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Re: Local ID TH140601112 / TH201406003089 FU (1)
Thank you for reporting to us a serious 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 – Pulmonary edema, involving a male patient, 84 Yrs who was subscribed Forteo, reported the event to Lilly on 09/JUN/2014.
Please, try to contact the patient to obtain HCP information (phone number and address). After that, please try to obtain the following information from HCP:
1. Did the patient receive any concomitant medication?
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2. When did the event start?
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3. Did the event of pulmonary edema worsened or it was a new clinical episode?
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4. When was the initial date of the hospitalization?
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5. Did the patient receive any corrective treatment due to the event?
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6. Did the patient undergo any investigation? If yes, please provide: name, date, results and normal range.
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7. Was the patient discharged from the hospital? If yes, please provide the date.
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8. Did the patient recover from the event? If yes, what was the recovery date?
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9. When was the restart date of teriparatide?
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10. What was the relatedness opinion?
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Thanks
Yours sincerely,
ELI LILLY AND COMPANY
Sasithorn Suntharo
Pharmacovigilance Associate
HCP’s signature:
Date:
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For Eli Lilly internal use only
Date of Confirmation of FU request sent to HCP:
Name and Designation: