Share on Facebook
Share on Twitter
Share on LinkedIn
Share by Email
Print
Orfadin Oral Suspension Generic Name & Formulations
Legal Class
Rx
General Description
Nitisinone 4mg/mL; strawberry-flavored; contains glycerol 500mg/mL and sodium 0.7mg/mL.
Pharmacological Class
4-hydroxyphenylpyruvate dioxygenase inhibitor.
See Also
How Supplied
Caps—60; Oral susp—90mL
Manufacturer
Generic Availability
NO
Orfadin Oral Suspension Indications
Indications
Treatment of hereditary tyrosinemia type 1 (HT-1) in combination with dietary restriction of tyrosine and phenylalanine.
Orfadin Oral Suspension Dosage and Administration
Adults and Children
Caps: take ≥1hr before or 2hrs after a meal. May open and mix contents in water, formula, or applesauce if difficulty swallowing caps or intolerant to oral susp. Initially 0.5mg/kg twice daily. Titrate individually as needed based on response. Monitor plasma and/or urine succinylacetone levels, liver function, and alpha-fetoprotein levels. Increase to 0.75mg/kg twice daily if succinylacetone is still detectable 1 month after treatment initiation; max 2mg/kg total daily dose may be needed. Maintenance: ≥5yrs with undetectable succinylacetone levels after a minimum of 4wks therapy on a stable dose: may give total daily dose once daily (eg, 1–2mg/kg once daily).
Orfadin Oral Suspension Contraindications
Not Applicable
Orfadin Oral Suspension Boxed Warnings
Not Applicable
Orfadin Oral Suspension Warnings/Precautions
Warnings/Precautions
Maintain dietary restriction of tyrosine and phenylalanine during therapy. Do not adjust dose to lower plasma tyrosine levels (maintain levels at <500μmol/L). Perform baseline eye exams (including slit-lamp test) prior to starting therapy and regularly thereafter; reevaluate and measure plasma tyrosine levels if ocular symptoms develop. Perform lab tests (including plasma tyrosine levels) if abrupt change in neurologic status occurs. Monitor platelets, WBC counts during therapy. Oral susp: glycerol content (>20mL as a single-dose) may increase risk of adverse effects (eg, headache, upset stomach, diarrhea). Elderly. Pregnancy. Nursing mothers.
Orfadin Oral Suspension Pharmacokinetics
See Literature
Orfadin Oral Suspension Interactions
Interactions
Potentiates sensitive CYP2C9 substrates (eg, celecoxib, tolbutamide) or CYP2C9 substrates with a narrow therapeutic index (eg, phenytoin, warfarin); reduce dose of these substrates by ½ or as needed. Potentiates OAT1/OAT3 substrates (eg, adefovir, ganciclovir, methotrexate); monitor.
Orfadin Oral Suspension Adverse Reactions
Adverse Reactions
Elevated tyrosine levels, thrombocytopenia, leukopenia, conjunctivitis, corneal opacity, keratitis, photophobia, eye pain, blepharitis, cataracts, granulocytopenia, epistaxis, pruritus, exfoliative dermatitis, dry skin, maculopapular rash, alopecia; hyperkeratotic plaques on the soles and palms.
Orfadin Oral Suspension Clinical Trials
See Literature
Orfadin Oral Suspension Note
Not Applicable
Orfadin Oral Suspension Patient Counseling
See Literature
