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

Microlite

Active Ingredient:
Ethinylestradiol, Levonorgestrel
Origin:
EU

Microlite (Ethinylestradiol, Levonorgestrel)

Ethinylestradiol and Levonorgestrel, the active ingredients in Microlite, are a combined oral contraceptive presented as an oral tablet for oral use. It prevents pregnancy in women of reproductive age by suppressing ovulation and altering cervical mucus.

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

Manufacturer / TM Owner

Bayer Ltd

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Indications & Clinical Uses

Microlite, a combined oral contraceptive, is indicated for hormonal contraception to prevent unintended pregnancy.

  • Pregnancy prevention: provides reliable contraception by inhibiting ovulation and preventing implantation.
  • Menstrual cycle regulation: helps achieve more predictable bleeding patterns and reduces menstrual discomfort.
  • Acne improvement: may lessen androgen‑related skin lesions in some women.

How It Works

  • Microlite contains ethinylestradiol and levonorgestrel, which bind to estrogen and progesterone receptors respectively. The combination suppresses the mid‑cycle surge of luteinising hormone (LH) and follicle‑stimulating hormone (FSH), thereby inhibiting ovulation. It also thickens cervical mucus and induces endometrial changes that reduce the likelihood of sperm penetration and implantation.

Side Effects

Common Side Effects

  • Nausea: mild to moderate stomach upset.
  • Headache: tension‑type or migraine‑like pain.
  • Breast tenderness: temporary swelling or discomfort.
  • Spotting: irregular breakthrough bleeding.
  • Weight fluctuation: mild fluid retention.
  • Mood changes: irritability or mild depression.

Serious or Rare Side Effects

  • Thromboembolic events: deep vein thrombosis or pulmonary embolism.
  • Hypertensive crisis: sudden severe high blood pressure.
  • Liver dysfunction: jaundice or abnormal liver enzymes.
  • Severe allergic reaction: rash, swelling, or anaphylaxis.
  • Vision changes: sudden loss of vision or eye pain.
  • Gallbladder disease: inflammation or stones.

Precautions & Warnings

Before using Microlite, consider the following precautions to ensure safe and effective use.

  • Smoking status: avoid use if over 35 and a smoker due to increased cardiovascular risk.
  • Cardiovascular history: assess for hypertension, stroke, or clotting disorders.
  • Liver disease: use with caution in patients with hepatic impairment.
  • Migraine with aura: contraindicated because of stroke risk.
  • Breast cancer history: avoid as hormones may stimulate tumor growth.
  • Store at ambient temperature: keep below 25 °C, in the original packaging, protected from moisture and light.

Avoid Interactions

Microlite can interact with several medicines that alter its effectiveness or increase adverse risks.

Major Interactions (Avoid)

  • Anticoagulants (e.g., warfarin): may reduce contraceptive efficacy and alter clotting.
  • Certain antiepileptics (e.g., carbamazepine, phenytoin): increase hormone metabolism, lowering effectiveness.
  • Rifampicin: induces hepatic enzymes, decreasing plasma levels of ethinylestradiol and levonorgestrel.

Moderate Interactions (Monitor Closely)

  • Antifungals (e.g., ketoconazole): may increase hormone concentrations, raising side‑effect risk.
  • St. John’s wort: can reduce contraceptive effectiveness.
  • Certain antibiotics (e.g., tetracycline): may slightly diminish hormone levels.

Frequently Asked Questions

Microlite is a combined oral contraceptive containing ethinylestradiol and levonorgestrel. It is prescribed to prevent pregnancy in women of reproductive age by inhibiting ovulation and creating cervical mucus conditions that are unfavorable for sperm.

Ethinylestradiol, an estrogen component, binds to estrogen receptors and works together with levonorgestrel to suppress the mid‑cycle surge of luteinising hormone (LH) and follicle‑stimulating hormone (FSH). This prevents the release of an egg and also stabilises the endometrial lining.

The specific dosing regimen for Microlite is determined by the prescribing clinician based on the product’s labeling and the patient’s individual health profile. Patients should follow the prescriber’s instructions and not alter the dose on their own.

Microlite is classified as pregnancy category X, meaning it must not be used during pregnancy because it can cause fetal harm. It is also not recommended while breastfeeding, as hormones may pass into breast milk and affect the infant.

To order Microlite, 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.

Microlite contains the standard dose combination of ethinylestradiol and levonorgestrel, which is widely used and well‑studied. Compared with other formulations that may use different progestins or estrogen doses, Microlite offers a balance of efficacy and tolerability that aligns with many clinical guidelines.

Microlite 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.

Microlite is taken orally, usually once daily at the same time each day. The tablet is swallowed with water and should be started on the first day of the menstrual cycle or as directed by a healthcare professional.

The most serious risks include thromboembolic events such as deep‑vein thrombosis or pulmonary embolism, severe hypertension, and rare liver disorders. Patients should seek immediate medical attention if they experience unexplained leg pain, shortness of breath, severe headache, or jaundice.

Microlite is contraindicated in women who are pregnant, have a history of thromboembolic disease, uncontrolled hypertension, certain cancers (e.g., estrogen‑dependent breast cancer), liver disease, or who are smokers over the age of 35. It should also be avoided in individuals with known hypersensitivity to any component of the tablet.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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