- Staat
- NJ
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 28.02.2023
- Impfdatum
- 21.02.2023
- Beginn
- 21.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Cardiac function test normal
Cold sweat
Disorientation
Dizziness
Fall
Pain in extremity
Pallor
Petit mal epilepsy
Seizure
Swelling of eyelid
Syncope
Tremor
Symptomtext
AFTER VACCINES ADMINSTRATION TEEN TOOK A FEW STEPS AND REPORTED FEELING DIZZY. I TRIED GUIDING HIM TO FLOOR, BUT COLLAPSED HE FELT COLD , PALE, AND CLAMMY. HE CONTINUE FALLING ON TO MY LEFT. ON THE FLOOR FACE DOWN CHILD HAS 3-4 SECOND PETITE MAL SEIZURE. HE WAS DISORIENTED & DID NOT KNOW DATE AND YEAR., BUT KNEW HIS AND MOTHER'S NAME. EMS WAS CALLED AT 1:21PM VITASL WERE CHECKED AT 1:21PM PULSE 83, OX99%,BP 112/75 RA. PT SAT UP ON FLOOR AND CONTINUO HAVING MILD TREMORS IN EXTREMITIES. AFTER SEIZURE MOM REPORTED A SYNCOPE EPIZODE 2 MOTHS PRIOR TO VACCINE, CHILD DISPUTED MOM'S CLAIMS AND SAID IT WAS DIZZINESS. CHILD WAS TAKEN BY ABULANCE TO HOSPITAL AT 1:50PM. PT REPORTED REMEMBERING THE WHOLE EPISODE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- ON 2/28/23 MOTHER REPORTED, TEEN HEART WAS CHECKED AND WERE TOLD EVERYTING IS OK. MOM REPORT TEEN EYE LIDS WERE SWOLLEN FOR 4 DAYS AFTER EPISODE. AND LEFT ARM PAIN FOR 3 DAYS.
- Aktuelle Erkrankungen
- TEEN FELT DIZZINES TWO MONTHS PRIOR, AS PER MOM
- Vorgeschichte
- NONE AS MOM
- Andere Medikamente
- NONE REPORTED, AS PER MOM
- Allergien
- NON EREPORTED, AS PER MOM
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 16.12.2022
- Impfdatum
- 10.12.2022
- Beginn
- 10.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Loss of consciousness
Syncope
Symptomtext
syncope -- Pt fainted after receiving both vaccines approximately 5 minutes after administration. Pt recovered and regained consciousness in 10-15 seconds. 911 dispatch was called. EMT team worked up patient and took vitals. Everything resulted within normal limits. Pt reportedly hadn't eaten anything since the night prior and EMT team lead assessed it was the most probable reason for syncope. Lead EMT felt comfortable letting the patient go home with a designated driver, with no further reported incident.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 22.08.2022
- Impfdatum
- 10.08.2022
- Beginn
- 10.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Confusional state
Hyperhidrosis
Pain in extremity
Pallor
Presyncope
Syncope
Wheelchair user
Symptomtext
After applying the band aid following the last immunization (Tdap), Patient fainted in her chair for about 3 seconds. Other nurses were called by CMA and mother. Patient was waking up but confused. Patient was diaphoretic and pale. Blood pressure was monitored as well as O2 and heart rate. Patient was given sips of coca cola and a couple bites of a muffin. Patient started to feel better and was complaining of arm pain. Mom was asked if she would like an ambulance called to transport to the ER and she opted to drive her herself. Patient was helped into a wheelchair and was taken to ER by parents. The next day, we called mom to find out how she was. Mom said the Doctor didn't think it was a vaccine reaction. They thought it was a vasovagal reaction. They gave her the ok to continue getting he vaccinations but to lay down in the future to prevent this from occuring.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 28.02.2023
- Impfdatum
- 27.02.2023
- Beginn
- 27.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Dizziness
Hyperventilation
Paraesthesia
Vomiting
Symptomtext
Pt reported about 1 hour after receiving vaccine symptoms of vomiting x4, dizziness and weakness, tingling hands, and hyperventilation pt reported relief after vomiting - dizziness and weakness lasted for about 1 hour
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- hypertension (recent diagnosis)
- Andere Medikamente
- telmisartan 20mg daily duloxetine 30mg daily
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 28.02.2023
- Impfdatum
- 24.02.2023
- Beginn
- 24.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood thyroid stimulating hormone normal
Full blood count normal
Metabolic function test
Tachycardia
Symptomtext
pt described tachycardia, requiring longer recovery period of heartrate after exercise (about 6 hours) resting heartrate 20 BPM more than normal all data from patient's watch
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tachycardia
- Hospital-Tage
- -
- Labordaten
- CBC, CMP, TSH were tested on 2/27/2023 all WNL for patient
- Aktuelle Erkrankungen
- hematuria
- Vorgeschichte
- Afib, OSA
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 12.10.2022
- Impfdatum
- 11.10.2022
- Beginn
- 11.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Feeling jittery
Oropharyngeal discomfort
Paraesthesia
Pharyngeal swelling
Symptomtext
5 minutes after the 5 vaccines, She felt an abnormal feeling in her throat like it was maybe swollen, tingling sensation in both arms, lightheaded feeling, jittery. HR and BP was good, no fever, breathing sounds remained clear. Patient was laid down and within 5 minutes or less 50 mg of IM Benadryl was given. Within 5 minutes or less, she felt the swelling sensation in throat get better. She slowly got better over the next 1 to 1.5 hours and left feeling well, not excessively tired.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- GERD- well controlled.
