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NUPLAZID™ (pimavanserin) tablets
2016-05-13 10:20:53 来源: 作者: 【 】 浏览:391次 评论:0
  • HIGHLIGHTS OF PRESCRIBING INFORMATION
    These highlights do not include all the information needed to use NUPLAZID safely and effectively. See full prescribing information for NUPLAZID.
    NUPLAZID™ (pimavanserin) tablets, for oral use
    Initial U.S. Approval: 2016
    WARNING: INCREASED MORTALITY IN ELDERLY PATIENTS WITH DEMENTIA-RELATED PSYCHOSIS
    See full prescribing information for complete boxed warning.
    • Elderly patients with dementia-related psychosis treated with antipsychotic drugs are at an increased risk of death.
    • NUPLAZID is not approved for the treatment of patients with dementia-related psychosis unrelated to the hallucinations and delusions associated with Parkinson's disease psychosis. (5.1)
    INDICATIONS AND USAGE

    NUPLAZID is an atypical antipsychotic indicated for the treatment of hallucinations and delusions associated with Parkinson's disease psychosis. (1)
    DOSAGE AND ADMINISTRATION

    • Recommended dose is 34 mg, taken orally as two 17 mg tablets once daily, without titration. (2)
    • Can be taken with or without food. (2)
    DOSAGE FORMS AND STRENGTHS

    Tablets: 17 mg. (3)
    CONTRAINDICATIONS

    None. (4)
    WARNINGS AND PRECAUTIONS

    • QT Interval Prolongation: Increases in QT interval; avoid use with drugs that also increase the QT interval and in patients with risk factors for prolonged QT interval. (5.2)
    ADVERSE REACTIONS

    Most common adverse reactions (≥5% and twice the rate of placebo): peripheral edema and confusional state. (6.1)

    To report SUSPECTED ADVERSE REACTIONS, contact ACADIA Pharmaceuticals Inc. at 1-844-422-2342 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

    DRUG INTERACTIONS
    • Strong CYP3A4 Inhibitors (e.g., ketoconazole): Reduce NUPLAZID dose by one-half. (2.2, 7.1)
    • Strong CYP3A4 Inducers: Monitor for reduced efficacy. Increase in NUPLAZID dosage may be needed. (2.2, 7.1)
    USE IN SPECIFIC POPULATIONS
    • Renal Impairment: No dosage adjustment for NUPLAZID is needed in patients with mild to moderate renal impairment. Use of NUPLAZID is not recommended in patients with severe renal impairment. (8.6)
    • Hepatic Impairment: Use of NUPLAZID is not recommended in patients with hepatic impairment. (8.7)
    See 17 for PATIENT COUNSELING INFORMATION.

    Revised: 4/2016

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

    NUPLAZID™ is indicated for the treatment of hallucinations and delusions associated with Parkinson's disease psychosis [see Clinical Studies (14)].

  • 2 DOSAGE AND ADMINISTRATION

     

    2.1 General Dosing Information

    The recommended dose of NUPLAZID is 34 mg, taken orally as two 17 mg strength tablets once daily, without titration.

    NUPLAZID can be taken with or without food.

    2.2 Dosage Modifications for Concomitant Use with CYP3A4 Inhibitors and Inducers

     

    • Coadministration with Strong CYP3A4 Inhibitors
      The recommended dose of NUPLAZID when coadministered with strong CYP3A4 inhibitors (e.g., ketoconazole) is 17 mg, taken orally as one tablet once daily [see Drug Interactions (7.1)].

     

    • Coadministration with Strong CYP3A4 Inducers
      Monitor patients for reduced efficacy if NUPLAZID is used concomitantly with strong CYP3A4 inducers; an increase in NUPLAZID dosage may be needed [see Drug Interactions (7.1)].
  • 3 DOSAGE FORMS AND STRENGTHS

    NUPLAZID (pimavanserin) is available as 17 mg strength tablets. The white to off-white, round, coated tablets are debossed on one side with a "P" and "17" on the reverse side.

  • 4 CONTRAINDICATIONS

    None.

  • 5 WARNINGS AND PRECAUTIONS

     

    5.1 Increased Mortality in Elderly Patients with Dementia-Related Psychosis

    Antipsychotic drugs increase the all-cause risk of death in elderly patients with dementia-related psychosis. Analyses of 17 dementia-related psychosis placebo-controlled trials (modal duration of 10 weeks and largely in patients taking atypical antipsychotic drugs) revealed a risk of death in the drug-treated patients of between 1.6- to 1.7-times that in placebo-treated patients. Over the course of a typical 10-week controlled trial, the rate of death in drug-treated patients was about 4.5%, compared to a rate of about 2.6% in placebo-treated patients.

    Although the causes of death were varied, most of the deaths appeared to be either cardiovascular (e.g., heart failure, sudden death) or infectious (e.g., pneumonia) in nature. NUPLAZID is not approved for the treatment of patients with dementia-related psychosis unrelated to the hallucinations and delusions associated with Parkinson's disease psychosis [see Boxed Warning].

    5.2 QT Interval Prolongation

    NUPLAZID prolongs the QT interval. The use of NUPLAZID should be avoided in patients with known QT prolongation or in combination with other drugs known to prolong QT interval including Class 1A antiarrhythmics (e.g., quinidine, procainamide) or Class 3 antiarrhythmics (e.g., amiodarone, sotalol), certain antipsychotic medications (e.g., ziprasidone, chlorpromazine, thioridazine), and certain antibiotics (e.g., gatifloxacin, moxifloxacin) [see Drug Interactions (7.1)]. NUPLAZID should also be avoided in patients with a history of cardiac arrhythmias, as well as other circumstances that may increase the risk of the occurrence of torsade de pointes and/or sudden death, including symptomatic bradycardia, hypokalemia or hypomagnesemia, and the presence of congenital prolongation of the QT interval [see Clinical Pharmacology (12.2)].

  • 6 ADVERSE REACTIONS

    The following serious adverse reactions are discussed elsewhere in the labeling:

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