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

Keriette

Active Ingredient:
Ethinylestradiol, Levonorgestrel
Origin:
EU

Keriette (Ethinylestradiol, Levonorgestrel)

Ethinylestradiol and Levonorgestrel, the active ingredients in Keriette, are a combined oral contraceptive presented as a tablet for oral use. It treats contraception and helps regulate menstrual cycles in women of reproductive age.

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

Manufacturer / TM Owner

Kern Pharma, S.L.

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Indications & Clinical Uses

Keriette is a combined hormonal contraceptive used to prevent pregnancy and manage menstrual cycle disorders.

  • Contraception: provides reliable prevention of pregnancy when taken as prescribed.
  • Menstrual cycle regulation: helps achieve more predictable bleeding patterns.
  • Menstrual irregularities: reduces heavy or prolonged bleeding and improves cycle regularity.

How It Works

  • Keriette combines ethinylestradiol, a synthetic estrogen, with levonorgestrel, a progestogen. The estrogen component suppresses the mid‑cycle surge of luteinising hormone (LH) and follicle‑stimulating hormone (FSH), while the progestogen inhibits ovulation, thickens cervical mucus and alters the endometrial lining, collectively preventing fertilisation and implantation.

Side Effects

Keriette may cause a range of adverse reactions. Common side effects are usually mild and transient.

Common Side Effects

  • Nausea: mild stomach upset, often improves with continued use.
  • Breast tenderness: temporary swelling or discomfort of the breasts.
  • Headache: mild to moderate intensity, may respond to simple analgesics.
  • Spotting: irregular light bleeding between periods.

Serious or Rare Side Effects

  • Deep vein thrombosis: blood clot formation in the legs, requiring immediate medical attention.
  • Pulmonary embolism: clot migration to the lungs, a life‑threatening emergency.
  • Stroke or myocardial infarction: rare cardiovascular events, especially in high‑risk individuals.
  • Severe allergic reaction: rash, swelling, or difficulty breathing.
  • Liver dysfunction: jaundice or abnormal liver enzymes.
  • Vision changes: sudden loss of vision or visual disturbances.

Precautions & Warnings

Before prescribing Keriette, clinicians should evaluate individual risk factors and counsel patients on safe use.

  • Thromboembolic risk assessment: avoid in women with history of clotting disorders.
  • Cardiovascular evaluation: caution in smokers over 35 or those with hypertension.
  • Liver disease monitoring: use with care in patients with hepatic impairment.
  • Breast cancer history: consider alternative contraception for survivors.
  • Pregnancy testing: ensure patient is not pregnant before initiation.
  • Store at ambient temperature: keep tablets in original packaging, protect from moisture and heat.

Avoid Interactions

Keriette can interact with other medicines, affecting its efficacy or safety.

Major Interactions (Avoid)

  • Enzyme‑inducing anticonvulsants (e.g., carbamazepine, phenytoin): markedly reduce contraceptive effectiveness.
  • Rifampin or rifabutin: potent inducers that may lead to contraceptive failure.
  • St. John’s wort: herbal supplement that can decrease hormone levels.

Moderate Interactions (Monitor Closely)

  • Certain antibiotics (e.g., tetracycline, metronidazole): may slightly reduce contraceptive reliability.
  • Antifungal agents (e.g., fluconazole, itraconazole): can increase hormone concentrations.
  • Antiretroviral drugs (e.g., protease inhibitors): may alter hormone metabolism, requiring additional contraceptive measures.

Frequently Asked Questions

Keriette is a combined oral contraceptive containing ethinylestradiol and levonorgestrel. It is prescribed to prevent pregnancy and to help regulate menstrual cycles, providing reliable birth control and more predictable bleeding patterns for women of reproductive age.

Ethinylestradiol suppresses the mid‑cycle surge of luteinising hormone and follicle‑stimulating hormone, while levonorgestrel inhibits ovulation, thickens cervical mucus, and alters the endometrial lining. Together they prevent fertilisation and implantation, delivering effective contraception.

The dosing regimen for Keriette is determined by the prescribing healthcare professional. Typically, it is taken as a daily oral tablet following the specific schedule indicated on the prescription label.

Keriette is intended for use only when pregnancy is not present. If pregnancy occurs, the product should be discontinued and medical advice sought. Safety during breastfeeding has not been established; women should consult their physician before using any hormonal contraceptive while nursing.

To order Keriette, 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.

Keriette contains the standard dose combination of ethinylestradiol and levonorgestrel, a widely used regimen in combined oral contraceptives. Its efficacy and safety profile are comparable to other products in the same class, with differences mainly in pill formulation, packaging and brand‑specific excipients.

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

Keriette is taken orally, usually once daily at the same time each day. The tablet is swallowed whole with water, following the dosing schedule provided by the prescriber, which may include a placebo week to allow withdrawal bleeding.

Serious risks include thromboembolic events such as deep vein thrombosis, pulmonary embolism, stroke, and myocardial infarction. Women with a history of clotting disorders, cardiovascular disease, smoking over age 35, or certain cancers should discuss alternative contraception with their healthcare provider.

Keriette is contraindicated in women with known or suspected pregnancy, active or past thromboembolic disease, certain hormone‑dependent cancers, severe liver disease, uncontrolled hypertension, or those who are breastfeeding without medical guidance. A thorough medical assessment is essential before initiation.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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