Product image of Kestrelle (Desogestrel) supplied by GNH India

Kestrelle

Active Ingredient:
Desogestrel
Origin:
EU

Kestrelle (Desogestrel)

Desogestrel, the active ingredient in Kestrelle, is a progestin presented as an oral tablet for oral use. It is used as a hormonal contraceptive to prevent pregnancy in women of reproductive age.

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

Manufacturer / TM Owner

Farmitalia S.R.L.

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Indications & Clinical Uses

Desogestrel is a progestin used in hormonal contraception to prevent pregnancy.

  • Contraception: prevents ovulation and thereby reduces the chance of pregnancy.
  • Family planning: offers a daily oral option for women seeking a reversible method of birth control.
  • Menstrual cycle regulation: can help achieve more predictable bleeding patterns in some users.

How It Works

  • Desogestrel acts as a selective progesterone receptor agonist. By binding to progesterone receptors in the hypothalamus, it suppresses the luteinizing hormone surge, thereby inhibiting ovulation. The drug also induces changes in the cervical mucus, making it less permeable to sperm, and alters the endometrial lining to reduce the likelihood of implantation.

Side Effects

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

Common Side Effects

  • Nausea: mild stomach upset that usually resolves with continued use.
  • Headache: occasional tension‑type headaches.
  • Breast tenderness: mild discomfort or swelling of the breasts.
  • Irregular bleeding: spotting or changes in menstrual flow.
  • Mood changes: slight fluctuations in mood or emotional state.
  • Weight gain: modest increase in body weight in some users.

Serious or Rare Side Effects

  • Deep vein thrombosis: formation of blood clots in the legs.
  • Pulmonary embolism: clot migration to the lungs, a medical emergency.
  • Liver tumor: rare benign hepatic adenoma.
  • Severe allergic reaction: rash, swelling, or anaphylaxis.
  • Hyperglycemia: elevated blood sugar levels.
  • Hypertension: increase in blood pressure.

Precautions & Warnings

Before prescribing Desogestrel, clinicians should evaluate individual risk factors and advise patients on safe use.

  • Medical history review: assess for thromboembolic disorders, liver disease, or hormone‑sensitive cancers.
  • Smoking status: avoid use in women over 35 who smoke.
  • Liver function: monitor in patients with hepatic impairment.
  • Drug interactions: review concomitant medications that may affect efficacy.
  • Pregnancy and lactation: not indicated for use during pregnancy; discuss breastfeeding considerations.
  • Store at ambient temperature: keep below 25°C, in the original packaging, and protect from moisture.

Avoid Interactions

Desogestrel can interact with several medicines, altering its contraceptive effectiveness or increasing adverse effects.

Major Interactions (Avoid)

  • Antiepileptic enzyme inducers (e.g., carbamazepine, phenytoin): may markedly reduce contraceptive efficacy.
  • Rifampicin: decreases plasma concentrations of desogestrel.
  • Protease inhibitor antiretrovirals: can affect hormone metabolism.
  • St. John’s wort: herbal inducer that lowers drug levels.
  • Azole antifungals (e.g., ketoconazole): may increase desogestrel exposure.

Moderate Interactions (Monitor Closely)

  • Antibiotics such as tetracycline: possible modest reduction in effectiveness.
  • SSRIs (selective serotonin reuptake inhibitors): may increase risk of bleeding.
  • Diuretics: may influence fluid balance and blood pressure.
  • Antihypertensives: monitor blood pressure for additive effects.
  • Herbal supplements like ginseng: potential pharmacodynamic interactions.

Frequently Asked Questions

Kestrelle contains desogestrel, a progestin‑only hormone that is prescribed as a contraceptive to prevent pregnancy. It is taken daily by women of reproductive age who desire a reliable, reversible method of birth control.

Desogestrel acts as a selective progesterone receptor agonist. By binding to receptors in the hypothalamus, it suppresses the luteinizing hormone surge, which prevents ovulation. It also thickens cervical mucus and alters the endometrium, creating an environment that is unfavorable for sperm and implantation.

The dosing regimen for Kestrelle is determined by the prescribing clinician based on the patient’s medical history and individual needs. Typically, it is taken as one tablet daily at the same time each day, but the exact dose and schedule should follow the prescriber’s instructions.

Kestrelle is not intended for use during pregnancy because it is a contraceptive. Women who become pregnant while taking the product should discontinue it and consult a healthcare professional. Limited data are available for breastfeeding; clinicians should weigh potential risks and benefits before prescribing.

To place an order, 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.

Kestrelle (desogestrel) is a progestin‑only pill, offering a daily oral alternative to combined estrogen‑progestin contraceptives. It avoids estrogen‑related risks such as increased clotting, making it suitable for women who cannot take estrogen. Compared with long‑acting methods, it requires daily adherence but provides flexibility to stop use at any time.

Kestrelle tablets should be stored at ambient temperature, below 25 °C. Keep them in the original blister pack, protect from moisture and direct sunlight, and store out of reach of children.

Kestrelle is taken orally, usually as a single tablet each day. It should be swallowed with water at roughly the same time each day to maintain consistent hormone levels and maximize contraceptive effectiveness.

The most serious risks include rare but potentially life‑threatening blood clots such as deep vein thrombosis and pulmonary embolism, as well as liver tumors and severe allergic reactions. Patients should seek immediate medical attention if they experience unexplained leg pain, shortness of breath, severe abdominal pain, or signs of an allergic reaction.

Kestrelle is contraindicated in women with known or suspected pregnancy, active liver disease, a history of thromboembolic disorders, hormone‑sensitive cancers, or those who are over 35 and smoke heavily. It should also be avoided in individuals with known hypersensitivity to desogestrel or any tablet excipients.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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