__________________________________________________________________________________________
Re: Local ID TH140104733 / TH201407003022 FU (1)
Thank you for reporting to us an adverse event related to Lilly product.
We would like to collect more information to better understanding the reported event.
Please respond to following questions regarding the adverse event – Dizziness, Nausea, Vomit and worsening renal test value, involving a female patient who was subscribed Forteo, reported the event to Lilly on 09/JAN/2014.
Please attempt to obtain the contact information of the HCP of the patient. If HCP contact information is obtained, please send the following questions:
1. Please provide the laboratory results, with dates and units, related to the event of worsening renal test value:
____________________________________________________________________________
____________________________________________________________________________
____________________________________________________________________________
2. Was the renal test value wrong before starting Forteo?
____________________________________________________________________________
____________________________________________________________________________
____________________________________________________________________________
3. It was reported that the patient was reducing the pain relief pill, why was the pain relief pill being reduced?
____________________________________________________________________________
____________________________________________________________________________
____________________________________________________________________________
4. What was the name of the pain relief pill?
____________________________________________________________________________
____________________________________________________________________________
____________________________________________________________________________
5. What was the dosage regimen and start date of Forteo?
____________________________________________________________________________
____________________________________________________________________________
____________________________________________________________________________
6. Were the following events related to Forteo?
____________________________________________________________________________
____________________________________________________________________________
____________________________________________________________________________
7. Please provide rationale of:
- Dizziness:
____________________________________________________________________________
____________________________________________________________________________
____________________________________________________________________________
- Vomiting:
____________________________________________________________________________
____________________________________________________________________________
____________________________________________________________________________
- Nausea:
____________________________________________________________________________
____________________________________________________________________________
____________________________________________________________________________
- Worsening renal test value:
____________________________________________________________________________
____________________________________________________________________________
____________________________________________________________________________
Thanks
Yours sincerely,
ELI LILLY AND COMPANY
Sasithorn Suntharo
Pharmacovigilance Associate
HCP’s signature:
Date:
__________________________________________________________________________________
For Eli Lilly internal use only
Date of Confirmation of FU request sent to HCP:
Name and Designation:
__________________________________________________________________________________________
Re: Local ID TH140104733 / TH201407003022 FU (1)
Thank you for reporting to us an adverse event related to Lilly product.
We would like to collect more information to better understanding the reported event.
Please respond to following questions regarding the adverse event – Dizziness, Nausea, Vomit and worsening renal test value, involving a female patient who was subscribed Forteo, reported the event to Lilly on 09/JAN/2014.
Please attempt to obtain the contact information of the HCP of the patient. If HCP contact information is obtained, please send the following questions:
1. Please provide the laboratory results, with dates and units, related to the event of worsening renal test value:
____________________________________________________________________________
____________________________________________________________________________
____________________________________________________________________________
2. Was the renal test value wrong before starting Forteo?
____________________________________________________________________________
____________________________________________________________________________
____________________________________________________________________________
3. It was reported that the patient was reducing the pain relief pill, why was the pain relief pill being reduced?
____________________________________________________________________________
____________________________________________________________________________
____________________________________________________________________________
4. What was the name of the pain relief pill?
____________________________________________________________________________
____________________________________________________________________________
____________________________________________________________________________
5. What was the dosage regimen and start date of Forteo?
____________________________________________________________________________
____________________________________________________________________________
____________________________________________________________________________
6. Were the following events related to Forteo?
____________________________________________________________________________
____________________________________________________________________________
____________________________________________________________________________
7. Please provide rationale of:
- Dizziness:
____________________________________________________________________________
____________________________________________________________________________
____________________________________________________________________________
- Vomiting:
____________________________________________________________________________
____________________________________________________________________________
____________________________________________________________________________
- Nausea:
____________________________________________________________________________
____________________________________________________________________________
____________________________________________________________________________
- Worsening renal test value:
____________________________________________________________________________
____________________________________________________________________________
____________________________________________________________________________
Thanks
Yours sincerely,
ELI LILLY AND COMPANY
Sasithorn Suntharo
Pharmacovigilance Associate
HCP’s signature:
Date:
__________________________________________________________________________________
For Eli Lilly internal use only
Date of Confirmation of FU request sent to HCP:
Name and Designation:
การแปล กรุณารอสักครู่..