Product image of Lamotrigina Teva (Lamotrigine) supplied by GNH India

Lamotrigina Teva

Active Ingredient:
Lamotrigine
Origin:
EU

Lamotrigina Teva (Lamotrigine)

Lamotrigine, the active ingredient in Lamotrigina Teva, is a sodium channel blocker presented as an oral tablet for oral use. It is prescribed for the treatment of epilepsy, including partial and generalized tonic‑clonic seizures, and for maintenance therapy in bipolar disorder.

GNH India supplies Lamotrigina Teva as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides regulatory support for global distribution, offering reliable sourcing, batch traceability, and responsive technical assistance.

Manufacturer / TM Owner

Teva Pharma – Produtos Farmacêuticos Lda

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Indications & Clinical Uses

Lamotrigine is used in neurological and psychiatric disorders that involve abnormal neuronal excitability.

  • Partial seizures: decreases frequency of focal seizures.
  • Generalized tonic‑clonic seizures: reduces occurrence of convulsive seizures.
  • Bipolar disorder (maintenance): helps maintain mood stability and prevent relapse.

How It Works

  • Lamotrigine inhibits voltage‑gated sodium channels in neuronal membranes, preferentially stabilizing the inactive state of the channel. This reduces the rapid influx of sodium ions during depolarization, limiting repetitive neuronal firing. The drug also diminishes release of excitatory neurotransmitters such as glutamate, contributing to its antiepileptic and mood‑stabilising effects. By modulating these pathways, lamotrigine lowers neuronal hyperexcitability without significant impact on cardiac conduction or hormonal systems.

Side Effects

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

Common Side Effects

  • Rash: mild skin irritation or erythema.
  • Headache: transient cranial pain.
  • Dizziness: sensation of light‑headedness.
  • Nausea: mild gastrointestinal upset.
  • Fatigue: feeling of tiredness or reduced energy.
  • Tremor: fine shaking of hands or limbs.

Serious or Rare Side Effects

  • Stevens‑Johnson syndrome: severe skin reaction with blistering.
  • Toxic epidermal necrolysis: life‑threatening skin detachment.
  • Aseptic meningitis: inflammation of meninges without infection.
  • Hematologic abnormalities: such as agranulocytosis or aplastic anemia.
  • Hepatic failure: severe liver injury.
  • Suicidal ideation: emergence of thoughts of self‑harm.

Precautions & Warnings

When prescribing lamotrigine, several safety considerations are recommended.

  • Initiate therapy: start at low dose and titrate slowly to reduce rash risk.
  • Monitor skin: discontinue immediately if a rash develops.
  • Assess hepatic function: use caution in patients with liver impairment.
  • Review psychiatric history: monitor for mood changes or suicidal thoughts.
  • Avoid abrupt discontinuation: taper dose to prevent seizure recurrence.
  • Store at ambient temperature: keep below 25°C in original container, protect from moisture.

Avoid Interactions

Lamotrigine interacts with several medicines; clinicians should evaluate potential effects.

Major Interactions (Avoid)

  • Valproic acid: markedly increases lamotrigine plasma levels, risk of toxicity.
  • Carbamazepine, phenytoin, phenobarbital: reduce lamotrigine concentrations, may diminish efficacy.
  • Oral contraceptives: estrogen‑containing pills lower lamotrigine levels, may require dose adjustment.

Moderate Interactions (Monitor Closely)

  • Serotonergic agents: potential for increased serotonergic effects.
  • Other antiepileptic drugs (e.g., levetiracetam): may require therapeutic monitoring.
  • Antacids containing aluminum or magnesium: may slightly decrease absorption.

Frequently Asked Questions

Lamotrigina Teva, containing lamotrigine, is indicated for the treatment of epilepsy—including partial seizures and generalized tonic‑clonic seizures—and for maintenance therapy in bipolar disorder to help stabilize mood and prevent relapse.

Lamotrigine blocks voltage‑gated sodium channels on neurons, stabilizing the inactive channel state and reducing rapid sodium influx. This limits repetitive neuronal firing and decreases the release of excitatory neurotransmitters such as glutamate, which underlies its antiepileptic and mood‑stabilising actions.

The appropriate dose of Lamotrigina Teva is individualized by the prescribing clinician based on the patient’s specific condition, age, renal and hepatic function, and any concomitant medications. Dosage titration is typically gradual to minimise the risk of skin reactions.

Lamotrigine’s safety in pregnancy is classified as unknown, and limited data are available. It may be used if the potential benefit outweighs the risk, but clinicians usually monitor plasma levels closely. Lamotrigine does pass into breast milk, so breastfeeding decisions should be made with medical guidance.

To request Lamotrigina Teva, 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 (including any cold‑chain requirements), and necessary import documentation.

Both lamotrigine and carbamazepine are sodium channel blockers used for epilepsy, but lamotrigine has a broader indication that includes bipolar disorder maintenance. Lamotrigine generally has a lower risk of drug‑induced hyponatremia and fewer cognitive side effects, while carbamazepine can induce hepatic enzymes more strongly, affecting the metabolism of other drugs.

Lamotrigina Teva should be stored at ambient temperature, preferably below 25 °C. Keep the tablets in the original packaging, protect them from moisture and direct sunlight, and ensure they are out of reach of children.

Lamotrigina Teva is taken orally, usually as a tablet. The medication is swallowed whole with water and can be taken with or without food, following the dosing schedule set by the prescriber.

The most serious adverse reactions include severe skin conditions such as Stevens‑Johnson syndrome or toxic epidermal necrolysis, aseptic meningitis, hematologic abnormalities like agranulocytosis, hepatic failure, and the emergence of suicidal thoughts. Immediate medical attention is required if any of these occur.

Lamotrigine should be avoided in individuals with a known hypersensitivity to the drug or any of its components. Patients with a history of severe rash to other antiepileptic agents, uncontrolled liver disease, or those taking contraindicated interacting medicines (e.g., certain enzyme inducers) should not use it without specialist supervision.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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