Product image of Lesiplus (Drospirenone, Ethinylestradiol | Lactose) supplied by GNH India

Lesiplus

Active Ingredient:
Drospirenone, Ethinylestradiol | Lactose
Origin:
EU

Lesiplus (Drospirenone, Ethinylestradiol | Lactose)

Drospirenone, the active ingredient in Lesiplus, is a combined oral contraceptive presented as a tablet for oral use. Together with ethinylestradiol, it forms a hormonal contraceptive that inhibits ovulation, alters cervical mucus, and induces endometrial changes to prevent pregnancy in women of reproductive age.

GNH India supplies Lesiplus as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, providing reliable access to this EU‑approved medication.

Manufacturer / TM Owner

Theramex Ireland Limited

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Indications & Clinical Uses

Lesiplus, a combined oral contraceptive, acts on the hormonal regulation pathway to prevent unintended pregnancy.

  • Prevention of pregnancy: provides reliable hormonal contraception for women of reproductive age.
  • Menstrual cycle regulation: helps achieve more predictable menstrual bleeding patterns.
  • Reduction of ovarian cysts: may decrease the formation of functional ovarian cysts.

How It Works

  • Drospirenone and ethinylestradiol work together to suppress the hypothalamic‑pituitary‑ovarian axis, preventing the mid‑cycle surge of luteinizing hormone that triggers ovulation. The progestogenic component also thickens cervical mucus, creating a barrier to sperm, while the estrogen component stabilizes the endometrial lining, reducing breakthrough bleeding and enhancing contraceptive efficacy.

Side Effects

Lesiplus may cause a range of adverse reactions, most of which are mild and transient.

Common Side Effects

  • Nausea: mild to moderate stomach upset.
  • Headache: tension‑type or migraine‑like pain.
  • Breast tenderness: soreness or swelling of breast tissue.
  • Weight gain: modest increase in body weight.
  • Mood changes: irritability or mood swings.
  • Spotting: irregular vaginal bleeding between periods.

Serious or Rare Side Effects

  • Venous thromboembolism: deep vein thrombosis or pulmonary embolism.
  • Hypertension: significant increase in blood pressure.
  • Liver disorders: jaundice or abnormal liver function tests.
  • Gallbladder disease: formation of gallstones or cholecystitis.
  • Severe allergic reaction: rash, swelling, or anaphylaxis.
  • Visual disturbances: sudden vision loss or retinal vein occlusion.

Precautions & Warnings

Before prescribing Lesiplus, clinicians should assess individual risk factors and consider contraindications.

  • Smoking: avoid use in women over 35 who smoke heavily.
  • Cardiovascular disease: contraindicated in patients with history of stroke, myocardial infarction, or uncontrolled hypertension.
  • Liver disease: use with caution in patients with active liver disease.
  • Migraine with aura: avoid in women who experience migraine headaches with visual disturbances.
  • Pregnancy and lactation: not recommended during pregnancy or while breastfeeding.
  • Store at ambient temperature: keep below 25 °C, retain in original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Lesiplus can interact with several medications, altering its efficacy or safety profile.

Major Interactions (Avoid)

  • Antiepileptic drugs (e.g., carbamazepine, phenytoin): may reduce contraceptive effectiveness.
  • Rifampin and other strong enzyme inducers: significantly decrease hormone levels.
  • Certain antivirals (e.g., ritonavir): may lower contraceptive efficacy.

Moderate Interactions (Monitor Closely)

  • Antifungal agents (e.g., fluconazole): may increase hormone concentrations.
  • St. John’s wort: may modestly reduce contraceptive effect.
  • Diuretics (e.g., thiazides): may affect fluid balance and blood pressure.

Frequently Asked Questions

Lesiplus is a combined oral contraceptive tablet containing drospirenone and ethinylestradiol. It is prescribed to prevent unintended pregnancy in women of reproductive age by providing reliable hormonal contraception.

The drospirenone component suppresses ovulation and thickens cervical mucus, while ethinylestradiol stabilizes the endometrial lining. Together they inhibit the hormonal surge needed for egg release and create a hostile environment for sperm, thereby preventing pregnancy.

The dosing regimen for Lesiplus is determined by the prescribing healthcare professional. Typically, it is taken once daily at the same time for a 21‑day active phase followed by a hormone‑free interval, but the exact schedule should follow the prescriber’s instructions.

Lesiplus is not intended for use during pregnancy and should be discontinued if pregnancy occurs. Its safety during breastfeeding has not been established, so healthcare providers usually advise against use while nursing.

To order Lesiplus, 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 institutional credentials, and then provides pricing, availability, shipping details, and necessary import documentation.

Lesiplus contains drospirenone, a progestin with anti‑androgenic and mild diuretic properties, which may offer benefits such as reduced water retention and improved acne compared with some other progestins. Its efficacy and safety profile are comparable to other FDA‑approved combined oral contraceptives.

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

Lesiplus is taken orally, usually once daily at the same time each day. The typical regimen involves 21 consecutive active tablets followed by a 7‑day hormone‑free interval, during which withdrawal bleeding occurs.

Serious risks include venous thromboembolism (deep‑vein thrombosis or pulmonary embolism), arterial thrombosis (stroke or heart attack), hypertension, and rare liver disorders. Patients should be monitored for signs of blood clots, severe headaches, or visual changes.

Lesiplus is contraindicated in women who are pregnant, breastfeeding, have a history of thromboembolic events, uncontrolled hypertension, severe liver disease, known or suspected estrogen‑dependent tumors, or who are smokers over age 35.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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