Product image of Mytulip (Chlormadinone Acetate, Ethinylestradiol) supplied by GNH India

Mytulip

Active Ingredient:
Chlormadinone Acetate, Ethinylestradiol
Origin:
EU

Mytulip (Chlormadinone Acetate, Ethinylestradiol)

Chlormadinone acetate and ethinylestradiol, the active ingredients in Mytulip, are a combined oral contraceptive presented as a tablet for oral use. They prevent pregnancy in women of reproductive age by suppressing ovulation and altering cervical mucus and the endometrium. Mytulip is marketed in the European Union and complies with EU pharmaceutical standards.

GNH India supplies Mytulip 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

  • Mytulip, a combined oral contraceptive, is indicated for hormonal regulation to prevent pregnancy.
  • Prevention of pregnancy: provides reliable contraceptive protection by inhibiting ovulation and inducing cervical mucus and endometrial changes that prevent fertilisation and implantation.

How It Works

  • Mytulip combines chlormadinone acetate, a progestogenic agent, with ethinylestradiol, a synthetic estrogen. The estrogen component suppresses the hypothalamic‑pituitary‑ovarian axis, reducing follicle‑stimulating hormone release, while the progestogen further inhibits luteinising hormone surge, preventing ovulation. Both hormones also thicken cervical mucus and modify the endometrium, creating an environment hostile to sperm penetration and implantation.

Side Effects

Mytulip may cause a range of adverse reactions. Common side effects are usually mild and transient, while serious or rare events require immediate medical attention.

Common Side Effects

  • Nausea: mild stomach upset that often resolves with continued use.
  • Breast tenderness: temporary swelling or discomfort of the breasts.
  • Headache: mild to moderate headache episodes.
  • Irregular vaginal bleeding: spotting or breakthrough bleeding between periods.

Serious or Rare Side Effects

  • Blood clots (deep‑vein thrombosis, pulmonary embolism): sudden leg pain, swelling, or shortness of breath.
  • Severe hypertension: markedly elevated blood pressure, headache, or visual changes.
  • Liver disorders (cholestatic jaundice): yellowing of skin or eyes, dark urine, itching.

Precautions & Warnings

Before prescribing Mytulip, clinicians should evaluate several safety considerations.

  • Contraindicated in pregnancy: product is category X and must not be used by pregnant women.
  • History of thromboembolic disease: avoid due to increased clotting risk.
  • Uncontrolled hypertension: assess blood pressure and treat before initiation.
  • Estrogen‑sensitive tumors: contraindicated in known or suspected breast or endometrial cancer.
  • Smoking in women over 35 years: heightened cardiovascular risk; advise cessation.
  • Store at room temperature below 25°C: keep in the original packaging, protect from moisture and light.

Avoid Interactions

Mytulip can interact with other medicines, altering its effectiveness or safety profile.

Major Interactions (Avoid)

  • Enzyme‑inducing anticonvulsants (e.g., carbamazepine, phenytoin): markedly reduce contraceptive efficacy.
  • Rifampin or rifabutin: decrease hormone levels, increasing risk of unintended pregnancy.
  • Protease inhibitor ritonavir: may raise estrogen concentrations, heightening side‑effect risk.

Moderate Interactions (Monitor Closely)

  • Broad‑spectrum antibiotics (e.g., tetracycline, fluoroquinolones): possible modest reduction in contraceptive effect.
  • St. John’s wort: may lower hormone levels, requiring additional contraceptive measures.
  • Selective serotonin reuptake inhibitors: may increase incidence of mood‑related side effects.

Frequently Asked Questions

Mytulip is a combined oral contraceptive that contains chlormadinone acetate and ethinylestradiol. It is prescribed to prevent pregnancy in women of reproductive age by inhibiting ovulation and creating cervical mucus and endometrial conditions that are unfavorable for fertilisation and implantation.

Chlormadinone acetate is a synthetic progestogen that suppresses the hypothalamic‑pituitary‑ovarian axis, reducing the luteinising hormone surge needed for ovulation. Together with ethinylestradiol, it also thickens cervical mucus and alters the endometrium, providing multiple mechanisms that prevent conception.

The dosing regimen for Mytulip is determined by the prescribing healthcare professional. Typically, combined oral contraceptives are taken once daily for a specified cycle, but the exact schedule, tablet strength and duration must be set by the prescriber based on individual patient needs.

Mytulip is classified as pregnancy category X, meaning it must not be used during pregnancy because it can cause fetal harm. It is also not recommended while breastfeeding, as hormonal components may pass into breast milk and affect the infant. Women should discontinue use if they become pregnant.

To order Mytulip, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide. After the request, the sales team will verify trade or institutional credentials, then provide pricing, availability, shipping details and any necessary import documentation.

Mytulip contains chlormadinone acetate, a progestogen with a slightly higher anti‑androgenic profile, combined with ethinylestradiol. Compared with other combined pills that use levonorgestrel or desogestrel, Mytulip may offer different bleeding pattern profiles and a comparable efficacy, but the choice depends on individual risk factors, tolerability and clinician preference.

Mytulip tablets should be stored at room temperature below 25 °C. Keep them in the original blister pack or container, protect from moisture and direct light, and ensure they are out of reach of children.

Mytulip is taken orally, usually once daily at the same time each day. The tablets are swallowed with water and should be started according to the prescriber's instructions, often on the first day of the menstrual period or after a hormone‑free interval.

The most serious risks include venous or arterial thromboembolism, severe hypertension, and liver disorders such as cholestatic jaundice. Women with a history of clotting disorders, uncontrolled high blood pressure, smoking over age 35, or estrogen‑sensitive cancers should be evaluated carefully before using Mytulip.

Mytulip is contraindicated in pregnant women, individuals with known or suspected estrogen‑dependent tumors (e.g., breast cancer), active or past thromboembolic disease, severe uncontrolled hypertension, liver disease, and women over 35 who smoke. It should also be avoided in patients with known hypersensitivity to either chlormadinone acetate or ethinylestradiol.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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