- Staat
- AK
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 12.08.2023
- Impfdatum
- 11.08.2023
- Beginn
- 11.08.2023
- Tage bis Beginn
- 0,0
- Dosis
- 7+
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Cough
Headache
Lip pruritus
Mobility decreased
Symptomtext
Slight headache in left temple a few minutes after - thought it might be my imagination Allergy cough on the drive home - no other triggers Itchy lips about 20 minutes after - took a claritin Next day - mid morning while driving - knuckle on middle finger of left hand got sharp pain and couldn?t bend - very out of nowhere - no recent injuries and no physical activities to cause it, no history of arthritis in fingers, but I have had flare ups in knees.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Cold type virus three weeks prior
- Vorgeschichte
- Recently diagnosed celiac disease
- Andere Medikamente
- Vitamin D Calcium Magnesium Colostrum
- Allergien
- Celiac Disease Allergic to grasses, pollens, molds, animal dander Sensitive to raw fruits and vegetables
- Vorherige Impfungen
- Reactions to Covid Vaccines and Zoster - out sick feeling, fatigued, light fevers for 2-3 days
- Staat
- WI
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 13.06.2023
- Impfdatum
- 05.06.2023
- Beginn
- 09.06.2023
- Tage bis Beginn
- 4,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injected limb mobility decreased
Pain in extremity
Symptomtext
Patient reports that she had the vaccine on 06/05/23 following a cut on her right hand. Friday the pain peaked in the left arm and she continues to have pain and limited range of motion in the left arm. She was advised to be evaluated by a provider and appointment was scheduled for mid-day 06/13/23.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- To be determined at upcoming appointment.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- acne
- Andere Medikamente
- Tretinoin cream Junel FE 1/20 Bupropion XL spironolactone cetirizine
- Allergien
- Augmentin latex nickel
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 11.05.2023
- Impfdatum
- 15.04.2023
- Beginn
- 17.04.2023
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Inflammation
Pain in extremity
Paraesthesia
Symptomtext
Vaccine administered 4/15 experienced normal soreness in right arm. 4/17 started to experience a burning/tingling sensation near shoulder on right side. I was not sure if this was normal or not since I did not receive a vaccine information statement. I went back to clinic that administered vaccine 4/27. They were not able to tell me what was wrong. They stated they never saw anything like this before. They prescribed Meloxicam for pain and inflammation. As well as referred me to fill out this form and speak with the Department of Health. I spoke with them and I need a referral from my PCP to be seen. I called my PCP and I am waiting to hear back from them. Almost a month later I am still experiencing a burning/tingling sensation near my shoulder on the right side of my body.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- They have not suggested any tests to be ran as of 5/11/2023.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Depression/anxiety
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 01.11.2023
- Impfdatum
- 01.11.2023
- Beginn
- 01.11.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Dizziness
Hyperhidrosis
Nausea
Symptomtext
Pt. received 5 vaccines with 3 in the left deltoid and 2 vaccines in the right deltoid. After giving the last two vaccines Polio and HPV at 1156am in the right deltoid. The patient began to feel dizzy, nauseated, sweaty, weak. Vitals were taken at 11:57. BP 79/ 57 p- 63 O2 sats 99% temp. 97.8 Vitals were retaken again by provider and she retook them at 12:04 pm 96/63 p- 71, O2 sats 99%. Vitals retaken again at 12:07 pm, BP 99/66, p- 69, O2 sats 99, temp 97.9. Provider stated patient is at baseline. Her baseline vitals are 99/58. Patient ambulated out of the clinic with mother with the steady gait.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 8,0
- Geschlecht
- M
- Eingang
- 07.09.2023
- Impfdatum
- 21.08.2023
- Beginn
- 02.09.2023
- Tage bis Beginn
- 12,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Rash morbilliform
Rash papular
Rash pruritic
Symptomtext
