. Denied headstrike. Returned to clinic where I gave the pt water, monitored BP and pt status for ~15 minutes. Pt left in stable condition, no longer experiencing any symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 25.07.2022
- Impfdatum
- 22.07.2022
- Beginn
- 22.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Febrile convulsion
Symptomtext
Febrile Seizure, Tmax 102F, 911 called, brought to local hospital, treated with acetaminophen, no recurrence
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Febrile convulsion
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Conjunctivitis 6/30/22
- Vorgeschichte
- Atopic dermatitis Chronic otitis media requiring tubes
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 22.07.2022
- Impfdatum
- 19.07.2022
- Beginn
- 19.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Body temperature increased
Condition aggravated
Seizure
Symptomtext
Patient is a(an) 4 y.o. male who is here with parent, an additional history source. Patient had febrile seizure in May. It was associated with HFMD, had a fever and then had a seizure which was still happening when they got to the ED. He recovered. 2 nights ago he was playing video game and had a seizure that lasted 2 minutes and was generalized. He had 103 temp at the time.he got MMRV, DTaP-IPV and Pfizer COVID vaccine 8 hours prior to the seizure. After the seizure mom gave ibuprofen, he fell asleep for about 20 min, and awoke afebrile and was acting normal. He has been normal since.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Had one previous febrile seizure
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 1,4
- Geschlecht
- M
- Eingang
- 12.07.2022
- Impfdatum
- 11.07.2022
- Beginn
- 11.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LL
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Body temperature increased
Febrile convulsion
Feeling abnormal
Lethargy
Loss of consciousness
Seizure
Skin warm
Unresponsive to stimuli
Viral test negative
Symptomtext
After receiving vaccination, patient was out of it for approximately ~15 mins, after that period seemed lethargic but otherwise normal. Patient showed no other adverse reaction until time for his nap at 12:40p, when he felt warm to the touch but underarm temperature reading was 98.7. He woke up atypically early at 2:50p, but laid in crib seemingly playing quietly. At 3:56p, mother heard whimpering sound and went to check on patient who was convulsing and unconscious until EMS arrived at 4:03p, he was very hot but EMS was unable to get an accurate temperature reading. Convulsions stopped when paramedics arrived at approx. 4:03p and patient was unresponsive for an additional approx. 10 mins. Patient was placed under ice by EMS and had a temperature reading of 102.4 when he arrived Hospital in approx 20-30 mins later.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Febrile convulsion
- Hospital-Tage
- -
- Labordaten
- Virology panel was all negative.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 07.07.2022
- Impfdatum
- 07.07.2022
- Beginn
- 07.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 6
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Headache
Loss of consciousness
Neck pain
Pallor
Symptomtext
Patient was here today scheduled in the Covid clinic for his first Pfizer-BioNTech COVID-19 Vaccine injection. Injection was given 0.2mL into right thigh at approx 11:00am, I had entered vaccine info into computer, scheduled next appt and dad, the patient and other person were waiting their 15-20min. I had checked on them twice during their wait period and he was doing fine. At around the 20min mark, dad hollared for a nurse. When I entered the room, patient was in dads arms, feet on floor, color was pale/ grayish. I took Him and layed him on the exam room table. He was breathing and starting to move around some. dad watched him until I grabbed stethascope and cuff. His BP lying down was 100/62, 2 Providers came in to check on him. Dad said he had complained of his head and neck hurting and then feeling weak prior to passing out. The Provider continued to assess patient, asked pt/dad questions, listened to lung sounds, etc. When pt was sat up, his BP was 96/64. We gave him cool compress, and then an ice pack to apply to back of neck and a cup of cold water. After patient was feeling better he was able to go home and was advised to take it easy and relax the rest of the day. ( also Dad had mentioned earlier when I was in the room with them, that they live in/near forest/woods- They had removed a very small tick from between his toes within the last day or so) Pfizer- Covid- 6mo-4yr (Maroon top) Lot # FT9142 exp 9/7/22 Sodium Chloride 0.9% lot# 6024132 Exp 5/31/23 (2.2mL mixed with vial) Vial opened and mixed at 7:57am on 7/7/22- good for 6 hours
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- cellulitis of right eyelid, tick bite
- Vorgeschichte
- no
- Andere Medikamente
- None reported prior to vaccination, after reviewing chart, possibly cefdinir
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 01.07.2022
- Impfdatum
- 01.07.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood test
Fall
Hyporesponsive to stimuli
Loss of consciousness
Pallor
Unresponsive to stimuli
Vision blurred
Symptomtext
Pfizer 6mo-4yo EUA, health surveillance program, and screening form reviewed with mother, no concerns. Mother requesting client to be vaccinated in vastus lateralis instead of deltoid. Issued immunization record card. Began 15 minute observation after administration. Five minutes after administration, client fell. RN observed client brace with arms and knees, did not hit head. Client slow to respond to mother calling client's name. Client stood up unassisted and mother picked up into lap, then client's eyes became unfocused, lip color paled, skin paled, and client became unresponsive. After five seconds, client spontaneously became alert and went to sit up. Mother and RN encouraged client to remain lying down. Water and graham crackers provided; client able to tolerate. Mother stated client has passed out before with vaccines; mother also admitted personal history of passing out with vaccines, blood draws, and medical procedures. Client answers questions appropriately and engaging with mother and RN. After five minutes, mother encouraged client to try sitting up. Client able to tolerate sitting up. Lip color pink and skin color returned to normal. After five minutes of sitting, mother asked client if client feels okay. Client stated feeling okay. RN escorted mother and client from clinic to private vehicle.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Has had a prior syncopal episode with vaccination.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- Mother stated client has had syncopal episode with vaccines in the past but could not remember at what age or visit.
- Staat
- MN
- Alter
- 0,9
- Geschlecht
- F
- Eingang
- 29.06.2022
- Impfdatum
- 27.06.2022
- Beginn
- 28.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Electroencephalogram
Intensive care
Seizure
Symptomtext
Seizure within 48 hours of vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Intensive care
- Hospital-Tage
- -
- Labordaten
- EEG ongoing. Pt admitted to ICU
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Microcephaly, encephalomalacia with cerebral infarction
- Andere Medikamente
- Melatonin 1mg po HS
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 28.06.2023
- Impfdatum
- 26.09.2022
- Beginn
- 21.04.2023
- Tage bis Beginn
- 207,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthma
Condition aggravated
Hypoxia
Symptomtext
R09.02 HYPOXIA 4/20/2023 ASTHMA, UNSPECIFIED W ACUTE EXACERBATION
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 0,8
- Geschlecht
- M
- Eingang
- 08.05.2023
- Impfdatum
- 02.11.2022
- Beginn
- 22.11.2022
- Tage bis Beginn
- 20,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dehydration
Diarrhoea
Ear disorder
Ear infection
Hand-foot-and-mouth disease
Malaise
SARS-CoV-2 test negative
Symptomtext
He got sick on 11/08/22. We took him to the doctor was diagnosed with an ear infection and was prescribed Amoxicillin. He still had the ear infection on 11/22/22, so we went back to the doctor, and he was also diagnosed with hands foot and mouth as well. He was prescribed Amoxicillin-Pot Clavulanate. He got better, then we went back on 12/2/23, because he was having ear trouble again and was having diarrhea. Due to being dehydrated, we stopped taking Amoxicillin until his stomach got better and then we started Amoxicillin again. This lasted until 12/31/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dehydration
- Hospital-Tage
- -
- Labordaten
- 08NOV2022 COVID-19 Test - Negative; 02DEC2022 COVID-19 Test - Negative; 22DEC2022 COVID-19 Test - Negative
- Aktuelle Erkrankungen
- RSV
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Cow's Milk Protein
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 10.04.2023
- Impfdatum
- 07.10.2022
- Beginn
- 01.04.2023
- Tage bis Beginn
- 176,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest X-ray abnormal
Cough
Decreased appetite
Norovirus infection
Pneumonia
Pneumonia bacterial
Pyrexia
Symptomtext
My daughter initially had a cough. She was recovering from the Norovirus, but she had a cough that lingered. She developed a fever on the evening of 4/1/2023, and her fever worsened and spiked for a few days. At its lowest point, the fever was 100.8; at its highest, it was 102. I occasionally gave her TYLENOL to treat the fever, and it helped for a little while. It helped overnight and into the morning, but then she would get a fever again in the mid- to late afternoon or evening. On 4/4/2023, I took her the pediatric NP. The NP checked her lungs and determined that she needed a chest X-ray, which my daughter underwent at the radiology lab that day. It was determined that my daughter had bacterial bronchial pneumonia. The NP prescribed a ten-day course of amoxicillin. She also said that if my daughter needed TYLENOL for relief, it was okay to also give that to her. We were also advised to make sure she was getting plenty of fluids and that we should give her water or PEDIALYTE. We came home and followed the NP's orders. The fever went away as of the morning of 4/7/2023. My daughter then progressively got better. My daughter has regained about 85% of her appetite. She coughs less frequently now, but it's still persistent. We were told that this would probably happen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pneumonia
- Hospital-Tage
- -
- Labordaten
- 04APR2023 Chest X-Ray, Bacterial Bronchial Pneumonia detected
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 1,6
- Geschlecht
- F
- Eingang
- 30.03.2023
- Impfdatum
- 29.03.2023
- Beginn
- 29.03.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injected limb mobility decreased
Injection site pain
Injection site swelling
Symptomtext
Family called in to triage nurse at clinic 3/30/23 that patient had increased swelling and pain to right thigh with reduced motion of right thigh, more than expected with previous vaccines. No respiratory distress or GI distress.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Atopic dermatitis, lactose intolerance
- Andere Medikamente
- none
- Allergien
- lactose intolerance
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 28.12.2022
- Impfdatum
- 24.09.2022
- Beginn
- 09.12.2022
- Tage bis Beginn
- 76,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Ear infection
Pneumonia
Urinary tract infection
Symptomtext
Initial ILI followed by partial pneumonia (right), bilateral ear infection, and UTI.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pneumonia
- Hospital-Tage
- -
- Labordaten
- Physical exam
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 22.12.2022
- Impfdatum
- 29.08.2022
- Beginn
- 11.11.2022
- Tage bis Beginn
- 74,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Ear infection
Erythema
Peripheral swelling
Pneumonia
Pyrexia
Type IV hypersensitivity reaction
Symptomtext
A month after COVID-19 vaccine, went to 4 year old Pediatric appointment and received Influenza, MMR and DTaP vaccinations. Three days later arm became red and swollen; Four days later he started running high fevers, as high as 105. Pediatrician said the the MMR vaccine can have a delayed response of up to two weeks. A month later he developed Pneumonia with an ear infection. Went to urgent care and was given amoxicillin.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pneumonia
- Hospital-Tage
- -
- Labordaten
- Regular exam.
- Aktuelle Erkrankungen
- Had a cold 1 week before COVID-19 vaccine.
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- U
- Eingang
- 13.12.2022
- Impfdatum
- 07.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
AST/ALT ratio
Alanine aminotransferase increased
Aspartate aminotransferase increased
Bronchiolitis
Chest X-ray
Cough
Full blood count
Metabolic function test
Nasal congestion
Overdose
Pneumonia
Product preparation issue
Product use issue
Respiratory syncytial virus infection
White blood cell count increased
Symptomtext
FluZone Sanofi Date: 07Oct22; Pneumonia; She accidentally mixed the vial with 1.3 ml of diluent instead of 2.2 ml and realized this after she had administered 5 doses; She accidentally mixed the vial with 1.3 ml of diluent instead of 2.2 ml; Infiltrate on bronchiolitis; High WBC; High AST & ALT; High AST & ALT; RSV; Cough; Nasal congestion; This is a spontaneous report received from a contactable reporter(s) (Nurse) from medical information team. A 3-year-old patient received BNT162b2 (BNT162B2), on 07Oct2022 as dose 1 (maroon cap), single (Lot number: FT9142, Expiration Date: 31Dec2022), in right thigh for covid-19 immunisation; influenza vaccine (FLUZONE [INFLUENZA VACCINE]), on 07Oct2022 as dose 4, single (Lot number: UT7680MA) intramuscular, in left thigh. The patient's relevant medical history included: "Mom did not inform office staff patient developed hive", start date: 06Oct2022 (unspecified if ongoing), notes: Mom did not inform office staff patient developed hive on 06Oct2022.; "Cough", start date: 17Sep2022, stop date: 23Oct2022, notes: covid vaccine did not affect patient condition patient were improving, prior to receiving vaccine.; "Nasal congestion", start date: 17Sep2022, stop date: 23Oct2022, notes: covid vaccine did not affect patient condition patient were improving, prior to receiving vaccine.; "as patient(s) mom did not notify RN of rash which developed the night before patient received covid vaccine" (unspecified if ongoing), notes: developed the night before patient received covid vaccine. The patient's concomitant medications were not reported. The following information was reported: COUGH (non-serious) with onset 2022, outcome "recovered"; NASAL CONGESTION (non-serious) with onset 2022, outcome "recovered"; PRODUCT PREPARATION ISSUE (hospitalization, medically significant) with onset 07Oct2022, outcome "unknown", described as "She accidentally mixed the vial with 1.3 ml of diluent instead of 2.2 ml"; OVERDOSE (hospitalization, medically significant) with onset 07Oct2022, outcome "unknown", described as "She accidentally mixed the vial with 1.3 ml of diluent instead of 2.2 ml and realized this after she had administered 5 doses"; PNEUMONIA (hospitalization, medically significant) with onset 13Oct2022, outcome "not recovered"; RESPIRATORY SYNCYTIAL VIRUS INFECTION (non-serious) with onset 13Oct2022, outcome "not recovered", described as "RSV"; PRODUCT USE ISSUE (hospitalization, medically significant), outcome "unknown", described as "FluZone Sanofi Date: 07Oct22"; BRONCHIOLITIS (medically significant), outcome "unknown", described as "Infiltrate on bronchiolitis"; WHITE BLOOD CELL COUNT INCREASED (non-serious), outcome "unknown", described as "High WBC"; ASPARTATE AMINOTRANSFERASE INCREASED (non-serious), ALANINE AMINOTRANSFERASE INCREASED (non-serious), outcome "unknown" and all described as "High AST & ALT". The patient underwent the following laboratory tests and procedures: AST/ALT ratio (0-35): (13Oct2022) 82 uL, notes: Result: High AST& ALT; (13Oct2022) 105 uL, notes: Result: High AST& ALT; Chest X-ray: (13Oct2022) Plus RSV & Pneumonia, notes: Comments: Infiltrate on bronchiolitis; Full blood count (5.0-17.0): (13Oct2022) 20.7, notes: Result: High WBC. Units: Thou/uL; Metabolic function test: (13Oct2022) 20.7, notes: Result: WNL. Units: Thou/uL. Therapeutic measures were taken as a result of pneumonia. Additional information: The nurse reported a vaccination error involving the Pfizer COVID-19 vaccine maroon cap for 6 months to under 5 years. She was running a COVID clinic today for little ones and she had consulted the COVID vaccine prep and administration summaries from the CDC website and she had gotten confused about the diluent amount and accidentally mixed the vial with 1.3 ml of diluent instead of 2.2 ml and realized this after she had administered 5 doses and could not draw anymore, up to 5 kids (1 is almost 2, 1 patient is 2, 1 patient is 3, 1 patient is 15 months and 1 patient is 6 months) were administered with the vaccine; she stated that it was the last vaccine for 2 of the patients. The nurse made this mistake and sent an email to VAERS but didn't know what she should advise the patient's parents and if they should be worried about anything. On 06Dec2022, it was reported that contributing factors to the medication error was not having appropriate vaccine preparation and administration summary form from CDC website infront of nurse when reconstituting vaccine/not being able to draw up all vaccine doses at one time before administering to patients/nurse fulfilling regular office responsibilities (i.e. rooming patients, taking recording vitals, administering routine vaccines, answering/triaging phone calls, etc.) as well as running covid vaccine clinic alone. covid vaccine did not affect patient(s) condition patient was known to be sick with cough & congestion, which were improving to RN(s) knowledge, prior to receiving vaccine. Patient likely had RSV for 4-5 weeks which progressed into pneumonia independently from vaccine effects, as patient(s) mom did not notify RN of rash which developed the night before patient received covid vaccine. RN would not have given vaccine if aware of rash the night before. The Pfizer product did not had a causal effect to the adverse event. Pertinent details: Mom did not inform office staff patient developed hive on 06Oct2022. Improved at well visit on 06Oct2022 was not on vaccine questionnaire; did not notify RN when asked if patient(s) illness had changed since apt before receiving vaccine. Treated with 1 dose of IV ceftriaxone (600mg), then home with PO amoxicillin, 400mg/5mL; 7.4mL PO q 12h x10 days for pneumonia. Patient hospitalization d/t pneumonia is unrelated to patient receiving covid vaccine. Follow-up (10Oct2022): This is a spontaneous follow-up report received in response to the mail trail sent regarding the confirmation below mentioned query. The response included: Additional information: reporter phone number. Follow-up (06Dec2022): This is a spontaneous follow-up report from a contactable nurse. This nurse reported in response to HCP follow-up letter sent that included: Updated information included: Primary reporter suffix added. Primary reporter alternative phone number added. Age at vaccination added. Dose number added. Dose description updated. Route of administration added. Co-suspect added. Co-suspect (vaccination date, lot number, route of administration, dose number, dose description, anatomical location) added. Vaccine administered at private facility added. Other medical history added. Lab tests added. New events added. Event outcomes added.; Sender's Comments: Based on the available information in the case, the causal association between the event Pneumonia, Vaccine overdose, Inappropriate dilution of medication, Drug use for unapproved combination and the suspect drug BNT162B2 cannot be excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.,Linked Report(s) : US-PFIZER INC-202201212961 same reporter/drug/event, different patient;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pneumonia
- Hospital-Tage
- -
- Labordaten
- Test Date: 20221013; Test Name: RUQ PANEL; Test Result: 82 uL; Comments: Result: High AST& ALT; Test Date: 20221013; Test Name: RUQ PANEL; Test Result: 105 uL; Comments: Result: High AST& ALT; Test Date: 20221013; Test Name: Chest X-Ray; Result Unstructured Data: Test Result:Plus RSV & Pneumonia; Comments: Comments: Infiltrate on bronchiolitis; Test Date: 20221013; Test Name: CBC &Diff; Result Unstructured Data: Test Result:20.7; Comments: Result: High WBC Units: Thou/uL; Test Date: 20221013; Test Name: BMP; Result Unstructured Data: Test Result:20.7; Comments: Result: WNL Units: Thou/uL
- Aktuelle Erkrankungen
- Cough (covid vaccine did not affect patient condition patient were improving, prior to receiving vaccine.); Nasal congestion (covid vaccine did not affect patient condition patient were improving, prior to receiving vaccine.)
- Vorgeschichte
- Medical History/Concurrent Conditions: Hives (Mom did not inform office staff patient developed hive on 06Oct2022.); Rash (developed the night before patient received covid vaccine.)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 11.12.2022
- Impfdatum
- 06.12.2022
- Beginn
- 07.12.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal pain
Arthralgia
Face oedema
Gait inability
Inflammatory marker increased
Mobility decreased
Pain
Pyrexia
Rash pruritic
Urticaria
Symptomtext
diffuse/generalized migrating rash severely pruritic, facial edema, elevated inflammatory markers, severe arthralgia limiting ability to ambulate, fever. Started as joint pain and hives about 22 hrs after vaccination. Progressed to urticarial appearing rash and inability to walk due to pain about 12 hrs later. Rash and arthralgia waxed and waned. Peak severity of rash on day 3, accompanied by severe sudden onset abdominal pain and fever 101.5.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Flu vaccine given simultaneously
- Allergien
- Ampicillin
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 15.11.2022
- Impfdatum
- 12.08.2022
- Beginn
- 14.08.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LG
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Bronchiolitis
Chest X-ray abnormal
Cough
Dyspnoea
Speech disorder
Symptomtext
She had a small cough that developed that Sunday, and I gave her medicine. She was having a hard time breathing so I took her to the emergency room. They checked her oxygen which was at 98%. They gave her a breathing treatment. So, they gave prescription for steroids along albuterol inhaler. She took the albuterol inhaler for 3 days. She was diagnosed Bronchiolitis. Her symptoms improved after about a week. It took 3 days for her to be able to speak in full sentences. I do believe it is completely recovered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- X-Ray of lungs, Bronchiolitis discovered August 14, 2022.
- Aktuelle Erkrankungen
- Cold; runny nose; mild fever on the Monday prior to vaccination
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 07.11.2022
- Impfdatum
- 14.07.2022
- Beginn
- 14.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LG
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal discomfort
Abdominal pain upper
Blood test normal
Malaise
Migraine
Nausea
Oral pain
Pain in extremity
Pyrexia
Ultrasound scan normal
Symptomtext
We waited 15 minutes after and proceeded to the parking lot and he started not feeling well. He felt like he would throw up and was sick to his stomach. He woke up later that night to severe headache like migraine, fever and this lasted several days. He also had mouth pain he said it hurt really bad and was sore. This lasted a few weeks. And then he would complain of stomach pain for weeks and then spiked a high fever for 24 hours then fever for a week. He's been tested and no virus. Since July he's been complaining of severe stomach pains. Doctors have been unsure of what's going on and the only connection is that he's been having these issues since his first vaccination. He still complains about 1 leg hurting and chronic stomach pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- Blood work normal; Ultrasound normal
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- None
- Allergien
- Apple juice; apple sauce; fructose intolerance
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 12.10.2022
- Impfdatum
- 22.09.2022
- Beginn
- 05.10.2022
- Tage bis Beginn
- 13,0
- Dosis
- 2
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Dehydration
Diarrhoea
Hypophagia
Lethargy
Pyrexia
SARS-CoV-2 test positive
Vomiting
Symptomtext
My daughter had excessive diarrhea, she was very lethargic, feverish, had a cough, and she threw up. We tested on Sunday for COVID-19 and she was negative but we tested her again on 10/05/2022 and it came back positive. We called a nurse and she encouraged Pedialyte and fluids, but no prescriptions. She would not really eat or drink, it took a while to get her rehydrated. She is doing better and we are testing again tomorrow.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dehydration
- Hospital-Tage
- -
- Labordaten
- 02OCT2022 COVID-19 Test ? Negative 05OCT2022 COVID-19 Test ? Positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Multivitamin
- Allergien
- Lactose
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 07.10.2022
- Impfdatum
- 14.09.2022
- Beginn
- 15.09.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Chest X-ray abnormal
Chills
Cough
Croup infectious
Oxygen saturation decreased
Pneumonia
Pyrexia
Rash
SARS-CoV-2 test negative
Streptococcus test negative
Symptomtext
One day after receiving the 3rd dose of COVID-19 got a fever of 101; Gave tylenol and was seemed better the next day; Two days later had another high fever of over 103 this time; Planned on seeing Pediatrician first thing on monday, but then he also started to develop a rash on legs and feet and was alternating between fever and chills after taking fever reducers; Used an oximeter to check his oxygen and it was really low; Went to Urgent Care, given a breathing treatment and was tested for COVID-19 and Strep, both were negative; The Breathing Treatment wasn't helping, was rushed to the hospital by an ambulance; Given a chest X-ray and was diagnosed with Pneumonia; Given more breathing treatments, and was hospitalized for 1 night and was given Amoxicillin through his IV; Released the next day and sent home an Albuterol Inhaler and Amoxicillin;. A few days later he developed a heavy cough; Went back to Urgent Care and was told he had Croup; Went to Pediatrician and was given Dexamethasone. Seems to be doing better now.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pneumonia
- Hospital-Tage
- 1,0
- Labordaten
- COVID-19 test - negative; Strep test - negative; Chest X-ray - Pneumonia
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- Zyrtec
- Allergien
- Lactose Intolerant
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 2,0
- Geschlecht
- M
- Eingang
- 05.10.2022
- Impfdatum
- 27.09.2022
- Beginn
- 03.10.2022
- Tage bis Beginn
- 6,0
- Dosis
- 3
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest X-ray
Cough
Dyspnoea
Influenza virus test
Respiratory syncytial virus test
Respiratory tract congestion
SARS-CoV-2 test
Wheezing
Symptomtext
Trouble breathing, (wheezing, raspy), congested, coughing
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Covid-19, Flu, RSV X-Ray chest
- Aktuelle Erkrankungen
- No other vaccines prior Norovirus
- Vorgeschichte
- None
- Andere Medikamente
- Zyrtec - 2.5 mL daily Daily Vitamin - 1 daily
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 08.09.2022
- Impfdatum
- 23.08.2022
- Beginn
- 29.08.2022
- Tage bis Beginn
- 6,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Abdominal pain
Anticoagulant therapy
COVID-19
Diarrhoea
Headache
Activated partial thromboplastin time
C-reactive protein increased
Conjunctivitis
Electrocardiogram abnormal
Erythema
Fibrin D dimer increased
Inflammatory marker increased
International normalised ratio normal
Kawasaki's disease
Leukopenia
Hepatic enzyme increased
Illness
Immunoglobulin therapy
Symptomtext
Case-patient had first Pfizer vaccine on 8/2/22, acute COVID-19 infection with positive antigen test on 8/8/22, and second Pfizer vaccine on 8/23/22. Case-patient developed symptoms for Multisystem Inflammatory System (MIS-C) on 8/29/22. Case met case definition for MIS-C with evidence of clinically severe illness requiring hospitalization, fever, multisystem involvement (cardiac, hematologic, gastrointestinal, dermatologic). The case experience abdominal pain, diarrhea, elevated liver enzymes, thrombocytopenia, headache, conjunctival injection, shotty cervical lymphadenopathy and various elevated inflammatory markers (see box 19). Case-patient was treated with IVIG, ASA, and steroids, and survived.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Sinus tachycardia
- Hospital-Tage
- -
- Labordaten
- COVID-19 Ab nucleocapsid and spike positive (9/2/22), COVID-19 home antigen test positive (8/8/22), elevated inflammatory markers (9/1/22-9/4/22)
- Aktuelle Erkrankungen
- COVID-19 positive August 8th, 6 days after 1st COVID vax
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 08.09.2022
- Impfdatum
- 23.08.2022
- Beginn
- 29.08.2022
- Tage bis Beginn
- 6,0
- Dosis
- 2
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Abdominal pain
Anticoagulant therapy
COVID-19
Diarrhoea
Headache
Activated partial thromboplastin time
C-reactive protein increased
Conjunctivitis
Electrocardiogram abnormal
Erythema
Fibrin D dimer increased
Inflammatory marker increased
International normalised ratio normal
Kawasaki's disease
Leukopenia
Hepatic enzyme increased
Illness
Immunoglobulin therapy
Symptomtext
Case-patient had first Pfizer vaccine on 8/2/22, acute COVID-19 infection with positive antigen test on 8/8/22, and second Pfizer vaccine on 8/23/22. Case-patient developed symptoms for Multisystem Inflammatory System (MIS-C) on 8/29/22. Case met case definition for MIS-C with evidence of clinically severe illness requiring hospitalization, fever, multisystem involvement (cardiac, hematologic, gastrointestinal, dermatologic). The case experience abdominal pain, diarrhea, elevated liver enzymes, thrombocytopenia, headache, conjunctival injection, shotty cervical lymphadenopathy and various elevated inflammatory markers (see box 19). Case-patient was treated with IVIG, ASA, and steroids, and survived.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Sinus tachycardia
- Hospital-Tage
- -
- Labordaten
- COVID-19 Ab nucleocapsid and spike positive (9/2/22), COVID-19 home antigen test positive (8/8/22), elevated inflammatory markers (9/1/22-9/4/22)
- Aktuelle Erkrankungen
- COVID-19 positive August 8th, 6 days after 1st COVID vax
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 07.09.2022
- Impfdatum
- 04.09.2022
- Beginn
- 04.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- AZ
- Alter
- 0,9
- Geschlecht
- M
- Eingang
- 26.08.2022
- Impfdatum
- 25.08.2022
- Beginn
- 25.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Crying
Decreased appetite
Dyspnoea
Fatigue
Fluid intake reduced
Grunting
Mobility decreased
Respiratory rate increased
Somnolence
Symptomtext
Mom called concerned stating that patient received 2nd Covid vaccine this morning and is now having trouble breathing. Mom stated that patient was seen on 08/25/2022 for second Covid vaccine and was normal after vaccine that morning. Mom stated that she took patient to daycare afterwards and patient fell asleep on the care ride. Mom said that this was out of character for the patient especially since the patient slept all the way through the night. Mom stated that she dropped patient off at daycare and at 1400 mom received a call from the daycare. According to mom, the daycare told her that the patient was having abnormal breathing and told her to come pick patient up. Mom stated that patient breathing is abnormal but his face has not changed color. Triage nurse listened over the phone to the patient breathing and the patient was grunting with each breath for periods of time and then breathing normally. Mom stated that she believed patient respiration rate is high but every time she set him down to count it, he started crying. Mom denied patient having slow/shallow breathing, cyanosis, retractions, wheezing, or vomiting. Mom stated that patient activity level, eating, and drinking are decreased. Mom stated that she did not know if patient had been regularly urinating and when his last urination was because she had just picked patient up from daycare. Mom stated that patient eyes seemed to be glazed over as if he was taking medications and is more tired than normal. Mom was advised per provider to be seen in the emergency room for further and more immediate evaluation. Outcome is unknown as follow up has not been scheduled and patient was taken local Hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Left Acute Suppurative Otitis Media, Rash
- Vorgeschichte
- No known medical problems
- Andere Medikamente
- Amoxicillin-Pot Clavulanate 600-42.9MG/5ML Oral Suspension Reconstituted, 3.5 ML two times daily
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- XB
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 14.08.2022
- Impfdatum
- 02.08.2022
- Beginn
- 04.08.2022
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chills
Fatigue
General physical condition abnormal
Influenza virus test negative
Pyrexia
Rhinitis
Rhinorrhoea
SARS-CoV-2 test negative
Streptococcus test negative
Tachycardia
Tremor
Vomiting
Wheezing
Symptomtext
Pt received 2nd COVID Vx on 8/2/22. On 8/4/22, she developed fever, chills, fatigue, rhinitis & rhinorrhea, tachycardia, wheezing. Her mother brought her in to urgent care 8/6 for evaluation (ill-appearing, febrile with shaking chills; T 102.7F, pulse 160, RR 26, 97% O2). Pt was given Tylenol in clinic. She immediately vomited. Replacement dose was given. Pt tested negative for COVID, flu, and Strep. Pt was discharged with Orapred Rx with instructions to monitor closely for worsening. Mother was advised to follow up with PCP and to take her to ER if any worsening.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tachycardia
- Hospital-Tage
- -
- Labordaten
- COVID antigen test, rapid Strep test, flu test - all negative 8/6/22
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 2,0
- Geschlecht
- M
- Eingang
- 05.08.2022
- Impfdatum
- 16.07.2022
- Beginn
- 17.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dyspnoea
Symptomtext
difficulty breathing; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the parent. A 2-year-old male patient received BNT162b2 (BNT162B2), on 16Jul2022 at 11:00 as dose 2, single (Lot number: FT9142) at the age of 2 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "He has had the flu before" (unspecified if ongoing), notes: Know it is something viral. He has had the flu before, but it wasn't anything like this.; "he has an underlying condition, like asthma" (unspecified if ongoing), notes: Doctor is presuming that he has an underlying condition. There were no concomitant medications. Vaccination history included: BNT162b2 (Dose-1, LOT: FT9142, Expiry date:31Dec2022), administration date: 23Jun2022, when the patient was 2-year-old, for COVID-19 immunization, reaction(s): "Drug ineffective", "Doctor is presuming he had Covid when he got the second vaccine\ antigen Covid test was negative", "amoxicillin to prevent pneumonia", "respiratory distress", "being sick when he got the second vaccine", "runny yellow nose and cough they are assuming he has Covid because he is presenting the same way he did in Apr2022", "runny yellow nose and cough they are assuming he has Covid because he is presenting the same way he did in Apr2022", "Still wheezy and everything today", "occurrence of the difficulty breathing". The following information was reported: DYSPNOEA (medically significant) with onset 17Jul2022 at 01:30, outcome "recovering", described as "difficulty breathing". The event "difficulty breathing" required physician office visit. Therapeutic measures were taken as a result of dyspnoea. Clinical course: This report was not related to a study or programme. The reporter (mother) was calling because her three year old son received second dose of COVID-19 vaccine on Sat 16Jul2022 and the following morning they had to take him to urgent care because he had difficulty breathing and they gave him a dose of Decadron. The child's doctor thought he had COVID, but it did not present itself until the next day. Verified the above information with the caller. Called to see if there was any data on whether or not her son should get the third vaccine in September. If him being sick when he got the second vaccine could possibly affect the building of the antibodies from this past dose on 16Jul2022. Difficulty breathing: Started about 1:30am on 17Jul2022. The reporter needed to take him to the hospital with breathing issues before. Back in Jun2022, he woke up in respiratory distress and they had to take him to the urgent care then as well. With this occurrence of the difficulty breathing, he was being treated with nebulizers of albuterol sulfate 4 times a day, amoxicillin to prevent pneumonia, 5 days of prednisone, Cetirizine HCL. Still wheezy and everything today, but better. Doctor was presuming that he had an underlying condition, like asthma that was contributing to all this. Doctor was presuming he had COVID when he got the second vaccine, the symptoms just hadn't presented yet. In Apr2022, he was PCR positive, but his antigen test was negative. This time, his antigen COVID test was negative, but they did not do a PCR. Based on the presentation of his symptoms, like his runny yellow nose and cough they are assuming he had Covid because he was presenting the same way he did in Apr2022. Know it was something viral. He had the flu before, but it was not anything like this. Does not think it was the vaccine. It was just bad timing when he got the vaccine. The doctor of the patient recommendation was that he get a booster again in Nov2022 after the third dose was Sep2022. Concern was that because he seems to be very susceptible based on being in the hospital in Apr and then this issue with the breathing. Hopefully, the vaccine will keep him out of the hospital. As of right now, this was the plan they will go for. If there was any other data or guidance feel free to reach out. She was calling to see if there are other recommendations for getting a booster early in these cases. Her son was not one of those kids that gets sick, coughs twice, and gets better. She wants to keep him as protected as possible.There were no additional Vaccines Administered on Same Date of the Pfizer. This event did not require a visit to Emergency Room. The patient went to urgent care on 17Jul2022. Has been to PCP three times and has a follow up scheduled for 3 weeks. The patient did not receive any other vaccines within four weeks prior to the vaccination. There were no adverse events prior vaccinations. Patient medical history including any illness at time of vaccination was none and other conditions were No. The family medical history were not provided. There were no relevant tests and investigations.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Asthma (Doctor is presuming that he has an underlying condition); Flu (Know it is something viral. He has had the flu before, but it wasn't anything like this.)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 28.07.2022
- Impfdatum
- 27.07.2022
- Beginn
- 27.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Peripheral swelling
Rash
Symptomtext
Patient developed rash 2 hours after vaccine while at home. They worsened x 12 hours and patient developed mild swelling on hands and feet. Denies difficulty breathing, swelling of mouth, difficulty swallowing, etc. No medication given. Mother gave a tepid bath which improved rash.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 0,6
- Geschlecht
- M
- Eingang
- 26.07.2022
- Impfdatum
- 20.07.2022
- Beginn
- 23.07.2022
- Tage bis Beginn
- 3,0
- Dosis
- 2
- Route/Site
- SYR / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Conjunctivitis
Ear infection
Eye discharge
Insomnia
Symptomtext
07/23/2022 A few days after the second vaccine he woke up very happy and feeling normal however later that night he started to form gunk in his eye and since he had pink eye after his first vaccination we were familiar with it. Putting him down to sleep he was having a terrible time trying to sleep and on the 25th of July we decided to take him in to the doctor that day. We were advised that he did have pink eye in both eyes and a double ear infection again, and so he was given a new antibiotic called cefdinir to try out. He seems to have slept throughout the night okay.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Physical examination
- Aktuelle Erkrankungen
- Double pink eye; ear infections; fever
- Vorgeschichte
- Umbilical Hernia; Aurelio Sickening
- Andere Medikamente
- AUGMENTIN
- Allergien
- Peanut
- Vorherige Impfungen
- Pfizer #1: Lot: FT9142 Date: 06/29/2022: A week after the 1st vaccination he started to have pink eye in both eyes and ear infec
- Staat
- FL
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 06.07.2022
- Impfdatum
- 30.06.2022
- Beginn
- 30.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / OT
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bacterial infection
Body temperature increased
Chest X-ray
Cough
Dehydration
Fatigue
Lethargy
Nasopharyngitis
Pyrexia
Rhinorrhoea
SARS-CoV-2 test
Urine analysis
Symptomtext
Patient received her vaccine Thursday morning, June 30, 2022, about 9:00 AM. She had a cold starting 5-6 days prior, just runny nose and cough. Within 20-30 minutes, she said she was tired and wanted to sleep. She was falling asleep in the car. She had a temperature of 100.5. An hour post vaccine, she was 101.9. I medicated her with TYLENOL. Three hours post vaccine, her fever broke. Fever started to spike again in the evening, to 102. Friday morning she woke up with 100.5. I medicated her with TYLENYOL and sent her to school. She was fine all day until the evening again. This fever went on and I called her pediatrician on Sunday. She said if fever more than 5 days, we will see her. I took her in yesterday, she was lethargic and dehydrated. She started antibiotics last night and is fever free this morning. She clearly has a bacterial infection. We believe the vaccine activated her immune system.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dehydration
- Hospital-Tage
- -
- Labordaten
- July 5, 2022 - Chest X-ray; UA; Three COVID-19 tests
- Aktuelle Erkrankungen
- Upper Respiratory; Common Cold
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 1,3
- Geschlecht
- M
- Eingang
- 30.06.2022
- Impfdatum
- 22.06.2022
- Beginn
- 25.06.2022
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- IM / LG
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Agitation
Basophil count normal
Basophil percentage
Blood albumin decreased
Blood culture negative
Blood sodium decreased
C-reactive protein increased
Echocardiogram normal
Eosinophil count decreased
Eosinophil percentage decreased
Dyspnoea
Erythema
Pyrexia
Urticaria
Erythema multiforme
Granulocyte percentage
Haematocrit normal
Haemoglobin normal
Symptomtext
3 days following immunization patient developed fever and rash. 4 days following immunization fever continued and rash spread. Was evaluated at urgent care. Augmentin stopped. Same day rash continued to spread and seen in ER. Patient given prednisolone po and benadryl. 5 days following immunization patient continued prednisolone and rash continued to spread 6 days following immunization patient diagnosed by me with erythema multiforme with significant facial, body, and extremity swelling. Sent to ER. Lab evaluation significant for low albumin, low sodium, elevated ESR, elevated CRP. Patient given solumedrol IV x1 with mild improvement in rash and sent home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 6/28/2022 15:03 White Blood Cell Count: 10.03 Hemoglobin: 12.6 Hematocrit: 38.5 Red Blood Cell Count: 4.49 Mean Corpuscular Volume: 85.7 Mean Corpuscular Hemoglobin: 28.1 MCH Concentration: 32.7 Red Cell Distribution Width-SD: 47.0 Red Cell Distribution Width-CV: 15.3 Platelet Count, Auto: 317 Mean Platelet Volume: 10.5 Nucleated RBC%, automated: 0.0 Absolute Nucleated RBC Count: 0.00 Neutrophil Percent, Auto: 35.7 Lymphocyte Percent, Auto: 56.7 Monocyte Percent, Auto: 6.2 Eosinophil Percent, Auto: 0.2 Basophil Percent, Auto: 0.9 Immature Granulocytes%: 0.3 Absolute Neut Count: 3.58 Absolute Mono Count: 0.62 Absolute Lymphocyte Count: 5.69 Absolute Baso Count: 0.09 Absolute Eos Count: 0.02 Absolute Immature Gran Count: 0.03 6/28/2022 14:57 Sedimentation rate, Erythrocyte: 17 (H) C-Reactive Protein: 5.9 (H) blood culture negative to date ECHO 6/29 CONCLUSIONS 1. Unsedated, agitated 16 month old M with fever, initial evaluation. Mild technical limitations from unsedation 2. Normal SDS cardiac segmental anatomy 3. No CHD or CM identified. 4. Origin of the coronary arteries appear normal with no aneurysms or ectasia. 5. Good biventricular systolic function 6. No pericardial effusion.
