1,933 reports of this reaction
3.5% of all IXAZOMIB reports
#5 most reported adverse reaction
PNEUMONIA is the #5 most commonly reported adverse reaction for IXAZOMIB, manufactured by Takeda Pharmaceuticals America, Inc.. There are 1,933 FDA adverse event reports linking IXAZOMIB to PNEUMONIA. This represents approximately 3.5% of all 55,273 adverse event reports for this drug.
Patients taking IXAZOMIB 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 IXAZOMIB users, representing a notable but not dominant share of adverse events.
In addition to pneumonia, the following adverse reactions have been reported for IXAZOMIB:
The following drugs have also been linked to pneumonia in FDA adverse event reports:
PNEUMONIA has been reported as an adverse event in 1,933 FDA reports for IXAZOMIB. This does not prove causation, but indicates an association observed in post-market surveillance data.
PNEUMONIA accounts for approximately 3.5% of all adverse event reports for IXAZOMIB, making it a notable side effect.
If you experience pneumonia while taking IXAZOMIB, 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.