The most recent study was published June 25 in JAMA Ophthalmology. Researchers found a correlation between use of rivaroxaban and a risk of spontaneous vitreous hemorrhage, although they noted that all three patients who developed the eye hemorrhage were also taking an additional anticoagulant at the time.
“The risk of hemorrhage may be particularly elevated during the transition period when patients are switched from baseline anticoagulant to rivaroxaban therapy and are taking both anticoagulants simultaneously,” researchers wrote.
According to Reuters (6/26/15), all three patients who experienced vitreous hemorrhage were males over the age of 70 who experienced the hemorrhage in their right eye. All three were taking warfarin and rivaroxaban at the same time and all three discontinued the warfarin when the hemorrhage developed. All three recovered from the hemorrhage within two months of the event and did not suffer any significant vision damage.
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“Although rates of gastrointestinal bleeding seem to be similar in this commercially insured sample of adults in the United States, we cannot rule out…a more than twofold higher risk of bleeding with rivaroxaban compared with warfarin.”
As lawsuits filed against the makers of Xarelto work their way through the courts, more lawsuits are being added to the multidistrict litigation. As of July 15, 2015, 805 lawsuits had been consolidated in MDL 2592 (In Re: Xarelto Products Liability Litigation) before US District Judge Eldon E. Fallon. In June there were 552 such lawsuits consolidated. Consolidation for pretrial proceedings is not a comment on the merits of the lawsuits, it is an acknowledgement that the lawsuits share similar questions of fact.