> Hello, I have Lupus and was perscribed Trexall which is the same as
> Methotrexate. At the time my Platlets would drop for unknow reasons
[quoted text clipped - 6 lines]
> Be well
> shortie
Hello and welcome,
Someone else here (who has not been posting lately and was not on MTX)
Lupus affects her blood, so her blood counts go low.
On the other hand, some here on MTX mention that the first 24 hours is the
worst (after the injection), so maybe that's when their blood counts go
low, so thanks for the heads up.
It does say leukopenia here (whiich I think means low blood counts)
http://www.rxlist.com/cgi/generic/mtx_ad.htm
In general,the incidence and severiity of acute side effects are related
to dose and frequency of administration.
Side Effects with methotrexate
The most frequently reported adverse reactions include ulcerative
stomatitis, leukopenia, nausea, and abdominal distress. Other frequently
reported adverse effects are malaise, undue fatigue, chills and fever,
dizziness and decreased resistance to infection.
Other adverse reactions that have been reported with methotrexate are
listed below by organ system. In the oncology setting, concomitant
treatment and the underlying disease make specific attribution of a
reaction to methotrexate difficult.
> Hello, I have Lupus
Hello.
I see you also have scleroderma and Pulmonary Hypertension and Raynaud's
and Dermatomyositis.
On oxygen all the time eh?
My lung function is not good and my fingers go blue a lot these days.
I've had Raynaud's since childhood (secondary I think) due to frostbite.
Keep in touch and let us know how youre doing, ok?
Hugs
J
shortie - 10 Feb 2006 02:36 GMT
Hello J, I don't have low platlets anymore my doctor infused me with 4
doses of Rituxan and put my platlets in remission for over a yr now.
Which is great, and I hope anybody reading this or knowing anyone this
information will help them. I have (MCTD) secondary pulmomary
hypertension 4-5 L all the time when doing any thing that is exerting,
if I am sitting and reading or watching tv I don't need it. I take a
medicine called tracleer which helps alot and soon hope to start a new
drug its called Revatio it is a drug that is in Viagra.That is the drug
that has been approved for pulmonary hypertension. Are you on any drugs
for your bad lung function?So is your Raynauds really bad in the winter
and no effect in the summer? How do you keep your hands warm?What kind
of Lupus do you have?
Be well all
shortie
J - 15 Feb 2006 08:57 GMT
> Hello J, I don't have low platlets anymore my doctor infused me with 4
> doses of Rituxan and put my platlets in remission for over a yr now.
[quoted text clipped - 10 lines]
> Be well all
> shortie
No drugs for lung function. I don't have family doctor and walkin clinic
doctor has no time to discuss things; only have brief encounters with him.
Good luck with new meds.
Raynaud's is worse in winter. I wear several layers of mitts, so if fingers
get cold i can bend fingers to warm in palm of my hand; sometimes wear
gloves in house as well. Put hands between legs to warm hands and thick
loose socks to keep feet warm
i don't have Lupus. My uncle did. A work collegue did. My brother might.
Met a lady on fibro newsgoup, she has Lupus; and we were both posting here.
She doesn't post anymore,but I stayed because I like the newsgroup (people,
topics, friendly) and made other friends here. :)
Keep in touch and let us know how you're doing, ok?
J