Parent called to report patient has rash on face, neck, chest, back, arms, and legs. Rask is raised, itchy, no fluid/drainage, no redness. Parent reported she asked her mom to look at rash and stated rash looked like measles. Parent reported she has not used any OTC meds (topical or oral) for rash and has only bathed child with DOVE body wash. Advised parent to take child to Urgent Care for evaluation of rash, and she may use mild OTC treatment for itching (e.g., calamine lotion, Benadryl topical cream/ointment, Aveeno bath). Also explained to parent that a VAERS report would be filed to report the reaction she has reported patient had to the vaccines.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash morbilliform
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none reported
- Vorgeschichte
- none reported
- Andere Medikamente
- unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 30.08.2023
- Impfdatum
- 29.08.2023
- Beginn
- 29.08.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Discomfort
Nausea
Pain
Pyrexia
Vomiting
Symptomtext
Within 1hr following vaccination: Fevers, Chills, Rigors, Body Aches, Nausea, Vomiting. Taking Tylenol for fever and discomfort
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Erythromycin
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 05.07.2023
- Impfdatum
- 12.06.2023
- Beginn
- 13.06.2023
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Feeling abnormal
Nausea
Pyrexia
Symptomtext
Donor reported that he had a fever and nausea as well as what he described as " A spacey feeling" the day after his immunization at the donation center. He stated that his symptoms lasted 4 days and he did not report this information to us until 06/27/2023. Donor on this date reported that he was free from all symptoms and an internal donor adverse report was initiated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- As our donation center falls under a pharmaceutical manufacturer and not a health care provider no labs on donor were obtained but donor was suggested to see his personal health care provider for further evaluation.
- Aktuelle Erkrankungen
- None reported
- Vorgeschichte
- None reported.
- Andere Medikamente
- None reported
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 15.06.2023
- Impfdatum
- 01.06.2023
- Beginn
- 14.06.2023
- Tage bis Beginn
- 13,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site bruising
Injection site erythema
Injection site pain
Injection site swelling
Symptomtext
Pt reported a red circle 1 day after injection, on day 2 she comes in and shows a small bruise at injection site and a lump about 1/2 " below that measures about 1" x 1/2 ". This is sore to the pt, no redness noted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- Joint soreness, fatigue, headaches, stiffness
- Vorgeschichte
- eczema, prediabetes
- Andere Medikamente
- unknown
- Allergien
- bee pollen, hydrocodone, hydroxyzine, morphine, oxycodone, wathermellon
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 09.06.2023
- Impfdatum
- 01.06.2023
- Beginn
- 02.06.2023
- Tage bis Beginn
- 1,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Injection site erythema
Injection site pruritus
Injection site swelling
Symptomtext
Patient received the TD vaccine on 06/01/2023 and noticed the next day, 06/02/2023 that her left deltoid area around the injection side was raised and red "like a mosquito" bite. The area proceeded to grow in redness and size, along with becoming itchy and the patient decided to be seen for these symptoms on 06/08/2023.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 08.06.2023
- Impfdatum
- 03.06.2023
- Beginn
- 03.06.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Hyperhidrosis
Pallor
Symptomtext
On 06/03/2023 a approximately 15:01 the donor was pale in color, sweating and reports feeling lightheaded/dizzy and feeling of faint. Ice Pack was applied to the back of the donor's neck and Propel water given. Donor began to pink up and report that he is feeling better at 1505, skin dry to touch. Donor reported he felt faint upon during his previous tetanus immunization (1st dose). Donor leaves facility with a steady gait and in stable condition at 1513.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- Blood pressure and pulses taken by the treating medical staff member: At 15:01 Blood pressure was 87/61, pulse 57. At 15:05, blood pressure was 90/67, pulse 61. At 15:10 blood pressure was 100/72, pulse 71.
- Aktuelle Erkrankungen
- Donor disclosed no health conditions or illnesses.
- Vorgeschichte
- Donor disclosed no health conditions or illnesses.
- Andere Medikamente
- Donor has no medications recorded. Centers do not record OTC meds, supplements, etc.
- Allergien
- No known allergies.
