301 reports of this reaction
1.9% of all BLEOMYCIN SULFATE reports
#12 most reported adverse reaction
RESPIRATORY FAILURE is the #12 most commonly reported adverse reaction for BLEOMYCIN SULFATE, manufactured by Fresenius Kabi USA, LLC. There are 301 FDA adverse event reports linking BLEOMYCIN SULFATE to RESPIRATORY FAILURE. This represents approximately 1.9% of all 16,267 adverse event reports for this drug.
Patients taking BLEOMYCIN SULFATE who experience respiratory failure should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
RESPIRATORY FAILURE is a less commonly reported adverse event for BLEOMYCIN SULFATE, but still significant enough to appear in the safety profile.
In addition to respiratory failure, the following adverse reactions have been reported for BLEOMYCIN SULFATE:
The following drugs have also been linked to respiratory failure in FDA adverse event reports:
RESPIRATORY FAILURE has been reported as an adverse event in 301 FDA reports for BLEOMYCIN SULFATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
RESPIRATORY FAILURE accounts for approximately 1.9% of all adverse event reports for BLEOMYCIN SULFATE, making it a notable side effect.
If you experience respiratory failure while taking BLEOMYCIN SULFATE, 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.