Clinical drug

phenoxybenzamine hydrochloride 10 MG Oral Capsule [Dibenzyline]

10 MG · Oral Capsule · oral

A form of phenoxybenzamine

phenoxybenzamine hydrochloride 10 MG Oral Capsule [Dibenzyline] — Other peripheral vasodilators. INDICATION AND USAGE Phenoxybenzamine hydrochloride capsules are indicated in the treatment of pheochromocytoma, to control episodes of hypertension a

phenoxybenzamine hydrochloride 10 MG Oral Capsule [Dibenzyline]

Active ingredient

Classification

Other peripheral vasodilatorsalpha-Adrenergic Blocker

Drug interactions

Phenoxybenzamine may interact with certain adrenergic compounds leading to significant cardiovascular effects.

  • majorepinephrine — exaggerated hypotensive response and tachycardia
  • unknownlevarterenol — blocks hyperthermia production
  • unknownreserpine — blocks hypothermia production

Indications

INDICATION AND USAGE Phenoxybenzamine hydrochloride capsules are indicated in the treatment of pheochromocytoma, to control episodes of hypertension and sweating. If tachycardia is excessive, it may be necessary to use a beta -blocking agent concomitantly.

Dosage

DOSAGE AND ADMINISTRATION The dosage should be adjusted to fit the needs of each patient. Small initial doses should be slowly increased until the desired effect is obtained or the side effects from blockade become troublesome. After each increase, the patient should be observed on that level before instituting another increase . The dosage should be carried to a point where symptomatic relief and/or objective improvement are obtained, but not so high that the side effects from blockade become troublesome. Initially, 10 mg of phenoxybenzamine hydrochloride twice a day. Dosage should be increased every other day, usually to 20 to 40 mg 2 or 3 times a day, until an optimal dosage is obtained, as judged by blood pressure control. Long-term use of phenoxybenzamine is not recommended (see PRECAUTIONS Carcinogenesis and Mutagenesis ). STORAGE Store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature]. Dispense in a tight container.

Warnings

WARNINGS Phenoxybenzamine hydrochloride-induced alpha -adrenergic blockade leaves beta -adrenergic receptors unopposed. Compounds that stimulate both types of receptors may, therefore, produce an exaggerated hypotensive response and tachycardia.

Contraindications

CONTRAINDICATIONS Conditions where a fall in blood pressure may be undesirable; hypersensitivity to the phenoxybenzamine hydrochloride capsules, or any of its components.

Mechanism of action

CLINICAL PHARMACOLOGY Phenoxybenzamine hydrochloride is a long-acting, adrenergic, alpha -receptor-blocking agent, which can produce and maintain “chemical sympathectomy” by oral administration. It increases blood flow to the skin, mucosa and abdominal viscera, and lowers both supine and erect blood pressures. It has no effect on the parasympathetic system. 20 percent to 30 percent of orally administered phenoxybenzamine appears to be absorbed in the active form 1 . The half-life of orally administered phenoxybenzamine hydrochloride is not known; however, the half-life of intravenously administered phenoxybenzamine hydrochloride is approximately 24 hours. Demonstrable effects with intravenous administration persist for at least 3 to 4 days, and the effects of daily administration are cumulative for nearly a week 1 .

Indicated ICD-10 codes

Source: RxNorm + openFDA + RxClass + FAERS · 2026

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