- Aktuelle Erkrankungen
- Otitis media Viral URI
- Vorgeschichte
- Recurrent otitis media
- Andere Medikamente
- Augmentin
- Allergien
- No known
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 1,3
- Geschlecht
- M
- Eingang
- 30.06.2022
- Impfdatum
- 22.06.2022
- Beginn
- 25.06.2022
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- SYR / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Agitation
Basophil count normal
Basophil percentage
Blood albumin decreased
Blood culture negative
Blood sodium decreased
C-reactive protein increased
Echocardiogram normal
Eosinophil count decreased
Eosinophil percentage decreased
Dyspnoea
Erythema
Pyrexia
Urticaria
Erythema multiforme
Granulocyte percentage
Haematocrit normal
Haemoglobin normal
Symptomtext
3 days following immunization patient developed fever and rash. 4 days following immunization fever continued and rash spread. Was evaluated at urgent care. Augmentin stopped. Same day rash continued to spread and seen in ER. Patient given prednisolone po and benadryl. 5 days following immunization patient continued prednisolone and rash continued to spread 6 days following immunization patient diagnosed by me with erythema multiforme with significant facial, body, and extremity swelling. Sent to ER. Lab evaluation significant for low albumin, low sodium, elevated ESR, elevated CRP. Patient given solumedrol IV x1 with mild improvement in rash and sent home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 6/28/2022 15:03 White Blood Cell Count: 10.03 Hemoglobin: 12.6 Hematocrit: 38.5 Red Blood Cell Count: 4.49 Mean Corpuscular Volume: 85.7 Mean Corpuscular Hemoglobin: 28.1 MCH Concentration: 32.7 Red Cell Distribution Width-SD: 47.0 Red Cell Distribution Width-CV: 15.3 Platelet Count, Auto: 317 Mean Platelet Volume: 10.5 Nucleated RBC%, automated: 0.0 Absolute Nucleated RBC Count: 0.00 Neutrophil Percent, Auto: 35.7 Lymphocyte Percent, Auto: 56.7 Monocyte Percent, Auto: 6.2 Eosinophil Percent, Auto: 0.2 Basophil Percent, Auto: 0.9 Immature Granulocytes%: 0.3 Absolute Neut Count: 3.58 Absolute Mono Count: 0.62 Absolute Lymphocyte Count: 5.69 Absolute Baso Count: 0.09 Absolute Eos Count: 0.02 Absolute Immature Gran Count: 0.03 6/28/2022 14:57 Sedimentation rate, Erythrocyte: 17 (H) C-Reactive Protein: 5.9 (H) blood culture negative to date ECHO 6/29 CONCLUSIONS 1. Unsedated, agitated 16 month old M with fever, initial evaluation. Mild technical limitations from unsedation 2. Normal SDS cardiac segmental anatomy 3. No CHD or CM identified. 4. Origin of the coronary arteries appear normal with no aneurysms or ectasia. 5. Good biventricular systolic function 6. No pericardial effusion.
- Aktuelle Erkrankungen
- Otitis media Viral URI
- Vorgeschichte
- Recurrent otitis media
- Andere Medikamente
- Augmentin
- Allergien
- No known
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 09.05.2023
- Impfdatum
- 16.09.2022
- Beginn
- 16.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Crying
Erythema
Urticaria
Vomiting
Symptomtext
Child was crying continually after getting the shot. Within a few minutes developed a hive on the left forearm. 5mg of Zyrtec was given shortly afterward but since he was so upset he vomited prior to first attempt to give it to him. After the Zyrtec was given he developed red patches on his upper extremities. There was no further vomiting and at no time in over a half hour of observation did he have any difficulty breathing, coughing or wheezing or any other symptoms. He did calm down however and went home with both parents who are RNs. His 4 year old brother had the same vaccine without any immediate reaction.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- Egg. Hives
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 25.04.2023
- Impfdatum
- 24.10.2022
- Beginn
- 26.03.2023
- Tage bis Beginn
- 153,0
- Dosis
- 3
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Diarrhoea
Loss of personal independence in daily activities
Stool analysis
Vomiting
Symptomtext
Starting early in the morning 28MAR2023 my Daughter had a vomiting episode early in the morning around four AM that lasted on and off for three hours. I kept her home from school that day it was shortly followed by diarrheas and the she seemed to bounce back fine My husband AND i assumed it was a stomach bug and then it happened again two nights later and we thought she just ate something bad it occurred again over the week around 02APR2023 by the morning of 05APR2023 she had her fourth episode in over a week. That morning we took her to Urgent care and the doctor could not determine the cause of her symptoms, we told to simply monitor her since we were unsure of the source and we were sent home with a stool sample kit for the diarrhea and a prescription of Flumodine to help calm the stomach. For about one week she seemed to be doing better until 13APR2023 she threw up two nights in a row after the first night I was able yo collect a stool sample to send to Urgent care and after the third night I made an appoint with our Pediatrician Dr he determined due to the incidents being isolated with no other symptom than vomiting or diarrhea the caudle was food related.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 10.04.2023
- Impfdatum
- 23.03.2023
- Beginn
- 29.03.2023
- Tage bis Beginn
- 6,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Abdominal pain
Oropharyngeal pain
Specific gravity urine
Streptococcus test negative
Urine analysis abnormal
Urine analysis normal
Urine ketone body present
Viral test negative
Vomiting
Symptomtext
Patient presented to urgent care with abdominal pain, intractable vomiting x 4 days on 4/2/23. +sore throat.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- Rapid strep, strep pcr, and viral panel testing negative. Urinalysis negative except showing large ketones, and spec grav 1.030
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- none
- Andere Medikamente
- unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- -
- Geschlecht
- M
- Eingang
- 04.04.2023
- Impfdatum
- 13.10.2022
- Beginn
- 14.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Exposure to communicable disease
Extra dose administered
Loss of personal independence in daily activities
Pain in extremity
Pyrexia
Symptomtext
Loss of personal independence in daily activities; Exposure to communicable disease; Pain in extremity; Extra dose administered; Pyrexia; This case was retrieved during the Vaccines Adverse Event Reporting System (VAERS) monitoring on 12-JAN-2023 with the following VAERS Primary ID 2480320-1. The original narrative from the sender is the following: Child got varicella vaccine 2 days in a row. On 11-OCT-2022 exposed to varicella at school. On 12-OCT-2022 vaccinated at school with Varivax with father's consent (name spelled different and 2nd last name omitted on consent) present during education and consent completion. On 13-OCT-2022 mother brings child to vaccine clinic and screening had occurred on 11-OCT-2022. Mother consented through which indicated child needed varicella vaccination. Error was not noted until entry after clinic. Call to mother 14-OCT-2022, child had mild fever treated with acetaminophen on 13-OCT-2022 and mother kept him home from school next day due to arm pain, but states child is eating and paying normally 24 hours after vaccination. The reporter did not provide an assessment of causal relationship between Vaxelis and the reported events "Loss of personal independence in daily activities", "Pyrexia" and "Pain in extremity". The causal relationship between Vaxelis and the reported events "Exposure to communicable disease (Child exposed at school)" and "Extra dose administered" were assessed as not related and not applicable respectively, due to the nature of these events. No further information is expected
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Prophylaxis
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 27.03.2023
- Impfdatum
- 23.09.2022
- Beginn
- 23.10.2022
- Tage bis Beginn
- 30,0
- Dosis
- 3
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Croup infectious
Ear infection
Fatigue
Herpangina
Loss of personal independence in daily activities
Pain in extremity
Scarlet fever
Streptococcus test positive
Symptomtext
After receiving the third dose, she experienced a sore arm and fatigue. On October 23, 2022, she had Herpangina and missed preschool for a week. She saw the doctor twice that week for it. On January 11, 2023, she was diagnosed with Scarlet Fever. The doctor prescribed Amoxycillin for 10 days. On March 23, 2023, she was diagnosed with a Double Ear Infection and Croup. She is taking Amoxycillin for 10 days for that as well.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 01/11/2023 Strep Test - Positive
- Aktuelle Erkrankungen
- Double Ear Infection
- Vorgeschichte
- None
- Andere Medikamente
- Multivitamin with Fluoride
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 2,0
- Geschlecht
- M
- Eingang
- 24.03.2023
- Impfdatum
- 22.09.2022
- Beginn
- 30.01.2023
- Tage bis Beginn
- 130,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Ear infection
Ear pain
Pyrexia
Rhinorrhoea
SARS-CoV-2 test negative
Symptomtext
On 01/30/2023, he started with a fever that day and also had runny nose and right ear pain. He tested negative for COVID-19. We took him to the doctor, he had an ear infection and took antibiotics. He is better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ear pain
- Hospital-Tage
- -
- Labordaten
- 02FEB2023-- COVID 19 Test -- Negative
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 0,8
- Geschlecht
- F
- Eingang
- 23.03.2023
- Impfdatum
- 15.09.2022
- Beginn
- 11.01.2023
- Tage bis Beginn
- 118,0
- Dosis
- 3
- Route/Site
- IM / LG
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Conjunctivitis viral
Cough
Decreased appetite
Fatigue
Illness
Influenza A virus test positive
Loss of personal independence in daily activities
Nasal congestion
Pyrexia
SARS-CoV-2 test negative
Streptococcus test negative
Symptomtext
On January 11, 2023, she woke up with a fever. The highest her fever got throughout the course of the illness was 103-degrees. We alternated TYLENOL and ibuprofen for the fever. We made an appointment with her pediatrician who saw her that same day. They tested her for Flu, Strep, and COVID-19. She tested positive for Influenza A. She was prescribed TAMIFLU. Her only symptoms for the first two or three days were a fever. Around day three or four, she began to develop nasal congestion and cough. She also developed Viral Conjunctivitis, fatigue, and decreased appetite. She was out of school a little over a week. She returned to school on Friday, January 20, 2023.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 01/11/2023 COVID-19 test negative; 01/11/2023 Strep test negative; 01/11/2023 Flu test positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 20.03.2023
- Impfdatum
- 13.09.2022
- Beginn
- 24.01.2023
- Tage bis Beginn
- 133,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Influenza virus test negative
Pyrexia
Respiratory syncytial virus test positive
Rhinorrhoea
SARS-CoV-2 test negative
Symptomtext
She developed a runny nose around January 24, 2023. She also developed a cough around January 27, 2023. She ran 100.5-degree fever January 27 and 28, 2023. She was still coughing and had a runny nose on January 31, 2023. I took her to see the doctor. They tested her for RSV and the Flu. She tested positive for RSV. The doctor did not prescribe medication but told us to continue the humidifier and ibuprofen as needed. She also suggested wearing a mask around older family members. She began feeling better around February 4, 2023. Her symptoms almost completely resolved by February 9, 2023. She continues to have a slight cough first thing in the morning. She has a follow-up appointment to address that issue today.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- 01/29/2023 at home COVID-19 test negative; 01/31/2023 RSV test positive; 01/31/2023 Flu test negative
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- 2mm hole in right eardrum and mild hearing loss in right ear
- Andere Medikamente
- ZYRTEC; probiotic
- Allergien
- Seasonal
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 2,0
- Geschlecht
- M
- Eingang
- 13.03.2023
- Impfdatum
- 24.06.2022
- Beginn
- 15.07.2022
- Tage bis Beginn
- 21,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site discolouration
Symptomtext
On approximately 07/15/2022, in the morning, we noticed a white spot, about the size of a nickel, at the injection site. We showed the doctor at his well check-up in August. We thought it may be a fungal infection, we put cream on it, and it is still there. I showed it to the doctor again last week.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site discolouration
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Omega 3 DHA Supplement
- Allergien
- Egg
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 13.03.2023
- Impfdatum
- 15.07.2022
- Beginn
- 10.01.2023
- Tage bis Beginn
- 179,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Diarrhoea
Food allergy
Symptomtext
My son has had loose stools and intermittent diarrhea with occasional regular stools. This began around 1/10/2023. He doesn't seem to have pain, because he says his tummy doesn't hurt. We have tried isolating foods from his diet, such as milk and fruit, as was recommended by his pediatrician. On 2/24/2023, we took him to his physician, who suggested that we continue isolating certain foods. She said his symptoms were likely caused by a food allergy. She asked us if we had had any tummy bugs in the family at any point, and we confirmed that we had, though my son is the only one with an ongoing problem. She also suggested skin and blood tests for allergies for my son. My son has not yet undergone any tests, though. Since we have begun isolating foods, my son's symptoms have improved. The symptoms are still present, though less frequent.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- 24FEB2023 - Basic Physical Examination - No Abdominal Pain Detected, Good Health Indicated
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- None
- Andere Medikamente
- Children's Chewable Multivitamin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 0,5
- Geschlecht
- F
- Eingang
- 13.03.2023
- Impfdatum
- 12.09.2022
- Beginn
- 12.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site reaction
Skin reaction
Symptomtext
Have a tiny mark where it was given. Has been six months and looks like a tiny pen mark. No redness, no irritation, no issues. Mom asking to submit vears given it not gone away.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site reaction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Vitamin D
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 2,0
- Geschlecht
- M
- Eingang
- 13.03.2023
- Impfdatum
- 10.09.2022
- Beginn
- 01.02.2023
- Tage bis Beginn
- 144,0
- Dosis
- 3
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cough
Ear infection
Ear pain
Nasopharyngitis
Pyrexia
Rhinorrhoea
Symptomtext
On approximately 02/01/2023, he began having ear infections and colds. His ears hurt and he had coughing, runny nose, and mild fever. We went to the doctor for two sick visits and were prescribed a different antibiotic each time. As far as we know, he has recovered. He is in preschool.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ear pain
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Vitamin D
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 13.03.2023
- Impfdatum
- 09.09.2022
- Beginn
- 19.02.2023
- Tage bis Beginn
- 163,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Ear infection
Ear pain
Pyrexia
Vomiting
Symptomtext
On the morning of 02/19/2023, she woke up vomiting. On the next 2 days, she had a low grade fever and sore left ear. We went to the doctor on 02/22/2023, and she had an ear infection. She was prescribed amoxicillin. She went though that course and seemed to make a full recovery.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ear pain
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Multivitamin
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 01.03.2023
- Impfdatum
- 28.10.2022
- Beginn
- 28.10.2022
- 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 haemorrhage
No adverse event
Symptomtext
Patient was being vaccinated with Fluarix on right arm when patient moved. PHN removed needle from patient's arm to prevent any injury. No fluid was injected from syringe. PHN did not note any bleeding on arm when needle was removed. RN, PHN reviewed with patient's mother the importance stabilizing patient's extremity for safe injection of vaccine. Mother verbalized understanding. PHN replaced needle tip with a new needle and upon return to vaccine table, patient's mother Mother stated that patient was bleeding at injection site. PHN observed slight bleeding at injection site, and noted that bleeding stopped after a few seconds. Bleeding ceased from injection site and no redness or swelling was observed by , PHN. Patient was vaccinated with Fluarix on right deltoid, one inch below the first injection attempt, per CDC guidelines to separate injection sites by one inch. Mother and patient waited in post-vaccination observation area and no adverse symptoms were noted or reported by mother. Mother was educated by PHN on emergency precautions and when to seek emergency care for patient. Mother verbalized understanding
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site haemorrhage
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 24.01.2023
- Impfdatum
- 05.01.2023
- Beginn
- 05.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Feeling hot
Immediate post-injection reaction
Oropharyngeal pain
Vomiting
Symptomtext
Patients mother called the oncall of physician noted to inquire about symptoms that arose immediatly after vaccination (while under observation. The parent did not report this to the vaccinating facility.) Patient told mother that his throat was sore, and he felt hot. Patient then went home and vomited all within an hour of vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Unk
- Vorgeschichte
- Unk
- Andere Medikamente
- Unk
- Allergien
- Unk
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 19.01.2023
- Impfdatum
- 16.07.2022
- Beginn
- 21.11.2022
- Tage bis Beginn
- 128,0
- Dosis
- 2
- Route/Site
- SYR / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Influenza virus test negative
Pyrexia
Respiratory syncytial virus test positive
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
She had a runny nose and developed a cough on 11/26/2022 and this lasted two to three weeks a RSV was positive, Influenza and COVID-19 tests were negative, then around 12/25/2022 the same conditions started including a fever up to 101 degrees a COVID-19 test was negative.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- COVID-19 test one positive and one negative.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Reactive airway disease; Umbilical hernia
- Andere Medikamente
- Tylenol; Albuterol; Advil; Budesonide
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 0,8
- Geschlecht
- F
- Eingang
- 18.01.2023
- Impfdatum
- 18.01.2023
- Beginn
- 18.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Symptomtext
child checked after 15 minute observation and right upper leg/thigh area was red- no rash noted. no respiratory distress. APN in room to check child and Benadryl ordered and administered. child discharged home with instructions- verbal by APN
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- -
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 16.01.2023
- Impfdatum
- 26.09.2022
- Beginn
- 08.01.2023
- Tage bis Beginn
- 104,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Fatigue
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
He ran a low-grade fever for one night and a cough with chest congestion. He tested positive on December 8, 2022 for COVID-19. Since then, he has been really tired and has a congested cough.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19, positive, 12/08/2022
- Aktuelle Erkrankungen
- He was getting over a cold the day he got the vaccine.
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 1,5
- Geschlecht
- F
- Eingang
- 12.01.2023
- Impfdatum
- 02.12.2022
- Beginn
- 10.01.2023
- Tage bis Beginn
- 39,0
- Dosis
- 1
- Route/Site
- IM / LG
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test negative
Symptomtext
She had a fever and was tugging at her ears. She was also very congested. I contacted her doctor and he prescribed cefdinir. She is still dealing with these symptoms at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- 10JAN2023 COVID-19 test negative
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 1,3
- Geschlecht
- F
- Eingang
- 06.01.2023
- Impfdatum
- 07.12.2022
- Beginn
- 15.12.2022
- Tage bis Beginn
- 8,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Administration site rash
Drug eruption
Skin discolouration
Symptomtext
Drug eruption rash started 12/15/22 and continued to progress 1/5/23. Turned purple hue around end of December. Spreading down thigh and beginning to show on bil upper arms. Denies fevers, limping, decreased activity, decreased appetite. Second dose given 12/28/22 (due to unknown it was from the COVID vaccine) and now rash has begun on R leg (administration site) as well.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Administration site rash
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 1,3
- Geschlecht
- F
- Eingang
- 06.01.2023
- Impfdatum
- 07.12.2022
- Beginn
- 15.12.2022
- Tage bis Beginn
- 8,0
- Dosis
- 2
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Administration site rash
Drug eruption
Skin discolouration
Symptomtext
Drug eruption rash started 12/15/22 and continued to progress 1/5/23. Turned purple hue around end of December. Spreading down thigh and beginning to show on bil upper arms. Denies fevers, limping, decreased activity, decreased appetite. Second dose given 12/28/22 (due to unknown it was from the COVID vaccine) and now rash has begun on R leg (administration site) as well.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Administration site rash
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 0,5
- Geschlecht
- M
- Eingang
- 29.12.2022
- Impfdatum
- 29.06.2022
- Beginn
- 16.12.2022
- Tage bis Beginn
- 170,0
- Dosis
- 1
- Route/Site
- IM / LG
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pyrexia
Symptomtext
Dec 16 around 3:00 began running low grade fever. Over the next couple days it got up to 102.5 without meds. Spoke with PCP and was told to keep an eye on him and give him TYLENOL to keep him comfortable. Fever resolved on it's own by 12/20/2022. Received pneumococcal, MMR, and Varicella vaccines on 12/08 and we were told it could possibly cause rash and fever.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Confirmed COVID-19 on May 23
- Vorgeschichte
- None
- Andere Medikamente
- Vitamin D3 drops
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 1,3
- Geschlecht
- F
- Eingang
- 29.12.2022
- Impfdatum
- 08.12.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- N/A
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Influenza A virus test
Pyrexia
SARS-CoV-2 test
Streptococcus test
Symptomtext
Patient was given an extra dose of the Covid vaccine. She got 2 doses of Moderna in July and August 2022 and was given a dose of Pfizer in December 2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- On 12/13/22 Patient was tested for strep, influenza A, and Covid due to a fever of 102.0 F.
- Aktuelle Erkrankungen
- Ear infection in the month prior
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- Hives following her flu shot on 11/10/2022.
- Staat
- MI
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 24.12.2022
- Impfdatum
- 26.07.2022
- Beginn
- 04.11.2022
- Tage bis Beginn
- 101,0
- Dosis
- 1
- Route/Site
- SYR / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain upper
COVID-19
Diarrhoea
Exposure to SARS-CoV-2
Gastric dilatation
SARS-CoV-2 test positive
Vaccine breakthrough infection
Vomiting
Symptomtext
We had been quarantined since 10/31/2022 due to my husband?s COVID diagnosis. Patient had a breakthrough case of COVID with initial positive test on 11/04/2022. Patient had severe vomiting and diarrhea that started that night. The diarrhea was intermittent throughout the following weeks but the vomiting did not fully subside until November 25, 2022. On November 15th the vomiting was for 12 hours straight. The other days it was once a night around 7-8 pm. He would vomit up all of his daily food intake. His stomach would hurt and be distended until he vomited, which is out of the ordinary for him. The contents of his stomach would still contain items he ate for breakfast 12 hours prior. Patient was seen by his pediatrician on 11/18/2022 for this condition.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 23.12.2022
- Impfdatum
- 15.12.2022
- Beginn
- 16.12.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Breath odour
Fatigue
Nausea
Pyrexia
SARS-CoV-2 test negative
Streptococcal infection
Streptococcus test positive
Symptomtext
My son received his 3rd dose of Pfizer on 12/15/2022. His Strep symptoms started around 05:00PM on 12/16/2022. He had fever and normally he doesn't sleep early but that day he went to bed early. This wasn't normal for him. On 12/17/2022 he had a fever of 104, nausea, tiredness, his breath was smelling. I work at a hospital so I knew it was Strep. I started giving him TYLENOL and MOTRIN to reduce his fever. I realized that the TYLENOL wasn't helping so I only gave him MOTRIN. On 12/22/2022 I took him to the clinic around 12:30PM. They tested him for COVID-19 which was negative but he was positive for Strep. They prescribed him amoxicillin for 10 days. Now he is more active and slowly recovering from Strep.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 23DEC2022 COVID-19 test negative
- Aktuelle Erkrankungen
- Diarrhea for 2-3 days a week earlier
- Vorgeschichte
- Apraxia
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- 2nd dose COVID-19 behavior changed
- Staat
- TX
- Alter
- 2,0
- Geschlecht
- M
- Eingang
- 22.12.2022
- Impfdatum
- 07.09.2022
- Beginn
- 07.12.2022
- Tage bis Beginn
- 91,0
- Dosis
- 3
- Route/Site
- IM / LG
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Ear infection
Otorrhoea
Pyrexia
Symptomtext
He had a fever, and drainage in his ear. This lasted for a couple days and then we decided to take him to urgent care and they diagnosed him with an ear infection. They prescribed ofloxacin and amoxicillin. He started feeling better after taking the medication for 2 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 16.12.2022
- Impfdatum
- 02.12.2022
- Beginn
- 01.12.2022
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Body height
Body temperature
Decreased appetite
Eye discharge
Irritability
Incorrect dose administered
Product preparation issue
Pyrexia
Lethargy
Overdose
Product preparation error
Sleep terror
Weight
Symptomtext
night terrors; irritable; lethargic; High fevers; his eyes like a gooky something; received 0.2 mL of undiluted COVID-19 vaccine on 02Dec2022; received 0.2 mL of undiluted COVID-19 vaccine on 02Dec2022; decreased appetite; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team, Program ID. The reporter is the parent. A 3-year-old male patient received BNT162b2 (BNT162B2), on 02Dec2022 at 10:15 as dose 2 (maroon cap), 0.2 ml single (Lot number: FT9142, Expiration Date: 31Dec2022) at the age of 3 years, in left arm for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: BNT162b2 (DOSE 1; , Lot Number: FT9142), administration date: 11Nov2022, when the patient was 3-year-old, for COVID-19 immunization. The following information was reported: PRODUCT PREPARATION ERROR (non-serious) with onset 02Dec2022, outcome "recovered" (02Dec2022), OVERDOSE (non-serious) with onset 02Dec2022 at 10:15, outcome "recovered" (02Dec2022) and all described as "received 0.2 mL of undiluted COVID-19 vaccine on 02Dec2022"; PYREXIA (non-serious) with onset 02Dec2022 at 14:00, outcome "recovered" (03Dec2022), described as "High fevers"; EYE DISCHARGE (non-serious) with onset 02Dec2022 at 14:00, outcome "recovered" (04Dec2022), described as "his eyes like a gooky something"; LETHARGY (non-serious) with onset 02Dec2022 at 14:00, outcome "recovered" (06Dec2022), described as "lethargic"; IRRITABILITY (non-serious) with onset 03Dec2022 at 07:00, outcome "recovered" (06Dec2022), described as "irritable"; SLEEP TERROR (non-serious) with onset 04Dec2022, outcome "recovered" (07Dec2022), described as "night terrors"; DECREASED APPETITE (non-serious) with onset Dec2022, outcome "recovered" (08Dec2022). Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of pyrexia. Therapeutic measures were not taken as a result of decreased appetite, lethargy, irritability, sleep terror, eye discharge. Additional information: Has a caregiver who reported that her 3 year old son received an undiluted dose of the Covid 19 vaccine. Information confirmed as provided. Color of the cap was unknown. Was for his second dose. Was trying to understand what amount of undiluted vaccine would be in what he received if it was appropriately diluted. Wanted to know how many times the actual dose of vaccine that he received. Later provided that he was sick having symptoms from Friday to yesterday. Provided symptoms of high fevers, decreased appetite, very lethargic, irritable and having night terrors and having discharge from his eyes like a gooky something. Patient details: Clarified age of onset was 3 years, 2 months approximately. Weight is 35 pounds, 6 ounces. Height is approximately 3 feet, 1 inch. Event details: High fevers: Started Friday afternoon at 2:00pm. Had high fevers on Friday and Saturday. Treatment: Gave Tylenol and fluids. Had him drink more water and stuff. Decreased appetite: Started Friday or Saturday and his appetite came back yesterday. Treatment: None. Very lethargic: Started Friday and he bounced back Tuesday. Treatment: None. Irritable: Started Friday and that kind of recovered by Tuesday; Treatment: None. Having night terrors: Last night was his first night without. Wednesday was his last night of night terrors. Treatment: None. Having discharge from his eyes like a gooky something: Started Friday evening 02Dec2022 through Sunday 04Dec2022. Treatment: None. Product details: Had his first dose of Pfizer Covid 19 vaccine on 11Nov2022 with a lot of FT9142 and unknown expiration date. Pfizer/BioNTech COVID-19 Vaccine Follow-up, Questionnaire 1. Patient Details: Patient Age at Time of Vaccination (Years): 3 years, 2 months 2.Pfizer/BioNtech COVID-19 Vaccine Details: 1st dose: Date: 11Nov2022 Time: Not provided. Anatomical Site of injection: Not provided, Route of Administration: if other, please specify: Not provided Batch/Lot number: FT9142 4. For Only: Vaccination Facility Type: Pharmacy. Vaccine Administered at Military Facility? No 5. 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): None 6. Concomitant Drugs: List below concomitant drugs taken within two weeks before the event onset. Exclude all drugs only administered more than two weeks before the event, and any drug used to treat the event or taken after event onset: None 7. Patient's Medical History (including any illness at time of vaccination): None 8. Family Medical History Relevant to Adverse Events (AEs): None 9. Relevant Tests: None 10. Specific Relevant Test: For Thromboembolic events with Thrombocytopenia: Not applicable 11. Adverse Events: Note: For Thromboembolic Events with Thrombocytopenia Include specific relevant test above: AE Term: second dose: son received an undiluted dose of the Covid 19 vaccine. Onset Time: approximately 1015. AE required visit to: followed up with physician's office on 05Dec2022 for general check up, AE Term: high fevers, Onset Time: 1400. AE required visit to: None. AE Term: decreased appetite, Onset Time: 1400; caller clarified the start date for decreased appetite was 02Dec2022 or 03Dec2022. AE required visit to: None. AE Term: very lethargic, Onset Time: 1400, AE required visit to: None. AE Term: irritable, Onset Time: 0700, AE required visit to: None, AE Term: having discharge from his eyes like a gooky something, Onset Time: 1400, AE required visit to: None 12. Autopsy Information: In case of death, was an autopsy done? Not applicable 13. Comments/Narrative: provide clear narrative description of the sequence of event(s), diagnosis, treatment, and any other relevant details: Not applicable. Caller would like to know how much of the actual compound (RNA) his son received after he received an undiluted 0.2 mL dose of the COVID-19 vaccine. Question: Caller thinks we should provide this information and also that the company is withholding information. Question: Caller would like to know how much diluent is added to each vial. Question: Caller would like to know how many mcg of RNA her son was administered. The information on the batch/lot number for BNT162b2 has been requested and will be submitted if and when received. Follow-up (09Dec2022): New information received from a contactable consumer reported for a patient which included: reporter slider #02, patient details (Ethnicity, height, weight), relevant medical history, historical vaccine, lab data, product details (lot no., expiry date, anatomical location) vaccination information (best doctor, vaccine facility information), event onset date, stop date, outcome, new event and clinical information was added.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- Test Name: Height; Result Unstructured Data: Test Result:3 feet, 1 inch.; Comments: Height is approximately 3 feet, 1 inch.; Test Name: Fever; Result Unstructured Data: Test Result:High; Comments: High fever; Test Name: weight; Result Unstructured Data: Test Result:35 pounds, 6 ounces; Comments: Weight is 35 pounds, 6 ounces.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other Conditions: No
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 2,0
- Geschlecht
- U
- Eingang
- 15.12.2022
- Impfdatum
- 07.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Overdose
Product preparation issue
Symptomtext
fatigue; She accidentally mixed the vial with 1.3 ml of diluent instead of 2.2 ml and realized this after she had administered 5 doses; She accidentally mixed the vial with 1.3 ml of diluent instead of 2.2 ml; This is a spontaneous report received from a contactable reporter(s) (Nurse) from medical information team. A 24-month-old patient received BNT162b2 (BNT162B2), on 07Oct2022 at 08:54 as dose 1 (maroon cap), single (Lot number: FT9142, Expiration Date: 31Dec2022) at the age of 24 months intramuscular, in left thigh for covid-19 immunisation. The patient's relevant medical history included: "GERD", start date: 13Jul2021 (ongoing), notes: Pertinent details: N/A. The patient's concomitant medications were not reported. Vaccination history included: pentacel (Manufacture: Sanofi, Batch/lot: UJ641AAA, Route: IM, Anatomical site of injection: Left thigh, No. of previous doses: 3), administration date: 14Sep2022; prevnar 13 (Manufacture: Pfizer, Batch/lot: FF7356, Route: IM, Anatomical site of injection: Right thigh, No. of previous doses: 3), administration date: 14Sep2022; fluzone (Manufacture: Sanofi, Batch/lot: UT7680MA, Route: IM, Anatomical site of injection: Left thigh, No. of previous doses: 2), administration date: 14Sep2022. The following information was reported: PRODUCT PREPARATION ISSUE (non-serious) with onset 07Oct2022 at 08:54, outcome "unknown", described as "She accidentally mixed the vial with 1.3 ml of diluent instead of 2.2 ml"; OVERDOSE (non-serious) with onset 07Oct2022 at 08:54, outcome "unknown", described as "She accidentally mixed the vial with 1.3 ml of diluent instead of 2.2 ml and realized this after she had administered 5 doses"; FATIGUE (non-serious) with onset 08Oct2022, outcome "recovered" (09Oct2022). Therapeutic measures were not taken as a result of fatigue. Additional information: The nurse reported a vaccination error involving the Pfizer COVID-19 vaccine maroon cap for 6 months to under 5 years. She was running a COVID clinic for little ones and she had consulted the COVID vaccine prep and administration summaries from the CDC website and she had gotten confused about the diluent amount and accidentally mixed the vial with 1.3 ml of diluent instead of 2.2 ml and realized that after she had administered 5 doses and could not draw anymore, up to 5 kids (1 was almost 2, 1 patient was 2, 1 patient was 3, 1 patient was 15 months and 1 patient was 6 months) were administered with the vaccine; she stated that it was the last vaccine for 2 of the patients. The reporter considered that the Pfizer product had a causal effect to the adverse event. Relevant tests were not done. Follow-up (10Oct2022): This is a spontaneous follow-up report received in response to the mail trail sent regarding the confirmation of query. The response included: Updated information: Reporter information updated. Follow-up (14Oct2022): Follow-up attempts are completed. No further information is expected. Follow-up (09Dec2022): This is a spontaneous follow-up report received from the same contactable Nurse. This Nurse reported for the patient in response to HCP letter sent via follow-up letter which included that: Updated information included: Reporter's details, historical vaccine details, suspect product details and additional information were updated.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202201213448 same reporter, drug, and event; different patient;US-PFIZER INC-202201213449 same reporter, drug, and event; different patient;US-PFIZER INC-202201213450 same reporter, drug, and event; different patient;US-PFIZER INC-202201213451 same reporter, drug, and event; different patient;US-PFIZER INC-PV202200122002 Same patient/drug, different dose/event;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- GERD (Pertinent details: N/A)
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 13.12.2022
- Impfdatum
- 02.12.2022
- Beginn
- 02.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
Overdose
Product preparation error
Pyrexia
Symptomtext
given the pfizer maroon cap vaccine without diluent; 0.2ml (undiluted); high fever; This is a spontaneous report received from a contactable reporter(s) (Pharmacist) from medical information team, Program ID. A 3-year-old male patient received BNT162b2 (BNT162B2), on 02Dec2022 as dose 2 (maroon cap), 0.2 ml single (Lot number: FT9142, Expiration Date: 31Dec2022) at the age of 3 years for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Dose: 1; Manufacturer unknown), for COVID-19 immunization. The following information was reported: OVERDOSE (non-serious) with onset 02Dec2022, outcome "unknown", described as "0.2ml (undiluted)"; PRODUCT PREPARATION ERROR (non-serious) with onset 02Dec2022, outcome "unknown", described as "given the pfizer maroon cap vaccine without diluent"; PYREXIA (non-serious) with onset 02Dec2022, outcome "unknown", described as "high fever". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of pyrexia. Additional information: States there was an incident in which a toddler was given the pfizer maroon cap vaccine without diluent. States she needs information on how much the dosage would have been. States she followed up with the mom, so far the child had a high fever one day after the vaccine was administered. States the child was given Motrin which brought it back down and seems to be ok right now. Confirms dose volume that was administered to the 3 yr old male patient was 0.2ml. NDC number of Pfizer Covid vaccine: 59267007801. The Pfizer covid vaccine that was administered for toddlers age 3-4 and she had made a report with interaction; they had a 2nd dose administered on a toddler and it was given without the diluent at the dose of 0.2mL and she did file this information in an initial report but did not know if there was any other information as far as what to look for and side effects and this happened on the 02Dec.It was said they had a toddler that received his second dose without the dose being diluted. Caller asking what they need to do. It was mentioned that they had a toddler that received his second dose without the dose being diluted. Reported that they do have a patient who received the second dose of Pfizer covid-19 maroon cap without diluent.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- Test Name: Fever; Result Unstructured Data: Test Result:Unknown results
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 08.12.2022
- Impfdatum
- 21.11.2022
- Beginn
- 06.12.2022
- Tage bis Beginn
- 15,0
- Dosis
- 1
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Contusion
Nasopharyngitis
Pyrexia
Respiratory symptom
Urticaria
Vomiting
Symptomtext
On 12/6 at 7am patient woke up with hives on her inner thighs, back of armpits, insides/backs of legs. The hives spread quickly to all of legs, arms, belly, hands, and face. We gave her Benedryl at 830am which did help the hives subside, but by 4pm they came back with increased amount. We brought her to urgent care at 5pm. The doctor evaluated her with no clear diagnosis, diagnosed uticaria and told to f/u with PCP. She has had upper respiratory s/s, fever, vomiting, and cold symptoms intermittently for the past 4-6 weeks, which I reported to the doctor. She was prescribed Prednisone, benadryl, and pepcid. Following day, PCP was called - we were advised to change benadryl to oral Zyrtec instead. We don't know if these hives are from one of the vaccines from 11/21/22 or from circulating Flu/RSV/viral illnesses in the community. Today, 12/8/22, she now has superficial bruising to her abdomen, legs, and buttocks. Her disposition and appetite are normal. She does not appear to be overtly itchy or uncomfortable.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- Sickle cell trait, reactive airway disease
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- Pediarix (DTap, HepB, IPV) - 13 months old, large 8 inch diameter warm/raised circumcised area
- Staat
- -
- Alter
- 1,3
- Geschlecht
- M
- Eingang
- 07.12.2022
- Impfdatum
- 07.12.2022
- Beginn
- 07.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Immediate post-injection reaction
Rash
Symptomtext
Patient developed rash over torso, back, abdomen, neck, and face 10 minutes after receiving first dose of Pfizer COVID Vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Chronic Rhinitis
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 1,8
- Geschlecht
- F
- Eingang
- 05.12.2022
- Impfdatum
- 13.09.2022
- Beginn
- 13.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Crying
Rash
Rash erythematous
Swelling face
Symptomtext
22 month old patient came in to receive her 2nd dose of Covid Vaccine. Administered Pfizer Peds 6mos-4yrs covid vaccine at 1610. Patient started crying and was inconsolable 5 minutes after. I checked the injection site and there is no redness or swelling. Ten minutes after the injection, mom noticed patient's face is swollen. Noticed patchy red rash around the cheek area. Temp is 99.8F, tympanic. Notified RN Manager and Peds On-Call, give Benadryl 0.2mL. Administered Benadryl 0.2mL at 1643. Ice pack placed on the injection site. VS at 1655 as follows: BP 125/74 (crying), HR 116. Patient monitored for 30 minutes after Benadryl was given. Patient is more calm, asleep and in no signs of distress. Face is not swollen anymore and rash is nearly resolved. No audible wheezing. MD advised parents to follow-up with patient's PCP. At 1715, MD cleared patient to be discharged.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 05.12.2022
- Impfdatum
- 02.12.2022
- Beginn
- 02.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Aphasia
Nausea
Pallor
Peripheral coldness
Vomiting
Symptomtext
Patient was here with her mother for influenza vaccine and Covid vaccination - Pfizer #1. Pt healthy and talkative when presented to room. Was fussing that she "didn`t want a shot" just prior to immunizations. After vaccinations, pt was talking, choosing stickers, conversing with her mother, reading a book, walking around the room, ate some candy. Pt was seated in hallway near nurses' desk with mother for the 15 min observation time. At 1555, patient became pale, nauseated, vomited undigested food from lunch on the chair in the hallway. Given oral care. Lying down on the chair in hallway. Pt was moved to an individual pt room and assisted to lie down on the mat. Ice pack to posterior neck area for comfort. Pt was quiet, skin pale and cool. Still nauseated. Was able to focus on mother to commands, but would not verbalize to questions asked of her. O2 Sat was 95%. Pulse 84. T97.4. Heart auscultated, apical pulse strong and regular. Peds BP cuff too large for pt - unable to obtain reading. Within 10 min, pt was talking and answering questions. Skin color improving, to normal pink color. 911 called at beginning of event, but since pt was improving, and after consulting with mother, mother opted not to have patient taken to ER by ambulance. Mother feels comfortable continuing to watch her at home. Mother instructed on signs and sx to watch for. Continued observation here 15 more minutes. Pt was up, jumping and playing on the mat. Sat with mother on chair, talking about Christmas presents. Laughing and playing game with staff. Tried to recheck pt O2 sat but her hands were too cold from ice pack and she was very mobile. Nurses present.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 01.12.2022
- Impfdatum
- 30.11.2022
- Beginn
- 30.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lip swelling
Pruritus
Rash
Rash erythematous
Symptomtext
Patient received the shot at about 3:30pm. In the left thigh. At about 8:45pm, parent noticed several flesh tone bumps on the patient?s left thigh (back). Parent thought it was mosquito bites. In the morning, the next day at 6:55am, noticed flash tone bumps all over the legs, arms, and trunk. Gave her 5ml of Zyrtec. There were also several red bumps throughout the body. Then later in the day the bumps spread to the ear and face. At 4:45pm, noticed the lips were swollen. Also saw that all the flesh stone bumps were now all red bumps. There was also a significant number of bumps compared to the morning. The patient was acting normal throughout the entire day and also eating and drinking. There is some itching in some of the places on the body such as the thigh area (left and right) and the ankle (right). Took the patient to see a physician at 6:00pm. At this time noticed there were red bumps around the lips. The doctor didn?t find anything wrong after performing an examination besides the bumps on the body and advised to continue giving Zyrtec and that the side effects could last weeks. The doctor did inform the parents of signs to look out for that would warrant a need to go to the ER. The doctor also advised to speak to another doctor. Allergist and primary physician to determine if we should continue with the 3rd dose of Covid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- Ear infection 9 days prior to the vaccination. Taking amoxicillin and was on the 9th day of the medication.
- Vorgeschichte
- None
- Andere Medikamente
- Amoxicillin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 01.12.2022
- Impfdatum
- 30.11.2022
- Beginn
- 01.12.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Pyrexia
Symptomtext
Fatigue, Fever
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 30.11.2022
- Impfdatum
- 28.11.2022
- Beginn
- 28.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Ear swelling
Erythema
Eye swelling
Lip swelling
Oropharyngeal pain
Pruritus
Urticaria
Symptomtext
5 mins after receiving vaccines patient reported his throat was "hurting" his neck at skin was red and itchy. He was obsereved in the office for 20 mins and symptoms resolved. Within an hour of recieving the vaccines, when family was back at home, his eyes/ears/lips were swollen, he had widespread hives from head to toe and his body was bright red per mother. Mom took patient to the ED where they administered Benadryl and observed patient for 3 hours. Patient is doing well today.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Flu 11/17/22
- Vorgeschichte
- Tetralogy of Fallot
- Andere Medikamente
- No
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 29.11.2022
- Impfdatum
- 14.07.2022
- Beginn
- 16.07.2022
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Rash
Symptomtext
4-year-old rash. Based on history and clinical exam low suspicion for cellulitis, impetigo, zoster. Differential includes contact dermatitis, viral exanthem. allergic reaction (though with no hives). Plan for PO cetirizine. Close outpatient follow-up. Discharged in stable condition.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- exposed to shingles 2 weeks prior to vaccination
- Vorgeschichte
- Autism
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 21.11.2022
- Impfdatum
- 19.08.2022
- Beginn
- 24.08.2022
- Tage bis Beginn
- 5,0
- Dosis
- 2
- Route/Site
- SYR / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Decreased appetite
Fatigue
Malaise
Pyrexia
Symptomtext
She was very tired and was on the sofa all the time and didn't want to eat, and had a fever. After that on the following day I called the doctor, I thought she was a bit better and planned to take her to the doctor. As the day progressed she was getting better Mon/Tuesday. By Wednesday morning my other child started feeling ill, so I took them to the doctor and got her tested. Each child was sick for about 2 days, then I got COVID-19 and then my husband.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- None
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 18.11.2022
- Impfdatum
- 16.11.2022
- Beginn
- 18.11.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Diarrhoea
Symptomtext
Diarrhea after vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Runny nose within last month
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 18.11.2022
- Impfdatum
- 18.11.2022
- Beginn
- 18.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pruritus
Rash
Rash erythematous
Symptomtext
Pt developed red patches on bilateral forearms to elbow, reported a slight itch which resolved within about 5 minutes with a cold pack. Pt reported that her arms were itchy earlier in the day but patches were not present to arm at time of injection. Pt assessed by Nurse Practitioner in office who advised additional 15 minute monitoring in office . Pt reported itch had resolved. Nurse Practitioner in patient room for reassessment who had ok'd pt to leave office and recommended Benadryl as needed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 18.11.2022
- Impfdatum
- 18.07.2022
- Beginn
- 05.08.2022
- Tage bis Beginn
- 18,0
- Dosis
- 2
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Nasal congestion
Pain in extremity
Pyrexia
SARS-CoV-2 test positive
Symptomtext
After the vaccine, she complained of arm soreness for a day or two. She tested positive for COVID-19 on 08/05/2022. We alternated between MOTRIN and TYLENOL for her symptoms. She had a fever, mild cough and mild nasal congestion which lasted about 48 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- 05AUG2022 COVID-19 test positive
- Aktuelle Erkrankungen
- Cold
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 17.11.2022
- Impfdatum
- 09.11.2022
- Beginn
- 10.11.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Cough
Decreased appetite
Ear pain
Lacrimation increased
Nasal congestion
Ocular hyperaemia
Symptomtext
red and watery eyes; red and watery eyes; cough; nasal congestion; earache; lack of appetite; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). A 4-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 09Nov2022 at 15:30 as dose 1 (maroon cap), single (Lot number: FT9142) at the age of 4 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Covid-19" (unspecified if ongoing), notes: If covid prior vaccination: Yes. There were no concomitant medications. The following information was reported: COUGH (non-serious) with onset 10Nov2022 at 18:00, outcome "recovering"; EAR PAIN (non-serious) with onset 10Nov2022 at 18:00, outcome "recovering", described as "earache"; DECREASED APPETITE (non-serious) with onset 10Nov2022 at 18:00, outcome "recovering", described as "lack of appetite"; NASAL CONGESTION (non-serious) with onset 10Nov2022 at 18:00, outcome "recovering"; OCULAR HYPERAEMIA (non-serious), LACRIMATION INCREASED (non-serious) all with onset 10Nov2022 at 18:00, outcome "recovering" and all described as "red and watery eyes". The events "red and watery eyes", "cough", "nasal congestion", "earache" and "lack of appetite" required emergency room visit. Therapeutic measures were taken as a result of ocular hyperaemia, lacrimation increased, ear pain. Additional Information: The patient did not receive other vaccines within four weeks prior to COVID vaccine. The events resulted in doctor or other healthcare professional office/clinic visit, and emergency room/department or urgent care. Ear infection was treated with Amoxicillin. Prior to vaccination, the patient was diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ear pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19 (If covid prior vaccination: Yes)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 15.11.2022
- Impfdatum
- 28.10.2022
- Beginn
- 04.11.2022
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- IM / LG
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Ear infection
Ear pain
Pyrexia
Symptomtext
Night of 11/04/2022 woke up several times complaining of earache. Called doctor on 11/05/2022, went in to office and was diagnosed with an ear infection. Was prescribed amoxicillin. Spiked a fever on 11/06/2022 of 101. Has one dose antibiotic left. Has recovered from ear infection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ear pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 09.11.2022
- Impfdatum
- 08.11.2022
- Beginn
- 09.11.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Rash
Symptomtext
Mother indicates, minor began to present rash and itching in the area of the hands.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 04.11.2022
- Impfdatum
- 01.11.2022
- Beginn
- 01.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Malaise
Product preparation error
Pyrexia
Symptomtext
In addition to the 4 vaccines given above, see #17 - Covid 19 Pfizer-BioNTeck Vaccine 0.2 ml dose given (age 6 mo to less than 5 years old). Dose given was not diluted, resulting in 15 mcg being administered instead of 3 mcg which is the normal diluted dose. MD was notified assoon as discovered the day the dose administered, but after the patient left the clinic. There was no reaction in the 15 min observation period in the clinic after administration. MD documented 11/4/22 reassessment of patient via phone call with parents who denied any side effects other than 1-2 days febrile and feeling acutely ill, which is now fully resolved. MD recommended follow up in 304 months for rest of her vaccines.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none (avoids dairy)
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 1,3
- Geschlecht
- M
- Eingang
- 02.11.2022
- Impfdatum
- 29.09.2022
- Beginn
- 05.10.2022
- Tage bis Beginn
- 6,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Cardiomegaly
Chest X-ray abnormal
Pyrexia
Rash
Symptomtext
Patient got fever on day 3(10/01/2022), on October 5th patients fever was 104 pt. was seen in ER , rash developed . X-ray showed mild cardiomegaly
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- Chest X-ray 10/05/2022
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE at time of vaccine
- Andere Medikamente
- NONE
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 02.11.2022
- Impfdatum
- 30.09.2022
- Beginn
- 04.10.2022
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Rash
Viral rash
Symptomtext
Child received third dose of Pfizer vaccine and Seasonal Flu vaccine on 9/30 at 5:30PM. On 10/4 at 12:30PM, child presented with a mild rash on torso and legs. Pediatrician diagnosed with viral exanthem on 10/4. Rash worsened and spread to face and arms by 10/5. Rash cleared by 10/8/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Cough and ear infection (9/16-9/21)- Prescribed amoxicillin 400 mg/5 ml oral suspension; Completed medication on 9/29.
- Vorgeschichte
- None
- Andere Medikamente
- Completed amoxicillin 400 mg/5 ml oral suspension on 9/29 (day prior to vaccination)
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 02.11.2022
- Impfdatum
- 28.10.2022
- Beginn
- 28.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pain
Symptomtext
Site: Pain at Injection Site-Severe, Site: Redness at Injection Site-Severe, Additional Details: Ice pack administered to child. Advised mother to give motrin as needed for pain. Counseled mom to continue to monitor and seek higher level of care if worsening.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 1,8
- Geschlecht
- M
- Eingang
- 02.11.2022
- Impfdatum
- 26.10.2022
- Beginn
- 28.10.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema multiforme
Rash
Symptomtext
Erythema multiforme minor- rash on the face, thighs, abdomen and arms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Mild URI noted on 10/28/22
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 1,8
- Geschlecht
- F
- Eingang
- 01.11.2022
- Impfdatum
- 28.06.2022
- Beginn
- 30.06.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- SYR / LG
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Urticaria
Symptomtext
Two days after receiving dose one of the vaccine she erupted in hives all over her body. We sought care from her primary care physician at that time. The hives persisted throughout the following weeks and worsened significantly after her third dose of the vaccine. At that time we also sought care from her pediatric allergy specialist. The consensus amongst her providers was that she was having a hives immune response to the vaccine, NOT an allergic response and that she was not in danger at any point as a result of receiving this vaccine. Her daily allergy medication dosage was increased, at which point the hives resolved and have not returned.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Zyrtec
- Allergien
- Tree Nut Allergy
- Vorherige Impfungen
- She routinely breaks out in a rash following vaccine administration.
- Staat
- MA
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 01.11.2022
- Impfdatum
- 29.10.2022
- Beginn
- 01.11.2022
- Tage bis Beginn
- 3,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Pyrexia
Respiratory failure
Status epilepticus
Symptomtext
Hospitalization for status epilepticus and associated respiratory failure. Febrile to 106.9.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HIE, seizure disorder, developmental delay, feeding tube dependence
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 0,5
- Geschlecht
- M
- Eingang
- 01.11.2022
- Impfdatum
- 27.10.2022
- Beginn
- 28.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Injection site bruising
Petechiae
Platelet count decreased
Symptomtext
Petechial rash beginning 10/28/22 1 day after vaccination & significant bruising on body on body @ injection site. Twin sibling vaccinated same day (not identical) is fine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- 10/31 Platelet ct 15K, PT 13.7/PTT 44.3 see attached lab results
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Probiotic
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 31.10.2022
- Impfdatum
- 27.10.2022
- Beginn
- 27.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Injection site rash
Pyrexia
Symptomtext
MOTHE CALLLED ON 10/31/2022 REPORTED PATIENT HAD LOW GRADE FEVER ON 10/27/2022, WAS GIVEN TYLENOL. SHE ALSO STATED PATIENT DEVELOPED A RASH TO INJECTION SITE ON 10/30/2022. SHE STATES TODAY RASH LOOKS LIKE IT IS CLEARING UP SOME, NOT AS RED. MOTHER WAS INSTRUCTED IF SYMPTOMS WORSEN, GO TO ER.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Runny nose
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 27.10.2022
- Impfdatum
- 25.10.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Injection site pain
No adverse event
Symptomtext
There has been no adverse reaction to date. This dose was given too soon. Instead of 8 weeks between the 2nd and 3rd dose there was only 4 weeks. Only symptom experienced was soreness at the site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Sodium Fluoride 0. 5 mg Daily
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 25.10.2022
- Impfdatum
- 24.10.2022
- Beginn
- 24.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site pain
Product preparation issue
Symptomtext
Pt was given 0.2 undiluted dose of the 2-5 yr COVID vaccine. The Nurse manager called and spoke with mom, mom stated that pt had some soreness at the injection site, but no other symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- pneumonia viral illness
- Vorgeschichte
- dysphagia hypoxic ischemic encephalopathy
- Andere Medikamente
- amoxicillin
- Allergien
- none known
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 1,8
- Geschlecht
- F
- Eingang
- 25.10.2022
- Impfdatum
- 16.09.2022
- Beginn
- 20.10.2022
- Tage bis Beginn
- 34,0
- Dosis
- 3
- Route/Site
- IM / LG
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cough
Croup infectious
Pyrexia
Wheezing
Symptomtext
Agency woke up with a fever of 102 degrees Fahrenheit on 10/20/22 along with cough and wheezing. She was taken to urgent care the following day and was diagnosed with croup and treated with oral dexamethasone. I don?t believe this is an adverse reaction from the vaccine. She just got sick with a virus from daycare that caused her croup.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- None.
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 24.10.2022
- Impfdatum
- 15.09.2022
- Beginn
- 15.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Rash papular
Symptomtext
Pt developed diffuse papular rash 9 days after vaccine. no other smyptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash papular
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 22.10.2022
- Impfdatum
- 14.10.2022
- Beginn
- 14.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Overdose
Pain in extremity
Product preparation error
Symptomtext
sore arm; the vaccine was administered undiluted to a 3 year old female patient; the vaccine was administered undiluted to a 3 year old female patient; This is a spontaneous report received from a contactable reporter(s) (Pharmacist). A 3-year-old female patient received BNT162b2 (BNT162B2), on 14Oct2022 as dose 3 (maroon cap; booster), single (Lot number: FT9142) at the age of 3 years for covid-19 immunisation. The patient's relevant medical history included: "antibiotic" (unspecified if ongoing). Concomitant medication(s) included: BACTRIM PAEDIATRIC taken for antibiotic therapy, start date: 08Aug2022. Vaccination history included: BNT162b2 (DOSE 1, SINGLE), administration date: 29Jul2022, for Covid-19 immunization; BNT162b2 (DOSE 2, SINGLE), administration date: 19Aug2022, for Covid-19 immunization. The following information was reported: OVERDOSE (non-serious), PRODUCT PREPARATION ERROR (non-serious) all with onset 14Oct2022, outcome "unknown" and all described as "the vaccine was administered undiluted to a 3 year old female patient"; PAIN IN EXTREMITY (non-serious) with onset 15Oct2022, outcome "recovered" (16Oct2022), described as "sore arm". Additional information: A non-diluted covid vaccine was administered to a 3-year-old patient. Forgot to dilute in sodium chloride. The reporter was asking for advice on what to inform patient and what to do next. It was clarified that the type of medication error was overdose. The stage of medication error was preparation and administration. It was reported that pharmacy student comes once a week and was very busy and made the mistake. The overdose event was for the 3rd dose of the vaccine. The reporter called the patient 4-5 times since the overdose incident to check on them. Friday, 14Oct2022, the day of the overdose, the patient was fine and did not need any medical evaluation or treatment. Saturday (15Oct2022) she called the patient at 10:00 and the mom said the patient had a sore arm. Sunday (16Oct2022) she called the patient at 9:30 and the mom said the arm was arm still a little sore, but by 17:00 on Sunday no more sore arm. She called the patient on Monday (17Oct2022) and the patient was fine. The information on the batch/lot number for BNT162b2 has been requested and will be submitted if and when received. Follow-up (18Oct2022): This is a spontaneous follow-up report received from a contactable Pharmacist. This pharmacist reported in response to HCP telephonic follow-up activity. Updated information included: Historical vaccines (dose 1 and dose 2 added), medical history (antibiotic therapy added), Suspected vaccine (lot number FT9142, vaccination date, Dosage regimen, Vaccination facility details for dose 3), concomitant (Bactrim paediatric added), event data (Pain in arm added, onset date for vaccine overdose and product concentrate not diluted added) and additional information updated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Antibiotic therapy
- Andere Medikamente
- BACTRIM PAEDIATRIC
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 21.10.2022
- Impfdatum
- 15.09.2022
- Beginn
- 16.09.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash pruritic
Urticaria
Symptomtext
My daughter is on week 5 of ring shaped hives that all over her body: torso, legs, feet, hands, arms, face and ears. Given it was unkown at first, pediatrician, prescribed a round of oral liquid prednisone, 4ml twice a day for 3 days (9/20-9/22). This appeared to make the hives disappear after the last dose, but they came back and multiplied in less than 24 hrs later. We were told this was a rebound and she was placed back on prednisone this time once a day for 14 days. We saw no improvement this time, and by the end of the first of the 2nd round of prednisone, the pediatrician referred us to a dermatologist who confirmed (10/13) the itchy patches were hives, likely resulting from the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash pruritic
- Hospital-Tage
- -
- Labordaten
- Only visual test by dermatologist on 10/13
- Aktuelle Erkrankungen
- Skeeter Syndrome allergic reaction to mosquito bite on 9/2
- Vorgeschichte
- none
- Andere Medikamente
- multivitatin gummy
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 21.10.2022
- Impfdatum
- 30.09.2022
- Beginn
- 30.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Irritability
Off label use
Overdose
Product preparation error
Product preparation issue
Product use issue
Vaccination site pain
Symptomtext
The child received 10 doses.; administered the full vial, undiluted; Off label use; Product use for unapproved combination; had soreness at her right arm injection site; a little fatigued and cranky; a little fatigued and cranky; This is a spontaneous report received from contactable reporter(s) (Other HCP) from medical information team. A 3-year-old female patient received BNT162b2 (BNT162B2), on 30Sep2022 at 11:00 as dose 2 (maroon cap), single (Lot number: FT9142, Expiration Date: 01Nov2022) at the age of 3 years, in left arm for covid-19 immunisation; influenza vaccine (FLU VACCINE VII), on 30Sep2022 as dose number unknown, single (Batch/Lot number: unknown) for immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. Vaccination history included: BNT162b2 (DOSE 1 (MAROON CAP), SINGLE, NCD: 59267-0078-1, lot: FT9142, Pfizer), administration date: 01Sep2022, when the patient was 3-year-old, for Covid-19 Immunization. The following information was reported: IRRITABILITY (non-serious), FATIGUE (non-serious) all with onset 30Sep2022, outcome "recovered" (02Oct2022) and all described as "a little fatigued and cranky"; VACCINATION SITE PAIN (non-serious) with onset 30Sep2022, outcome "recovered" (02Oct2022), described as "had soreness at her right arm injection site"; OFF LABEL USE (non-serious) with onset 30Sep2022 at 11:00, outcome "unknown"; PRODUCT USE ISSUE (non-serious) with onset 30Sep2022 at 11:00, outcome "unknown", described as "Product use for unapproved combination"; OVERDOSE (non-serious) with onset 30Sep2022 at 11:00, outcome "unknown", described as "The child received 10 doses."; PRODUCT PREPARATION ERROR (non-serious) with onset 30Sep2022 at 11:00, outcome "unknown", described as "administered the full vial, undiluted". Additional Information: Warm transfer from (name) Pfizer Medical Information INT-#. Reporting an incident with one of their patients. It was a 3-year-old girl patient. She has received the COVID vaccine from Pfizer -maroon cap. The nurse administered the full vial, undiluted. The child received 10 doses. The child is fine. The caller confirmed the details provided by the transferring agent. This happened during the immunizations clinic.This occurred about 11 am this morning 30Sep2022. Seriousness: it is serious to have a med error like this, but the baby is fine. She was fine during the 15-minute observation. It is not disabling at this time. They are expecting an increased systemic response. She also received the flu shot today. This was her second dose of the COVID vaccine. She didn't have any medications listed on her consent form .Patient's Medical History (including any illness at time of vaccination): 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: no. Relevant Tests: List other relevant diagnostic and confirmatory test results for event(s), for example, from blood tests, cerebrospinal fluid culture, bacterial sero-type, diagnostic imaging, (e.g., chest X-ray, MRI): no. Caller is an Manager with (city name) (state name) health department. One of her nurses administered 1 full vial of undiluted Pfizer BioNtech Covid vaccine maroon cap to a 3yo girl. Child waited customary 15min post vaccine dose and was fine. Error was noticed later when they were counting the doses. Child received 10 doses of the undiluted product. Event occurred today. Wants to know the procedure to follow post administration. On 03Oct2022, according to the call recording, the reporter stated that a 3-year-old female patient was administered the contents of a full undiluted vial, which contains 10 doses; so, 1 child received 10 doses. Upon follow up on 17Oct2022, it was reported that the phone out 3:15pm. Phone answered by reporter who provided an update. She spoke to the parents who said the patient had soreness at her right arm injection site and was a little fatigued and cranky that Friday. By Sunday she was back to her normal self and running around playing and was fine now. Follow-up (03Oct2022): This is a spontaneous follow-up report received in response to the mail trail sent confirming that 1 child received 10 doses. Updated information includes: additional clinical details. Follow-up attempts are completed. No further information is expected. Follow-up (17Oct2022): This is a spontaneous follow-up report from a contactable Other HCP. This Other HCP reported in response to HCP letter sent via telephonic follow-up activity. Updated information included: New events (Product use for unapproved combination, Off label use vaccination site pain, irritability, and fatigue) and Additional information added. Follow-up attempts are completed. No further information is expected.; Sender's Comments: The event of Overdose is assessed as related to suspect drug BNT162b2
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 21.10.2022
- Impfdatum
- 30.09.2022
- Beginn
- 30.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Irritability
Off label use
Overdose
Product preparation error
Product preparation issue
Product use issue
Vaccination site pain
Symptomtext
The child received 10 doses.; administered the full vial, undiluted; Off label use; Product use for unapproved combination; had soreness at her right arm injection site; a little fatigued and cranky; a little fatigued and cranky; This is a spontaneous report received from contactable reporter(s) (Other HCP) from medical information team. A 3-year-old female patient received BNT162b2 (BNT162B2), on 30Sep2022 at 11:00 as dose 2 (maroon cap), single (Lot number: FT9142, Expiration Date: 01Nov2022) at the age of 3 years, in left arm for covid-19 immunisation; influenza vaccine (FLU VACCINE VII), on 30Sep2022 as dose number unknown, single (Batch/Lot number: unknown) for immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. Vaccination history included: BNT162b2 (DOSE 1 (MAROON CAP), SINGLE, NCD: 59267-0078-1, lot: FT9142, Pfizer), administration date: 01Sep2022, when the patient was 3-year-old, for Covid-19 Immunization. The following information was reported: IRRITABILITY (non-serious), FATIGUE (non-serious) all with onset 30Sep2022, outcome "recovered" (02Oct2022) and all described as "a little fatigued and cranky"; VACCINATION SITE PAIN (non-serious) with onset 30Sep2022, outcome "recovered" (02Oct2022), described as "had soreness at her right arm injection site"; OFF LABEL USE (non-serious) with onset 30Sep2022 at 11:00, outcome "unknown"; PRODUCT USE ISSUE (non-serious) with onset 30Sep2022 at 11:00, outcome "unknown", described as "Product use for unapproved combination"; OVERDOSE (non-serious) with onset 30Sep2022 at 11:00, outcome "unknown", described as "The child received 10 doses."; PRODUCT PREPARATION ERROR (non-serious) with onset 30Sep2022 at 11:00, outcome "unknown", described as "administered the full vial, undiluted". Additional Information: Warm transfer from (name) Pfizer Medical Information INT-#. Reporting an incident with one of their patients. It was a 3-year-old girl patient. She has received the COVID vaccine from Pfizer -maroon cap. The nurse administered the full vial, undiluted. The child received 10 doses. The child is fine. The caller confirmed the details provided by the transferring agent. This happened during the immunizations clinic.This occurred about 11 am this morning 30Sep2022. Seriousness: it is serious to have a med error like this, but the baby is fine. She was fine during the 15-minute observation. It is not disabling at this time. They are expecting an increased systemic response. She also received the flu shot today. This was her second dose of the COVID vaccine. She didn't have any medications listed on her consent form .Patient's Medical History (including any illness at time of vaccination): 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: no. Relevant Tests: List other relevant diagnostic and confirmatory test results for event(s), for example, from blood tests, cerebrospinal fluid culture, bacterial sero-type, diagnostic imaging, (e.g., chest X-ray, MRI): no. Caller is an Manager with (city name) (state name) health department. One of her nurses administered 1 full vial of undiluted Pfizer BioNtech Covid vaccine maroon cap to a 3yo girl. Child waited customary 15min post vaccine dose and was fine. Error was noticed later when they were counting the doses. Child received 10 doses of the undiluted product. Event occurred today. Wants to know the procedure to follow post administration. On 03Oct2022, according to the call recording, the reporter stated that a 3-year-old female patient was administered the contents of a full undiluted vial, which contains 10 doses; so, 1 child received 10 doses. Upon follow up on 17Oct2022, it was reported that the phone out 3:15pm. Phone answered by reporter who provided an update. She spoke to the parents who said the patient had soreness at her right arm injection site and was a little fatigued and cranky that Friday. By Sunday she was back to her normal self and running around playing and was fine now. Follow-up (03Oct2022): This is a spontaneous follow-up report received in response to the mail trail sent confirming that 1 child received 10 doses. Updated information includes: additional clinical details. Follow-up attempts are completed. No further information is expected. Follow-up (17Oct2022): This is a spontaneous follow-up report from a contactable Other HCP. This Other HCP reported in response to HCP letter sent via telephonic follow-up activity. Updated information included: New events (Product use for unapproved combination, Off label use vaccination site pain, irritability, and fatigue) and Additional information added. Follow-up attempts are completed. No further information is expected.; Sender's Comments: The event of Overdose is assessed as related to suspect drug BNT162b2
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 0,8
- Geschlecht
- M
- Eingang
- 20.10.2022
- Impfdatum
- 13.10.2022
- Beginn
- 14.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Diarrhoea
Infant irritability
Symptomtext
diarrhea and irritability developed 24 hours after immunizations; no fever or vomiting or rash; no weight loss; slowly improved over 7 days
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 19.10.2022
- Impfdatum
- 06.09.2022
- Beginn
- 10.09.2022
- Tage bis Beginn
- 4,0
- Dosis
- 2
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dermatitis diaper
Rash
Symptomtext
I noticed that a few days after the vaccine she developed a rash on her bottom, and I thought it was a diaper rash and it didn't improve. I then tried CETAPHIL and that didn't work. I called the doctor, and he prescribed a steroidal antifungal cream. He said if that didn't work, we would have to follow up with a Dermatologist. She is still dealing with the rash at this time. I still don't know if it is coincidental or related to the vaccine. There were no changes in detergent or anything like that.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- LIL CRITTERS multivitamin gummy
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 12.10.2022
- Impfdatum
- 12.10.2022
- Beginn
- 12.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Cough
Crying
Emotional distress
Erythema
Oropharyngeal pain
Pruritus
Urticaria
Wheezing
Symptomtext
Patient received vaccines at 1225 as ordered. Patient remained in room for 30 minutes post monitoring due to history of anaphylaxis to eggs. RN continued to check in on patient and MOC. 1255: RN noticed patient sitting on the bed looking very upset. Patient was scratching and MOC consoling. RN assessed and noted small, red, circular hives noted on back and neck. RN immediately brought CPNP to bedside for further assessment. 1300: Patient began coughing and stated his throat was hurting. NP listened to lung sounds and noted wheezing + called MD to bedside. IM Epi given to right thigh and patient placed on continuous pulse ox. Patient crying and hives spreading to face. 1303: RN gave PO benadryl as ordered. Breathing exercises completed with patient and patient tolerated PO benadryl well. Patient maintaining O2 sats 95% - 98% on room air. Wheezing continued, but breath sounds and hives improving. 1312: RN and NP continued monitoring closely at bedside and transferred patient + MOC safely to ED with second Epi pen dose on hand. 1320: Patient sitting up in wagon, continues to report throat hurting, but NAD and calm, breathing normally, awake and alert at this time. Hives fully subsided from face and decreased on back. Patient is no longer wheezing or coughing at this time. Patient checked in to ED; report given to ED RN by NP, and patient brought back to ED room safely with ED RN and MOC.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 1,1
- Geschlecht
- M
- Eingang
- 10.10.2022
- Impfdatum
- 06.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pyrexia
Rash
Rash erythematous
Rash maculo-papular
Symptomtext
He had fever the next day, and also developed a generalized erythematous maculopapular rash involving, trunk, extremities and face 3 days after the first dose of COVCID-19 vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- no
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- no
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 1,3
- Geschlecht
- M
- Eingang
- 08.10.2022
- Impfdatum
- 27.09.2022
- Beginn
- 02.10.2022
- Tage bis Beginn
- 5,0
- Dosis
- 3
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Anaemia
Blood culture
Blood lactic acid
Culture urine
Full blood count
Glucose urine present
Hyperglycaemia
Metabolic function test
Rash
Red blood cell sedimentation rate
SARS-CoV-2 test
Streptococcus test
Urine analysis abnormal
Symptomtext
4 days after dose 3 of Pfizer vaccine, patient seen in ED for wide spread rash, incidental finding of glucose in urine, hyperglycemia, anemia.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- 10/2/2022: ED had performed blood culture, urine culture, ua, strep and covid pcr nasal tests, cbcd, cmp, sed rate, lactate.
- Aktuelle Erkrankungen
- otitis media ; fever 6 days prior to dose 3 of Pfizer covid vaccine for under 5 years old.
- Vorgeschichte
- none
- Andere Medikamente
- amoxicillin day 9 of 10
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 07.10.2022
- Impfdatum
- 07.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 7+
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Crying
Rash macular
Symptomtext
mom notified nurse during waiting period of possible rash developing on patient's face. Patient had been crying hard during vaccination, blotching around eyes and cheeks visible, no hives. injection site clear, no visible rash or hives on abdomen or back, airway is unobstructed. Mom requested Benedryl to be given. Benedryl 12.5 mg given po at 1340. 1350 Patients blotches improved 1400 patient's face clear
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash macular
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- seasonal allergies
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 07.10.2022
- Impfdatum
- 06.10.2022
- Beginn
- 06.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pain in extremity
Product preparation issue
Symptomtext
no adverse reaction but the vaccine was not dilute properly prior to administration. pt reports arm pain and nothing else
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 04.10.2022
- Impfdatum
- 03.01.2022
- Beginn
- 03.10.2022
- Tage bis Beginn
- 273,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Nausea
Symptomtext
Vaccine was given by (RN), Client didn't seem sick or overly nervous. She sat on moms lap while mom answered questions about previous vaccinations. Pfizers 6mo-4 yr covid shot was given 0.2 mL in RD. Client did not appear to be in distress after vaccination and walked out of room for 15 min wait. During wait, mother states Patient begin to show symptoms of wanting to vomit. Mother states client never vomited and was showing signs of feeling better when we arrived to the car. Vital signs were taken, and snacks and orange juice were given. Mom stated client may have just been upset that father was unable to go with them to get vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 2,0
- Geschlecht
- M
- Eingang
- 03.10.2022
- Impfdatum
- 30.09.2022
- Beginn
- 30.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Fluid intake reduced
Hypersomnia
Hypophagia
Peripheral coldness
Skin warm
Vomiting
Symptomtext
Mom states that child went to sleep around 10pm and then slept for 14 hours after the vaccination. When he woke up he was not eating or barley drinking anything. When she gave him the bottle he threw up his milk and was in white chunks. She states his fever was 99.2 . Dad gave him a steamy bath and after gave him a cool damp rag because his body was warm to to touch and his feet was ice cold.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vomiting
- Hospital-Tage
- -
- Labordaten
- unknown, called her this morning and she states that she was taking him to the emergency room.
