5,027 reports of this reaction
2.0% of all MYCOPHENOLATE MOFETIL reports
#6 most reported adverse reaction
PNEUMONIA is the #6 most commonly reported adverse reaction for MYCOPHENOLATE MOFETIL, manufactured by Genentech, Inc.. There are 5,027 FDA adverse event reports linking MYCOPHENOLATE MOFETIL to PNEUMONIA. This represents approximately 2.0% of all 256,184 adverse event reports for this drug.
MYCOPHENOLATE MOFETIL has an overall safety score of 85 out of 100. Patients taking MYCOPHENOLATE MOFETIL who experience pneumonia should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
PNEUMONIA is a less commonly reported adverse event for MYCOPHENOLATE MOFETIL, but still significant enough to appear in the safety profile.
In addition to pneumonia, the following adverse reactions have been reported for MYCOPHENOLATE MOFETIL:
The following drugs have also been linked to pneumonia in FDA adverse event reports:
PNEUMONIA has been reported as an adverse event in 5,027 FDA reports for MYCOPHENOLATE MOFETIL. This does not prove causation, but indicates an association observed in post-market surveillance data.
PNEUMONIA accounts for approximately 2.0% of all adverse event reports for MYCOPHENOLATE MOFETIL, making it a notable side effect.
If you experience pneumonia while taking MYCOPHENOLATE MOFETIL, contact your healthcare provider. They can evaluate whether the symptom is related to your medication and discuss potential adjustments to your treatment plan. Do not stop taking prescribed medication without consulting your doctor.