Product image of Natriumoxybat Accord (Sodium Oxybate) supplied by GNH India

Natriumoxybat Accord

Active Ingredient:
Sodium Oxybate
Origin:
EU

Natriumoxybat Accord (Sodium Oxybate)

Sodium Oxybate, the active ingredient in Natriumoxybat Accord, is a gamma‑hydroxybutyrate (GHB) CNS depressant presented as an oral formulation for oral use. It is indicated for the treatment of narcolepsy, specifically addressing cataplexy and excessive daytime sleepiness in affected patients.

GNH India supplies Natriumoxybat Accord as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Accord Healthcare B.V.

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Indications & Clinical Uses

Sodium Oxybate is used in the management of narcolepsy and its related symptom complex.

  • Narcolepsy with cataplexy: reduces the frequency and severity of cataplexy episodes.
  • Excessive daytime sleepiness (narcolepsy): improves wakefulness and reduces daytime sleepiness.
  • Nighttime sleep quality (narcolepsy): enhances slow‑wave sleep, leading to more restorative sleep.

How It Works

  • Sodium Oxybate acts as an agonist at both GHB receptors and GABA_B receptors in the central nervous system. Activation of these receptors increases slow‑wave (deep) sleep and modulates neurotransmission, which together diminish cataplexy attacks and improve daytime alertness in patients with narcolepsy.

Side Effects

Sodium Oxybate may cause a range of adverse reactions, which are categorized by frequency and severity.

Common Side Effects

  • Nausea: mild to moderate stomach upset.
  • Headache: transient cranial discomfort.
  • Dizziness: sensation of light‑headedness.
  • Nasal congestion: blockage or runny nose.

Serious or Rare Side Effects

  • Respiratory depression: reduced breathing effort, potentially life‑threatening.
  • Seizures: occurrence of convulsive episodes.
  • Severe hypotension: marked drop in blood pressure causing faintness.

Precautions & Warnings

When prescribing Sodium Oxybate, clinicians should observe several safety precautions.

  • Contraindication: avoid use in patients with known hypersensitivity to sodium oxybate or GHB.
  • Respiratory risk: monitor patients with compromised breathing or sleep‑disordered breathing.
  • Alcohol interaction: advise patients to abstain from alcohol while on therapy.
  • Pregnancy and lactation: use only if potential benefit justifies potential risk; discuss with obstetrician.
  • Store at ambient temperature: keep below 25 °C in the original container, protected from moisture and light.

Avoid Interactions

Sodium Oxybate can interact with other medicines, requiring careful management.

Major Interactions (Avoid)

  • Central nervous system depressants (e.g., benzodiazepines, opioids): additive sedation and respiratory depression.
  • Sodium‑containing medications (e.g., high‑dose sodium bicarbonate): risk of sodium overload and hypertension.

Moderate Interactions (Monitor Closely)

  • Antidepressants (especially SSRIs): may increase risk of serotonin syndrome.
  • Antihypertensive agents: potential enhancement of blood‑pressure‑lowering effect.
  • Anticonvulsants: possible alteration of seizure threshold.

Frequently Asked Questions

Natriumoxybat Accord contains sodium oxybate and is prescribed for patients with narcolepsy to treat cataplexy episodes and to reduce excessive daytime sleepiness, helping improve overall wakefulness and nighttime sleep quality.

Sodium oxybate binds to GHB and GABA_B receptors in the brain, promoting deep slow‑wave sleep and modulating neurotransmitter activity. This dual action lessens cataplexy attacks and enhances daytime alertness in people with narcolepsy.

The exact dose of sodium oxybate is individualized and set by the prescribing clinician based on the patient’s age, weight, severity of symptoms, and response to therapy. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

Safety data are limited; sodium oxybate should be used during pregnancy or lactation only if the potential benefit outweighs the possible risk to the fetus or infant. Healthcare providers should discuss these considerations with the patient and a obstetric specialist.

To 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 necessary import documentation.

The primary alternative, modafinil, is a wake‑promoting agent that does not address cataplexy. Sodium oxybate, by contrast, improves both nighttime sleep architecture and cataplexy control, offering a broader therapeutic effect for patients whose primary issue includes cataplexy.

Store Natriumoxybat Accord at ambient temperature, preferably below 25 °C. Keep the product in its original packaging, protect it from moisture and direct light, and ensure the container is tightly closed when not in use.

The medication is taken orally, usually in divided doses at night as directed by the prescriber. It is important to follow the exact timing and dosing schedule to achieve optimal therapeutic benefit and to minimize adverse effects.

Serious risks include respiratory depression, severe hypotension, and seizures. Patients should be monitored for signs of breathing difficulty, sudden drops in blood pressure, or convulsive activity, and should seek immediate medical attention if any of these occur.

Individuals with known hypersensitivity to sodium oxybate or other GHB compounds, those with severe respiratory disorders, and patients who consume alcohol heavily should avoid this medication. It is also contraindicated in patients for whom the risks outweigh the therapeutic benefits.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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