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VIOKACE TAB(pancrelipase)
2017-03-21 10:52:31 来源: 作者: 【 】 浏览:686次 评论:0
  • HIGHLIGHTS OF PRESCRIBING INFORMATION
    These highlights do not include all the information needed to use VIOKACE safely and effectively. See full prescribing information for VIOKACE.
    Initial U.S. Approval: 2012
    INDICATIONS AND USAGE
    VIOKACE™ is a combination of porcine-derived lipases, proteases, and amylases. VIOKACE, in combination with a proton pump inhibitor, is indicated in adults for the treatment of exocrine pancreatic insufficiency due to chronic pancreatitis or pancreatectomy. (1)
    DOSAGE AND ADMINISTRATION
    VIOKACE is not interchangeable with any other pancrelipase product.
    VIOKACE tablets should be swallowed whole. Do not crush or chew tablets. (2.1)   Dosing should not exceed the recommended maximum dosage set forth by the Cystic Fibrosis Foundation Consensus Conferences Guidelines. (2.2)
    • Begin with 500 lipase units/kg of body weight per meal to a maximum of 2,500 lipase units/kg of body weight per meal (or less than or equal to 10,000 lipase units/kg of body weight per day), or less than 4,000 lipase units/g fat ingested per day. (2.2)
    • Individualize dosage based on clinical symptoms, the degree of steatorrhea present and the fat content of the diet. (2.2)
    DOSAGE FORMS AND STRENGTHS

    Tablets: 10,440 USP units of lipase; 39,150 USP units of protease; 39,150 USP units of amylase (3)

    Tablets: 20,880 USP units of lipase; 78,300 USP units of protease; 78,300 USP units of amylase (3
    CONTRAINDICATIONS

    • None. (4)

    WARNINGS AND PRECAUTIONS

    • Fibrosing colonopathy is associated with high-dose use of pancreatic enzyme replacement. Exercise caution when doses of VIOKACE exceed 2,500 lipase units/kg of body weight per meal (or greater than 10,000 lipase units/kg of body weight per day). (5.1)
    • To avoid irritation of oral mucosa, do not chew VIOKACE or retain in the mouth. (5.2)
    • Exercise caution when prescribing VIOKACE to patients with gout, renal impairment, or hyperuricemia. (5.3)
    • There is theoretical risk of viral transmission with all pancreatic enzyme products including VIOKACE. (5.4)
    • Exercise caution when administering pancrelipase to a patient with a known allergy to proteins of porcine origin. (5.5)

    ADVERSE REACTIONS

    • Adverse reactions occurring in at least 2 chronic pancreatitis or pancreatectomy patients (greater than or equal to 7%) receiving VIOKACE are biliary tract stones and anal pruritus. (6.1)

    To report SUSPECTED ADVERSE REACTIONS, contact APTALIS Pharma US, Inc. at 1-800-472-2634 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

    USE IN SPECIFIC POPULATIONS
    • The safety and effectiveness of VIOKACE in pediatric patients have not been established. (8.4)
    • VIOKACE use in pediatric patients may result in suboptimal growth due to tablet degradation in the gastric environment. In general, delayed-release (enteric-coated) capsules should be used for pediatric patients. (8.4)
    See 17 for PATIENT COUNSELING INFORMATION and Medication Guide.

    Revised: 3/2012

  • FULL PRESCRIBING INFORMATION: CONTENTS*
  • 1 INDICATIONS AND USAGE

    VIOKACE (pancrelipase) tablets, in combination with a proton pump inhibitor, is indicated in adults for the treatment of exocrine pancreatic insufficiency due to chronic pancreatitis or pancreatectomy.

  • 2 DOSAGE AND ADMINISTRATION

    VIOKACE is not interchangeable with any other pancrelipase product.

    VIOKACE is orally administered. Therapy should be initiated at the lowest recommended dose and gradually increased. The dosage of VIOKACE should be individualized based on clinical symptoms, the degree of steatorrhea present, and the fat content of the diet as described in the Limitations on Dosing below [see Dosage and Administration (2.2) and Warnings and Precautions (5.1)].

    2.1 Administration

    Since VIOKACE is not enteric-coated, it should be taken in combination with a proton pump inhibitor [see Indications and Usage (1)].

    VIOKACE should be taken during meals or snacks, with sufficient fluid. Tablets should be swallowed whole. Do not crush or chew tablets. Care should be taken to ensure that no drug is retained in the mouth to avoid mucosal irritation.

    2.2 Dosage

    Dosage recommendations for pancreatic enzyme replacement therapy were published following the Cystic Fibrosis Foundation Consensus Conferences.1,2,3 VIOKACE should be administered in a manner consistent with the recommendations of the Conferences provided in the following paragraph. Only the adult dosing guidelines are shown below. Patients may be dosed on a fat ingestion-based or actual body weight-based dosing scheme.

    Additional recommendations for pancreatic enzyme therapy in patients with exocrine pancreatic insufficiency due to chronic pancreatitis or pancreatectomy are based on a clinical trial conducted in these populations.

    Enzyme dosing should begin with 500 lipase units/kg of body weight per meal to a maximum of 2,500 lipase units/kg of body weight per meal (or less than or equal to 10,000 lipase units/kg of body weight per day), or less than 4,000 lipase units/g fat ingested per day.

    Usually, half of the prescribed VIOKACE dose for an individualize

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