Product image of Nitrazepam "dak" (Nitrazepam) supplied by GNH India

Nitrazepam "dak"

Active Ingredient:
Nitrazepam
Origin:
EU

Nitrazepam "dak" (Nitrazepam)

Nitrazepam, the active ingredient in Nitrazepam dak, is a benzodiazepine presented as an oral tablet for oral administration. It exerts sedative, anxiolytic, muscle‑relaxant and anticonvulsant actions, and is indicated for the short‑term treatment of insomnia, the management of anxiety disorders, and the control of certain epileptic seizures in adult patients.

GNH India supplies Nitrazepam dak as a licensed, GDP‑compliant product sourced from the EU, providing reliable access to hospitals, pharmacies and clinics worldwide. The company adheres to international quality standards and offers comprehensive regulatory support for cross‑border distribution.

Manufacturer / TM Owner

Orifarm Healthcare A/S

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Indications & Clinical Uses

Nitrazepam is a benzodiazepine that acts on the central nervous system to modulate GABA activity.

  • Insomnia: improves sleep onset and maintenance in patients with short‑term sleep disturbance.
  • Anxiety disorders: reduces excessive anxiety, tension and associated autonomic symptoms.
  • Epileptic seizures: helps control certain seizure types, particularly absence and myoclonic seizures, when used as adjunct therapy.

How It Works

  • Nitrazepam binds to an allosteric site on the GABA‑A receptor complex, increasing the frequency of chloride channel opening in response to GABA. This enhances chloride influx, hyperpolarising neuronal membranes and producing sedative, anxiolytic, muscle‑relaxant and anticonvulsant effects throughout the central nervous system.

Side Effects

Nitrazepam may cause a range of adverse reactions, from mild to severe.

Common Side Effects

  • Drowsiness: feeling unusually sleepy during daytime activities.
  • Dizziness: sensation of light‑headedness or unsteadiness.
  • Impaired coordination: reduced motor control affecting tasks such as driving.
  • Memory impairment: difficulty recalling recent events.

Serious or Rare Side Effects

  • Respiratory depression: slowed breathing that may be life‑threatening.
  • Severe allergic reactions: rash, swelling, or anaphylaxis.
  • Withdrawal seizures: seizures occurring after abrupt discontinuation.
  • Mood changes: depression, suicidal thoughts, or paradoxical aggression.

Precautions & Warnings

When prescribing nitrazepam, clinicians should consider several safety measures.

  • Dose adjustment in elderly: start with the lowest effective dose due to increased sensitivity.
  • Avoid abrupt discontinuation: taper under medical supervision to prevent withdrawal phenomena.
  • Use with caution in hepatic impairment: monitor plasma levels and clinical response.
  • Avoid concomitant CNS depressants: increased risk of profound sedation and respiratory depression.
  • Pregnancy and lactation: contraindicated; classified as Category D.
  • Store at ambient temperature: keep below 25°C in the original container, protect from moisture and light.

Avoid Interactions

Nitrazepam can interact with other medicines, altering its safety profile.

Major Interactions (Avoid)

  • Opioids: additive respiratory depression and profound sedation.
  • Alcohol: synergistic CNS depression leading to marked drowsiness.
  • Other benzodiazepines: cumulative sedative effect and increased overdose risk.

Moderate Interactions (Monitor Closely)

  • Antidepressants (SSRIs): may enhance sedation and dizziness.
  • Antihistamines: increased drowsiness and impaired psychomotor performance.
  • CYP3A4 inhibitors (e.g., erythromycin, ketoconazole): may raise nitrazepam plasma concentrations.

Frequently Asked Questions

Nitrazepam dak contains the benzodiazepine nitrazepam and is prescribed for the short‑term treatment of insomnia, the management of anxiety disorders, and as an adjunct in controlling certain types of epileptic seizures, particularly absence and myoclonic seizures.

Nitrazepam binds to a specific site on the GABA‑A receptor, increasing the frequency of chloride channel opening when GABA is present. This enhances inhibitory neurotransmission, leading to sedation, anxiolysis, muscle relaxation and anticonvulsant effects.

The appropriate dose of nitrazepam is individualized by the prescribing clinician based on the patient’s age, clinical condition, and response to therapy. Dosage adjustments may be required for elderly patients or those with hepatic impairment.

Nitrazepam is classified as Pregnancy Category D, indicating evidence of fetal risk. It is generally contraindicated during pregnancy and lactation because it can cross the placenta and enter breast milk, potentially causing sedation or withdrawal in the infant.

To request Nitrazepam dak, 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.

Nitrazepam shares the core mechanism of GABA‑A modulation with other benzodiazepines but has a relatively long half‑life, which can provide sustained sleep promotion. Compared with shorter‑acting agents, it may carry a higher risk of daytime sedation and accumulation in the elderly.

Store Nitrazepam dak at ambient temperature, preferably below 25 °C, in its original blister pack or container. Protect it from moisture, direct sunlight and excessive heat to maintain potency and prevent degradation.

Nitrazepam dak is taken orally, usually with a glass of water. It may be administered with or without food, but patients should follow the prescriber’s instructions regarding timing relative to meals to ensure consistent absorption.

Serious risks include respiratory depression, especially when combined with other CNS depressants, severe allergic reactions, withdrawal seizures after abrupt discontinuation, and profound sedation that can impair driving or operating machinery.

Nitrazepam is contraindicated in patients with known hypersensitivity to benzodiazepines, severe respiratory insufficiency, acute narrow‑angle glaucoma, and in pregnant or breastfeeding women. Caution is also advised for individuals with severe hepatic impairment or a history of substance dependence.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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