Adverese side effects of generic cellcept.? I am a kidney transplant patient. Has any one using cellcept and then going to the generic form had any negative side effects/ FDrom the Generic Equivalent Drug!
kelly d replied: "generic drugs are the same as brand, its exactly the same ingredient that is going to make you feel better"
Cellcept (mycophenolate mofetil) side effect? Hi, I had a liver transplant 12 years ago due to PSC and been on Tacrolimus (prograf) since. no problem with the medication. recently kidneys got really bad and now I am in hospital. dr are planning to change my Tacrolimus to cellcept but I am so upset. 12 years I was with tacrolimus and I trust it so much. how can I change it and feel comfortable. I am worry about all the unknown side effect of it. is it any WEIGHT GAINE associated with it? its only cellcept and NOT combine with steroid. can some one please help me and answer my question?
abijann replied: "I definitely understand how hard it is to change from a drug, like Prograf...that you feel so secure and comfortable with taking ...to another anti rejection drug. It kinds of makes you half scared to death.
People who have had liver transplants are usually placed on all three drugs:
Prograf, Cellcept, and Prednisone and then later the Cellcept is taken away.
Prograf has always been known to develop a problem with the kidneys while taking it. They try to get a patient off of it before it can do more damage.
There are two types of mycophenolate drugs: Cellcept (mofetil) and then a time release type known as Myfortic (mycophenolate sodium).
The main thing with Cellcept is not to try to become pregnant when on this drug.
I would keep a close eye on your White Cell count also...if you see it start to go down alot, you may need to be placed on Prednisone with it.
These two sites will explain more about the side effects of this drugs and any interactions with other drugs that may develop:
--d03839a1.html
They don't usually place someone on a new
anti rejection drug without following them very closely when they do this. For awhile, they may request more blood testing to be sure you are doing well.
However, with Prograf, you have to be tested often to make sure the level in your blood stays in a certain range all the time...with Cellcept, you may be freed up of having so much blood testing done, in the long run.
If you are in the hospital,now, then they may not let you leave until they are sure this change is okay for you.
All drugs have side effects, and it depends alot on your other medical conditions and your past and present medical history...to see how you might do while on this drug and whether these side effects may or may not take place. If it was me, I would ask to speak to your TOP doctor about this and discuss with him your concerns...not the nurses or interns there. I found this out the hard way.
It will take time, if the drug does work for you,
that you will start to feel secure again.
Best wishes to you...wish I could be of
more help."
Liver medication side effects? I've been taking 3 medications for my liver for several years now. Cellcept, Urso and Prednisone. Just curious if anyone (male) taking these had or are having any sexual side effects?
phantomlimb7 replied: "If you are taking cellcept, I am presuming that you've had a liver transplant (since it's an antirejection drug) and ursodiol is to prevent the formation of gallstones. Prednisone is also used to prevent tissue rejection, as it's a steroid.
Prednisone is the most likely culprit to sexual dysfunction in the form of lack of desire, or fluid shifts which can cause circulatory interference. It can also cause diabetes with long term use, and that can also lead to erectile dysfunction and lowered libido. It can also cause depression, which leads to lowered sex drive. I don't know what other factors you may have with your liver disease, but I would suggest that you talk to your primary care physician or your immunologist or transplant doc to address the loss of libido (lack of drive or desire) or loss of erectile function."
Is there anyone taking CellCept? If so, how long did you take it and what symptoms did you have? SERIOUS REPLIES ONLY. THANKS!
Hi, I was diagnosed with lupus almost 2 years ago after over 11 years of dealing with various symptoms and flares and kidney disease. Right now I am only taking 1/2 a 250 mg chloroquine tablet once a day but I still have pain and fatigue and my sed rate is going up slowly, which it does during seasonal changes. My doctor wants me to start chemo or steroids, which scares the crap out of me. I saw online that there is something called CellCept that may work to reduce lupus symptoms that may have more tolerable symptoms than chemo, but I don't want to jump into anything. Can someone who has lupus who has or is using CellCept tell me if it works, how long it works, if you experienced any really bad side effects and if so did you recover? And did the lupus come back? Thank you for your help.
DaBoomvang replied: "Hi
I do not have Lupus, but I do have a similar auto-immune disease. I can imagine we take the same drugs for the same reasons, because our auto-immune systems are out of controll and need to be supressed,
I have been taking methotrexate (aka chemo), and it's been absolutely horrible. The side effects of nausea and vomiting were miserable. Plus, I was sooooo tired. I would sleep for 18 hours, get up, and need a nap within 2 hours.
