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

Myprimose

Active Ingredient:
Ethinylestradiol, Etonogestrel
Origin:
EU

Myprimose (Ethinylestradiol, Etonogestrel)

Ethinylestradiol, the active ingredient in Myprimose, is a combined estrogen‑progestogen contraceptive presented as a vaginal formulation for contraceptive use. It works to prevent pregnancy by suppressing ovulation and altering cervical mucus and the endometrial lining.

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

Manufacturer / TM Owner

Exeltis Italia Srl

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Indications & Clinical Uses

Myprimose, a combined estrogen‑progestogen contraceptive, is indicated for preventing unintended pregnancy. It is used within the hormonal contraception pathway.

  • Contraception: provides reliable prevention of pregnancy when used as directed.
  • Menstrual cycle regulation: helps achieve more predictable bleeding patterns for many users.
  • Treatment of hormonally‑responsive conditions: may be employed to manage symptoms such as dysmenorrhea or acne associated with hormonal imbalance.

How It Works

  • Ethinylestradiol and etonogestrel act together to suppress the hypothalamic‑pituitary‑ovarian axis, preventing the mid‑cycle surge of luteinizing hormone that triggers ovulation. The estrogen component stabilises the endometrial lining, while the progestogen thickens cervical mucus and further modifies the endometrium, creating an environment unsuitable for fertilisation and implantation.

Side Effects

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

Common Side Effects

  • Nausea or mild gastrointestinal upset.
  • Breast tenderness or enlargement.
  • Headache or migraine episodes.
  • Spotting or breakthrough bleeding.
  • Mood changes or irritability.
  • Weight fluctuation or fluid retention.

Serious or Rare Side Effects

  • Venous thromboembolism (deep‑vein thrombosis, pulmonary embolism).
  • Arterial thrombosis (stroke, myocardial infarction).
  • Severe hypertension.
  • Liver disorders, including benign tumors.
  • Allergic reactions such as rash, angioedema, or anaphylaxis.
  • Ectopic pregnancy if contraception fails.

Precautions & Warnings

Before initiating Myprimose, clinicians should evaluate individual risk factors and counsel patients on safe use.

  • Cardiovascular assessment: review history of thromboembolic events, hypertension, or smoking.
  • Hepatic function: assess liver disease, as metabolism may be impaired.
  • Smoking status: advise against use in women over 35 who smoke.
  • Pregnancy avoidance: confirm negative pregnancy test before starting and advise immediate discontinuation if pregnancy occurs.
  • Missed dose guidance: provide clear instructions on what to do after a missed application.
  • Storage: Store at room temperature: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Myprimose can interact with several medicines that affect hormone metabolism or clotting risk.

Major Interactions (Avoid)

  • Strong CYP3A4 inducers (e.g., rifampin, carbamazepine, phenytoin) which may reduce contraceptive efficacy.
  • Certain antiretroviral agents (e.g., efavirenz) that lower hormone levels.
  • St. John’s wort, a herbal inducer of hepatic enzymes.
  • Antifungal agents like ketoconazole when used at high doses.

Moderate Interactions (Monitor Closely)

  • Antidepressants (SSRIs) that may increase bleeding tendencies.
  • Antihypertensive drugs, especially ACE inhibitors, which may affect blood pressure control.
  • Diuretics, which can alter electrolyte balance.
  • Anticonvulsants with moderate enzyme‑inducing properties (e.g., valproate).
  • Herbal supplements such as ginseng that may have variable effects on hormone levels.

Frequently Asked Questions

Myprimose is a prescription‑only combined estrogen‑progestogen contraceptive designed to prevent unintended pregnancy. It works by inhibiting ovulation and creating cervical mucus and endometrial changes that reduce the chance of fertilisation and implantation.

The ethinyloestradiol component stabilises the endometrial lining, while etonogestrel suppresses the hypothalamic‑pituitary‑ovarian axis, preventing the luteinising hormone surge needed for ovulation. Together they also thicken cervical mucus and alter the uterine lining, providing multiple barriers to pregnancy.

The specific dosing regimen for Myprimose is determined by the prescribing healthcare professional based on the product’s formulation and the patient’s individual needs. Patients should follow the prescriber’s instructions and not alter the schedule without medical advice.

Myprimose is classified as Pregnancy Category X, meaning it must not be used during pregnancy because it can harm the fetus. It is also not recommended while breastfeeding, as hormonal exposure may affect milk production and infant development.

To order Myprimose, 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 necessary import documentation.

Myprimose delivers the same active ingredients—ethinylestradiol and etonogestrel—as many oral combined pills, but it is formulated for vaginal administration. This route may offer more consistent hormone absorption for some users, while the efficacy and safety profile remain comparable to other combined hormonal methods.

Myprimose should be stored at room temperature, below 25 °C, in its original packaging. Keep the product away from moisture, direct sunlight, and extreme temperature fluctuations to maintain its stability and effectiveness.

Myprimose is a vaginal formulation that is inserted according to the prescribing information, typically using an applicator or pre‑filled device. The exact administration schedule—such as frequency and duration—must be followed as directed by the healthcare provider.

The most serious risks include venous or arterial thromboembolism (e.g., deep‑vein thrombosis, pulmonary embolism, stroke), severe hypertension, liver disorders, and rare allergic reactions. Patients should seek immediate medical attention if they experience symptoms such as sudden chest pain, shortness of breath, severe headache, or unexplained swelling.

Myprimose is contraindicated in women who are pregnant, have a known or suspected thromboembolic disorder, uncontrolled hypertension, active liver disease, or a history of estrogen‑dependent tumors. It should also be avoided by smokers over 35 years of age and anyone with a known hypersensitivity to ethinylestradiol, etonogestrel, or any excipients.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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