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

Lamotrigin Al

Active Ingredient:
Lamotrigine
Origin:
EU

Lamotrigin Al (Lamotrigine)

Lamotrigine, the active ingredient in Lamotrigin Al, is an anticonvulsant presented as an oral tablet for oral use. It treats epilepsy, including partial and generalized seizures, and is used as maintenance therapy for bipolar disorder in adults.
GNH India supplies Lamotrigin Al as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Aliud Pharma Gmbh

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Indications & Clinical Uses

Lamotrigine is an anticonvulsant that acts on seizure activity and mood regulation.

  • Epilepsy (partial seizures): Reduces the frequency of partial seizures in adults and children.
  • Epilepsy (generalized tonic‑clonic seizures): Prevents occurrence of generalized tonic‑clonic seizures.
  • Epilepsy (secondary generalized seizures): Decreases risk of seizure generalisation.
  • Bipolar disorder (maintenance therapy): Helps maintain mood stability and prevents recurrence of depressive or manic episodes.

How It Works

  • Lamotrigine inhibits voltage‑gated sodium channels, stabilising neuronal membranes and diminishing the release of excitatory neurotransmitters such as glutamate. This reduction in neuronal hyper‑excitability underlies its antiepileptic and mood‑stabilising effects.

Side Effects

Lamotrigine may cause a range of adverse reactions, most of which are mild and transient.

Common Side Effects

  • Dizziness: Light‑headed sensation, often transient.
  • Headache: Mild to moderate cranial pain.
  • Nausea: Stomach upset, sometimes with mild vomiting.
  • Rash: Skin redness or itching, usually limited.
  • Blurred vision: Temporary visual disturbances.
  • Insomnia: Difficulty falling or staying asleep.

Serious or Rare Side Effects

  • Stevens‑Johnson syndrome: Severe skin reaction requiring immediate medical attention.
  • Toxic epidermal necrolysis: Life‑threatening skin detachment.
  • Blood dyscrasias: Aplastic anaemia or agranulocytosis.
  • Hepatic failure: Marked liver enzyme elevation or liver injury.
  • Suicidal thoughts: Emergence of depressive or suicidal ideation.
  • Severe rash with mucosal involvement: Requires urgent evaluation.

Precautions & Warnings

When prescribing Lamotrigin Al, clinicians should consider several safety measures.

  • Dose titration: Initiate at a low dose and increase gradually as directed.
  • Renal impairment: Adjust dose in patients with reduced renal function.
  • Hepatic impairment: Use caution in liver disease and monitor function.
  • Concomitant valproate: May increase lamotrigine levels, raising toxicity risk.
  • Pregnancy: Discuss potential risks with the prescriber; data are limited.
  • Store at ambient temperature: Keep below 25°C in the original pack, protect from moisture.

Avoid Interactions

Lamotrigin Al interacts with several medicines that can alter its plasma concentration.

Major Interactions (Avoid)

  • Valproic acid: Increases lamotrigine levels, heightening toxicity risk.
  • Carbamazepine: Decreases lamotrigine levels, potentially reducing efficacy.
  • Phenobarbital: Lowers lamotrigine concentrations, may require dose increase.
  • Phenytoin: Reduces lamotrigine exposure, risking seizure breakthrough.

Moderate Interactions (Monitor Closely)

  • Oral contraceptives: May lower lamotrigine levels; monitor seizure control.
  • Serotonergic agents: Potential for serotonin syndrome; observe for symptoms.
  • Other antiepileptics: May necessitate dose adjustments based on therapeutic response.

Frequently Asked Questions

Lamotrigin Al contains lamotrigine, which is prescribed for the treatment of epilepsy—including partial, generalized tonic‑clonic and secondary generalized seizures—and as maintenance therapy to stabilize mood in adults with bipolar disorder.

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

The appropriate dose of Lamotrigin Al is determined individually by the prescribing clinician based on the patient’s condition, age, renal function and any concomitant medications. Patients should follow the prescriber’s instructions exactly.

Safety data for lamotrigine in pregnancy and lactation are limited. Healthcare providers weigh potential benefits against risks, and women who are pregnant, planning pregnancy, or breastfeeding should discuss treatment options with their prescriber.

To request Lamotrigin Al, 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.

Lamotrigin Al differs from many antiepileptics by primarily targeting sodium channels without significant enzyme induction. Compared with carbamazepine or phenytoin, it has a lower risk of drug‑induced liver enzyme elevation but may require careful monitoring when combined with valproic acid or oral contraceptives.

Lamotrigin Al should be stored at ambient temperature, preferably below 25 °C, in its original packaging to protect it from moisture and light. Keep the product out of reach of children.

Lamotrigin Al is taken orally, usually as a tablet, with or without food. The prescriber will advise the exact dosing schedule, which may involve gradual titration to minimise adverse effects.

Serious risks include severe skin reactions such as Stevens‑Johnson syndrome or toxic epidermal necrolysis, blood disorders like agranulocytosis, liver injury, and the emergence of suicidal thoughts. Immediate medical attention is required if any of these occur.

Lamotrigin Al is contraindicated in patients with a known hypersensitivity to lamotrigine or any component of the formulation. Caution is also advised for individuals with severe hepatic or renal impairment, and it should be avoided in pregnancy unless clearly indicated by a healthcare professional.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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