Predictable pharmacodynamics and pharmacokinetics. |
Standardized tests for monitoring of DOAC activity are not easily available, when it is necessary in liver and kidney injury. |
Low drug-drug and food interactions. |
Currently lack a universal antidote |
No dietary restriction. |
High cost (in some countries) |
Rapid onset and offset, short half life. |
Experience limited to a decade |
No need of regular laboratory monitoring unlike VKA |
Needed dose modification in renal dysfunction |
Wide therapeutic window. |
Superiority against VKA for efficacy is yet to be achieved |
DOACs can be started without LMWH due to their rapid onset. |
Not indicated in pregnancy |
Low rates of ICH (50% reduction) |
|