Kc. Oberg et al., FOCUS ON RETEPLASE - A NEWLY APPROVED 3RD-GENERATION THROMBOLYTIC AGENT FOR THE TREATMENT OF ACUTE MYOCARDIAL-INFARCTION, Formulary, 32(1), 1997, pp. 37
Reteplase (Retavase) is a genetically engineered third-generation thro
mbolytic agent recently approved by the FDA for the treatment of acute
myocardial infarction (AMI). Its several domain modifications of the
tissue-type plasminogen activator gene have given reteplase enhanced p
harmacologic properties, including a threefold-longer half-life, which
allows for a simplified thrombolytic dosing regimen. Reteplase is giv
en as a 10-U intravenous bolus followed 30 minutes later by a second 1
0-U bolus. Several comparative trials have shown reteplase to be as ef
fective and well tolerated as streptokinase and to achieve more rapid,
complete, and sustained thrombolysis than alteplase. As with other th
rombolytics, the most serious adverse effect reported with reteplase i
s bleeding. Reteplase may offer a useful alternative to existing throm
bolytic therapy in AMI.