Product image of Пропес (Dinoprostone) supplied by GNH India

Пропес

Active Ingredient:
Dinoprostone
Origin:
EU

Пропес (Dinoprostone)

Пропес (Dinoprostone) is a prostaglandin E2 used to help prepare the cervix for labor induction. This medication supports cervical ripening in late-term pregnancies. It is administered vaginally under medical supervision. Suitable for patients requiring labor induction assistance.

Manufacturer / TM Owner

Ferring Gmbh

1
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Indications & Clinical Uses

  • Пропес (Dinoprostone) is used to help soften and dilate the cervix before labor begins. It is prescribed when labor needs to be induced for medical reasons, such as post-term pregnancy or when the mother’s or baby’s health requires delivery. This medication works by mimicking natural prostaglandins to prepare the cervix. It is not used for routine labor induction.

Side Effects

  • Пропес may cause mild uterine contractions as the cervix begins to soften and open. Some patients report localized warmth or discomfort at the application site. Headaches or mild fever are occasionally observed. These effects are typically temporary and monitored by healthcare providers during administration.

Precautions & Warnings

  • Пропес should only be used under direct medical supervision in a clinical setting. Patients with a history of difficult deliveries, uterine surgery, or certain medical conditions may not be suitable candidates. Continuous fetal monitoring is required during administration. Inform your healthcare provider of all current medications and health conditions before use.

Avoid Interactions

  • Concurrent use with other oxytocic agents may increase the risk of excessive uterine contractions. Medications that affect prostaglandin metabolism, such as NSAIDs, could alter the effectiveness of dinoprostone. Avoid combining with other cervical ripening agents unless directed by a physician. Always disclose all medications to your healthcare provider.

Frequently Asked Questions

It is used to help prepare the cervix for labor induction in late-term pregnancies.

It is administered vaginally by a healthcare professional in a clinical setting.

No, it must be used under direct medical supervision in a hospital or clinic.

Mild uterine contractions, localized warmth, headaches, or low-grade fever may occur.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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