Product image of Naxalgan (Pregabalin) supplied by GNH India

Naxalgan

Active Ingredient:
Pregabalin
Origin:
EU

Naxalgan (Pregabalin)

Pregabalin, the active ingredient in Naxalgan, is a gabapentinoid presented as an oral tablet for oral administration. It is used to manage neuropathic pain conditions such as diabetic peripheral neuropathy and post‑herpetic neuralgia, to control partial‑onset seizures, and to treat generalized anxiety disorder in adult patients.

GNH India supplies Naxalgan as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, ensuring quality and regulatory compliance across EU and global markets. The product conforms to EU GMP standards and is available for bulk and retail distribution.

Manufacturer / TM Owner

Vipharm S.A.

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Indications & Clinical Uses

Pregabalin is employed to treat conditions involving neuropathic pain, seizures, and anxiety.

  • Diabetic peripheral neuropathic pain: reduces pain intensity and improves sensory function.
  • Postherpetic neuralgia: alleviates chronic burning and stabbing pain after shingles.
  • Fibromyalgia: lessens widespread musculoskeletal pain and fatigue.
  • Partial onset seizures: decreases seizure frequency in adults.
  • Generalized anxiety disorder: diminishes excessive worry and associated symptoms.

How It Works

  • Pregabalin binds selectively to the α2‑δ subunit of voltage‑gated calcium channels in the central nervous system. This binding reduces calcium influx into presynaptic neurons, which in turn decreases the release of excitatory neurotransmitters such as glutamate, norepinephrine, and substance P, leading to diminished neuronal hyperexcitability associated with pain, seizures, and anxiety.

Side Effects

Pregabalin may cause a range of adverse reactions, varying from mild to serious.

Common Side Effects

  • Dizziness: sensation of light‑headedness or unsteadiness.
  • Somnolence: increased sleepiness or fatigue.
  • Peripheral edema: swelling of the lower extremities.
  • Weight gain: gradual increase in body weight.

Serious or Rare Side Effects

  • Angioedema: rapid swelling of face, lips, tongue, or throat.
  • Severe hypersensitivity: rash, itching, or anaphylactic reactions.
  • Suicidal thoughts: emergence of depressive symptoms or suicidal ideation.

Precautions & Warnings

Before prescribing Naxalgan, clinicians should consider several safety aspects.

  • Renal impairment: dose adjustment may be required in patients with reduced kidney function.
  • Elderly patients: monitor for increased dizziness or falls.
  • Concomitant CNS depressants: avoid excessive sedation when combined with alcohol or opioids.
  • Pregnancy and lactation: use only if the potential benefit justifies the potential risk to the fetus or infant.
  • Store at ambient temperature: keep below 25°C in the original packaging, protected from moisture and direct sunlight.

Avoid Interactions

Pregabalin can interact with other medicines, affecting efficacy or safety.

Major Interactions (Avoid)

  • Opioids: combined use may cause profound respiratory depression and profound sedation.
  • CNS depressants (e.g., benzodiazepines): may result in excessive drowsiness or impaired coordination.

Moderate Interactions (Monitor Closely)

  • Antihypertensives: pregabalin may enhance blood‑pressure‑lowering effects.
  • Diuretics: monitor for increased risk of peripheral edema.
  • ACE inhibitors or ARBs: watch for additive effects on renal function in susceptible patients.

Frequently Asked Questions

Naxalgan contains pregabalin, which is prescribed for diabetic peripheral neuropathic pain, post‑herpetic neuralgia, fibromyalgia, partial‑onset seizures, and generalized anxiety disorder in adult patients.

Pregabalin binds to the α2‑δ subunit of voltage‑gated calcium channels, reducing calcium entry into nerve terminals and thereby decreasing the release of excitatory neurotransmitters that contribute to pain, seizure activity, and anxiety.

The appropriate dose of Naxalgan is determined by the prescribing healthcare professional based on the patient’s specific condition, response, and renal function. Dosage adjustments are made individually.

Pregabalin’s safety in pregnancy and lactation has not been fully established. It should only be used if the potential benefit outweighs the possible risk to the fetus or infant, and the decision must be made by a qualified clinician.

To request Naxalgan, 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.

Naxalgan (pregabalin) shares a similar mechanism with gabapentin but generally offers more predictable pharmacokinetics, higher potency, and a faster onset of action, which can translate into more consistent symptom control for neuropathic pain and seizures.

Naxalgan should be stored at ambient temperature, below 25 °C, in its original blister pack or container, protected from moisture, heat and direct sunlight to maintain stability.

Naxalgan is taken orally, usually with or without food, as directed by the prescriber. Tablets should be swallowed whole with water and not crushed or chewed unless specifically instructed.

Serious risks include angioedema, severe hypersensitivity reactions, and the emergence of suicidal thoughts or behaviors. Patients should be monitored closely for any signs of swelling, rash, or mood changes.

Naxalgan is contraindicated in patients with known hypersensitivity to pregabalin or any component of the formulation. Caution is also advised for individuals with severe renal impairment who have not had dose adjustments.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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