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Re: Local ID TH140900412 / TH201409001531 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 – tired, dizzy, nauseous and feverish , involving a female patient, 80 Yrs. who was subscribed Forteo, reported the event to Lilly on 02/SEP/2014.
Please ask initial reporter in the following questions:
1. Relevant medical history
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2. It was reported patient felt feverish, did she took her temperature? If so, please mention it.
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3. Was Forteo restarted? If so please provide restart date.
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4. If Forteo was restarted, did the events re-appear or worsened after it was restarted?
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5. Please provide corrective treatment for each event.
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6. Please provide current outcome for each event.
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7. Please provide current status of Forteo.
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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: