唯代若靜脈輸注液

Pays: Taïwan

Langue: chinois

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

Ingrédients actifs:

POLY(O-2 HYDROXYETHYL )STARCH;;SODIUM ACETATE TRIHYDRATE (EQ TO SODIUM ACETATE 3H2O );;SODIUM CHLORIDE;;POTASSIUM CHLORIDE;;CALCIUM CHLORIDE DIHYDRATE;;MAGNESIUM CHLORIDE HEXAHYDRATE (EQ TO MAGNESIUM CHLORIDE 6H2O)

Disponible depuis:

和聯生技藥業股份有限公司 台北市敦化北路３１１號５樓 (04270075)

Code ATC:

B05AA07

forme pharmaceutique:

注射劑

Composition:

SODIUM ACETATE TRIHYDRATE (EQ TO SODIUM ACETATE 3H2O ) (4008000670) MG; CALCIUM CHLORIDE DIHYDRATE (4012000350) MG; MAGNESIUM CHLORIDE HEXAHYDRATE (EQ TO MAGNESIUM CHLORIDE 6H2O) (4012001550) MG; POTASSIUM CHLORIDE (4012001800) MG; SODIUM CHLORIDE (4012002100) MG; POLY(O-2 HYDROXYETHYL )STARCH (9600030283) (molar substitution 0.42, MW130,000)MG

Unités en paquet:

塑膠軟袋裝

classe:

製　劑

Type d'ordonnance:

限由醫師使用

Fabriqué par:

SERUMWERK BERNBURG AG HALLESCHE LANDSTRABE 105B, 06406 BERNBURG, GERMANY DE

Domaine thérapeutique:

hydroxyethylstarch

indications thérapeutiques:

預防及治療血容積低下及休克

Descriptif du produit:

註銷日期: 2016/06/01; 註銷理由: 許可證已逾有效期; 有效日期: 2016/01/13; 英文品名: Vitafusal Solution for Infusion

Statut de autorisation:

已註銷

Date de l'autorisation:

2011-01-13