174 reports of this reaction
1.5% of all BARICITINIB reports
#17 most reported adverse reaction
URINARY TRACT INFECTION is the #17 most commonly reported adverse reaction for BARICITINIB, manufactured by Eli Lilly and Company. There are 174 FDA adverse event reports linking BARICITINIB to URINARY TRACT INFECTION. This represents approximately 1.5% of all 11,538 adverse event reports for this drug.
Patients taking BARICITINIB who experience urinary tract infection should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
URINARY TRACT INFECTION is a less commonly reported adverse event for BARICITINIB, but still significant enough to appear in the safety profile.
In addition to urinary tract infection, the following adverse reactions have been reported for BARICITINIB:
The following drugs have also been linked to urinary tract infection in FDA adverse event reports:
URINARY TRACT INFECTION has been reported as an adverse event in 174 FDA reports for BARICITINIB. This does not prove causation, but indicates an association observed in post-market surveillance data.
URINARY TRACT INFECTION accounts for approximately 1.5% of all adverse event reports for BARICITINIB, making it a notable side effect.
If you experience urinary tract infection while taking BARICITINIB, 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.