Product image of Moventig (Naloxegol) supplied by GNH India

Moventig

Active Ingredient:
Naloxegol
Origin:
EU

Moventig (Naloxegol)

Naloxegol, the active ingredient in Moventig, is a peripheral opioid receptor antagonist presented as an oral dosage form for oral use. It is approved in the European Union for the treatment of opioid‑induced constipation in adult patients receiving opioid therapy.

GNH India supplies Moventig as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides regulatory‑approved products to a global customer base.

Manufacturer / TM Owner

Grünenthal Gmbh

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Indications & Clinical Uses

Naloxegol is used to manage opioid‑induced constipation, a gastrointestinal disorder associated with opioid therapy.

  • Opioid‑induced constipation: restores normal bowel movements in adults on chronic opioid therapy.
  • Opioid‑related gastrointestinal hypomotility: improves intestinal transit and reduces stool retention.
  • Patients receiving strong analgesics: alleviates constipation symptoms without affecting analgesia.

How It Works

  • Naloxegol selectively antagonizes μ‑opioid receptors located in the gastrointestinal tract while remaining excluded from the central nervous system. By blocking opioid binding peripherally, it prevents opioid‑mediated reduction of intestinal motility, thereby enhancing bowel transit and facilitating normal stool formation in patients receiving opioid therapy.

Side Effects

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

Common Side Effects

  • Abdominal pain: mild to moderate discomfort in the abdomen.
  • Diarrhea: increased frequency of loose stools.
  • Nausea: feeling of sickness or urge to vomit.
  • Flatulence: excess gas and bloating.
  • Vomiting: expulsion of stomach contents.
  • Constipation: occasional paradoxical worsening of bowel movements.

Serious or Rare Side Effects

  • Intestinal obstruction: signs of blockage requiring medical attention.
  • Severe abdominal pain: persistent or worsening pain.
  • Allergic reactions: rash, itching, swelling, or difficulty breathing.
  • Hepatic enzyme elevation: abnormal liver function tests.
  • Pancreatitis: inflammation of the pancreas presenting with upper abdominal pain.

Precautions & Warnings

Before initiating therapy, clinicians should evaluate patient-specific factors and monitor for potential complications.

  • Assess renal function: avoid or adjust use in severe renal impairment.
  • Monitor for abdominal pain: discontinue if signs of obstruction appear.
  • Avoid in known hypersensitivity: do not prescribe to patients with documented allergy to naloxegol.
  • Caution in gastrointestinal disorders: use carefully in patients with Crohn's disease or ulcerative colitis.
  • Store at ambient temperature: keep in the original packaging, protect from moisture and light.

Avoid Interactions

Naloxegol can interact with other medicines that affect its metabolism or transport.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors: may markedly increase naloxegol exposure and risk of adverse events.
  • Concomitant opioid antagonists: can reduce the intended effect on constipation.
  • P‑glycoprotein inhibitors: may raise systemic concentrations.

Moderate Interactions (Monitor Closely)

  • Moderate CYP3A4 inhibitors: may require dose adjustment or closer monitoring.
  • P‑glycoprotein inducers: could lower naloxegol effectiveness.
  • Anticholinergic agents: may exacerbate constipation if used together.

Frequently Asked Questions

Moventig contains naloxegol and is indicated for the treatment of opioid‑induced constipation in adult patients who are receiving opioid therapy. It helps restore normal bowel function by counteracting the constipating effects of opioids on the gastrointestinal tract.

Naloxegol is a selective peripheral μ‑opioid receptor antagonist. It blocks opioid binding in the gut without crossing the blood‑brain barrier, thereby preventing opioid‑mediated reduction of intestinal motility and promoting normal bowel movements.

The dosage of Moventig is determined by the prescribing healthcare professional based on the patient’s clinical condition, renal function, and response to therapy. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

Safety data for naloxegol in pregnancy and lactation are limited. It should only be used if the potential benefit justifies the potential risk to the fetus or infant, and the decision should be made by a qualified healthcare provider.

To order Moventig, submit an enquiry on the product page at gnhindia.com specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any required import documentation.

Moventig (naloxegol) is a peripheral μ‑opioid receptor antagonist, differing from laxatives that act locally or systemically. Compared with other antagonists such as methylnaltrexone, naloxegol is administered orally and does not affect central analgesia, offering a convenient option for many patients.

Moventig should be stored at ambient temperature, below 25 °C, in its original packaging. Keep the product away from moisture and direct sunlight to maintain stability and potency.

Moventig is taken orally, usually once daily, with or without food, as directed by the prescribing clinician. The tablet should be swallowed whole with a glass of water and not chewed or crushed.

Serious risks include intestinal obstruction, severe abdominal pain, and rare allergic reactions such as rash or breathing difficulties. Patients should seek immediate medical attention if they experience signs of blockage or severe discomfort.

Moventig is contraindicated in patients with known hypersensitivity to naloxegol or any component of the formulation, and it should be used with caution in individuals with severe renal impairment or existing gastrointestinal obstruction.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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