Monograph Details

Central Nervous System > Parkinsonism
ZELAPAR
Manufacturer
Valeant Pharmaceuticals, Inc
Legal Classification
Rx
Pharmacological Class
MAO-B inhibitor.
Generic Name
Selegiline 1.25mg; orally-disintegrating tabs; contains phenylalanine.
Indications
Adjunct in Parkinson's disease in patients with deteriorating response to levodopa/carbidopa.
Children
<16yrs: not recommended.
Adults
Take (without liquids) in the AM before breakfast; do not eat/drink within 5 minutes (before or after). Place tablet on tongue, do not swallow. ≥16 yrs: 1.25mg once daily for at least 6 weeks; if needed, may increase to max 2.5mg once daily if tolerated. Do not exceed max dose. Not bioequivalent to other forms of selegiline.
Contraindications
During or within 2 weeks of meperidine, MAOIs (eg, other forms of selegiline). Concomitant tramadol, methadone, propoxyphene, dextromethorphan.
Precautions
Renal or hepatic impairment. Monitor for melanoma. Elderly (higher risk of orthostatic hypotension). Pregnancy (Cat.C). Nursing mothers: not recommended.
Interactions
See Contraindications. Avoid sympathomimetic amines, tricyclics, SSRIs, SNRIs; allow at least 14 days after discontinuing selegiline before starting an SSRI (eg, fluoxetine), tricyclic or SNRI; allow 5 weeks after discontinuing fluoxetine before starting selegiline. Caution with CYP3A4 inducers (eg, phenobarbital, phenytoin, carbamazepine, nafcillin, rifampin). Consider reducing concomitant levodopa/carbidopa dose if dyskinesia occurs.
Adverse Reactions
Postural hypotension (usually transient), dizziness, GI upset, pain, headache, insomnia, rhinitis, stomatitis, hypertension, ECG abnormality, hallucinations.
How Supplied
Tabs—60
Additional Resources
Related Prescribing Note