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Re: Global ID / Local ID: TH201412006669/ TH141202269 FU (2)
Thank you for reporting to us an adverse event related to Lilly product(s).
We would like to collect more information to better understanding the reported event.
Please respond to following question regarding the adverse event – Sepsis associated with SLE, involving a female patient, aged 59, who was subscribed Forteo, reported the event to Lilly on 15-Dec-2014.
Please provide the informatoin for following:
1. Please provide the reason teriparatide was discontinued; the date patient passed away; the cause of death.
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2. Did the patient experience worsening of SLE?
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3. Relatedness to teriparatide.
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4. Date of SLE diagnosis? Other medical history.
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5. Concomitant medications.
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6. What was the cause of death listed on the death certificate? Please provide a copy of the death certificate.
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7. What was the basis for the diagnosis of sepsis (clinical features, multiorgan failure, presence of hypotension etc – please enumerate)?
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8. Was there a primary focus of infection (please provide details)?
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9. What was the patient's baseline WBC count? At the time when the WBCs were destroyed?
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10. Please provide any diagnostic and lab results such as M, CT, EEG, Blood gases, CBC, etc.
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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: