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30/JUN/2014
Re: Local ID TH140101604 / TH201401005858 FU (2)
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 – Right ankle swelling, swelling around injection site, involving a female patient, age 69 yrs who was subscribed Forteo, reported the event to Lilly on 13/JAN/2014.
Please, contact the initial reporter and ask:
1. What was the patient s medical history?
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2. What was the patient concomitant medication?
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3. Why have patient been hospitalized in Nov-2013? Please, provide dates of admission and discharge as well as much information regarding this hospitalization as possible.
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4. Did patient started teriparatide treatment while hospitalization?
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5. Was osteoarthritis a preexisting condition to patient or did she developed the disease while on teriparatide treatment?
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6. Did patient undergo to the draining procedure? Did she receive any other corrective treatment for ankle swelling?
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7. Have patient been hospitalized after beginning treatment with teriparatide besides that hospitalization in Nov2013?
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8. Did patient recover from the events?
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9. 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: