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#518220 - 02/09/18 03:48 AM Confused - which drug to take
PFMarconi Offline

Registered: 07/10/13
Posts: 4
Hi, I'm writing to ask for some advice
Having been diagnosed in 2004, my AS has only recently started to become a painful problem which appears to be slowly spreading.
My rheumatologist has suggested I move from Naproxen onto Cosentyx, but having read about the different side effects people are suffering from - and they seem to be plenty - I'm not so sure.
What do other people take and what are the pros and cons you've faced.

Many thanks

#518221 - 02/09/18 07:13 AM Re: Confused - which drug to take [Re: PFMarconi]
Frederick Offline

Registered: 03/28/06
Posts: 254
Naproxen and Cosentyx are a couple of drugs I haven't been on so perhaps I am not the one to answer this.
However I have always taken the attitude that as long as my rheumatologist is happy for me to try some new
drug or other then I will give it a go. If you are on medication for A.S. long term the chances are that sooner
or latter you will get side affects from your medication. You then decide what is the worst is it the side effects
of the new drug or the pain of the A.S. assuming that is that the new drug is of at least some benefit to you. Phone your rheumatology helpline if you have such problems and they are sure to put you right on such things.

Over the years I have on the whole been rather lucky as I have had very few side effects from whatever medication
I have been on. It takes a while for most drugs to take affect be that good or bad. So if possible try and put up with
any side effects at least till you have spoken to your clinic or G.P. Read the literature that comes with the medication
and obviously stop immediately if you read of any possible dangerous side effects that you start to suffer from.
As a matter of interest what country are you posting from?

#518229 - 02/10/18 06:13 AM Re: Confused - which drug to take [Re: Frederick]
PFMarconi Offline

Registered: 07/10/13
Posts: 4
Thanks for your comments Frederick.
I live in the UK.

#518233 - 02/10/18 04:28 PM Re: Confused - which drug to take [Re: PFMarconi]
Winter Offline

Registered: 12/01/10
Posts: 448
Hi Paul - I have been on Cosentyx for three months and it is helping my AS. It took over two months to really kick in. I went through four TNF biologics prior to Cosentyx. Prior to Cosentyx, my body was a mess. I was requiring high dose steroids and cortisone shots for flare ups, couldn’t sleep and was having difficulty walking, doing basic chores at home, etc.. I was giving up the fight. I am back to doing things I enjoy again, can sleep at night, walk for exercise and I can do housework again. When I over do, my body is recovering with sleep now. I wish I would have had Cosentyx 15 years ago but glad I have it now. My only complaint is that it has caused constipation because I have irritable bowel syndrome but doc put me on Linzess and no more constipation. I would recommend giving it a try. Keep us posted.
Meds -Prednisone 2 mg , Cosentyx and topical NSAID

#518241 - 02/12/18 04:34 AM Re: Confused - which drug to take [Re: Winter]
PFMarconi Offline

Registered: 07/10/13
Posts: 4
Thanks very much for your comments Winter. Very reassuring to read such positive stuff. I think this will be the drug I'll opt for so no doubt I'll send a future post.

#518250 - 02/13/18 02:11 PM Re: Confused - which drug to take [Re: PFMarconi]
Winter Offline

Registered: 12/01/10
Posts: 448
Paul - Hope you get to feeling better soon. .

Meds -Prednisone 2 mg , Cosentyx and topical NSAID

#518254 - 02/14/18 04:55 AM Re: Confused - which drug to take [Re: PFMarconi]
PFMarconi Offline

Registered: 07/10/13
Posts: 4
Many thanks to everyone for your comments.
After a lot of thought - coupled with a rough few days and the belief that the condition is worsening - I'm meeting my Rheum. next week as a first step to taking Cosentyx. 
Overall I feel positive about things and look forward to my beloved AS being held in check.
Thanks once more.

#518260 - 02/16/18 06:58 AM Re: Confused - which drug to take [Re: PFMarconi]
Sue22 Offline

Registered: 01/13/08
Posts: 21326
Loc: Upstate NY
I've been on Humira for my spondy since june 2013 and have only had good results. The shot hurts, but that's it.

It isn't perfect, sometimes my flares are stronger than the Humira, and then I take some Aleve (but that quickly causes gastritis and edema for me) and once or twice a year I seem to need a short course of methylpred.

but stating how much it has helped every single symptom would fill up several pages.

i am cautious (maybe too cautious) about taking it if I think I might be getting sick or when taking the methylpred, so maybe that is why I haven't had infection issues. I also take vitamin C (500-1000 mg daily) and LDN (low dose naltrexone), eat a healthy whole foods diet, try to get enough sleep, try to walk most days and stay as active as I can, all things to keep my immune system healthy so that the Humira won't depress it too much.

So, really, I only have good things to say about it; Humira gave me my life back.


Spondyloarthropathy, HLAB27 negative
Humira (still methylprednisone for flares, just not as often. Aleve if needed, rarely.)
LDN/zanaflex/flector patches over SI/ice
vits C, D. probiotics. hyaluronic acid. CoQ, Mg, Ca, K.
walk, bike
no dairy (casein sensitivity), limited eggs, limited yeast (bread)


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