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CETYLEV (acetylcysteine) effervescent tablets
2017-02-09 07:22:51 来源: 作者: 【 】 浏览:568次 评论:0
  • HIGHLIGHTS OF PRESCRIBING INFORMATION
    These highlights do not include all the information needed to use CETYLEV™ safely and effectively. See full prescribing information for CETYLEV.
    CETYLEV (acetylcysteine) effervescent tablets for oral solution
    Initial U.S. Approval: 1963
    INDICATIONS AND USAGE

    CETYLEV is an antidote for acetaminophen overdose indicated to prevent or lessen hepatic injury after ingestion of a potentially hepatotoxic quantity of acetaminophen in patients with acute ingestion or from repeated supratherapeutic ingestion. (1)
    DOSAGE AND ADMINISTRATION

    Pre-Treatment Assessment Following Acute Ingestion (2.1):

    Obtain a plasma or serum sample to assay for acetaminophen concentration at least 4 hours after ingestion.

    • If the time of acetaminophen ingestion is unknown:
      • Administer a loading dose of CETYLEV immediately
      • Obtain an acetaminophen concentration to determine the need for continued treatment
    • If the acetaminophen concentration cannot be obtained (or is unavailable or uninterpretable) within the 8-hour time interval after acetaminophen ingestion or there is clinical evidence of acetaminophen toxicity:
      • Administer a loading dose of CETYLEV immediately and continue treatment for a total of 17 doses.
    • If the patient presents more than 8 hours after ingestion and the time of acute acetaminophen ingestion is known:
      • Administer a loading dose of CETYLEV immediately
      • Obtain acetaminophen concentration to determine need for continued treatment
    • If the patient presents less than 8 hours after ingestion and the time of acute acetaminophen ingestion is known and the acetaminophen concentration is known:
      • Use the Rumack-Matthew nomogram (Figure 1) to determine whether or not to initiate treatment with CETYLEV (2.2)

    Nomogram for Estimating Potential for Hepatotoxicity from Acute Acetaminophen Ingestion (2.2):

    • See the Full Prescribing Information for instructions on how to use the nomogram to determine the need for loading and maintenance dosing.

    Recommended Adult and Pediatric Dosage (2.3):

    • CETYLEV is for oral administration only; not for nebulization or intratracheal instillation
    • Loading dose: 140 mg/kg
    • Maintenance doses: 70 mg/kg repeated every 4 hours for a total of 17 doses.
    • See Full Prescribing Information for weight-based dosage and preparation and administration instructions.

    Repeated Supratherapeutic Acetaminophen Ingestion (2.4):

    • Obtain acetaminophen concentration and other laboratory tests to guide treatment; Rumack-Matthew nomogram does not apply.
    DOSAGE FORMS AND STRENGTHS

    Effervescent tablets: 500 mg and 2.5 grams (3)
    CONTRAINDICATIONS

    None (4)
    WARNINGS AND PRECAUTIONS

    • Hypersensitivity Reactions, Including Urticaria: Discontinue CETYLEV unless deemed essential to patient management and the reactions can be otherwise controlled (5.1)
    • Risk of Upper Gastrointestinal Hemorrhage: Consider the risk/benefit for patients at risk of hemorrhage (e.g., those with esophageal varices, peptic ulcers, etc.) versus the risk of developing hepatic toxicity, and treat with CETYLEV accordingly.(5.2)
    ADVERSE REACTIONS

    Most common adverse reactions are nausea and vomiting, other gastrointestinal symptoms, and rash with or without fever. (6)
    To report SUSPECTED ADVERSE REACTIONS, contact Arbor Pharmaceuticals LLC at 1- 866-516-4950 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

    See 17 for PATIENT COUNSELING INFORMATION and FDA-approved patient labeling.

    Revised: 1/2016

  • FULL PRESCRIBING INFORMATION: CONTENTS*

    1 INDICATIONS AND USAGE

    2 DOSAGE AND ADMINISTRATION

    2.1 Pretreatment Assessment and Testing Following Acute Acetaminophen Ingestion

    2.2 Nomogram for Estimating Potential for Hepatotoxicity from Acute Acetaminophen Ingestion and Need for CETYLEV Treatment

    2.3 Recommended Dosage and Preparation and Administration Instructions in Adults and Pediatrics for Acute Acetaminophen Ingestion

    2.4 Recommendations for Repeated Supratherapeutic Acetaminophen Ingestion

    3 DOSAGE FORMS AND STRENGTHS

    4 CONTRAINDICATIONS

    5 WARNINGS AND PRECAUTIONS

    5.1 Hypersensitivity Reactions

    5.2 Risk of Upper Gastrointestinal Hemorrhage

    6 ADVERSE REACTIONS

    8 USE IN SPECIFIC POPULATIONS

    8.1 Pregnancy

    8.2 Lactation

    8.4 Pediatric Use

    8.5 Geriatric Use

    8.6 Patients Sensitive to High Sodium Intake

    11 DESCRIPTION

    12 CLINICAL PHARMACOLOGY

    12.1 Mechanism of Action

    12.3 Pharmacokinetics

    13 NONCLINICAL TOXICOLOGY

    13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility

    16 HOW SUPPLIED/STORAGE AND HANDLING

    17 PATIENT COUNSELING INFORMATION

    *Sections or subsections omitted from the full prescribing information are not listed.
  • 1 INDICATIONS AND USAGE

    CETYLEV is indicated to prevent or lessen hepatic injury after ingestion of a potentially hepatotoxic quantity of acetaminophen in patients with acute ingestion or from repeated supratherapeutic ingestion (RSI).

