देश: सिंगापुर
भाषा: अंग्रेज़ी
स्रोत: HSA (Health Sciences Authority)
GRANISETRON HCl EQV GRANISETRON
DKSH SINGAPORE PTE. LTD.
A04AA02
1.12 mg (eqv 1 mg)
TABLET, FILM COATED
GRANISETRON HCl EQV GRANISETRON 1 mg
ORAL
Prescription Only
Delpharm Milano s.r.l.
ACTIVE
1994-07-21
1 KYTRIL® Granisetron COMPOSITION _Active ingredient_: granisetron. _ _ _Ampoules _ Clear glass ampoules, each containing 1 mg granisetron present as the hydrochloride in 1 ml isotonic saline as a clear, colourless liquid. Clear glass ampoules, each containing 3 mg granisetron present as the hydrochloride in 3 ml isotonic saline as a clear, colourless liquid. _Excipients_: ampoules also contain sodium chloride, citric acid monohydrate and water for injections Ph. Eur. _ _ _Tablets _ White triangular film-coated tablets, each containing 1 mg granisetron present as the hydrochloride. _Excipients_: tablets also contain lactose monohydrate, hypromellose, sodium starch glycolate, cellulose, magnesium stearate, titanium dioxide E171, macrogol 400 and polysorbate 80. PROPERTIES AND EFFECTS Granisetron is a potent and highly selective 5-hydroxytryptamine (5- HT3) receptor antagonist with anti-emetic activity. PHARMACOKINETICS _Absorption _ Absorption of Kytril is generally not influenced by food and is rapid and complete, though oral bioavailability is reduced to around 60% as a result of first pass metabolism. _ _ _Distribution _ Kytril is widely distributed with a mean volume of distribution of approximately 3 liters/kg; plasma protein binding is approximately 65%._ _ _ _ _Metabolism _ Biotransformation pathways involve N-demethylation and aromatic ring oxidation followed by conjugation._ _ _ _ _Elimination _ Clearance is predominantly by hepatic metabolism. Urinary excretion of unchanged Kytril averages 12% of dose whilst that of metabolites amounts to about 47% of पूरा दस्तावेज़ पढ़ें
1 KYTRIL® Granisetron COMPOSITION _Active ingredient_ : granisetron. _ _ _Ampoules _ Clear glass ampoules, each containing 1 mg granisetron present as the hydrochloride in 1 ml isotonic saline as a clear, colourless liquid. Clear glass ampoules, each containing 3 mg granisetron present as the hydrochloride in 3 ml isotonic saline as a clear, colourless liquid. _Excipients_ : ampoules also contain sodium chloride, citric acid monohydrate and water for injections Ph. Eur. _ _ _Tab_ _lets _ White triangular film-coated tablets, each containing 1 mg granisetron present as the hydrochloride. _Excipients_ : tablets also contain lactose monohydrate, hypromellose, sodium starch glycolate, cellulose, magnesium stearate, titanium dioxide E171, macrogol 400 and polysorbate 80. PROPERTIES AND EFFECTS Granisetron is a potent and highly selective 5-hydroxytryptamine (5- HT3) receptor antagonist with anti-emetic activity. PHARMACOKINETICS _Absorption _ Absorption of Kytril is generally not influenced by food and is rapid and complete, though oral bioavailability is reduced to around 60% as a result of first pass metabolism. _ _ _Distribution _ Kytril is widely distributed with a mean volume of distribution of approximately 3 liters/kg; plasma protein binding is approximately 65%. _ _ _ _ _Metabolism _ Biotransformation pathways involve N-demethylation and aromatic ring oxidation followed by conjugation. _ _ _ _ _Elimination _ Clearance is predominantly by hepatic metabolism. Urinary excretion of unchanged Kytril averages 12% of dose whilst that of metabolites amounts to about 47% of dose. The remainder is excreted in feces as metabolites. Mean plasma half-life in patients is approximately nine hours, with a wide inter-subject variability. INDICATIONS AND USAGE Tablets Kytril is indicated for the prevention of nausea and vomiting induced by cytostatic therapy. Ampoules Kytril is indicated for the prevention or treatment of nausea and vomiting induced by cytostatic therapy and for the prevention and treatment of post-operative n पूरा दस्तावेज़ पढ़ें