- Staat
- AL
- Alter
- 11,0
- Geschlecht
- F
- Eingang
- 19.06.2023
- Impfdatum
- 26.05.2023
- Beginn
- 26.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syncope
Symptomtext
syncope, no treatment required. Patient ambulated to PV independently.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 11,0
- Geschlecht
- F
- Eingang
- 25.05.2023
- Impfdatum
- 25.05.2023
- Beginn
- 25.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syncope
Symptomtext
vasovagal syncope
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- viral URI 4/24/23
- Vorgeschichte
- -
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 03.01.2023
- Impfdatum
- 03.01.2023
- Beginn
- 03.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dizziness
Syncope
Vomiting
Symptomtext
SYNCOPE EPISODE LASTED 5-8 SECONDS VOMIT ONCE DIZZINESS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- AMOXICILLIN
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 06.03.2023
- Impfdatum
- 03.03.2023
- Beginn
- 03.03.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Nervousness
Pallor
Tremor
Symptomtext
Pt was administered IM menquadfi at 2:15 pm after completing physical. At that time patient was anxious about vaccination and I offered pt water. Pt declined and I administered vaccination and gave pt ice pack after administration. Pt jumped right off of table, I discussed with patient and stepmom and brother (who also received menquadfi) that they should move arms around and can use tylenol later for any remaining pain. Approximately 10 minutes later receptionist from front desk called to state pt was feeling faint. RNs went up to pt first to assess. Pt was pale and shaking but sitting in chair, complaining of dizziness. I brought the BP machine and water to pt, RN applied ice packs to patient's neck and forehead. V/s in waiting room were 122/73, pulse 88 and pulseox 98%. After water and ice packs patient did state he felt improvement in symptoms. Had patient sit in chair for 15 minutes. Able to stand up, pt stated he felt fine though he was still shaky. Able to walk off floor with assistance from stepmom and dad who came up from car.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Developmentally delayed, PKU
- Andere Medikamente
- None
- Allergien
- Augmentin, Shellfish
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 15.09.2023
- Impfdatum
- 14.09.2023
- Beginn
- 14.09.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Hyperhidrosis
Symptomtext
Client had reaction after vaccination- client became light headed and sweaty, water was given, VS were taken, P60, BP110/70, SPO2 97%. Client recovered and left after sitting 15 minute in waiting area.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- PCN
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 06.06.2023
- Impfdatum
- 02.06.2023
- Beginn
- 02.06.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Urticaria
Symptomtext
All 3 vaccines were given at 10:15am, patient released from waiting room with mother at 10:30am. about 11am staff reported mother came back to clinic and knocked on the door to the department, pt noted to have hives on both lower forearms. No shortness of breath noted. MD called to room to check on patient and order received to given Benadryl 14mls which was given at 11:09am. Mother and patient kept in exam room back to pediatrics for close monitoring for about 1 hours. Rash was gone by the time mother and patient was released from the clinic and mother reported no problems noted once home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- per mother toward end of school year pt complaining of stomach pains
- Vorgeschichte
- none per mother
- Andere Medikamente
- none
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 19.05.2023
- Impfdatum
- 04.05.2023
- Beginn
- 08.05.2023
- Tage bis Beginn
- 4,0
- Dosis
- 1
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site swelling
Injection site warmth
Symptomtext
Site red and swollen. Site initally red, warm and raised to the touch. member asymptomatic and voices no complaints. cardio respiratory unremarkable. vitals 129/84 bp72 rr16 spo2 99%. member advised to seark immediate care for any concerning syptoms that may arise approximatly 4 days out from recieving vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 19.05.2023
- Impfdatum
- 14.05.2023
- Beginn
- 14.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Flushing
Hyperhidrosis
Loss of personal independence in daily activities
Symptomtext
Systemic: Dizziness / Lightheadness-Mild, Systemic: Flushed / Sweating-Mild, Additional Details: 5 mins after receiving vaccine, patient complained of lightheadedness and became diaphoretic. Was assisted to supine position on the examining table with legs elevated. Vital signs continuously monitored and pulse was in the 40's and 50's. EMS activated after 20 mins of no resolution in symptoms. Patient discharged home after evaluation by EMS personnel. Called patient today 05/15/2023 and he sated he is felling better and is back at school
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 24.03.2023
- Impfdatum
- 08.11.2022
- Beginn
- 18.11.2022
- Tage bis Beginn
- 10,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Aphasia
Malaise
Pallor
Skin discolouration
Symptomtext
1619 MenQuadfi administeredin right deltoid. 1620: Client reported not feeling well after vaccine administration. Client dropped her head. Client's color became very pale, with blue/purple coloration noted around eyes and mouth. Head repositioned, arms noted to be drawing in towards her body, unable to speak. Moved to the floor by staff. + void noted. EMS called, requested EMS transport. 1621 Client noted to have a heart rate and breathing. Oxygen via nasal canula. 1622 VS obtained: BP: 111/66, P: 127, RR: 24, SPO2: 99%, temp:98.7. Client able to sit up, no verbal response. Moved to room with assistance from staff. Client remained pale in color. Client's mother at the bedside. 1627 EMS arrived in room with client. Care taken over by EMS. BP:113/72, R: 130, RR: 22, SPO2: 99%,. 1635 Client moved to EMS stretcher 1637 Client awake and talking with EMS staff. To ambulance by EMS stretcher. 1640 EMS departed facility en route to Hospital Emergency room
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none known
- Vorgeschichte
- none known
- Andere Medikamente
- none known
- Allergien
- nkda
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 25.01.2023
- Impfdatum
- 16.01.2023
- Beginn
- 16.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Dyskinesia
Fall
Immediate post-injection reaction
Symptomtext
Patient sat on the examination table, and received 3 vaccinations -2 on left arrm, and the last one on right arm. Immediately after the 3rd injection, patient said that she felt dizzy, and slouched forwards. She was placed flat on the examination table immediately. Dr. was summoned from the next examination room, and attended to the patient immediately. The patient was then noticed to have jerking movements of both upper extremities, lasting 15 to 20 seconds. No color changes, no bradycardia, no tachycardia. Soon after the jerking movements stopped, the patient opened her eyes. Dr. asked the patient --- > "Who am I ? ". The patient responded --- > "Dr.". Patient was observed for 45 minutes, then sent home
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- Headaches, on and off, for one month:
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- Possibly allergic to shrimp
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 04.01.2023
- Impfdatum
- 09.12.2022
- Beginn
- 12.12.2022
- Tage bis Beginn
- 3,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site erythema
Injection site pruritus
Injection site swelling
Injection site warmth
Symptomtext
Itching , redness, swelling of left upper arm, was warm to touch ; Taking benadryl and ibuprofen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Lo-estrin FE
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 11,0
- Geschlecht
- F
- Eingang
- 23.12.2022
- Impfdatum
- 23.12.2022
- Beginn
- 23.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Immediate post-injection reaction
Malaise
Visual impairment
Vomiting
Symptomtext
Immediately after receiving MenQuadfi patient stated, she felt sick and dizzy. Afterwards she stated she felt her eyes "go black" for a couple of seconds. She did not faint but did vomit. After recovering she did receive Tdap in lying position. She had no issues directly after vaccine and rested for 10 minutes. While out at the desk she started feeling dizzy and had another feeling of her eyes "going black". She did not faint. She rested for about 15 minutes and was able to leave the clinic with no issue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 9,0
- Geschlecht
- F
- Eingang
- 28.09.2023
- Impfdatum
- 27.09.2023
- Beginn
- 27.09.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- IL
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 20.02.2023
- Impfdatum
- 13.02.2023
- Beginn
- 13.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Medication error
No adverse event
Product storage error
Symptomtext
patient was administered Menquadfi after temperature excursion deemed vaccines non-viable for usage with no reported adverse event; lowest temperature it reached was 30.9f for a total duration out of range of 4 hours and 30 minutes with no reported adverse event; Initial information received on 15-Feb-2023 regarding an unsolicited valid non-serious case received from a other health professional. This case involves 12 years old male patient who was administered Menquadfi (meningococcal a-c-y-w135 (t conj) vaccine ) after temperature excursion deemed vaccines non-viable for usage with no reported adverse event and lowest temperature it reached was 30.9f for a total duration out of range of 4 hours and 30 minutes with no reported adverse event The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 13-Feb-2023, the patient received a 0.5 ml dose of suspect meningococcal a-c-y-w135 (t conj) vaccine Suspension for injection (strength were not reported) (lot U7450AA and expiry date- 10-Oct-2024) via intramuscular route in the left deltoid for Immunization after temperature excursion deemed vaccines non-viable for usage with no reported adverse event (poor quality product administered) (latency: same day) On 13-Feb-2023 , vaccine has lowest temperature it reached was 30.9f for a total duration out of range of 4 hours and 30 minutes with no reported adverse event (product storage error) (latency: same day) Action taken was not applicable. At time of reporting, the outcome was Unknown for the 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 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
- IL
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 20.02.2023
- Impfdatum
- 13.02.2023
- Beginn
- 13.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Medication error
No adverse event
Product storage error
Symptomtext
patient received vaccine that was administered post temperature excursion with no reported adverse event; patient received vaccine that was administered post temperature excursion with no reported adverse event; Initial information received on 15-Feb-2023 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 17 years old female patient who received Meningococcal A-C-Y-W135 (T CONJ) vaccine [Menquadfi] vaccine that was administered post temperature excursion with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 13-Feb-2023, the patient received a dose 1 of 0.5 ml once of suspect Meningococcal A-C-Y-W135 (T CONJ) vaccine Solution for injection that was administered post temperature excursion with no reported adverse event (poor quality product administered) (latency: same day) (lot: U7450AA, expiry date: 10-Oct-2024) via intramuscular route in the right deltoid with unknown strength for immunization. On an unknown date the patient received vaccine that was administered post temperature excursion with no reported adverse event (product storage error) (latency: unknown). 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 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
- TN
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 02.02.2023
- Impfdatum
- 01.02.2023
- Beginn
- 01.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
HEPA VACCINE ADMINISTERED AND WAS OUT OF DATE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- PEANUT OIL
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 26.01.2023
- Beginn
- 26.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
Male patient 18 years of age, came into the clinic to receive vaccines. He was registered and verified. When patient arrived to the nurse to receive multiple vaccines; nurse asked patient if he had any shot record; patient stated no. Nurse asked patient had he ever received any vaccines before he stated yes but had no proof. Patient was vaccinated with MCV4 and HPV. After being vaccinated the school nurse produced shot records that were not provided prior. After reviewing records, patient was explained that he did not need to receive MCV4 because he had received a previous dose. Explain the side effects and allergic reactions. Advised patient if he has any problems please seek medical attention immediately.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- nkda
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 28.01.2023
- Impfdatum
- 21.01.2023
- Beginn
- 21.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
No adverse event
Symptomtext
MENQUADFI was given before it was due with no advesre event; Initial information received on 24-Jan-2023 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 13 years old male patient who experienced Meningococcal A-C-Y-W135 (T Conj) vaccine [Menquadfi] was given before it was due with no advesre event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included Influenza vaccine (Influenza vaccine) for Prophylactic vaccination; and Diphtheria vaccine toxoid, pertussis vaccine acellular 3-Component, Tetanus vaccine toxoid (Boostrix) for Prophylactic vaccination. On 21-Jan-2023, the patient received a 0.5 ml dose once 1 of suspect Meningococcal A-C-Y-W135 (T Conj) vaccine Solution for injection was given before it was due with no advesre event (inappropriate schedule of product administration) of standard strength (lot: U7450AA) via intramuscular route in the right deltoid with unknown expiry date for Immunization. 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 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
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 21.01.2023
- Impfdatum
- 21.01.2023
- Beginn
- 21.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Wrong product administered
Symptomtext
He was given Meningococcal conjugate in error. He already got a dose on september 2022. No adverse reaction observed. Patient alert and oriented. Stayed for 15 minutes observation
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 07.12.2022
- Impfdatum
- 07.12.2022
- Beginn
- 07.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Wrong product administered
Symptomtext
None reported at this time; received MenQuadFi by mistake (had only asked for MMR)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 16.11.2022
- Impfdatum
- 08.11.2022
- Beginn
- 08.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Medication error
No adverse event
Wrong product administered
Symptomtext
a patient inadvertently received a dose of MENQUADFI instead of TRUMEMBA with no reported adverse event; Initial information received on 08-Nov-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 17 years old male patient inadvertently received a dose of MENINGOCOCCAL A-C-Y-W135 (T CONJ) VACCINE [MENQUADFI] instead of trumemba with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 08-Nov-2022, the patient received a dose of suspect MENINGOCOCCAL A-C-Y-W135 (T CONJ) VACCINE (lot U7450AA; 10-OCT-2024) via intramuscular route in the left arm for prophylactic vaccination. On 08-NOV-2022 the patient reported a non-serious event a patient inadvertently received a dose of MENINGOCOCCAL A-C-Y-W135 (T CONJ) VACCINE instead of trumemba with no reported adverse event (wrong product administered). Action taken: not applicable. At time of reporting, the outcome was Unknown for the 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.; Sender's Comments: 01358281:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Medication error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 02.11.2022
- Impfdatum
- 01.11.2022
- Beginn
- 01.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Symptomtext
No adverse reaction noted or reported to the clinic.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asthma without complications, ADHD Allergic Rhinitis, Mixed Anxiety and Depressive Disorder
- Andere Medikamente
- Vyvanse, Clonidine, Risperdal, Flonase, Cetirizine, Singular
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 26.10.2022
- Impfdatum
- 24.10.2022
- Beginn
- 25.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Burning sensation
Erythema
Hypersensitivity
Peripheral swelling
Symptomtext
Pt got the Menactra at 11 year no reaction gave the Menquadfi for 2 dose at 16 years and had allergic reaction with swelling, red and burning on the left arm On the right arm trumenba had the same reaction not as bad as the menquadfi. We informed them that the menquadfi doesnt need another dose so we dont have to worry about that on but the trumenba needs a booster so we asked them to keep an eye on that arm to see if it gets bigger if it gets to big we might not be able to give the booster asked them to take pictures. Told them to take cetirizine and called in a steroid cream.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Burning sensation
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Asthma and numbs in fingers
- Vorgeschichte
- Asthma
- Andere Medikamente
- Albuterol, fluticasone, L- methylfolate, singulair, ventolin and cetirizine
- Allergien
- NKDA, Dustmites and Grass
- Vorherige Impfungen
- -