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Indication & Dosage
 
 
Oral
ADVANCED OVARIAN CARCINOMA
Adult: When used as a single agent in previously untreated patients, 400 mg/m2 BSA by IV infusion over 15-60 min on day 1 at 4-wkly intervals. May repeat course if neutrophil count is at least 2000 and platelet count is at least 100,000. For use as a single agent in previously treated patients, initiate at 360 mg/m2. When used with cyclophosphamide in previously untreated patients, initiate at 300 mg/m2.
   
Precautions Neonates; diminished renal function; neurotoxicity; liver function impairment.
   
Potentially Life-threatening 
Adverse Drug Reactions
Thrombocytopenia, neutropenia, leukopenia, anaemia; nausea, vomiting, central neurotoxicity, peripheral neuropathies, ototoxicity; elevation of ALT, AST, blood urea and bilirubin levels, electrolyte disturbances; alopecia; asthenia, pain; cardiac failure, embolism and cerebrovascular accidents may occur; mucositis.
   
Adverse Drug Reactions Bone marrow suppression and anaphylactic reactions.
   
Interactions Increased risk of ototoxicity when used with aminoglycosides.
   
   
 

 

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