Riluzole

A to Z Drug Facts

Riluzole

  Action
  Indications
  Contraindications
  Route/Dosage
  Interactions
  Lab Test Interferences
  Adverse Reactions
  Precautions
Patient Care Considerations
  Administration/Storage
  Assessment/Interventions
  Patient/Family Education


(RILL-you-zole)
Rilutek
Class: Neuroprotective

 Action Unknown; however, the following properties may be related to effects: Inhibits glutamate release; inactivates voltage-dependent sodium channels; interferes with intra-cellular events following transmitter binding at excitatory amino acid receptors. These effects may protect neural tissues against degenerative changes.

 Indications Treatment of patients with amyotrophic lateral sclerosis (ALS; Lou Gehrig's disease).

 Contraindications Standard considerations.

 Route/Dosage

ADULTS: PO 50 mg q 12 hr.

 Interactions

Caffeine, theophylline, amitriptyline, quinolones: May reduce riluzole elimination. Cigarette smoke, rifampin, omeprazole: May enhance riluzole elimination.

 Lab Test Interferences None well documented.

 Adverse Reactions

CV: Hypertension; tachycardia; palpitations; peripheral edema. CNS: Headache; hypertonia; depression; dizziness; insomnia; somnolence; vertigo; circumoral paresthesia; aggravation reaction; agitation; tremor. DERM: Pruritus; eczema; alopecia; exfoliative dermatitis. EENT: Rhinitis; sinusitis. HEPA: Abnormal liver function tests. GI: Nausea; vomiting; dyspepsia; anorexia; diarrhea; constipation; flatulence; abdominal pain; stomatitis; dry mouth; oral moniliasis. GU: Urinary tract infection; dysuria. META: Weight loss. RESP: Decreased lung function; cough. OTHER: Asthenia; arthralgia; back pain; malaise.

 Precautions

Pregnancy: Category C. Lactation: Undetermined. Children: Safety and efficacy not established. Elderly: Age-related compromised renal and hepatic function may cause a decrease in clearance of riluzole. Renal impairment: Use with caution in patients with renal impairment. Hepatic function impairment: Use with caution in patients with current evidence or history of abnormal liver function indicated by significant elevations of liver enzymes. Baseline elevations of several LFTs (especially elevated bilirubin) should preclude use of riluzole. Monitoring: Measure serum aminotransferases before and during therapy. Evaluate serum SGPT levels every month during the first 3 months of treatment, every 3 months during the remainder of the first yr and periodically thereafter. Special populations: Females and Japanese patients may possess a lower metabolic capacity to eliminate riluzole as compared to males and Caucasian subjects respectively.


PATIENT CARE CONSIDERATIONS


 Administration/Storage

 Assessment/Interventions

OVERDOSAGE: SIGNS & SYMPTOMS
  None reported

 Patient/Family Education

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Copyright
© 2003 Facts and Comparisons
David S. Tatro
A to Z Drug Facts