Indications & Dose:
Symptomatic chronic heart failure with reduced ejection fraction (in patients not currently taking an ACE inhibitor or angiotensin II receptor antagonist, or stabilised on low doses of either of these agents)
Symptomatic chronic heart failure with reduced ejection fraction (in patients currently stabilised on an ACE inhibitor or angiotensin II receptor antagonist)
Adult: Initially 51/49 mg twice daily for 2–4 weeks, increased if tolerated to 103/97 mg twice daily, consider a starting dose of 26/24 mg if systolic blood pressure less than 110mmHg
Contraindications:
Concomitant use of ACE inhibitor (separate administration by 36 hours) . systolic blood pressure less than 100 mmHg
Side Effects:
Common or very common Anaemia . diarrhoea . gastritis . hypoglycaemia . hypokalaemia . nausea . vertigo
PREGNANCY Manufacturer advises avoid— toxicity with sacubitril in animal studies.
BREAST FEEDING Manufacturer advises avoid— present in milk in animal studies.
HEPATIC IMPAIRMENT Manufacturer advises starting dose of 26/24 mg twice daily in moderate impairment. Contraindicated in severe impairment.
RENAL IMPAIRMENT Manufacturer recommends a starting dose of 26/24mg twice daily if eGFR less than 30 mL/minute/1.73m2. Also consider this starting dose if eGFR 30 to 60 mL/minute/1.73m2.
Cautions:
Precautions:
Interaction:
Appendix 1 (angiotensin-II receptor antagonists, sacubitril)
Warnings:
Adverse Effects:
Lactations:
Special Precautions:
Counselling:
Side Effects Or Adverse Reactions:
Patient And Carer Advice:
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