"The U.S. Food and Drug Administration today approved Vimizim (elosulfase alfa), the first FDA-approved treatment for Mucopolysaccharidosis Type IVA (Morquio A syndrome). Morquio A syndrome is a rare, autosomal recessive lysosomal storage disease "...
DOSAGE AND ADMINISTRATION
The dosage of Visken ® (pindolol) should be individualized. The recommended initial dose of Visken® (pindolol) is 5 mg b.i.d. alone or in combination with other antihypertensive agents. An antihypertensive response usually occurs within the first week of treatment. Maximal response, however, may take as long as or occasionally longer than 2 weeks. If a satisfactory reduction in blood pressure does not occur within 3-4 weeks, the dose may be adjusted in increments of 10 mg/day at these intervals up to a maximum of 60 mg/day.
Visken ® (pindolol) tablets, USP
White, uncoated, heart-shaped tablets; 5 mg and 10 mg, packages of 100. 5 mg tablets engraved "VISKEN (pindolol) 5'' on one side, and embossed "V'' on other side (NDC 0078-0111-05). 10 mg tablets engraved "VISKEN (pindolol) 10'' on one side, and embossed "V'' on other side (NDC 0078-0073-05).
Store and Dispense
Below 86°F (30°C); tight, light-resistant container.
Manufactured by: Novartis Pharmaceuticals Canada Inc. Dorval (Quebec) Canada H9R 4P5. Distributed by: Novartis Pharmaceuticals Corporation, East Hanover, New Jersey 07936. REV: MAY 2007. FDA Rev date: 10/27/2007
Last reviewed on RxList: 2/13/2008
This monograph has been modified to include the generic and brand name in many instances.
Additional Visken Information
Visken - User Reviews
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