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Organ toxicity? cardiotoxicity

Cumulative organ toxicity also presents a significant obstacle for effective chemotherapy. In many cases, the severity of the toxicity impedes the broader use of an agent. Other specific toxicities are associated with specific agents, for example cardiotoxicity with adriamycin (32), renal toxicity with i7j -platinum (28), and neurotoxicity with vincristine (49). [Pg.444]

A number of quinolones had to be taken off the market due to toxic effects on the liver, heart, or other organs, that became recognized only after marketing (e.g. temafloxacin, trovafloxacin, grepafloxacin). A risk for severe cardiotoxicity, hepatotoxicity, or phototoxicity is... [Pg.1058]

Drug interactions Proleukin may affect central nervous system function. Therefore interactions could occur following concomitant administration of psychotropic drugs. Concurrent administration of drugs possessing nephrotoxic, myelotoxic, cardiotoxic, or hepatotoxic effects with Proleukin may increase toxicity in these organ systems. Reduced kidney and liver function secondary to Proleukin treatment may delay elimination of concomitant medications and increase the risk of adverse events from those drugs. Beta-blockers and other antihypertensives may potentiate the hypotension seen with Proleukin. [Pg.201]


See other pages where Organ toxicity? cardiotoxicity is mentioned: [Pg.444]    [Pg.518]    [Pg.340]    [Pg.326]    [Pg.419]    [Pg.18]    [Pg.93]    [Pg.93]    [Pg.96]    [Pg.313]    [Pg.347]    [Pg.31]    [Pg.174]    [Pg.1930]    [Pg.40]    [Pg.478]    [Pg.10]    [Pg.595]    [Pg.808]    [Pg.340]    [Pg.665]    [Pg.377]    [Pg.501]    [Pg.808]    [Pg.346]    [Pg.356]    [Pg.377]    [Pg.148]    [Pg.148]    [Pg.135]   
See also in sourсe #XX -- [ Pg.256 ]




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