WeHaveLupus.com Forum Index WeHaveLupus.com
Lupus Erythematosus Support Forum
 

 FAQFAQ SearchSearch Free GamesMake a Donation  UsergroupsUsergroups Free GamesForum Rules ProfileContact RegisterRegister 
ProfileWebsite News Log inSubmit Articles  ProfileProfile Log in to check your private messagesLog in to check your private messages Log inLog in 

Plaquenil did not work starting chemotherapy



 
Post new topic   Reply to topic    WeHaveLupus.com Forum Index -> Lauri's Lounge
Author Message
TMWeaver
Sea Monkey
Sea Monkey



Joined: 30 May 2003
Posts: 11


PostPosted: Tue Oct 28, 2003 7:51 pm    Post subject: Plaquenil did not work starting chemotherapy Reply with quote

My doctor advised me today that I have not responded to the plaquenil so my next step is chemo. I am not looking forward to the side affects. Has anyone been on Methotrexate? Does it work?

Crying or Very sad
Back to top
View user's profile Send private message
muriate
Little Guppy
Little Guppy



Joined: 09 Feb 2003
Posts: 35


PostPosted: Tue Oct 28, 2003 8:06 pm    Post subject: Reply with quote

Hello,
I am on plaquenil. But a friend of mine has been on methotrexate for years. It has worked for her. She has had little of side effects. Here is some info I found on it.

The most common side effect of methotrexate is nausea. The nausea from methotrexate use often disappears on its own though and may be controlled by lowering the dose or spreading the dose out.

The drug can cause hidden problems too and tests are done to monitor whether or not these problems are occurring. Complete blood counts are done since methotrexate can suppress the production of new blood cells and lead to severe forms of anemia. Liver-chemistry profiles are done to watch for possible effects on the liver. Liver damage is among the worst potential problems since once the damage is done it is irreversible. Since most serious damage to the liver is not revealed in a blood test, a liver biopsy may be recommended periodically.

Another potential threat from methotrexate use is lung disease. Dry cough accompanied by fever and shortness of breath could indicate such a problem. Some people who use methotrexate develop sores on their skin and inside their mouths. These are signs of a toxic reaction to the drug and its use may need to be discontinued.

Wish you the best,
Write if you need anything
Muriate
Back to top
View user's profile Send private message Send e-mail
JenHa55
Little Hamster
Little Hamster



Joined: 30 Aug 2003
Posts: 75

Location: British Columbia, Canada

PostPosted: Fri Dec 26, 2003 9:45 pm    Post subject: Reply with quote

After my most recent hospital visit, they have decided to put me on chemo as well (aka methotrexate). I'm pretty new at this one drug as well. Let me know how it goes and I will do the same. Some people I know have side effects from it but better then Prednisone is what I hear. We'll see...

Best of luck to you. Sending you good thoughts.
Back to top
View user's profile Send private message MSN Messenger
tinajee
Tadpole
Tadpole



Joined: 23 Dec 2003
Posts: 21

Location: Cleveland, Mississippi

PostPosted: Fri Dec 26, 2003 10:13 pm    Post subject: Reply with quote

Hi I am on Methatrexate now and the nausea was bad at first but after being on it for a while your body kinda gets use to it and it's not so bad. But with me the medicine has still not put me in remission. I have been on both Plaquenil and Methatrexate for about a year now and no remission yet. So I pray you have better luck than me. Good news the factor of losing hair on it is not that bad either. And always remember it will grow back. Good luck!!!!!!!
Back to top
View user's profile Send private message Send e-mail
annette
Sea Monkey
Sea Monkey



Joined: 14 Feb 2004
Posts: 12


PostPosted: Sat Mar 06, 2004 10:18 am    Post subject: Cellcept for the Treatment of S.L.E. Reply with quote

Hey guys,has anyone been on cellcept? My docter wants me to go on this new drug.I have had Lupus (Diffuse Proliferative Glumorulinephritis) for 16years.And have been on prednisone and plaquneil for 16years as well.But my Nephrologist say i need for drugs to keep my lupus in remission. Thanks

Love,
Annette
Back to top
View user's profile Send private message
Display posts from previous:   
Post new topic   Reply to topic    WeHaveLupus.com Forum Index -> Lauri's Lounge All times are GMT - 8 Hours
Page 1 of 1

 

© 2001-2007