Class |
Phenylalkylamine |
Dihydropyridine |
Benzothiazepine |
Uses |
SVT, excluding AF with WPW |
HTN, Angina |
Angina, HTN, SVT, Raynaud's, migraine, oesophageal dysmotility |
Presentation |
20-240mg tablet, PO solution, IV at 2.5mg.ml-1 |
Tablet |
Tablet |
Isomerism |
Racemic preparation. The D-isomer also has some local anaesthetic activity |
|
|
Route of Administration |
PO/IV |
PO |
PO |
Dosing |
80-160mg BD/TDS |
2.5-10mg daily |
30-120mg TDS |
Absorption |
20% bioavailability |
60% bioavailability |
40% bioavailability |
Distribution |
90% protein bound |
90% protein bound, lipid insoluble. |
80% protein bound |
Metabolism |
Hepatic to active norverapamil |
Hepatic to inactive metabolites |
Hepatic to active metabolites |
Elimination |
Renal elimination of active metabolites |
Renal of inactive metabolites |
Renal of active metabolites. t1/2 2-7 hours |
CVS |
↓ HR via ↓ SA and ↓ AV nodal conduction, ↓ inotropy, ↓ SVR, ↓ BP, arrhythmia including HB |
↓ SVR, ↓ BP, with reflexive ↑ HR, ↑ inotropy, ↑ CO |
↓ AV nodal conduction but typically stable HR, ↓ SVR, ↓ CVR, ↓ MVO2, ↑ CO |
CNS |
↓ Cerebral vascular resistance |
↓ Cerebral vascular resistance with nimodipine |
|
GIT |
|
|
↓ LOS tone |
Interactions |
Contraindicated with concurrent β-blocker use due to profound ↓ HR, ↓ inotropy |
|
Contraindicated with concurrent β-blocker use due to profound ↓ HR, ↓ inotropy |