menopur multidose

menopur multidose Uses, Dosage, Side Effects, Food Interaction and all others data.

menopur multidose contains follicle stimulating hormone (FSH) and luteinizing hormone (LH) purified from the urine of postmenopausal women. It is used as a fertility medication that is injected either subcutaneously or intramuscularly. It is composed of LH with 2 subunits, alpha = 92 residues, beta = 121 residues and FSH with 2 subunits, alpha = 92 residues, beta=111 residues.

Used to treat female infertility, menopur multidose stimulates late follicular maturation and resumption of oocyte meiosis, and initiates rupture of the pre-ovulatory ovarian follicle. menopur multidose bind to the LH/hCG/FSH receptor of the granulosa and theca cells of the ovary to effect these changes in the absence of an endogenous LH surge.

menopur multidose
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Uses during Pregnancy
Uses during Breastfeeding
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Trade Name	menopur multidose
Availability	Prescription only
Generic	Menotropins
Menotropins Other Names	Human menopausal gonadotrophin, Menotrophin, Menotropin, Menotropina, Menotropins (FSH;LH)
Related Drugs	progesterone, clomiphene, Clomid, chorionic gonadotropin (hcg), Pregnyl, Menopur, Gonal-f, Follistim, Follistim AQ
Weight	600iu, 1200iu,
Type	Powder, For Solution
Formula	C₁₀₁₄H₁₆₀₉N₂₈₇O₂₉₄S₂₇
Weight	23390.3 Da
Groups	Approved
Therapeutic Class
Manufacturer	Ferring
Available Country	Saudi Arabia, Switzerland
Last Updated:	September 19, 2023 at 7:00 am

Uses

menopur multidose is a purified combination of human luteinizing hormone and follicle stimulating hormone used to treat female infertility.

For the treatment of female infertility

menopur multidose is also used to associated treatment for these conditions: Assisted Reproductive Technology therapy

How menopur multidose works

Being a combination drug, menopur multidose bind to the follicle stimulating hormone receptor (FSH), which results in ovulation in the absence of sufficient endogenous luteinizing hormone (LH). It also binds the LH receptor, thereby stimulating proper hormone release. The drug contains both FSH and LH, therefore, it induces ovarian follicular growth and development as well as gonadal steroid production in women who do not have ovarian failure. FSH is the primary driver of follicular recruitment and growth in early folliculogenesis, while LH is important for ovarian steroidogenesis and is involved in the physiological events leading to development of a competent pre-ovulatory follicle.