63 reports of this reaction
1.3% of all AMPICILLIN SODIUM AND SULBACTAM SODIUM reports
#19 most reported adverse reaction
HEPATIC FUNCTION ABNORMAL is the #19 most commonly reported adverse reaction for AMPICILLIN SODIUM AND SULBACTAM SODIUM, manufactured by Roerig. There are 63 FDA adverse event reports linking AMPICILLIN SODIUM AND SULBACTAM SODIUM to HEPATIC FUNCTION ABNORMAL. This represents approximately 1.3% of all 4,969 adverse event reports for this drug.
Patients taking AMPICILLIN SODIUM AND SULBACTAM SODIUM who experience hepatic function abnormal should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
HEPATIC FUNCTION ABNORMAL is a less commonly reported adverse event for AMPICILLIN SODIUM AND SULBACTAM SODIUM, but still significant enough to appear in the safety profile.
In addition to hepatic function abnormal, the following adverse reactions have been reported for AMPICILLIN SODIUM AND SULBACTAM SODIUM:
The following drugs have also been linked to hepatic function abnormal in FDA adverse event reports:
HEPATIC FUNCTION ABNORMAL has been reported as an adverse event in 63 FDA reports for AMPICILLIN SODIUM AND SULBACTAM SODIUM. This does not prove causation, but indicates an association observed in post-market surveillance data.
HEPATIC FUNCTION ABNORMAL accounts for approximately 1.3% of all adverse event reports for AMPICILLIN SODIUM AND SULBACTAM SODIUM, making it a notable side effect.
If you experience hepatic function abnormal while taking AMPICILLIN SODIUM AND SULBACTAM SODIUM, 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.