Product image of Noodanticonceptie Ulipristal Etos (Ulipristal Acetate) supplied by GNH India

Noodanticonceptie Ulipristal Etos

Active Ingredient:
Ulipristal Acetate
Origin:
EU

Noodanticonceptie Ulipristal Etos (Ulipristal Acetate)

Ulipristal acetate, the active ingredient in Noodanticonceptie Ulipristal Etos, is a selective progesterone receptor modulator presented as an oral tablet for oral use. It is employed as emergency contraception to prevent pregnancy when taken up to five days after unprotected intercourse in women of reproductive age.

GNH India supplies Noodanticonceptie Ulipristal Etos as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, with a focus on quality assurance, regulatory compliance and reliable global logistics, and timely delivery.

Manufacturer / TM Owner

Healthypharm B.V.

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Indications & Clinical Uses

  • Ulipristal acetate is a selective progesterone receptor modulator used in the emergency contraception pathway.
  • Emergency contraception (up to 5 days after unprotected intercourse): provides a non‑surgical option to prevent pregnancy by delaying or inhibiting ovulation.
  • Contraceptive failure management: used when regular hormonal contraception fails, offering rapid pregnancy prevention.
  • Missed oral contraceptive dose rescue: effective after a missed scheduled pill, reducing the risk of unintended conception.

How It Works

  • Ulipristal acetate binds competitively to progesterone receptors in the hypothalamus, ovary and endometrium, blocking progesterone‑mediated signaling. This antagonism prevents the luteinizing hormone surge, thereby inhibiting or delaying ovulation, and also alters endometrial receptivity, reducing the likelihood of implantation if fertilization has occurred.

Side Effects

Ulipristal acetate is generally well tolerated, but several adverse reactions have been reported.

Common Side Effects

  • Nausea
  • Headache
  • Abdominal or pelvic pain
  • Fatigue or dizziness
  • Menstrual irregularities (early, delayed or heavier bleeding)
  • Mild allergic skin reactions (rash, itching)

Serious or Rare Side Effects

  • Anaphylactic or severe allergic reaction
  • Severe abdominal pain suggesting ectopic pregnancy
  • Liver enzyme elevation or hepatic injury
  • Persistent or worsening menstrual bleeding
  • Thromboembolic events (very rare)
  • Vision changes or severe headache indicating possible intracranial pressure changes

Precautions & Warnings

  • When prescribing or dispensing Ulipristal acetate, consider the following safety measures.
  • Timing of administration: take as soon as possible, preferably within 120 hours after unprotected intercourse.
  • Pregnancy status: avoid use if a confirmed pregnancy is present.
  • Breastfeeding: consult a healthcare professional before use.
  • Drug interactions: be aware of enzyme‑inducing agents that may lower effectiveness.
  • Medical conditions: use with caution in patients with hepatic impairment.
  • Store at ambient temperature: keep in the original packaging, protect from moisture and heat.

Avoid Interactions

Ulipristal acetate may interact with several concomitant medications.

Major Interactions (Avoid)

  • Rifampicin: strong enzyme inducer that markedly reduces efficacy.
  • St. John's wort: herbal inducer decreasing plasma levels.
  • Anticonvulsants (e.g., carbamazepine, phenytoin): lower drug exposure.

Moderate Interactions (Monitor Closely)

  • Hormonal contraceptives: may experience reduced effectiveness when taken together.
  • Antifungal azoles (e.g., ketoconazole): can increase ulipristal levels.
  • Certain antibiotics (e.g., tetracycline): minimal effect but monitoring is advised.

Frequently Asked Questions

Noodanticonceptie Ulipristal Etos contains ulipristal acetate and is used as an emergency contraceptive. It is intended to prevent pregnancy when taken within five days after unprotected sexual intercourse or when a regular contraceptive method fails.

Ulipristal acetate works by binding to progesterone receptors, blocking the hormone’s action. This prevents the luteinizing hormone surge needed for ovulation and also makes the uterine lining less receptive to a fertilized egg, thereby reducing the chance of implantation.

The specific dose and regimen are determined by the prescribing healthcare professional. Typically, a single oral tablet is administered, but the exact dosage must be confirmed by a qualified prescriber based on individual clinical circumstances.

Ulipristal acetate is not intended for use during an established pregnancy. Its safety in breastfeeding has not been fully established, so women who are nursing should discuss potential risks and benefits with their healthcare provider before use.

To place an order, 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 required import documentation.

Ulipristal acetate remains effective up to 120 hours after intercourse, whereas levonorgestrel’s efficacy declines sharply after 72 hours. Ulipristal also works by directly antagonizing progesterone receptors, offering a higher efficacy in later windows of the emergency contraception timeframe.

Store the tablets at ambient temperature, below 25 °C, in the original blister pack. Keep them away from moisture, direct sunlight and excessive heat to maintain product stability.

The medication is taken orally as a single tablet with water. It should be swallowed whole and not chewed. For optimal absorption, it can be taken with or without food, but the tablet must be ingested promptly after the prescribed time window.

Serious risks include severe allergic reactions such as anaphylaxis, possible hepatic injury, and rare cases of ectopic pregnancy that may present with persistent abdominal pain. Any signs of a severe reaction or unusual symptoms should prompt immediate medical attention.

Women with a known pregnancy, those with severe liver disease, or individuals who have had a hypersensitivity reaction to ulipristal acetate or any component of the tablet should avoid using this product. Consultation with a healthcare professional is essential before use.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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