- Staat
- NY
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 02.10.2023
- Impfdatum
- 02.10.2023
- Beginn
- 02.10.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Seizure like phenomena
Symptomtext
Other nurse was alerted to patient experiencing "seizure like" activity in the waiting area at approximately 1430. Per nurse patient appeared lucid and conscious upon her immediate response. Writer arrived for unrelated reason and saw other nurse was already tending to patient. Patient noted to have legs elevated, and a cool towel on head. nurse asked student nurse to get a snack and gatorade while writer was looking for cold compress on arrival. Writer provided nurse with a cold compress and she placed it on patient's chest approximately one minute after arrival. After 2 minutes of lying down with feet elevated patient stated he wanted to sit up in a chair. Writer and nurse assisted to chair. Writer observed patient for approximately 10 minutes. Patient stated he was feeling better. Patient's representative was instructed to have patient wait another 10 minutes in observation area. Both patient and patient's representative verbalized understanding.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure like phenomena
- Hospital-Tage
- -
- Labordaten
- no medical tests or labs taken at this time .
- Aktuelle Erkrankungen
- denied illness at time of vaccination, unknown if illness one month prior
- Vorgeschichte
- denies long term health problems at time of vaccination
- Andere Medikamente
- unknown
- Allergien
- no known allergies
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 25.09.2023
- Impfdatum
- 23.09.2023
- Beginn
- 23.09.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pallor
Syncope
Symptomtext
Patient experienced syncope after receiving Hep A, influenza, MenACWY, Tdap, and varicella vaccines. Briefly unresponsive, pale complexion. Recovered quickly; monitored for almost 1 hour.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 18.08.2023
- Impfdatum
- 17.08.2023
- Beginn
- 18.08.2023
- Tage bis Beginn
- 1,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abnormal sensation in eye
Bell's palsy
Borrelia test
Eyelid ptosis
Full blood count
Herpes zoster
Malaise
Metabolic function test
Palpitations
Symptomtext
felt ill about 12:30 am the night after immunization, felt heart was pounding. In the morning was very worried, noted left upper eyelid ptosis and an unusual feeling around the eye. Presented to Health Services and heart rate and auscultation were normal, but there was ptosis L and unusual sensation but not numbness from left eye to upper cheek. Referred for immediate eye exam, preliminary diagnosis zoster vs bells palsy, empiric prednisone and valacyclovir prescribed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bell's palsy
- Hospital-Tage
- -
- Labordaten
- 8/18/23 lyme titer (due to insect reaction about 2 weeks previous), CBC, CMP ordered, no results yet available
- Aktuelle Erkrankungen
- insect bite reaction 8/8/23
- Vorgeschichte
- anxiety not formally diagnosed per chart
- Andere Medikamente
- none
- Allergien
- none known
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 11,0
- Geschlecht
- F
- Eingang
- 26.07.2023
- Impfdatum
- 25.07.2023
- Beginn
- 25.07.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fall
Head injury
Pain in extremity
Syncope
Symptomtext
Pt fainted about 8-10 minutes after receiving vaccine. Pt had reported she was fine but her arm was sore after vaccination. Pt was standing to leave awaiting paperwork and fainted hitting her head on floor. Pt was evaluated by nursing staff and EMS, noting not with redness on back of head, but no laceration or bleeding from site. Observed pt arm, no skin reaction noted from vaccine administration site. Pt denied any difficulty breathing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 12.04.2023
- Impfdatum
- 20.03.2023
- Beginn
- 20.03.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Medication error
Syncope
Symptomtext
syncope; extra dose of MENQUADFI was administered to a patient; Initial information received on 07-Apr-2023 regarding an unsolicited valid serious case received from a consumer/non-hcp (Non-healthcare professional). This case involves a 17 years old female patient who was administered an extra dose of Meningococcal A-C-Y-W135 (T Conj) Vaccine [Menquadfi] and experienced syncope. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 20-Mar-2023, the patient received 0.5 ml (Dose 3) of suspect Meningococcal A-C-Y-W135 (T Conj) Vaccine Solution for injection (lot number: U7449AA, Expiry date: 23-SEP-2024) (Frequency-once; Strength- standard) via intramuscular route in the left deltoid for prophylactic vaccination (Immunisation). On 20-Mar-2023, the patient was administered an extra dose of Meningococcal A-C-Y-W135 (T Conj) Vaccine (extra dose administered) (Latency: same day) and experienced syncope (syncope) (Latency: same day). Supervisor reported an extra dose of MENQUADFI was administered to a patient who had a syncope episode after the administration. Caller is inquiring about safety information. This situation is reported as a medication error due to an extra dose of MENQUADFI being administered. Action taken: not applicable. It was not reported if the patient received a corrective treatment for the events (syncope) Outcome: Unknown for the reported event 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. Seriousness Criteria: Medically significant for syncope.; Sender's Comments: Sanofi company comment dated 11-Apr-2023: This case involves a 17 years old female patient who was administered an extra dose of Meningococcal A-C-Y-W135 (T Conj) Vaccine [Menquadfi] and experienced syncope. Furthermore, information regarding condition at the time of vaccination excluding other predisposing etiologies would be needed for complete assessment of the case. Based upon the reported information, the role of the suspect vaccine cannot be assessed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 31.03.2023