- Vorherige Impfungen
- Donor left nurses office after receiving a tetanus vaccination and fell down. Donor stated that he began not feeling great befor
- Staat
- VA
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 03.06.2023
- Impfdatum
- 24.05.2023
- Beginn
- 24.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Injection site swelling
Product administered at inappropriate site
Symptomtext
Site: Pain at Injection Site-Severe, Site: Swelling at Injection Site-Medium, Additional Details: pt called and complained that vaccine was given too high on her arm and she is feeling pain and swelling
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 17.05.2023
- Impfdatum
- 04.04.2023
- Beginn
- 05.04.2023
- Tage bis Beginn
- 1,0
- Dosis
- N/A
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pain in extremity
Peripheral swelling
Product administered at inappropriate site
Skin warm
Symptomtext
Pt states that her vaccine was placed to low on the arm. A day or 2 after vaccine the arm swelled was arm to touch and painful. Since has resovled.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 28.12.2023
- Impfdatum
- 28.12.2023
- Beginn
- 28.12.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Feeling hot
Flushing
Symptomtext
Influenza and Td IM given per protocol observing proper technique. Patient tolerated procedure well. Observed for 15 min. felt flushed and hot at 2 pm and asked for water. Pt. stated she has not eaten breakfast nor lunch as well. Felt better at 2:17 pm, no fainting, not in any distress. Vital signs stable. Oxygen saturation on room air 98%. Awake/alert, oriented to person, place and time. NP notified of events, and pt. cleared to go home. At 2:35 pm Pt. stated she felt completely better, no dizziness, no other complaints. Vital signs stable. Instructed to go to Emergency room or call EMS if symptoms return. Pt. verbalized understanding. Discharged with mother, in stable condition.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Feeling hot
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 7,0
- Geschlecht
- M
- Eingang
- 13.12.2023
- Impfdatum
- 12.12.2023
- Beginn
- 12.12.2023
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Wrong product administered
Symptomtext
Patient should have recieved a Tdap vaccine instead of a Td vaccine (Tenivac).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- No illness at the time. Unknow for up to one month prior
- Vorgeschichte
- None reported
- Andere Medikamente
- unknown
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 13.12.2023
- Impfdatum
- 12.12.2023
- Beginn
- 12.12.2023
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Wrong product administered
Symptomtext
Patient should have received Tdap (Boostix) vaccine not Td Absorbed (Tenivac). No treatment. Outcome: Patient will receive Tdap vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- No illness at the time of vaccination. Unknown about up to one month prior.
- Vorgeschichte
- None reported
- Andere Medikamente
- Unknown
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 06.11.2023
- Impfdatum
- 06.11.2023
- Beginn
- 06.11.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
No adverse event
Symptomtext
Extra dose of Varivax administered. Vaccine was not necessary, no symptoms reported
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 7,0
- Geschlecht
- M
- Eingang
- 03.10.2023
- Impfdatum
- 05.09.2023
- Beginn
- 05.09.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 10,0
- Geschlecht
- M
- Eingang
- 03.10.2023
- Impfdatum
- 05.09.2023
- Beginn
- 05.09.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 8,0
- Geschlecht
- F
- Eingang
- 29.09.2023
- Impfdatum
- 06.09.2023
- Beginn
- 06.09.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 0,8
- Geschlecht
- F
- Eingang
- 16.09.2023
- Impfdatum
- 07.09.2023
- Beginn
- 07.09.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Medication error
No adverse event
Product administered to patient of inappropriate age
Symptomtext
9 month old patient was administered TENIVAC with no reported adverse event; Initial information received on 07-Sep-2023 regarding an unsolicited valid non-serious case received from a consumer/non-healthcare professional. This case involves 9-month-old patient was administered diphtheria-2/tetanus-5 adsorbed toxoids NO preservative adult [Tenivac] with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 07-Sep-2023, the patient received a dose of suspect Diphtheria-2/Tetanus-5 Adsorbed Toxoids No Preservative Adult Suspension for injection lot U7745AA expiry date: 20-May-2025 via unknown route in the right thigh for immunization and 9 month old patient was administered tenivac with no reported adverse event (product administered to patient of inappropriate age) on the same day following the administration of Diphtheria-2/Tetanus-5 Adsorbed Toxoids No Preservative Adult. Action taken was not applicable. At time of reporting, the outcome was Unknown for the event 9 month old patient was administered tenivac 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
