Product image of Leverette 28 (Ethinylestradiol, Levonorgestrel | Lactose) supplied by GNH India

Leverette 28

Active Ingredient:
Ethinylestradiol, Levonorgestrel | Lactose
Origin:
EU

Leverette 28 (Ethinylestradiol, Levonorgestrel | Lactose)

Ethinylestradiol, the active ingredient in Leverette 28, is a combined oral contraceptive presented as a tablet for oral use. It prevents pregnancy in women of reproductive age. Leverette 28 also contains levonorgestrel, a progestogenic component that enhances contraceptive efficacy.

GNH India supplies Leverette 28 as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Exeltis Healthcare S.L

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Indications & Clinical Uses

Leverette 28 is a combined oral contraceptive that acts on the hormonal regulation of the menstrual cycle to prevent unintended pregnancy.

  • Contraception: prevents pregnancy in women of reproductive age.
  • Menstrual cycle regulation: helps establish a regular monthly bleeding pattern.
  • Acne management: may improve hormonal acne in some users.

How It Works

  • Ethinylestradiol and levonorgestrel bind to estrogen and progesterone receptors, respectively, suppressing the hypothalamic‑pituitary‑ovarian axis. This inhibition prevents the mid‑cycle surge of luteinizing hormone, thereby blocking ovulation. In addition, the progestin thickens cervical mucus and the estrogen component alters the endometrial lining, creating an environment hostile to fertilization and implantation.

Side Effects

Leverette 28 may cause a range of adverse reactions. Patients should be aware of both common and serious possibilities.

Common Side Effects

  • Nausea: mild to moderate stomach upset.
  • Headache: tension‑type or migraine‑like pain.
  • Breast tenderness: swelling or discomfort of the breasts.
  • Spotting between periods: light vaginal bleeding.

Serious or Rare Side Effects

  • Blood clots: deep vein thrombosis or pulmonary embolism.
  • Stroke: neurological deficits due to cerebrovascular occlusion.
  • Severe allergic reaction: rash, swelling, or anaphylaxis.

Precautions & Warnings

Before prescribing Leverette 28, clinicians should evaluate individual risk factors and advise patients accordingly.

  • Assess thromboembolic risk: review personal and family history of clotting disorders.
  • Monitor cardiovascular health: avoid use in uncontrolled hypertension or smoking over age 35.
  • Evaluate hepatic function: caution in patients with liver disease.
  • Review medication history: certain enzyme‑inducing drugs may reduce effectiveness.
  • Store at room temperature below 25°C: keep in the original pack, protect from moisture and light.

Avoid Interactions

Leverette 28 can interact with several drug classes, altering its contraceptive efficacy or increasing adverse effects.

Major Interactions (Avoid)

  • Antiepileptic enzyme inducers (e.g., phenytoin, carbamazepine, phenobarbital): markedly reduce hormone levels.
  • Rifampin and other strong antibiotics: decrease contraceptive effectiveness.
  • St. John's wort: herbal inducer that may compromise efficacy.

Moderate Interactions (Monitor Closely)

  • Antifungal agents (e.g., ketoconazole, itraconazole): may increase hormone concentrations.
  • HIV protease inhibitors (e.g., ritonavir): can affect hormone metabolism.
  • Certain antidepressants (e.g., SSRIs): may modestly alter plasma levels.
  • Ginkgo biloba: potential additive effect on bleeding risk.

Frequently Asked Questions

Leverette 28 is a combined oral contraceptive containing ethinyloestradiol and levonorgestrel. It is prescribed to prevent pregnancy in women of reproductive age and may also help regulate menstrual cycles and improve hormonal acne in some patients.

Ethinyloestradiol and levonorgestrel act on estrogen and progesterone receptors to suppress the hypothalamic‑pituitary‑ovarian axis, preventing the luteinizing hormone surge that triggers ovulation. The progestin also thickens cervical mucus and the estrogen modifies the endometrial lining, reducing the chance of fertilization and implantation.

The prescribing clinician determines the dosing schedule. Typically, Leverette 28 is taken as one tablet daily for 21 consecutive days followed by a hormone‑free interval, but the exact regimen may vary based on individual medical assessment.

Leverette 28 is intended for use in women who are not pregnant. If pregnancy occurs, the product should be discontinued. Limited data exist on safety during breastfeeding; women should discuss potential risks with their healthcare provider before use.

To order Leverette 28, 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.

Leverette 28 offers efficacy comparable to other combined oral contraceptives. Its formulation uses levonorgestrel as the progestin, which has a well‑established safety profile. Differences among products generally relate to the estrogen dose, type of progestin, and specific side‑effect profiles.

Store Leverette 28 at room temperature below 25 °C. Keep the tablets in their original packaging, protect them from moisture and direct light, and ensure the container is tightly closed to maintain product stability.

Leverette 28 is taken orally with a glass of water. It is usually recommended to take the tablet at the same time each day, with or without food, to maintain consistent hormone levels.

Rare but serious risks include venous thromboembolism (deep‑vein thrombosis or pulmonary embolism), stroke, myocardial infarction, and severe allergic reactions such as anaphylaxis. Patients should seek immediate medical attention if they experience symptoms such as sudden chest pain, shortness of breath, severe headache, or swelling of the limbs.

Leverette 28 should be avoided by women with a history of thromboembolic disorders, estrogen‑dependent cancers, uncontrolled hypertension, smoking over age 35, or known hypersensitivity to any component of the tablet. Consultation with a healthcare professional is essential before initiating therapy.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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