Methatrexate?: Is this drug prescribed for lupus in... - LUPUS UK

LUPUS UK

32,241 members28,596 posts

Methatrexate?

roobarb profile image
14 Replies

Is this drug prescribed for lupus in general, or for those people with both lupus & RA?

Written by
roobarb profile image
roobarb
To view profiles and participate in discussions please or .
Read more about...
14 Replies

It is prescribed for lupus. And it is prescribed for RA. I expect if you have both conditions, it may be prescribed because the root cause of both diseases is a malfunctioning immune system, and MTX works, like other lupus and RA drugs, by damping down the immune system.

roobarb profile image
roobarb in reply to

Thanks Maggie, I have SLE, but not RA. I cannot tolerate oral meds, so I am trying to find an injectable alternative to suggest to my rheumy. I had good results with oral azathioprine initially, but this is very expensive as IM injection. I will obviously discuss it with rheumy & see what she says, but wanted to get other lupies feed back first. X

mstr profile image
mstr

Hi Roobarb, I have just been prescribed this for lupus and polymyositis, I'm guessing it for the reason Maggie said to dampen down the immune system.

roobarb profile image
roobarb in reply tomstr

Really hope it works for you mstr. Will you let me know how you get on?

mstr profile image
mstr in reply toroobarb

Hi Roobarb, So far after my first dose I seem to be fine, bit nauseous on day after taking it but nothing unbearable and headachy a bit. I read to drink lots of water to flush the toxins out and don't know if this is true but it did seem to help the head. I can honestly say it's the first time for 6 months that I feel normal. The pains under my ribs/stomach area are gone and my head feels clear. I thin

mstr profile image
mstr in reply tomstr

sorry I pressed enter too early. I know it is early days and I have to increase my dosage fortnightly so there may be some dodgy days ahead whilst I try to adjust. I also know it's about lifestyle changes too so am eating healthy, back to etc. So far so good but I am fearful to say that just in case and I'm aware the flare ups/symptoms can return. No doubt whatsoever I needed something stronger though and I guess all I can suggest is anything your consultant recommends to try. I was nervous completely and expected to be up half the night vomitting (and that may happen so I'm still prepared). For the first time in months I feel like me. Hope you are ok too xxx

roobarb profile image
roobarb in reply tomstr

It must be nice to feel almost normal again! I met a guy who had been on long term metha last week who had some tips to deal with the sickness, if it does became bothersome for you. He said folic acid did the trick for him. Were you prescribed an ant acid with it also? I think that's standard practice with this drug.

mstr profile image
mstr in reply toroobarb

Hi there, yes I was and was told to take it 3 days after to prevent side effects. If I have any bother I have to ring the rheumy nurse who will recommend more folic acid to take. I still feel it's all a bit of a learning curve and I really must find out whether I will be on this long term. It seems this illness brings new questions each time.

roobarb profile image
roobarb in reply tomstr

It sounds like you have a good team looking after you. Take care & I hope you continue to make good progress. X

mstr profile image
mstr in reply toroobarb

Thanks and to you too x

Purpletop profile image
Purpletop

Both. Lupus medication is mainly 'borrowed' from treatments for other illnesses. MTX was originally used for RA, immunosuppressants were initially used for transplants, antimalarials were used as their name suggests, even now the research is applied to existing drugs, as bringing a new drug on the market is a very expensive and long process.

roobarb profile image
roobarb in reply toPurpletop

Thanks purple top, sounds like it might a possible alternative for me. I'm getting a bit desperate!

Purpletop profile image
Purpletop in reply toroobarb

It isn't that effective for organ involvement, mainly used for joint/connective tissue pain and vasculitis. Do you have any organ involvement?

roobarb profile image
roobarb in reply toPurpletop

No organ involvement, thanks goodness. But possible peripheral vasculitis, awaiting test results. The problem is, I can't tolerate oral meds, so need an alternative & metha is commonly given as IM injection.

I feel like I'm going in circles with local rheumies, but have been told about a good lupus specialist. So I think that's my next step, as they will have more experience, & hopefully other ideas of what might be suitable for me. Thanks for your valuable input. X

Not what you're looking for?

You may also like...

hydroxychloroquine/ Methatrexate

Hi looking for advice please.Two weeks ago I was put on 20mg Methatrexate for Sjorgens syndrome...
Den73 profile image

Methatrexate hangover

Hi not posted for a bit but just wanted to know if when you take methatrexate (injections) are you...

Methatrexate and sickness

Hi I’ve not posted for a long time I’ve had a very good run the Meds seem to be working very well...
Ianrussell69 profile image

Blood test for query lupus. Road to diagnosis

I have family history of lupus and I have been experiencing lupus symptoms and it was made worse...
Cutiecutie profile image

Addenbrooke’s Hospital awarded LUPUS UK Centre of Excellence

LUPUS UK has named Addenbrooke’s Hospital as a LUPUS UK Centre of Excellence in recognition of...
Paul_Howard profile image
Partner

Moderation team

See all
Debbie_kinsey profile image
Debbie_kinseyAdministrator
chelseawong profile image
chelseawongAdministrator
michaellasmith profile image
michaellasmithAdministrator

Top community tags

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.