Where to Order Acetadote

Contact your wholesaler or our customer service center to order Acetadote.

Customer Service Center:

Phone: (877) 274-7200
Fax: (614) 652-9127

IV Acetadote may be the right choice for your patients
  • Approved for adult and pediatric dosing
  • Patient's level of consciousness does not limit IV administration
  • Patients with acetaminophen overdose often present with nausea and vomiting – IV administration
    may allow for accurate dosing

How Supplied

Acetadote (acetylcysteine) injection is available as a 20% solution (200 mg/mL) in 30 mL single dose vials. Acetadote is sterile and can be used for IV administration. It is available as follows:

  • 30 mL vials, carton of 4 (NDC 66220-207-30)

Do not use previously opened vials for IV administration.

Available by Prescription Only
HCPS code J0132 (Please refer to your coding department for complete billing information.)


Indication

Acetadote, administered intravenously within 8 to 10 hours after ingestion of a potentially hepatotoxic quantity of acetaminophen, is indicated to prevent or lessen hepatic injury.

For maximal protection against hepatic injury, administer Acetadote within 8 hours post-ingestion.

Efficacy diminishes progressively after 8 hours and treatment initiation between 15 and 24 hours post-ingestion of acetaminophen yields limited efficacy.

Important Safety Information

Acetadote is contraindicated in patients with hypersensitivity or previous anaphylactoid reactions to acetylcysteine or any components of the preparation. Serious anaphylactoid reactions, including death in a patient with asthma, have been reported in patients administered acetylcysteine intravenously.

Acetadote should be used with caution in patients with asthma, or where there is a history of bronchospasm. The total volume administered should be adjusted for patients less than 40 kg and for those requiring fluid restriction. To avoid fluid overload, the volume of diluent should be reduced as needed. If volume is not adjusted, fluid overload can occur, potentially resulting in hyponatremia, seizure, and death.

In the literature, the most frequently reported adverse reactions attributed to IV acetylcysteine administration were rash, urticaria and pruritus. The frequency of adverse reactions has been reported to be between 0.2% and 20.8%, and they most commonly occur during the initial loading dose of acetylcysteine.

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