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HCL hairy-cell leukemia; human cultured lymphoblasts
HCl hydrogen chloride
PSVT Paroxysmal Supra-Ventricular Tachycardia
  ? Tx
    1. Carotid ...
WPW Syndrome Wolff-Parkinson-White Syndrome
  ? CIx
    1. Drugs; AV Conduct...
CONVINCE Controlled Onset Verapamil Investigation of Cardiovascular Endpoints
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V Verapamil
VER Verapamil
VP Verapamil
VRP Verapamil
VPL verapamil
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verapamil <drug> A calcium channel blocking drug, used as a coronary vasodilator and antiarrhythmic.
Pharmacologic action: Calcium channel blockade, direct, potent negative chronotrope and inotrope, slows conduction in AV node, systemic and coronary vasodilation.
Uses: Supraventricular tachycardias.
Dose: 2.5 - 5.0 mg IV over 1-2 minutes May repeat at 5.0 - 10 mg every 15-30 minutes until 30 mg total dose.
Onset: 3 - 5 min.
Potential complications: Hypotension due to vasodilation and depressed contractility. Treat with calcium; bradycardia, AV block can be exacerbated, contraindicated with congestive heart failure, synergistic interaction with beta blockers.
Note: Administration of verapamil to a patient with ventricular tachycardia can be lethal. Verapamil can accelerate heart rate and decrease blood pressure, especially in patients with Wolff-Parkinson-White and wide-complex tachycardia.
(12 Mar 2000)
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