In the US, TheraSphere® is authorized by Federal Law for use in radiation treatment or as a neoadjuvant to surgery or transplantation in patients with unresectable hepatocellular carcinoma (HCC) who can have placement of appropriately positioned hepatic arterial catheters. The device is also indicated for HCC patients with partial or branch portal vein thrombosis/occlusion, when clinical evaluation warrants the treatment. The effectiveness of this device for this use has not been demonstrated. Humanitarian Device.1
Common adverse effects include fatigue, pain, and nausea. The majority of adverse effects were mild to moderate in severity and were manageable or resolved over time. For details on rare or more severe adverse effects, please refer to the TheraSphere® Package Insert. 1,3,5
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Corporate press releases are selected from information communicated on www.btgplc.com and are selected because the information relates to BTG products available in various countries. The information is not being shared to advocate use of a product outside of its locally approved indication for use.
Noteworthy News articles are selected from information communicated on websites external to BTG and are selected because the information relates to BTG products available in various countries. The information is not being shared to advocate use of a product outside of its locally approved indication for use.
Not all products and/or indications are available in the US and certain other territories. LC Bead and Bead Block are trademarks and/or registered trademarks of Biocompatibles UK Ltd. EKOS, the EKOS logo, Acoustic Pulse Thrombolysis and EkoSonic are trademarks and/or registered trademarks of EKOS Corporation. TheraSphere® is manufactured for Biocompatibles UK Ltd. TheraSphere is a registered trademark of Theragenics Corporation used under license by Biocompatibles UK Ltd. Varithena is a registered trademark of Provensis Ltd. PneumRx and RePneu are trademarks of PneumRx. PneumRx is a registered trademark in the US and certain other territories. The RePneu Coils are not approved for commercial sale in the United States, and are restricted by US law to investigational use only in the U.S. ‘See more. Reach further. Treat smarter’ and ‘Imagine where we can go’ are trademarks of BTG International Ltd. BTG and the BTG roundel logo are registered trademarks of BTG International Ltd. Biocompatibles UK Ltd, EKOS Corporation, Provensis Ltd and PneumRx Corporation are BTG International group companies. For full prescribing information please click here Bead Block™, EKOS®, LC Bead®, TheraSphere®, Varithena®, PneumRx © Copyright 2015 BTG International Ltd. All rights reserved.”