Table 3.
Antihypertensive Class | Specific Classes/Agents | Drug Interactions | Notes |
---|---|---|---|
Diuretics [194] | thiazides, thiazide-like, loop, potassium-sparing | Unlikely to occur | Metabolized outside CYP450 |
β-blockers [195-201] | Hepatically metabolized: propranolol, metoprolol | PIs, EFV | Increased concentrations of β-blockers: prolong effect, increase risk of adverse effects |
Hydophilic: nadolol, atenolol | Not thought to exist | Excreted in the urine | |
Calcium channel blockers (CCB) [202-204] |
Verapamil, diltiazem, amlodipine, nifedipine | PIs, NNRTIs | PIs: increased concentrations of CCB, prolonged effect NNRTIs: reduced bioavailability of CCB |
Angiotensin-converting enzyme inhibitors [205-208] | Not expected to occur | Metabolized outside CYP450 | |
Angiotensin II receptor blockers [209-216] | Losartan | CYP2C9 inhibitors, PIs | CYP2C9 inhibitors: Decreased losartan efficacy PIs: increased losartan serum concentrations |
Candesartan, irbesartan | Not thought to exist | Undergo hepatic metabolism, do not require biotransformation | |
Eprosartan, olmesartan, telmisartan, valsartan | Not thought to exist | Metabolized outside CYP450 |
PIs protease inhibitors, EFV efavirenz, NNRTIs non-nucleoside reverse transcriptase inhibitors, CCB calcium channel blockers.