Bernstein L S
Can Med Assoc J. 1975 Jun 14;112(13 Spec No):96-8.
Since trimethoprim-sulfamethoxazole (TMP-SMX) was first marked occasional reviews have surveyed the pattern of adverse reactions. Skin rashes characteristic of sulfonamide sensitivity have predominated, with relatively few of a serious exfoliative nature. Hematologic adverse reactions recorded follow the pattern known to occur with sulfonamides, with a few cases related to the action of trimethoprim on human folate metabolism. Such an effect is more likely to occur when the patient's folate status is already jeopardized; it is rare in relation to the widespread use of the drug combination. Long-term administration does not per se seem to represent an additional hazard provided the dose is the correct one and the hematologic monitoring of the patient is performed regularly. The suggestion that TMP-SMX has a toxic effect on the kidney has not been substantiated. An estimated 250 million "standard treatment courses" have been given in the first 6 years of marketing and, overall, the picture of adverse reactions corresponds with that expected from a sulfonamide of relatively low toxicity.
自从甲氧苄啶-磺胺甲恶唑(TMP-SMX)首次上市以来,不时有综述对其不良反应模式进行调查。磺胺类药物敏感性特有的皮疹最为常见,严重的剥脱性皮疹相对较少。所记录的血液学不良反应遵循磺胺类药物已知的发生模式,少数病例与甲氧苄啶对人体叶酸代谢的作用有关。当患者的叶酸状态已经受到损害时,这种效应更有可能发生;相对于该药物组合的广泛使用而言,这种情况很少见。只要剂量正确且对患者进行定期血液学监测,长期给药本身似乎并不构成额外风险。关于TMP-SMX对肾脏有毒性作用的说法尚未得到证实。在上市后的头6年里,估计已开出了2.5亿个“标准疗程”,总体而言,不良反应情况与预期的低毒性磺胺类药物相符。