February 13, 2016
Recommended Topic Related To:

Zanosar

"On December 16, 2014, the U. S. Food and Drug Administration approved lanreotide (Somatuline Depot Injection, Ipsen Pharma) for the treatment of patients with unresectable, well or moderately differentiated, locally advanced or metastatic gastroe"...

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Zanosar




PATIENT INFORMATION

Confusion, lethargy, and depression have been reported in a limited number of patients receiving continuous intravenous infusion of ZANOSAR for 5 days. Patients should be informed that there may be a potential risk in driving or using complex machinery.

Last reviewed on RxList: 2/2/2015
This monograph has been modified to include the generic and brand name in many instances.

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