Product image of Leverette 21 (Ethinylestradiol, Levonorgestrel) supplied by GNH India

Leverette 21

Active Ingredient:
Ethinylestradiol, Levonorgestrel
Origin:
EU

Leverette 21 (Ethinylestradiol, Levonorgestrel)

Ethinylestradiol, the active ingredient in Leverette 21, is a combined oral contraceptive presented as a tablet for oral use. Combined with levonorgestrel, the formulation provides estrogen and progestogen activity to reliably prevent pregnancy in women of reproductive age.

GNH India supplies Leverette 21 as a licensed, GDP‑compliant international pharmaceutical supplier, providing the product to hospitals, pharmacies and clinics across global markets with consistent quality and regulatory compliance.

Manufacturer / TM Owner

Exeltis Healthcare S.L

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Indications & Clinical Uses

Leverette 21, a combined oral contraceptive, is used within the hormonal contraception pathway to prevent unintended pregnancy and manage related menstrual conditions.

  • Contraception: prevention of unintended pregnancy in women of reproductive age.
  • Menstrual cycle regulation: reduction of irregular bleeding and stabilization of cycle length.
  • Acne management: improvement of moderate acne associated with androgen excess.

How It Works

  • Ethinylestradiol binds to estrogen receptors, delivering negative feedback to the hypothalamic‑pituitary axis, while levonorgestrel activates progesterone receptors, suppressing the luteinizing hormone surge. The combined action inhibits ovulation, thickens cervical mucus, and induces endometrial changes that together prevent fertilization and implantation. Additionally, the progestogenic component reduces endometrial proliferation, contributing to contraceptive efficacy.

Side Effects

Leverette 21 may cause a range of adverse reactions, which are categorized by frequency and severity.

Common Side Effects

  • Nausea: mild to moderate stomach upset.
  • Breast tenderness: discomfort or swelling of the breasts.
  • Headache: transient cranial pain.
  • Spotting or breakthrough bleeding: irregular light bleeding.
  • Weight gain: modest increase in body weight.
  • Mood changes: irritability or emotional fluctuations.

Serious or Rare Side Effects

  • Venous thromboembolism: deep vein thrombosis or pulmonary embolism.
  • Stroke: cerebrovascular accident, especially in high‑risk individuals.
  • Myocardial infarction: heart attack due to arterial blockage.
  • Severe hypertension: sudden rise in blood pressure.
  • Allergic reaction: rash, swelling, or anaphylaxis.
  • Liver dysfunction: jaundice or abnormal liver enzymes.

Precautions & Warnings

Before prescribing Leverette 21, clinicians should consider several safety precautions to minimize risk.

  • Pregnancy contraindication: must not be used during pregnancy (Category X).
  • Smoking restriction: avoid in women over 35 who smoke.
  • Thromboembolic history: contraindicated in patients with past venous or arterial clotting events.
  • Hypertension: caution in uncontrolled high blood pressure.
  • Liver disease: avoid in active liver disease or severe hepatic impairment.
  • Store at ambient temperature: keep below 25 °C in the original packaging, protected from moisture and light.

Avoid Interactions

Leverette 21 can interact with other medicines, altering its effectiveness or safety profile.

Major Interactions (Avoid)

  • Enzyme‑inducing anticonvulsants (e.g., carbamazepine, phenytoin): reduce contraceptive efficacy.
  • Rifampicin and other rifamycins: markedly decrease hormone levels.
  • Protease inhibitors (e.g., ritonavir): increase risk of hormonal side effects.
  • St John’s wort: may lower contraceptive effectiveness.
  • Certain antiretrovirals (e.g., efavirenz): diminish hormone exposure.

Moderate Interactions (Monitor Closely)

  • Antifungal agents (e.g., ketoconazole): may increase hormone concentrations.
  • SSRIs (e.g., fluoxetine): possible alteration of bleeding patterns.
  • Antihypertensives (e.g., beta‑blockers): monitor blood pressure changes.
  • Diuretics: may affect electrolyte balance and blood pressure.
  • Herbal supplements (e.g., ginseng): observe for reduced contraceptive reliability.

Frequently Asked Questions

Leverette 21 is a combined oral contraceptive containing ethinylestradiol and levonorgestrel. It is prescribed to prevent unintended pregnancy in women of reproductive age and may also be used to help regulate menstrual cycles and improve moderate acne linked to hormonal imbalance.

Ethinylestradiol acts as a synthetic estrogen, binding to estrogen receptors and providing negative feedback to the hypothalamus and pituitary gland. This suppresses the release of luteinizing hormone and follicle‑stimulating hormone, helping to inhibit ovulation when combined with the progestogenic action of levonorgestrel.

The dosing regimen for Leverette 21 is determined by the prescribing healthcare professional. Typically, it is taken as a daily tablet according to a cycle defined by the prescriber, but exact strength and schedule should follow the clinician’s instructions and the product label.

Leverette 21 is classified as Pregnancy Category X, meaning it must not be used during pregnancy because it can harm the fetus. Breastfeeding mothers should consult their physician, as hormonal contraceptives can affect milk production and infant exposure.

To order Leverette 21, 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 21 contains the standard dose combination of ethinylestradiol and levonorgestrel, a widely used regimen offering reliable contraception. Compared with newer formulations that may use different progestins or lower estrogen doses, Leverette 21 provides a well‑characterized efficacy and safety profile familiar to clinicians.

Store Leverette 21 tablets at ambient temperature, preferably below 25 °C. Keep the blister pack in its original container, protect it from moisture and direct sunlight, and ensure the packaging remains sealed until use.

Leverette 21 is taken orally, usually once daily at the same time each day. The tablet is swallowed whole with water and should be started according to the prescriber’s schedule, often on the first day of the menstrual period or as directed.

The most serious risks include venous thromboembolism, 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 high blood pressure.

Leverette 21 is contraindicated in women who are pregnant, have a history of thromboembolic disease, uncontrolled hypertension, active liver disease, known estrogen‑dependent tumors, or who are over 35 years old and smoke. 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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