- Staat
- AZ
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 04.10.2023
- Impfdatum
- 03.10.2023
- Beginn
- 03.10.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cold sweat
Lethargy
Pallor
Slow response to stimuli
Syncope
Symptomtext
Patient experienced syncope in car. By the time nurse arrived to patients side he had regained consciousness. Patient was alert and oriented but lethargic and slow to answer basic questions. Patients vitals checked and were within normal range. Skin pale and clammy. Ice pack was placed on back of head, and fluids provided. Patient did not fully recover within 15 minutes, EMS call was placed. Nurse remained with patient till arrival and report given to paramedics. Paramedics evaluated patient vitals rechecked and still within range, EKG normal. Paramedics determined patient was ok to go home and be monitored by parent. Parent advised to monitor patient and to call EMS, if it needed. Parent verbalized understanding and agreed with plan.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- EKG- normal
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 11,0
- Geschlecht
- F
- Eingang
- 31.03.2023
- Impfdatum
- 29.03.2023
- Beginn
- 29.03.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dizziness
Feeling hot
Immediate post-injection reaction
Syncope
Symptomtext
The Dtap and MenQuadFi were administered first. Immediately after administering the third vaccine (HPV) vaccine, pt. c/o feeling lightheaded and then fainted. RN lowered her to a laying position and elevated her legs. Patient opened her eyes right away and stated that she felt very warm. Patient remained laying down for 10 minutes and then slowly sat up after reporting feeling better. Pt. sat for an additional 5 minutes without dizziness or complaint. Pt. was able to stand and walk out of the office unassisted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None at visit
- Vorgeschichte
- None
- Andere Medikamente
- Multivitamin
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 06.02.2023
- Impfdatum
- 02.02.2023
- Beginn
- 02.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Seizure like phenomena
Syncope
Symptomtext
Patient had a syncopal episode followed by a brief seizure-like episode (5-10 seconds long). Was back to baseline after.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure like phenomena
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 23.08.2022
- Impfdatum
- 17.08.2022
- Beginn
- 17.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Syncope
Symptomtext
Vasovagal syncope. Started at 0933. Patient instructed to stay laying on floor. Sat up when able and drank juice. At 0950, patient was assisted to parent's car when he stated he felt better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 17.02.2023
- Impfdatum
- 15.02.2023
- Beginn
- 15.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Chest pain
Extra dose administered
Symptomtext
Patient inadvertently received two doses of varicella vaccine an subsequently experienced chest pain. Sent to ED for further evaluation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Amoxicillin
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 14.06.2023
- Impfdatum
- -
- Beginn
- 02.06.2023
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Discomfort
Headache
Symptomtext
Patient received Meningococcal vaccine on 6/2/23. Mom states that patient has had headache and still next x3days (since 6/11/23). She reached out to her pediatrician, who stated that the discomfort may be from an ear infection. As of 6/14/23, the symptoms are continuing and mom fears the vaccine is the problem. Mother has been advised to reach back out to her pediatrician for further evaluation of her son.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- ibuprofen
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 11,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 27.12.2022
- Beginn
- 28.12.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site erythema
Injection site induration
Injection site urticaria
Pyrexia
Symptomtext
erythematous wheal with induration on left arm( Menquadfi) site, 4"X4"TDaP site also with mild erythema and induration .