- Medication error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 24.07.2023
- Impfdatum
- 24.07.2023
- Beginn
- 24.07.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Fluoxetine HCI 20 mg capsule
- Allergien
- Sulfamethoxzaole, Penicillin G Benzathine
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 14.07.2023
- Impfdatum
- 13.07.2023
- Beginn
- 13.07.2023
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Symptomtext
Tdap booster due and Td given
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- F
- Eingang
- 07.07.2023
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Exposure during pregnancy
Medication error
Wrong product administered
Symptomtext
pregnant patient came into the clinic wanting to receive boostrix, however the patient was administered tenivac instead with no reported adverse event; pregnant patient came into the clinic wanting to receive boostrix, however the patient was administered tenivac instead with no reported adverse event; Initial information received on 05-Jul-2023 regarding an unsolicited valid non-serious case received from a pharmacist. This case involves an unknown age female patient who was pregnant and was exposed to Diphtheria-2/Tetanus-5 Adsorbed Toxoids No Preservative Adult [Tenivac] and Diphtheria Vaccine Toxoid, Pertussis Vaccine Acellular 3-Component, Tetanus Vaccine Toxoid (Boostrix). Data regarding this pregnancy were received prospectively, i.e. before pregnancy outcome was known. The date of last menstrual period was not reported. The estimated due date was not reported. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. The patient had unknown previous pregnancy/ies. On an unknown date, the patient received 0.5 ml of suspect Diphtheria-2/Tetanus-5 Adsorbed Toxoids No Preservative Adult Suspension for injection (lot number: U7745AA; Expiry date: 20-May-2024) (Frequency: Once; Strength: Standard) via intramuscular route in the right side (Site unspecified) for immunization. On an unknown date, the patient received an unknown dose of suspect Diphtheria Vaccine Toxoid, Pertussis Vaccine Acellular 3-Component, Tetanus Vaccine Toxoid not produced by Sanofi Pasteur (with an unknown formulation, strength, expiry date and lot number) via unknown route in unknown administration site for prophylactic vaccination (Immunisation). On an unknown date, the pregnant patient came into the clinic wanting to receive Diphtheria Vaccine Toxoid, Pertussis Vaccine Acellular 3-Component, Tetanus Vaccine Toxoid, however the patient was administered Diphtheria-2/Tetanus-5 Adsorbed Toxoids No Preservative Adult instead with no reported adverse event (exposure during pregnancy) (wrong product administered) (latency: same day). It was reported, calling on behalf of patient regarding administration of Tenivac. Caller stated that she has questions regarding the administration of Tenivac and another product for a pregnant patient. Caller states that a pregnant patient came into the clinic wanting to receive Boostrix, however the patient was administered TENIVAC instead. Caller would like to know if there is a minimum time interval before Tdap can be administered? Caller would like to know if there is any concern for fetal toxicity/harm with receiving two doses of diphtheria and tetanus? Action taken: not applicable for both suspects Outcome: Unknown Additionally, at time of reporting, the outcome of the pregnancy is unknown. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in the Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Exposure during pregnancy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 24.03.2023
- Impfdatum
- 21.03.2023
- Beginn
- 23.03.2023
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Oedema peripheral
Swelling
Symptomtext
pt stated swelling under arm pit up to her neck swelling started 3-23-23
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oedema peripheral
- Hospital-Tage
- -
- Labordaten
- Pt visit with MD/Primary care was told by MD everything was fine
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- Asthma Acute Bronchitis Pain Vertigo
- Andere Medikamente
- Metoprolol Hydroxyzine Pam Difulcan 150 Escitalopram Triamcinolone Premarin Vag cream
- Allergien
- Macrolide Ketolides
- Vorherige Impfungen
- -