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- none
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 03.10.2022
- Impfdatum
- 16.09.2022
- Beginn
- 19.09.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Decreased appetite
Fatigue
Irritability
Pyrexia
Rash
Rash erythematous
SARS-CoV-2 test negative
Streptococcus test negative
Symptomtext
Crankiness, fatigue, loss of appetite started ~1 day post vaccine (9/17/22). Fever of ~102 F started around 3 days post vaccine (9/19/22). Controlled with Tylenol. Mild rash started on neck ~6 days post vaccine (9/22/22) and continued to get worse over several days. Rash (looked like moderate sunburn in circular patches on face, legs, arms, back... not raised, no weeping, no itching or pain). Fever varied around 99-102 F for several days. No elevated temperature as of 9/29/22. As of 10/02/22, fatigue and lack of appetite has persisted and has just started to get better. Rash significantly improved as of 10/02/22 - rashes began to fade from center of circle outward.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Doctor's visit on 9/22/22 and again on 9/29/22; COVID-19 test negative (patient and one family member both negative); Strep test negative
- Aktuelle Erkrankungen
- None known
- Vorgeschichte
- None known
- Andere Medikamente
- Vitamin B-12, Vitamin D, Omega-3
- Allergien
- None known
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 0,7
- Geschlecht
- M
- Eingang
- 30.09.2022
- Impfdatum
- 24.09.2022
- Beginn
- 28.09.2022
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- SYR / LG
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Decreased appetite
Ear infection
Irritability
Poor quality sleep
Pyrexia
Symptomtext
On Wednesday afternoon, he had a fever of 101.7 degrees and was very cranky. He was pulling at his ears and and a decrease in appetite. He did not sleep well Wednesday night. He was fussy again Thursday morning. I took him to the doctor's office. He was diagnosed with an ear infection. They prescribed amoxycillin. He seems to be feeling better today.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Cold
- Vorgeschichte
- None
- Andere Medikamente
- BIOGAIA probiotic
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 27.09.2022
- Impfdatum
- 23.09.2022
- Beginn
- 24.09.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Rash
Urticaria
Symptomtext
Patient took vaccination on 23rd Sept 2022 (4:30 pm ) and from next day around 12:00 pm he started developing hives ,rashes with itchiness. Hives,rashes would come and go after 1-2 hours and randomly re-appear on other parts of body(arms,hips,thighs,face,neck). We haven't given him any medication yet except Tylenol which we gave him after vaccination around 9:00 pm. We are still seeing symptoms as of 09/27/2022 9:55 pm CT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- He had common cold a week before he took vaccination .He recovered from it in 2 days.
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 2,0
- Geschlecht
- M
- Eingang
- 27.09.2022
- Impfdatum
- 01.09.2022
- Beginn
- 02.09.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Rash
Urticaria
Symptomtext
URTICARIA treated with Benadryl and topical hydrocortisone Patient seen in office 9/7, symptoms started 9/2. Diffuse rash. Improved with treatment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 2,0
- Geschlecht
- M
- Eingang
- 22.09.2022
- Impfdatum
- 16.09.2022
- Beginn
- 17.09.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SC / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Eye discharge
Rash erythematous
Symptomtext
He had pfizer COVID vaccine on Friday 9/16 and then got the rash on 9/17/22. It was tiny pink bumps on arms, legs and trunk as well. It did not bother him. The rash is flat. It was never bumpy. They were very small spots, like 1 mm. There were not migratory. It seemed to appear everywhere at once, and has not changed location since. No blistering nor sloughing of skin. No change in skin products nor soaps. On 9/17 he woke up with some gunk in the eyes and then it cleared up over that weekend. His eyes were not appreciably pink. He was not sick in any other way at that time. He was sick the week prior but was definitely on the mend for many days and then the eye symptoms happened somewhat out of the blue. No runny nose nor seeming in pain/sore throat nor cough at that time. The eyes were better within a few days. They were dabbing some tea bags on the eyes which helped. No tongue swelling nor lip swelling. No abnormal breathing nor funny noises with breathing. No vomiting. Rash is about the same since (this visit was 5 days from vaccination)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash erythematous
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Sick on approximately 9/10/22 with mild viral illness that was improving. Then on 9/17 he had some discharge in the eyes without other symptoms and that cleared up over a few days. No conjunctivitis.
- Vorgeschichte
- Recurrent otitis media
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 20.09.2022
- Impfdatum
- 13.09.2022
- Beginn
- 13.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Rash erythematous
Respiratory tract congestion
Symptomtext
He developed red goosebump-size bumps primarily on his core, chest, back, and down both arms. The redness has faded, but he still has raised bumps. They have diminished in size, but they are still present. He did not develop a fever and the bumps did not itch. He also has a cough and congestion, but I think that is due to having a cold.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash erythematous
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Flintstone Gummy Vitamins
- Allergien
- Seasonal Allergy
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 0,5
- Geschlecht
- M
- Eingang
- 20.09.2022
- Impfdatum
- 16.09.2022
- Beginn
- 16.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Symptomtext
Patient developed a slight rash approximately 30- 40 minutes after vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- None-Patient was seen in office the same day afterwards.
- Aktuelle Erkrankungen
- Urticaria, Ear Infection, Eye Drainage
- Vorgeschichte
- GERD
- Andere Medikamente
- Pepcid (6.4mg total)
- Allergien
- Lactose
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 19.09.2022
- Impfdatum
- 03.08.2022
- Beginn
- 01.09.2022
- Tage bis Beginn
- 29,0
- Dosis
- 2
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Pruritus
Rash
Skin irritation
Urticaria
Symptomtext
He has a heavy, dry cough a couple of weeks after receiving his vaccine. Days after that, he started having hives on his arm and really bad itching like something was irritated him. I contacted his doctor about it and they informed me to put hydrocortisone cream on it to see if it would reduce the itch and hive outbreak. They told me if the coughing and hives persist to wear he can't breathe to take him to the emergency room. He still does his normal daily activities, but the cough won't subside since receiving his vaccine. When he's having a breakout, the pediatrician told me to give him an allergy medication (I alternate between BENADRYL and ZYRTEC to help the breakout as well).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 19.09.2022
- Impfdatum
- 27.06.2022
- Beginn
- 27.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Agitation
Anger
Headache
Symptomtext
Both times headaches, anger and agitation for up to 2 weeks after the vaccine. DUE FOR DOSE 3 ON 9/21/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 1,2
- Geschlecht
- M
- Eingang
- 19.09.2022
- Impfdatum
- 15.09.2022
- Beginn
- 17.09.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Decreased appetite
Fatigue
Feeling abnormal
Irritability
Pyrexia
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test negative
Symptomtext
He started having a runny nose, congestion, fatigue, loss of appetite, irritable, coughing and a low grade fever. They just told me to give him MOTRIN and TYLENOL. He hasn't been feeling good since the night of the vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 test- negative- 9/17/22.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Seizures
- Andere Medikamente
- KEPPRA; TYLENOL; MOTRIN
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 18.09.2022
- Impfdatum
- 15.09.2022
- Beginn
- 15.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Oropharyngeal pain
Pyrexia
Symptomtext
Dose #3 given too early. Dose #1 was given on 7/28/2022. Dose #2 was given on 8/25/2022. Parent aware. Mom reported that patient had a sore throat and fever the night of 9/15/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- 8/19/22 Strep Throat and took a course of Amoxicillin
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 18.09.2022
- Impfdatum
- 15.09.2022
- Beginn
- 15.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Delirium
Feeling cold
Vomiting
Symptomtext
7:00 PM: Described feeling cold, but no detectable fever. 9:00 PM: Awoken from sleep and deliriously walking through the hall. 11:30 PM: Vomited, Provided Tylenol 4:00 AM: Vomited
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vomiting
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- Minor cold with fever.
- Vorgeschichte
- -
- Andere Medikamente
- Zyrtec (5mL), Probiotic Gummies, 2x Daily Pepcid
- Allergien
- Egg, Peanut, Tree Nuts, Sesame
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 1,0
- Geschlecht
- F
- Eingang
- 17.09.2022
- Impfdatum
- 17.09.2022
- Beginn
- 17.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site cellulitis
Symptomtext
Right thigh cellulitis noted on 9/17/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site cellulitis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Cholecalciferol oral drops
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 16.09.2022
- Impfdatum
- 03.08.2022
- Beginn
- 03.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site discolouration
Symptomtext
After receiving his first Covid vaccine, mom noticed a very small bluish/black dot at the injection site. It was not swollen or painful. We were using a different brand needles than our usual so unsure if the spot was left from the needle or the vaccine itself.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site discolouration
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- none
- Allergien
- none known
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 1,3
- Geschlecht
- F
- Eingang
- 15.09.2022
- Impfdatum
- 14.09.2022
- Beginn
- 14.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cough
Hypersomnia
Injection site erythema
Rash
Symptomtext
Patient came in to office for her 2nd covid dose, successful vaccination given in left thigh, pt observed after injection for 15min, Pt injection site was checked before being discharged from office and nurse and mom notice redness at diaper line that was not present prior to injection. Dr. came in to observe injection site, benadryl 7ml was order and pt was observed in office for additional 25-30min. During observation Rash did become a littler more prounced and spreading to arms but after calmed down and could see improvement occuring with redness. Also while observing patient she started to cough which was not present per mom prior to visit. Dr. ordered steroid dexamethasone 0.9 ml inj to be given ot pt observed for additional 20-30 min, outcome was good pt looked great, pt discharged with mom and dad home. Pt contacted today RE: follow up call, mom states pt did well after visit, slept alot, mom didn't have to take her to take her to ER/urgent care.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- per mom none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- N.K.D.A
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 0,9
- Geschlecht
- M
- Eingang
- 14.09.2022
- Impfdatum
- 30.07.2022
- Beginn
- 30.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Discomfort
Ear infection
Nasal congestion
Pain
Vomiting
Symptomtext
On 7/30/22 he vomited 3x and had no fever, several wet diapers. On 8/3/22 he had nasal congestion, cough, and was feeling uncomfortable and was in pain. Took him to Pediatrician the next day and he diagnosed with a double ear infection and just kind of looked like most allergies. They prescribed antibiotics for the ear infections.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Vitamin D3
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 1,5
- Geschlecht
- M
- Eingang
- 12.09.2022
- Impfdatum
- 17.08.2022
- Beginn
- 18.08.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Urticaria
Symptomtext
Hives one day after vaccination on 8/17/22 Taken to urgent care & prescribed Benadryl
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Sodium Fluoride
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 12.09.2022
- Impfdatum
- 23.08.2022
- Beginn
- 24.08.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site erythema
Injection site swelling
Symptomtext
Large erythematous swollen area at the injection site the day after her shot. Resolved over 3 days w/ antihistamine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- vitamins
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 12.09.2022
- Impfdatum
- 29.08.2022
- Beginn
- 01.09.2022
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Angular cheilitis
Rash maculo-papular
Symptomtext
Maculopapular rash onset about 3 days after receiving vaccine. Generalized over body. Self resolved after about 1 week (dried up per MOC). Also with angular cheilitis that self resolved at the same time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash maculo-papular
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Infantile eczema
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 2,0
- Geschlecht
- M
- Eingang
- 12.09.2022
- Impfdatum
- 08.09.2022
- Beginn
- 09.09.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Body temperature increased
Diarrhoea
Vomiting
Symptomtext
Loose stool, vomiting, and temp 102 F.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 2,0
- Geschlecht
- M
- Eingang
- 09.09.2022
- Impfdatum
- 17.08.2022
- Beginn
- 17.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Injection site rash
Injection site urticaria
Lip pruritus
Lip swelling
Urticaria
Symptomtext
Patient had Pfizer vaccine on 08/17/2022 on his right thigh and 15 minutes later mom reported rash on right thigh on the site of the vaccine and provider evaluated patient and diagnosis urticaria right thigh and right buttock and prescribed Benadryl 5 ml and patient took it. After 10 minutes, mom reported patient with lips itchy and provider found slight swollen lip and patient had EpiPen Jr one dose and he was sent to the Emergency room. In ER, got PO steroids, observed, symptoms resolved, didn't recur.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 0,7
- Geschlecht
- M
- Eingang
- 09.09.2022
- Impfdatum
- 20.08.2022
- Beginn
- 21.08.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Symptomtext
Diffuse rash the day after vaccination not responsive to diphenhydramine that lasted less than 1 week.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- None; was evaluated in the office.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Vitamin D 400 IU daily
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 2,3
- Geschlecht
- M
- Eingang
- 08.09.2022
- Impfdatum
- 24.08.2022
- Beginn
- 03.09.2022
- Tage bis Beginn
- 10,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Conjunctivitis
Cough
Ear infection
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test negative
Symptomtext
Starting on 9/3/22, 10 days after receiving the second dose of the pfizer covid vaccine, patient had conjunctivitis, congestion and slight cough.Also, there was a pontential covid exposure on 9/1/22 and a at home test was performed results were negative. Due to the holiday weekend of labor day we took patient in to be seen by his primary Doctor on 9/6/22. He was diagnosis with a double ear infection. His doctor prescibed a course of antibotic, augment. On 9/7/22 he developed a fever of 101, we have treated with tylenol. Unsure if this is a true adverse reaction to the vaccine, or simply a child who got sick.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- At home Covid test performed on 9/4/22 Results Negative. Covid Rapid test again 9/6/22 results negtaive. PCR covid test performed 9/6/22 results negative.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none known at this time.
- Andere Medikamente
- none, at the time of vaccination
- Allergien
- none known at this time.
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 06.09.2022
- Impfdatum
- 02.09.2022
- Beginn
- 03.09.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Pyrexia
Symptomtext
Patient's mother stated that they have been monitoring his fever for 4 days, alternating ibuprofen and tylenol. Mother stated that patient has no other symptoms, but started a dry, occasional cough on 9/5/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- unknown
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 06.09.2022
- Impfdatum
- 08.07.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Vaccination site pain
Symptomtext
Pain at the injection site, sore arm; This is a spontaneous report received from a contactable reporter(s) (Nurse). A 4-year-old male patient received BNT162b2 (BNT162B2), on 08Jul2022 as dose 1, single (Lot number: FT9142, Expiration Date: Jan2023) at the age of 4 years, in right arm for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: VACCINATION SITE PAIN (non-serious) with onset 2022, outcome "unknown", described as "Pain at the injection site, sore arm". Additional Information: The patient had pain at the injection site, sore arm, with the first dose. No additional vaccines was administered on same date of the Pfizer suspect. The patient did not receive other vaccines within four weeks prior to COVID vaccine. No adverse event following prior vaccinations. The NDC number was 59267007804.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site 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
- AZ
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 06.09.2022
- Impfdatum
- 23.08.2022
- Beginn
- 23.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Body temperature
Overdose
Product preparation error
Pyrexia
Symptomtext
fever 101.3; administered to a patient without being diluted; administered to a patient without being diluted; This is a spontaneous report received from contactable reporter(s) (Other HCP and Physician) from medical information team, Program ID. A 2-year-old female patient received BNT162b2 (BNT162B2), on 23Aug2022 at 10:54 as dose 2 (maroon cap), 0.2 ml single (Lot number: FT9142, Expiration Date: 31Dec2022) at the age of 2 years intramuscular, in left deltoid for covid-19 immunisation. The patient's relevant medical history included: "allergies" (unspecified if ongoing), notes: diagnosed allergies; "compromised immune status" (unspecified if ongoing); "respiratory illness" (unspecified if ongoing); "genetic/chromosomal abnormalities" (unspecified if ongoing); "endocrine abnormalities (including diabetes)" (unspecified if ongoing); "endocrine abnormalities (including diabetes)" (unspecified if ongoing); "obesity" (unspecified if ongoing). There were no concomitant medications. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE), for COVID-19 immunization. The following information was reported: OVERDOSE (non-serious), PRODUCT PREPARATION ERROR (non-serious) all with onset 23Aug2022 at 10:54, outcome "unknown" and all described as "administered to a patient without being diluted"; PYREXIA (non-serious) with onset 24Aug2022, outcome "recovered", described as "fever 101.3". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of pyrexia. Additional information: patient age at time of vaccination in years: 2 years 9 months. This report is related to a study or programme. Vaccine name was unknown since not their patient. Concomitant drugs: drug name (trade and generic) was none. Patient(s) medical history: illness/ae was unknown. Reporter said the overdose event was the 2nd dose. The first dose was given in (withheld), so they don't have any information on the experience with prior dose. They are a walk in clinic, so the patient is not a regular patient. The patient has not reported any adverse events to them so far. Reporter clarified that she is a medical assistant who called on behalf of (withheld)-pediatrician, only provided by inbound transfer agent as unknown type of healthcare professional. She clarified that she did not call about the gray cap formulation; she called about the pfizer covid-19 vaccine, maroon cap 2-5 years of age formulation. She mentioned that this formulation is what they use for age 6 months to 4 years of age. She clarified that this patient was administered an undiluted dose of the product. She asked if they need to be aware if the patient could have any reactions relative to this event. Administered undiluted dose: there have been no associated adverse events or lasting effects with this event to caller's awareness. First dose, date of administration was unknown, reporter believes this suspect product dose was patient's second dose, but has no information to provide on what would have been her first dose. Vaccination facility type was clinic. Vaccine was not administered at military facility. 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) and reporter don't know about it. 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 was none. Reporter was not aware of emergency room, physician office, 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), ae(s) following prior vaccinations, patient's medical history (including any illness at time of vaccination) 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, family medical history relevant to ae(s) and relevant tests. Other conditions, investigations and other products was given as no. It was reported that, the day after the vaccine the patient had a fever 101.3 and she gave her Motrin to lower the temperature and the fever resolved. She had been eating and sleeping well. Follow-up (23Aug2022): This is a spontaneous follow-up report received from a contactable Other-HCP. Program Id. This Other-HCP reported for a 2 year old Female patient that: Updated Information: Reporter information, patient details, suspect details, relevant medical history and additional information. Follow-up (31Aug2022): This is a spontaneous follow-up report received from a contactable Other HCP. This Other HCP reported in response to HCP telephonic follow-up activity which included that: Updated information included: Lab data, event details (new event of fever, start date and treatment received were added) and additional information updated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- Test Name: fever; Result Unstructured Data: Test Result:101.3
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Allergy (diagnosed allergies); Chromosomal abnormality NOS; Diabetes; Endocrine disorder; Immune system disorder; Obesity; Respiratory disorder NOS neonatal
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 0,8
- Geschlecht
- F
- Eingang
- 05.09.2022
- Impfdatum
- 02.09.2022
- Beginn
- 03.09.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site rash
Rash
Symptomtext
rash. worst at location site, but also all over body: legs vagina, stomach chest, cheeks, arms
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- ear infection
- Vorgeschichte
- n/a
- Andere Medikamente
- Amoxocillin
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 02.09.2022
- Impfdatum
- 15.07.2022
- Beginn
- 15.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain
Body temperature
Dysphonia
Influenza virus test
Oropharyngeal pain
Poor quality product administered
Pyrexia
Streptococcus test
Wrong technique in product usage process
Symptomtext
This is a spontaneous report received from a contactable reporter(s) (Other HCP) from medical information team. A 4-year-old female patient received BNT162b2 (BNT162B2), on 15Jul2022 at 11:00 as dose 1, single (Lot number: FT9142) at the age of 4 years intramuscular for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. The following information was reported: WRONG TECHNIQUE IN PRODUCT USAGE PROCESS (non-serious) with onset 15Jul2022 at 11:00, outcome "unknown", described as "given incorrectly...The nurse drew up the diluent, 2.2ml, into a syringe and pulled 0.2ml from the vaccine vial into the syringe. It was mixed in the syringe and not in the vial."; POOR QUALITY PRODUCT ADMINISTERED (non-serious) with onset 15Jul2022 at 11:00, outcome "unknown", described as "it was given incorrectly. The nurse drew up the diluent, 2.2ml, into a syringe and pulled 0.2ml from the vaccine vial into the syringe. It was mixed in the syrin"; ABDOMINAL PAIN (non-serious) with onset 19Jul2022, outcome "unknown"; PYREXIA (non-serious) with onset 19Jul2022, outcome "unknown", described as "fever 101-102"; DYSPHONIA (non-serious) with onset 19Jul2022, outcome "unknown", described as "hoarse voice"; OROPHARYNGEAL PAIN (non-serious) with onset 19Jul2022, outcome "unknown", described as "sore throat". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of oropharyngeal pain, abdominal pain, pyrexia, dysphonia. Additional Information: Caller was an office manager calling on behalf of a pediatric clinic. The product was given incorrectly. Caller was not sure if she had time to do a report. The mother of the patient was getting antsy and had already been there for 30 minutes. Caller clarified that she did not have time to do a report at that time. Caller clarified how it was given incorrectly. The nurse drew up the diluent, 2.2ml, into a syringe and pulled 0.2ml from the vaccine vial into the syringe. The patient did not receive prior vaccinations within 4 weeks. It was mixed in the syringe and not in the vial. Follow-up (30Aug2022): This is a spontaneous follow-up report received from a contactable Other HCP. This Other HCP reported in response to HCP letter sent. Updated information: Vaccine Information (dose number, lot number, route of administration), information on concomitant medication, lab test, treatment received, vaccine administration facility information and new adverse events added.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220719; Test Name: Fever; Result Unstructured Data: Test Result:101-102; Test Date: 20220719; Test Name: FLU Rapid; Result Unstructured Data: Test Result:Negative; Test Date: 20220719; Test Name: Strep Rapid; Result Unstructured Data: Test Result:Negative
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 01.09.2022
- Impfdatum
- 22.08.2022
- Beginn
- 23.08.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
Dysarthria
Pyrexia
SARS-CoV-2 test
Symptomtext
very high fever 104 degrees/low grade fever (99/100 degrees); speech has been slurred; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the parent. A 4-year-old male patient received BNT162b2 (BNT162B2), on 22Aug2022 at 17:00 as dose 2, single (Lot number: FT9142) at the age of 4 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Covid-19" (unspecified if ongoing), notes: If covid prior vaccination: yes. There were no concomitant medications. Vaccination history included: BNT162b2 (Dose Number: 1, Batch/Lot No: FT9142, Location of injection: Arm Left, Vaccine Administration Time: 02:30 PM), administration date: 01Aug2022, when the patient was 4-year-old, for Covid-19 immunization. The following information was reported: DYSARTHRIA (non-serious) with onset 23Aug2022 at 16:30, outcome "recovering", described as "speech has been slurred"; PYREXIA (non-serious) with onset 23Aug2022 at 16:30, outcome "recovering", described as "very high fever 104 degrees/low grade fever (99/100 degrees)". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of pyrexia. Additional information: It was reported that, almost exactly 24 hours after the shot his son had a very high fever 104 degrees and fever reducers (tylenol & advil) at times only brought it down to 103 so they had to use ice packs to lower his fever in addition to the fever reducers. His fever lasted 32 hours and he then had a low grade fever (99/100 degrees). they noticed the day after his fever that his speech had been slurred. Patient recieved treatment fever reducers. Patient had covid prior vaccination. Patient did not test covid positive post vaccination no. Patient has no known allergies. Patient had no other vaccine in four weeks. Patient had no other medications in two weeks.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220823; Test Name: Fever; Result Unstructured Data: Test Result:104 degrees; Comments: after the shot my son had a very high fever 104 degrees; Test Date: 20220823; Test Name: Fever; Result Unstructured Data: Test Result:103; Comments: fever reducers (tylenol & advil) at times only brought it down to 103 so we had to use ice packs to lower his fever in addition to the fever reducers; Test Date: 20220823; Test Name: Fever; Result Unstructured Data: Test Result:(99/100 degrees).; Comments: His fever lasted 32 hours and he then had a low grade fever (99/100 degrees).; Test Name: Covid-19 test; Result Unstructured Data: Test Result:Yes; Comments: If Covid prior vaccination: Yes; Test Name: Covid-19 test; Result Unstructured Data: Test Result:No; Comments: If Covid tested post vaccination: No
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19 (If covid prior vaccination: yes)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 31.08.2022
- Impfdatum
- 18.08.2022
- Beginn
- 27.08.2022
- Tage bis Beginn
- 9,0
- Dosis
- 2
- Route/Site
- SYR / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Malaise
Pyrexia
SARS-CoV-2 test negative
Vomiting
Symptomtext
Three year old. Nine days after vaccination she had a fever of 101.9, and threw up. Took her to the Dr., and upon examination the Dr. didn't think it was a reaction to the vaccine. Given a COVID-19 test and it was negative. Took her home and gave her TYLENOL. She was sick for about 3 days, and is better now.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- COVID-19 test - negative
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Fluoride
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 30.08.2022
- Impfdatum
- 26.08.2022
- Beginn
- 26.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dermatitis allergic
Injection site pruritus
Injection site rash
Rash
Rash papular
Symptomtext
Site: Itching at Injection Site-Mild, Systemic: Allergic: Rash (specify: facial area, extremeties)-Mild, Systemic: IM given in right thigh, after 10 minutes pt developed small papular rash on right leg and to lesser extent on left leg.-Mild, Additional Details: Pt was reassessed and given 2.5 ml of Benadryl, rash only appeared on lower ext. Pt continued to be active with no other symptoms. Pt was watched for additional 20 minutes after initial 15minutes. no other symptoms arose. Discussed with parent signs and symptoms to watch for over the next 24 hours and seek medical help if necessary.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 29.08.2022
- Impfdatum
- 10.08.2022
- Beginn
- 12.08.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- SYR / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fall
Nasopharyngitis
Pain in extremity
Weight bearing difficulty
Symptomtext
Tolerated vaccine well. 2 days after vaccine, patient fell several times while playing. Patient then c/o pain in affected leg, and for a brief time could not bear weight at all. After resting for a short time, was able to bear partial weight. Afebrile, no visible swelling, no known injury to area. He recovered within a few hours of rest and after taking Motrin. He fell again once early the next morning, but did not c/o pain at that time. He also woke up with mild cold symptoms that morning. No further issues, and was able to bear weight normally. Since issue resolved on its own with symptomatic treatment, did not have him seen by a doctor.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- Hospitalized for respiratory distress/reactive airway on 7/11/22-7/12/22. Symptoms had resolved fully prior to incident.
- Vorgeschichte
- Asthma Cat allergy
- Andere Medikamente
- Flovent HFA 44mcg, 2 puffs bid
- Allergien
- Cats, slight varied environmental allergies
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 1,3
- Geschlecht
- M
- Eingang
- 29.08.2022
- Impfdatum
- 17.08.2022
- Beginn
- 21.08.2022
- Tage bis Beginn
- 4,0
- Dosis
- UNK
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Joint swelling
Rash
Rash macular
Respiratory viral panel
Symptomtext
~ 90 h after vaccine developed diffuse E-M minor rash w R wrist, L knee swelling. Pt. did not improve on Zyrtec, and Orapred (prednisolone) given 15mg daily. Pt had a quick improvement and these were discontinued after 4d
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- VRP
- Aktuelle Erkrankungen
- Rhino/Enterovirus + VRP
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 27.08.2022
- Impfdatum
- 27.08.2022
- Beginn
- 27.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Vaccine positive rechallenge
Symptomtext
Patient complain of dizziness 5 minutes after receiving 2nd dose of vaccine. Parents states that she only have seasonal allergies, no other know allergies. Patient had similar reaction to 1st dose. Vital signs monitored within normal limits. Offered juice, cracker and water. Dad at bedside. Patient was able to verbalized her needs. Alert and Oriented 4x.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- n/a
- Allergien
- seasonal allergies
- Vorherige Impfungen
- Dizziness from 1st dose of Covid Pfizer vaccine August 3, 2022
- Staat
- MN
- Alter
- 2,0
- Geschlecht
- M
- Eingang
- 27.08.2022
- Impfdatum
- 13.08.2022
- Beginn
- 13.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered at inappropriate site
Vaccination site pruritus
Vaccination site rash
Symptomtext
This is a spontaneous report received from a contactable reporter(s) (Physician). A 2-year-old male patient received BNT162b2 (BNT162B2), on 13Aug2022 at 11:00 as dose 1, single (Lot number: FT9142) at the age of 2 years, in right leg for covid-19 immunisation. The patient's relevant medical history included: "Face skin itching" (unspecified if ongoing), notes: Other medical history: Face skin itching since age 6 month. There were no concomitant medications. The following information was reported: PRODUCT ADMINISTERED AT INAPPROPRIATE SITE (non-serious) with onset 13Aug2022 at 11:00, outcome "unknown", described as "Vaccine site location Right leg (site of vaccination)"; VACCINATION SITE RASH (non-serious), VACCINATION SITE PRURITUS (non-serious) all with onset 15Aug2022 at 12:00, outcome "recovered with sequelae" and all described as "Itching rash of the right thigh (site of vaccination)". Therapeutic measures were not taken as a result of vaccination site rash, vaccination site pruritus, product administered at inappropriate site. Additional information: Patient recovered with lasting effects. No treatment was given for adverse event. No covid prior and post vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Itching (Other medical history: Face skin itching since age 6 month)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- -
- Geschlecht
- F
- Eingang
- 27.08.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Increased appetite
Nasal oedema
Pyrexia
Rash
Weight
Symptomtext
This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the parent. A 14-month-old female patient received BNT162b2 (BNT162B2), as dose 1, single (Lot number: FT9142) for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. The following information was reported: PYREXIA (non-serious), outcome "unknown", described as "Fever"; RASH (non-serious), outcome "unknown"; NASAL OEDEMA (non-serious), outcome "unknown", described as "Swollen up nose"; INCREASED APPETITE (non-serious), outcome "unknown". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of pyrexia, rash, nasal edema, increased appetite. Additional information: Reporter stated, calling to report an adverse side effect for Pfizer vaccine for reporter's one year old. Later when probed for age at onset of events, reporter stated, 14 months. When probed for the side effects, reporter stated, fever, rash, swollen up nose, increased appetite. Height and weight: Reporter stated, not sure about the height and the weight was probably around 25 pounds. Expiration date: Reporter stated, It was not on the form. Reporter do not see it on the form. Treatment: Reporter stated, No. Prior vaccinations: Reporter stated, She did not. No other products. Reporter queried, Okay was she safe to get Tylenol for her fever or was she safe to get a second dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- Test Name: weight; Result Unstructured Data: Test Result:around 25 lbs; Comments: Reporter stated, not sure about the height and the weight was probably around 25 pounds.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 26.08.2022
- Impfdatum
- 19.08.2022
- Beginn
- 19.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Pain in extremity
Symptomtext
Doses 1 and 2 were previously given correctly. Dose 2 given on 07/22/2022. Pt. came in for her 3rd dose. This nurse mistakenly understood she was giving the 2nd dose. It was discovered today, 08/26/22,that this was pt's 3rd dose. 3rd dose was given 4 weeks early. Mother reports pt. did fine with the 3rd dose given on 08/19/22 except having a sore arm. Sore arm resolved and pt. is doing fine today, has done fine since 08/19/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 26.08.2022
- Impfdatum
- 28.07.2022
- Beginn
- 28.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Lethargy
Pyrexia
Vomiting
Symptomtext
Mom states that after patients first covid vaccine on 07/28/22, that within 30 minutes he became lethargic, within an hour and half he was vomiting and proceeded to vomit 5 times within a 24 hour period. Mom also states he spiked a 102 fever within that time as well. Patient was taken to urgent care for observation and then sent home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Seizures Delayed Milestones Intracranial Hemorrhage Acquired Nystagmus Developmental Delay Bilateral Cerebral Palsy
- Andere Medikamente
- None
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 25.08.2022
- Impfdatum
- 25.08.2022
- Beginn
- 25.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Urticaria
Symptomtext
Mild case of hives to face, abdomen and legs. Benadryl given with improvement.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- None known
- Andere Medikamente
- None
- Allergien
- None known
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 2,0
- Geschlecht
- M
- Eingang
- 25.08.2022
- Impfdatum
- 22.08.2022
- Beginn
- 22.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Pruritus
Urticaria
Symptomtext
He had the vaccination on 08/22/2022. I noticed that afternoon hives inside both wrists, elbows and knees. I gave him a full dose of ZYRTEC. On 08/23/2022, he was fine in the morning. But by that evening he couldn't stop scratching his foot and going to sleep. He had hives all over his extremities. We gave him more ZYRTEC. In the morning I called the nurse line 08/24/2022. We took him to the ER. Barely visible hive on left cheek. Gave steroid to drink. I picked up children's BENADRYL on the way home. 08/25/2022 patient had hives all over his body. The progression of the hives seem to be working through his body. He is home from daycare today. We are treating with BENADRYL and ZYRTEC. We don't know a plan going forward with the 3rd vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Cold
- Vorgeschichte
- Eczema from corn products
- Andere Medikamente
- N/A
- Allergien
- Eggs
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 1,7
- Geschlecht
- F
- Eingang
- 25.08.2022
- Impfdatum
- 04.08.2022
- Beginn
- 21.08.2022
- Tage bis Beginn
- 17,0
- Dosis
- 2
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Rash
Urticaria
Symptomtext
Possible rash/hives on bilateral legs, arms and buttocks
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- None reported
- Aktuelle Erkrankungen
- None reported
- Vorgeschichte
- None reported
- Andere Medikamente
- None reported
- Allergien
- None reported
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 2,0
- Geschlecht
- M
- Eingang
- 24.08.2022
- Impfdatum
- 13.08.2022
- Beginn
- 15.08.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Vaccination site pruritus
Vaccination site rash
Symptomtext
ITCHING RASH ON THE RIGHT TIGH, AROUND THE VACCINATION SITE NO TREATMENT DONE RECOVERED AFTER 10 DAYS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site pruritus
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE COVID-19 ON DEC. 2021
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- FACE ITCHING SINCE AGE 6 MONTH (UNKNOWN CAUSE) ALLERGY TEST NEVER DONE, TOO YOUNG.
