Product image of Microgynon (Ethinylestradiol, Levonorgestrel) supplied by GNH India

Microgynon

Active Ingredient:
Ethinylestradiol, Levonorgestrel
Origin:
EU

Microgynon (Ethinylestradiol, Levonorgestrel)

Ethinylestradiol and Levonorgestrel, the active ingredients in Microgynon, are combined oral contraceptives presented as tablets for oral use. They prevent pregnancy by inhibiting ovulation, thickening cervical mucus and altering the endometrial lining.

GNH India supplies Microgynon as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Bayer Ag

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Indications & Clinical Uses

Microgynon, a combined oral contraceptive, is used to prevent pregnancy by modulating the hormonal regulation of the menstrual cycle.

  • Contraception (prevention of pregnancy): suppresses ovulation and creates an environment that reduces fertilisation.
  • Cycle regulation: provides predictable withdrawal bleeding each month.
  • Acne management: reduces androgen‑driven skin lesions in women when prescribed for this purpose.

How It Works

  • Microgynon contains ethinylestradiol, a synthetic estrogen, and levonorgestrel, a progestogen. The estrogen component stabilises the endometrial lining while the progestogen suppresses the mid‑cycle luteinising hormone surge, preventing follicular rupture. Together they thicken cervical mucus and alter the endometrium, making implantation unlikely.

Side Effects

Microgynon may cause a range of adverse reactions, most of which are mild and transient.

Common Side Effects

  • Nausea: mild stomach upset, often resolves with continued use.
  • Headache: tension‑type or migraine‑like pain.
  • Breast tenderness: temporary swelling or soreness.
  • Spotting: irregular light bleeding between periods.
  • Mood changes: irritability or mild depression.
  • Weight fluctuation: modest fluid retention.

Serious or Rare Side Effects

  • Deep vein thrombosis: painful swelling in a leg, requires urgent care.
  • Pulmonary embolism: sudden shortness of breath, chest pain.
  • Stroke: neurological deficits, facial droop, speech difficulty.
  • Myocardial infarction: chest discomfort, radiating pain.
  • Severe allergic reaction: rash, swelling, difficulty breathing.
  • Liver tumor: abnormal liver function tests, abdominal pain.

Precautions & Warnings

Before prescribing Microgynon, clinicians should evaluate individual risk factors and counsel patients on safe use.

  • Smoking: avoid use in women over 35 who smoke, due to increased thrombotic risk.
  • History of thromboembolism: contraindicated in patients with prior deep vein thrombosis or pulmonary embolism.
  • Pregnancy: discontinue immediately if pregnancy is confirmed; the product is not indicated during pregnancy.
  • Breastfeeding: consult a healthcare professional before use, as hormones may affect milk production.
  • Blood pressure monitoring: check regularly, especially in patients with hypertension.
  • Store at ambient temperature: keep below 25 °C, retain in original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Microgynon can interact with several medicines, altering its effectiveness or increasing adverse event risk.

Major Interactions (Avoid)

  • Rifampicin and other enzyme‑inducing antibiotics: reduce contraceptive efficacy.
  • Anticonvulsants such as phenytoin or carbamazepine: may diminish hormone levels.
  • HIV protease inhibitors (e.g., ritonavir): can increase hormone concentrations, raising side‑effect risk.

Moderate Interactions (Monitor Closely)

  • Antifungal agents like ketoconazole: may increase plasma levels of ethinylestradiol.
  • Selective serotonin reuptake inhibitors (SSRIs): can slightly elevate risk of bleeding.
  • Diuretics: may affect electrolyte balance, requiring periodic monitoring.

Frequently Asked Questions

Microgynon is a combined oral contraceptive tablet containing ethinylestradiol and levonorgestrel. It is prescribed to prevent pregnancy by inhibiting ovulation, thickening cervical mucus, and altering the uterine lining, providing reliable hormonal birth control for women of reproductive age.

Ethinylestradiol, a synthetic estrogen, stabilises the endometrial lining, while levonorgestrel, a progestogen, suppresses the mid‑cycle luteinising hormone surge, preventing follicular rupture. Together they also thicken cervical mucus and modify the uterine environment, making fertilisation and implantation unlikely.

The dosing regimen for Microgynon is determined by the prescribing healthcare professional. Typically, it is taken as one tablet daily for a 21‑day active phase followed by a hormone‑free interval, but the exact schedule should be confirmed with the prescriber.

Microgynon is not intended for use during pregnancy and should be discontinued if pregnancy occurs. While limited data exist for breastfeeding, the decision to use hormonal contraception while nursing should be made in consultation with a healthcare provider, weighing potential benefits and risks.

To request Microgynon, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.

Microgynon contains a specific dose of ethinylestradiol and levonorgestrel, offering a balance of efficacy and tolerability comparable to other second‑generation combined oral contraceptives. Compared with newer formulations, it may have a slightly higher risk of estrogen‑related side effects, but its clinical effectiveness in preventing pregnancy remains consistent.

Microgynon tablets should be stored at ambient temperature, preferably below 25 °C. Keep them in the original blister pack, protect from moisture and direct sunlight, and ensure the container is tightly closed to maintain product stability throughout its shelf life.

Microgynon is taken orally, with or without food, once each day at the same time. Patients should swallow the tablet whole with water and follow the prescribed cycle, typically 21 consecutive active tablets followed by a hormone‑free interval.

The most serious risks include thromboembolic events such as deep vein thrombosis, pulmonary embolism, stroke, and myocardial infarction. These events are more likely in women who smoke, are over 35, or have a personal or family history of clotting disorders. Prompt medical attention is required if symptoms arise.

Microgynon is contraindicated in women with a known hypersensitivity to its components, current pregnancy, uncontrolled hypertension, a history of thromboembolic disease, certain hormone‑dependent cancers, and in smokers over the age of 35. A thorough medical assessment is essential before initiating therapy.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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