- Impfdatum
- 29.03.2023
- Beginn
- 29.03.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bradycardia
Dizziness
Flushing
Nausea
Pallor
Tinnitus
Presyncope
Symptomtext
Patient had office visit today where she received the meningococcal vaccine. Upon leaving, she started to get dizzy, nauseas, lightheaded and felt flushed with ringing ears. Triage was called for her in the lobby and I was asked to assist. Evaluated patient in the lobby where she was noted to be alert, sitting in a chair but mildly pale. She endorsed the above symptoms. She was mildly bradycardic to the 50's and initial BP was in the 70's systolic. Suspected to have had a vasovagal response so she was brought into an exam room and layed down with feet elevated. This improved her symptoms and vitals. She was given an ice pack, glass of water and allowed to rest. After resting for several minutes, patient's symptoms dramatically improved, vitals stabilized and she was discharged to home in stable condition.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Asthma
- Andere Medikamente
- Albuterol Inhaler
- Allergien
- No Allergies
- Vorherige Impfungen
- -
- 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 / RA
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
- IN
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 03.12.2022
- Impfdatum
- 03.12.2022
- Beginn
- 03.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Feeling abnormal
Loss of consciousness
Pallor
Peripheral coldness
Pulse abnormal
Skin warm
Symptomtext
about 5 minutes after injection patient said she didn't feel right and was pale. Her hands were cold and neck was warm. I had technician call emergency services. Patient then lots consciousness for a brief moment and mother and I tried to keep her talking. I took her blood pressure (143/45) and O2 98%. Her pulse was erratic and hard to read. Fire department arrived and provided oxygen and retook her BP and O2. EMTs arrived and transported patient to the hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- 12/03/2022@2:10pm BP=143/45 and O2 98%
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- History of POTS
- Andere Medikamente
- Unknown
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 23.11.2022
- Impfdatum
- 20.09.2022
- Beginn
- 21.10.2022
- Tage bis Beginn
- 31,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Ear pain
Electromyogram
Guillain-Barre syndrome
Hypoaesthesia
Laboratory test abnormal
Magnetic resonance imaging
Motor dysfunction
Nerve conduction studies
Otitis media
Paraesthesia
Pharyngitis
Pyrexia
Rheumatoid factor increased
Sensory loss
Symptomtext
Patient received MenQuadfi booster vaccine administered on 09/20/2022. Patient developed fever and ear pain on 10/05/2022, a PCP visit was completed, and patient diagnosed with left otitis media, acute pharyngitis, and prescribed Amoxicillin 875 mg to be taken twice per day for 7 days. A few weeks later, around 10/21/2022, patient began noticing tingling sensation in toes. This progressed to numbness, which then progressed to the hands as well. About 1 week later motor deficit symptoms began to develop. Presented to ED on 11/6/22, notes indicate diminished sensations along hands, arms, feet and legs. Most of the labs were unremarkable and no other symptoms present. Patient did have an elevated rheumatoid factor. Patient Discharged home with Gabapentin 100 mg prescribed orally to be taken three times per day. Over the next few weeks symptoms were persistent with no improvement on medication. Patient was direct admitted from an outpatient neurology follow up appointment. Patient admitted to Hospital on 11/10/2022 and discharged home on 11/18/2022 with a diagnosis of Guillain Barre Syndrome.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Guillain-Barre syndrome
- Hospital-Tage
- 8,0
- Labordaten
- Multiple blood tests, MRI, EMG, Nerve conduction study
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Scoliosis
- Andere Medikamente
- Zyrtec 10 mg tablets Daily
- Allergien
- Pollen-Food Allergy
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 03.11.2022
- Impfdatum
- 01.11.2022
- Beginn
- 01.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syncope
Symptomtext
Pt experienced syncopal event 4 min after immunization received. Slight movement noted of left arm and left leg for 15 seconds while syncopal event lasted. Pt regained consciousness 30 seconds after syncopal event started. Applied cold towel to forehead and cheeks, Pt maintained a pulse during syncopal event.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None reported by Parent
- Vorgeschichte
- None reported by Parent at time of Immunization.