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 0,6
- Geschlecht
- F
- Eingang
- 24.08.2022
- Impfdatum
- 17.08.2022
- Beginn
- 20.08.2022
- Tage bis Beginn
- 3,0
- Dosis
- 2
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Vomiting
Symptomtext
After both COVID-19 vaccines (7/27/2022 and 8/17/2022 - same lot#), 3 days later had a few hours of repeated vomiting. OK before and afterward.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vomiting
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 2,0
- Geschlecht
- M
- Eingang
- 23.08.2022
- Impfdatum
- 19.08.2022
- Beginn
- 19.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Conjunctivitis
Cough
Fatigue
Malaise
Pyrexia
Respiratory tract congestion
Symptomtext
Symptoms include fever, congestion, cough, conjunctivitis (both eyes), fatigue, malaise. Onset was one day following vaccine for conjunctivitis, three days for remaining symptoms. I am reporting at day five and symptoms have worsened.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 23.08.2022
- Impfdatum
- 22.08.2022
- Beginn
- 22.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Rash
Rash erythematous
Symptomtext
Patient's mother noticed a red rash behind both knees about 2-3 hours after receiving vaccine. Pt's mother states that the rash did not appear to be bothersome to patient. Today, the patient's mother states that the rash is diminishing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 22.08.2022
- Impfdatum
- 18.08.2022
- Beginn
- 20.08.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pruritus
Urticaria
Symptomtext
Large itchy hives for 24 hours
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 22.08.2022
- Impfdatum
- 19.08.2022
- Beginn
- 19.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Rash erythematous
Rash macular
Symptomtext
Approximately 10 minutes after the vaccine was administered, mom notified staff that she saw a red/blotchy rash across her chest and upper arms. No other symptoms noted: no swelling, no vomiting, no other complaints. Mother and child stayed in the waiting area and patient was given a fruit punch juice box and scooby doo snack pouch. By 5pm, approximately 31 minutes after administration of vaccine, no rash or redness was seen on patient. No other complaints noted. No medications were given.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash erythematous
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- sinus infection, had covid November 2021
- Vorgeschichte
- umbilical hernia, jaundice, picu stay for infection around the belly button at birth, chronic ear/sinus infections (will need ear tubes placed if she has one more ear infection)
- Andere Medikamente
- allergy medication Zyrtec every morning, albuterol nebulizer PRN
- Allergien
- seasonal allergies in the summer (never had formal allergy testing)
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 20.08.2022
- Impfdatum
- 04.08.2022
- Beginn
- 04.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Haemorrhage
Injection site erythema
Injury associated with device
No adverse event
Scratch
Symptomtext
Site: Redness at Injection Site-Mild, Systemic: see notes-Mild, Error: Patient accidentally stuck by needle. Additional details: As provider was pulling out the needle from patient's thigh, patient slapped his hand across the syringe and caused needle to scrape the top of his thigh. Superficial scrape about 1 inch in length with minimal bleeding. Band-Aids applied. No other adverse effects noted. Patient's father stated he will apply Polysporin at home and clean the area. Encouraged parent to monitor and follow-up as needed. Patient scheduled in 21 days for 2nd dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 20.08.2022
- Impfdatum
- 08.08.2022
- Beginn
- 08.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Overdose
Pain in extremity
Product preparation error
Symptomtext
His leg was sore; Given undiluted dose of vaccine; Given undiluted dose of vaccine; This is a spontaneous report received from contactable reporter(s) (Pharmacist and Consumer or other non HCP) from medical information team, Program ID. A 3-year-old male patient received BNT162b2 (BNT162B2), on 08Aug2022 as dose 1, single (Lot number: FT9142) at the age of 3 years for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: OVERDOSE (non-serious), PRODUCT PREPARATION ERROR (non-serious) all with onset 08Aug2022, outcome "unknown" and all described as "Given undiluted dose of vaccine"; PAIN IN EXTREMITY (non-serious), outcome "unknown", described as "His leg was sore". Additional Information: The reporter was a pharmacist calling about the COVID-19 vaccine. The reporter reported that, it was administered to a patient without being diluted. Reporter came into the line and verified information received from the transferring agent. Reporter stated that the COVID 19 vaccine she was calling about had a dark red cap. Reporter stated that she was looking for guidance on this situation. Stated that she had not contacted the parents of the patient yet, she wanted to contact Pfizer first. Reporter began to cry and stated that she felt bad that this happened. The reporter was asking about a 3-year-old male patient who received his first dose of dark red cap vaccine, not diluted. She was looking for guidance. The pharmacist reported it was human error. The vaccines are too overwhelming. Every vaccine has different dosage amounts, different age groups, different dilution instructions, different dosages. It was too much and she goes slow when preparing but it was too many variations and calculations and the mistake happened with the overdose. The patient did not receive any prior vaccinations within 4 weeks. Information regarding concomitant drugs and medical history was reported as unknown. The reporter did call the mother after the overdose event and the mother was a physician which was helpful for monitoring the patient. The mother said he was fine but acting like his leg was sore but considered it a normal reaction. No other adverse events reported beyond that one. Follow-up (10Aug2022): This is a spontaneous follow-up report received from a contactable consumer. Updated information: reporter information (primary reporters email address and new secondary reporter added) and patient details (age at vaccination captured). Follow-up (17Aug2022): This is a spontaneous follow-up report received from a contactable pharmacist. Updated Information: suspect drug (vaccine facility information added), reaction data (added new event of his leg was sore) and additional information updated with details of clinical course.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 19.08.2022
- Impfdatum
- 12.08.2022
- Beginn
- 12.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
Product administered at inappropriate site
Pyrexia
Symptomtext
Patient developed a fever; Vaccine location: Left leg; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A 2-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 12Aug2022 at 12:00 as dose 1, single (Lot number: FT9142) at the age of 2 years intramuscular, in left leg for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: PRODUCT ADMINISTERED AT INAPPROPRIATE SITE (non-serious) with onset 12Aug2022 at 12:00, outcome "unknown", described as "Vaccine location: Left leg"; PYREXIA (non-serious) with onset 13Aug2022 at 17:00, outcome "not recovered", described as "Patient developed a fever". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of pyrexia. Additional information: It was reported that the patient developed a fever in the afternoon on 13Aug2022. Fever got to 102 Fahrenheit and was treated with Tylenol; the patient still had temperature in the morning on 16Aug2022. Tylenol did decrease the temperature. There was nothing known about patient's allergies. The patient did not receive any other vaccine in four weeks. The patient did not have Covid prior to vaccination. The patient was not tested for Covid post vaccination. AE did not result in physician office visit or emergency room visit. The reporter classified the event as non serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220812; Test Name: Body temperature; Result Unstructured Data: Test Result:102 Fahrenheit
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other medical history: No
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 0,8
- Geschlecht
- F
- Eingang
- 18.08.2022
- Impfdatum
- 06.07.2022
- Beginn
- 10.07.2022
- Tage bis Beginn
- 4,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Diarrhoea
Rash
Rash erythematous
Symptomtext
Diffuse red rash that started on face and spread down body. Also had several episodes of diarrhea. Rash resolved within 8 days. Diarrhea lasted 2 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Nasal congestion week prior
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 1,4
- Geschlecht
- F
- Eingang
- 17.08.2022
- Impfdatum
- 06.08.2022
- Beginn
- 10.08.2022
- Tage bis Beginn
- 4,0
- Dosis
- 2
- Route/Site
- SYR / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abnormal behaviour
Crying
Fatigue
Hypersomnia
Irritability
Loss of personal independence in daily activities
Pyrexia
Viral infection
Symptomtext
Four days after vaccination, 8-10-2022, she started having a fever up to 102.2, crying and mildly irritable with fatigue. She did not want to play with any of her toys at daycare. There was no lump or swelling at vaccine site. I called the nurse at my primary care physicians office and she suggested Tylenol if temp up to 102 and to increase oral fluids. She advised that the fever was probably due to a virus instead of the vaccine. The following day, her temp was still 101.6. She still had excessive sleeping periods. She missed 2 days of daycare. There was no fever on 8-12 and seemed to be much better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Roseola Virus within 1 month
- Vorgeschichte
- None
- Andere Medikamente
- Vitamin D supplement
- Allergien
- Seasonal Allergies
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 1,3
- Geschlecht
- M
- Eingang
- 16.08.2022
- Impfdatum
- 12.08.2022
- Beginn
- 12.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Vomiting
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vomiting
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 0,5
- Geschlecht
- M
- Eingang
- 15.08.2022
- Impfdatum
- 09.08.2022
- Beginn
- 11.08.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Eczema
Poor quality sleep
Rash macular
Symptomtext
My son did not sleep well during the night and the next morning when I changed him he had big red blotches on his back. I called his doctor and were able to get in. She doctor did an exam and was stating she thought it was eczema but wanted to make sure it was not hand foot and mouth which is going around. He does not go to day care or anything so that was ruled out. She gave us a cream for the rash and in about two days it cleared up. He did get other vaccines the same day but I do not have all the information for them but he also got DTAP, Pneumonia, and Hep B on the 9th when he got his COVID-19 vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash macular
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Propranolol; vitamin D drops
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 15.08.2022
- Impfdatum
- 05.08.2022
- Beginn
- 05.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Abdominal pain
Vomiting
Symptomtext
Last Friday (5 Aug 2022) I took Patient to a Pharmacy local to me for his first dose of the Pfizer COVID-19 vaccine for kids 4 and under. He complained of a tummy ache and threw up in the car about 20 minutes after his shot, so I took him to Urgent Care. The urgent care intake staff triaged him and recommended hydration and monitoring for any other symptoms. He initially had a temp of 99.6F, was able to sip water & a little bit of pedialite and fell asleep for about three hours (continued?).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Mild persistent childhood asthma
- Andere Medikamente
- Flovent
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 1,1
- Geschlecht
- M
- Eingang
- 12.08.2022
- Impfdatum
- 28.07.2022
- Beginn
- 30.07.2022
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Cardiac telemetry abnormal
Cyanosis
Diarrhoea
Discomfort
Faeces discoloured
Feeling abnormal
Heart rate increased
Influenza virus test negative
Pyrexia
Respiratory syncytial virus test negative
Respiratory viral panel
SARS-CoV-2 test negative
Skin discolouration
Ventricular extrasystoles
Symptomtext
Patient had his second covid vaccine on Thursday afternoon, July 28. He had worsening diarrhea (turned liquid from being soft and was darker) the next day on July 29. On Saturday morning July 30, he woke up at 4:30 in the morning with a fever of 103.5. He seemed pretty draggy and uncomfortable all morning, although his fever was responsive to Tylenol. A little later that morning he looked a little blue around his lips, and his hands and feet were dusky with slow capillary refill. He was not in distress, just continued to seem under the weather and have fevers when the medicine wore off. We took him to an Emergency Room because of lack of availability of a dr's office appointment on Saturday. They checked his vitals which were normal other than a slightly elevated HR and the fever (back up at 103.4), gave some Motrin, and think he probably had a viral GI bug. They would have tested his stool but he didn't have an episode while we were there. They did a covid and respiratory panel which was negative. patient's fever and diarrhea resolved over the next couple days and he was quickly back to his normal self.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- Labs: Respiratory panel was negative for COVID-19, influenza, and RSV. Tele strip: Normal sinus rhythm other than 1 noted.
- Aktuelle Erkrankungen
- Diarrhea started day of vaccination
- Vorgeschichte
- n/a
- Andere Medikamente
- Multivitamin + iron
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 0,8
- Geschlecht
- F
- Eingang
- 12.08.2022
- Impfdatum
- 29.06.2022
- Beginn
- 06.08.2022
- Tage bis Beginn
- 38,0
- Dosis
- 1
- Route/Site
- IM / LG
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cough
Pyrexia
Rhinorrhoea
Symptomtext
High fever, cough, and runny nose. The fever started 8/7/22 and was 101 and then got up to 102. The cough started on Saturday 8/6/22. They recommended alternating TYLENOL and MOTRIN. She is back to her normal self other than the cough.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Vitamin D
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 12.08.2022
- Impfdatum
- 05.08.2022
- Beginn
- 05.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Intentional medical device removal by patient
Product administration interrupted
Skin laceration
Symptomtext
Site: Pain at Injection Site-Mild, Additional Details: pt received laceration to left leg after kicking while attempting to inject covid vaccine, no vaccine administered, vaccine was administered in arm instead
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 2,0
- Geschlecht
- M
- Eingang
- 11.08.2022
- Impfdatum
- 04.08.2022
- Beginn
- 05.08.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Diarrhoea
Fatigue
Hypersomnia
Influenza virus test negative
Oropharyngeal pain
Pyrexia
Respiratory syncytial virus test negative
Respiratory tract congestion
SARS-CoV-2 test negative
Sinus congestion
Streptococcus test negative
Symptomtext
Fever for almost 4 days (range 101.5-103.5). Diarrhea (green in color). Sore throat. Head congestion. Chest congestion. Very tired and slept a lot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- Covid test, RSV test, Strep test. Flu test. They were all negitive
- Aktuelle Erkrankungen
- none. maybe runny nose here and there
- Vorgeschichte
- none
- Andere Medikamente
- Flintstones complete childrens multivitamin supplement (1/2 tablet onces per day). Culturelle Kids Purely Probiotics chewables (one tablet per day).
- Allergien
- none known
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 1,5
- Geschlecht
- F
- Eingang
- 11.08.2022
- Impfdatum
- 10.08.2022
- Beginn
- 10.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Injection site pruritus
Injection site reaction
Rash
Rash macular
Swelling face
Symptomtext
Situation Note: Called to see a 18 month old female for eval after WCC for possible allergic reaction after administration of vaccines. Both COVID-19 and Hepatitis A vaccine administered in right thigh. Right thigh after a few minutes +blotchy, patient scratching at it. After a few minutes, patient was sitting watching a video, and face started swelling. IM epinephrine given and EMS called. 5min after epi, rash on thigh and face swelling improved, EMS arrived.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pruritus
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 11.08.2022
- Impfdatum
- 10.08.2022
- Beginn
- 11.08.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Vomiting
Symptomtext
Within 24hours vomiting , no medical treatment at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vomiting
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Pink eye and strep in the month prior
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A potential allergy to peanuts
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 11.08.2022
- Impfdatum
- 10.08.2022
- Beginn
- 11.08.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Urticaria
Symptomtext
Raised hives on inside of right thigh and both arms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 10.08.2022
- Impfdatum
- 12.07.2022
- Beginn
- 05.08.2022
- Tage bis Beginn
- 24,0
- Dosis
- 2
- Route/Site
- IM / LG
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Influenza virus test negative
Pyrexia
SARS-CoV-2 test negative
Vomiting
Symptomtext
She developed a fever to 101 on Friday August 5th. Fever returned on 8/6/2022, last fever was on the evening of 8/6/2022. Resolved with motrin and tylenol. Two episodes of emesis one am on 8/6 and another in the middle of the night on 8/7/22. Went to pediatric urgent care 8/6/22. Afebrile, no abnormal findings, flu and covid negative. Doctor believed it be a virus and that it would resolve with rest, fluids, tylenol.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- Flu test negative, Covid 19 rapid and pcr negative, all on 8/6/2022
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 1,1
- Geschlecht
- M
- Eingang
- 10.08.2022
- Impfdatum
- 05.08.2022
- Beginn
- 06.08.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Clumsiness
Coordination abnormal
Gait disturbance
Pyrexia
Symptomtext
Within 24 hours of receiving his 2nd Covid vaccine dose (Pfizer), our son developed a fever of 102.5. He also displayed some loss of coordination - tripping, and noticeably more unsteady on his feet than he was prior to the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- None were taken. We notified his pediatrician's office and received guidance about treating the fever at the time. We notified them in writing about the loss of coordination after the fact, but did not seek any further help for that. Patient recovered from his fever within about 36 hours, but is still wobbly on his feet. (This is why I'm checking "unknown" for item 20).
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- None.
- Allergien
- Slight rashy reaction to egg - possible allergy? Has not been tested.
- Vorherige Impfungen
- Within 12 hours of his 1st Covid vaccine dose (Pfizer), Patient developed a wet cough and slight fever of 101 degrees.
- Staat
- CA
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 09.08.2022
- Impfdatum
- 05.08.2022
- Beginn
- 07.08.2022
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Diarrhoea
Pyrexia
SARS-CoV-2 test negative
Therapeutic response decreased
Symptomtext
Low grade fever on Sunday night (100.5) progressed to high fever Monday morning at 102.8. Fever was not responsive to medications and remained around 101 until 5pm when it started to come back down. Patient also had diarrhea on Saturday and Monday
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- COVID antigen test negative
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Constipation
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- High fever and febrile seizure plus rash after MMR vaccine.
- Staat
- NC
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 09.08.2022
- Impfdatum
- 20.07.2022
- Beginn
- 20.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cough
Diarrhoea
Fatigue
Pyrexia
Rhinorrhoea
SARS-CoV-2 test negative
Viral infection
Symptomtext
1) Diarrhea - evening after vaccine & next day (7/20 - 7/21) 2) Fever, runny nose, cough, fatigue (7/29-8/5) - negative for COVID x2. Pediatrician (8/2) advised likely just a bad virus. OTC ibuprofen, fluids, rest. Returned to daycare on 8/2 after being symptomatic for a full week.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- COVID PCR test - 7/29 negative COVID rapid test - 8/1 negative COVID PCR test - 8/2 negative
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 09.08.2022
- Impfdatum
- 02.08.2022
- Beginn
- 02.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Overdose
Pain in extremity
Product preparation error
Pyrexia
Product preparation issue
Symptomtext
This is a spontaneous report received from contactable reporter(s) (Nurse) from medical information team, Program ID: A 3-year-old male patient received BNT162b2 (BNT162B2), on 02Aug2022 as dose 2 (maroon cap), single (Lot number: FT9142, Expiration Date: 01Sep2022) at the age of 3 years intramuscular, in left deltoid for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. Vaccination history included: BNT162b2 (Dose 1, Batch/Lot#: FT9142, Anatomical Site of Injection: Left deltoid), administration date: 12Jul2022, for COVID-19 immunization. The following information was reported: PRODUCT PREPARATION ERROR (non-serious), OVERDOSE (non-serious) all with onset 02Aug2022, outcome "unknown" and all described as "The dose was not diluted"; PAIN IN EXTREMITY (non-serious) with onset 02Aug2022, outcome "recovered" (2022), described as "arm sore the evening of the overdose"; PYREXIA (non-serious) with onset 03Aug2022, outcome "recovered" (2022), described as "had fever last night (temperature not provided)". Additional information: It was reported by RN about a three-year-old male patient who received his second dose of the maroon cap. Warm transfer from [withheld] with Support, CEP: 159558 with a health care provider/vaccine provider on the line to report adverse event where they had a patient who was administered the Pfizer COVID-19 vaccine maroon cap without a diluent. They have a medical information question, want to ask for some guidance to notify the family of the patient. She clarified that she was a nurse, provided by inbound transfer agent only as healthcare provider/vaccine provider. She clarified that this patient was administered a dose without diluent of Pfizer COVID-19 vaccine, maroon cap formulation. She clarified that their medical director will probably want to know a little more, so she wanted to get guidance regarding this event to provide to the medical director. She reported there has been no testing, treatment or medical intervention relative to this event that she was aware of. Upon follow-up on 04Aug2022, she spoke with the mom this morning who reported that the patient's arm sore the evening of the overdose and he also had fever last night (temperature not provided). Mom said he was fine today, so the reporter considered the events resolved. No follow-up attempts are possible. No further information is expected. Follow-up (04Aug2022): New information received from a contactable Nurse. This Nurse reported in response to HCP telephonic follow-up activity which included. Updated information included: New reporter slider added. New historical vaccine (none) and historical vaccine notes. Vaccine Facility Information, new events added (Pain in arm and Fever) were added. 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
- MN
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 09.08.2022
- Impfdatum
- 02.08.2022
- Beginn
- 02.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Overdose
Pain in extremity
Product preparation error
Pyrexia
Product preparation issue
Symptomtext
This is a spontaneous report received from contactable reporter(s) (Nurse) from medical information team, Program ID: A 3-year-old male patient received BNT162b2 (BNT162B2), on 02Aug2022 as dose 2 (maroon cap), single (Lot number: FT9142, Expiration Date: 01Sep2022) at the age of 3 years intramuscular, in left deltoid for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. Vaccination history included: BNT162b2 (Dose 1, Batch/Lot#: FT9142, Anatomical Site of Injection: Left deltoid), administration date: 12Jul2022, for COVID-19 immunization. The following information was reported: PRODUCT PREPARATION ERROR (non-serious), OVERDOSE (non-serious) all with onset 02Aug2022, outcome "unknown" and all described as "The dose was not diluted"; PAIN IN EXTREMITY (non-serious) with onset 02Aug2022, outcome "recovered" (2022), described as "arm sore the evening of the overdose"; PYREXIA (non-serious) with onset 03Aug2022, outcome "recovered" (2022), described as "had fever last night (temperature not provided)". Additional information: It was reported by RN about a three-year-old male patient who received his second dose of the maroon cap. Warm transfer from [withheld] with Support, CEP: 159558 with a health care provider/vaccine provider on the line to report adverse event where they had a patient who was administered the Pfizer COVID-19 vaccine maroon cap without a diluent. They have a medical information question, want to ask for some guidance to notify the family of the patient. She clarified that she was a nurse, provided by inbound transfer agent only as healthcare provider/vaccine provider. She clarified that this patient was administered a dose without diluent of Pfizer COVID-19 vaccine, maroon cap formulation. She clarified that their medical director will probably want to know a little more, so she wanted to get guidance regarding this event to provide to the medical director. She reported there has been no testing, treatment or medical intervention relative to this event that she was aware of. Upon follow-up on 04Aug2022, she spoke with the mom this morning who reported that the patient's arm sore the evening of the overdose and he also had fever last night (temperature not provided). Mom said he was fine today, so the reporter considered the events resolved. No follow-up attempts are possible. No further information is expected. Follow-up (04Aug2022): New information received from a contactable Nurse. This Nurse reported in response to HCP telephonic follow-up activity which included. Updated information included: New reporter slider added. New historical vaccine (none) and historical vaccine notes. Vaccine Facility Information, new events added (Pain in arm and Fever) were added. 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
- 1,1
- Geschlecht
- M
- Eingang
- 08.08.2022
- Impfdatum
- 09.07.2022
- Beginn
- 31.07.2022
- Tage bis Beginn
- 22,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Irritability
Pyrexia
Rash
SARS-CoV-2 test negative
Symptomtext
He experienced a high fever of 103.8, irritability and rash on his back.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- COVID-19 test which was negative.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 08.08.2022
- Impfdatum
- 01.08.2022
- Beginn
- 03.08.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Infection
Injection site erythema
Injection site swelling
Symptomtext
Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Additional Details: Patient evaluated by PCP who determined she had an infection and started on antibiotics, but didn't think related to the vaccine injection per mother's report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 06.08.2022
- Impfdatum
- 06.08.2022
- Beginn
- 06.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Crying
Vomiting
Symptomtext
Patient vomited in waiting room. He was brought back into the exam room and assessed. VS stable and exam unremarkable. His father thought the patient threw up due to crying while getting the vaccine. Patient reported that he no longer felt like he needed to through up and that he felt "good".
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vomiting
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 05.08.2022
- Impfdatum
- 04.08.2022
- Beginn
- 05.08.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Symptomtext
Developed a rash on face morning after receiving vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- One month prior had fever and other family members had confirmed mononucleosis. With all the same symptoms we assume he had mono also.
- Vorgeschichte
- None
- Andere Medikamente
- Multivitamin flint stones; Vitamin C gummies
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 05.08.2022
- Impfdatum
- 15.07.2022
- Beginn
- 16.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Rash erythematous
Rash pruritic
Symptomtext
Red, patchy, itchy rash on base of both palms. Started within 24 hours of dose, became apparent on third day, and has persisted from date of dose to present (August 5, 2022). No other symptoms. Patient on claritin for seasonal allergies but has no effect on rash and itchiness. Persistent, wakes up itching palms. If not resolved before second dose on August 18, 2022, clinic visit will be scheduled.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 05.08.2022
- Impfdatum
- 05.08.2022
- Beginn
- 05.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash erythematous
Symptomtext
Patient was given a shot at 0930 stayed for 15 mins experiencing no signs or symptoms of an allergic reaction. Patient then went to Dunkin Donuts and MOP notice red spots on the Patient's Arm and Leg. MOP of Patient then brought Patient back to the immunization treatment and was assessed by a provider. Provider continued to monitor for 15 more minutes and prescribed oral diphenhydramine for current reaction. MOP was educated if reactions gets worse to go to the closer emergency room.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash erythematous
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- None
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 1,0
- Geschlecht
- F
- Eingang
- 04.08.2022
- Impfdatum
- 03.08.2022
- Beginn
- 04.08.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Hypophagia
Influenza virus test negative
Irritability
Pallor
Rash macular
SARS-CoV-2 test negative
Symptomtext
Crankiness day of vaccination. Today (day after vaccination), diffuse blanching macular rash mostly concentrated on the face/torso/upper legs. Refusing food, drinking well and cranky today.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash macular
- Hospital-Tage
- -
- Labordaten
- COVID-19/flu PCR negative.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None. Patient took Motrin following vaccine administration.
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 02.08.2022
- Impfdatum
- 02.08.2022
- Beginn
- 02.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Symptomtext
Rash on legs, torso and upper arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- URI 10 days prior.
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 1,8
- Geschlecht
- F
- Eingang
- 02.08.2022
- Impfdatum
- 19.07.2022
- Beginn
- 20.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Erythema
Lethargy
Peripheral swelling
Pyrexia
Symptomtext
15 hours after shot: swelling and redness in left hand, right arm, and both legs (calves). Prednisone was prescribed but she couldn?t keep it down. Swelling and redness resolved independently within 3-4 days. 5 days after shot, woke up with fever (102), very lethargic. Gave Tylenol, was better for a few hours. Lethargic again in the afternoon, better by the next day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None known
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 02.08.2022
- Impfdatum
- 27.07.2022
- Beginn
- 28.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Miliaria
Rash
Rash erythematous
Viral infection
Symptomtext
Pt was playing at the park the day following her vaccine. It was a very humid and hot day. We were at the park for about an hour when we were getting ready to leave I notice her face was red with a rash. I then checked her stomach, back, and arms. They all were covered with red bumps but only her stomach looked like it was heat rash. After cooling down, her rash did not subside. I contacted her doctor they said to give Benedryl and send photos. I sent photos and was told it was most likely a viral infection and continue Benedryl or do Claritin. We switched to Claritin and after day 5 her rash started to fade.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- n/a - just sent photos to doctor
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- Lactulose
- Allergien
- allergic to pollen
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 0,8
- Geschlecht
- F
- Eingang
- 02.08.2022
- Impfdatum
- 23.07.2022
- Beginn
- 26.07.2022
- Tage bis Beginn
- 3,0
- Dosis
- 2
- Route/Site
- SYR / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Hypersensitivity
Rash
Symptomtext
07/26/2022 we began to notice bumps forming around her face. I did contact her doctor and they said to monitor it. Over the weekend we rubbed Benadryl on it and it started to improve. However, when she went into day care it came back as well. We took her to the ER and they stated that she is most likely having an allergic reaction to something however they don't believe that it was due to the vaccination. Since going to the ER her symptoms are improving dramatically and the rash on her face is getting a lot better. She also has a twin that received the exact same vaccines at the same time and she is doing completely fine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Seasonal Cold
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Amoxicillin
- Vorherige Impfungen
- T-DAP and HIV shot on 10/25/2021 came down with a 102 fever not even 12 hours after vaccinations received.
- Staat
- CT
- Alter
- 1,3
- Geschlecht
- F
- Eingang
- 01.08.2022
- Impfdatum
- 13.07.2022
- Beginn
- 25.07.2022
- Tage bis Beginn
- 12,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Contusion
Injection site rash
Pallor
Rash
Rash macular
Rash pruritic
Skin discolouration
Urticaria
Symptomtext
Approximately 12 days after the injection small round dots (similar to mosquito bites) appeared on legs. 12 hours later there were more dots and they were slightly larger and had spread to other parts of the body, but still mostly concentrated on legs. Within 24 hours the rash had spread to her entire body, the dots varied in size and appeared to be behaving like hives (itchy, blanched when touched, worsened/joined together when itched). The rash calmed down after 4 days but evidence of the rash remains a full week later (faded, flat brownish/bruise colored remnants).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site rash
- Hospital-Tage
- -
- Labordaten
- Visual inspection by physician on 7/25 and 7/27.
- Aktuelle Erkrankungen
- Coxsackie infection; flu infection; unspecified virus from daycare; ear infection (antibiotics started 7/18)
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 01.08.2022
- Impfdatum
- 20.07.2022
- Beginn
- 22.07.2022
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- SYR / LG
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Diarrhoea
Symptomtext
Diarrhea starting 7/22/22 and continuing through 7/28/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma
- Andere Medikamente
- None
- Allergien
- Amoxicillin
- Vorherige Impfungen
- Diarrhea after Pfizer COVID vaccine dose 1 on 6/29/22
- Staat
- MI
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 01.08.2022
- Impfdatum
- 22.07.2022
- Beginn
- 22.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Rash
Rash pruritic
Symptomtext
Noticed a rash starting behind his left ear. From there it spread to his posterior, groin, back, chest, and face. Most noticeable on posterior, penis and stomach. Rash itches and burns when cleaned with soap. Rash continues to today. Saw doctor 7/31 about rash. Prescribed prednisone.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Asthma; Allergies
- Andere Medikamente
- Cephalexin
- Allergien
- No
- Vorherige Impfungen
- Throat swelled after 1st dose of Pfizer Covid 19 vaccine on 7/1/2022.
- Staat
- MA
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 31.07.2022
- Impfdatum
- 26.07.2022
- Beginn
- 26.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Pyrexia
Symptomtext
Daily chills and low grade fever every late evening around 7pm since first night of vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Allergies as mentioned above
- Andere Medikamente
- Xyxal
- Allergien
- Tree nuts, shellfish
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 31.07.2022
- Impfdatum
- 21.07.2022
- Beginn
- 26.07.2022
- Tage bis Beginn
- 5,0
- Dosis
- 2
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Aphthous ulcer
Oral pain
Symptomtext
Painful canker sores found out on July 26th on left inside cheek Went to urgent care on 07/26/2022 and prescribed ibuprofen and triamcinolone Followed up with the PCP on 07/28/2022 As of 07/30/2022, canker sores still present (left and right inside cheek)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oral pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None that is known of
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 29.07.2022
- Impfdatum
- 29.07.2022
- Beginn
- 29.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Urticaria
Symptomtext
Hives appearing all over the body within hours of getting shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Probiotics, Multivitamin
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 29.07.2022
- Impfdatum
- 07.07.2022
- Beginn
- 25.07.2022
- Tage bis Beginn
- 18,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Nausea
Oropharyngeal pain
Pain
Pyrexia
SARS-CoV-2 test positive
Vomiting
Symptomtext
He tested positive for COVID-19 on 7/25/22. He had a cough, fever of 105 that day, and went down to 103 the next day, vomiting, sore throat, and body aches. We took him to the hospital because he was vomiting and had such a high fever. He continues to have a cough. He took 1 dose of TYLENOL at the hospital and ondansetron for nausea.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- COVID-19 test- 7/25/22- positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 1,6
- Geschlecht
- F
- Eingang
- 29.07.2022
- Impfdatum
- 17.07.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Diarrhoea
Product administered at inappropriate site
Pyrexia
Rash
Symptomtext
patient received BNT162B2 in left leg; She had a rash over her body; high fever; excessive diarrhea; This is a spontaneous report received from a contactable reporter (Consumer). The reporter is the parent. A 19-month-old female patient received BNT162b2 on 17Jul2022 as dose 2 (maroon cap), 0.2 ml single (Lot number: FT9142) at the age of 19 months, in left leg for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: BNT162b2 (DOSE 1 (MAROON CAP), 0.2 ML SINGLE, Lot no: FT9142), administration date: 26Jun2022, when the patient was 18-month-old, for Covid-19 immunization. The following information was reported: PYREXIA (medically significant) with onset Jul2022, outcome "not recovered", described as "high fever"; RASH (medically significant) with onset Jul2022, outcome "not recovered", described as "She had a rash over her body"; DIARRHOEA (medically significant) with onset Jul2022, outcome "not recovered", described as "excessive diarrhea"; PRODUCT ADMINISTERED AT INAPPROPRIATE SITE (non-serious) with onset 17Jul2022, outcome "unknown", described as "patient received BNT162B2 in left leg". Therapeutic measures were not taken as a result of rash, pyrexia, diarrhoea. Parents did not know what to give her. Parents were going to take her to the hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- 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
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 28.07.2022
- Impfdatum
- 22.07.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Swelling face
Urticaria
Symptomtext
face was puffy/she went to bed with the face still puffy/woke up and it was fine; face was covered in hives/spots started to disappear/woke up and it was fine; This spontaneous case was reported by a consumer and describes the occurrence of SWELLING FACE (face was puffy/she went to bed with the face still puffy/woke up and it was fine) and URTICARIA (face was covered in hives/spots started to disappear/woke up and it was fine) in a 3-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. FT9142) for COVID-19 prophylaxis. Concurrent medical conditions included Milk allergy (not anaphylaxis but when she drank cows milk, she breaks out in hives). Concomitant products included CYPROHEPTADINE HYDROCHLORIDE (PERIACTIN) and FAMOTIDINE for an unknown indication. On 22-Jul-2022, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In July 2022, the patient experienced SWELLING FACE (face was puffy/she went to bed with the face still puffy/woke up and it was fine) and URTICARIA (face was covered in hives/spots started to disappear/woke up and it was fine). The patient was treated with CETIRIZINE HYDROCHLORIDE (EQUATE ALLERGY RELIEF [CETIRIZINE HYDROCHLORIDE]) for Allergy, at a dose of 2.5 milliliter. At the time of the report, SWELLING FACE (face was puffy/she went to bed with the face still puffy/woke up and it was fine) and URTICARIA (face was covered in hives/spots started to disappear/woke up and it was fine) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Past medical history included J2 dependent. It was reported that paitent received the vaccine yesterday last night and did not see anything, but 40 minutes later after they drive home, her face was covered in hives and face was puffy. Caller reported the primary care doctor told her to gave an allergy medicine and all she had was Equate brand cetirizine hydrochloride 2.5 ml. Caller told it helped, the spots started to disappear an hour after and then she went to bed with the face still puffy and then woke up and it was fine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Milk allergy (not anaphylaxis but when she drank cows milk, she breaks out in hives)
- Vorgeschichte
- -
- Andere Medikamente
- PERIACTIN; FAMOTIDINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 1,5
- Geschlecht
- F
- Eingang
- 27.07.2022
- Impfdatum
- 20.07.2022
- Beginn
- 26.07.2022
- Tage bis Beginn
- 6,0
- Dosis
- 2
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Sleep disorder
Sneezing
Symptomtext
She started getting symptoms around 2AM with a high fever of 101.6. I did give her children's TYLENOL. She now has a runny nose and sneezing. She is also having trouble sleeping. I took her to a facility and had a rapid COVID-19 test that was positive.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- COVID-19 test - positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 27.07.2022
- Impfdatum
- 21.07.2022
- Beginn
- 21.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Rash
Urticaria
Symptomtext
Systemic: Allergic: Itch (specify: facial area, extremeties)-Mild, Systemic: Allergic: Itch Generalized-Mild, Systemic: Allergic: Rash (specify: facial area, extremeties)-Mild, Systemic: Allergic: Rash Generalized-Mild, Additional Details: Per patient's mother, symptoms began on 07/21/2022 night. Patient's mother reported patient told her she was "itchy" under her arm on the side that the vaccine was given. Per the mother the next afternoon the patient had developed hives to her face, forehead, neck, chest, abdomen, right hip. Per the mother the child had no new foods, lotions, fragrances, been around any new animals that day. Per the mother she spoke with a Pharmacist and the patient's Pediatrician.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 26.07.2022
- Impfdatum
- 15.07.2022
- Beginn
- 24.07.2022
- Tage bis Beginn
- 9,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Eye swelling
Rash
Symptomtext
He had the vaccination on 07/15/2022. We noticed the rash on 07/24/2022 on the back of his neck, back and both legs. It progressed the following day and his left eye was swollen and more rash on his upper chest. We gave over the counter ZYRTEC but it doesn't seem to be working. We sent the doctor office a message and waiting to hear back.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Peanut allergy; He was prescribed an EPIPEN at time of vaccination but we did not have to use.
- Andere Medikamente
- N/A
- Allergien
- Peanuts
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 26.07.2022
- Impfdatum
- 21.07.2022
- Beginn
- 21.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
C-reactive protein normal
Fatigue
Full blood count
Neutropenia
Pyrexia
Red blood cell sedimentation rate normal
White blood cell count decreased
Symptomtext
low grade fever (~99), fatigue, neutropenia
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 7/24/22 CBC (WBC 2.2), CRP <0.1, P1, Sed Rate 11
- Aktuelle Erkrankungen
- 6/29/22 vomiting
- Vorgeschichte
- none
- Andere Medikamente
- N/A
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 0,9
- Geschlecht
- F
- Eingang
- 26.07.2022
- Impfdatum
- 26.07.2022
- Beginn
- 26.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Vomiting
Symptomtext
Multiple episodes of vomiting 1.5 hours after vaccination, no other symptoms. Given benadryl IM. Normal exam in office. Observed for 30 minutes, tolerated nursing. Discharged home with close observation by parent.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vomiting
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- None
- Allergien
- No known
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- -
- Geschlecht
- M
- Eingang
- 26.07.2022
- Impfdatum
- 24.07.2022
- Beginn
- 26.07.2022
- Tage bis Beginn
- 2,0
- Dosis
- UNK
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Decreased appetite
Influenza virus test
Pyrexia
Respiratory syncytial virus test
Rhinorrhoea
SARS-CoV-2 test
Streptococcus test
Vomiting
Symptomtext
Fever, vomiting, cough, runny nose. Poor appetite
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- covid test 07/26/22 flu 07/26/22 rsv 07/26/22 strep07/26/22
- Aktuelle Erkrankungen
- yes ear infection diagnosed on 07/01/22
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 25.07.2022
- Impfdatum
- 21.07.2022
- Beginn
- 24.07.2022
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Rash erythematous
Rash maculo-papular
Symptomtext
Received vaccine on 07/21/2022 On 07/24/2022 mother noted rash of body Seen by MD, who is primary care provider, at Pediatrics- Erythematous, maculopapular rash of most of body. Lower legs, soles and palms spared
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- No
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 25.07.2022
- Impfdatum
- 16.07.2022
- Beginn
- 18.07.2022
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Oropharyngeal pain
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test negative
Symptomtext
7/18/2022 She had a headache and I gave her some Ibuprofen. The next couple of days she would complain occasionally about a headache and sore throat, no fever or other symptoms. On 7/21/2022 she began having a runny nose and congestion and continued having a sore throat and headaches. 0n 7/22/2022 I took her to the doctor, and they said she looked okay. We started her on Zyrtec that evening. An at home COVID test on 7/24/2022 which was negative. She is still having a runny nose and has not complained of a headache or sore throat for the last few days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- At home COVID test, negative
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Alopecia
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 23.07.2022
- Impfdatum
- 22.07.2022
- Beginn
- 22.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypersensitivity
Injection site erythema
Injection site rash
Injection site warmth
Symptomtext
The patient's mother informed my team lead of an allergic reaction. The patient developed a rash on her left, lateral, lower leg. The rash was warm to touch with red, raised bumps. The child was not in distress, she had no pain and responded no when asked if it itched. After doing a head to toe exam, I found the patient was A/Ox3, PMS x3 and airway was open. The patient was administered (1) children's chewable benadryl. The mother was advised to follow up with a pediatrician and monitor her child for any other developing symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 23.07.2022
- Impfdatum
- 23.07.2022
- Beginn
- 23.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Agitation
Rash
Symptomtext
? 0940-Child vaccinated with 1st dose Pediatric Pfizer COVID 19 Vaccine(6 months-4years) in right vastus lateralis by RN. Child extremely agitated before and during vaccination. ? 1000-Dad noticed rash on thighs and SO notified by OBS staff. ? Non-raised rash noted by SO on bilateral thighs and anterior/posterior trunk. ? No swelling of lips, no hives, color pink, child in NAD, bilateral BS nl, no wheezing, moving air bilaterally without difficulty, awake and alert. "Acting normal" per dad. ? Dad declined EMS activation. SO requested dad to stay additional OBS time for total of 30 minutes and to notify OBS staff of any change in child's condition. ? 1015-Dad ready to leave OBS. ? SO assessment at this time: rash-no change. ? Child in NAD, color nl, no swelling noted, no hives, bilateral BS nl, no wheezing, moving air bilaterally without difficulty. ? Instructed father in s/s anaphylactic rxn and potential latent rxn, contact 911 if s/s respiratory distress/swelling of lips/tongue, contact PCP with any other concerns post-vaccination. Dad verbalized understanding of all instructions and says he would like to continue to monitor child at home at this time. ? Child awake and alert, carried by dad from vaccination clinic @1020.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- None reported by father during pre-vaccination screening.
