Finished product reference
Contraceptive De
Tablet · Oral · 0.15 mg/30 µg
- List code
- 21746
- Pharmacologic class
- Combined oral contraceptive (monophasic, desogestrel + ethinylestradiol)
What it is and how it works
A monophasic combined oral contraceptive containing the third-generation progestogen desogestrel with ethinylestradiol (typically 150 micrograms/30 micrograms). It suppresses gonadotrophin release and ovulation, thickens cervical mucus and alters the endometrium.
Indications
Oral contraception.
Dosage and administration (summary)
One tablet daily at about the same time for 21 days, followed by a 7-day tablet-free interval (or as directed by the specific pack).
Contraindications
Current or past venous or arterial thromboembolism, known thrombophilia, migraine with aura, severe or multiple cardiovascular risk factors (including smoking over 35 years), severe hepatic disease or liver tumours, known or suspected sex-steroid-dependent malignancy, and undiagnosed vaginal bleeding.
Warnings and precautions
Combined hormonal contraceptives increase the risk of venous thromboembolism, and desogestrel-containing products carry a higher risk than levonorgestrel-containing ones. Blood pressure should be checked before and during use. Efficacy may be reduced by vomiting, diarrhoea and enzyme-inducing drugs.
Pregnancy
Not indicated in pregnancy; discontinue if pregnancy occurs.
Storage and supply
Store below 25 °C in the original package.
Source: reference summary prepared from the EU SmPC/EPAR, BNF and WHO Model Formulary. The approved product information in Iran governs.
Other presentations of the same active ingredient
Reference information for professional sourcing and registration enquiries, not medical advice or a promotion. Drug information is condensed from US FDA prescribing information (public domain, via openFDA and DailyMed) and does not replace the product’s approved labelling in Iran. Availability, origin and documentation are confirmed per enquiry.
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