GO TO CMA Home
GO TO Inside CMA
GO TO Advocacy and Communications
GO TO Member Services
GO TO Publications
GO TO Professional Development
GO TO Clinical Resources

GO TO What's New
GO TO Contact CMA
GO TO Web Site Search
GO TO Web Site Map


CMAJ
CMAJ - August 24, 1999JAMC - le 24 août 1999

Tuberculosis: 9. Treatment

Table 2: Doses of and common adverse reactions* to second-line antituberculosis drugs*

  Daily dose inadults and children    
 
   
Drug Usual Maximal Recommended
  regular monitoring 
Adverse reactions†

Cycloserine  150–250  
    mg
500 mg Mental status Neurologic and psychiatric disturbance, convulsions, rash
Ethionamide 15–20 mg/kg 750 mg Hepatic enzymes Gastrointestinal disturbance, hepatotoxicity, hypersensitivity
Capreomycin 15–30 mg/kg 1 g Vestibular function, audiometry, blood urea nitrogen, creatinine Auditory, vestibular and renal toxic effects
Kanamycin, amikacin 15–30 mg/kg 1 g Vestibular function, audiometry, blood urea nitrogen, creatinine, hepatic enzymes Auditory and renal toxic effects; rarely, vestibular toxic effects
Fluoroquinolones        
Ciprofloxacin 500–750 mg twice daily 1 g   Gastrointestinal upset
Ofloxacin 600–800 mg 1 g   Gastrointestinal upset
Levofloxacin 500 mg 750 mg   Gastrointestinal upset
Sparfloxacin 200 mg     Gastrointestinal upset

Note: Second-line drugs are more difficult to use than first-line drugs. They should be used only when necessary and should be given and monitored by health care providers experienced in their use.
*Adapted from the Tuberculosis Committee of the Canadian Thoracic Society,17 and the American Thoracic Society.18
†All of these drugs may cause rash, nausea and fever.

[Return to text]