Classes
DEA Class; Rx
Common Brand Names; Tekturna
- Renin Inhibitors
Description
Direct renin inhibitor
Used for hypertension
Black box warning for pregnancy
Indications
Indicated for treatment of hypertension in adults and children ≥6 years
Contraindications
Hypersensitivity
Coadministration with ARBs or ACE inhibitors in patients with diabetes mellitus
Children <2 years
Adverse Effects
- Diarrhea (2.3%)
- Cough (1.1%)
- Rash (1%)
- Increase in serum creatinine (<7%)
- Hyperkalemia (<1%)
- Angioedema
- Headache
- Gout
- Renal stones
- Seizure
- Severe hypotension
- Rhabomyolysis
- Toxic epidermal necrolysis
- Increase in uric acid
- Angina
- Peripheral edema
- Increased serum creatinine
- Nausea/vomiting
- Hyponatremia
Warnings
Symptomatic hypotension may occur after initiation of treatment in patients with marked volume depletion, patients with salt depletion, or with combined use of other agents acting on the renin angiotensin-aldosterone system (RAAS); the volume or salt depletion should be corrected prior to administration of treatment, or the treatment should start under close medical supervision; transient hypotensive response is not a contraindication to further treatment, which usually can be continued without difficulty once the blood pressure has stabilized.
Monitor renal function periodically; changes in renal function, including acute renal failure, can be caused by drugs that affect the RAAS; patients whose renal function may depend in part on activity of the RAAS (eg, patients with renal artery stenosis, severe heart failure, post-myocardial infarction or volume depletion) or patients receiving ARB, ACE inhibitors or nonsteroidal anti-inflammatory drug (NSAID), including selective cyclooxygenase-2 inhibitors (COX-2 inhibitors)], therapy may be at particular risk of developing acute renal failure; monitor renal function periodically (see Black Box Warnings)
Pregnancy and Lactation
Fetal harm may occur when administered to a pregnant woman
Use of drugs that act on the renin-angiotensin system during the second and third trimesters of pregnancy reduces fetal renal function and increases fetal and neonatal morbidity and death
There is no information regarding the presence of aliskiren in human milk, the effects on the breastfed infant, or the effects on milk production
Maximum Dosage
300 mg/day PO.
300 mg/day PO.
Weighing 50 kg or more: 300 mg/day PO
Weighing 20 kg to 49 kg: 150 mg/day PO
6 to 12 years weighing 50 kg or more: 300 mg/day PO.
6 to 12 years weighing 20 kg to 49 kg: 150 mg/day PO. Not indicated; lack of appropriate dosage form available.
2 to 5 years: Not recommended
Younger than 2 years: Contraindicated.
Contraindicated.
Contraindicated.
How supplied
Aliskiren
tablet
- 150mg
- 300mg
oral pellets in capsules
- 37.5mg