- Andere Medikamente
- None reported by Parent
- Allergien
- None reported by Parent
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 17.10.2022
- Impfdatum
- 13.10.2022
- Beginn
- 13.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dizziness
Dizziness postural
Fall
Loss of consciousness
Pallor
Symptomtext
Upon completion of HPV vaccine to right arm (last vaccine given) RN was talking with patient assessing how he was feeling as RN was completing documentation. Patient stating he was feeling well and was ready to leave clinic. After appx 2-3 minutes of talking, patient started to stand up and became pale and dizzy and fell to his left into the wall and slid down onto the floor. He was completely passed out and RN yelled for help as she rolled patient onto his back. He awoke immediate upon rolling into supine position. His feet were elevated and a cool compress applied. It took appx 5-10 minutes for dizziness to completely resolve. Patient was monitored for appx 20 minutes total before being allowed to leave clinic with his mother.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 03.10.2022
- Impfdatum
- 27.09.2022
- Beginn
- 30.09.2022
- Tage bis Beginn
- 3,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Computerised tomogram
Electroencephalogram
Seizure
Symptomtext
Patient has reported series of seizures 4 days after receiving meningitis vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- Patient has had Cat scan, EEG and blood work while at the ER.
- Aktuelle Erkrankungen
- no know history of disease
- Vorgeschichte
- no know history of disease
- Andere Medikamente
- Folic Acid 1 mg Vitamin D 1.25 mg
- Allergien
- no know drug allergies
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 26.10.2022
- Impfdatum
- 26.10.2022
- Beginn
- 26.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Blood pressure increased
Chills
Dizziness
Headache
Heart rate increased
Rash macular
Tremor
Symptomtext
Patient received vaccines in office and was fine when left and went on to school. Mom called the office one and a half hours later and stated that he was in the school nurse office shaking uncontrollably and dizzy. Told mom to bring him by the office and we would check him out. When child got to the office he was light headed, dizzy, had a headache, shaking uncontrollable, had a blotchy rash and rigor. Patients blood pressure and pulse was elevated. Provider came into office and evaluated patient. We kept him in office for about 30 minutes after coming back to clinic, Provider advised mom to take him to the emergency room to continue to be evaluated to make sure no other symptoms occur, mom was in agreeance.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- None in the clinic on 10/26/2022
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Cetirizine 10 mg, Singulair 10 mg
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 06.10.2022
- Impfdatum
- 04.10.2022
- Beginn
- 04.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Echocardiogram normal
Ejection fraction normal
Electrocardiogram ST segment elevation
Electrocardiogram ST-T segment abnormal
Magnetic resonance imaging heart
Troponin increased
Symptomtext
Started having chest pain within minutes of vaccine. Presented to ED 2 days later, admitted with elevated troponins with concern for myocarditis.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- 2,0
- Labordaten
- Troponin (normal limit <77): 275 (10/5) > 451 (10/6) > 10,915 EKG (10/5 & 10/6): Sinus rhythm, Borderline ST elevation, inferior leads Echocardiogram (10/5): SUMMARY: Normal left ventricle size, wall thickness, and systolic function. -LVEF 69% by Teicholz method -Borderline abnormal LV global longitudinal strain: -17.6% Normal right ventricle size, wall thickness, and systolic function. Normal intracardiac connections with no apparent septal defects. Normal valve structure and function. No aortic arch abnormalities demonstrated. No evidence of pulmonary hypertension. No pericardial or obvious pleural effusion. Cardiac MRI pending, currently admitted
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 17.01.2023
