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 dosage form for oral administration. It is indicated for the treatment of partial onset seizures, diabetic peripheral neuropathic pain, postherpetic neuralgia, fibromyalgia, and generalized anxiety disorder, providing symptom relief in adult patients across these therapeutic areas.

GNH India supplies Naxalgan as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, ensuring quality and regulatory conformity for global distribution. Our supply chain adheres to stringent quality standards and supports timely delivery to healthcare providers.

Manufacturer / TM Owner

Vipharm S.A.

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Indications & Clinical Uses

Pregabalin acts on the nervous system to reduce abnormal neuronal firing associated with seizures and neuropathic pain.

  • Partial onset seizures: reduces seizure frequency in patients with epilepsy.
  • Diabetic peripheral neuropathic pain: alleviates pain and improves sensory function in diabetic patients.
  • Postherpetic neuralgia: decreases persistent pain following shingles.
  • Fibromyalgia: lessens widespread musculoskeletal pain and improves quality of life.
  • Generalized anxiety disorder: diminishes anxiety symptoms and promotes calmness.

How It Works

  • Pregabalin binds selectively to the α2δ subunit of voltage‑gated calcium channels in the central nervous system, decreasing calcium influx into presynaptic neurons. This action reduces the release of excitatory neurotransmitters such as glutamate, norepinephrine, and substance P, thereby dampening neuronal hyperexcitability that underlies seizures, neuropathic pain, and anxiety.

Side Effects

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

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.
  • Dry mouth: reduced salivation leading to oral discomfort.
  • Blurred vision: temporary visual disturbances.

Serious or Rare Side Effects

  • Angioedema: rapid swelling of face, lips, tongue, or throat requiring emergency care.
  • Severe skin reactions: such as Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Suicidal thoughts: emergence of depressive symptoms or suicidal ideation.
  • Respiratory depression: especially when combined with other CNS depressants.
  • Cardiac failure: worsening of pre‑existing heart failure symptoms.

Precautions & Warnings

Before initiating therapy, clinicians should evaluate patient‑specific factors and monitor for potential risks.

  • Assess renal function: adjust dose in patients with impaired clearance.
  • Monitor for suicidal ideation: counsel patients and caregivers about mood changes.
  • Avoid abrupt discontinuation: taper dose under medical supervision to prevent withdrawal.
  • Use caution in pregnancy: limited data; weigh benefits against potential risks.
  • Evaluate for hypersensitivity: discontinue if rash or angioedema develops.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Pregabalin can interact with other medicines, altering its efficacy or safety profile.

Major Interactions (Avoid)

  • Opioids: combined use may increase risk of respiratory depression and profound sedation.
  • Central nervous system depressants (e.g., benzodiazepines, alcohol): may enhance sedative effects and impair cognition.

Moderate Interactions (Monitor Closely)

  • Antacids containing aluminum or magnesium: may reduce pregabalin absorption; separate dosing by at least 2 hours.
  • Diuretics: can raise serum pregabalin concentrations, requiring monitoring for side effects.
  • NSAIDs: may potentiate peripheral edema; observe for swelling.

Frequently Asked Questions

Naxalgan contains pregabalin and is prescribed for partial onset seizures, diabetic peripheral neuropathic pain, postherpetic neuralgia, fibromyalgia, and generalized anxiety disorder. It helps control seizure activity, relieve various types of neuropathic pain, and reduce anxiety symptoms in adult patients.

Pregabalin binds to the α2δ subunit of voltage‑gated calcium channels in the central nervous system. This binding reduces calcium entry into nerve terminals, which in turn lowers the release of excitatory neurotransmitters such as glutamate, norepinephrine, and substance P, dampening neuronal hyperexcitability that contributes to seizures, pain, and anxiety.

The appropriate dose of Naxalgan is determined individually by a qualified prescriber based on the patient’s condition, renal function, and response to therapy. Clinicians start with a low dose and may adjust it gradually, following current clinical guidelines and patient tolerance.

Safety data for pregabalin in pregnancy and lactation are limited. It should only be used when the potential benefit justifies any potential risk to the fetus. Women who are breastfeeding should discuss possible infant exposure with their healthcare provider, as pregabalin may be present in breast milk.

To place an order, submit an enquiry on the Naxalgan 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 (including any cold‑chain requirements), and necessary import documentation.

The primary alternative to pregabalin is gabapentin, another gabapentinoid. Both agents share a similar mechanism but pregabalin generally has higher potency, more predictable absorption, and may achieve therapeutic levels faster. Clinical choice depends on efficacy, tolerability, patient-specific factors, and prescribing physician preference.

Naxalgan should be stored at room temperature, below 25 °C, in its original packaging. Protect the product from moisture, excessive heat, and direct sunlight. Keep it out of reach of children and do not use after the expiration date.

Naxalgan is taken orally, usually with or without food, as directed by the prescribing clinician. The tablets (or capsules) should be swallowed whole with a glass of water and not crushed or chewed unless specifically instructed.

Serious risks include angioedema (rapid swelling of the face, lips, tongue, or throat), severe skin reactions such as Stevens‑Johnson syndrome, emergence of suicidal thoughts or depressive symptoms, respiratory depression when combined with other CNS depressants, and worsening of heart failure due to fluid retention.

Naxalgan is contraindicated in patients with known hypersensitivity to pregabalin or any of its excipients. Caution is advised for individuals with severe renal impairment, uncontrolled heart failure, or a history of suicidal behavior. Pregnant or breastfeeding women should only use it when clearly needed and after consulting a healthcare professional.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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