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* Six percent (n=2/36) of patients taking
BARACLUDE and 15 percent
(n=5/33) of patients taking adefovir
experienced a Grade 3-4 adverse
event.
* Three percent (n=1/36) of patients taking
BARACLUDE experienced a
serious adverse event (elevated ALT
that resolved with continued
treatment). Nine percent (n=3/33) of
patients taking adefovir
experienced a serious adverse event
(one patient had elevated ALT that
resolved with continued treatment;
one patient had acute hepatitis with
ALT flare [ALT flare defined as
greater than two times baseline and
greater than 10 times the upper
limit of normal]; one patient was
involved in a motor vehicle
accident).
* There were no deaths in either arm and one
patient discontinued
treatment due to an adverse
event.
About BARACLUDE(R) (entecavir)Discovered at Bristol-Myers Squibb, BARACLUDE(R) (entecavir) is a nucleoside analogue indicated for the treatment of chronic hepatitis B virus infection in adults with evidence of active viral replication with either evidence of persistent elevations in serum aminotransferases (ALT or AST) or histologically active disease. BARACLUDE has been approved in more than 60 countries and regions around the world.
Important Information About BARACLUDE(R) (entecavir) 0.5mg/1mg Tablets
BARACLUDE(R) (entecavir) is a prescription medicine used for
chronic infection with hepatitis B virus (HBV) in adults
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