Just today, I am starting a new medication... Cellcept!
I am hoping for the best. I dont know what to expect. I dont know what side effects to expect either. I can let you know though!
The worst drug I've ever had to take though, was prednisone (steropids). I would recommend you do ANYTHING to avoid taking it! I gained 20 pounds in weeks on it, and it was not because of over eating! The drug makes you gain weight. AND... it redistributes your fat into your belly - so now I have a beer belly. :o( I gained 3 inches in my waistline. Dieting wont help - there is nothing you can do to avoid it.
I wish you the best as you battle your fight! I hope you fight the fight! Good luck,"
mgnysgtcappo replied: "My wife has been taking cellcept for her Lupus for the last two and a half years with little side effects. She was a little sick to her stomach at first but now it really doesn't affect her. It has done wonders for her Lupus flare ups though. She hasn't had kidney involvement since being on the drug and she is only taking 5 mg of prednisone right now. She also has antiocardiolipid syndrome and takes coumadin to thin her blood. If you have any more questions or would like some more detailed info please feel free to email me"
Who do some medications cause rashes or acne? For example a possible side effect of Cellcept is a rash and in some casesn Prednisone causes acne...
Thanks
vim4you2 replied: "http://www.skincarephysicians.com/rosaceanet/whatis.html
...
Or it could be lots of sugar. sugar does it to me, like dough nuts, and too much chocolate at once...
oh and milk, definitely milk, does it to me too.
good luck"
Effects of new Meds? My dr. prescribed "cellcept" and the side effects are pretty bad. I was wondering if anyone else had taken this drug and if they had any side effects.
Its an autoimmune suppressant and its generally used for people who have had organ transplants.
msmaryanne1 replied: "What's it for?"
Am I able to take adipex-p if I am diagnosed with a type of kidney disease? I was diagnosed with lupus nephritis and I am currently prescribed CellCept. What interactions and side effects could occur?
N replied: "You should ask your doctor about this. It doesn't seem to have any obvious interactions with cellcept or with kidney function but you should double check with your doctor."
mgunnycappo replied: "Here's the deal. There isn't necessarily an contraindication with Cellcept. However, adipex-p is known to increase blood pressure and shouldn't be taken by anyone with high blood pressure. Because you have Lupus Nephritis you are prone to high blood pressure due to your renal function. Has a doctor actually prescribed adipex-p to you? I would find it hard to believe that an MD who knows your Lupus Nephritis diagnosis would prescribe this medication for you. How overweight are you? What is your diet like? Do you exercise? These are all better options than taking a 'fat' pill. You need to be careful because taking these kinds of medications put stress on the body and we all know that stress causes Lupus flares. If I were you I would avoid this medication like the plague, but at the very least discuss it with your nephrologist and your rheumatologist prior to taking it."
cellcept for Lupus? Anyone here had a bad reaction from the drug cellcept. Also, anyone taking cellcept and prednisone for their Lupus. Have you experienced any negative side effects with both drugs as well.
Linda R replied: "I took prednisone from February 2003 to April 2006. I was constantly hungry, very irritable, had trouble sleeping and cried easily.
I have been on Cellcept since October 2003 and am now on a low dose (250mg), At first I had increased fatigue when I took the morning dose of 500mg but that subsided. I am happy because it controls my nephropathy and many of the symptoms of lupus."
christibro40 replied: "Hi, I am a lupus Paitent. and owner of a Lupus online support group. I have not been on cell cept YET, but it is being disscused. I have been on prednison, and had horrible side effects I could not tolerate, insulan dependant diabetes, weight gain, mood changes, moon face, I won't take, others do, without the side effects I have. I just got off 6 months of IV cytoxin, which is in the same class of cell cept, but to my inderstanding a bit harsher. I did have side effects, a bit of loss of hair, weakness, fatigue etc. Lupus is difficult, we dont have many options. I go to my dr this week, and cell cept may be part of the disscussion again. From my groups file however I did pull this article regarding cell cept and Lupus. Maybe you can gain some insight into the drug. It is an immunosuppresent, which cytoxin kinda is, it was originally classified a chemotherapy, and used for cancer, but now there are stronger cancer drugs. Cell Cept is one of the great new hopes for those of us with moderate to severe Lupus.
Here is the article
New use for immunosuppressive drug offers hope,
quality of life to
patients.
A promising new treatment for lupus challenges
the way physicians
currently treat patients suffering with lupus
kidney disease,
according to researchers at the State University
of New York (SUNY)
Downstate Medical Center.