- Impfdatum
- 17.01.2023
- Beginn
- 17.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Rash
Symptomtext
Patient developed rash on hands bilaterally 30 minutes after receiving MenQuadfi vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 07.12.2022
- Impfdatum
- 13.10.2022
- Beginn
- 13.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site swelling
Peripheral swelling
Symptomtext
Swelling of the left arm/shoulder at injection site for 3 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site swelling
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asthma
- Andere Medikamente
- -
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 28.11.2022
- Impfdatum
- 22.11.2022
- Beginn
- 22.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dizziness
Feeling hot
Visual impairment
Symptomtext
Following vaccinations patient began to feel warm and got dizzy. Distress button was pushed by MA staff. Immediate response by RN staff, MA staff, and providers. Lowered patient slowly and gently to the ground and elevated feet. Cold compress applied. Patient was orientated to person and place but did report fuzzy vision. Vitals taken. After approximately 10 minutes patient did improve and was able to sit up. He drank apple juice and continued to improve. Stayed for an additional 10 minutes with no further incidents.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 15.11.2022
- Impfdatum
- 04.11.2022
- Beginn
- 05.11.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Back pain
Chills
Eye swelling
Immunisation reaction
Lacrimation increased
Ocular discomfort
Ocular hyperaemia
Pain
Swelling of eyelid
Symptomtext
The night he received his vaccines (Bivalent, HPV, MCV4, Flu) - he had the chills and back pain. No temperature was taken He was given ibuprofen to help with the pain The next day, his left eye started to become swollen, he noticed it when he woke - both lids were swollen Possible erythema, white part of the eye was red, no pain but a little uncomfortable, there was some tearing, no other discharge He went to the UC that day - was told that it was from the vaccines - given benadryl and antibiotics Family did not start the otic antibiotics The swelling improved by the time he was seen at the UC and completely resolved in 2 days. The benadryl helped. No swelling at the site of injection of any of the vaccines Minimal pain that resolved in 2 days and did not need treatment No erythema at the site of injections on either arm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Respiratory : Exercise induced bronchospasm--Medium Genitourinary: Tight foreskin---Medium Other : Child in welfare custody---Medium Allergic rhinitis---Medium Delayed immunizations
- Andere Medikamente
- ? albuterol 108 (90 Base) MCG/ACT inhaler, Inhale 2 puffs every 6 (six) hours if needed for wheezing or shortness of breath (night cough, 10-15 min before exercise). Use with spacer, Disp: 18 g, Rfl: 3 ? betamethasone, augmented, (Diprole
- Allergien
- ? Watermelon [Citrullus Vulgaris] Itching and Swelling Pt states throat closed and he needed his inhaler the last time he ate watermelon. ? Pineapple Itching
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 31.10.2022
- Impfdatum
- 31.10.2022
- Beginn
- 31.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blindness
Deafness unilateral
Feeling hot
Hyperhidrosis
Immediate post-injection reaction
Malaise
Retching
Symptomtext
Patient received first vaccine in Left Deltoid(T-Dap). Patient did well with that vaccine. Then patient had MCV4(MenQuadfi) injected in Rt arm. Immediately patient stated that he could not see & hear out of Rt ear. He was profusely sweating & hot. I started talking with him & had mom to keep speaking with him. We used a cold compress on neck & cold wet compress on forehead. Patient did state he thought he was going to get sick. He did dry heave in the trash can. We than got him a juice & crackers. He sipped slowly on the juice & ate crackers. Patient never passed out. He started feeling better after the juice & crackers.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- A few weeks prior had a detached retina.
- Vorgeschichte
- No
- Andere Medikamente
- Unknown
- Allergien
- No known Allergies
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 07.08.2023
- Impfdatum
- 17.07.2023
- Beginn
- 17.07.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Medication error
No adverse event
Wrong product administered
Symptomtext
accidently given a menactra instead of the bexsero dose with no reported adverse event; Initial information received on 02-Aug-2023 regarding an unsolicited valid non-serious case received from a pharmacist. This case involves a 18 years old male patient who was accidently given a menactra instead of the bexsero dose 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 booster dose of tozinameran (pfizer biontech covid-19 vaccine) for Immunisation. On 17-Jul-2023, the patient received 0.5 ml (dose 3) of suspect meningococcal A-C-Y-W135 (D CONJ) Vaccine, Solution for injection lot U7449AA via intramuscular route in the right deltoid for immunization (strength, expiry date: unknown) and suspect meningococcal vaccine B RFHBP/NADA/NHBA OMV not produced by Sanofi Pasteur lot number not reported via unknown route in unknown administration site for prophylactic vaccination (strength, formulation, dose, batch number, expiry date: unknown), the patient was accidently given a menactra instead of the bexsero dose with no reported adverse event (wrong product administered)(latency same day). Action taken: not applicable. It was not reported if the patient received a corrective treatment for the event (wrong product administered). Outcome was Unknown for the event wrong product administered. 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
- Medication error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- PFIZER BIONTECH COVID-19 VACCINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 12,0
- Geschlecht
- U
- Eingang
- 26.07.2023
- Impfdatum
- 25.07.2023
- Beginn
- 25.07.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Wrong product administered
Symptomtext
Patient given wrong Meningococcal (Men B) vaccine by CMA, did not have RN or Dr. check her vaccines. Mother was called and patient returned to clinic. No redness, edema, no adverse reaction noted at site. Correct Vaccine paper and Meningococcal4 acwy given by RN in opposite Deltoid Right after reviewing CDC recommendations. Observed for 20min after vaccine to ensure no A/R - none.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- NKDA, None
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- -
- Geschlecht
- M
- Eingang
- 27.06.2023
- Impfdatum
- 22.03.2023
- Beginn
- 22.03.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product administered to patient of inappropriate age
Symptomtext
No adverse event; Product administered to patient of inappropriate age (13 years old); This case was retrieved during the monitoring on 12-APR-2023 with the following Primary ID 2602334-1. The original narrative from the sender is as follows: No symptoms or adverse effects. Due to the nature of the event, the causal relationship between Vaxelis and "no symptoms or adverse effects and Product administered to patient of inappropriate age (13 years old)" was not applicable. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Prophylaxis
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 28.04.2023
- Impfdatum
- 17.04.2023
- Beginn
- 17.04.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
No adverse event
Wrong product administered
Symptomtext
patient received their first dose of MENQUADFI in October 2022, and then inadvertently received another dose of MENQUADFI early with no reported adverse event; the patient was supposed to receive the HPV vaccine, but she was inadvertently administered a second dose of MENQUADFI with no reported adverse event; Initial information received on 21-Apr-2023 regarding an unsolicited valid non-serious case received via other health professional. This case involves a 12 years old female patient who received their first dose of menquadfi in october 2022, and then inadvertently received another dose of menquadfi early and the patient was supposed to receive the hpv vaccine, but she was inadvertently administered a second dose of meningococcal a-c-y-w135 (t conj) vaccine [Menquadfi] with no reported adverse event. The patient's past medical history, medical treatment(s), concomitant(s) and family history were not provided. On 17-Apr-2023, the patient received suspect meningococcal a-c-y-w135 (t conj) vaccine Solution for injection lot dose number 2 at dose of 0.25 ml (batch number: U7449AA, Expiry date: 23-Sep-2024) via intramuscular route in the left arm for prophylactic vaccination (immunization) and TB skin test (skin test) On 17-Apr-2023 , patient received their first dose of menquadfi in october 2022, and then inadvertently received another dose of menquadfi early (incorrect dose administered) , patient was supposed to receive the hpv vaccine, but she was inadvertently administered a second dose of menquadfi (wrong product administered) (same day latency) with no reported adverse event. Action taken was not applicable. 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
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 26.04.2023
- Impfdatum
- 17.04.2023
- Beginn
- 17.04.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Medication error
No adverse event
Wrong product administered
Symptomtext
Patient in clinic for immunization revisit. Patient scheduled to receive HPV vaccine. Manquadfi immunization inadvertently given to administered. Contacted mother of patient on 04/20/2023 and advised her of the medication error. Discussed the conditions of the patient. Mother advised the patient was fine with no adverse reactions noted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Medication error
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 14.04.2023
- Impfdatum
- 14.04.2023
- Beginn
- 14.04.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Hepatitis B antibody negative
