Sabitar 24 mg+26 mg (Tablet)

Unit Price: ৳ 45.00 (3 x 10: ৳ 1,350.00)
Strip Price: ৳ 450.00

Medicine Details

Indications

  • Reduces cardiovascular death risk
  • Reduces hospitalization risk for heart failure
  • For chronic heart failure (NYHA Class ll-IV)
  • For symptomatic heart failure in pediatric patients (aged one year and older)
  • Administered in conjunction with other heart failure therapies
  • Usable in place of an angiotensin-converting enzyme inhibitor (ACEi) or other ARB

Pharmacology

  • Contains neprilysin inhibitor (sacubitril) and angiotensin receptor blocker (valsartan)
  • Inhibits neprilysin (neutral endopeptidase) via LBQ657
  • Blocks angiotensin II type-1 (AT1) receptor via valsartan
  • Increases levels of peptides degraded by neprilysin
  • Simultaneously inhibits effects of angiotensin II by valsartan

Dosage & Administration

  • Recommended starting dose for adult heart failure: 49/51 mg orally twice daily
  • Target maintenance dose for adult heart failure: 97/103 mg twice daily
  • Pediatric patients aged one year and older have different dose recommendations
  • Dosage adjustment for patients with severe renal impairment
  • Dosage titration based on pediatric patient weight

Interaction

  • Should not be used with ACEi, aliskiren in patients with diabetes
  • Use with ARB should be avoided
  • Potassium-sparing diuretics may increase serum potassium level
  • NSAIDs may increase risk of renal impairment
  • Increased risk of lithium toxicity when used with lithium

Contraindications

  • Hypersensitivity to any component
  • History of angioedema related to previous ACE inhibitor or ARB therapy
  • Concomitant use of ACE inhibitors or aliskiren in patients with diabetes

Side Effects

  • Angioedema
  • Hypotension
  • Impaired renal function
  • Hyperkalemia
  • Cough
  • Dizziness

Pregnancy & Lactation

  • Safety and effectiveness not established in pediatric patients less than 1 year of age
  • No relevant pharmacokinetic differences observed in elderly patients
  • No dose adjustment required for mild hepatic impairment
  • Not recommended in patients with severe hepatic impairment
  • No dose adjustment required in patients with mild to moderate renal impairment
  • Recommended starting dose for patients with severe renal impairment

Precautions & Warnings

  • May cause angioedema
  • May lower blood pressure and cause symptomatic hypotension
  • Monitor serum creatinine
  • Monitor serum potassium periodically and treat appropriately

Use in Special Populations

  • Safety and effectiveness not established in pediatric patients
  • No relevant pharmacokinetic differences observed in elderly patients
  • Different starting dose recommendations for patients with renal or hepatic impairment

Overdose Effects

  • Hypotension likely result of overdosage
  • Symptomatic treatment should be provided

Storage Conditions

  • Keep in a dry place
  • Store below 30°C
  • Protect from moisture
  • Keep out of the reach of children

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