Product image of Oxycodone/Naloxone Stada (Naloxone, Oxycodone) supplied by GNH India

Oxycodone/Naloxone Stada

Active Ingredient:
Naloxone, Oxycodone
Origin:
EU

Oxycodone/Naloxone Stada (Naloxone, Oxycodone)

Naloxone, the active ingredient in Oxycodone/Naloxone Stada, is an opioid antagonist presented as a combination formulation for oral use. It is paired with oxycodone to manage pain while reducing opioid‑induced constipation. GNH India supplies Oxycodone/Naloxone Stada as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals and pharmacies worldwide.

GNH India supplies Oxycodone/Naloxone Stada as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals and pharmacies worldwide.

Manufacturer / TM Owner

Stada Arzneimittel Ag

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Indications & Clinical Uses

Oxycodone/Naloxone Stada is used in the management of moderate to severe pain where opioid therapy is required and constipation is a concern.

  • Chronic non‑cancer pain: provides analgesia while mitigating opioid‑induced bowel dysfunction.
  • Cancer‑related pain: delivers strong pain relief with reduced risk of constipation.
  • Post‑operative pain: controls acute pain after surgery and helps maintain bowel function.
  • Pain in opioid‑tolerant patients: offers effective analgesia with a built‑in antagonist to limit excess opioid effects.

How It Works

  • The combination works by delivering oxycodone, a µ‑opioid receptor agonist that produces analgesia, together with naloxone, a peripheral µ‑opioid receptor antagonist that remains largely inactive systemically when taken orally but blocks opioid receptors in the gastrointestinal tract, thereby reducing constipation while preserving central pain relief.

Side Effects

Side effects are reported for both components of the combination, with the naloxone component primarily influencing gastrointestinal tolerance.

Common Side Effects

  • Nausea: mild to moderate upset stomach.
  • Constipation: reduced bowel movements despite naloxone.
  • Dizziness: light‑headed sensation.
  • Somnolence: sleepiness or fatigue.
  • Dry mouth: reduced salivation.
  • Headache: mild cranial pain.

Serious or Rare Side Effects

  • Respiratory depression: slowed breathing, potentially life‑threatening.
  • Severe hypotension: marked drop in blood pressure.
  • Acute opioid withdrawal: agitation, sweating, vomiting when naloxone effect dominates.
  • Hepatic dysfunction: elevated liver enzymes.
  • Allergic reactions: rash, itching, swelling, or anaphylaxis.
  • Seizures: rare convulsive episodes.

Precautions & Warnings

When prescribing Oxycodone/Naloxone Stada, clinicians should consider patient history and monitor for adverse reactions.

  • Assess renal and hepatic function: adjust use if impairment is present.
  • Evaluate gastrointestinal history: patients with severe bowel obstruction may need alternative therapy.
  • Monitor for signs of opioid dependence or abuse: use with caution in at‑risk individuals.
  • Avoid concurrent strong CYP3A4 inhibitors: may increase oxycodone levels.
  • Educate patients on proper dosing and risks: ensure understanding of when to seek medical help.
  • Store at ambient temperature: keep in original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Oxycodone/Naloxone Stada can interact with several drug classes, requiring careful management.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may raise oxycodone concentrations and increase toxicity risk.
  • CNS depressants (e.g., benzodiazepines, barbiturates, alcohol): additive sedation and respiratory depression.
  • MAO inhibitors: can precipitate severe hypertension or serotonin syndrome.

Moderate Interactions (Monitor Closely)

  • Moderate CYP3A4 inhibitors (e.g., erythromycin): may modestly increase oxycodone exposure.
  • Diuretics: can enhance hypotensive effects.
  • Anticholinergics: may worsen constipation despite naloxone component.

Frequently Asked Questions

Oxycodone/Naloxone Stada is indicated for the treatment of moderate to severe pain when opioid therapy is needed and there is a concern about opioid‑induced constipation. It is used in chronic non‑cancer pain, cancer‑related pain, post‑operative pain and in patients who are already tolerant to opioids.

Naloxone is a peripheral µ‑opioid receptor antagonist that, when taken orally, remains largely confined to the gastrointestinal tract. It blocks opioid receptors there, reducing constipation, while allowing oxycodone to act centrally on µ‑receptors to provide analgesia.

The specific dose and dosing schedule are determined by the prescribing clinician based on the patient’s pain severity, prior opioid exposure, renal and hepatic function, and overall clinical condition. No standard dose is provided here.

Both oxycodone and naloxone cross the placenta and can be present in breast milk. Use is generally discouraged unless the potential benefit justifies the potential risk to the fetus or infant, and it should only be prescribed after careful risk‑benefit assessment by a qualified health professional.

To place an order, submit an enquiry on the product page at gnhindia.com with 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 necessary import documentation.

Compared with plain oxycodone tablets, the combination adds naloxone to actively counteract opioid‑induced constipation, offering similar analgesic efficacy with a lower incidence of bowel‑related side effects. This can improve patient comfort and adherence compared with opioid‑only regimens.

Store the tablets at ambient temperature, preferably below 25 °C, in the original container to protect them from moisture and direct sunlight. Keep out of reach of children and do not use if the packaging is damaged.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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