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

Myloop

Active Ingredient:
Ethinylestradiol, Etonogestrel
Origin:
EU

Myloop (Ethinylestradiol, Etonogestrel)

Ethinylestradiol, the active ingredient in Myloop, is a combined estrogen‑progestogen contraceptive presented as a vaginal ring for vaginal use. It prevents pregnancy by delivering continuous hormone levels to women of reproductive age, and the ring also contains etonogestrel, a progestogen that works synergistically with ethinylestradiol to maintain contraceptive efficacy.

GNH India supplies Myloop as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, ensuring quality and regulatory compliance across markets. The company provides reliable logistics and documentation for cross‑border procurement.

Manufacturer / TM Owner

Ceres Pharma Nv

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Indications & Clinical Uses

Myloop, a combined estrogen‑progestogen contraceptive, is indicated for hormonal contraception.

  • Contraception (prevention of pregnancy): provides reliable reversible birth control for women of reproductive age.
  • Family planning: enables controlled spacing of pregnancies to support reproductive health goals.
  • Menstrual cycle regulation: may reduce menstrual bleeding and dysmenorrhea while maintaining contraceptive protection.

How It Works

  • The vaginal ring releases ethinylestradiol and etonogestrel at a steady rate, maintaining serum concentrations that suppress the hypothalamic‑pituitary‑gonadal axis. Ethinylestradiol provides estrogenic feedback that inhibits follicular development, while etonogestrel binds progesterone receptors to prevent ovulation, thicken cervical mucus, and induce endometrial changes, collectively preventing pregnancy.

Side Effects

Myloop may be associated with a range of adverse reactions, which are generally categorized by frequency and severity.

Common Side Effects

  • Vaginal irritation or discharge: mild irritation, spotting or increased discharge at the insertion site.
  • Headache: transient tension‑type or migraine‑like headaches.
  • Nausea or abdominal discomfort: mild gastrointestinal upset.
  • Breast tenderness: temporary swelling or sensitivity of the breasts.

Serious or Rare Side Effects

  • Thromboembolic events: deep‑vein thrombosis or pulmonary embolism, requiring immediate medical attention.
  • Hepatic disorders: liver enzyme elevation or rare hepatic adenoma.
  • Severe allergic reaction: anaphylaxis, angioedema, or Stevens‑Johnson syndrome.

Precautions & Warnings

Before prescribing Myloop, healthcare professionals should consider several precautionary measures to ensure patient safety.

  • Pregnancy contraindication: do not use in women who are or may become pregnant.
  • Smoking restriction: avoid use in women who smoke more than 15 cigarettes per day.
  • History of thromboembolism: contraindicated in patients with prior venous or arterial clotting events.
  • Liver disease: use with caution in patients with active liver disease or tumors.
  • Breast cancer: contraindicated in current or past estrogen‑dependent breast cancer.
  • Store at room temperature: keep in original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Myloop can interact with other medicines, altering its contraceptive effectiveness or increasing adverse effect risk.

Major Interactions (Avoid)

  • Enzyme‑inducing anticonvulsants (e.g., carbamazepine, phenytoin, phenobarbital): markedly reduce hormone levels, risking contraceptive failure.
  • Rifampin and other strong CYP3A4 inducers: decrease ethinylestradiol and etonogestrel concentrations.
  • St. John’s wort (hypericum perforatum): herbal inducer that may compromise contraceptive efficacy.

Moderate Interactions (Monitor Closely)

  • Antifungal agents such as ketoconazole or itraconazole: may increase hormone exposure, requiring monitoring for side effects.
  • Selective serotonin reuptake inhibitors (SSRIs): can modestly increase risk of mood changes or bleeding.
  • Antihypertensive drugs (e.g., ACE inhibitors): may require blood pressure monitoring due to possible fluid retention.

Frequently Asked Questions

Myloop is a prescription vaginal ring that provides hormonal contraception. It delivers a continuous combination of ethinylestradiol and etonogestrel to prevent ovulation, thicken cervical mucus, and alter the endometrium, thereby reducing the risk of unintended pregnancy for women of reproductive age.

Ethinylestradiol is a synthetic estrogen that supplies negative feedback to the hypothalamus and pituitary, suppressing the release of gonadotropins. This inhibition prevents the growth of ovarian follicles and reduces the likelihood of ovulation, which is a key step in the contraceptive action of Myloop.

The dosing regimen for Myloop is determined by the prescribing clinician. Typically, the vaginal ring is inserted and left in place for three consecutive weeks, followed by a one‑week ring‑free interval during which withdrawal bleeding occurs. Exact timing and any adjustments are individualized.

Myloop is contraindicated in pregnancy; it must not be used by women who are pregnant or may become pregnant. While limited data exist for breastfeeding, most guidelines advise against using combined hormonal contraceptives during lactation, especially in the early postpartum period, unless the benefits outweigh the risks.

To order 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 (including any cold‑chain requirements) and the necessary import documentation.

Compared with oral combined pills, Myloop offers a steady hormone release without daily dosing, which can improve adherence. Unlike implants or intrauterine devices, it is non‑invasive and removable by the user. Its efficacy is comparable to other combined hormonal methods, but individual choice should consider lifestyle, side‑effect profile and medical history.

Myloop should be stored at room temperature, ideally below 25 °C, in its original packaging. The packaging protects the ring from moisture and light. Do not expose the device to extreme heat or humidity, and keep it out of reach of children.

Myloop is a flexible vaginal ring that is inserted into the upper vagina by the patient or a healthcare professional. Once placed, it remains in situ for three weeks, delivering continuous hormone levels, after which it is 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, hepatic disorders including rare liver tumors, and severe allergic reactions like anaphylaxis or Stevens‑Johnson syndrome. Prompt medical attention is required if any of these symptoms occur.

Myloop is contraindicated in women who are pregnant, have a history of thromboembolic disease, active liver disease or liver tumors, estrogen‑dependent breast cancer, or who smoke heavily (more than 15 cigarettes per day). It should also be avoided in individuals with known hypersensitivity to any component of the ring.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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