Product image of Leverette (Ethinylestradiol, Levonorgestrel | Lactose) supplied by GNH India

Leverette

Active Ingredient:
Ethinylestradiol, Levonorgestrel | Lactose
Origin:
EU

Leverette (Ethinylestradiol, Levonorgestrel | Lactose)

Ethinylestradiol / Levonorgestrel, the active ingredient in Leverette, is a combined estrogen‑progestogen oral contraceptive presented as a tablet for oral use. It works to prevent pregnancy by inhibiting ovulation, thickening cervical mucus and altering the endometrial lining in women of reproductive age.

GNH India supplies Leverette as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, providing reliable access to this hormonal contraceptive for qualified prescribers. The company adheres to EU quality standards and offers comprehensive logistics support for global distribution.

Manufacturer / TM Owner

Exeltis Czech S.R.O.

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Indications & Clinical Uses

Leverette, a combined estrogen‑progestogen oral contraceptive, is indicated for hormonal contraception.

  • Prevention of pregnancy: provides reliable reversible contraception for women of reproductive age.
  • Family planning: enables planned intervals between pregnancies.
  • Hormonal contraception: suppresses ovulation and modifies cervical mucus to reduce fertilisation risk.

How It Works

  • Ethinylestradiol and levonorgestrel bind to estrogen and progesterone receptors, respectively, producing negative feedback on the hypothalamic‑pituitary‑ovarian axis. This suppresses the mid‑cycle surge of luteinising hormone, preventing ovulation, while also thickening cervical mucus and inducing endometrial changes that hinder sperm penetration and implantation.

Side Effects

Leverette may cause a range of adverse reactions. The frequency and severity vary among individuals.

Common Side Effects

  • Nausea: mild to moderate stomach upset, especially during the first cycles.
  • Breast tenderness: temporary swelling or discomfort of the breasts.
  • Headache: occasional mild to moderate headache.
  • Spotting or breakthrough bleeding: irregular light bleeding between periods.
  • Mood changes: mild fluctuations in mood or emotional state.
  • Weight fluctuation: slight changes in body weight or fluid retention.

Serious or Rare Side Effects

  • Thromboembolic events: deep‑vein thrombosis or pulmonary embolism, particularly in high‑risk individuals.
  • Hypertension: new‑onset or worsening high blood pressure.
  • Hepatic adenoma: rare benign liver tumor.
  • Visual disturbances: sudden loss of vision or eye pain.
  • Severe allergic reaction: anaphylaxis, rash, or swelling of the face and throat.
  • Cardiovascular events: myocardial infarction or stroke in susceptible patients.

Precautions & Warnings

Before prescribing Leverette, clinicians should evaluate patient history and risk factors.

  • Cardiovascular risk assessment: avoid in women with a history of thromboembolism or uncontrolled hypertension.
  • Smoking status: contraindicated for smokers over 35 years of age.
  • Liver function: assess hepatic disease, as metabolism may be impaired.
  • Pregnancy contraindication: do not use during known or suspected pregnancy.
  • Store at ambient temperature: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Leverette can interact with several drug classes, affecting its efficacy or safety.

Major Interactions (Avoid)

  • Enzyme‑inducing anticonvulsants (e.g., carbamazepine, phenytoin): may markedly reduce contraceptive effectiveness.
  • Rifampicin or other rifamycins: strong induction of hepatic enzymes can lower hormone levels.
  • St. John's wort: herbal inducer that can compromise contraceptive reliability.

Moderate Interactions (Monitor Closely)

  • Certain antibiotics (e.g., tetracycline, metronidazole): may slightly diminish contraceptive effect.
  • Antifungal agents (e.g., fluconazole): can increase hormone concentrations, raising side‑effect risk.
  • Antiretroviral drugs (e.g., protease inhibitors): may alter hormone metabolism, requiring clinical monitoring.

Frequently Asked Questions

Leverette is a combined estrogen‑progestogen oral tablet indicated for the prevention of pregnancy. It provides a reversible, hormone‑based method of contraception for women of reproductive age when taken as prescribed.

Ethinylestradiol and levonorgestrel act on estrogen and progesterone receptors, creating negative feedback that suppresses the luteinising hormone surge, thereby preventing ovulation. The hormones also thicken cervical mucus and modify the endometrial lining, making fertilisation and implantation unlikely.

The dosing regimen for Leverette is determined by the prescribing clinician. Typically, the product is taken once daily at the same time each day, but the exact schedule and duration are individualized based on the patient’s medical profile and treatment plan.

Leverette is contraindicated during pregnancy because it is designed to prevent conception. Limited data are available for breastfeeding; if a woman chooses to breastfeed, the prescriber should evaluate the risk‑benefit balance and may recommend an alternative method of contraception.

To order Leverette, 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.

Leverette contains the standard doses of ethinylestradiol and levonorgestrel found in many combined oral contraceptives, offering comparable efficacy and safety profiles. Differences among products usually relate to tablet size, inactive ingredients, or specific dosing schedules, but the core mechanism of preventing ovulation remains consistent.

Leverette tablets should be stored at ambient temperature, below 25 °C, in the original blister pack or container. Protect them from moisture, excessive heat and direct sunlight to maintain potency throughout the shelf life.

Leverette is taken orally, usually as one tablet each day. Patients should start on the first day of their menstrual cycle or as directed by their healthcare provider, and continue daily without missing doses to maintain contraceptive effectiveness.

The most serious risks include thromboembolic events such as deep‑vein thrombosis or pulmonary embolism, especially in women with cardiovascular risk factors, and hypertension‑related complications. Rare but severe adverse events may involve hepatic adenoma, myocardial infarction, stroke, or severe allergic reactions.

Leverette should not be used by women with a known history of thromboembolic disorders, uncontrolled hypertension, active liver disease, or known hypersensitivity to any component of the tablet. It is also contraindicated in smokers over 35 years of age and in anyone who is pregnant.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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