Larocent
Generic Name
larocent-25-mg-capsule
Manufacturer
Unspecified Pharma Ltd.
Country
Bangladesh
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Price Details
Current market pricing information
| Variant | Unit Price | Strip Price |
|---|---|---|
| larocent 25 mg capsule | ৳ 400.00 | ৳ 2,400.00 |
Description
Overview of the medicine
Larocent 25 mg Capsule is an antihistamine used to relieve symptoms associated with allergic rhinitis and chronic urticaria. It helps to reduce sneezing, runny nose, itchy or watery eyes, and itching. The active ingredient is Loratadine.
Uses & Indications
Dosage
Adults
The usual adult dose of Loratadine is 10 mg once daily. For Larocent 25 mg capsule, the recommended dose is 25 mg once daily, or as directed by a physician, particularly for more severe symptoms or specific formulations.
Elderly
No dosage adjustment is generally required for elderly patients with normal renal and hepatic function. For patients with significant impairment, a starting dose of 10 mg every other day is often advised for standard Loratadine, which may need adjustment for 25 mg.
Renal_impairment
For patients with severe renal impairment (creatinine clearance < 30 mL/min), a starting dose of 10 mg every other day is recommended for standard Loratadine. For 25 mg, caution and physician consultation are advised.
How to Take
Larocent 25 mg Capsule should be taken orally with or without food, preferably at the same time each day.
Mechanism of Action
Loratadine, the active ingredient, selectively blocks peripheral H1-receptors, preventing histamine from binding and thereby reducing allergic symptoms. It has minimal sedative effects due to its low penetration of the blood-brain barrier.
Pharmacokinetics
Onset
Within 1-3 hours
Excretion
Approximately 40% excreted in urine and 42% in feces over a 10-day period, primarily as conjugated metabolites.
Half life
Plasma half-life: 8.4 hours (range 3-20 hours). Descarboethoxyloratadine (active metabolite) half-life: 28 hours (range 8.8-92 hours).
Absorption
Rapidly absorbed after oral administration. Food may slightly delay absorption but does not significantly affect overall bioavailability.
Metabolism
Extensively metabolized in the liver by cytochrome P450 3A4 and 2D6 to descarboethoxyloratadine (active metabolite).
Side Effects
Contraindications
- •Known hypersensitivity to Loratadine or any component of the formulation.
- •Children under 2 years of age (general recommendation for Loratadine, specific formulations may vary).
Drug Interactions
Cimetidine, Ketoconazole, Erythromycin
May increase plasma concentrations of Loratadine and its active metabolite, though usually without clinical significance.
Other CNS depressants (e.g., alcohol, sedatives)
Loratadine has minimal sedative effects, but caution is advised when co-administered with other CNS depressants.
Storage
Store below 30°C in a dry place, away from light and moisture. Keep out of reach of children.
Overdose
Symptoms of overdose include somnolence, tachycardia, and headache. Management should be symptomatic and supportive, including gastric lavage and activated charcoal if appropriate.
Pregnancy & Lactation
Pregnancy Category B. Loratadine is excreted in breast milk; therefore, caution should be exercised when administered to a nursing woman.
Frequently Asked Questions
Common questions about this medicine
Pack Sizes
Shelf Life
24 to 36 months from the date of manufacture, depending on storage conditions.
Availability
Available in pharmacies nationwide
Approval Status
Approved by relevant national regulatory authorities
Patent Status
Generic versions available, patent expired
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