1,535 reports of this reaction
1.4% of all APIXABAN reports
#19 most reported adverse reaction
GASTROINTESTINAL HAEMORRHAGE is the #19 most commonly reported adverse reaction for APIXABAN, manufactured by Amneal Pharmaceuticals of New York LLC. There are 1,535 FDA adverse event reports linking APIXABAN to GASTROINTESTINAL HAEMORRHAGE. This represents approximately 1.4% of all 106,298 adverse event reports for this drug.
Patients taking APIXABAN who experience gastrointestinal haemorrhage should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
GASTROINTESTINAL HAEMORRHAGE is a less commonly reported adverse event for APIXABAN, but still significant enough to appear in the safety profile.
In addition to gastrointestinal haemorrhage, the following adverse reactions have been reported for APIXABAN:
The following drugs have also been linked to gastrointestinal haemorrhage in FDA adverse event reports:
GASTROINTESTINAL HAEMORRHAGE has been reported as an adverse event in 1,535 FDA reports for APIXABAN. This does not prove causation, but indicates an association observed in post-market surveillance data.
GASTROINTESTINAL HAEMORRHAGE accounts for approximately 1.4% of all adverse event reports for APIXABAN, making it a notable side effect.
If you experience gastrointestinal haemorrhage while taking APIXABAN, 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.