Mail gekregen van Allergan
Geplaatst: 19 aug 2020 08:15
Ik heb een klacht ingediend bij Allergan en kreeg zojuist de volgende reactie:
Thank you for reporting the adverse event to us and sorry to hear about the problems you have experienced.
This case has now been logged under Allergan Reference: PR 2247499 & PR 2247501. Please could you kindly quote this Allergan reference number in all future correspondence.
I work in Product Surveillance and my department collects safety information with regards to Allergan Medical devices and reporting adverse events to regulatory authorities. In order to progress your complaint, please could I request your consent to collect the following information:
· Date the adverse event on your breast implants (left and right) was first noticed? How did the adverse event occur?
· Breast Device Details (Serial Number/Lot Number/CatLog Number)
· Left
· Right
· Name of Implanting Surgeon?
· Name of Implanting Institution?
· Explanting Date (If you have one scheduled with your surgeon, if not please advise)?
· Name of Explanting Surgeon?
· Name of Explanting Institution?
· Contact details of both surgeons/secretary’s details? (please include email address if available)*
· Permission to contact both surgeons/secretary’s details?*
*Please note without your permission to contact your physicians and their contact details we will be unable to proceed any further with your complaint. Once permission and details are provided we will contact them directly to progress the complaint with their assistance. Your physicians should remain your primary point of contact.
Kind Regards,
cid:image005.jpg@01D63554.9C744980
LORENZ AGUJETAS
WIPRO Contingent Worker for and on behalf of
Wie heeft dit ook gedaan en weet wat er nu verder gaat gebeuren?
Ik heb trouwens gewoon antwoord gegeven op alles.
Thank you for reporting the adverse event to us and sorry to hear about the problems you have experienced.
This case has now been logged under Allergan Reference: PR 2247499 & PR 2247501. Please could you kindly quote this Allergan reference number in all future correspondence.
I work in Product Surveillance and my department collects safety information with regards to Allergan Medical devices and reporting adverse events to regulatory authorities. In order to progress your complaint, please could I request your consent to collect the following information:
· Date the adverse event on your breast implants (left and right) was first noticed? How did the adverse event occur?
· Breast Device Details (Serial Number/Lot Number/CatLog Number)
· Left
· Right
· Name of Implanting Surgeon?
· Name of Implanting Institution?
· Explanting Date (If you have one scheduled with your surgeon, if not please advise)?
· Name of Explanting Surgeon?
· Name of Explanting Institution?
· Contact details of both surgeons/secretary’s details? (please include email address if available)*
· Permission to contact both surgeons/secretary’s details?*
*Please note without your permission to contact your physicians and their contact details we will be unable to proceed any further with your complaint. Once permission and details are provided we will contact them directly to progress the complaint with their assistance. Your physicians should remain your primary point of contact.
Kind Regards,
cid:image005.jpg@01D63554.9C744980
LORENZ AGUJETAS
WIPRO Contingent Worker for and on behalf of
Wie heeft dit ook gedaan en weet wat er nu verder gaat gebeuren?
Ik heb trouwens gewoon antwoord gegeven op alles.
