Inhouse product
Dydrogesterone
Hormone Replacement Treatment: To counteract the effects of unopposed oestrogen on the endometrium in women with problems owing to natural or surgically induced menopause who have an intact uterus when using hormone replacement therapy.
Dydrogesterone is an orally active progestogen that creates a full secretory endometrium in an oestrogen-primed uterus, hence protecting against oestrogen-induced endometrial hypertrophy and carcinogenesis. It's used to treat endogenous progesterone insufficiency in all situations. Dydrogesterone doesn't have any oestrogenic, androgenic, thermogenic, anabolic, or corticoid properties.
Always take Presentation 10 mg tablet exactly as your doctor has prescribed.
Presentationerone deficiencies:
Hormone Replacement Therapy: In combination with continuous oestrogentherapy, take one tablet daily for 14 consecutive days of a 28 day cycle. In combination with cyclical oestrogen therapy take one tablet daily during the last 12 to 14 days of oestrogen therapy. For doctors: If endometrial biopsies or ultrasound reveal inadequate Presentationational response, 20 mg Dydrogesterone should be prescribed. For patients: If you are not sure what type of oestrogen therapy you are on, talk to your Doctor before taking Presentation. There is no relevant use of Dydrogesterone before menarche. The safety and efficacy of Dydrogesterone in adolescents aged 12 to 18 years has not been established.
Hypersensitivity to the active ingredient or any of the excipients is known. Progestogen-dependent neoplasms that are known or suspected (e.g. meningioma).
Migraines/headaches, nausea, menstruation abnormalities, and breast pain/tenderness are the most commonly reported adverse medication responses in patients treated with Dydrogesterone in clinical studies of reasons without oestrogen therapy.
More than 10 million pregnancies are thought to have been exposed to Dydrogesterone. There have been no reports of Dydrogesterone use during pregnancy causing harm. Dydrogesterone excretion in mother's milk is unknown. Progestogens and their metabolites transfer to the mother's milk in tiny amounts, according to previous experience with other progestogens. It's unclear whether the child is in danger. As a result, Dydrogesterone should be avoided during lactation.
The etiology of irregular bleeding should be determined prior to starting dydrogesterone medication. During the first several months of treatment, you may experience breakthrough bleeding and spotting. If breakthrough bleeding or spotting occurs after a period of treatment or persists after treatment has been stopped, the cause should be examined, which may include an endometrial biopsy to rule out endometrial cancer. Stopping the medication should be considered if one of the following disorders appears for the first time or worsens during use.
Female Sex hormones
Store below 30°C in a dry, light-protected location. Keep out of children's reach.
Incepta Pharmaceuticals Ltd.
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