- Andere Medikamente
- testosterone, progesterone, pantaprozole
- Allergien
- morphine, Pfizer COVID-19 Vaccine
- Vorherige Impfungen
- 04/20/2021- She had 2nd Pfizer covid-19 vaccine and it caused mild difficulty breathing.
- Staat
- MO
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 26.06.2023
- Impfdatum
- 26.06.2023
- Beginn
- 26.06.2023
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Symptomtext
Patient came to receive updated Tdap. Patient called an hour later to describe a few bumps that were itching on arm and chest area. No other s/s described. Patient stated that he took 50 mg of Benadryl. Patient recommended to contact PCP for further follow up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Not during time of vaccination but was sick a few weeks ago.
- Vorgeschichte
- none
- Andere Medikamente
- None
- Allergien
- none
- Vorherige Impfungen
- Menveo-patient described flu like symptoms
- Staat
- MO
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 01.03.2023
- Impfdatum
- 24.02.2023
- Beginn
- 24.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pain in extremity
Product administered to patient of inappropriate age
Product administration error
Symptomtext
PT GIVEN HIGH DOSE FLU VACCINE IN ERROR, PT REPORTED NO SIDE EFFECTS ASIDE FROM SORE ARM. DENIED ANY FURTHER QUESTIONS OR CONCERNS AT THIS TIME
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- MUSHROOM, PAPAYA
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 28.02.2023
- Impfdatum
- 20.02.2023
- Beginn
- 20.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Injection site pain
Neck pain
Pain
Symptomtext
Pt stated that when the tdap vaccine was given she felt a sharp pain in her arm and then in the last 8 days since receiving the vaccine, pt states her pain is traveling up towards her neck/back.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 11,0
- Geschlecht
- F
- Eingang
- 22.08.2022
- Impfdatum
- 09.08.2022
- Beginn
- 09.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Injection site warmth
Pyrexia
Symptomtext
Fever and tiredness hours after the short that lasted for approx 12-18 hours; Very Hot Arm Around the Injection Site for over 5 days post shot
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 03.08.2023
- Impfdatum
- 31.07.2023
- Beginn
- 31.07.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Wrong product administered
Symptomtext
Client received MMRV instead of just MMR. Client also received Varicella. Client is older then 12 years old and client received Varicella vaccine the same day. Dr. for Dept. of Health made aware and recommendation received to give client MMR vaccine & Varicella vaccine # 2 at his return appointment on 8/28/23. No report of any adverse side effects from client.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 13.02.2023
- Impfdatum
- 13.02.2023
- Beginn
- 13.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
Adacel vaccine, indicated for ages 10-64, was chosen for patient when inputted. Patient is over the age of 64 and would be indicated for Boostrix vaccine, which is indicated for 10+. Error was not caught before administration. Patient received Adacel vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- N/a
- Aktuelle Erkrankungen
- N/a
- Vorgeschichte
- N/a
- Andere Medikamente
- Advair, ProAir, Losartan, Carvedilol, Levothyroxine, Citalopram, Atorvastatin
- Allergien
- N/a
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 1,2
- Geschlecht
- F
- Eingang
- 29.11.2022
- Impfdatum
- 29.11.2022
- Beginn
- 29.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Wrong product administered
Symptomtext
no adverse reaction at this time, child was given Tdap instead of Dtap
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- peanuts
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 26.10.2022
- Impfdatum
- 21.09.2022
- Beginn
- 21.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Underdose
Symptomtext
Patient came into the clinic to receive the Moderna Bivalent but was inadvertently given the Moderna pediatric 0.5 mL dose. KDHE, CDC and Moderna Helpline were notified this same day for guidance. Patient was notified same day of the error.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 19.10.2022
- Impfdatum
- 11.10.2022
- Beginn
