Adult: 10 mg once daily. Child: 2-11 years ≥10-<25 kg: 2.5 mg once daily; ≥25 kg: 5 mg once daily. ≥12 years Same as adult dose.
Administration
May be taken with or without food.
Special Precautions
Patient with known QTc interval prolongation, predisposition to arrhythmias (e.g. uncorrected hypokalaemia, bradycardia, acute myocardial ischaemia). Hepatic and renal impairment. Children and elderly. Pregnancy and lactation. Avoid concomitant use with strong CYP3A4 inhibitors.
Adverse Reactions
Significant: Rarely, QTc interval prolongation, torsade de pointes, hypersensitivity reactions (e.g. anaphylaxis, angioedema). Blood and lymphatic system disorders: Eosinophilia, neutropenia (children). Gastrointestinal disorders: Vomiting, dry mouth, oropharyngeal pain, dry throat, abdominal pain, diarrhoea, dyspepsia, nausea, constipation. General disorders and administration site conditions: Fatigue, asthenia, irritability, thirst; night sweats (children). Investigations: Increased ALT, AST, blood creatine phosphokinase, weight; abnormal LFT. Metabolism and nutrition disorders: Increased appetite. Musculoskeletal, connective tissues, and bone disorders: Arthralgia, myalgia, back pain. Nervous system disorders: Somnolence, headache, dizziness, disturbance in attention. Respiratory, thoracic and mediastinal disorders: Cough, rhinitis, pharyngitis, nasal dryness, epistaxis, tonsillitis.
Drug Interactions
May increase the plasma concentrations of CYP3A4 substrates (e.g. simvastatin, lovastatin, midazolam) and CYP3A4 substrates with narrow therapeutic index (e.g. ciclosporin, tacrolimus, sirolimus, everolimus, cisapride). Increased plasma concentrations with CYP3A4 strong inhibitors (e.g. itraconazole, ketoconazole, voriconazole, posaconazole, HIV protease inhibitors, clarithromycin, nefazodone) and moderate inhibitors (e.g. erythromycin, fluconazole, diltiazem).
Food Interaction
Increased systemic exposure with grapefruit juice; avoid concomitant administration. May increase the CNS depressant effect of alcohol.
Action
Description: Rupatadine is a long-acting, 2nd generation antihistamine that possesses selective peripheral H1 receptor and platelet activating factor (PAF) antagonistic activities. At high concentrations, it was noted to prevent the degranulation of mast cells and release of cytokines, specifically TNFα in human mast cells and monocytes. Onset: 1-2 hours. Duration: Antihistaminic activity: 24 hours. Pharmacokinetics: Absorption: Rapidly absorbed from the gastrointestinal tract. Time to peak plasma concentration: 0.75-1 hour. Distribution: Volume of distribution: 9,799 L. Plasma protein binding: 98.5-99%. Metabolism: Almost completely metabolised in the liver via oxidation, N-dealkylation, and hydroxylation mainly by CYP3A4 isoenzyme, and to a lesser extent by CYP2C9, CYP2C19, and CYP2D6, into active metabolites, desloratadine and its hydroxylated derivatives. Excretion: Via faeces (60.9%); urine (34.6%). Elimination half-life: 4.04-6.07 hours.
Chemical Structure
Rupatadine Source: National Center for Biotechnology Information. PubChem Compound Summary for CID 133017, Rupatadine. https://pubchem.ncbi.nlm.nih.gov/compound/Rupatadine. Accessed Nov. 24, 2020.