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![CMAJ - August 24, 1999](issue-4.gif) ![](../../../images-site/navbar-8space.gif) ![](../../../images-site/nav-linksub.gif)
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 |
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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. |
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