Ranozex 500 mg (Tablet (Extended Release))

Unit Price: ৳ 16.00 (3 x 10: ৳ 480.00)
Strip Price: ৳ 160.00

Medicine Details

Category Details
Generic Ranolazine
Company Sun pharmaceutical bangladesh ltd

Title

Ranozex Medicine

Category

  • Cardiovascular Medicine
  • Anti-anginal
  • Anti-ischaemic

Description

Ranozex is indicated for the treatment of chronic angina. It may be used with beta-blockers, nitrates, calcium channel blockers, anti-platelet therapy, lipid-lowering therapy, ACE inhibitors, and angiotensin receptor blockers.

Color Options

  • White

Dimensions

Standard tablet size

Dosage

Initiate at 500 mg twice daily and increase to 1000 mg twice daily, if needed, based on clinical symptoms

Administration

Swallow whole; do not crush, break, or chew. Take with or without meals.

Interaction

  • CYP 3A Inhibitors: Do not use with strong CYP 3A inhibitors. Limit maximum dose to 500 mg twice daily with moderate CYP 3A inhibitors
  • CYP 3A Inducers: Do not use with inducers
  • P-gp Inhibitors: May need to lower the dose based on clinical response
  • Drugs Transported by P-gp or Metabolized by CYP2D6: May need reduced doses when used with Ranozex

Contraindications

  • Pre-existing QT prolongation
  • Hepatic impairment
  • Taking QT prolonging drugs
  • Taking potent and moderately potent CYP3A inhibitors

Side Effects

  • Bradycardia
  • Palpitations
  • Tinnitus
  • Vertigo
  • Abdominal pain
  • Dry mouth
  • Vomiting
  • Peripheral edema
  • Dyspnea
  • Hypotension
  • Orthostatic hypotension

Pregnancy & Lactation

  • Pregnancy Category: C
  • Effect on Fetus: Unknown
  • Effect on Nursing Infants: Serious adverse reactions possible

Mode of Action

  • Effect: Anti-ischemic and anti-anginal effects
  • Mechanism: Inhibition of cardiac late sodium current (I_Na), QT prolongation effect by inhibition of I_Kr

Precautions & Warnings

Blocks QTc and prolongs the QTc interval, caution with co-administration of P-gp inhibitors

Overdose Effects

  • Dizziness
  • Nausea
  • Vomiting
  • Diplopia
  • Paresthesia
  • Confusion
  • Syncope

Absorption

  • Cmax: 2-5 hours
  • Half-life: 6-22 hours
  • Distribution: Approximately 62% bound to human plasma proteins
  • Metabolism and Excretion: Metabolized mainly by CYP3A and to a lesser extent by CYP2D6, excreted primarily in urine and feces

Therapeutic Class

Other Anti-anginal & Anti-ischaemic drugs

Storage Conditions

Keep below 30°C temperature, away from light & moisture. Keep out of the reach of children.

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