998 reports of this reaction
3.3% of all AZACITIDINE FOR reports
#7 most reported adverse reaction
PNEUMONIA is the #7 most commonly reported adverse reaction for AZACITIDINE FOR, manufactured by Accord Healthcare Inc.. There are 998 FDA adverse event reports linking AZACITIDINE FOR to PNEUMONIA. This represents approximately 3.3% of all 29,877 adverse event reports for this drug.
Patients taking AZACITIDINE FOR 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 moderately reported among AZACITIDINE FOR users, representing a notable but not dominant share of adverse events.
In addition to pneumonia, the following adverse reactions have been reported for AZACITIDINE FOR:
The following drugs have also been linked to pneumonia in FDA adverse event reports:
PNEUMONIA has been reported as an adverse event in 998 FDA reports for AZACITIDINE FOR. This does not prove causation, but indicates an association observed in post-market surveillance data.
PNEUMONIA accounts for approximately 3.3% of all adverse event reports for AZACITIDINE FOR, making it a notable side effect.
If you experience pneumonia while taking AZACITIDINE FOR, 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.