Inhouse product
Indications
D-gest tablet is
indicated in-
Progesterone deficiencies:
Hormone Replacement
Therapy: To counteract the
effects of unopposed oestrogen on the endometrium in hormone replacement
therapy for women with disorders due to natural or surgical induced menopause
with an intact uterus.
* রেজিস্টার্ড চিকিৎসকের পরামর্শ মোতাবেক ঔষধ সেবন করুন'
Pharmacology
Dydrogesterone is an
orally-active progestogen which produces a complete secretory endometrium in an
estrogen-primed uterus thereby providing protection against the increased risk
for endometrium hyperplasia and carcinogenesis induced by estrogens. It is indicated
in all cases of endogenous progesterone deficiency. Dydrogesterone has no
estrogenic, no androgenic, no thermogenic, no anabolic and no corticoid
activity.
Dosage &
Administration
Progesterone
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.
* রেজিস্টার্ড চিকিৎসকের পরামর্শ মোতাবেক ঔষধ সেবন করুন'
Interaction
No interaction studies
have been performed.
Contraindications
Side Effects
The most commonly reported
adverse drug reactions of patients treated with D-gest in clinical trials of
indications without oestrogen treatment are
Pregnancy &
Lactation
So far there were no
indications of a harmful effect of Dydrogesterone use during pregnancy.
Dydrogesterone is excreted in the milk of nursing mothers. A risk to the
breastfed child cannot be excluded. Dydrogesterone should not be used during
breast-feeding. There is no evidence that Dydrogesterone decreases fertility.
Precautions &
Warnings
Before initiating
D-gest treatment for abnormal bleeding the etiology for the bleeding should be
clarified. Breakthrough bleeding and spotting may occur during the first months
of treatment. If breakthrough bleeding or spotting appears after some time on
therapy, or continues after treatment has been discontinued, the reason should
be investigated, which may include endometrial biopsy to exclude endometrial
malignancy.
If one of the following disorders occurs during use for the first time or gets
worse, stopping the treatment should be considered.
In cases of habitual
or threatened abortion, the viability of the fetus should be ascertained. It is
also necessary to monitor during treatment whether the pregnancy is still
progressing and whether the embryo is still alive. Treatment with D-gest has infrequently
been associated with alterations in liver function, sometimes accompanied by
clinical symptoms. Thus, D-gest should be used with caution in patients with
acute liver disease or a history of liver disease as long as liver function
tests have failed to return to normal. In cases of severe hepatic impairment
treatment should be discontinued.
Patients with a history of depression must be carefully monitored; if severe
depression recurs, treatment with D-gest must be stopped.
Overdose Effects
D-gest was well
tolerated after oral dosing (maximum daily dose is 360 mg). No reports of ill
effects from overdose have been recorded. If a large overdose is discovered
within two or three hours and treatment seems desirable, gastric lavage is
recommended. There are no specific antidotes and treatment should be
symptomatic. Aforementioned information is also applicable for overdosing in
children.
Therapeutic Class
Female Sex hormones
Storage Conditions
Store at below 30°C in
a dry place protected from light. Keep out of reach of children.
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