Free delivery nationwide for orders above ₱800

 
RXDRUG-DRP-3340-1pc

MOTRIGINE Lamotrigine 50mg Tablet 1's

Selling for 2820
In stock
+
Add to wish list
Discreet Packaging
FDA-registered Products
FDA-licensed Pharmacies
Description

Indications/Uses

As monotherapy and adjunct to treatment with other antiepileptics for partial seizure and primary and secondary generalized tonic-clonic seizures. Prophylaxis of bipolar disorders.

Dosage/Direction for Use

Adults: Initial Dose: Monotherapy: 25 mg once daily for 2 weeks followed by 50 mg once daily for 2 weeks; thereafter the dose is increased by maximum of 50-100 mg every 1-2 weeks. Maintenance Dose: 100-200 mg daily.
Bipolar Disorder: 100-200 mg daily.

Administration

May be taken with or without food.

Contraindications

Hypersensitivity to lamotrigine or to any of the excipients of Motrigine/Motrigine 100.

Special Precautions

Lamotrigine should be given with caution to patients with hepatic or renal impairment. Patients receiving lamotrigine should be closely monitored especially for changes in hepatic, renal and clotting functions.
Use in pregnancy: The use of Lamotrigine is not recommended for use in pregnancy.
Use in lactation: Lamotrigine is distributed into breast milk and therefore, should be avoided during breastfeeding.

Use In Pregnancy & Lactation

Use in pregnancy: The use of Lamotrigine is not recommended for use in pregnancy.
Use in lactation: Lamotrigine is distributed into breast milk and therefore, should be avoided during breastfeeding.

Adverse Reactions

Skin rashes may occur during therapy with lamotrigine. Severe skin reactions including Stevens-Johnson syndrome were reported especially in children and usually occur within 8 weeks of starting lamotrigine.
Symptoms eg, fever, malaise, flu-like symptoms, drowsiness, lymphadenopathy, facial edema, and rarely, hepatic dysfunction, leukopenia and thrombocytopenia have also been reported with rashes as part of hypersensitivity syndrome.
Other adverse effects include angioedema and photosensitivity, diplopia, blurred vision and conjunctivitis and dizziness, drowsiness, insomnia, headache, ataxia, nystagmus, tremor, tiredness, nausea and vomiting, irritability and aggression, hallucinations, agitation and confusion. Very rarely, lupus-like reactions have been reported.

Drug Interactions

There are complex interactions between antiepileptic and toxicity may be enhanced by the enzyme inducers carbamazepine, phenytoin, phenobarbital and primidone, and inhibited by valproate.

Storage

Store at temperatures not exceeding 30°C.
Shelf-Life: 36 months.

Action

Pharmacology: Pharmacokinetics: Lamotrigine is well-absorbed from the gastrointestinal tract and peak plasma concentrations (Cmax) occur approximately 2.5 hrs after oral dose. It is widely distributed in the body and is reported to be about 55% bound to plasma proteins. It is extensively metabolized in the liver and excreted almost entirely conjugate. It slightly induces its own metabolism and the t½ at conjugate. It slightly induces its own metabolism and the t½ in urine, principally as a glucuronide conjugate. It slightly induces its own metabolism and the t½ at steady state is reported to be about 24 hrs. Lamotrigine is distributed in breast milk.

MedsGo Class

Anticonvulsants

Features

Brand
MOTRIGINE
Full Details
Dosage Strength
50 mg
Drug Ingredients
  • Lamotrigine
Drug Packaging
Tablet 1's
Generic Name
Lamotrigine
Dosage Form
Tablet
Registration Number
DRP-3340
Drug Classification
Prescription Drug (RX)
Find similar

View all variations as list

  CODE Dosage Strength Drug Packaging Availability Price  
MOTRIGINE Lamotrigine 50mg Tablet 1's, Dosage Strength: 50 mg, Drug Packaging: Tablet 1's
RXDRUG-DRP-3340-1pc
50 mg Tablet 1's
In stock
2820
+