  • 2 DOSAGE AND ADMINISTRATION

     

    2.1 Pretreatment Assessment and Testing Following Acute Acetaminophen Ingestion

    The following recommendations are related to acute acetaminophen ingestion. For recommendations related to repeated supratherapeutic exposure see Dosage and Administration (2.4).

    1. Assess the history and timing of acetaminophen ingestion as an overdose.
      • The reported history of the quantity of acetaminophen ingested as an overdose is often inaccurate and is not a reliable guide to therapy.
    2. Obtain the following laboratory tests to monitor hepatic and renal function and electrolyte and fluid balance: aspartate aminotransferase (AST), alanine aminotransferase (ALT), bilirubin, international normalized ratio (INR), creatinine, blood urea nitrogen (BUN), blood glucose, and electrolytes.
    3. Obtain a plasma or serum sample to assay for acetaminophen concentration at least 4 hours after ingestion. Acetaminophen concentrations obtained earlier than 4 hours post-ingestion may be misleading as they may not represent maximum acetaminophen concentrations.
    4. If the time of acute acetaminophen ingestion is unknown:
    5. If the acetaminophen concentration cannot be obtained (or is unavailable or uninterpretable) within the 8-hour time interval after acetaminophen ingestion or there is clinical evidence of acetaminophen toxicity:
    6. If the patient presents more than 8 hours after ingestion and the time of acute acetaminophen ingestion is known:
    7. If the patient presents less than 8 hours after ingestion and the time of acute acetaminophen ingestion is known and the acetaminophen concentration is known:

    2.2 Nomogram for Estimating Potential for Hepatotoxicity from Acute Acetaminophen Ingestion and Need for CETYLEV Treatment

    If the timing of the acute acetaminophen ingestion is known and the results of the acetaminophen assay are available within 8 hours:

    • Refer to the Rumack-Matthew nomogram (see Figure 1) to determine whether or not to initiate treatment with CETYLEV.
    • Initiation of CETYLEV depends on the acetaminophen concentration and also the clinical presentation of the patient.

    The nomogram may underestimate the hepatotoxicity risk in patients with chronic alcoholism, malnutrition, or CYP2E1 enzyme inducing drugs (e.g., isoniazid), and consideration should be given to treating these patients even if the acetaminophen concentrations are in the nontoxic range.

    Loading Dose

    For patients whose acetaminophen concentrations are at or above the "possible" toxicity line (dotted line in nomogram):

    For patients with an acute overdose due to an extended-release acetaminophen, if the acetaminophen concentration at 4 hours post ingestion is below the possible toxicity line then obtain a second sample for acetaminophen concentration 8 to 10 hours after the acute ingestion. If the second value is at or above the "possible" toxicity line (dotted line in nomogram):

    For patients whose values are below the "possible" toxicity line, but time of ingestion was unknown or sample was obtained less than 4 hours after ingestion:

    For patients whose values are below the "possible" toxicity line and time of ingestion is known and the sample was obtained more than 4 hours after ingestion, do not administer CETYLEV because there is minimal risk of hepatotoxicity.

       Figure 1 Rumack-Matthew Nomogram for Estimating Potential for Hepatotoxicity from Acetaminophen Poisoning – Plasma or Serum Acetaminophen Concentration versus Time (hours) Post-acetaminophen Ingestion (Adapted from Rumack and Matthew, Pediatrics 1975; 55:871−876.)
     Figure 1

    Maintenance Dose

    Determine need for continued treatment with CETYLEV after the loading dose. Choose ONE of the following based on the acetaminophen concentration:

    The acetaminophen concentration is above the possible toxicity line according to the nomogram (see Figure 1):

    • Continue CETYLEV treatment with the maintenance dose for 17 doses [see Dosage and Administration (2.3)].
    • Monitor hepatic and renal function and electrolytes throughout treatment.

    The acetaminophen concentration could not be obtained:

    • Continue CETYLEV treatment with the maintenance dose for 17 doses [see Dosage and Administration (2.3)].
    • Monitor hepatic and renal function and electrolytes throughout treatment.

    For patients whose acetaminophen concentration is below the "possible" toxicity line (see Figure 1) and time of ingestion is known and the sample was obtained more than 4 hours after ingestion:

    • Discontinue CETYLEV.

    The acetaminophen concentration was in the non-toxic range, but time of ingestion was unknown or less than 4 hours:

    • Obtain a second sample for acetaminophen concentration and consider the patient's clinical status to decide whether or not to continue CETYLEV treatment.
    • If there is any uncertainty as to patient's risk of developing hepatotoxicity, it is recommended to administer a complete treatment course.

    Continued Therapy After Completion of Loading and Maintenance Doses

    In cases of suspected massive overdose, or with concomitant ingestion of other substances, or in patients with preexisting liver disease; the absorption and/or the half-life of acetaminophen may be prolonged. In such cases, consideration should be given to the need for continued treatment with CETYLEV beyond a total of 17 maintenance doses.

    Acetaminophen levels and ALT/AST and INR should be checked after the last maintenance dose. If acetaminophen levels are still detectable, or if the ALT/AST are still increasing or the INR remains elevated; the maintenance doses should be continued and the treating physician should contact a US regional poison center at 1-800-222-1222, or alternatively, a "special health professional assistance line for acetaminophen overdose" at 1-800-525-6115 for assistance with dosing recommendations.

    2.3 Recommended Dosage and Preparation and Administration Instructions in Adults and Pediatrics for Acute Acetaminophen Ingestion

    • CETYLEV is for oral administration only; not for nebulization or intratracheal instillation.
    • After appropriate preparation and dilu
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