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在药品的包装和说明书中,竟然有135个品种违反《药品管理法》及相关法规。这是最近卫生部组织的一项审查结果。审查结果显示,有的药品包装内没有附上说明书,仅在药品外包装上印了简单的说明;有的药品说明书内容与卫生部批准的说明书不一致,夸大药品使用范围,更改“用法用量”、“禁忌症”及“注意事项”等;有的使用商品名的药品不印制药品通用
In the pharmaceutical packaging and brochures, there are actually 135 varieties in violation of “Drug Administration Law” and related laws and regulations. This is the result of a recent review organized by the Ministry of Health. The examination results showed that some pharmaceutical packaging did not attach instructions, only printed on the drug packaging a brief description; some drug instructions and the Ministry of Health approved the instructions inconsistent, exaggerate the scope of the use of drugs, change the “usage and dosage” “Contraindications” and “precautions” and so on; some use of trade names of drugs do not print generic drugs