Rupatadine is indicated for the symptomatic treatment of Seasonal & Perennial Allergic Rhinitis & Urticaria.
H1-histamine receptor antagonist
Rupatadine is a long-acting, non-sedative antagonist of histamine H1-receptors. It also antagonizes the platelet activating factor (PAF). Both histamine and PAF cause broncho constriction which leads to an increase in the vascular permeability and act as a mediator in the inflammatory process. With the dual mode of action, Rupatadine shows better therapeutic effect than an isolated antihistamine. Rupatadine possesses other anti allergic properties such as the inhibition of the degranulation of mast cells induced by immunological and non immunological stimuli and inhibition of the release of cytokines, particularly of the tumor necrosis factor alpha (TNF α) in human mastocytes and monocytes.
Adults and adolescents (above 12 years) - The recommended dosage is 10 mg once daily, with or without food.
With medicine: The concomitant administration of Rupatadine 20 mg and ketoconazole or erythromycin increases the systemic exposure. Rupatadine should be used with caution when it is administered concomitantly with these drug substances and other inhibitors of the isozyme CYP3A4. Rupatadine should be used with caution when it is co-administered with statins, CNS depressants or alcohol.
With food: Grapefruit and Grapefruit juice should not be taken simultaneously with Rupatadine
Hypersensitivity to Rupatadine or to any of the excipients. Rupatadine should be used with caution in patients with known prolongation of the QT interval, patients with uncorrected hypokalemia, patients with ongoing proarrhythmic conditions, such as clinically significant bradycardia or acute myocardial ischemia.Rupatadine should be used with caution in elderly patients (65 years and older) due to little clinical data. As there is no clinical experience in patients with impaired kidney or liver function, the use of rupatadine 10 mg tablets is at present not recommended in these patients.
Sleepiness, headache, dizziness, dry mouth, fatigue, asthenia.
No adequate data available. Caution should be exercised when prescribing rupatadine to pregnant or lactating women; it is unknown whether rupatadine is excreted into breast milk.
The most common adverse reaction was somnolence. If accidental ingestion of very high doses occurs, symptomatic treatment together with the required supportive measures should be given.
Store in cool & dry place below 30°C, protect from light & moisture. Keep out of reach of children.