"The European Medicines Agency's Committee for Medicinal Products for Human Use (CHMP) has recommended the marketing of selexipag (Uptravi, Actelion Registration Ltd) for the treatment of adults with pulmonary arterial hypertension (PAH)./"...
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 Dibenzyline (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).
Store at 25°C (77°F); excursions permitted to 15°- 30°C (59°- 86°F) [See USP Controlled Room Temperature].
Dibenzyline (phenoxybenzamine hydrochloride) capsules, 10 mg, in bottles of 100 (NDC 65197- 001-01).
** Available as Levophed® Bitartrate (brand of norepinephrine bitartrate) from Abbott Laboratories.
DATE OF ISSUANCE: MARCH 2008. Manufactured for WellSpring Pharmaceutical Corporation, Bradenton, FL 34202-4101, USA. By WellSpring Pharmaceutical Canada Corp. Oakville, Ontario L6H 1M5 Canada. Rev. 03/08. FDA rev date: 4/3/2008This monograph has been modified to include the generic and brand name in many instances.
Last reviewed on RxList: 5/14/2008
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