1,142 reports of this reaction
2.8% of all MOXIFLOXACIN reports
#4 most reported adverse reaction
PNEUMONIA is the #4 most commonly reported adverse reaction for MOXIFLOXACIN, manufactured by Lifestar Pharma LLC. There are 1,142 FDA adverse event reports linking MOXIFLOXACIN to PNEUMONIA. This represents approximately 2.8% of all 40,887 adverse event reports for this drug.
Patients taking MOXIFLOXACIN 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 MOXIFLOXACIN, but still significant enough to appear in the safety profile.
In addition to pneumonia, the following adverse reactions have been reported for MOXIFLOXACIN:
The following drugs have also been linked to pneumonia in FDA adverse event reports:
PNEUMONIA has been reported as an adverse event in 1,142 FDA reports for MOXIFLOXACIN. This does not prove causation, but indicates an association observed in post-market surveillance data.
PNEUMONIA accounts for approximately 2.8% of all adverse event reports for MOXIFLOXACIN, making it a notable side effect.
If you experience pneumonia while taking MOXIFLOXACIN, 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.