Stable angina
Adult: Initially, 375 mg bid, increase after 2-4 wk to 500 mg bid. Max: 750 mg bid.
Elderly: Dose titration needed.
Elderly: Dose titration needed.
Indications and Dosage
Oral
Stable angina Adult: Initially, 375 mg bid, increase after 2-4 wk to 500 mg bid. Max: 750 mg bid.
Elderly: Dose titration needed. |
Renal Impairment
Mild to moderate (CrCl 30-80 mL/min): Dose titration needed. Severe (CrCl <30 mL/min): Contraindicated.
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Hepatic Impairment
Mild: Dose titration needed. Moderate to severe: Contraindicated.
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Administration
May be taken with or without food.
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Contraindications
Concomitant admin w/ potent CYP3A4 inhibitors, CYP3A4 inducers and class 1A or class III antiarrhythmics other than amiodarone. Moderate to severe hepatic and severe renal impairment (CrCl <30 mL/min).
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Special Precautions
Patient w/ history of long QT syndrome, known acquired QT interval prolongation, moderate to severe CHF (NYHA Class III-IV), low wt (<60 kg). Mild hepatic and mild to moderate renal impairment (CrCl 30-80 mL/min). Elderly. Pregnancy and lactation.
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Adverse Reactions
QT interval prolongation, acute renal failure, nausea, constipation, dizziness, headache, palpitations, tinnitus, vertigo, dry mouth, abdominal pain, vomiting, peripheral oedema, dyspnoea, bradycardia, haematuria, paraesthesia, hypotension, blurred vision.
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Patient Counseling Information
May impair ability to drive or operate machinery.
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Monitoring Parameters
Baseline and follow up ECG to evaluate QT interval; monitor renal function in patients w/ moderate to severe renal impairment, BP in patients w/ renal dysfunction; serum K levels.
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Overdosage
Symptoms: Dizziness, nausea, vomiting, diplopia, lethargy, syncope, severe tremor, incoordination, dysplasia, hallucination. Management: Symptomatic and supportive treatment.
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Drug Interactions
Increased plasma levels w/ moderate CYP3A4 inhibitors (e.g. diltiazem, fluconazole, erythromycin), P-glycoprotein inhibitors (e.g. verapamil, ciclosporin) and CYP2D6 inhibitors (e.g. paroxetine). May increase plasma digoxin concentrations. May increase risk of rhabdomyolysis w/ simvastatin. May increase plasma concentrations of atorvastatin, other statins (e.g. lovastatin) and CYP3A4 substrates w/ narrow therapeutic range (e.g. tacrolimus, sirolimus, everolimus). May increase plasma exposure of metformin. Increased risk of ventricular arrhythmias w/ other drugs that prolong QT interval (e.g. terfenadine, astemizole, mizolastine).
Potentially Fatal: Increased plasma concentrations leading to increased adverse effects w/ CYP3A4 inhibitors (e.g. itraconazole, ketoconazole, HIV protease inhibitors, clarithromycin, telithromycin, nefazodone). Decreased plasma concentration w/ CYP3A4 inducers (e.g. rifampicin, phenytoin, phenobarbital, carbamazepine). Increased risk of QT interval prolongation w/ class 1A (e.g. quinidine) or class III (e.g. dofetilide, sotalol) antiarrhythmics other than amiodarone. |
Food Interaction
Increased plasma concentrations w/ grapefruit juice. Decreased plasma concentrations w/ St John's wort.
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Action
Description: Ranolazine exert its antianginal and anti-ischaemic effects through concentration-, voltage-, and frequency-dependent inhibition of the late Na current and other cardiac ion channels and transporters. It may decrease the magnitude of the late Na current resulting in a net reduction in intracellular Na concentrations, reversal of Ca overload, restoration of ventricular pump function, and prevention of ischaemia-induced arrhythmias. Its antianginal effects are not dependent upon reductions in heart rate or BP and QT interval prolongation effect is caused by inhibition of rapid delayed rectifier K current (IKr), which prolongs the ventricular action potential.
Pharmacokinetics: Absorption: Highly variable. Time to peak plasma concentration: Approx 2-5 hr. Distribution: Plasma protein binding: Approx 62%. Metabolism: Extensively metabolised in GI tract and liver by CYP3A4 (major) and CYP2D6 (minor) isoenzymes. Excretion: Via urine (approx 75%) and the remainder in faeces (<5% as unchanged drug). Terminal half-life: 7 hr. |
Storage
Store at 25°C.
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MIMS Class
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References
Anon. Ranolazine. Lexicomp Online. Hudson, Ohio. Wolters Kluwer Clinical Drug Information, Inc. https://online.lexi.com. Accessed 05/08/2014. Buckingham R (ed). Ranolazine. Martindale: The Complete Drug Reference [online]. London. Pharmaceutical Press. https://www.medicinescomplete.com. Accessed 05/08/2014. McEvoy GK, Snow EK, Miller J et al (eds). Ranolazine. AHFS Drug Information (AHFS DI) [online]. American Society of Health-System Pharmacists (ASHP). https://www.medicinescomplete.com. Accessed 05/08/2014. Ranexa Extended-Release Tablets. U.S. FDA. https://www.fda.gov/. Accessed 05/08/2014. Ranexa Tablet, Film Coated, Extended Release (Gilead Sciences, Inc.). DailyMed. Source: U.S. National Library of Medicine. https://dailymed.nlm.nih.gov/dailymed/. Accessed 05/08/2014.
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