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LIALDA(mesalamine)delayed-release tablets
2016-11-19 07:40:11 来源: 作者: 【 】 浏览:336次 评论:0
  • HIGHLIGHTS OF PRESCRIBING INFORMATION
    These highlights do not include all the information needed to use LIALDA safely and effectively. See full prescribing information for LIALDA.
    LIALDA ® (mesalamine) delayed-release tablets, for oral use
    Initial U.S. Approval: 1987
    INDICATIONS AND USAGE
    LIALDA is a locally acting 5-aminosalicylic acid (5-ASA) indicated for the induction of remission in adults with active, mild to moderate ulcerative colitis and for the maintenance of remission of ulcerative colitis. ( 1)
    DOSAGE AND ADMINISTRATION
    For induction of remission of active, mild to moderate ulcerative colitis, two to four 1.2 g tablets taken once daily with food. ( 1, 2)
    For maintenance of remission of ulcerative colitis, two 1.2 g tablets taken once daily with food. ( 1, 2)
    DOSAGE FORMS AND STRENGTHS
    Delayed-Release Tablets: 1.2 g ( 3)
    CONTRAINDICATIONS
    Patients with known hypersensitivity to salicylates or aminosalicylates or to any of the ingredients of LIALDA tablets. ( 4)
    WARNINGS AND PRECAUTIONS
    • Renal impairment may occur. Assess renal function at the beginning of treatment and periodically during treatment. ( 5.1)
    • Mesalamine-induced acute intolerance syndrome has been reported. Observe patients closely for worsening of these symptoms while on treatment. ( 5.2)
    • Use caution when treating patients who are hypersensitive to sulfasalazine. ( 5.3)
    • Mesalamine-induced cardiac hypersensitivity reactions (myocarditis and pericarditis) have been reported. ( 5.3)
    • Hepatic failure has been reported in patients with pre-existing liver disease. Use caution when treating patients with liver disease. ( 5.4)
    • Upper GI tract obstruction may delay onset of action. ( 5.5)
    • Use of mesalamine may lead to spuriously elevated test results when measuring urinary normetanephrine by liquid chromatography with electrochemical detection. ( 5.6)
    ADVERSE REACTIONS
    • The most common adverse reactions (incidence ≥ 2%) are ulcerative colitis, headache, flatulence, liver function test abnormality, and abdominal pain. ( 6.1)

    To report SUSPECTED ADVERSE REACTIONS, contact Shire US Inc. at 1-800-828-2088 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch
    DRUG INTERACTIONS

    • Nephrotoxic agents including NSAIDs: renal reactions have been reported. ( 7.1)
    • Azathioprine or 6-mercaptopurine: blood disorders have been reported. ( 7.2)
    USE IN SPECIFIC POPULATIONS
    • Renal impairment: Use LIALDA with caution in patients with a history of renal disease. ( 5.1, 7.1, 8.5, 13.2)
    • Nursing Women: Caution should be exercised when administered to a nursing woman. ( 8.3)
    • Geriatric Patients: Monitor blood cell counts in geriatric patients. ( 8.5)
    See 17 for PATIENT COUNSELING INFORMATION.

    Revised: 11/2015

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

    LIALDA is indicated for the induction of remission in patients with active, mild to moderate ulcerative colitis and for the maintenance of remission of ulcerative colitis.

  • 2 DOSAGE AND ADMINISTRATION

    The recommended dosage for the induction of remission in adult patients with active, mild to moderate ulcerative colitis is two to four 1.2 g tablets taken once daily with a meal for a total daily dose of 2.4 g or 4.8 g. The recommended dosage for the maintenance of remission is two 1.2 g tablets taken once daily with a meal for a total daily dose of 2.4 g.

  • 3 DOSAGE FORMS AND STRENGTHS

    The red-brown ellipsoidal delayed-release tablet containing 1.2 g mesalamine is debossed on one side and imprinted with S476.

  • 4 CONTRAINDICATIONS

    LIALDA is contraindicated in patients with known hypersensitivity to salicylates or aminosalicylates or to any of the ingredients of LIALDA [see Warnings and Precautions (5.3)Description (11)Adverse Reactions (6.2)].

  • 5 WARNINGS AND PRECAUTIONS

     

    5.1 Renal Impairment

    Renal impairment, including minimal change nephropathy, acute and chronic interstitial nephritis, and, rarely, renal failure, has been reported in patients given products such as LIALDA that contain mesalamine or are converted to mesalamine.

    It is recommended that patients have an eva luation of renal function prior to initiation of LIALDA therapy and periodically while on therapy. Exercise caution when using LIALDA in patients with known renal dysfunction or a history of renal disease.

