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Ranolazine

Brand: Ranexa (US/EU) / Ranozex (IN) / Ranolaz (BD)
Antianginal Late sodium-current inhibitor

Chemistry

Molecular Formula C24H33N3O4
PubChem CID: 56959
Open in PubChem
Structure
structure

Pharmacokinetics

Half-life 7 hours
Tmax 2 h
Bioavailability 35 % (approx)
Protein Binding 62 %
Volume of Distribution 1.8 L/kg (approx)
Clearance Route hepatic
Active Metabolites yes
Notes Metabolized mainly by CYP3A4 and partially by CYP2D6; substrate of P-glycoprotein. Avoid strong CYP3A inhibitors/inducers (e.g., ketoconazole, rifampin). Steady state reached in ~3 days.

⚠️ Safety & Warnings

Severity: Moderate

Adverse Effects:
Dizziness, constipation, nausea, headache, QT interval prolongation

Contraindications:
Pre-existing QT prolongation, hepatic impairment, concomitant use of strong CYP3A inhibitors

Precautions:
Monitor ECG for QT interval; adjust dose in moderate renal impairment; avoid grapefruit products; caution with other QT-prolonging drugs