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 0,8
- Geschlecht
- M
- Eingang
- 23.07.2022
- Impfdatum
- 21.07.2022
- Beginn
- 21.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
C-reactive protein increased
Carbon dioxide decreased
Erythema multiforme
Full blood count abnormal
Leukocytosis
Malaise
Metabolic acidosis
Metabolic function test
Metabolic function test abnormal
Pyrexia
Rash
Rash erythematous
Rash pruritic
White blood cell count increased
Symptomtext
Rash onset within hours of vaccination on 7/21/22 with itchy red bumps, progressed over 2 days to widespread cutaneous erythema multiforme (approx 30% BSA), fever, malaise. No mucosal involvement, no sloughing when examined on 7/23/22. D/w pediatric infectious disease specialist, decided to closely monitor outpatient, start oral steroids. Note: maternal hx SJS, suspect genetic predisposition, but no HLA subtyping done to date
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- CBC showed leukocytosis, WBC 15.8, CMP showed mild metabolic acidosis (CO2 16), otherwise within normal limits. CRP elevated 93.4 mg/L
- Aktuelle Erkrankungen
- acute otits media 7/12/22 (was on amox day #9 at time of covid #2)
- Vorgeschichte
- none
- Andere Medikamente
- Amoxicillin
- Allergien
- nkda
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 2,0
- Geschlecht
- M
- Eingang
- 23.07.2022
- Impfdatum
- 22.07.2022
- Beginn
- 23.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LG
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Gait disturbance
Irritability
Oedema peripheral
Pain
Skin oedema
Pain in extremity
Peripheral swelling
Sleep disorder
Urticaria
Weight bearing difficulty
Symptomtext
Patient got his 2nd Covid vaccine and his 2nd Hep A vaccine around 4pm in afternoon 7/22. Parents gave motrin before bed. He woke up around midnight, wide awake, whiney and wanting to sleep with parents. He did the same thing after his 1st covid vaccine but not after other vaccinations. Morning of 7/23 woke up around 6 am and had edema of hands, feet - skin taught - didnt want to bear weight or walk and said that it hurt. Otherwise happy, ate normally, acting normally. Came into office at 9am with newly developed urticarial rash on body. Not itchy. No swelling of lips, tongue, face. No difficulty breathing, vomiting, fever, irritability. Swelling from hands and feet had gone down a little and he was walking, climbing per usual.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Conjunctivitis on 6/29
- Vorgeschichte
- Atopic Dermatitis Reactive Airway Disease
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 2,0
- Geschlecht
- M
- Eingang
- 23.07.2022
- Impfdatum
- 22.07.2022
- Beginn
- 23.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LG
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Gait disturbance
Irritability
Oedema peripheral
Pain
Skin oedema
Pain in extremity
Peripheral swelling
Sleep disorder
Urticaria
Weight bearing difficulty
Symptomtext
Patient got his 2nd Covid vaccine and his 2nd Hep A vaccine around 4pm in afternoon 7/22. Parents gave motrin before bed. He woke up around midnight, wide awake, whiney and wanting to sleep with parents. He did the same thing after his 1st covid vaccine but not after other vaccinations. Morning of 7/23 woke up around 6 am and had edema of hands, feet - skin taught - didnt want to bear weight or walk and said that it hurt. Otherwise happy, ate normally, acting normally. Came into office at 9am with newly developed urticarial rash on body. Not itchy. No swelling of lips, tongue, face. No difficulty breathing, vomiting, fever, irritability. Swelling from hands and feet had gone down a little and he was walking, climbing per usual.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Conjunctivitis on 6/29
- Vorgeschichte
- Atopic Dermatitis Reactive Airway Disease
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 22.07.2022
- Impfdatum
- 09.07.2022
- Beginn
- 09.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypersensitivity
Rash
Rash pruritic
Symptomtext
Patient seen due to rash immediately following first COVID vaccine (Pfizer, 6mo to 4 year dose). Pinpoint rash on arms up to shoulders. None on trunk, few on legs. Itchy but he was not scratching at them. No prior reaction to vaccines or other allergies. Benadryl given. Normal vitals, normal physical examination. Observed for 1 hour with repeat vitals and examination, again normal. Adverse reaction added to allergies.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 22.07.2022
- Impfdatum
- 22.07.2022
- Beginn
- 22.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Nausea
Vomiting
Symptomtext
Nausea. Vomitted x1.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 21.07.2022
- Impfdatum
- 18.07.2022
- Beginn
- 19.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain
Asthenia
Chills
Decreased appetite
Headache
Lethargy
Oropharyngeal pain
Pyrexia
SARS-CoV-2 test negative
Vomiting
Symptomtext
Fever, chills, and lethargy rapidly developed late morning after the vaccine was administered had little appetite. Several hours later, child vomited. Fever reached over 102F and did not always respond to medicine (Tylenol and/or Motrin). Fever, chills, lethargy, lack of appetite, and intermittent belly and throat pain continued for several days. Headache developed around 1.5 days after vaccine. By 2.5 days after the vaccine, the chills/fever dissipated and energy was much improved. Throat pain remained through to day 3. No one else who was exposed to the child became ill, and the timing seems suspect, which led us to believe it was a vaccine reaction.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- Home antigen COVID tests administered 7/19 and 7/21 were negative. Doctor examined child but did not think COVID PCR test nor flu test was appropriate.
- Aktuelle Erkrankungen
- Possible COVID 2 weeks prior - never tested positive but developed an intermittent cough. Everyone else in the house had symptomatic COVID. We waited for everyone to recover and cough to fade before vaccinating her.
- Vorgeschichte
- Eczema, seasonal allergies
- Andere Medikamente
- Claritin, fluoride supplement,s Align probiotic
- Allergien
- Possible fish allergy (FPIES)
- Vorherige Impfungen
- 2? red welt at vaccine site in response to seasonal flu vaccine at least twice in her life
- Staat
- PA
- Alter
- 10,0
- Geschlecht
- F
- Eingang
- 21.07.2022
- Impfdatum
- 19.07.2022
- Beginn
- 20.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Incorrect dose administered
Pain in extremity
Symptomtext
Patient received the 6 mos to 4yr Pfizer vaccine dose instead of the 5-11 yr dose accidentally. Patient had mild arm soreness and the chills after receiving the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None known
- Vorgeschichte
- None known
- Andere Medikamente
- None known
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 8,0
- Geschlecht
- F
- Eingang
- 21.07.2022
- Impfdatum
- 19.07.2022
- Beginn
- 20.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Pain in extremity
Symptomtext
Patient received the 6 month -4 yr Pfizer vaccine dose instead of the 5-11 year vaccine accidentally. She had mild arm soreness the day after the vaccine given.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None known
- Vorgeschichte
- None known
- Andere Medikamente
- None known
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 21.07.2022
- Impfdatum
- 19.07.2022
- Beginn
- 20.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Axillary pain
Incorrect dose administered
Myalgia
Pain in extremity
Pyrexia
Symptomtext
Patient received the COVID vaccine for the 6 month-4 yr age group instead of the 5-11 yr age group dose. He had mild soreness of arm muscles, arm pit and low grade temp =100 the day after the vaccine given.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None known
- Vorgeschichte
- Mild intermittent asthma Tree nut allergy Seasonal allergic rhinitis Allergic colitis
- Andere Medikamente
- None
- Allergien
- Allergy to tree nut
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 9,0
- Geschlecht
- F
- Eingang
- 21.07.2022
- Impfdatum
- 19.07.2022
- Beginn
- 20.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Axillary pain
Incorrect dose administered
Injection site pain
Symptomtext
Patient accidentally was given the wrong dose of vaccine- a Pfizer 6mos to 4 yr dose. No adverse events. She had mild arm soreness at site of injection and arm pit soreness in the 1-2 days after the injection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Mild intermittent asthma
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 20.07.2022
- Impfdatum
- 02.07.2022
- Beginn
- 11.07.2022
- Tage bis Beginn
- 9,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Culture positive
Rash
Staphylococcus test positive
Varicella virus test positive
Symptomtext
Patient developed a rash on his left thigh.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- Swab results from skin rash: SP SOURCE Skin - swab VZV DNA PCR POSITIVE Abnormal ROUTINE CULT RSLT Abnormal Final Report Heavy growth Staphylococcus aureus
- Aktuelle Erkrankungen
- Lab confirmed Covid on 6/2/2022
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 20.07.2022
- Impfdatum
- 15.07.2022
- Beginn
- 15.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain
Body temperature increased
Culture
Dysphonia
Illness
Immunisation reaction
Incorrect dose administered
Influenza A virus test negative
Influenza B virus test
Oropharyngeal pain
Product preparation error
Streptococcus test negative
Viral infection
Symptomtext
Patient given invalid dose of COVID-19 vaccine. This was caught after being administered but prior to the patient leaving. Staff member drew-up 2.2mL of diluent in syringe with 0.2mL of vaccine and administered to the patient. Patient asked to wait 20 mins before leaving the office. Doctor spoke with the patient's mother and advised of precautions. Spoke with Pfizer. They recommended redoing series since it was invalid, but mom and office wanted to hold-off at this time. Office visit 7/19/2022: Episode onset: 2 days ago. Maximum temperature: Temperature yesterday of 101?F - 102?F. Associated symptoms include abdominal pain and a sore throat. Pertinent negatives include no congestion, coughing, ear pain or rhinorrhea. Associated symptoms comments: Voice sounds hoarse. She tried NSAIDs for the symptoms of sore throat. Suspect viral illness or due to recent COVID-19 vaccine, though that is less likely as other family members have been ill recently.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- Rapid strep negative. Will call if culture is positive. Flu A and B were negative.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 1,1
- Geschlecht
- F
- Eingang
- 20.07.2022
- Impfdatum
- 19.07.2022
- Beginn
- 19.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Rash
Rash macular
Symptomtext
Maybe thirty minutes later at home she was having a spotty rash through out her body. It was on her hands legs and on her chest. It did not seem to bother her. We do not assume it was itchy or painful. We contacted her PCP via tele conference at 05:15pm. They said to give 2ml of Children's Benadryl. The medicine seemed to work and she went to sleep. As of today the rash is completely gone.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Children's Benadryl
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 20.07.2022
- Impfdatum
- 19.07.2022
- Beginn
- 20.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Vomiting
Symptomtext
Sudden onset of vomiting at 23 hours post vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vomiting
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 2,0
- Geschlecht
- M
- Eingang
- 19.07.2022
- Impfdatum
- 15.07.2022
- Beginn
- 18.07.2022
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Gait disturbance
Joint swelling
Pruritus
Urticaria
Symptomtext
Patient started with urticarial rash on inner thighs on 7/18/22 (3 days after vaccination). Rash progressed over the next 24 hours and then he had swelling of bilateral wrists/ankles with refusal to walk on right foot on 7/19/22. Was also on Amoxicillin for otitis at the time of rash and mom had given dose of amoxicillin on the morning that rash began. Patient treated with Zyrtec/Benadryl for itching from rash. No fever or other systemic symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Otitis media - bilateral
- Vorgeschichte
- None
- Andere Medikamente
- Amoxicillin
- Allergien
- None known
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 5,0
- Geschlecht
- F
- Eingang
- 19.07.2022
- Impfdatum
- 03.07.2022
- Beginn
- 06.07.2022
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain
Constipation
Decreased appetite
Influenza virus test negative
Respiratory syncytial virus test negative
SARS-CoV-2 test negative
Streptococcus test negative
Vomiting
Symptomtext
Started experiencing abdominal pain x 2 days. Started giving her Miralax as she had been previously constipated. On day 3 she returned to school and vomited twice. For the following 4 days she had no appetite. I took her to Urgent care where she was tested for Influenza, Strep, RSV and COVID, all were negative. The following day I took her to the Pediatrician practice. The Nurse Practitioner stated that it was an adverse reaction to the vaccine and if she
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- Influenza, Strep, RSV and COVID 19
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Miralax as needed
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 19.07.2022
- Impfdatum
- 14.07.2022
- Beginn
- 17.07.2022
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- IM / LG
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Pyrexia
SARS-CoV-2 test positive
Symptomtext
He received his COVID-19 vaccine on 07/14/2022. He didn't show any signs of discomfort. The first signs of anything wrong was on 07/17/2022 he had a high fever. He responded well to Tylenol and Ibuprofen to break his fever. We had a telehealth visit with his doctor, they recommended that he should be seen at an urgent care center. He tested positive for COVID-19 on 07/18/2022. They recommended to keep comfortable by taking Tylenol, Ibuprofen and stay hydrated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- Tested for COVID-19 for at the urgent care center and it was positive.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- DE
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 19.07.2022
- Impfdatum
- 16.07.2022
- Beginn
- 17.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Rash
Urticaria
Symptomtext
24 hours after shot given developed hives to L leg, L back, and a few hives to R leg. Hives resolved around 36 hours after injection then reappeared on B/L legs about 54 hours after injection with erythema to B/L legs an B/L arms, all of which resolved within 8 hours. pt has never had hives or rash before.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- -
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 19.07.2022
- Impfdatum
- 02.07.2022
- Beginn
- 03.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthropod bite
Erythema
Injection site reaction
Pallor
Rash erythematous
Erythema multiforme
Rash macular
Rash papular
Rash pruritic
Skin discolouration
Skin lesion
Urticaria
Symptomtext
Seen on 7/18/22 and diagnosed with erythema multiforme. Pt has areas of bluish circular hues around thighs on lateral bilateral thighs, inner left thigh has two circular lesions with circumferential erythema and central pallor. Symptoms started day after vaccine. Mom noticed four red welts near her diaper area on 7/3/22. Spots persisted. On 7/16/22, the rash had spreading redness with central pallor and a red raised circular redness that is itchy. The first ones on her lateral thighs improved after using hydrocortisone topically, but other ones the next day increased.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site reaction
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Tethered cord s/p repair 9/2020; Congenital hydronephrosis; Anorectal malformation; Hyperbilirubinemia; Recto-vestibular fistula; Prematurity; Pelviectasis of kidney
- Andere Medikamente
- Senna
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 19.07.2022
- Impfdatum
- 02.07.2022
- Beginn
- 03.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthropod bite
Erythema
Injection site reaction
Pallor
Rash erythematous
Erythema multiforme
Rash macular
Rash papular
Rash pruritic
Skin discolouration
Skin lesion
Urticaria
Symptomtext
Seen on 7/18/22 and diagnosed with erythema multiforme. Pt has areas of bluish circular hues around thighs on lateral bilateral thighs, inner left thigh has two circular lesions with circumferential erythema and central pallor. Symptoms started day after vaccine. Mom noticed four red welts near her diaper area on 7/3/22. Spots persisted. On 7/16/22, the rash had spreading redness with central pallor and a red raised circular redness that is itchy. The first ones on her lateral thighs improved after using hydrocortisone topically, but other ones the next day increased.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site reaction
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Tethered cord s/p repair 9/2020; Congenital hydronephrosis; Anorectal malformation; Hyperbilirubinemia; Recto-vestibular fistula; Prematurity; Pelviectasis of kidney
- Andere Medikamente
- Senna
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 0,8
- Geschlecht
- F
- Eingang
- 18.07.2022
- Impfdatum
- 15.07.2022
- Beginn
- 17.07.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Urticaria
Symptomtext
Rash/Hives all over body
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 18.07.2022
- Impfdatum
- 24.06.2022
- Beginn
- 08.07.2022
- Tage bis Beginn
- 14,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Exposure to SARS-CoV-2
Pyrexia
SARS-CoV-2 test positive
Symptomtext
I believe my daughter was exposed to COVID-19 at camp where not everyone was masked. She came down with a high fever on 07/07/2022 but tested negative for COVID-19 with an at home test. That night she was coughing throughout the night so I retested her the next day and the results were positive. Her fever got up to 103. I reached out to her doctor who advised to give her cough syrup and to treat her fever with over the counter medication. Her fever went away for a few days by 07/12 but returned a few days later so I spoke with her pediatrician again who thought that she may have exposed to a secondary virus. At this point on 7/18/22 she is still running mild fevers at around 99 degrees.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- At home COVID-19 test 07/08/22-positive
- Aktuelle Erkrankungen
- Virus in early June. 06/08/2022-06/10/2022
- Vorgeschichte
- None.
- Andere Medikamente
- Children's Multivitamin.
- Allergien
- Peanuts; Wheat.
- Vorherige Impfungen
- D-TAP-swollen leg-Age: 18 months. Date: Unknown.
- Staat
- MD
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 18.07.2022
- Impfdatum
- 14.07.2022
- Beginn
- 17.07.2022
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Enanthema
Induration
Nikolsky's sign
Petechiae
Rash
Rash erythematous
Rash papular
Rash pruritic
Rash vesicular
Scab
Skin lesion
Skin plaque
Symptomtext
Rapid onset, full-body rash starting 3 days after co-administration of COVID mRNA and MMRV vaccines in a healthy 4 year old male Rash is varicelliform, consisting of Indurated, vesicular, erythematous rash Several hundred lesions in total, many closely grouped, becoming confluent and forming hard plaques in several areas, especially the distal extremities Each lesion appears to start as flesh-colored or erythematous papules which grow, becoming indurated and erythematous. These then rapidly form a scab in the center of a an erythematous ring Lesions of multiple ages found in same areas Does not seem to have an ordered progression from one area to the next, i.e. not centripetal, but rather all seemed to crop up at once in multiple areas, Involves the entire body surface, worst on extremities and throat, and rather mild on trunk and scalp, but spares no surface completely It was extremely pruritic on day 1 but this seems to have abated somewhat by today (day 2) There is no oozing, crusting, bleeding, pus, or other signs of bacterial superinfection Negative Nikolsky sign and there are no areas of skin maceration Positive for enanthem consisting of petechiae on the soft palate and a few small vesicles on the soft palate and posterior pharynx Patient denies dysphagia He is otherwise very well. There is no involvement of the eyes or TMs or nasal sinuses and no significant lymphadenopathy. No fever, normal energy, no cough or rhinorrhea, no abdominal pain, no dysuria The remainder of the ROS and PE are unremarkable.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- No tests ordered
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Eczema
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 0,8
- Geschlecht
- F
- Eingang
- 18.07.2022
- Impfdatum
- 22.06.2022
- Beginn
- 14.07.2022
- Tage bis Beginn
- 22,0
- Dosis
- 1
- Route/Site
- SYR / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Discomfort
Drainage
Feeling hot
Irritability
Pyrexia
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
She woke up on the 14th and had some sniffles. I took her to day care, and they called around 3pm and they said she had a fever of 101.7. I went and picked her up, and she was very uncomfortable, warm, and fussy. And she was having a lot of drainage from her nose. I gave her some ibuprofen and made her more comfortable. She slept through the night, and the next morning she still had congestion. It didn?t look like she had any fever that day. She has had some congestion the past few days, and that?s about it.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- Rapid COVID-19 Test 07/13/2022 - Negative; PCR COVID-19 Test 07/14/2022 - Positive
- Aktuelle Erkrankungen
- RSV 06/14/2022
- Vorgeschichte
- None
- Andere Medikamente
- Vitamin D
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 0,8
- Geschlecht
- M
- Eingang
- 18.07.2022
- Impfdatum
- 12.07.2022
- Beginn
- 16.07.2022
- Tage bis Beginn
- 4,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypophagia
Irritability
Pyrexia
SARS-CoV-2 test
Symptomtext
It was Saturday but he may have been a little more fussy because mom was away. Saturday around noon dad notices the baby wouldn't eat or drink and had fever of 101. Dad then call doctors and the doctors told him to come to the campus. No medication was given from the doctor. We were just instructed to give him Tylenol. Today he seems happy and back to normal but yesterday was pretty rough.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- COVID-19 test
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 18.07.2022
- Impfdatum
- 15.07.2022
- Beginn
- 15.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Rash
Urticaria
Symptomtext
Patient noted to have new rash antecubital fossa, back of neck, behind knees, erythematous, hive like on back of neck starting approx 20 min after receiving vaccine. Given benadryl and watched for additional 15 minutes after the benadryl without changes. However, review of our clinic policy showed ER recommendation so sent to ER for extended monitoring which was normal.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 2,0
- Geschlecht
- M
- Eingang
- 17.07.2022
- Impfdatum
- 14.07.2022
- Beginn
- 15.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Vomiting
Symptomtext
Vomiting - 5:30am, 6:30am, 7:30am, 8:30am, & 9:30am on Friday 7/15. One episode of vomiting Sunday 7/17 at 8:30am.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vomiting
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Multivitamin
- Allergien
- Penicillin allergy
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 16.07.2022
- Impfdatum
- 06.07.2022
- Beginn
- 07.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain upper
Body temperature
Body temperature increased
Vomiting
Abdominal pain
Injection site pain
Malaise
Nausea
Symptomtext
temperature 101; Stomach pain; threw up; This is a spontaneous report received from contactable reporter(s) (Nurse). The reporter is the parent. A 3-year-old male patient received BNT162b2 (BNT162B2), on 06Jul2022 at 09:15 as dose 1, single (Lot number: FT9142) at the age of 3 years, in left leg for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: ABDOMINAL PAIN UPPER (non-serious) with onset 07Jul2022, outcome "not recovered", described as "Stomach pain"; BODY TEMPERATURE INCREASED (non-serious) with onset 07Jul2022, outcome "not recovered", described as "temperature 101"; VOMITING (non-serious) with onset 07Jul2022, outcome "not recovered", described as "threw up". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of body temperature increased, abdominal pain upper, vomiting. Additional information: The patient had no other conditions (including medical history/ any illness at time of vaccination), investigations (relevant test) and did not receive any other products. The patient had no previous immunization with the Pfizer vaccine and no additional vaccines administered on same date of the Pfizer suspect. The patient did not have any prior vaccinations (within 4 weeks) and no events following them. Family history included father was diabetic. Reporter stated that her son and their family of 5 all had the Pfizer vaccines and had not had any problems at all. The patient seemed perfectly fine the morning when he got up. On the day of the report, her husband had to pick up their son from day care because he had a temperature 101 and was complaining of stomach pain and threw up. He seems to be progressing as the day goes on. Husband just went to pick son up and reporter had not actually seen him yet. Hasn't actually seen him throwing up. The events did not require a visit to emergency room or Physician office.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220707; Test Name: temperature; Result Unstructured Data: Test Result:101
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other Conditions: No. Patient's Medical History (including any illness at time of vaccination)? None.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 16.07.2022
- Impfdatum
- 06.07.2022
- Beginn
- 07.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain upper
Body temperature
Body temperature increased
Vomiting
Abdominal pain
Injection site pain
Malaise
Nausea
Symptomtext
temperature 101; Stomach pain; threw up; This is a spontaneous report received from contactable reporter(s) (Nurse). The reporter is the parent. A 3-year-old male patient received BNT162b2 (BNT162B2), on 06Jul2022 at 09:15 as dose 1, single (Lot number: FT9142) at the age of 3 years, in left leg for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: ABDOMINAL PAIN UPPER (non-serious) with onset 07Jul2022, outcome "not recovered", described as "Stomach pain"; BODY TEMPERATURE INCREASED (non-serious) with onset 07Jul2022, outcome "not recovered", described as "temperature 101"; VOMITING (non-serious) with onset 07Jul2022, outcome "not recovered", described as "threw up". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of body temperature increased, abdominal pain upper, vomiting. Additional information: The patient had no other conditions (including medical history/ any illness at time of vaccination), investigations (relevant test) and did not receive any other products. The patient had no previous immunization with the Pfizer vaccine and no additional vaccines administered on same date of the Pfizer suspect. The patient did not have any prior vaccinations (within 4 weeks) and no events following them. Family history included father was diabetic. Reporter stated that her son and their family of 5 all had the Pfizer vaccines and had not had any problems at all. The patient seemed perfectly fine the morning when he got up. On the day of the report, her husband had to pick up their son from day care because he had a temperature 101 and was complaining of stomach pain and threw up. He seems to be progressing as the day goes on. Husband just went to pick son up and reporter had not actually seen him yet. Hasn't actually seen him throwing up. The events did not require a visit to emergency room or Physician office.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220707; Test Name: temperature; Result Unstructured Data: Test Result:101
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other Conditions: No. Patient's Medical History (including any illness at time of vaccination)? None.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 15.07.2022
- Impfdatum
- 07.07.2022
- Beginn
- 11.07.2022
- Tage bis Beginn
- 4,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Decreased appetite
Listless
Pyrexia
Symptomtext
Fever lasting two days that started *four days after* injection. Fever ranged between 100.5 - 101. General listlessness, loss of appetite.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 15.07.2022
- Impfdatum
- 07.07.2022
- Beginn
- 13.07.2022
- Tage bis Beginn
- 6,0
- Dosis
- 1
- Route/Site
- SYR / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
COVID-19
Decreased appetite
Fatigue
Pyrexia
SARS-CoV-2 test positive
Symptomtext
Her two most significant symptoms are fever and fatigue. It started with fatigue, and we checked for a fever at 100.7. Wednesday afternoon it was at 101.7. We gave her 5 ml of MOTRIN and went to bed at 6:15PM. The next morning, her fever was at 104 and we gave her more MOTRIN. She was very low energy and went back to sleep until about 10AM. We've been alternating MOTRIN and TYLENOL every 3 hours since yesterday morning. Yesterday afternoon about 4PM her fever was at 102.6. We stayed on the schedule with the medication, and she went back to bed at 6:30PM. This morning her fever was at 102.7. We gave her MOTRIN again. Her appetite wasn't that great but she's eating better today and had a bowel movement. She doesn't have high energy, but she is playing today and seems to be improving. She doesn't have a cough or much congestion. Her main symptoms are fever and fatigue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- At home COVID-19 test 07/13/2022 - positive; COVID-19 PCR test 07/13/2022 - positive.
- Aktuelle Erkrankungen
- Influenza B 10 days prior to vaccination
- Vorgeschichte
- None
- Andere Medikamente
- FLINTSTONE vitamin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 15.07.2022
- Impfdatum
- 23.06.2022
- Beginn
- 09.07.2022
- Tage bis Beginn
- 16,0
- Dosis
- 1
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
COVID-19
Cough
Glassy eyes
Irritability
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Sneezing
Symptomtext
07/10/2022 Around 2:00 PM she became super cranky, her eyes became glassy, her nose started running, she was sneezing and coughing. I tested her with a home COVID test which was positive. Her temperature was 101.5 and we called her transplant team who told us to give her TYLENOL and increase her fluids. 07/11/2022 I called her pediatrician to let them know she had tested positive. They agreed to continue her palliative care, to try a NETTY POT, and continue TYLENOL and fluids. 07/11/2022 She seemed fine. Around 3:00 PM or 4:00 PM she was out of energy. 7/12/2022 She was a little sicker that morning and her fever went up. We gave TYLENOL and she was fine for the rest of the day. 7/13/2022 she seemed fine. Yesterday she seemed a little sicker. Throughout, her nose has been very runny and she has a deep cough. She has not recovered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- COVID home test, positive
- Aktuelle Erkrankungen
- Prior to vaccine runny nose; cough
- Vorgeschichte
- Biliary Atresia; liver transplant
- Andere Medikamente
- Tacrolimus; vitamin D3; cetirizine
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 15.07.2022
- Impfdatum
- 23.06.2022
- Beginn
- 27.06.2022
- Tage bis Beginn
- 4,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Anaemia
Arthralgia
Aspartate aminotransferase increased
C-reactive protein increased
Epstein-Barr virus test negative
Pyrexia
Urticaria
Full blood count abnormal
Inflammatory marker increased
Joint swelling
Pain in extremity
Peripheral swelling
Rash
Rash erythematous
Red blood cell sedimentation rate increased
Respiratory viral panel
SARS-CoV-2 test negative
Urine analysis normal
Symptomtext
Had fever, hives & joint pains 3 days after vaccination. Lasting 9 days total.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- N/a
- Allergien
- N/a
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 15.07.2022
- Impfdatum
- 23.06.2022
- Beginn
- 27.06.2022
- Tage bis Beginn
- 4,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Anaemia
Arthralgia
Aspartate aminotransferase increased
C-reactive protein increased
Epstein-Barr virus test negative
Pyrexia
Urticaria
Full blood count abnormal
Inflammatory marker increased
Joint swelling
Pain in extremity
Peripheral swelling
Rash
Rash erythematous
Red blood cell sedimentation rate increased
Respiratory viral panel
SARS-CoV-2 test negative
Urine analysis normal
Symptomtext
Had fever, hives & joint pains 3 days after vaccination. Lasting 9 days total.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- N/a
- Allergien
- N/a
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 0,9
- Geschlecht
- F
- Eingang
- 14.07.2022
- Impfdatum
- 14.07.2022
- Beginn
- 14.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Symptomtext
Skin rashes all over the back, as well as the abdomal area of the patient
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 14.07.2022
- Impfdatum
- 11.07.2022
- Beginn
- 13.07.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Mouth swelling
Rash
Symptomtext
Generalized rash, mouth swelling began 7/13/22. Took OTC antihistamine. Prescribed steroids.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- ear infection
- Vorgeschichte
- Denies
- Andere Medikamente
- Augmentin
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 14.07.2022
- Impfdatum
- 08.07.2022
- Beginn
- 08.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Headache
Influenza virus test negative
Pyrexia
SARS-CoV-2 test negative
Streptococcus test negative
Symptomtext
Right away she did have a headache and was fatigued. The next day she seemed pretty normal. On 07/13/2022 She did come down with fatigue, a headache, low grade fever, and overall tiredness. We took her to her pediatrician the same day, they did evaluate for strep, flu, and COVID-19 and all tests came back negative. As of today she is doing completely fine and is back to her normal self.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Strep test: negative, flu test: negative, COVID-19: negative.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Multivitamin
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 13.07.2022
- Impfdatum
- 07.07.2022
- Beginn
- 09.07.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Diarrhoea
Symptomtext
Moderate diarrhea lasted 2 days
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 13.07.2022
- Impfdatum
- 07.07.2022
- Beginn
- 07.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal pain upper
Blood test normal
Borrelia test
Culture
Culture urine negative
Fatigue
Pyrexia
Urine output decreased
Symptomtext
On the evening of 07/07/2022 started running low grade fever from then until 07/11/2022. On 07/12/22 fever spiked up to 102.9 and the on the evening of 07/12/2022 she had stomach ache, fever up to 105.0, fatigued and low urine out put. She was taken to the ER at the Hospital and had normal blood and urine cultures. The Lyme/Tick cultures are still out and have not received the results yet. As of today she is still running a 99.0 fever.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- Blood Culture; Urine Culture on 07/12/2022 Normal Tick/Lyme Disease Culture on 07/12/2022 Not Results Yet
- Aktuelle Erkrankungen
- Constipation
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 0,8
- Geschlecht
- M
- Eingang
- 13.07.2022
- Impfdatum
- 24.06.2022
- Beginn
- 06.07.2022
- Tage bis Beginn
- 12,0
- Dosis
- 1
- Route/Site
- SYR / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Ear infection
Hypersomnia
Infant irritability
Lethargy
Pyrexia
SARS-CoV-2 test positive
Symptomtext
06/24/2022 Vaccination 07/02/2022 Patient had an ear infection, lethargic, extended naps which is unusual for him and spiked a fever of 103.2. I called Pedicatrian. We were out of town and to give him Motrin. It went down to 101 degrees. 07/03/2022 No fever. 07/06/2022 Patient was pretty fussy that afternoon. I asked the daycare to keep eye on him if he seemed more fussier. They called me and said they think something is wrong. I went to pick up Patient. 07/06/2022 Went to Pediatrician's office for Ear Infection. Tested POSITIVE for COVID-19. I don't know if symptoms were due to the ear infection or COVID-19. He's doing better with Amoxicillin and Motrin. 07/11/2022 COVID-19 NEGATIVE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- COVID-19
- Aktuelle Erkrankungen
- Ear Infection
- Vorgeschichte
- N/A
- Andere Medikamente
- Vitamin D drops
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 13.07.2022
- Impfdatum
- 09.07.2022
- Beginn
- 10.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Pyrexia
SARS-CoV-2 test negative
Vomiting
Symptomtext
We started to notice that after lunch she vomited out her entire lunch while driving over to a friends house. After that, she seemed fine and played in the pool for a bit and everything was normal she did sleep over an hour and a half and seemed a little more tired than usual. After getting home later that evening we noticed that she began to run a small fever. We did not give her anything for the symptoms and she seemed to be fine and slept the entire night through. We then took her to the pediatrician the next day she still had a fever of 100, and at the visit they measured a temperature at 101. COVID-19 test was done and came back negative, they said she was well hydrated, everything else looked great. After getting home she took a two hour nap. Tylenol was given in the middle of the afternoon and fever went down and she seemed completely fine. As of the 12th, she has been completely fine and non symptomatic.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 Test: Negative
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Topical Cream for Eczema
- Allergien
- Peanuts; Cashews
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 12.07.2022
- Impfdatum
- 06.07.2022
- Beginn
- 06.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Rash
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 12.07.2022
- Impfdatum
- 07.07.2022
- Beginn
- 07.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site extravasation
Vaccination error
Symptomtext
Patient was present in the clinic on 7/7/2022 for her 1st dose of Pfizer (6 months ? 4yrs formulation, lot number FT9142). RN, the vaccinator, went ahead to vaccinated on the right vastus lateralis, however when the needle (25G vanishing point) was 1/4 of the way piercing into the child skin; the child moved. The vaccinator attempted to follow and continue to insert the needle. Upon injecting, the dose was leaking at the injection site. Vaccinator and parent were able to witness that almost none of the dose enter the site. RN was able to assess the site for any scratching or bruising as well assessed for any bleeding. RN notified the Charge nurse, who was able to educate parent on the need for repeating dose on different site (left vastus lateralis) per our protocol, since less than half ? or rather none of the dose had entered the site. The parent was educated on watching the child for any bruising and that the child can be given children?s Tylenol for comfort. Parent expressed understanding and consented to re-administration of dose in opposite site. Client was able to successfully receive dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site extravasation
- Hospital-Tage
- -
- Labordaten
- unknown
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 2,0
- Geschlecht
- M
- Eingang
- 11.07.2022
- Impfdatum
- 07.07.2022
- Beginn
- 08.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Urticaria
Symptomtext
Urticaria noted on trunk less than 24 hours after vaccine resolved with use of Benadryl.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Unknown
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 1,1
- Geschlecht
- F
- Eingang
- 09.07.2022
- Impfdatum
- 23.06.2022
- Beginn
- 23.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Body temperature
Product administered at inappropriate site
Pyrexia
Symptomtext
prolonged high fever; Anatomical Location of Administration of Pfizer vaccine considered as suspect: Left Thigh; This is a spontaneous report received from contactable reporter(s) (Pharmacist) from medical information team. The reporter is the parent. A 13-month-old female patient received BNT162b2 (BNT162B2), on 23Jun2022 at 11:45 as dose 1, single (Lot number: FT9142) at the age of 13 months, in left thigh for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: mmr, administration date: 05May2022, when the patient was 12-month-old, for Immunisation, reaction(s): "Diarrhea". The following information was reported: PRODUCT ADMINISTERED AT INAPPROPRIATE SITE (non-serious) with onset 23Jun2022 at 11:45, outcome "unknown", described as "Anatomical Location of Administration of Pfizer vaccine considered as suspect: Left Thigh"; PYREXIA (medically significant) with onset 25Jun2022, outcome "not recovered", described as "prolonged high fever". The event "prolonged high fever" required emergency room visit. The patient underwent the following laboratory tests and procedures: Body temperature: (01Jul2022) gone down, notes: almost 105 degrees to 102 degrees. The patient did not receive any other vaccines within four weeks prior to the vaccination. 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)was none reported.; Sender's Comments: Based on the information in the case report and a plausible temporal relationship, a possible causal association between the events and suspect drug BNT162B2 cannot be excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220701; Test Name: fever; Result Unstructured Data: Test Result:gone down; Comments: almost 105 degrees to 102 degrees
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Patient's Medical History (including any illness at time of vaccination): None
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 1,8
- Geschlecht
- M
- Eingang
- 08.07.2022
- Impfdatum
- 08.07.2022
- Beginn
- 08.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Blood glucose normal
Cardiac monitoring
Crying
Decreased appetite
Eye movement disorder
Fatigue
Muscle rigidity
Pyrexia
Skin discolouration
Symptomtext
Woke up after nap very tired. Cried getting diaper changed. Refused snack/drink. Started to fall, eyes rolled back, skin tone looked gray/blue, body went rigid for about 2 minutes. EMS arrived within 10 min. HR at 180 bpm. Febrile 102F. Blood sugar 112 mg/dL
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- EMS measured blood pressure, temperature, blood sugar, and put some leads on his body to monitor his heart. ED measured temperature, O2 level, and heart rate.
