IRON SUPPLEMENTS - A COMMON CAUSE OF DRUG-INTERACTIONS

被引:80
作者
CAMPBELL, NRC
HASINOFF, BB
机构
[1] MEM UNIV NEWFOUNDLAND,FAC MED,ST JOHNS A1B 3V6,NEWFOUNDLAND,CANADA
[2] MEM UNIV NEWFOUNDLAND,DEPT CHEM,ST JOHNS A1B 3V6,NEWFOUNDLAND,CANADA
关键词
IRON; DRUG INTERACTION;
D O I
10.1111/j.1365-2125.1991.tb05525.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Iron-drug interactions of clinical significance may occur in many patients and involve a large number of therapies. Concurrent ingestion of iron causes marked decreases in the bioavailability of a number of drugs. The affected drugs, tetracycline, tetracycline derivatives (doxycycline, methacycline and oxytetracycline), penicillamine, methyldopa, levodopa, carbidopa and ciprofloxacin have diverse chemical structures and clinical effects. The major mechanism of these drugs interactions is the formation of iron-drug complexes (chelation or binding of iron by the involved drug). A large number of other important and commonly used drugs such as thyroxine, captopril and folic acid have been demonstrated to form stable complexes with iron. There is little known about the effects of concurrent therapy with iron supplements for most of the drugs.
引用
收藏
页码:251 / 255
页数:5
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