A study published in the New England Journal
of Medicine (NEJM) this
week shows promising results of the use of
mycophenolate mofetil
(MMF), an immunosuppressive drug used primarily
to combat organ
rejection in transplant patients, in induction
therapy for patients
suffering from lupus nephritis (lupus kidney disease).
Marketed as CellCept, which is approved by the
U.S. Food and Drug
Administration (FDA) for use in kidney, heart and
liver organ
transplant patients, MMF has been shown to
play a major role in
controlling lupus nephritis. The research published
in NEJM found
that lupus patients using orally administered MMF
demonstrated better
clinical response and did not experience many
of the severe side
effects associated with the current standard-of-care,
intravenous
cyclophosphamide (IVC), a form of chemotherapy,
which has been used
to treat patients with lupus kidney disease
since the 1970s.
For patients and physicians, these landmark
findings offer a
choice. "With no FDA-approved drugs for the
treatment of lupus
nephritis for the past 30 years, we have been
limited in our options
for patients," said Ellen Ginzler, M.D.,
Professor of Medicine and
Chief of Rheumatology, SUNY Downstate, Brooklyn,
NY, and lead
investigator in the study. "For some patients,
the side effects
associated with intravenous cyclophosphamide
treatment have been
worse than the disease itself."
The side effects of IVC therapy include nausea,
vomiting, hair loss
and infertility. Some patients, discouraged
by these side effects,
choose to forego treatment, putting themselves
at risk for kidney
failure and premature death.
Significant findings of the study include:
- - Induction therapy with MMF was superior to
IVC in inducing
complete remission of lupus nephritis
- - MMF appeared to be better tolerated than
IVC, with less severe
side effects
"These findings give us renewed confidence
in treating lupus kidney
disease and helping patients maintain their
quality of life," said
Sandra Raymond, president and CEO of the Lupus
Foundation of America,
the nation's leading non-profit organization
for lupus. "This is
encouraging news for the millions around the
world who are suffering
from the devastating effects of lupus."
Study Design
The NEJM report details the results of a
24-week randomized, open-
label study of 140 patients at 19 study sites
with systemic lupus
erythematosus who had advanced stages of lupus
nephritis.
Investigators compared the effectiveness of an
oral dose of MMF as
induction therapy to that of the IVC treatment.
At the start of the
study, 71 patients received MMF and 69 patients
received IVC;
patients failing to improve in at least one key
area after 12 weeks
were converted to the other regimen. A total of
24 patients were
withdrawn from the study; nine in the MMF group
and 15 in the IVC
group. There were 16 complete remissions; that
is, the disease became
inactive, on MMF and four complete remissions
on IVC; 21 partial
remissions, or improvement in the still active
disease, were recorded
in patients on MMF and 17 in patients on IVC.
Adverse Events
There were two deaths in the IVC group during
treatment; a third
patient declined IVC therapy and died from pulmonary
hemorrhage and
renal failure. There were no deaths in the MMF
group. Infection and
gastrointestinal side effects accounted for most
of the adverse
events in both patient groups. Severe infections
(e.g., pneumonia and
lung abscess, necrotizing fasciitis, gram-negative
sepsis) occurred
only in the IVC group. Pyogenic, or pus-producing,
infections were
significantly less frequent among patients
receiving MMF.
Hospitalizations for vomiting and dehydration
occurred in five
patients receiving IVC. Diarrhea occurred more
frequently among
patients in the MMF group.
About Lupus and Lupus Nephritis
According to the Lupus Foundation of America,
it is estimated that as
many as 1.5 million Americans suffer from lupus,
a chronic autoimmune
disease that causes inflammation and tissue damage
to virtually any
organ system in the body, especially the kidneys.
Although lupus can
strike in men and women of all ages, lupus occurs
10 to 15 times more
frequently in women. Symptoms vary and the cause
of lupus is not well
understood, though researchers cite a combination
of genetics and
environment as possible factors. Lupus nephritis
is a medical term
for lupus that affects the kidneys. It is the most
common severe
complication of lupus and affects approximately
one third of lupus
patients.
For more information about lupus, please
contact the Lupus Foundation
of America at 202-349-1155 or visit the
organization's website:.
About SUNY Downstate Medical Center
SUNY Downstate Medical Center is the only academic medical center in
Brooklyn, Queens, or Staten Island, comprising a College of Medicine,
a College of Nursing, a College of Health Related Professions, a
School of Graduate Studies, and University Hospital of Brooklyn.
About the Lupus Foundation of America
The Lupus Foundation of America is the nation's leading nonprofit
voluntary health organization dedicated to lupus. The LFA has a
nationwide network of nearly 300 chapters, branches and support
groups located throughout the United States. The National Office is
located in Washington, D.C.
