英和和英

出典:『Wikipedia』 (2011/06/06 12:19 UTC 版)

英語による解説

引用

The Adverse Event Reporting System (AERS) is a computerized information database designed to support the U.S. Food and Drug Administration's (FDA) post-marketing safety surveillance program for all approved drug and therapeutic biologic products. The FDA uses AERS to monitor for new adverse events and medication errors that might occur with these marketed products.