I was on Clexane 60 mg twice a day by prof Hughes. I am switching to Rivoraxaban or Xarelto 10 mg tabs. I am curious what dosages other patients are taking. I have taken it only once but I don't think it is stron enough. Unfortunately my hematologist does not have a lot of information for this drug & APS syndrome. Anyone Designer 16
? Is anyone taking Rivoraxaban or xar... - Hughes Syndrome A...
? Is anyone taking Rivoraxaban or xarelto
Hi, I was also on Clexane, 18 months ago changed to Xarelto 20mg. No problems and APS symptoms under control. Good luck.
10 mg is the dose required to prevent clots after hip and knee surgery, 20 mg is for treating DVT and PE - check with your Dr
I take Rivaroxaban 20mg daily (1 @ night) and 100 mg aspirin. Was on 80mg Clexane before switching nearly a year ago. So far no problems.
I just started zarelto a month ago 15mg's. went to the Hematologist and she is upping me to 20mg's. She did not want to start me out out on the higher dosage because I have kidney disease, but my creatnine has gone down since on this medication. I seem to be doing fine with it so far.
Hi
I started on rivaroxaban on 2nd April - 20mg at 6am with also 150mg pregabalin for Fibromyalga (???) Only side effect is can sleep flat out for 4 hours - !!! But in last 8 months I could sleep all day regardless - I am totally exhausted
I took fibromyalgia a few years ago. It made me very nervous. I know nerve medicine really mess with sleeping. My friends mom also had problems with sleep. I would talk to your doctor. Designer16
I understand that you have difficulties with your medicin. You live in the US and Prof Hughes in England. He has prescribed Clexane earlier but it costs a fortune to get your drug in USA. Now you have just started Rivaroxaban 10 mg.
Try as APsnotFab and Mary also had said earlier to get an APS-Specialist in your country if it is possible. You are allergic to some medicins and you are also talking of Fibromyalgia. You need an Expert!
I understand it is not easy but the new drug Rivaroxaban are not even licened for APS. Do you have had arterial or venous clots?
I feel sorry for you as I understand that you have a difficult situation. Hope you find your own APS-Specialist to talk to. You are a real fighter I think!
Kerstin in Stockholm Good Luck!
Hi
I am not taking fibromyalgia, I took it once several years ago before I saw Prof Hughes. I have tried to find a APS specialist in my area & it has proven to be a lost cause. I do have a hematologist monitoring me. I have been taking the xarelto for 3 days & seem to be OK. I have had a pulmonary embolism years ago & no new clots. I have a lot of neurological symptoms which are improving. I see prof Hughes 24 April & see what he says.
Thank you
Designer16