Wrong product administered
Symptomtext
PATIENT CAME FOR HEP B SERIES , AND RCEIVED MENQUADFI
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- UNKNOWN
- Allergien
- NONE
- Vorherige Impfungen
- MENNIGICOCCAL B ADVERSE REACTION BELLS PALSY
- Staat
- KY
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 23.03.2023
- Impfdatum
- 22.03.2023
- Beginn
- 22.03.2023
- 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 administered to patient of inappropriate age
Symptomtext
No symptoms or adverse effects
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
- KY
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 24.02.2023
- Impfdatum
- 20.02.2023
- Beginn
- 20.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Medication error
Product administered to patient of inappropriate age
Symptomtext
4 years had not elapsed between the last meningococcal vaccine with no reported adverse event; Initial information received on 21-Feb-2023 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 12 years old female patient who reported 4 years had not elapsed between the last meningococcal vaccine with no reported adverse event after receiving MENINGOCOCCAL A-C-Y-W135 (T CONJ) VACCINE [MENQUADFI]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included HPV VACCINE VLP RL1 9V (YEAST) (GARDASIL 9) for Immunisation. On 20-Feb-2023, the patient received 0.25 mL to 2 mL dose of suspect MENINGOCOCCAL A-C-Y-W135 (T CONJ) VACCINE solution for injection( lot number U7449AA ) and( expiry 24-Sep-2023) via intramuscular route in the right arm for Immunization On 20-FEB-2023 the patient had a non-serious event " 4 years had not elapsed between the last meningococcal vaccine with no reported adverse event" (product administered to patient of inappropriate age) following the administration of MENINGOCOCCAL A-C-Y-W135 (T CONJ) VACCINE ( latency : same day ) No lab data included Action taken with MENINGOCOCCAL VACCINE (MENQUADFI) was not applicable. At time of reporting, the outcome was Unknown for the event 4 years had not elapsed between the last meningococcal vaccine with no reported adverse event. 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 guidelines. 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
- Medication error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 20.02.2023
- Impfdatum
- 20.02.2023
- Beginn
- 20.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
No adverse event
Symptomtext
Provider submitted order for MenQuadfi and HPV, MA administered both MenQuadfi and HPV. Provider then realized patient did not require MenQuadfi booster since patient had already received a dose on 02/14/2022. Provider notified parent and patient of error. Attempted to call Sanofi Pasteur to receive guidance but closed due to holiday. No adverse reaction at the time of discharge.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None known
- Vorgeschichte
- None known
- Andere Medikamente
- No known medication
- Allergien
- Amoxicillin
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 22.12.2022
- Impfdatum
- 22.12.2022
- Beginn
- 01.12.2022
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
no known adverse event. Patient received duplicate vaccine 3 mos apart. No signs or symptoms 24hrs post receiving vaccines.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- KNA
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 14.12.2022
- Impfdatum
- 12.12.2022
- Beginn
- 12.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Unknown schedule of product administration
Symptomtext
Nurse failed to look in record and took word for it that this child was new and that we would have to start from scratch with the vaccination. Nurse had forgotten that this child had come into the office for the same shots back in September making two of them invalid due to spacing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unknown schedule of product administration
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None noted
- Vorgeschichte
- None noted
- Andere Medikamente
- None noted
- Allergien
- None noted
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 11,0
- Geschlecht
- F
- Eingang
- 06.12.2022
- Impfdatum
- 28.10.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product preparation issue
Symptomtext
Patient was given Pfizer COVID Vaccine, orange cap, 5-11 undiluted so it was not reconstituted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product preparation issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Viral Syndrome with Fever 09/01/2022
- Vorgeschichte
- Asthma Headaches
- Andere Medikamente
- Flovent inhaler Albuterol Inhaler Montelukast Rizatriptan
- Allergien
- Amoxicillin
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 5,0
- Geschlecht
- F
- Eingang
- 04.11.2022
- Impfdatum
- 20.10.2022
- Beginn
- 20.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Symptomtext
The provider spoke with MOC about the vaccine and gave mother all vaccine information and what she need to look out for. A few days after the incident provider called mother again to follow up on patient and mother stated patient is doing good. No reaction to vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 21.10.2022
- Impfdatum
- 14.10.2022
- Beginn
- 14.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Wrong product administered
Symptomtext
Gave MMRV vaccine instead of MMR. Separate Varicella vaccination also given. Patient did not have any adverse effects
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 20.10.2022
- Impfdatum
- 19.10.2022
- Beginn
- 19.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Patient received a dose of MCV4, as well as Varicella on 10/13/2022 and again on 10/19/2022. No symptoms, signs, etc reported
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- Not applicable
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- No known allergies
- Vorherige Impfungen
- -