    In animal studies, the kidney was the principal organ for toxicity. [See Drug Interactions (7.1) and Nonclinical Toxicology (13.2)]

    5.2 Mesalamine-Induced Acute Intolerance Syndrome

    Mesalamine has been associated with an acute intolerance syndrome that may be difficult to distinguish from an exacerbation of ulcerative colitis. Although the exact frequency of occurrence has not been determined, it has occurred in 3% of patients in controlled clinical trials of mesalamine or sulfasalazine. Symptoms include cramping, acute abdominal pain and bloody diarrhea, and sometimes fever, headache, and rash. Observe patients closely for worsening of these symptoms while on treatment. If acute intolerance syndrome is suspected, promptly discontinue treatment with LIALDA.

    5.3 Hypersensitivity Reactions

    Some patients who have experienced a hypersensitivity reaction to sulfasalazine may have a similar reaction to LIALDA tablets or to other compounds that contain or are converted to mesalamine.

    Mesalamine-induced cardiac hypersensitivity reactions (myocarditis and pericarditis) have been reported with LIALDA and other mesalamine medications. Caution should be taken in prescribing this medicine to patients with conditions predisposing them to the development of myocarditis or pericarditis.

    5.4 Hepatic Impairment

    There have been reports of hepatic failure in patients with pre-existing liver disease who have been administered mesalamine. Caution should be exercised when administering LIALDA to patients with liver disease.

    5.5 Upper GI Tract Obstruction

    Pyloric stenosis or other organic or functional obstruction in the upper gastrointestinal tract may cause prolonged gastric retention of LIALDA which would delay mesalamine release in the colon.

    5.6 Interference with Laboratory Tests

    Use of mesalamine may lead to spuriously elevated test results when measuring urinary normetanephrine by liquid chromatography with electrochemical detection because of the similarity in the chromatograms of normetanephrine and mesalamine's main metabolite, N-acetylaminosalicylic acid (N-Ac-5-ASA). An alternative, selective assay for normetanephrine should be considered.

  • 6 ADVERSE REACTIONS

    The most serious adverse reactions seen in Lialda clinical trials or with other products that contain or are metabolized to mesalamine are:

    6.1 Clinical Trials Experience

    Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice.

    LIALDA has been eva luated in 1368 ulcerative colitis patients in controlled and open-label trials.

    Induction of Remission

    In two 8-week placebo-controlled clinical trials involving 535 ulcerative colitis patients, 356 received 2.4 g/day or 4.8 g/day LIALDA tablets and 179 received placebo. The most frequent adverse reaction leading to discontinuation from LIALDA therapy was exacerbation of ulcerative colitis (0.8%). Pancreatitis occurred in less than 1% of patients during clinical trials and resulted in discontinuation of therapy with LIALDA in patients experiencing this event.

    Adverse reactions occurring in LIALDA or placebo groups at a frequency of at least 1% in two 8-week, double blind, placebo-controlled trials are listed in Table 1. The most common adverse reactions with LIALDA 2.4 g/day and 4.8 g/day were headache (5.6% and 3.4%, respectively) and flatulence (4% and 2.8%, respectively).

    Table 1: Adverse Reactions in Two Eight-Week Placebo-Controlled Trials Experienced by at Least 1% of the LIALDA Group and at a Rate Greater than Placebo a

    Adverse
    Reaction
    LIALDA
    2.4 g/day
    (n = 177)
    LIALDA
    4.8 g/day
    (n = 179)
    Placebo

    (n = 179)
      Headache 10 (5.6%) 6 (3.4%) 1 (0.6%)
      Flatulence 7 (4%)   5 (2.8%)   5 (2.8%) 
      Liver Function Test Abnormal   1 (0.6%)   4 (2.2%)   2 (1.1%)
      Alopecia   0   2 (1.1%)   0
      Pruritus   1 (0.6%)   2 (1.1%)   2 (1.1%)
      a: Adverse reactions for which the placebo rate equalled or exceeded the rate for at least one of the LIALDA treatment groups were abdominal pain, dizziness, dyspepsia, and nausea.

    The following adverse reactions, presented by body system, were reported infrequently (less than 1%) by LIALDA-treated ulcerative colitis patients in the two controlled trials.

    Cardiac Disorder: tachycardia

    Vascular Disorders: hypertension, hypotension

    Skin and Subcutaneous Tissue Disorders: acne, prurigo, rash, urticaria

    Gastrointestinal Disorders: abdominal distention, colitis, diarrhea, pancreatitis, rectal polyp, vomiting

    Investigations: decreased platelet count

    Musculoskeletal and Connective Tissue Disorders: arthralgia, back pain

    Nervous System Disorders: somnolence, tremor

    Respiratory, Thoracic and Mediastinal Disorders: pharyngolaryngeal pain

    General Disorders and Administrative Site Disorders: asthenia, face edema, fatigue, pyrexia

    Ear and Laby

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