Dinogest Tablet

Dinogest is indicated for the treatment of endometriosis. Dinogest belongs to the class of medications called progestins. Progestins reduce the effects of estrogen on tissues such as the endometrium (lining of the uterus) and the breast. By reducing the growth effect of estrogen on the endometrium, Dinogest helps to reduce the pelvic pain experienced by women with endometriosis.

Dienogest acts as an agonist at the progesterone receptor (PR) with weak affinity that is comparable to that of progesterone but has a very potent progestagenic effect in the endometrium, causing endometrial atrophy after prolonged use. It promotes antiproliferative, immunologic and antiangiogenic effects on endometrial tissue. Dienogest reduces the level of endogenous production of oestradiol and thereby suppressing the trophic effects of oestradiol on both the eutopic and ectopic endometrium. Continous administration of dienogest results in hyperprogestogenic and moderately hypoestrogenic endocrine environment, which causes initial decidualization of endometrial tissue. It is an antagonist at androgen receptors, improve androgenic symptoms such as acne and hirsutism [A16570].

Tablet-taking can be started on any day of the menstrual cycle. The dosage of Dienogest is 2 mg daily without any break, taken preferably at the same time each day with some liquid as needed. Tablet must be taken continuously without regard to vaginal bleeding. When a pack is finished, the next one should be started without interruption.

In the event of missed tablet(s), the woman should take 2 mg only, as soon as she remembers, and should then continue the next day to take the tablet at her usual time. A tablet not absorbed due to vomiting or diarrhea should likewise be replaced by 2 mg.

Progestogens including Dinogest are metabolized mainly by the cytochrome P450 3A4 system . Therefore, inducers or inhibitors of CYP3A4 may affect the progestogen drug metabolism. Known CYP3A4 inhibitors like azole antifungals (e.g, ketoconazole, itraconazole, fluconazole), cimetidine, verapamil, macrolides (e.g, erythromycin, clarithromycin and roxithromycin), diltiazem, protease inhibitors (e.g, ritonavir, saquinavir, indinavir, nelfinavir), antidepressants (e.g, nefazodone, fluvoxamine, fluoxetine) may increase plasma levels of progestogens and result in adverse reactions.

Hypersensitivity to dienogest or to any of the excipients of Dienogest. Dienogest should not be used in the presence of any of the conditions such as, Active venous thromboembolic disorder; arterial and cardiovascular disease, (e.g, myocardial infarction, cerebrovascular accident, ischemic heart disease); diabetes mellitus with vascular involvement; presence or history of severe hepatic disease as long as liver function values have not returned to normal; presence or history of liver tumors (benign or malignant); known or suspected sex hormone-dependent malignancies and undiagnosed vaginal bleeding.

Undesirable effects are more common during the 1st months after start of intake of Dinogest, and subside with duration of treatment. The following undesirable effects have been reported in users of Dinogest. The most frequently reported undesirable effects during treatment that were considered at least possibly related to Dinogest were headache (9%), breast discomfort (5.4%), depressed mood (5.1%) and acne (5.1%).

• Nervous System Disorders: Headache, migraine.
• Cardiac Disorders: Uncommon: Unspecified circulatory system disorder, palpitations.
• Vascular Disorders: Uncommon: Hypotension.
• Gastrointestinal Disorders: Common: Nausea, abdominal pain, flatulence.
• Metabolism and nutrition disorders: Weight increase (3.6%)
• Psychiatric Disorders: Depressed mood, irritability, nervousness, altered mood.

There are limited data from the use of Dienogest in pregnant women. Animal studies and data from women exposed to Dienogest during pregnancy reveal no special risks on pregnancy, embryonic/fetal development, birth or development after birth for humans. However, Dienogest should not be administered to pregnant women because there is no need to treat endometriosis during pregnancy.

Treatment with Dienogest during lactation is not recommended. Physiochemical properties and animal data indicate excretion of Dienogest in breast milk. A decision must be made whether to discontinue breastfeeding or to abstain from Dienogest therapy taking into account the benefit of breastfeeding for the child and the benefit of therapy for the woman.

Before starting Dinogest treatment, pregnancy must be excluded. During treatment, patients are advised to use nonhormonal methods of contraception (e.g, barrier method) if contraception is required.

As Dinogest is a progestogen-only preparation, it can be assumed that special warnings and special precautions for use of other progestogen-only preparations are also valid for the use of Dinogest .

• Changes in Bleeding Pattern: Dinogest treatment affects the menstrual bleeding pattern in the majority of women.
• Hepatic Impairment: Dinogest is contraindicated in patients with present or past severe hepatic disease.
• Impairment of Fertility: Based on available data, ovulation is inhibited in the majority of patients during treatment with Dinogest. However, Dinogest is not a contraceptive. If contraception is required, a nonhormonal method should be used.

Use in Children: Dinogest is not indicated in children prior to menarche. The safety and efficacy of Dinogest in adolescents (menarche to 18 years) has not yet been established.

Use in the Elderly: There is no relevant indication for the use of Dinogest in the geriatric population.

Acute toxicity studies performed with Dinogest did not indicate a risk of acute adverse effects in case of inadvertent intake of a multiple of the daily therapeutic dose. There is no specific antidote. Dinogest 20-30 mg/day (10-15 times higher dose than in Dinogest) over 24 weeks of use were very well tolerated.

Female Sex hormones

Keep below 30°C temperature, away from light & moisture. Keep out of the reach of children.