Product image of Lamotrigine Cf (Lamotrigine) supplied by GNH India

Lamotrigine Cf

Active Ingredient:
Lamotrigine
Origin:
EU

Lamotrigine Cf (Lamotrigine)

Lamotrigine, the active ingredient in Lamotrigine Cf, is an Anticonvulsant presented as a tablet for oral use. It treats epilepsy and bipolar disorder by stabilizing neuronal activity.
GNH India supplies Lamotrigine Cf as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Centrafarm B.V.

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Indications & Clinical Uses

  • Lamotrigine Cf is an antiepileptic drug that modulates neuronal excitability in seizure disorders and mood stabilization in affective illness.
  • Epilepsy: reduces the frequency and severity of focal and generalized seizures.
  • Bipolar disorder: helps maintain mood stability and prevents depressive episodes.
  • Partial seizures: decreases occurrence of focal onset seizures with or without secondary generalization.

How It Works

  • Lamotrigine inhibits voltage‑gated sodium channels, which stabilizes neuronal membranes and diminishes the release of excitatory neurotransmitters such as glutamate. This reduction in neuronal firing underlies its antiepileptic and mood‑stabilizing effects, making it effective for seizure control and bipolar disorder management.

Side Effects

Lamotrigine may cause a range of adverse reactions, from mild to severe. Monitoring for side effects is important during therapy.

Common Side Effects

  • Dizziness or light‑headedness
  • Headache
  • Nausea or vomiting
  • Rash or mild skin irritation
  • Blurred vision
  • Fatigue or somnolence

Serious or Rare Side Effects

  • Stevens‑Johnson syndrome or toxic epidermal necrolysis
  • Severe skin reactions (e.g., drug reaction with eosinophilia and systemic symptoms)
  • Hematologic abnormalities such as aplastic anemia or agranulocytosis
  • Hepatic dysfunction or failure
  • Suicidal thoughts or behavior
  • Severe hypersensitivity reactions

Precautions & Warnings

  • Before initiating lamotrigine therapy, clinicians should consider several safety measures.
  • Dose titration: increase gradually to minimise rash risk.
  • Skin reactions: monitor regularly for any rash or hypersensitivity.
  • Hepatic function: assess liver status in patients with hepatic impairment.
  • Renal function: adjust dosing in severe renal disease.
  • Pregnancy: use only when potential benefit justifies potential risk.
  • Store at ambient temperature: keep in original container, protect from moisture and light.

Avoid Interactions

Lamotrigine interacts with several medicines that can alter its plasma concentration or increase toxicity risk.

Major Interactions (Avoid)

  • Valproate: markedly raises lamotrigine levels, increasing toxicity.
  • Carbamazepine: lowers lamotrigine concentrations, potentially reducing efficacy.
  • Phenobarbital: reduces lamotrigine levels, may require dose adjustment.

Moderate Interactions (Monitor Closely)

  • Oral contraceptives: may decrease lamotrigine levels, necessitating monitoring.
  • Serotonergic agents: watch for signs of serotonin syndrome.
  • Other antiepileptics (e.g., phenytoin, primidone): may require dose modifications.

Frequently Asked Questions

Lamotrigine Cf is prescribed to control seizures in patients with epilepsy and to stabilize mood in individuals with bipolar disorder. It helps reduce the frequency of focal and generalized seizures and prevents depressive episodes in bipolar maintenance therapy.

Lamotrigine blocks voltage‑gated sodium channels in neuronal membranes, which reduces the release of excitatory neurotransmitters such as glutamate. This action dampens abnormal neuronal firing, providing seizure control and mood‑stabilising effects.

The specific dose of lamotrigine is determined by the prescribing clinician based on the patient’s condition, age, and concomitant medications. Dosing typically starts low and is gradually increased to minimise the risk of skin reactions.

Safety data for lamotrigine in pregnancy and lactation are limited. It should only be used when the potential therapeutic benefit outweighs any possible risk to the fetus or infant, and decisions are made in consultation with a healthcare professional.

To 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 necessary import documentation.

Compared with carbamazepine or valproate, lamotrigine has a lower incidence of cognitive side effects and is often better tolerated. However, it requires careful titration to avoid rash, and drug‑interaction profiles differ, especially with enzyme‑inducing agents.

Lamotrigine tablets should be stored at ambient temperature, below 25 °C, in the original blister pack or container. Protect them from moisture, excessive heat and direct sunlight to maintain potency.

Lamotrigine is taken orally, usually as a tablet, with or without food. The exact schedule—once or twice daily—depends on the prescriber’s plan and the patient’s individual response.

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

Lamotrigine is contraindicated in patients with a known hypersensitivity to the drug or any of its components. Caution is also advised for individuals with severe hepatic or renal impairment, and it should be avoided in pregnancy unless clearly indicated.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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