Classes
DEA Class; Rx
Common Brand Names; Exforge
- ARB/CCB Combos
Description
Dihydropyridine calcium-channel blocker (amlodipine) combined with angiotensin II antagonist (valsartan); both drugs have long half-lives allowing for qd dosing; used primarily for tx of HTN after titration of individual drugs.
Indications
Indicated for the treatment of hypertension.
Contraindications
Hypersensitivity to valsartan, amlodipine, or excipients
Concomitant administration with aliskiren in patients with diabetes mellitus
Adverse Effects
- Headache
- Increased BUN (6-17%)
- Peripheral edema (5-8%)
- Anxiety (3%)
- Nasopharyngitis (4%)
- Increased potassium (3%)
- Upper respiratory infection (3%)
- Dizziness (2%)
- Somnolence (3%)
- Diarrhea (3%)
- Nausea (3%)
- Abdominal pain (3%)
- Cough (2%)
- Orthostatic hypotension
- Syncope
- Visual disturbance
- Tinnitus
- Exanthema
- Rhabdomyolysis
Warnings
Drugs that inhibit renin-angiotensin system can cause hyperkalemia; monitor serum electrolytes periodically; some patients with heart failure have developed increases in potassium with valsartan therapy; these effects are usually minor and transient, and they are more likely to occur in patients with pre-existing renal impairment; dosage reduction and/or discontinuation of therapy may be required
Worsening angina and acute MI may occur after starting or increasing amlodipine dose, particularly with severe obstructive CAD
Peripheral edema may occur within 2-3 weeks of starting therapy (amlodipine)
Use caution in heart failure, severe aortic stenosis (amlodipine), hepatic impairment, renal artery stenosis, or hypertrophic cardiomyopathy
Dual blockade of the renin angiotensin system with ARBs, ACE inhibitors, or aliskiren associated with increased risk for hypotension, hyperkalemia, and renal function changes (including acute renal failure) compared to monotherapy; closely monitor blood pressure
Pregnancy and Lactation
The drug combination can cause fetal harm when administered to a pregnant woman; use of drugs that act on renin-angiotensin system during second and third trimesters of pregnancy reduces fetal renal function and increases fetal and neonatal morbidity and death
There is limited information regarding presence of drug combination in human milk, effects on breastfed infant, or on milk production; valsartan is present in rat milk; limited published studies report that amlodipine is present in human milk
Because of the potential for serious adverse reactions in breastfed infants, breastfeeding is not recommended during treatment with this drug combination
Maximum Dosage
10 mg/day PO amlodipine and 320 mg/day PO valsartan.
10 mg/day PO amlodipine and 320 mg/day PO valsartan.
Safety and efficacy have not been established.
Safety and efficacy have not been established.
How supplied
Amlodipine/valsartan
tablet
- 5mg/160mg
- 5mg/320mg
- 10mg/160mg
- 10mg/320mg