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Re: sulfasalazine??

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Carol,

I've been on Azulfadine with Remicade, Enbrel and Humira. Currently on 500

mg/3x a day with 50 mg Enbrel 2x a week. Seems to be doing the trick. But as

with all the biologicals, my experience is that a run of 1-2 years is about all

you can hope for before having to change biologicals, and upping the dosages.

-L

Carol <carolsmisc@...> wrote:

Hello

all I tried a search of this group and did not find to many good things

about this drug, I cant take MTX or imuran, and I take Enbrel, anyone

taking this get good results, or should I not get my hopes up?

Blessings

Carol

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Hi Carol,

I'm , age 32, had PA *even though it was originally diagnosed

as RA* for close to 12 years (will be in June that is). I lurk most of

the time, but your message drew me out of the darkness.

I had great success with Sulfasalazine many years ago. In fact, it put

me into a remission that lasted for quite a while and life was semi-

normal.

But it also seems I usually have a high-tolerance for these drugs. I

don't know why. Guess I'm just lucky in that respect.

For information purposes, the other drugs I have been on (from the

beginning to now) include: Indomethacin (? had bad headaches wasn't on

it long), Plaquenil (hydroxycloroquine), the usual Naproxen,

Sulfasalazine, Celebrex, Bextra (briefly), Methotrexate and Arava.

Now I'm on Enbrel and Methotrexate. The rheumy is slowly but surely

weening me off the Methotrexate. Here's hoping I can get off it

completely by the end of the year - even though I'm a bit leery of that

since he has said the Enbrel usually works best in tandem with

something else.

Jenn in Arkansas

>

> Hello

>

> all I tried a search of this group and did not find to many good

things

> about this drug, I cant take MTX or imuran, and I take Enbrel, anyone

> taking this get good results, or should I not get my hopes up?

>

> Blessings

> Carol

>

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I take enbrel 50 mg twice a week and have been persribed 500 mg

sulfasalazine 2 twice daily, I hope this works for me. Have you had

any side effects?

Carol

> Hello

>

> all I tried a search of this group and did not find to many good

things

> about this drug, I cant take MTX or imuran, and I take Enbrel,

anyone

> taking this get good results, or should I not get my hopes up?

>

> Blessings

> Carol

>

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Guest guest

I take enbrel as well but the MTX was toxic to me, my liver lipids

went into the 160's and I was throwing up if I got the least bit

warm, plus I had these knots under my arms that were like boils every

two weeks or so.....maybe this will work for me, I was just scared

cause all I read sounded worse than what I had....thanks for your

words....carol

>

> Hi Carol,

>

> I'm , age 32, had PA *even though it was originally

diagnosed

> as RA* for close to 12 years (will be in June that is). I lurk most

of

> the time, but your message drew me out of the darkness.

>

> I had great success with Sulfasalazine many years ago. In fact, it

put

> me into a remission that lasted for quite a while and life was semi-

> normal.

>

> But it also seems I usually have a high-tolerance for these drugs.

I

> don't know why. Guess I'm just lucky in that respect.

>

> For information purposes, the other drugs I have been on (from the

> beginning to now) include: Indomethacin (? had bad headaches wasn't

on

> it long), Plaquenil (hydroxycloroquine), the usual Naproxen,

> Sulfasalazine, Celebrex, Bextra (briefly), Methotrexate and Arava.

>

> Now I'm on Enbrel and Methotrexate. The rheumy is slowly but surely

> weening me off the Methotrexate. Here's hoping I can get off it

> completely by the end of the year - even though I'm a bit leery of

that

> since he has said the Enbrel usually works best in tandem with

> something else.

>

> Jenn in Arkansas

>

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No side effects that I've noticed.

-L

BlueWindWoman <carolsbluewind@...> wrote:

I take enbrel 50 mg twice a week and have been persribed 500 mg

sulfasalazine 2 twice daily, I hope this works for me. Have you had

any side effects?

Carol

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Hi Carol,

I am on Sulfasalizine (3 pills 2/day) and I haven't really noticed any side

effects except maybe a little constipation, but I'm not sure if that is the case

or not... Anyway, they took me off of MTX and Remicade in mid February and just

last Wednesday I started to flare in my right foot (3 months after my last

Remicade treatment)... Friday I left for Halifax Canada and ended up having to

have a treatment there Sunday morning before flying to Paris as there was no way

I would have been able to continue on our vacation. Within even a few hours the

pain began to lesson and by yesterday, the pain was gone along with most of the

swelling. I went from barely able to walk (with crutches) to walking all over

Paris!!

Anyway, not sure if the Sulfasalazine is having an effect and by now it should

be. Thinking of stopping it!!

Best of Luck,

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