Sacutril 24 mg+26 mg (Tablet)

Unit Price: ৳ 40.00 (2 x 10: ৳ 800.00)
Strip Price: ৳ 400.00

Medicine Details

Indications

  • Reduces risk of cardiovascular death and hospitalization for heart failure in patients with chronic heart failure (NYHA Class ll-IV) and reduced ejection fraction
  • Treats symptomatic heart failure with systemic left ventricular systolic dysfunction in pediatric patients aged one year and older
  • Administered in conjunction with other heart failure therapies
  • Administered in place of an angiotensin-converting enzyme inhibitor (ACEi) or other ARB

Pharmacology

  • Contains neprilysin inhibitor, sacubitril, and an angiotensin receptor blocker, valsartan
  • Inhibits neprilysin (neutral endopeptidase; NEP) via LBQ657, the active metabolite of the prodrug sacubitril
  • Blocks the angiotensin II type-1 (AT1) receptor via valsartan

Dosage & Administration

  • Recommended starting dose for adults: 49/51 mg orally twice daily
  • Recommended maintenance dose for adults: 97/103 mg twice daily
  • Recommended dose for pediatric patients aged one year and older

Interaction

  • Should not be used with an ACEi, aliskiren in patients with diabetes, and use with an ARB should be avoided
  • Potassium-sparing Diuretics may increase serum potassium level
  • NSAIDs may increase risk of renal impairment
  • Lithium may increase risk of lithium toxicity

Contraindications

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

Side Effects

  • Angioedema
  • Hypotension
  • Impaired Renal Function
  • Hyperkalemia
  • Cough
  • Dizziness

Pregnancy & Lactation

  • Safety and effectiveness in pediatric patients less than 1 year of age not established
  • No relevant pharmacokinetic differences in elderly patients observed
  • No dose adjustment required in patients with mild hepatic impairment

Precautions & Warnings

  • May cause angioedema
  • May lower blood pressure and cause symptomatic hypotension
  • Monitor serum creatinine in patients with decreased renal function
  • Monitor serum potassium periodically

Use in Special Populations

  • Safety and effectiveness in pediatric patients not established
  • No relevant pharmacokinetic differences in elderly or very elderly patients observed
  • Starting dose adjustment for patients with severe renal impairment and moderate hepatic impairment

Overdose Effects

  • Limited data available
  • Hypotension is the most likely result of overdosage
  • Symptomatic treatment recommended
  • Unlikely to be removed by hemodialysis

Storage Conditions

  • Store below 30°C
  • Protect from moisture
  • Keep out of the reach of children

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