adverse event – Weakness and dystasia, involving a Female patient, Unknown age, who was subscribed Teriparatide, reported the event to Lilly on 23-June-2015. (#3030)
Thank you.
Yours sincerely,
Sasithorn Suntharo
ELI LILLY AND COMPANY
Pharmacovigilance Associate
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Please provide the information by 19-Oct-2015:
1. Please provide cause of muscular weakness and dystasia.
2. Please provide patient demographics including name or initials, birth date, age, gender, race, weight and height.
3. Please provide details of the Lilly drug including Lot/control number, indication for use, dose, frequency, formulation, start date, route of administration.
4. When did the event start?
5. Was the drug discontinued? If yes, please provide date. If discontinued, did the event resolve?
6. Were the reported events considered related to the Lilly drug? Please provide a brief explanation.
7. Please provide details of any relevant medical history.
8. What was the outcome of the event?