Dabigatran Trial: Hi all, I found out... - Hughes Syndrome A...

Hughes Syndrome APS Forum

10,354 members10,542 posts

Dabigatran Trial

MASuk10 profile image
2 Replies

Hi all,

I found out yesterday, after 18 months, that my APS is my primary condition which is good news in a way. My consultant at Northampton Hospital has recommended me for the Dabigatran trial. I'm waiting for a call from London with more information.

In the meantime is anyone here on that trial?

:-)

Written by
MASuk10 profile image
MASuk10
To view profiles and participate in discussions please or .
Read more about...
2 Replies
chrissybell profile image
chrissybell

Not on a trial, but am on dabigatran - have been since August 12. Suits me we'll (primary APS - with previous multiple PEs! Good luck (only side effect is if I take it lying down I can get really bad indigestion, so when taking night time dose (2 x a day) I have to sit up for at least 15 minutes. Other than that it doesn't interfere in my life at all! Good luck

Manofmendip profile image
Manofmendip in reply to chrissybell

That sounds good, I'm on Fragmin but I hope that one day I will be on an oral Heparin like you are.

Dave

You may also like...

Dabigatran approved by NICE

be seeing information in the media about a new oral anticoagulant called Dabigatran which has been...

Dabigatran and tummy trouble

diarrhoea now for about a year. The gastro consultant has recommended Omeprazole, but I am...

Pradaxa/Dabigatran

Pradaxa being used for Hughes Syndrome? I first found out about this drug in relation to my...

Dabigatran and retinal bleeding

I have AF. 5 years ago I was prescribed Dabigatran after having a stroke, plus Fleicanide and...

Pradaxa (Dabigatran) V's Warfarin

says I could be a candidate for it and it could be more advantageous for me given my age and rather...