Angeliq regulatory Post-Marketing Surveillance (PMS) is to get data about safety and efficacy in real practice for the indication approved by Korea Food and Drug Administration (KFDA). This is non-interventional , prospective, multi-center study.Target number of patients is 4500.
Study Type
OBSERVATIONAL
Enrollment
4,078
Take one tablet daily, continuously
Unnamed facility
Many Locations, South Korea
Adverse event collection
Time frame: At each visit of patient during observational period (6 months)
Improvement of menopausal symptoms
Time frame: After 6 months or at discontinuation of Angeliq (At earlier point)
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