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- Started on amoxicilin due to fever - 12/29/2022
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 11.01.2023
- Impfdatum
- 07.01.2023
- Beginn
- 07.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Disorientation
Dizziness
Flushing
Head injury
Hyperhidrosis
Injection site pain
Injection site swelling
Posture abnormal
Symptomtext
Site: Pain at Injection Site-Mild, Site: Swelling at Injection Site-Mild, Systemic: Dizziness / Lightheadness-Medium, Systemic: Flushed / Sweating-Medium, Additional Details: All occured right after administration of both vaccines on 01/07/2023. Pt was sitting on the chair and was feeling light headed and tipped over on the chair and hit is head on the wall. Was disoriented for a few minutes and came to. Was able to breath and was sweating profusely. Mother wanted to contact her PCP before calling EMS. She decided to take her son to the ER herself without me contacting EMS. Epipen was not used due to the patient was not having anaphylaxsis and was able to breathe.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 03.01.2023
- Impfdatum
- 03.01.2023
- Beginn
- 03.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Immediate post-injection reaction
Symptomtext
On 01/03/2022 at 9:45 AM a 16 year old female client received 3 vaccines (Influenza, Hep A, MenACWY). Before vaccination, nurse verified that the client had no pre-existing conditions and no history of reactions to vaccines. Before vaccination, nurse also verified that the client had eaten breakfast before coming to the clinic. Immediately after receiving the vaccines, the client reported to nurse and Nurse, that she was feeling dizzy. The client was offered juice, water, and an ice pack to place on the back of her neck. Her vitals were taken at this time (9:45 AM) B/P: 74/39, HR: 62, RR: 18, A&Ox4. Client was lowered to lay down on a mat on the floor as a fall precaution. She responded to all questions from the nurses during this time. At 9:53 AM her second reading of vitals were taken and read: B/P: 97/67, HR: 76, RR: 13, A&Ox4. Client reported that she was "feeling better" and had "no dizziness". She denied any other symptoms. Client continued to be monitored by nurses. Her aunt/caregiver was brought into the clinic room and was updated on the client's status. Additional vitals were taken at10:03 AM. These vitals were as follows: B/P: 99/69, HR: 73, RR: 16, A&Ox4. Patient denied any symptoms at this time. At 10:20 AM vitals were: B/P: 86/55, HR: 70, RR: 18, A&Ox4. Patient denied any symptoms at this time. At 10:30 AM vitals were: B/P: 90/70 (manual), HR: 72, RR: 16, A&Ox4. At 10:32 AM client denied any signs or symptoms. Remaining vaccines were not administered, and nurse advised for client to return another day to receive vaccines. Client and aunt were educated by nurse for client to hydrate, eat, rest, and to seek medical attention if any signs or symptoms return or develop. Client left clinic at 10:33 AM, ambulating independently.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 10.09.2022
- Impfdatum
- 08.09.2022
- Beginn
- 09.09.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Lymphadenopathy
Symptomtext
Lymph node swelling and pain in left axilla
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none reported
- Vorgeschichte
- none
- Andere Medikamente
- none known
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 11.08.2022
- Impfdatum
- 11.08.2022
- Beginn
- 11.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cold sweat
Dizziness
Pallor
Symptomtext
Student felt dizzy three minutes after receiving vaccines. He looks pale and clammy. Denied any shortness of breath. Awake, alert, oriented, responds to verbal stimuli. Student is assisted to lay down on the cot with feet elevated. VS taken. O2 given. V/S 3:08PM BP 82/48 HR 64 O2 sat 94% Laying down 3:13pm BP 117/67 HR 80 O2 sat 97% Laying down. Normal color 3:16pm BP 119/64 HR 77 O2 sat 97% Sitting 3:30pm BP 114/70 HR 82 )2 sat 97% Sitting Student went home with his mother in no acute distress. Normal color. Denied any dizziness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- N/A
- Allergien
- NKDA/NKA
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 01.07.2022
- Impfdatum
- 29.06.2022
- Beginn
- 30.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cough
Decreased appetite
Fatigue
Headache
Injection site pain
Pain
Symptomtext
achiness, soreness at site, appetite down, tired, H/A, coughing Temp 99.5
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- NO
- Aktuelle Erkrankungen
- COVID- 1-2 weeks prior.
- Vorgeschichte
- None
- Andere Medikamente
- NONE
- Allergien
- Seasonal
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 7,0
- Geschlecht
- F
- Eingang
- 11.07.2023
- Impfdatum
- 21.06.2023
- Beginn
- 21.06.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Circumstance or information capable of leading to medication error
No adverse event
Symptomtext
The Medical Assistant thought she saw an order for MenQuadfi for the patient. She pulled the vaccine and administered the vaccine to the patient. The patient has not experienced any adverse reaction.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Circumstance or information capable of leading to medication error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Tylenol 10ml by mouth given in office
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 11,0
- Geschlecht
- F
- Eingang
- 14.04.2023
- Impfdatum
- 16.12.2022
- Beginn
- 17.02.2023
- Tage bis Beginn
- 63,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Full blood count
Immune thrombocytopenia
Platelet count decreased
Symptomtext
PT DEVELOPED SEVERE ITP IN FEBRUARY, UNCLEAR IF RELATED TO VACCINES
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Full blood count
- Hospital-Tage
- -
- Labordaten
- INITIAL PLATELET COUNT OF 5 (2/17/2023) CBC MULTIPLE DATES
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NO
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 21.03.2023
- Impfdatum
- 14.03.2023
- Beginn
- 21.03.2023
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Product administered to patient of inappropriate age
Symptomtext
Patient received a Pfizer bivalent booster for 12+ and patient should have received the Pfizer bivalent for ages 5-11.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Asthma, anxiety
