FDA approves DrugsMD company Bijuva for treatment of vascular movement disorders in menopausal patients
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Last Update: 2020-06-11
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Source: Internet
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Author: User
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about 43 million women in the U.Sare in menopause, and as the ovaries stop producing estrogen, estrogen levels in the blood circulation drop, leading to VMS, often characterized by hot flashes and night sweatsToday,
TheFDA(approved by the u.SFDA) to treat vasomotor movement disorders (vasomotor symptoms, VMS) in menopausal patients, usually characterized by hot flashes and night sweatsabout Bijuva
Bijuva is a fixed-dose compounddrug(capsule) consisting of 1 mg of estrogen and 100 mg of progesteroneThis is the first FDA-approved bio-identical combination hormone replacement therapy to treat menopausal symptoms in menopausal women due to decreased hormone levels in their own hormonesthe study
more than 700 menopausal women with VMS received Bijuva or placebo treatment in a randomized double-blind, placebo-controlled, multicenter phase 3 clinicaltrial(of which VMS was conducted)results show that Bijuva is able to statistically significantly reduce the frequency and severity of VMS in patients and demonstrate good safety Bijuva is expected to be available in the second quarter of 2019, and we hope it will reduce the problems of VMS for menopausal women
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