Détails du rapport Vaer
Âge: N/A
Genre: Female
Région : Outside US
- Patient décédé?
- Non
- Renseignements sur les vaccins
-
Nom: COVID19 (COVID19 (PFIZER-BIONTECH))
Type : Coronavirus 2019 vaccine
Fabricant: PFIZER
Lot: unknown
- Date de réception du rapport
- 2022-03-04
- Date à laquelle le formulaire est complèté
- Date de vaccination
- Date d’apparition
- 0
- Nombre de jours (date d’apparition – date de vaccination)
- 0
- Description de l’événement indésirable
-
my husband and i got sick and we were home together for weeks without separation; my husband and i got sick and we were home together for weeks without separation; i had mild symptoms, postcovid symptoms are fatigue, weakness, internal stress remained; i had mild symptoms, postcovid symptoms are fatigue, weakness, internal stress remained; i had mild symptoms, postcovid symptoms are fatigue, weakness, internal stress remained; i had mild symptoms, postcovid symptoms are fatigue, weakness, internal stress remained; i still breastfeed in the evenings, my little son will be 5 this year; i still breastfeed in the evenings, my little son will be 5 this year; this is a spontaneous report received from a contactable reporter(s) (consumer or other non hcp) from medical information team. the reporter is the patient. a 43 year-old female patient received bnt162b2 (comirnaty) (batch/lot number: unknown) as dose 3 (booster), single, (batch/lot number: unknown) as dose 2, single and (batch/lot number: unknown) as dose 1, single for covid-19 immunisation. relevant medical history included: "breast feeding" (ongoing). the patient's concomitant medications were not reported. the following information was reported: drug ineffective (medically significant), suspected covid-19 (medically significant), outcome "unknown" and all described as "my husband and i got sick and we were home together for weeks without separation"; post-acute covid-19 syndrome (non-serious), fatigue (non-serious), asthenia (non-serious), stress (non-serious), outcome "unknown" and all described as "i had mild symptoms, postcovid symptoms are fatigue, weakness, internal stress remained"; off label use (non-serious), product use issue (non-serious), outcome "unknown" and all described as "i still breastfeed in the evenings, my little son will be 5 this year". the clinical course was reported as follows: " i still breastfeed in the evenings; my little son will be 5 this year. i think we have done our best to prevent this thanks to this. my little boy is fine, even if he got it, he went through it asymptomatically. probably yes, because my husband and i got sick, we were home together for weeks without separation. i had mild symptoms, post covid symptoms are fatigue, weakness, internal stress remained". the lot number for bnt162b2 was not provided and will be requested during follow up. follow-up (14feb2022): this is a spontaneous follow-up report received from a contactable consumer (patient). updated information: new events (off label use, drug use in unapproved population, covid-19, drug ineffective, post-covid syndrome, fatigue, stress, weakness) and clinical course. the lot number for bnt162b2 was not provided and will be requested during follow up.; sender's comments: linked report(s) : hu-pfizer inc-202200290569 same vaccine/reporter, different dose/event/patient (child case)
- Données de laboratoire
-
na
- Liste des symptômes
-
drug ineffective fatigue asthenia product use issue off label use stress suspected covid-19 post-acute covid-19 syndrome
- Patient décédé?
- Non
- Date de décès
- N/A
- Anomalie congénitale
- false
- Vaccin administré par :
- Other
- Vaccin acheté par :
- Inconnu
- Visite d’un patient à l’urgence?
- Non
- Patient hospitalisé?
- Non
- Séjour à l’hôpital
- Non
- Nombre de jours à l’hôpital
- Non spécifié
- Invalidité permanente?
- Non
- Allergies:
-
na
- Maladie actuelle
-
breast feeding