Onfi Generic Name & Formulations
Legal Class
General Description
Pharmacological Class
See Also
How Supplied
Manufacturer
Generic Availability
Mechanism of Action
Onfi Indications
Indications
Onfi Dosage and Administration
Adults and Children
Onfi Contraindications
Not Applicable
Onfi Boxed Warnings
Boxed Warning
Onfi Warnings/Precautions
Warnings/Precautions
Increased risk of drug-related mortality from concomitant use with opioids. Monitor for the emergence or worsening of depression, suicidal thoughts/behavior, and/or unusual changes in mood or behavior. Monitor for signs/symptoms of serious skin reactions (eg, SJS, TEN), esp. during the first 8 weeks of initiation or when re-introducing therapy; discontinue at the first sign of rash unless it's not drug-related. Evaluate immediately if signs or symptoms of drug reaction with eosinophilia and systemic symptoms (DRESS)/multiorgan hypersensitivity develop; discontinue if alternative etiology cannot be established. Assess patient's risk for abuse, misuse, addiction prior to and during therapy. Avoid abrupt cessation; taper by decreasing total daily dose by 5–10mg/day on a weekly basis. Drug or alcohol abusers. Severe renal or hepatic impairment or ESRD. Elderly. Neonatal sedation and withdrawal syndrome; monitor neonates exposed during pregnancy or labor. Pregnancy (esp. late stage). Nursing mothers: monitor infants.
Onfi Pharmacokinetics
Absorption
Relative bioavailability of clobazam tablets vs oral solution is approximately 100%. Time to peak concentration: ranged from 0.5 to 4 hours (clobazam tablets); ranged from 0.5 to 2 hours (oral susp).
Distribution
The volume of distribution at steady state was ~100 L. The in vitro plasma protein binding of clobazam and N-desmethylclobazam is ~80–90% and 70%, respectively.
Elimination
Renal (82%), fecal (11%).
Onfi Interactions
Interactions
Onfi Adverse Reactions
Adverse Reactions
Onfi Clinical Trials
See Literature
Onfi Note
Not Applicable
Onfi Patient Counseling
See Literature
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