- 11.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Patient was given COVID Pfizer Bivalent Booster instead of the second dose of COVID Pfizer primary series vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Sinus infection
- Vorgeschichte
- Trisomy 21, Global developmental delay, Cognitive developmental delay, Agressive behavior, Oral aversion, Mixed hearing loss, bilateral, Eczema, Constipation
- Andere Medikamente
- Zyrtec 10mg daily, Benadryl 12.5mg PRN, Flonase 2 sprays daily, Cortaid 1% cream twice daily, Melatonin 10mg daily, Miralax 17g daily, Kenalog 0.1% cream twice daily, Viloxazine ER 200mg daily
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 06.10.2022
- Impfdatum
- 28.09.2022
- Beginn
- 28.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Medication error
No adverse event
Symptomtext
adacel was administered to patient after expiration date with no reported adverse event; Initial information received from on 28-Sep-2022 regarding an unsolicited valid non-serious case received from a consumer/non-hcp. This case involves a 50 years old male patient to whom diphtheria-2/tetanus/5 AC pertussis vaccine [Adacel] was administered to patient after expiration date with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included Influenza Vaccine Inact Split 4V (Fluzone Quadrivalent) for prophylactic vaccination. On 28-Sep-2022, the patient received a dose 2 at dose of 0.5ml once of suspect diphtheria-2/tetanus/5 AC pertussis vaccine (lot U7528BA; Expiration Date :29-Sep-2022) via intramuscular route in the left deltoid for immunization after expiration date with no reported adverse event (expired product administered) (latency : same day). Action taken : not applicable. Outcome: Unknown. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in the Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- FLUZONE QUADRIVALENT
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 03.10.2022
- Impfdatum
- 03.10.2022
- Beginn
- 03.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
No adverse event
Symptomtext
child was administered the wrong dose of vaccine - no reactions
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 24.09.2022
- Impfdatum
- 16.09.2022
- Beginn
- 19.09.2022
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Vaccination site erythema
Vaccination site swelling
Vaccination site warmth
Symptomtext
Patient reported erythema, swelling and warmness to the touch below the vaccine administration site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None stated
- Vorgeschichte
- None stated
- Andere Medikamente
- No
- Allergien
- No Known Allergies
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 1,3
- Geschlecht
- M
- Eingang
- 23.08.2022
- Impfdatum
- 17.08.2022
- Beginn
- 17.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product administered to patient of inappropriate age
Wrong product administered
Symptomtext
ADACEL being administered to a patient under 10 years of age with no adverse event; patient was given TDAP instead of the ordered DTAP with no adverse event; Initial information received on 17-Aug-2022 regarding an unsolicited valid non-serious case received via health professional. Agency number: 01238843 This case involves a 15-month-old male patient who reported to have Diphtheria-2/Tetanus/5 AC Pertussis Vaccine [Adacel] being administered to a patient under 10 years of age with no adverse event and patient was given tdap instead of the ordered Diphtheria-15/Tetanus/5 AC Pertussis Vaccine [Daptacel] (dtap) with no adverse event. Concomitant medications included HIB VACCINE CONJ (TET TOX) (ACTHIB). The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 17-Aug-2022, the 15-month-old patient received suspect Adacel vaccine of the ordered Daptacel at dose of 0.5ml once via intramuscular route in the right thigh (lot U7528BA) Immunization (product administered to patient of inappropriate age and wrong product administered) at same day latency. Action taken: Not applicable for both suspects. At time of reporting, the outcome was Unknown for both events. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in the Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- ACTHIB
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 14.08.2022
- Impfdatum
- 14.08.2022
- Beginn
- 14.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No.
- Vorgeschichte
- None.
- Andere Medikamente
- None.
- Allergien
- No.
- Vorherige Impfungen
- -