6,434 reports of this reaction
2.7% of all AMBRISENTAN reports
#8 most reported adverse reaction
NAUSEA is the #8 most commonly reported adverse reaction for AMBRISENTAN, manufactured by Gilead Sciences, Inc.. There are 6,434 FDA adverse event reports linking AMBRISENTAN to NAUSEA. This represents approximately 2.7% of all 240,584 adverse event reports for this drug.
Patients taking AMBRISENTAN who experience nausea should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
NAUSEA is a less commonly reported adverse event for AMBRISENTAN, but still significant enough to appear in the safety profile.
In addition to nausea, the following adverse reactions have been reported for AMBRISENTAN:
The following drugs have also been linked to nausea in FDA adverse event reports:
NAUSEA has been reported as an adverse event in 6,434 FDA reports for AMBRISENTAN. This does not prove causation, but indicates an association observed in post-market surveillance data.
NAUSEA accounts for approximately 2.7% of all adverse event reports for AMBRISENTAN, making it a notable side effect.
If you experience nausea while taking AMBRISENTAN, 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.