Product image of Myloop (Ethinylestradiol, Etonogestrel) supplied by GNH India

Myloop

Active Ingredient:
Ethinylestradiol, Etonogestrel
Origin:
EU

Myloop (Ethinylestradiol, Etonogestrel)

Ethinylestradiol/Etonogestrel, the active ingredient in Myloop, is a combined estrogen‑progestogen contraceptive presented as a vaginal ring for vaginal use. It provides hormonal contraception to prevent pregnancy in women of reproductive age. The device releases a steady dose of hormones over three weeks, after which it is removed and replaced with a new ring.

GNH India supplies Myloop as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company ensures quality control, proper packaging, and timely delivery to meet global demand.

Manufacturer / TM Owner

Ceres Pharma Nv

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Indications & Clinical Uses

Myloop, a combined estrogen‑progestogen vaginal ring, is indicated for hormonal contraception and related menstrual management.

  • Contraception: Prevents pregnancy in women of childbearing potential.
  • Menstrual cycle regulation: Promotes more predictable bleeding patterns and reduces irregular spotting.
  • Management of dysmenorrhea: Decreases menstrual pain associated with ovulation.

How It Works

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

Side Effects

Common Side Effects

  • Nausea: mild to moderate stomach upset.
  • Headache: tension‑type or migraine‑like pain.
  • Breast tenderness: swelling or discomfort.
  • Vaginal irritation: itching or discharge at the insertion site.
  • Spotting or breakthrough bleeding: irregular light bleeding.
  • Mood changes: irritability or mild depression.

Serious or Rare Side Effects

  • Thromboembolic events: deep‑vein thrombosis or pulmonary embolism.
  • Hepatic adenoma or tumor: abnormal liver growth.
  • Severe allergic reaction: rash, swelling, or anaphylaxis.
  • Hypertension: sudden increase in blood pressure.
  • Vision changes: blurred vision or visual disturbances.
  • Gallbladder disease: inflammation or stones.

Precautions & Warnings

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

  • Contraindicated in pregnancy: Category X, do not use during any stage of pregnancy.
  • Avoid in smokers over 35 years: increased risk of cardiovascular events.
  • Screen for history of thromboembolism: contraindicated in patients with prior clotting disorders.
  • Monitor blood pressure regularly: hormonal therapy may elevate blood pressure.
  • Assess liver function: caution in patients with active hepatic disease.
  • Store at ambient temperature: keep in original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Myloop may interact with other medicines that affect hormone metabolism or increase clotting risk.

Major Interactions (Avoid)

  • Enzyme‑inducing anticonvulsants (e.g., carbamazepine, phenytoin): may reduce contraceptive efficacy.
  • Antiretroviral protease inhibitors (e.g., ritonavir): may decrease hormone levels.
  • St. John's Wort: can lower plasma concentrations of the active hormones.

Moderate Interactions (Monitor Closely)

  • Antifungal agents (e.g., fluconazole): may increase hormone exposure.
  • Macrolide antibiotics (e.g., erythromycin): may affect hepatic metabolism.
  • Selective serotonin reuptake inhibitors (SSRIs): may heighten risk of mood‑related side effects.

Frequently Asked Questions

Myloop is a vaginal contraceptive ring that delivers a combination of ethinyloestradiol and etonogestrel to provide reliable hormonal birth control. It is prescribed to prevent pregnancy in women of reproductive age and can also help regulate menstrual bleeding patterns.

The two hormones act on the hypothalamic‑pituitary‑ovarian axis. Ethinyloestradiol provides estrogenic activity while etonogestrel supplies progestogenic effects. Together they suppress the luteinizing hormone surge, preventing ovulation, thicken cervical mucus, and modify the endometrial lining, making implantation unlikely.

The dosing schedule is determined by the prescribing clinician. Typically, a single Myloop ring is inserted into the vagina and left in place for three weeks, followed by a one‑week ring‑free interval before a new ring is placed.

Myloop is contraindicated during pregnancy (pregnancy category X) and must not be used by women who are or may become pregnant. It is also not recommended for breastfeeding mothers because hormonal exposure may affect milk production and infant exposure.

To request Myloop, 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.

Both Myloop and combined oral contraceptives contain the same hormone pair, but Myloop delivers them continuously via a vaginal ring, eliminating the need for daily dosing. This can improve adherence and provide more stable hormone levels, while oral pills require daily intake and may have more gastrointestinal side effects.

Myloop should be stored at ambient temperature, preferably below 25 °C. Keep the rings in their original packaging, protect them from moisture, direct sunlight, and extreme heat to maintain hormone stability throughout the shelf life.

A healthcare professional or the patient inserts the flexible vaginal ring into the upper vaginal fornix. The ring remains in place for three weeks, during which it continuously releases hormones, and is then removed for a one‑week break before a new ring is inserted.

The most serious risks include thromboembolic events such as deep‑vein thrombosis or pulmonary embolism, severe hypertension, hepatic adenoma, and rare allergic reactions. Patients should seek immediate medical attention if they experience unexplained leg pain, shortness of breath, severe headache, or signs of an allergic response.

Myloop is contraindicated in women who are pregnant, have a history of thromboembolic disorders, are smokers over 35 years of age, have uncontrolled hypertension, have active liver disease, or have known hypersensitivity to either ethinyloestradiol or etonogestrel.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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