
Nifedipine Pharmacology
Published on Jun 5
11:36
0:000:00
<p>Nifedipine is a dihydropyridine calcium channel blocker that selectively inhibits L-type calcium channels in vascular smooth muscle, leading to vasodilation and reduced peripheral vascular resistance.</p>
<p>The extended-release formulation of nifedipine provides more stable plasma concentrations and is preferred for chronic management of hypertension and angina.</p>
<p>Common adverse effects include headache, flushing, peripheral edema, and dizziness, all related to its vasodilatory action.</p>
<p>Nifedipine undergoes extensive first-pass metabolism in the liver, primarily via CYP3A4 enzymes, which significantly influences its bioavailability and potential drug interactions.</p>
<p>CYP3A4 inhibitors (e.g., ketoconazole, erythromycin, grapefruit juice) can increase plasma levels of nifedipine, raising the risk of hypotension and adverse effects.</p>
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