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

Leandra

Active Ingredient:
Ethinylestradiol, Levonorgestrel
Origin:
EU

Leandra (Ethinylestradiol, Levonorgestrel)

Ethinylestradiol, the active ingredient in Leandra, is a combined oral contraceptive presented as a tablet for oral use. It prevents pregnancy in women of reproductive age by suppressing ovulation and altering cervical mucus.
GNH India supplies Leandra as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Medrx Licences Limited

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Indications & Clinical Uses

Leandra, a combined oral contraceptive, acts on the hormonal regulation of the menstrual cycle.

  • Contraception: Prevents pregnancy by inhibiting ovulation and modifying cervical mucus.
  • Menstrual cycle regulation: Provides predictable monthly bleeding and reduces irregular periods.
  • Acne treatment: Improves moderate acne associated with androgen excess in women.

How It Works

  • Ethinylestradiol and levonorgestrel bind to estrogen and progesterone receptors, respectively, providing negative feedback to the hypothalamic‑pituitary axis. This suppresses the release of luteinizing hormone (LH) and follicle‑stimulating hormone (FSH), preventing follicular development and ovulation. The progestin component also thickens cervical mucus and induces endometrial changes that reduce the likelihood of implantation.

Side Effects

Leandra 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: swelling or discomfort in the breasts.
  • Spotting or breakthrough bleeding: irregular light bleeding.
  • Mood changes: irritability or mild depression.
  • Weight gain: modest increase in body weight.

Serious or Rare Side Effects

  • Venous thromboembolism: deep‑vein clot formation.
  • Pulmonary embolism: clot migration to the lungs.
  • Stroke: cerebrovascular accident, especially in high‑risk individuals.
  • Myocardial infarction: heart attack risk in susceptible patients.
  • Severe hypertension: sudden rise in blood pressure.
  • Liver tumor: benign hepatic adenoma development.

Precautions & Warnings

Before prescribing Leandra, clinicians should evaluate patient risk factors and counsel on safe use.

  • Smoking: avoid use in women over 35 who smoke due to increased clot risk.
  • History of thromboembolism: contraindicated in patients with prior clotting events.
  • Liver disease: use with caution in active liver disease or dysfunction.
  • Hypertension: monitor blood pressure regularly; discontinue if uncontrolled.
  • Drug interactions: review concomitant medications that may reduce efficacy.
  • Store at ambient temperature: keep below 25°C, protect from moisture and keep in original packaging.

Avoid Interactions

Leandra can interact with several medicines, altering its effectiveness or safety profile.

Major Interactions (Avoid)

  • Strong CYP3A4 inducers (e.g., rifampin, carbamazepine, phenytoin): may markedly reduce contraceptive efficacy.
  • Other estrogen‑containing products (e.g., hormone replacement therapy): increase risk of thrombotic events.
  • Anticoagulants (e.g., warfarin): may enhance clotting risk.

Moderate Interactions (Monitor Closely)

  • Antifungals such as ketoconazole: may increase hormone levels.
  • Antiretrovirals (e.g., efavirenz): may lower contraceptive effectiveness.
  • St. John's wort: may modestly reduce hormone concentrations.
  • Certain antibiotics (e.g., griseofulvin): may slightly diminish efficacy.

Frequently Asked Questions

Leandra is a combined oral contraceptive that is prescribed to prevent pregnancy and to help regulate the menstrual cycle in women of reproductive age. It works by delivering both estrogen and progestin to suppress ovulation and modify cervical mucus.

Ethinylestradiol, the estrogen component, binds to estrogen receptors and provides negative feedback to the hypothalamus and pituitary gland. This reduces the release of luteinizing hormone and follicle‑stimulating hormone, helping to prevent the surge that triggers ovulation.

The specific dosing regimen for Leandra is determined by the prescribing clinician based on the product’s labeling and the patient’s individual needs. Healthcare providers select the appropriate tablet strength and schedule according to standard contraceptive guidelines.

Leandra is intended for use only when a woman is not pregnant. If pregnancy occurs, the medication should be stopped immediately. Limited data are available for breastfeeding; clinicians usually advise against use while nursing unless the benefits outweigh potential risks.

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

Leandra contains the same active ingredients—ethinylestradiol and levonorgestrel—as many other combined oral contraceptives. Its efficacy, safety profile and side‑effect spectrum are comparable, with differences mainly in tablet formulation, packaging and regulatory approvals in specific markets.

Leandra 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 store out of reach of children.

Leandra is taken orally, usually once daily at the same time each day, following the regimen indicated on the product label (e.g., 21 active tablets followed by a pill‑free interval). Patients should swallow the tablet whole with water.

The most serious risks include venous thromboembolism, pulmonary embolism, stroke, myocardial infarction and severe hypertension. These events are rare but can be life‑threatening, especially in women with pre‑existing risk factors such as smoking, clotting disorders or uncontrolled hypertension.

Leandra is contraindicated in women who are pregnant, have a history of thromboembolic disease, uncontrolled hypertension, active liver disease, known or suspected breast cancer, or who are over 35 and smoke. It should also be avoided in patients with known hypersensitivity to any component of the tablet.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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