pregnancy (see complete product information). Adverse events
reported in more than 30% of renal, cardiac or liver transplant
patients receiving CellCept (in combination with cyclosporine and
corticosteroids) were pain, fever, headache, asthenia, anemia,
leucopenia (patients should be monitored for neutropenia; dosing
should be interrupted or the dose reduced if neutropenia develops),
thrombocytopenia, leukocytosis, urinary tract infection,
hypertension, hypotension, peripheral edema, hypercholesteremia,
hypokalemia, hyperglycemia, creatinine, BUN and cough increased,
hypomagnesemia, diarrhea, constipation, nausea, vomiting,
respiratory infection, dyspnea, lung disorder, pleural effusion,
tremor and insomnia. Patients receiving immunosuppressant regimens
are at increased risk of developing lymphomas and other
malignancies, particularly of the skin.
Warning: Increased susceptibility to infection and the possible
development of lymphoma may result from immunosuppression. Only
physicians experienced in immunosuppressive therapy and management
of renal, cardiac or hepatic transplant patients should use
CellCept. Patients receiving the drug should be managed in
facilities equipped and staffed with adequate laboratory and
supportive medical resources. The physician responsible for
maintenance therapy should have complete information requisite for
the follow-up of the patient.
About Aspreva Pharmaceuticals
Aspreva is a global pharmaceutical company focused on
identifying, developing, and, upon approval, commercializing
evidence-based medicines for patients living with less common
diseases. Aspreva common stock is traded on the NASDAQ Global
Select Market under the trading symbol "ASPV" and on the Toronto
Stock Exchange under the trading symbol "ASV". Learn more at
http://www.aspreva.com.
About Roche
Headquartered in Basel, Switzerland, Roche is one of the world's
lead
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