- Andere Medikamente
- veniafaxine 37.5 mg XR; hydrOXYzine 10 mg; Ventolin HFA 108 mcg/act inhaler
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 02.02.2023
- Impfdatum
- 02.02.2023
- Beginn
- 02.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Wrong product administered
Symptomtext
The patient received MenQuadfi IM when he had just received Menactra IM on 1/19/23 and was supposed to received one of the meningococcal B vaccines today (Trumenba or Bexsero). Wrong vaccine given
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Cancer
- Vorgeschichte
- -
- Andere Medikamente
- Unknown
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 28.01.2023
- Impfdatum
- 24.01.2023
- Beginn
- 24.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product storage error
Symptomtext
one dose of MENQUADFI was administered post excursion,with no reported adverse event; Initial information was received on 24-Jan-2023 regarding an unsolicited valid non-serious case received from a other health professional. This case involves 16 years old male patient who reported that one dose of menquadfi was administered post excursion,with no reported adverse event while receiving vaccine 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. On 24-Jan-2023, the patient received a 0.25 ml to 2 ml dose of suspect meningococcal a-c-y-w135 (t conj) vaccine(supsection for injection) (lot U7299AB,Expiry date:04-Aug-2024) (with unknown strength) via intramuscular route in the left arm for immunization. On 24-Jan-2023 the patient developed a non-serious event of one dose of menquadfi was administered post excursion,with no reported adverse event (wrong product administered) (latency: same day) following the administration of meningococcal a-c-y-w135 (t conj) vaccine. Action taken with meningococcal vaccine (Menquadfi) was not applicable. At time of reporting, the outcome was Unknown for the event one dose of menquadfi was administered post excursion,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 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
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 26.01.2023
- Impfdatum
- 24.01.2023
- Beginn
- 01.01.2023
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
No adverse event
Symptomtext
None. Patient was given the adult dosage of Havrix, Hep A, instead of the right dosage. He denied adverse symptoms appr. 45 minutes later. I phoned him today. He denies any adverse symptoms since receiving the dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- No.
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 19.12.2022
- Impfdatum
- 30.11.2022
- Beginn
- 30.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Feeling hot
Immediate post-injection reaction
Posture abnormal
Staring
Unresponsive to stimuli
Symptomtext
Patient was to receive HPV, Flu, Menningitis & TDAP. He was given HPV & Menningitis in Lt Deltoid then flu in Rt Deltoid. Immediately after 3rd injection he had blank stare, became unresponsive & went limp into Mothers arms as she was standing behind him. I called for help & as Dr. and PA came into room patient was coming to. Vitals were taken and were within acceptable limits. Patient complained of being hot so I placed fan in room which he stated helped. Within 10 minutes patient's color had improved, he was talking and responding appropriately. He remained in room sitting in chair talking & laughing with mother & sister as she was waiting her post vaccine shot time. Patient was then discharged in care of mother with normal vital signs and no appearnt distress.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Feeling hot
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 03.10.2022
- Impfdatum
- 29.09.2022
- Beginn
- 29.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
At a clinic, pt was administered Menquadfi and TDAP due to parent's requesting vaccination, however, pt wasn't due for vaccine yet.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- Autism
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 10.09.2022
- Impfdatum
- 26.08.2022
- Beginn
- 26.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
No adverse event
Symptomtext
No reported adverse event. 2nd COVID vaccine from primary series was given on day 15 instead of waiting for 21 days as recommended by guidelines
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- None reported
- Vorgeschichte
- None reported
- Andere Medikamente
- Non reported
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 16.07.2022
- Impfdatum
- 07.07.2022
- Beginn
- 07.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect route of product administration
No adverse event
Symptomtext
menactra was given subcutaneously in the right upper arm to a patient instead of intramuscularly, no reported adverse event; Initial information was received on 12-Jul-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 12 years old male patient who experienced menactra was given subcutaneously in the right upper arm to a patient instead of intramuscularly, no reported adverse event while receiving vaccine MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE [MENACTRA]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included DIPHTHERIA VACCINE TOXOID, PERTUSSIS VACCINE ACELLULAR, TETANUS VACCINE TOXOID (TDAP) for Prophylactic vaccination. On 07-Jul-2022, the patient received 0.5 ml of suspect MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE (lot U7299AB) (formulation, strength and expiry date: unknown) via subcutaneous route in the right upper arm for routine prophylactic vaccination. On 07-JUL-2022 the patient developed a non-serious menactra was given subcutaneously in the right upper arm to a patient instead of intramuscularly, no reported adverse event (incorrect route of product administration) (Latency same day) following the administration of MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE. Action taken: not applicable. At time of reporting, the outcome was Unknown for the event menactra was given subcutaneously in the right upper arm to a patient instead of intramuscularly, 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
- Incorrect route of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -