Product image of Lamotrigin Aurobindo (Lamotrigine) supplied by GNH India

Lamotrigin Aurobindo

Active Ingredient:
Lamotrigine
Origin:
EU

Lamotrigin Aurobindo (Lamotrigine)

Lamotrigine, the active ingredient in Lamotrigin Aurobindo, is a sodium channel blocker presented as an oral tablet for oral use. It is employed in the management of epilepsy and bipolar disorder, helping to control seizures and stabilize mood in adult patients with a generally favorable safety profile.

GNH India supplies Lamotrigin Aurobindo as a licensed, GDP‑compliant international pharmaceutical product serving hospitals, pharmacies and clinics worldwide through regulated distribution channels that meet local regulatory requirements, ensuring product integrity and timely delivery to end‑users.

Manufacturer / TM Owner

Puren Pharma Gmbh & Co. Kg

1
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Indications & Clinical Uses

Lamotrigine is an antiepileptic agent that modulates neuronal excitability.

  • Epilepsy (generalized and focal seizures): reduces seizure frequency and severity.
  • Bipolar disorder (maintenance therapy): stabilizes mood and helps prevent depressive episodes.
  • Adjunctive therapy for refractory seizures: provides additional seizure control when other antiepileptics are insufficient.

How It Works

  • Lamotrigine inhibits voltage‑gated sodium channels on neuronal membranes, decreasing the influx of sodium ions during depolarization. This stabilizes neuronal membranes, reduces the release of excitatory neurotransmitters such as glutamate, and dampens abnormal neuronal firing that underlies seizures and mood instability.

Side Effects

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

Common Side Effects

  • Dizziness: transient light‑headedness, especially after dose changes.
  • Headache: mild to moderate intensity, often improves with continued therapy.
  • Nausea: gastrointestinal upset that may lessen over time.
  • Rash: skin irritation that should be monitored for progression.
  • Blurred vision: temporary visual disturbances.
  • Fatigue: feeling of tiredness or reduced energy.

Serious or Rare Side Effects

  • Stevens‑Johnson syndrome: severe skin reaction requiring immediate medical attention.
  • Toxic epidermal necrolysis: life‑threatening skin detachment.
  • Blood dyscrasias: rare cases of aplastic anemia or agranulocytosis.
  • Hepatic failure: severe liver injury, though uncommon.
  • Suicidal ideation: emergence or worsening of depressive thoughts.

Precautions & Warnings

Lamotrigine requires careful monitoring and patient education.

  • Dose titration: increase gradually to minimise risk of rash.
  • Monitor skin: discontinue at first sign of widespread rash or hypersensitivity.
  • Assess hepatic function: adjust dose in patients with liver impairment.
  • Pregnancy: avoid unless benefits outweigh potential risks; discuss with a healthcare professional.
  • Store at room temperature: keep in the original pack, protect from moisture and light.

Avoid Interactions

Lamotrigine interacts with several medicines that can alter its plasma levels.

Major Interactions (Avoid)

  • Valproic acid: markedly increases lamotrigine concentrations, raising toxicity risk.
  • Carbamazepine: significantly reduces lamotrigine levels, potentially decreasing efficacy.
  • Phenytoin: lowers lamotrigine concentrations, requiring dose adjustment.

Moderate Interactions (Monitor Closely)

  • Oral contraceptives: may reduce lamotrigine levels, necessitating monitoring.
  • Serotonergic agents: combined use may increase risk of serotonin syndrome.
  • Phenobarbital: decreases lamotrigine exposure, possibly requiring dose increase.

Frequently Asked Questions

Lamotrigin Aurobindo contains lamotrigine, which is prescribed to control seizures in patients with epilepsy and to provide maintenance therapy for adults with bipolar disorder, helping to stabilise mood and prevent depressive episodes.

Lamotrigine blocks voltage‑gated sodium channels on neurons, reducing sodium influx during depolarisation. This stabilises neuronal membranes and limits the release of excitatory neurotransmitters such as glutamate, thereby decreasing abnormal electrical activity that leads to seizures and mood swings.

The dose of lamotrigine is individualised by the prescribing clinician based on the patient’s condition, age, concomitant medications and response. The prescriber determines the starting dose, titration schedule and maintenance dose, which may differ between epilepsy and bipolar disorder.

Lamotrigine is classified as pregnancy category unknown; it should only be used during pregnancy when the potential benefit justifies the potential risk to the fetus. Limited data exist for breastfeeding, and a healthcare professional should evaluate the risk‑benefit balance before use.

To place an 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.

Compared with older sodium‑channel blockers such as carbamazepine, lamotrigine has a lower risk of drug‑induced hyponatraemia and fewer cognitive side effects. Unlike valproic acid, it does not cause significant weight gain or teratogenicity, but it requires slower titration to avoid skin reactions.

Lamotrigin Aurobindo tablets should be stored at room temperature, below 25 °C, in the original container to protect them from moisture and light. Keep the product out of reach of children and avoid exposure to extreme temperatures.

The medication is taken orally, usually with a glass of water. It can be taken with or without food, but consistent administration with respect to meals helps maintain stable blood levels. Tablets should be swallowed whole and not crushed or chewed.

The most serious risks include severe skin reactions such as Stevens‑Johnson syndrome or toxic epidermal necrolysis, blood disorders like aplastic anaemia, hepatic failure, and the emergence of suicidal thoughts. Immediate medical attention is required if any of these symptoms appear.

Patients with a known hypersensitivity to lamotrigine or any component of the tablet should avoid the product. It is also contraindicated in individuals who have previously experienced severe skin reactions to lamotrigine or related compounds.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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