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Discard solution if particulate matter or discoloration is observed. As an alternative to the oral formulation, intravenous mycophenolate mofetil hydrochloride is recommended in patients who are unable to tolerate oral medications. The intravenous mycophenolate mofetil may be administered for up to 14 days.

Patients should be switched to the oral formulation as soon as possible. Avoid direct contact with the prepared solution.

Also, the product is vacuum-sealed and should retain a vacuum throughout its shelf life. During Y-site administration, mycophenolate is physically compatible and chemically stable with 0. Mycophenolate should be used cautiously in patients with active gastrointestinal disease.

Patients with active peptic ulcer disease were excluded from trials with mycophenolate. Serious GI adverse effects associated with oral mycophenolate administration may aggravate or complicate GI disease see Adverse Reactions.

These patients experience higher plasma concentrations and systemic exposure of mycophenolic acid and mycophenolic acid glucuronide MPAG as compared with patients that have normal renal function.

The safety of long-term exposure to increased MPAG concentrations is unknown. Patients with uremia can be expected to have an increased free MPA concentration due to drug displacement.

No data are available for cardiac or hepatic transplant patients with severe renal impairment or failure.

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Breast-feeding Mycophenolate mofetil has been shown to be excreted in the milk of lactating rats. No studies on the effects on the ability to drive and use machines have been performed. The following undesirable effects cover adverse reactions from clinical trials The principal adverse reactions associated with the administration of CellCept in combination with ciclosporin and corticosteroids include diarrhoea, leucopenia, sepsis and vomiting, and there is evidence of a higher frequency of certain types of infections see section 4.

The following undesirable effects cover adverse reactions from post-marketing experience The types of adverse reactions reported during post-marketing with CellCept are similar to those seen in the controlled renal, cardiac and hepatic transplant studies. Infections Serious life-threatening infections including meningitis, endocarditis, tuberculosis and atypical mycobacterial infection.

Pregnancy, puerperium and perinatal conditions Cases of spontaneous abortions have been reported in patients exposed to mycophenolate mofetil, mainly in the first trimester, see section 4.

Congenital disorders Congenital malformations have been observed post-marketing in children of patients exposed to CellCept in combination with other immunosuppressants, see section 4. Respiratory, thoracic and mediastinal disorders There have been isolated reports of interstitial lung disease and pulmonary fibrosis in patients treated with CellCept in combination with other immunosuppressants, some of which have been fatal.

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Don't know if it was the medication or the disease. Share your thoughts with the world Cecilia United States 1 Mar 26, 2006 I have a questin for you i just stared to take cellcept what are the side affects i am warry that im going to Again wait again i lost 100pound and with lupus is very hard to loose it whould i again wait thank you for your time.

Martha Priest River, ID 2 Jul 6, 2006 I have MS and taking Copaxone. Amber Troy, MI 3 Sep 10, 2006 Cecilia wrote: I have a questin for you i just stared to take cellcept what are the side affects i am warry that im going to Again wait again i lost 100pound and with lupus is very hard to loose it whould i again wait thank you for your time.

I have been taking cell cept for over a year now. At first i had a real hard time taking it and used to get nausea and have diahrea.

Now I am so use to it that I do not have any side effects.

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The measured value for renal clearance of MPAG indicates removal occurs by renal tubular secretion as well as glomerular filtration. Consistent with this, coadministration of probenecid, a known inhibitor of tubular secretion, with mycophenolate mofetil in monkeys results in a 3-fold increase in plasma MPAG AUC and a 2-fold increase in plasma MPA AUC.

Thus, other drugs known to undergo renal tubular secretion may compete with MPAG and thereby raise plasma concentrations of MPAG or the other drug undergoing tubular secretion. Drugs that alter the gastrointestinal flora may interact with mycophenolate mofetil by disrupting enterohepatic recirculation.

You are encouraged to report negative side effects of prescription drugs to the FDA.

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  • In addition, women can stop having periods when on Cytoxan.

  • This medicine is prescribed if there are too many relapses of Nephrotic Syndrome.

  • The Cellcept Mofetil that I take is only 500 MG and it does the trick.

  • Sexually active men are recommended to use condoms during treatment and for at least 90 days after cessation of treatment.

Which is why I've been on prednisone 3 times and cellcept 2 years, and placquenil 1 year, and numerous other drugs. And it has, thank you God, cleared up with the nutrition plan.

I just got back on cellcept after about a year,switched to cytoxin last October. I took cellcept for quite a while before they decided to try benlysta, and I never experienced back pain as a result of the cellcept.

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  • Because of this risk to your liver, you should not drink alcohol while taking leflunomide, and you should tell your doctor if you have had liver problems in the past.

  • Concomitant Medications It is recommended that CellCept not be administered concomitantly with azathioprine because both have the potential to cause bone marrow suppression and such concomitant administration has not been studied clinically.