血代

국가: 대만

언어: 중국어

출처: 衛生福利部食品藥物管理署 (Ministry of Health and Welfare, Food And Drug Administration)

유효 성분:

NITROGEN;;SODIUM ION;;POTASSIUM ION;;CALCIUM ION;;CHLORIDE ION;;PHOSPHATE ION;;SULFURIC ACID (EQ TO SULPHURIC ACID)

제공처:

臺灣安萬特藥品股份有限公司 台北巿敦化南路一段１０８號９樓 (97168356)

약제 형태:

注射劑

구성:

主成分 (COMPOSITION: 1000ML CONTAIN: DEGRADED **) ; NITROGEN (2804001000) 6.3GM; CALCIUM ION (4026000410) 6.25MMOLE; CHLORIDE ION (4026000510) 145MMOLE; PHOSPHATE ION (4026001410) TRACE; POTASSIUM ION (4026001510) 5.1MMOLE; SODIUM ION (4026001710) 145MMOLE; SULFURIC ACID (EQ TO SULPHURIC ACID) (4036000400) TRACE

패키지 단위:

瓶裝

수업:

製　劑

처방전 유형:

限由醫師使用

Manufactured by:

CENTEON PHARMA GMBH. KRUMMBOGEN 10, 35039 MARBURG GERMANYBRUNINGSRASSE 50,D-65926 FRANKFURT AM MAIN ,GERMANY DE

치료 징후:

由於失血、失血漿過量所引起之休克　＊＊ＧＥＬＡＴＩＮ　ＰＯＬＹＰＥＰＴＩＤＥＤ　ＣＲＯＳＳ－ＬＩＮＫＥＤ　ＶＩＡ　ＵＲＥＡ　ＢＲＩＤＧＥＳ

제품 요약:

註銷日期: 1987/04/20; 註銷理由: 移轉（申請商）; 有效日期: 1989/06/06; 英文品名: HAEMACCEL

승인 상태:

已註銷

승인 날짜:

1984-02-20