Jen Acer
Ketchum
ketchumcomms.co.uk
MIND YOU, CELL CEPT IS NOT ONLY USED IN LUPUS PAITENTS WITH KIDNEY INVOLVMENT. AND I KNOW OF NO ONE WHO HAS DIED WHILE ON IT.
Good Luck
If you need support come check us out the link for where the article came from in our files and our group is below.
Chris"
sistermegan replied: "I have not taken CellCept, but I have taken Prednisone, Methotrexate, Imuran and Cytoxan. I understand that CellCept is similar to Methotrexate, Imuran and Cytoxan since they are all Immunosuppressives.
Methotrexate is the least problematic of the three Immunosuppressives (to me). I still had fatigue, nausea, low blood counts and some other problems...
Prednisone made me hungry all the time (which was nice to me because usually I am nauseated and don't feel hungry at all) and it also made me feel "puffy". I was also really cranky and tired all of the time. Prednisone did make me feel better over the long run, but over the short term it was kinda a pain.
The thing is that you need to talk to your doctor about your treatment options... and don't be afraid to try out new medicines if your doctor recommends them... talk with him or her about your concerns, what side effects you don't mind and which ones you can't tolerate, and keep communication open during your entire treatment plan.
Don't be surprised if you begin taking a med and find out that you need to adjust the dose several times before you get to a good place. (You might even have to switch out meds.)
Good luck and I hope your treatment brings you health!"
Anyone can advise is there a problem if I stop taking cellcept? I had my kidney transplant 1 1/2yrs ago.? Recently I am taking cellcept 1000mg per day. Doctor advised me to stop taking cellcept because he said that it will bring side effect to my liver. I am a hepatitis B carrier. I am so reluctant to stop the cellcept because the doctor said if I stop cellcept, my kidney may reject or not. Honestly, I rather to sacrified my liver than my liver even though both organ is important but I have no choice. I hope anyone out there can guide me on this.
DrB replied: "Get a second opinion from a physician specializing in this area.."
Ashley T replied: "Gosh that would be a hard decision. I also take cellcept every day. However if you do stop taking the cellcept and they find that you are rejecting your kidney they can always give you prednisone to stop the rejection and up your other anti-rejection medicines. Point blank, all rejection medicines have a side effect. I haven't found one yet that doesn't have a bad side effect to it. But I would talk with your txp team about your concerns. But I would do what your doctor advises. They know what is best for you. Good luck!"
Rapamune (sirolimus) side effect? Hi, I had a liver transplant 12 years ago due to PSC and been on Tacrolimus (prograf) since. no problem with the medication. recently kidneys got really bad and now I am in hospital. dr are planning to change my Tacrolimus to sirolimus but I am so upset. 12 years I was with tacrolimus and I trust it so much. how can I change it and feel comfortable. I am worry about all the unknown side effect of it. is it any WEIGHT GAINE associated with it? its only sirolimus and NOT combine with steroid. can some one please help me and answer my question?
Last minute today they change their mind again (initial plan was cellcept). anyway, no difference as I am so scared no matter what?
I read abour odema (thats not nice to have especially this is a life time drug) does that mean I will Have peripheral odema for rest of my life?? :-(
abijann replied: "When a drug company develops these drugs,
they are then tested for a long periods of time
before they are made available through the
Federal Drug Administration to be used in
humans. They then are considered safe once
they are approved, even though some drugs
are taken off the market afterwards.
These drug companies have to list every possible side effects from their extensive
testing on these drugs. That doesn't mean
that everything that may be listed is what the
person will have. It just means that there is
a possibility that it will occur. All drugs have
sheets of side effects...you just don't see
them. The pharmacist gets these inserts on
the medication, but the patient doesn't...they
get a simple print out on what to watch for.
The Rapamune does list as being a possible
side effect of weight gain and swelling.
Here is a link to read on this medication:
--d04453a1.html#d04453a1-sideeffects
If you type Rapamune or sirolimus in your
search engine...you will find lots of places
with more information and also the drug
companies site for this drug.
The doctors will watch you closely during
this time. You can also get a copy of your
blood work results and see how it might change
while you are on this drug. It is your right
to have a copy of this.
If you are in the hospital and you cannot talk
to the doctor about this...ask the nurse more
about it. She deals with patients all the time
on this drug and maybe able to answer your
questions about this. If you are at home,
don't be afraid to call and ,if you cannot speak
to the doctor, ask to speak to his nurse there.
I hope you do well. It upset me, too, when
this had happened."
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