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testing

 
   
LOMTIN  LOMUSTINE  LUSTINE 
 



Indication & Dosage
 
 
Oral
BRAIN TUMOURS
Adult: 100-130 mg/m2 as a single dose every 6 wk. Readjust dose according to platelet and leukocyte counts. Compromised marrow function: 100 mg/m2 as a single dose every 6 wk.
 
Oral
BRAIN TUMOURS
Child: 75-150 mg/m2 as a single dose every 6 wk. Readjust dose according to platelet and leukocyte counts.
 
Oral
HODGKIN'S DISEASE, RESISTANT OR RELAPSED
Adult: 100-130 mg/m2 as a single dose every 6 wk. Readjust dose according to platelet and leukocyte counts. Compromised marrow function: 100 mg/m2 as a single dose every 6 wk.
 
Oral
HODGKIN'S DISEASE, RESISTANT OR RELAPSED
Child: 75-150 mg/m2 as a single dose every 6 wk. Readjust dose according to platelet and leukocyte counts.
 
Oral
MALIGNANT MELANOMA
Adult: 100-130 mg/m2 as a single dose every 6 wk. Readjust dose according to platelet and leukocyte counts. Compromised marrow function: 100 mg/m2 as a single dose every 6 wk.
 
Oral
MALIGNANT MELANOMA
Child: 75-150 mg/m2 as a single dose every 6 wk. Readjust dose according to platelet and leukocyte counts.
 
Oral
LUNG CANCER
Adult: 100-130 mg/m2 as a single dose every 6 wk. Readjust dose according to platelet and leukocyte counts. Compromised marrow function: 100 mg/m2 as a single dose every 6 wk.
 
Oral
LUNG CANCER
Child: 75-150 mg/m2 as a single dose every 6 wk. Readjust dose according to platelet and leukocyte counts.
   
Administration Should be taken on an empty stomach (i.e. At least one hour before food or four hours after food). (Take on an empty stomach. May be taken at bedtime to reduce occurrence of nausea.)
   
Precautions Monitor CBC with differential platelet count wkly for at least 6 wk after a dose. Periodically perform pulmonary function studies and LFTs.
   
Potentially Life-threatening 
Adverse Drug Reactions
Pulmonary infiltrates, pulmonary fibrosis, nausea, vomiting, hepatotoxicity, nephrotoxicity, stomatitis, alopecia, disorientation, lethargy, dysarthria, ataxia, visual disturbances.
   
Adverse Drug Reactions Delayed bone marrow suppression and permanent marrow damage following prolonged use.
   
Interactions Increased levels/effects with CYP2D6 inhibitors.
   
   
 

 

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