I have more docs telling me they are seeing breakthrough clots on patients with higher CHADs scores and excessive bleeding in patients taking their meds more frequently than Q12. Why doesn't pharmacy have a required label for patients or make a special alarm clock to ensure patients take the med every 12 hours on the dot to avoid this problem? And why is Pfizer keeping important safety information from the public? FDA is working on ANOTHER new Eliquis label update this fall. It's time to come clean with the public and avoid the problems you had burying data with Lyrica and Celebrex, prior to the lawsuits.
