480 reports of this reaction
1.8% of all GENTAMICIN SULFATE reports
#8 most reported adverse reaction
CONDITION AGGRAVATED is the #8 most commonly reported adverse reaction for GENTAMICIN SULFATE, manufactured by Fresenius Kabi USA, LLC. There are 480 FDA adverse event reports linking GENTAMICIN SULFATE to CONDITION AGGRAVATED. This represents approximately 1.8% of all 27,380 adverse event reports for this drug.
Patients taking GENTAMICIN SULFATE who experience condition aggravated should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
CONDITION AGGRAVATED is a less commonly reported adverse event for GENTAMICIN SULFATE, but still significant enough to appear in the safety profile.
In addition to condition aggravated, the following adverse reactions have been reported for GENTAMICIN SULFATE:
The following drugs have also been linked to condition aggravated in FDA adverse event reports:
CONDITION AGGRAVATED has been reported as an adverse event in 480 FDA reports for GENTAMICIN SULFATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
CONDITION AGGRAVATED accounts for approximately 1.8% of all adverse event reports for GENTAMICIN SULFATE, making it a notable side effect.
If you experience condition aggravated while taking GENTAMICIN 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.