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|a CADTH Canadian Drug Expert Committee recommendation: Ulipristal acetate (Fibristal -- Allergan Inc.)
|h Elektronische Ressource
|b indication: uterine fibroids
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|a Drug reimbursement recommendation ulipristal acetate (Fibristal)
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|a Ulipristal acetate (Fibristal -- Allergan Inc.)
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|a Version 1.0
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|a Ottawa (ON)
|b Canadian Agency for Drugs and Technologies in Health
|c November 2017, 2017
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|a 1 PDF file (8 pages)
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|a Insurance, Health, Reimbursement
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|a Canada
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|a Norpregnadienes / therapeutic use
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|a Cost-Benefit Analysis
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|a Leiomyoma / drug therapy
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|a CADTH Canadian Drug Expert Committee
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|a Canadian Agency for Drugs and Technologies in Health
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|a eng
|2 ISO 639-2
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|b NCBI
|a National Center for Biotechnology Information
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|a CADTH common drug review
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|a "Final.". - "This recommendation supersedes the CADTH Canadian Drug Expert Committee (CDEC) recommendation for this drug and indication dated November 15, 2013."
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|u https://www.ncbi.nlm.nih.gov/books/NBK540533
|3 Volltext
|n NLM Bookshelf Books
|3 Volltext
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|a 610
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|a The CADTH Canadian Drug Expert Committee (CDEC) recommends that ulipristal acetate be reimbursed for the treatment of moderate to severe signs and symptoms of uterine fibroids in adult women of reproductive age who are eligible for surgery, and the intermittent treatment of moderate to severe signs and symptoms of uterine fibroids in adult women of reproductive age, with the duration of each treatment course being three months, if the following conditions are met: Conditions: The patient is under the care of an obstetrician/gynecologist. Treatment should be limited to a maximum of four courses of therapy
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