- Aktuelle Erkrankungen
- None. Covid 5 weeks ago
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 0,6
- Geschlecht
- M
- Eingang
- 08.07.2022
- Impfdatum
- 05.07.2022
- Beginn
- 05.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Irritability
Vomiting
Symptomtext
PT REC'D COVID VACCINE LL IM 07/05/22 APPROX. 5MIN AFTER VACCINE WAS ADMINISTERED PATIENT VOMITED A LARGE AMOUNT. PATIENT WAS NOT WORKED UP FROM THE VACCINE PER MOTHER OF CHILD, PT WAS CALM WHEN VOMITING EPISODE HAPPENED. PATIENT WAS EXAMINED BY ONE OF OUR PHYSICIANS AND DURING EXAM HAD 2 MORE VOMITING EPISODES. ONE EPISODE PT WAS FUSSY. VITALS TAKEN & WERE STABLE, PHYSICAN WAS UNSURE IF HE FELT IT WAS TRULY VACCINE RELATED . PT IS SCHEDULED FOR HIS 2ND VACCINE 07/26/22. PROGRESS REPORT FROM MOM TODAY 07/08/22 STATES PT IS DOING WELL, BACK TO NORMAL AFTER LEAVING CLINIC 07/05/22, NO OTHER VOMITING EPISODES OR OTHER REACTIONS WERE NOTED BY PARENT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vomiting
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 2,0
- Geschlecht
- M
- Eingang
- 08.07.2022
- Impfdatum
- 22.06.2022
- Beginn
- 22.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered at inappropriate site
Urticaria
Vomiting
Symptomtext
non-irritating hive/Hives were noticed on arms, belly, back, face, legs; vomiting; Vaccine location Left leg; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A 2-year-old male patient received BNT162b2 (BNT162B2), on 22Jun2022 as dose 1, single (Lot number: FT9142) at the age of 2 years intramuscular, in left leg for covid-19 immunisation. The patient's relevant medical history included: "chronic ear infections" (unspecified if ongoing); "covid" (unspecified if ongoing), notes: Prior vaccination. There were no concomitant medications. The following information was reported: PRODUCT ADMINISTERED AT INAPPROPRIATE SITE (non-serious) with onset 22Jun2022, outcome "unknown", described as "Vaccine location Left leg"; URTICARIA (non-serious) with onset 30Jun2022, outcome "recovering", described as "non-irritating hive/Hives were noticed on arms, belly, back, face, legs"; VOMITING (non-serious) with onset 30Jun2022, outcome "recovering". The events "non-irritating hive/hives were noticed on arms, belly, back, face, legs" and "vomiting" required physician office visit. Therapeutic measures were not taken as a result of urticaria, vomiting. Additional information: No other vaccine in four weeks. No other medication in two weeks. Covid was not tested post vaccination. No known allergies. 8 days post covid vaccine, patient had non-irritating hives that came and went and returned sporadically over 2 days. Hives were noticed on arms, belly, back, face, legs. No other symptoms came along with hives or prior to hives except for 1 instance of vomiting on 30Jun2022 when hives started. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19 (Prior vaccination); Ear infection
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 1,0
- Geschlecht
- F
- Eingang
- 07.07.2022
- Impfdatum
- 22.06.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- 9,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cough
Exposure to SARS-CoV-2
Fatigue
Irritability
Symptomtext
She had cough that sounded different, it sounded wetter, was irritable, more tired. We did not do a home COVID-19 Test since my wife had tested positive. Doctor recommended that if needed to give her over the counter medication to control symptoms. We alternated with Motrin and Tylenol. She is back to her normal self since July 4, 2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- No
- Vorherige Impfungen
- In the NICU she had a reaction to one of her vaccines
- Staat
- NY
- Alter
- 0,8
- Geschlecht
- M
- Eingang
- 06.07.2022
- Impfdatum
- 26.06.2022
- Beginn
- 28.06.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Diarrhoea
Irritability
Somnolence
Symptomtext
36 hours post administration, had irritability, drowsiness and diarrhea; 36 hours post administration, had irritability, drowsiness and diarrhea; 36 hours post administration, had irritability, drowsiness and diarrhea; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A 9-month-old male patient received BNT162b2 (BNT162B2), on 26Jun2022 at 15:45 as dose 1, single (Lot number: FT9142) at the age of 9 months intramuscular, in left arm for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: DIARRHOEA (non-serious), IRRITABILITY (non-serious), SOMNOLENCE (non-serious) all with onset 28Jun2022 at 09:30, outcome "recovering" and all described as "36 hours post administration, had irritability, drowsiness and diarrhea". Therapeutic measures were not taken as a result of diarrhoea, irritability, somnolence. Additional information: No other vaccine in four weeks and no other medications in two weeks. No covid prior vaccination, no covid tested post vaccination, no known allergies and no other medical history.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: none, Comment: Other medical history: none.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 05.07.2022
- Impfdatum
- 05.07.2022
- Beginn
- 05.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Erythema
Injection site pruritus
Pruritus
Symptomtext
Within about 40 minutes of the shot, my daughter started complaining of being itchy at the injection site. Then it quickly turned into itchy everywhere - mainly right side of her body - arm, hand, thumb, neck, cheek, and then about 15 minutes later it was at her legs and feet. She developed a slight bump on her chin that was itchy but then it subsided within about 10 minutes. By the time it had been about 75 minutes since the injection, she seemed to be less red everywhere and was only occasionally itching. She wasn?t as bothered by it at that point. It?s now 6 hours later and she seems to be fine, with random itching intermittently.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pruritus
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- About 5 weeks ago she had Hand Foot and Mouth
- Vorgeschichte
- None
- Andere Medikamente
- Up and up brand kids multivitamin and Zarbees Elderberry kids gummies.
- Allergien
- None
- Vorherige Impfungen
- Also at age 4, she has a large red bump develop at the injection site after the MMR vaccine. That was in May 2022.
- Staat
- CA
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 05.07.2022
- Impfdatum
- 25.06.2022
- Beginn
- 30.06.2022
- Tage bis Beginn
- 5,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Feeling abnormal
Glassy eyes
Lethargy
Pyrexia
Respiratory tract congestion
Symptomtext
Fussy when he came home from daycare. His eyes appeared glossy. He developed a fever (38.9 Celsius), congestion and was very lethargic and then after 24 hours he was back to his normal self. We treated his at fever by alternating antihistamines Ibuprofen, Tylenol. These symptoms lasted for about 2 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- Cold 3 weeks ago
- Vorgeschichte
- NA
- Andere Medikamente
- NA
- Allergien
- NA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 05.07.2022
- Impfdatum
- 25.06.2022
- Beginn
- 04.07.2022
- Tage bis Beginn
- 9,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Symptomtext
rash on cheeks, ears, neck
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Levocetirizine
- Allergien
- no known
- Vorherige Impfungen
- swelling, redness at the injection site
- Staat
- MI
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 05.07.2022
- Impfdatum
- 02.07.2022
- Beginn
- 02.07.2022
- 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
Chills
Myalgia
Symptomtext
She had chills, muscle aches and abdominal pain
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Claritin
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 2,0
- Geschlecht
- M
- Eingang
- 04.07.2022
- Impfdatum
- 29.06.2022
- Beginn
- 29.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Rash
Symptomtext
generalized rash, looking like small pinsized red/dark pink dots on belly, back, surrounding penis, around mouth, and next to right eye; Age at Vaccination: 2 yo; This is a spontaneous report received from contactable reporter (Consumer or other non HCP). A 2-year-old male patient received BNT162b2 (Pfizer-BioNTech COVID-19), on 29Jun2022 at 13:45 as dose 1, single (Lot number: FT9142) at the age of 2 years, in left leg for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included(in two weeks): FLUORIDE [SODIUM FLUORIDE]. The following information was reported: PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (non-serious) with onset 29Jun2022 at 13:45, outcome "unknown", described as "Age at Vaccination: 2 yo"; RASH (non-serious) with onset 29Jun2022 at 15:45, outcome "not recovered", described as "generalized rash, looking like small pinsized red/dark pink dots on belly, back, surrounding penis, around mouth, and next to right eye". Therapeutic measures were not taken as a result of rash. Additional information: Within 2 hours of receiving vaccine, developed generalized rash, looking like small pinsized red/dark pink dots on belly, back, surrounding penis, around mouth, and next to right eye. Didn't seem to be itchy or bothersome. No fever. Patient had no known allergies. The patient had not received any other vaccine in four weeks. Patient had not been diagnosed with COVID-19 prior to vaccination and had not been tested since the vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other medical history: No.
- Andere Medikamente
- FLUORIDE [SODIUM FLUORIDE]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 2,0
- Geschlecht
- M
- Eingang
- 04.07.2022
- Impfdatum
- 29.06.2022
- Beginn
- 29.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Lip swelling
Rash
Symptomtext
PATIENT DEVELOPED SWOLLEN LIPS AND RASH ON B/L ARMS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- h/o mild eczema
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 24.06.2022
- Beginn
- 24.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered at inappropriate site
Vomiting
Symptomtext
Vomiting starting at 36 hours after vaccine administration, for around 6 hours off and on through the night. No fever, and otherwise healthy/happy.; vaccine Location=Left leg; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 2-year-old female patient received BNT162b2 (BNT162B2), on 24Jun2022 at 09:15 as dose 1, single (Lot number: FT9142) at the age of 2 years, in left leg for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. The following information was reported: PRODUCT ADMINISTERED AT INAPPROPRIATE SITE (non-serious) with onset 24Jun2022 at 09:15, outcome "unknown", described as "vaccine Location=Left leg"; VOMITING (non-serious) with onset 25Jun2022 at 22:00, outcome "recovered", described as "Vomiting starting at 36 hours after vaccine administration, for around 6 hours off and on through the night. No fever, and otherwise healthy/happy.". Therapeutic measures were not taken as a result of product administered at inappropriate site, vomiting. Additional information:Facility type vaccine: Doctor's office/urgent care, The patient did not receive other vaccine in fourweeks or any other medication in two weeks. The patient reported vomiting starting at 36 hours after vaccine administration, for around 6 hours off and on through the night. No fever, and otherwise healthy/happy. The patient did not receive covid prior vaccination or covid tested post vaccination. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vomiting
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 1,9
- Geschlecht
- M
- Eingang
- 03.07.2022
- Impfdatum
- 23.06.2022
- Beginn
- 25.06.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
Pyrexia
Symptomtext
Started running fever oof 102 about 48 hours after vaccine; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the parent. A 23-month-old male patient received BNT162b2 (BNT162B2), on 23Jun2022 as dose 1, single (Lot number: FT9142) at the age of 23 months for covid-19 immunisation. The patient's relevant medical history included: "Known allergies: penicillin" (unspecified if ongoing). There were no concomitant medications. The following information was reported: PYREXIA (non-serious) with onset 25Jun2022, outcome "not recovered", described as "Started running fever oof 102 about 48 hours after vaccine". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of pyrexia.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220625; Test Name: Fever; Result Unstructured Data: Test Result:102
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Penicillin allergy
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 03.07.2022
- Impfdatum
- 22.06.2022
- Beginn
- 22.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site pain
SARS-CoV-2 test
Symptomtext
injection site pain - pain in right arm; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A 4-year-old male patient received BNT162b2 (COMIRNATY), on 22Jun2022 at 17:15 as dose 1, single (Lot number: FT9142) at the age of 4 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "seasonal allergies" (unspecified if ongoing); "known allergis: Tree nuts" (unspecified if ongoing), notes: known allergies: Tree Nuts, Eggs; "known allergis: Eggs" (unspecified if ongoing), notes: known allergies: Tree Nuts, Eggs; "Covid-19" (unspecified if ongoing), notes: If Covid prior vaccination: Yes. Concomitant medication(s) included: CHILDREN'S ZYRTEC. The following information was reported: INJECTION SITE PAIN (non-serious) with onset 22Jun2022 at 20:30, outcome "recovered" (Jun2022), described as "injection site pain - pain in right arm". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of injection site pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220624; Test Name: Rapid Test; Test Result: Negative
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Allergy to nuts (known allergies: Tree Nuts, Eggs); COVID-19 (If Covid prior vaccination: Yes); Egg allergy (known allergies: Tree Nuts, Eggs); Seasonal allergy
- Andere Medikamente
- CHILDREN'S ZYRTEC
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 21.06.2022
- Beginn
- 22.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Decreased appetite
Vomiting
Symptomtext
One day after receiving the her first dose of the vaccine, my daughter was not eating and vomited; One day after receiving the her first dose of the vaccine, my daughter was not eating and vomited. Thus far she has only had one round of vomiting; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the parent. A 2-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 21Jun2022 as dose 1, single (Lot number: FT9142) at the age of 2 years intramuscular, in left arm for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: DECREASED APPETITE (non-serious) with onset 22Jun2022 at 18:00, outcome "recovering", described as "One day after receiving the her first dose of the vaccine, my daughter was not eating and vomited"; VOMITING (non-serious) with onset 22Jun2022 at 18:00, outcome "recovering", described as "One day after receiving the her first dose of the vaccine, my daughter was not eating and vomited. Thus far she has only had one round of vomiting". Therapeutic measures were not taken as a result of decreased appetite, vomiting. Additional information: It was reported that other medical history and known allergies were noted as no. Facility type vaccine was noted as pharmacy or drug store. The patient did not experience covid-19 prior to vaccination and the patient was not tested for covid-19 post vaccination. The patient did not receive other vaccine in four weeks and did not receive other medications in two weeks. One day after receiving the her first dose of the vaccine, the patient was not eating and vomited. Thus far she has only had one round of vomiting. Up to this point no one else in the house had been sick so a stomach bug seemed less likely. Reporter's other daughter (age 4) received her first shot on the same day and has not had any symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vomiting
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other medical history: No
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
COVID-19
Product administered to patient of inappropriate age
Pyrexia
SARS-CoV-2 antibody test
Symptomtext
Tested positive for COVID; A little bit of fever last night and then today or this morning, she has a higher fever around 101; Daughter is 2 and a half years old; 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 child female patient of age 2 and a half year-old received BNT162b2 (BNT162B2), as dose 1, single (Lot number: FT9142) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: COVID-19 (non-serious), outcome "unknown", described as "Tested positive for COVID"; PYREXIA (non-serious), outcome "unknown", described as "A little bit of fever last night and then today or this morning, she has a higher fever around 101"; PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (non-serious), outcome "unknown", described as "Daughter is 2 and a half years old". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: Transferring agent stated, I have a caller on the other line. His daughter received, his daughter was 2 and a half years old (not confirmed and clarified) and just received the first shot last night and she had a fever, a little bit of fever/ low grade fever last night and then today or this morning, she had a higher fever around 101. Caller wanted to know if the vaccine can cause a false positive result. On confirming if the reporter only wants to report or needs any information transferring agent stated, he would like to report that adverse event as well as his daughter tested positive as well for COVID. So he wants to know if the vaccine can cause the COVID-19. On paraphrasing the concern reporter stated, that was correct and she also, we just tested her and she did come up positive for the test. So I am just curious if that is possibly positive from the vaccine shot or it is actually a Covid test. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- Test Name: Body temperature; Result Unstructured Data: Test Result:101; Comments: she has a higher fever around 101.; Test Name: COVID test; Test Result: Positive ; Comments: tested positive for COVID.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 02.07.2022
- Impfdatum
- 23.06.2022
- Beginn
- 23.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Diarrhoea
Urticaria
Vomiting
Symptomtext
Vomiting starting 15 minutes after shot, continued for 2 days. Diarrhea lasting 4 days. Hives starting 4 days after shot. Hives have lasted 5 days (so far).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Possible stomach virus the week before vaccine
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 1,0
- Geschlecht
- M
- Eingang
- 01.07.2022
- Impfdatum
- 28.06.2022
- Beginn
- 29.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Urticaria
Symptomtext
mild urticarial rash noted face, trunk , extremities note the following day after vaccination. As of 7/1, rash comes and goes and disappears with Diphenhydramine. Child acting fine, no fever, eating, drinking and playing as normal
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- Otitis media diagnosed 6/17/22, treated with Amoxicillin x 10 days. COVID vaccine given in combination with other 12 month vaccines: MMR, Varivax and Hepatitis A
- Vorgeschichte
- none
- Andere Medikamente
- Amoxicillin started on 6/17 for ear infection - completed course day prior to vaccine
- Allergien
- None known
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 5,0
- Geschlecht
- F
- Eingang
- 01.07.2022
- Impfdatum
- 27.06.2022
- Beginn
- 27.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Pain in extremity
Product preparation error
Symptomtext
27 patients were scheduled for the day and provider did not have a nurse or medical assistant, to help with any tasks or check-in. several patients were siblings needing different vials of Pfizer, which required different dilution amounts. Small (1ml) syringes were on the counter, and provider accidentally drew up the wrong dilution amount and diluted the vials with 0.13 mL of NS instead of 1.3 mL. the does given was still 0.2mL Patient has a sore arm as the only side effect
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- 27 patients were scheduled for the day and provider did not have a nurse or medical assistant, to help with any tasks or check-in. several patients were siblings needing different vials of Pfizer, which required different dilution amounts.
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 6,0
- Geschlecht
- M
- Eingang
- 01.07.2022
- Impfdatum
- 27.06.2022
- Beginn
- 27.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site pain
Product preparation issue
Pyrexia
Symptomtext
27 patients were scheduled for the day and provider did not have a nurse or medical assistant, to help with any tasks or check-in. several patients were siblings needing different vials of Pfizer, which required different dilution amounts. Small (1ml) syringes were on the counter, and provider accidentally drew up the wrong dilution amount and diluted the vials with 0.22 mL of NS instead of 2.2 mL. the does given was still 0.2mL. outcome: he had a minor fever and pain at the injection site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 01.07.2022
- Impfdatum
- 23.06.2022
- Beginn
- 29.06.2022
- Tage bis Beginn
- 6,0
- Dosis
- 1
- Route/Site
- SYR / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Emotional distress
Hand-foot-and-mouth disease
Oral pain
Stomatitis
Symptomtext
She told me her mouth hurt and was covering her ears. She continued to be in distress and I took her to the doctor on 06/30/2022. She diagnosed with Hand, Foot, and Mouth disease, she had multiple sores in her mouth, two on her hand and foot, and a few on her bottom. she was not prescribed any medication and I was told she can take Children's Motrin and Tylenol.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oral pain
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Flintstone Vitamins
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 30.06.2022
- Impfdatum
- 30.06.2022
- Beginn
- 30.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Rash
Rash erythematous
Rash macular
Symptomtext
Rash down Left arm, macular, lacy, red-pink, also mildly on the Right arms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- VSS, alert, playful, no testing.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Celiac disease
- Andere Medikamente
- None
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 1,8
- Geschlecht
- F
- Eingang
- 30.06.2022
- Impfdatum
- 27.06.2022
- Beginn
- 28.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Decreased appetite
Lethargy
Urticaria
Symptomtext
After she received the vaccine she was lethargic and hardly had an appetite. She woke up the next day with hives on her foot and inner thigh. After 30 minutes they disappeared. Through out the course of the day hives were popping up on different places of her body. At 6:45PM I gave her some ZYRTEC. The next morning when she woke up the hives were gone. On June 29, 2022 I took her to the doctor. The doctor said that the hives could have been virally triggered or caused by the vaccine, and they recommended for her to not get the 2nd dose. The doctor said to see her allergist to see what they think. She also has no history of ever having hives before.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Cold; runny nose
- Vorgeschichte
- Eczema
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 1,0
- Geschlecht
- M
- Eingang
- 30.06.2022
- Impfdatum
- 25.06.2022
- Beginn
- 26.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LG
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Diarrhoea
Pyrexia
Rash
Rash erythematous
Rash macular
SARS-CoV-2 test negative
Symptomtext
The next day, he developed a fever on 6/26/2022 that continued until 6/27/2022. His fever got up to 101.8 at the highest. On 6/27/2022, he developed a rash that was in a couple of spots on his body. The rash progressed and spread all over. The rash was red with small botchy circles but not raised. On 6/29/2022 we took him to the doctor. The rash was worse on his stomach that looked like Rosacea but it looked different than on his face that looked more like hives. Today his rash looks better and it is resolving. He has also had Diarrhea since 6/26/2022 that has resolved today. The doctor did do a COVID-19 test that was negative.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- COVID-19 test - negative
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 30.06.2022
- Impfdatum
- 27.06.2022
- Beginn
- 28.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Diarrhoea
SARS-CoV-2 test negative
Vomiting
Symptomtext
vomiting only at night and diarrhea
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- negative covid test.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 1,9
- Geschlecht
- M
- Eingang
- 29.06.2022
- Impfdatum
- 24.06.2022
- Beginn
- 26.06.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Immunisation reaction
Injection site pain
Pyrexia
Symptomtext
My son got his first dose of the Pfizer vaccine for COVID-19 on 6/24/2022. He had pain at the site of the injection for 48 hours. Afterwards, he became intermittently feverish. He reached a fever of 102.3 on 6/28/2022 at 3:30 PM. We gave him Tylenol and called the pediatrician's office. The fever then went away. The pediatrician advised us to monitor his condition and told us to bring him to her office if his situation did not improve; she suspected that the fever was connected to the vaccine. Thankfully, there has not been a recurrence of the fever ever since, and there no longer appears to be pain at the injection site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- None.
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 28.06.2022
- Impfdatum
- 25.06.2022
- Beginn
- 25.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abnormal sleep-related event
Influenza virus test negative
Lethargy
Nasopharyngitis
Nausea
Pyrexia
Rhinorrhoea
SARS-CoV-2 test negative
Vomiting
Symptomtext
06/25/2022 at 03:15 vaccination. Within 20 minutes, became lethargic and vomited at the 25 minute mark. Placed in car, in which he fell asleep which is not normal for pt. in that short distance. Got home and his temp was 100. Called pediatrician office and referred to urgent care. Temp was 101.8 upon arrival. Highest temp was 102 in which pt. threw up 1x more time. Got nausea under control. Fever lasted Saturday into Sunday. 06/26/2022 sniffles started in the morning. Pediatrician stated that it could have been a cold 'brewing' prior to vaccination, lingering cold.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- COVID; neg. flu; neg.
- Aktuelle Erkrankungen
- Possible cold virus but hadn't exhibited symptoms yet
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Penicillin class
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 28.06.2022
- Impfdatum
- 25.06.2022
- Beginn
- 01.06.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Fatigue
Product preparation issue
Product administration error
Symptomtext
The vaccine was incorrectly administered to my 3-year old. Instead of diluting the vaccine with 2.2 mL of saline, the pharmacist only diluted it with 0.22 mL of saline. She displayed minimal side effects (most notably fatigue in the first 24-48 hours), but we were told to watch her for chest pain without being told for how long this needs to be checked.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 1,6
- Geschlecht
- F
- Eingang
- 27.06.2022
- Impfdatum
- 26.06.2022
- Beginn
- 26.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Injection site rash
Pyrexia
Vomiting
Symptomtext
Vomiting twice an hour to an hour and a half later. Chills and a fever as well. There was a small rash at injections site, inner elbow and other leg.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Cold
- Vorgeschichte
- Febrile seizure in October of 2021
- Andere Medikamente
- No
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 27.06.2022
- Impfdatum
- 24.06.2022
- Beginn
- 24.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Vomiting
Symptomtext
Systemic: Vomiting-Mild, Additional Details: pt vomited once
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vomiting
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 27.06.2022
- Impfdatum
- 23.06.2022
- Beginn
- 24.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Crying
Insomnia
Irritability
Pyrexia
SARS-CoV-2 test positive
Symptomtext
June 24, 2022 she woke up very weepy and cranky, and that progressed throughout the day. She is usually very cheerful. She also had trouble sleeping. The next day on she Saturday morning woke up with a fever. On June 26th her fever broke around 3:00PM.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- Covid Test- positive (6/25/2022)
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Miralax
- Allergien
- She used to have an egg allergy, but she out grew it.
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 1,8
- Geschlecht
- F
- Eingang
- 27.06.2022
- Impfdatum
- 25.06.2022
- Beginn
- 26.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Pyrexia
Rash papular
Symptomtext
fever to 101 and diffuse papulovesicular rash
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 26.06.2022
- Impfdatum
- 01.06.2022
- Beginn
- 25.06.2022
- Tage bis Beginn
- 24,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Decreased appetite
Fatigue
Headache
Irritability
Malaise
Rhinorrhoea
Sneezing
Symptomtext
Sneezing, Runny nose, headache, feeling unwell, irritability, decreased appetite, tiredness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 2,0
- Geschlecht
- M
- Eingang
- 25.06.2022
- Impfdatum
- 24.06.2022
- Beginn
- 24.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Decreased appetite
Pyrexia
Vomiting
Symptomtext
Low grade fever 101 F, vomiting, decreased appetite.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Cold
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Augmentin
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 25.06.2022
- Impfdatum
- 25.06.2022
- Beginn
- 25.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Rash erythematous
Rash papular
Symptomtext
Diffuse rash. Started on back of neck, spread down arms and legs. Bright red, papular, non-blanching. Not itching, no trouble breathing, no changes at site of vaccine, no complaints. Given Benadryl, but nothing changed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- None, but referred to allergist for dose two.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- eczema
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 1,0
- Geschlecht
- M
- Eingang
- 24.06.2022
- Impfdatum
- 24.06.2022
- Beginn
- 24.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Rash
Rash erythematous
Symptomtext
After 10 minutes after receiving vaccine, patient developed red rash on forehead and temples. Rash resolved after 15-20 minutes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- No allergies.
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 1,4
- Geschlecht
- F
- Eingang
- 29.09.2023
- Impfdatum
- 18.01.2023
- Beginn
- 18.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Patient received COVID 19 vaccine that had been stored beyond the Beyond Use Date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 29.09.2023
- Impfdatum
- 06.02.2023
- Beginn
- 06.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Patient received COVID 19 vaccine that had been stored beyond the Beyond Use Date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 29.09.2023
- Impfdatum
- 13.03.2023
- Beginn
- 13.03.2023
- 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
Patient received COVID 19 vaccine that had been stored beyond the Beyond Use Date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 28.09.2023
- Impfdatum
- 14.03.2023
- Beginn
- 14.03.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Patient received COVID 19 vaccine that had been stored beyond the Beyond Use Date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 29.08.2023
- Impfdatum
- 25.02.2023
- Beginn
- 25.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 29.08.2023
- Impfdatum
- 28.01.2023
- Beginn
- 28.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 29.08.2023
- Impfdatum
- 18.03.2023
- Beginn
- 18.03.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 29.08.2023
- Impfdatum
- 21.01.2023
- Beginn
- 21.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 29.08.2023
- Impfdatum
- 28.12.2022
- Beginn
- 28.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 0,8
- Geschlecht
- M
- Eingang
- 29.08.2023
- Impfdatum
- 10.12.2022
- Beginn
- 10.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 29.08.2023
- Impfdatum
- 10.12.2022
- Beginn
- 10.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 0,6
- Geschlecht
- M
- Eingang
- 29.08.2023
- Impfdatum
- 28.12.2022
- Beginn
- 28.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 1,5
- Geschlecht
- F
- Eingang
- 29.08.2023
- Impfdatum
- 10.12.2022
- Beginn
- 10.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 29.08.2023
- Impfdatum
- 28.01.2023
- Beginn
- 28.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 28.08.2023
- Impfdatum
- 14.01.2023
- Beginn
- 14.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 28.08.2023
- Impfdatum
- 17.12.2022
- Beginn
- 17.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 28.08.2023
- Impfdatum
- 18.02.2023
- Beginn
- 18.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 28.08.2023
- Impfdatum
- 21.01.2023
- Beginn
- 21.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 28.08.2023
- Impfdatum
- 18.02.2023
- Beginn
- 18.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 28.08.2023
- Impfdatum
- 07.01.2023
- Beginn
- 07.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 5,0
- Geschlecht
- F
- Eingang
- 28.08.2023
- Impfdatum
- 07.01.2023
- Beginn
- 07.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 28.08.2023
- Impfdatum
- 28.12.2022
- Beginn
- 28.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 0,8
- Geschlecht
- F
- Eingang
- 28.08.2023
- Impfdatum
- 07.01.2023
- Beginn
- 07.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 0,8
- Geschlecht
- F
- Eingang
- 28.08.2023
- Impfdatum
- 17.12.2022
- Beginn
- 17.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 0,8
- Geschlecht
- M
- Eingang
- 28.08.2023
- Impfdatum
- 07.01.2023
- Beginn
- 07.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 0,8
- Geschlecht
- M
- Eingang
- 28.08.2023
- Impfdatum
- 17.12.2022
- Beginn
- 17.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 0,8
- Geschlecht
- M
- Eingang
- 28.08.2023
- Impfdatum
- 07.01.2023
- Beginn
- 07.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 0,8
- Geschlecht
- M
- Eingang
- 28.08.2023
- Impfdatum
- 17.12.2022
- Beginn
- 17.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 6,0
- Geschlecht
- M
- Eingang
- 25.08.2023
- Impfdatum
- 07.01.2023
- Beginn
- 07.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 1,8
- Geschlecht
- F
- Eingang
- 25.08.2023
- Impfdatum
- 18.02.2023
- Beginn
- 18.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 1,7
- Geschlecht
- F
- Eingang
- 25.08.2023
- Impfdatum
- 14.01.2023
- Beginn
- 14.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 25.08.2023
- Impfdatum
- 04.02.2023
- Beginn
- 04.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 25.08.2023
- Impfdatum
- 14.01.2023
- Beginn
- 14.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 0,6
- Geschlecht
- M
- Eingang
- 25.08.2023
- Impfdatum
- 18.03.2023
- Beginn
- 18.03.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 0,4
- Geschlecht
- M
- Eingang
- 25.08.2023
- Impfdatum
- 04.02.2023
- Beginn
- 18.02.2023
- Tage bis Beginn
- 14,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 25.08.2023
- Impfdatum
- 04.02.2023
- Beginn
- 04.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 25.08.2023
- Impfdatum
- 14.01.2023
- Beginn
- 14.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 25.08.2023
- Impfdatum
- 10.12.2022
- Beginn
- 10.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 5,0
- Geschlecht
- M
- Eingang
- 25.08.2023
- Impfdatum
- 07.01.2023
- Beginn
- 07.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 2,0
- Geschlecht
- M
- Eingang
- 25.08.2023
- Impfdatum
- 18.03.2023
- Beginn
- 18.03.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 0,8
- Geschlecht
- M
- Eingang
- 25.08.2023
- Impfdatum
- 28.01.2023
- Beginn
- 28.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 0,8
- Geschlecht
- M
- Eingang
- 25.08.2023
- Impfdatum
- 07.01.2023
- Beginn
- 07.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 25.08.2023
- Impfdatum
- 17.12.2022
- Beginn
- 17.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 0,7
- Geschlecht
- F
- Eingang
- 25.08.2023
- Impfdatum
- 14.01.2023
- Beginn
- 14.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 0,5
- Geschlecht
- F
- Eingang
- 25.08.2023
- Impfdatum
- 10.12.2022
- Beginn
- 10.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 25.08.2023
- Impfdatum
- 28.01.2023
- Beginn
- 28.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 25.08.2023
- Impfdatum
- 07.01.2023
- Beginn
- 07.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 25.08.2023
- Impfdatum
- 07.01.2023
- Beginn
- 07.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 0,7
- Geschlecht
- F
- Eingang
- 25.08.2023
- Impfdatum
- 21.01.2023
- Beginn
- 21.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 0,6
- Geschlecht
- M
- Eingang
- 25.08.2023
- Impfdatum
- 18.03.2023
- Beginn
- 18.03.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 0,5
- Geschlecht
- M
- Eingang
- 25.08.2023
- Impfdatum
- 25.02.2023
- Beginn
- 25.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 1,3
- Geschlecht
- F
- Eingang
- 25.08.2023
- Impfdatum
- 18.03.2023
- Beginn
- 18.03.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 25.08.2023
- Impfdatum
- 21.01.2023
- Beginn
- 21.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 25.08.2023
- Impfdatum
- 17.12.2022
- Beginn
- 17.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 0,6
- Geschlecht
- F
- Eingang
- 23.08.2023
- Impfdatum
- 18.03.2023
- Beginn
- 18.03.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 0,5
- Geschlecht
- F
- Eingang
- 23.08.2023
- Impfdatum
- 18.02.2023
- Beginn
- 18.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 23.08.2023
- Impfdatum
- 18.02.2023
- Beginn
- 18.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 23.08.2023
- Impfdatum
- 21.01.2023
- Beginn
- 21.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 0,8
- Geschlecht
- M
- Eingang
- 23.08.2023
- Impfdatum
- 04.02.2023
- Beginn
- 04.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 0,7
- Geschlecht
- F
- Eingang
- 23.08.2023
- Impfdatum
- 10.12.2022
- Beginn
- 10.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 0,7
- Geschlecht
- M
- Eingang
- 23.08.2023
- Impfdatum
- 10.12.2022
- Beginn
- 10.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 23.08.2023
- Impfdatum
- 18.03.2023
- Beginn
- 18.03.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 23.08.2023
- Impfdatum
- 21.01.2023
- Beginn
- 21.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 23.08.2023
- Impfdatum
- 21.01.2023
- Beginn
- 21.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 22.08.2023
- Impfdatum
- 01.04.2023
- Beginn
- 01.04.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 1,0
- Geschlecht
- F
- Eingang
- 22.08.2023
- Impfdatum
- 01.04.2023
- Beginn
- 01.04.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 22.08.2023
- Impfdatum
- 01.04.2023
- Beginn
- 01.04.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 22.08.2023
- Impfdatum
- 18.02.2023
- Beginn
- 18.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 0,8
- Geschlecht
- M
- Eingang
- 22.08.2023
- Impfdatum
- 01.04.2023
- Beginn
- 01.04.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 1,4
- Geschlecht
- F
- Eingang
- 22.08.2023
- Impfdatum
- 01.04.2023
- Beginn
- 01.04.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 22.08.2023
- Impfdatum
- 18.03.2023
- Beginn
- 18.03.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 0,6
- Geschlecht
- M
- Eingang
- 22.08.2023
- Impfdatum
- 28.12.2022
- Beginn
- 28.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 0,7
- Geschlecht
- M
- Eingang
- 22.08.2023
- Impfdatum
- 21.01.2023
- Beginn
- 21.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 22.08.2023
- Impfdatum
- 04.03.2023
- Beginn
- 04.03.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 22.08.2023
- Impfdatum
- 04.02.2023
- Beginn
- 04.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 1,4
- Geschlecht
- M
- Eingang
- 22.08.2023
- Impfdatum
- 04.03.2023
- Beginn
- 04.03.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 1,3
- Geschlecht
- M
- Eingang
- 22.08.2023
- Impfdatum
- 04.02.2023
- Beginn
- 04.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 22.08.2023
- Impfdatum
- 04.02.2023
- Beginn
- 04.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 22.08.2023
- Impfdatum
- 25.02.2023
- Beginn
- 25.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 2,0
- Geschlecht
- M
- Eingang
- 22.08.2023
- Impfdatum
- 10.12.2022
- Beginn
- 10.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 0,8
- Geschlecht
- F
- Eingang
- 22.08.2023
- Impfdatum
- 07.01.2023
- Beginn
- 07.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 2,0
- Geschlecht
- M
- Eingang
- 22.08.2023
- Impfdatum
- 21.01.2023
- Beginn
- 21.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 0,8
- Geschlecht
- F
- Eingang
- 21.08.2023
- Impfdatum
- 10.12.2022
- Beginn
- 10.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 0,5
- Geschlecht
- M
- Eingang
- 21.08.2023
- Impfdatum
- 18.03.2023
- Beginn
- 18.03.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 21.08.2023
- Impfdatum
- 28.12.2022
- Beginn
- 24.05.2023
- Tage bis Beginn
- 147,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 21.08.2023
- Impfdatum
- 10.12.2022
- Beginn
- 24.05.2023
- Tage bis Beginn
- 165,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 21.08.2023
- Impfdatum
- 07.01.2023
- Beginn
- 24.05.2023
- Tage bis Beginn
- 137,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 21.08.2023
- Impfdatum
- 10.12.2022
- Beginn
- 24.05.2023
- Tage bis Beginn
- 165,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 21.08.2023
- Impfdatum
- 07.01.2023
- Beginn
- 24.05.2023
- Tage bis Beginn
- 137,0
- Dosis
- 2
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 21.08.2023
- Impfdatum
- 07.01.2023
- Beginn
- 24.05.2023
- Tage bis Beginn
- 137,0
- Dosis
- 2
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 2,5
- Geschlecht
- M
- Eingang
- 08.08.2023
- Impfdatum
- 27.10.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Patient received COVID short after beyond use date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- NKA/NKDA
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 1,0
- Geschlecht
- F
- Eingang
- 08.08.2023
- Impfdatum
- 28.10.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Patient received COVID shot after beyond use date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 1,3
- Geschlecht
- M
- Eingang
- 08.08.2023
- Impfdatum
- 28.10.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Patient received COVID shot after beyond use date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- NKA/NKDA
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 07.08.2023
- Impfdatum
- 15.12.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Patient received covid shot after before use date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- multi vitamin
- Allergien
- NKA/NKDA
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 1,0
- Geschlecht
- M
- Eingang
- 07.08.2023
- Impfdatum
- 15.12.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Patient received covid shot after beyond use date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- NKA/NKDA
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 2,0
- Geschlecht
- M
- Eingang
- 07.08.2023
- Impfdatum
- 15.12.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Patient received covid shot after beyond use date
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- NKA/NKDA
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 1,5
- Geschlecht
- F
- Eingang
- 07.08.2023
- Impfdatum
- 15.12.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Patient Received covid shot after beyond use date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- NKA/NKDA
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 1,3
- Geschlecht
- F
- Eingang
- 07.08.2023
- Impfdatum
- 15.12.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Patient received covid shot after beyond use date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- NKA/NKDA
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 1,0
- Geschlecht
- F
- Eingang
- 01.08.2023
- Impfdatum
- 24.04.2023
- Beginn
- 24.04.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Symptomtext
CALLED PFIZER. THERE WERE NO SIDE EFFECTS NOTED BY PATIENT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 1,0
- Geschlecht
- F
- Eingang
- 01.08.2023
- Impfdatum
- 03.04.2023
- Beginn
- 03.04.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Symptomtext
WE CALLED PFIZER. THERE WERE NO SIDE EFFECTS BROUGHT TO ATTENTION BY PATIENT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 1,6
- Geschlecht
- F
- Eingang
- 01.08.2023
- Impfdatum
- 22.03.2023
- Beginn
- 22.03.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Symptomtext
WE CONTACTED PFIZER. THERE WERE NO SIGN AND SYMPTOMS BROUGHT TO OUR ATTENTION BY PATIENT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- FLOVENT
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 31.07.2023
- Impfdatum
- 25.11.2022
- Beginn
- 25.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
SHOT WAS GIVEN 2 DAYS AFTER THE BEYOND USE DATE. THE DEYOND USE DATE W 11/22/2022. WE HAVE CONTACTED PFIZER.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 27.07.2023
- Impfdatum
- 07.12.2022
- Beginn
- 01.12.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Symptomtext
No adverse reaction reported
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Heterotaxy syndrome with polysplenia, situs inversus abdominalis, immunosuppressed, severe protein-caolrie malnutrition, ventilator dependent, global developmental
- Andere Medikamente
- Medications Valid as of: July 27, 2023 - 5:03 PM Generic Name Brand Name Tablet Size Instructions for use Acetaminophen (Suspension) Acetaminophen Childrens 160 MG/5ML Take 120 mg by mouth every 6 (six) hours as needed (pain, fever). Albu
- Allergien
- Lactose, Nsaids, Soy
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 26.07.2023
- Impfdatum
- 09.09.2022
- Beginn
- 05.01.2023
- Tage bis Beginn
- 118,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Hypoxia
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypoxia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 1,1
- Geschlecht
- M
- Eingang
- 25.07.2023
- Impfdatum
- 14.09.2022
- Beginn
- 09.02.2023
- Tage bis Beginn
- 148,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Hypoxia
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypoxia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 12.07.2023
- Impfdatum
- 17.11.2022
- Beginn
- 28.04.2023
- Tage bis Beginn
- 162,0
- Dosis
- 2
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Obstructive sleep apnoea syndrome
Symptomtext
G47.33 OBSTRUCTIVE SLEEP APNEA 4/28/2023 OBSTRUCTIVE SLEEP APNEA
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Obstructive sleep apnoea syndrome
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 11.07.2023
- Impfdatum
- 24.03.2023
- Beginn
- 24.03.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Otitis media
Upper respiratory tract infection
Symptomtext
Otitis Media; acute upper respiratory infection; This is a spontaneous report received from contactable reporter(s) (Other HCP). A 3-year-old male patient received BNT162b2 (BNT162B2), on 24Mar2023 as dose 2 (maroon cap), single (Lot number: FT9142) at the age of 3 years intramuscular, in left thigh for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: BNT162b2 (DOSE 1 (MAROON CAP),SINGLE, Anatomical site of injection: Left thigh, Route of administration: Intramuscular, Batch/Lot number: FX5095), administration date: 24Feb2023, when the patient was 3-year-old, for COVID-19 immunization, reaction(s): "they gave to patients that were used beyond use date/ patient received FX5095 BUD for first vaccine", "they gave to patients that were used beyond use date/ patient received FX5095 BUD for first vaccine"; flu vaccine (DOSE 1, SINGLE, Manufacturer: Sanofi, Batch/Lot#: UT7723MA, Route: Intramuscular, Anatomical site of injection: Left thigh, No. of previous doses: 0), administration date: 24Feb2023, when the patient was 3-year-old. The following information was reported: OTITIS MEDIA (non-serious) with onset 24Mar2023, outcome "unknown"; UPPER RESPIRATORY TRACT INFECTION (non-serious) with onset 24Mar2023, outcome "unknown", described as "acute upper respiratory infection". Additional information: No specific relevant test for thromboembolic events with thrombocytopenia was done and the patient did not provide information regarding the reported adverse event(s) with the use of the product.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300152548 Same reporter, patient, product, different dose and events;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Otitis media
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 2,0
- Geschlecht
- M
- Eingang
- 05.07.2023
- Impfdatum
- 25.11.2022
- Beginn
- 13.02.2023
- Tage bis Beginn
- 80,0
- Dosis
- 2
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Breathing-related sleep disorder
Obstructive sleep apnoea syndrome
Symptomtext
BREATHING RELATED SLEEP DISORDER OBSTRUCTIVE SLEEP APNEA
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Breathing-related sleep disorder
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 0,6
- Geschlecht
- F
- Eingang
- 27.06.2023
- Impfdatum
- 11.11.2022
- Beginn
- 28.12.2022
- Tage bis Beginn
- 47,0
- Dosis
- 2
- Route/Site
- OT / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dermatitis atopic
Symptomtext
Atopic dermatitis; The initial case was missing the following minimum criteria: specific number of patients. Upon receipt of follow-up information on 11Apr2023, this case now contains all required information to be considered valid. This is a spontaneous report received from contactable reporter(s) (Other HCP) from medical information team. A 7-month-old female patient received BNT162b2 (BNT162B2), on 11Nov2022 as dose 2 (maroon cap), single (Lot number: FT9142, Expiration Date: 28Dec2022) at the age of 7 months intramuscular, in left thigh for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: BNT162b2 (DOSE 1 (MAROON CAP), SINGLE, Date: 21Oct2022, Anatomical site of injection: Left thigh, Route of administration: Intramuscular, Batch/Lot number: FT9142, Expiration Date: 28Dec2022), administration date: 21Oct2022, when the patient was 6-month-old, for COVID-19 immunization. The following information was reported: DERMATITIS ATOPIC (non-serious) with onset 28Dec2022, outcome "unknown", described as "Atopic dermatitis". Additional information: The reporter stated that there was an audit and they found that there were doses that they gave to patients that were used beyond its use date. Reporter verified that one lot of FT9142 was administered for two batches of that same lot number as provided by transferring agent. Two patients received two of the vaccines Beyond use date. Both patients received FX5095 BUD for their first vaccine and BUD with lot FT9142 for their second vaccine. The reporter confirmed that vials were unpunctured prior to the administration of the vaccines. The caller stated she called before regarding 49 doses of the Pfizer Covid-19 vaccine that were given patients past the beyond-use-date. It was 49 doses but 47 patients, because two patients received 2 doses with the products that were past the beyond use-date. She stated they received 3 packets that require to be filled out but it looks like it is one packet per patient. She wanted to know if she should copy these forms for all 47 patients or if they only needed information on 3 patients. Upon Follow-up on 03May2023, Reporter stated, "I have a caller on the line, she is calling about the Pfizer COVID Vaccine all formulations, she has called before because 47 patients were given the vaccines after the beyond use date and they received a packet from drug safety but only received 3 packet and she have some questions about how to fill that out if she has so many patients only got 3 packet." When paraphrased the concern: And she has 47 patients but they were only given 3 packets of 47 patients. She did say it was 49 doses because 2 of the patients received 2 doses but she is not calling to report. Reporter stated, "I have the LOT numbers of the beyond use day and the dates they were given I don't have much information on hand right now. I already had called regarding these. I have FT9142 and it was 5 patients and then it is GK1657 9 patients. The paper work that I received do I also need to provide their names and birth dates on there too. My question is because of the packets that I received if I have to submit their information on mail do I have to give it to you by phone right now because it is 47 patients. I just wanted to see if on the paper work I have to submit their information. Reporter was informed to write all patient details and sent it back to Pfizer. Upon follow up on 23May2023, it was reported that 5 Patients received Lot FT9142, none received FX5095 as the 1st dose. Upon follow-up on 22Jun203, third Covid vaccine (Dose 3, Date: 06Jan2023, Anatomical site of injection: Left thigh, Route of administration: Intramuscular, Batch/Lot number: FT9142) was given after the beyond use date. Specific relevant test for thromboembolic events with thrombocytopenia was reported as none. Follow-up (03May2023): This is a spontaneous follow-up report received from the same contactable Other HCP. This Other HCP reported for a patient that: Updated information included: Additional information. Follow-up (23May2023): This is a spontaneous follow-up report from the same contactable Other HCP. Updated information Included: Historical vaccine lot number and Expiration Date, Suspect vaccine Expiration Date, Vaccine facility information and additional Information. Follow-up (21Jun2023): Follow-up attempts are completed. No further information is expected. Follow-up (22Jun2023): This is a spontaneous follow-up report from the same contactable Other HCP. This Other HCP reported in response to HCP letter sent included that: Updated information Included: reporter information, patient information, historical vaccine added, vaccine information, anatomical location. New event Atopic dermatitis was captured. Event onset date added. The events poor quality vaccine administered, and product administration error were deleted.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300150037 same reporter and event, different patient and drug formulation;US-PFIZER INC-202300151563 same reporter and event, different patient and drug formulation;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dermatitis atopic
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- U
- Eingang
- 27.06.2023
- Impfdatum
- 27.07.2022
- Beginn
- 30.03.2023
- Tage bis Beginn
- 246,0
- Dosis
- 2
- Route/Site
- OT / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
SARS-CoV-2 test
Umbilical hernia
Symptomtext
umbilical hernia; This is a spontaneous report received from a contactable reporter(s) (Other HCP). A child patient received BNT162b2 (BNT162B2), on 27Jul2022 at 17:11 as dose 2 (maroon cap), single (Lot number: FT9142) intramuscular, in left thigh for covid-19 immunisation. The patient's relevant medical history included: "Hx of SARS-CoV2", start date: 18May2022 (unspecified if ongoing); "Constipation", start date: 12May2022 (unspecified if ongoing), notes: Pertinent details: Referred to GI. Concomitant medication(s) included: DTAP intramuscular taken for immunisation, on 30Mar2023 as dose 4, single; INFLUENZA intramuscular taken for immunisation, on 30Mar2023 as dose 2, single. Vaccination history included: BNT162b2 (Dose 1, Single, Time: 17:06, Anatomical site of injection: Right Thigh, Route of administration: Intramuscular, Batch/Lot number: FT9142), administration date: 06Jul2022, for COVID-19 Immunization; Dtap (Manufacturer: Sanofi; No. of previous doses: 3), for Immunization; Influenza (Manufacturer: Sanofi; No. of previous doses: 1), for Immunization. The following information was reported: UMBILICAL HERNIA (non-serious) with onset 30Mar2023, outcome "not recovered". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: Specific Relevant Test for thromboembolic events with thrombocytopenia were none.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- SARS-CoV-2 test
- Hospital-Tage
- -
- Labordaten
- Test Date: 202205; Test Name: Covid test; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Constipation (Pertinent details: Referred to GI); COVID-19
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 15.06.2023
- Impfdatum
- 18.04.2023
- Beginn
- 13.06.2023
- Tage bis Beginn
- 56,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
Bivalent Covid vaccine administered to patient 8 weeks after 'beyond use date' and therefor dose is not valid. Patient did not have any adverse reactions after vaccine administration.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- speech delay, slow weigh gain
- Andere Medikamente
- n/a
- Allergien
- amoxicillin
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 08.06.2023
- Impfdatum
- 24.05.2023
- Beginn
- 24.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Discontinued product administered
Symptomtext
MONOVALENT ADMINISTERED AS PRIMARY AND SECONDARY DOSES
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Discontinued product administered
- Hospital-Tage
- -
- Labordaten
- NO
- Aktuelle Erkrankungen
- NO
- Vorgeschichte
- NO
- Andere Medikamente
- NO
- Allergien
- NO
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 2,0
- Geschlecht
- M
- Eingang
- 08.06.2023
- Impfdatum
- 17.05.2023
- Beginn
- 17.05.2023
- 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
MONOVALENT ADMINISTERED AS PRIMARY AND SECONDARY DOSE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- NO
- Aktuelle Erkrankungen
- NO
- Vorgeschichte
- , SCIMITAR, VACTERL, colonostomy and g-tube dependent Hx of prematurity, imperforate anus, Scimitar Syndrome, atrial septal defect, patent ductus arteriosus, sequestration of right lower lung, right pulmonary artery hypoplasia, partial anomalous pulmonary venous return of right lower pulmonary vein, and large aortopulmonary collateral arising from abdominal aorta to sequestered right lung.
- Andere Medikamente
- -
- Allergien
- NO
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 1,2
- Geschlecht
- M
- Eingang
- 08.06.2023
- Impfdatum
- 03.05.2023
- Beginn
- 03.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Discontinued product administered
Symptomtext
MONOVALENT ADMINISTERED AS SECOND DOSE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Discontinued product administered
- Hospital-Tage
- -
- Labordaten
- NO
- Aktuelle Erkrankungen
- NO
- Vorgeschichte
- NO
- Andere Medikamente
- NO
- Allergien
- NO
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 08.06.2023
- Impfdatum
- 19.04.2023
- Beginn
- 19.04.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Discontinued product administered
Symptomtext
MONOVALENT ADMINISTERED AS SECOND DOSE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Discontinued product administered
- Hospital-Tage
- -
- Labordaten
- NO
- Aktuelle Erkrankungen
- NO
- Vorgeschichte
- NO
- Andere Medikamente
- NONE
- Allergien
- NO
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 08.06.2023
- Impfdatum
- 05.04.2023
- Beginn
- 05.04.2023
- 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
monovalent administered as second dose
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- no
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NO
- Andere Medikamente
- NONE
- Allergien
- NO
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 1,8
- Geschlecht
- F
- Eingang
- 08.06.2023
- Impfdatum
- 17.05.2023
- Beginn
- 17.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Discontinued product administered
Symptomtext
MONOVALENT ADMINISTERED AS THIRD DOSE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Discontinued product administered
- Hospital-Tage
- -
- Labordaten
- NOOOONE
- Aktuelle Erkrankungen
- NO
- Vorgeschichte
- NO
- Andere Medikamente
- NONE
- Allergien
- NO
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 08.06.2023
- Impfdatum
- 17.05.2023
- Beginn
- 17.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Discontinued product administered
Symptomtext
MONOVALENT ADMINISTERED AS THIRD DOSE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Discontinued product administered
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NO
- Vorgeschichte
- NO
- Andere Medikamente
- NO
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 1,4
- Geschlecht
- F
- Eingang
- 08.06.2023
- Impfdatum
- 17.05.2023
- Beginn
- 17.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Discontinued product administered
Symptomtext
monovalent administered as 1st dose
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Discontinued product administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- NO
- Vorgeschichte
- NO
- Andere Medikamente
- NONE
- Allergien
- NO
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 1,9
- Geschlecht
- M
- Eingang
- 08.06.2023
- Impfdatum
- 05.04.2023
- Beginn
- 05.04.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
administered monovalent as third dose
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- NO
- Vorgeschichte
- NO
- Andere Medikamente
- NONE
- Allergien
- NO
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 08.06.2023
- Impfdatum
- 03.05.2023
- Beginn
- 03.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Discontinued product administered
Symptomtext
ADMINISTERED MONOVALENT AS SECOND DOSE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Discontinued product administered
- Hospital-Tage
- -
- Labordaten
- NO
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 06.06.2023
- Impfdatum
- 28.04.2023
- Beginn
- 28.04.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Discontinued product administered
No adverse event
Symptomtext
Patient was administered dose of the monovalent COVID-19 vaccine after they were no longer authorized. Patient's parents were notified and reported patient did not have any symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Discontinued product administered
- Hospital-Tage
- -
- Labordaten
- No medical test or labs were done.
- Aktuelle Erkrankungen
- No other illnesses
- Vorgeschichte
- No chronic or long-standing health conditions
- Andere Medikamente
- No prescriptions
- Allergien
- No allergies
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 01.06.2023
- Impfdatum
- 27.12.2022
- Beginn
- 27.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Symptomtext
No adverse effects but patient was given the correct age dose 6mo-4yrs on 12/27/22 when he was 4 years old but he was given the 5yr-11yrs dose on 1/18/23 (he turned 5 yrs old on 12/31/22).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 01.06.2023
- Impfdatum
- 15.10.2022
- Beginn
- 01.10.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Symptomtext
No adverse effects but patient given the 6month-4yr vaccine when she was 4 years 11 months old on 10/15/22 and when she turned 5 years old she was given the 5ys-11ys vaccine on 12/14/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Hx of pertussis/ Right congenital dacryostenosis
- Andere Medikamente
- none
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 0,6
- Geschlecht
- M
- Eingang
- 26.05.2023
- Impfdatum
- 20.01.2023
- Beginn
- 20.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anaemia
Constipation
Expired product administered
Gastrooesophageal reflux disease
Poor quality product administered
Product administration error
Symptomtext
anemia; constipation; They gave to patients that were used beyond use date; They gave to patients that were used beyond use date; Dose administration date: 20Jan2023/Expiration date: 28Dec2022; suspect gastro-esophageal reflux disease; The initial case was missing the following minimum criteria: unspecified number of patients. Upon receipt of follow-up information on 11Apr2023, this case now contains all required information to be considered valid. This is a spontaneous report received from a contactable reporter(s) (Other HCP) from medical information team. A 7-month-old male patient received BNT162b2 (BNT162B2), on 20Jan2023 at 09:34 as dose 2 (maroon cap), single (Lot number: FT9142, Expiration Date: 28Dec2022) at the age of 7 months intramuscular, in left thigh for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: BNT162b2 (Dose 1st, Time: 09:59, Anatomical site of injection: Left thigh, Route of administration: Intramuscular, Batch/Lot number: FT9142), administration date: 21Dec2022, when the patient was 6-month-old, for COVID-19 immunization; fluzone quadrivalent (Manufacturer: Sanofi, Batch/Lot# UT7695JA, Route: IM, Anatomical Site of Injection: Left thigh, No. of Previous Doses: 1), administration date: 21Dec2022, when the patient was 6-month-old, for Immunization. The following information was reported: GASTROOESOPHAGEAL REFLUX DISEASE (non-serious) with onset 20Jan2023, outcome "recovered" (21Mar2023), described as "suspect gastro-esophageal reflux disease"; EXPIRED PRODUCT ADMINISTERED (non-serious) with onset 20Jan2023 at 09:34, outcome "unknown", described as "Dose administration date: 20Jan2023/Expiration date: 28Dec2022"; POOR QUALITY PRODUCT ADMINISTERED (non-serious), PRODUCT ADMINISTRATION ERROR (non-serious) all with onset 20Jan2023 at 09:34, outcome "unknown" and all described as "They gave to patients that were used beyond use date"; ANAEMIA (non-serious) with onset 21Mar2023, outcome "not recovered", described as "anemia"; CONSTIPATION (non-serious) with onset 21Mar2023, outcome "not recovered". Additional information: Reporter confirmed that vials were unpunctured prior to the administration of the vaccines. 5 Patients received Lot# FT9142, none received FX5095 as the 1st dose. Covid-19 monovalent vaccine dose#02 given beyond use date. Follow-up (09May2023): Follow-up attempts are completed. No further information is expected. Follow-up (23May2023): This is a spontaneous follow-up report from the same contactable Other HCP. This Other HCP reported for a 07 Moths old male patient in response to HCP letter sent which included that: Updated Information Included: Patient Information (Initials. DOB. Age. Height. Weight), Historical vaccine, Vaccine information [Dose administration date/time. Route of administration. Expiration date. Drug taken beyond expiry date. Anatomical location], Vaccine Facility Information, Event onset date, New AEs (Expired vaccine used, Gastrooesophageal reflux disease, Anemia and Constipation) added and narrative updated.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300151563 same reporter/drug/event, different patient;US-PFIZER INC-202300151563 same reporter/drug/event, different patient;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anaemia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 1,6
- Geschlecht
- M
- Eingang
- 26.05.2023
- Impfdatum
- 23.05.2023
- Beginn
- 23.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Discontinued product administered
No adverse event
Symptomtext
NO ADVERSE EVENTS FOR PATIENT. MEDICAL ASSISTANT ACCIDENTALLY ADMINISTERED MONOVALENT PFIZER COVID 6 MONTHS - 4 YEARS DOSE INSTEAD OF BIVALENT PFIZER DOSE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Discontinued product administered
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 23.05.2023
- Impfdatum
- 31.08.2022
- Beginn
- 20.10.2022
- Tage bis Beginn
- 50,0
- Dosis
- 2
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Hypoxia
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypoxia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 0,7
- Geschlecht
- F
- Eingang
- 19.05.2023
- Impfdatum
- 20.04.2023
- Beginn
- 20.04.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Discontinued product administered
Symptomtext
Second dose of Monovalent Covid Vaccine was administered on 4/20 after the deauthorization was made.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Discontinued product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 8,0
- Geschlecht
- F
- Eingang
- 11.05.2023
- Impfdatum
- 05.07.2022
- Beginn
- 05.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Wrong product administered
Symptomtext
patient came to office for booster dose of Pfizer Covid-19 vaccine. Instead of getting .2ml of Pfizer Covid-19 5-11 dose she received .2ml of Pfizer Covid19 6m-4yr. Mother notified immed
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 5,0
- Geschlecht
- F
- Eingang
- 11.05.2023
- Impfdatum
- 09.08.2022
- Beginn
- 09.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Underdose
Symptomtext
N/A, Client receive Pfizer dose 6m-4y instead of 5m-11y
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 09.05.2023
- Impfdatum
- 08.03.2023
- Beginn
- 08.03.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
vaccine storage in inappropriate temperature range
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 09.05.2023
- Impfdatum
- 06.02.2023
- Beginn
- 09.03.2023
- Tage bis Beginn
- 31,0
- Dosis
- 3
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
vaccine storage in inappropriate temperature range
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 1,5
- Geschlecht
- M
- Eingang
- 09.05.2023
- Impfdatum
- 27.01.2023
- Beginn
- 09.03.2023
- Tage bis Beginn
- 41,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
vaccine storage in inappropriate temperature range
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 2,0
- Geschlecht
- M
- Eingang
- 09.05.2023
- Impfdatum
- 18.01.2023
- Beginn
- 09.03.2023
- Tage bis Beginn
- 50,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
vaccine stored out of recommended temperature range
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 04.05.2023
- Impfdatum
- 24.02.2023
- Beginn
- 24.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
No reaction. This vaccine was given after the beyond use by date. It was in the refrigerator past the 10 weeks recommended storage time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 0,5
- Geschlecht
- F
- Eingang
- 04.05.2023
- Impfdatum
- 08.03.2023
- Beginn
- 08.03.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
This patient was given a pfizer covid vaccine after the beyond use by date. No reaction.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N//A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 0,5
- Geschlecht
- F
- Eingang
- 04.05.2023
- Impfdatum
- 15.02.2023
- Beginn
- 15.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
None. The pfizer covid 19 was administered after the beyond use by date after being in the refrigerator for more than 10 weeks.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 1,3
- Geschlecht
- M
- Eingang
- 04.05.2023
- Impfdatum
- 24.02.2023
- Beginn
- 24.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product storage error
Symptomtext
This vaccine was administered after the beyond use date of 10 weeks in the refrigerator. There were no reactions to the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 1,0
- Geschlecht
- F
- Eingang
- 04.05.2023
- Impfdatum
- 18.04.2023
- Beginn
- 24.04.2023
- Tage bis Beginn
- 6,0
- Dosis
- 2
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Discontinued product administered
No adverse event
Symptomtext
Discontinued pfizer monovalent 6mo-4yr , No adverse reaction reported by parent.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Discontinued product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 1,0
- Geschlecht
- M
- Eingang
- 04.05.2023
- Impfdatum
- 24.04.2023
- Beginn
- 24.04.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Discontinued product administered
No adverse event
Symptomtext
Discontinued Pfizer Monovalent 6mo-4yr, No Adverse reactions reported by parent.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Discontinued product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 0,8
- Geschlecht
- F
- Eingang
- 26.04.2023
- Impfdatum
- 29.12.2022
- Beginn
- 29.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 0,7
- Geschlecht
- F
- Eingang
- 26.04.2023
- Impfdatum
- 18.11.2022
- Beginn
- 18.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 2,0
- Geschlecht
- M
- Eingang
- 26.04.2023
- Impfdatum
- 24.06.2022
- Beginn
- 24.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 0,6
- Geschlecht
- F
- Eingang
- 26.04.2023
- Impfdatum
- 27.06.2022
- Beginn
- 27.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 1,0
- Geschlecht
- F
- Eingang
- 26.04.2023
- Impfdatum
- 05.07.2022
- Beginn
- 05.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 2,0
- Geschlecht
- M
- Eingang
- 26.04.2023
- Impfdatum
- 22.07.2022
- Beginn
- 22.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 2,0
- Geschlecht
- M
- Eingang
- 26.04.2023
- Impfdatum
- 01.07.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 26.04.2023
- Impfdatum
- 02.08.2022
- Beginn
- 02.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 2,0
- Geschlecht
- M
- Eingang
- 26.04.2023
- Impfdatum
- 19.08.2022
- Beginn
- 19.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 26.04.2023
- Impfdatum
- 14.10.2022
- Beginn
- 14.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 26.04.2023
- Impfdatum
- 11.07.2022
- Beginn
- 11.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 26.04.2023
- Impfdatum
- 14.10.2022
- Beginn
- 14.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 26.04.2023
- Impfdatum
- 22.07.2022
- Beginn
- 22.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 26.04.2023
- Impfdatum
- 30.06.2022
- Beginn
- 30.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 1,9
- Geschlecht
- M
- Eingang
- 26.04.2023
- Impfdatum
- 20.10.2022
- Beginn
- 20.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 1,7
- Geschlecht
- M
- Eingang
- 26.04.2023
- Impfdatum
- 20.07.2022
- Beginn
- 20.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 1,2
- Geschlecht
- F
- Eingang
- 26.04.2023
- Impfdatum
- 18.11.2022
- Beginn
- 18.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 1,3
- Geschlecht
- M
- Eingang
- 26.04.2023
- Impfdatum
- 30.11.2022
- Beginn
- 30.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 1,3
- Geschlecht
- M
- Eingang
- 26.04.2023
- Impfdatum
- 28.10.2022
- Beginn
- 28.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 23.04.2023
- Impfdatum
- 28.10.2022
- Beginn
- 28.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
No adverse event Covid 19 vaccine expired 10/27/2022 Given 10/28/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 23.04.2023
- Impfdatum
- 28.10.2022
- Beginn
- 28.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
No adverse event Covid 19 vaccine expired 10/27/2022 Given 10/28/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 23.04.2023
- Impfdatum
- 01.11.2022
- Beginn
- 01.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
No adverse event Covid 19 vaccine expired 10/27/2022 Given 11-01-2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 2,0
- Geschlecht
- M
- Eingang
- 23.04.2023
- Impfdatum
- 01.11.2022
- Beginn
- 01.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
No adverse event Covid 19 vaccine expired 10/27/2022 Given 11-01-2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 23.04.2023
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
No adverse event Covid 19 vaccine expired 10/27/2022 Given 11-07-2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 0,6
- Geschlecht
- F
- Eingang
- 23.04.2023
- Impfdatum
- 10.11.2022
- Beginn
- 10.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
No adverse event Covid 19 vaccine expired 10/27/2022 Given 11-10-2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 23.04.2023
- Impfdatum
- 10.11.2022
- Beginn
- 10.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
No adverse event Covid 19 vaccine expired 10/27/2022 Given 11-10-2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 23.04.2023
- Impfdatum
- 11.11.2022
- Beginn
- 11.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
No adverse event Covid 19 vaccine expired 10/27/2022 Given 11-11-2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 23.04.2023
- Impfdatum
- 11.11.2022
- Beginn
- 11.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
No adverse event Covid 19 vaccine expired 10/27/2022 Given 11-11-2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 2,0
- Geschlecht
- M
- Eingang
- 23.04.2023
- Impfdatum
- 16.11.2022
- Beginn
- 16.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
No adverse event Covid 19 vaccine expired 10/27/2022 Given 11-16-2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 23.04.2023
- Impfdatum
- 16.11.2022
- Beginn
- 16.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
No adverse event Covid 19 vaccine expired 10/27/2022 Given 11-16-2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 23.04.2023
- Impfdatum
- 16.11.2022
- Beginn
- 16.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
no adverse event Covid 19 vaccine expired 10/27/2022 given 11/16/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 23.04.2023
- Impfdatum
- 21.11.2022
- Beginn
- 21.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 0,8
- Geschlecht
- F
- Eingang
- 23.04.2023
- Impfdatum
- 21.11.2022
- Beginn
- 21.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 0,9
- Geschlecht
- M
- Eingang
- 23.04.2023
- Impfdatum
- 02.12.2022
- Beginn
- 02.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 23.04.2023
- Impfdatum
- 02.12.2022
- Beginn
- 02.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 23.04.2023
- Impfdatum
- 03.12.2022
- Beginn
- 03.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 2,0
- Geschlecht
- M
- Eingang
- 23.04.2023
- Impfdatum
- 03.12.2022
- Beginn
- 03.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 1,2
- Geschlecht
- F
- Eingang
- 23.04.2023
- Impfdatum
- 05.12.2022
- Beginn
- 05.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 1,2
- Geschlecht
- F
- Eingang
- 23.04.2023
- Impfdatum
- 05.12.2022
- Beginn
- 05.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 1,1
- Geschlecht
- F
- Eingang
- 22.04.2023
- Impfdatum
- 08.12.2022
- Beginn
- 08.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 22.04.2023
- Impfdatum
- 09.12.2022
- Beginn
- 09.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 3,0
- Geschlecht
- F
- Eingang
- 22.04.2023
- Impfdatum
- 09.12.2022
- Beginn
- 09.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 0,6
- Geschlecht
- F
- Eingang
- 22.04.2023
- Impfdatum
- 09.12.2022
- Beginn
- 09.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 22.04.2023
- Impfdatum
- 09.12.2022
- Beginn
- 09.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- NONE.
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 21.04.2023
- Impfdatum
- 10.12.2022
- Beginn
- 10.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 0,7
- Geschlecht
- F
- Eingang
- 20.04.2023
- Impfdatum
- 12.12.2022
- Beginn
- 12.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 2,0
- Geschlecht
- F
- Eingang
- 20.04.2023
- Impfdatum
- 12.12.2022
- Beginn
- 12.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 2,0
- Geschlecht
- M
- Eingang
- 20.04.2023
- Impfdatum
- 12.12.2022
- Beginn
- 12.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SC / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect route of product administration
No adverse event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect route of product administration
- Hospital-Tage
- -
- Labordaten
- NKA ITEM20: Patient did not suffer any adverse event.
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 2,0
- Geschlecht
- M
- Eingang
- 18.04.2023
- Impfdatum
- 18.04.2023
- Beginn
- 18.04.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Product preparation issue
Symptomtext
Vaccine administered without the diluent.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 2,0
- Geschlecht
- M
- Eingang
- 17.04.2023
- Impfdatum
- 26.09.2022
- Beginn
- 26.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine was administered post use date. Patient's provider Dr. contacted parents or guardian on 02/22/23 stating manufacturer's vaccine activity at the time of administration. Manufacturer's Statement: Pfizer reviewed the stability of the vaccine you received and determined that it likely did not maintain the activity necessary to protect against COVID-19 at time of administration. Pfizer cannot guarantee the protection you may have received is equivalent to what was seen in studies and data is not available to support administering an additional dose of vaccine to you. However, if you wish to undergo revaccination, we will provide you access as outlined below.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 17.04.2023
- Impfdatum
- 03.09.2022
- Beginn
- 03.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine was administered post use date. Patient's provider Dr. contacted parents or guardian on 02/20/23 stating manufacturer's vaccine activity at the time of administration. Manufacturer Statement: Pfizer reviewed the stability of the vaccine you received and determined that it maintained the activity necessary to protect against COVID-19 at time of administration. Pfizer cannot guarantee the protection you have received is equivalent to what was seen in studies and data is not available to support administering an additional dose of vaccine to you. However, if you wish to undergo revaccination, we will provide you access as outlined below.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 5,0
- Geschlecht
- F
- Eingang
- 12.04.2023
- Impfdatum
- 11.04.2023
- Beginn
- 11.04.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Underdose
Symptomtext
Pt was inadvertently given pfizer covid monovalent for 6m-4year. Patient parent was notified.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 11.04.2023
- Impfdatum
- 10.04.2023
- Beginn
- 10.04.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
No adverse event
Symptomtext
Pt came in for third dose of Toddler series. Updated guidelines states that pt should have received Bivalent dose. Mom states no adverse reaction from vaccine. Notified parents to return in >8 weeks for bivalent vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 5,0
- Geschlecht
- F
- Eingang
- 04.04.2023
- Impfdatum
- 21.11.2022
- Beginn
- 21.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Underdose
Symptomtext
Pt turned age 5; Pt received Pfizer dose 3 monovalent 6 mo-4 y vaccine on 11/21/22. No adverse reactions.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Not known
- Vorgeschichte
- No
- Andere Medikamente
- Not known
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 0,8
- Geschlecht
- M
- Eingang
- 04.04.2023
- Impfdatum
- 21.02.2023
- Beginn
- 21.02.2023
- 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 administered at inappropriate site
Symptomtext
Patient was here for covid vaccine and inadvertently given IM injection in the arm instead of the thigh. Parent notified and was not upset and stated that the child had no adverse reaction to the vaccine. Nurse Immunization Coordinator notified.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- na
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- -
- Geschlecht
- M
- Eingang
- 04.04.2023
- Impfdatum
- 01.12.2022
- Beginn
- 01.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
After administration of COVID vaccine, it was discovered that the vaccine had expired.; This case was retrieve during the Vaccines Adverse Event Reporting System (VAERS) monitoring on 12-JAN-2023 with the following VAERS Primary ID 2526877-1. The original narrative from the sender is the following: After administration of COVID vaccine, it was discovered that the vaccine had expired. Vaccine diluted 11/30/22 at 11:35AM, expired 11/30/22 at 11:35PM. Vaccine administered 12/1/22 at 8:50PM, approximately 9 hours and 20 min after expiration. Pfizer contacted for stability report. No further information available. Pfizer recommending communicating with their supply chain department as they may have further stability report. Dr. called and informed mom of event. Pt doing well, no adverse symptoms. Received word from supply chain department that they do not have stability reports to support effectiveness of vaccine. Called and spoke with mom. Pt is doing well and does not appear to have any adverse symptoms from vaccine. The reporter did not provide an assessment of causal relationship between Vaxelis and the reported event "After administration of COVID vaccine, it was discovered that the vaccine had expired". No further information is expected
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Prophylaxis
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- -
- Geschlecht
- M
- Eingang
- 04.04.2023
- Impfdatum
- 01.12.2022
- Beginn
- 01.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
After administration of COVID vaccine, it was discovered that the vaccine had expired.; This case was retrieve during the Vaccines Adverse Event Reporting System (VAERS) monitoring on 12-JAN-2023 with the following VAERS Primary ID 2526877-1. The original narrative from the sender is the following: After administration of COVID vaccine, it was discovered that the vaccine had expired. Vaccine diluted 11/30/22 at 11:35AM, expired 11/30/22 at 11:35PM. Vaccine administered 12/1/22 at 8:50PM, approximately 9 hours and 20 min after expiration. Pfizer contacted for stability report. No further information available. Pfizer recommending communicating with their supply chain department as they may have further stability report. Dr. called and informed mom of event. Pt doing well, no adverse symptoms. Received word from supply chain department that they do not have stability reports to support effectiveness of vaccine. Called and spoke with mom. Pt is doing well and does not appear to have any adverse symptoms from vaccine. The reporter did not provide an assessment of causal relationship between Vaxelis and the reported event "After administration of COVID vaccine, it was discovered that the vaccine had expired". No further information is expected
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Prophylaxis
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 2,0
- Geschlecht
- M
- Eingang
- 03.04.2023
- Impfdatum
- 22.08.2022
- Beginn
- 22.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
COVID-19 Pfizer LOT #FT9142 kept in fridge BUD. Received 7/26/22 and administered 11/30/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -