2,259 reports of this reaction
5.8% of all Brilinta reports
#2 most reported adverse reaction
MYOCARDIAL INFARCTION is the #2 most commonly reported adverse reaction for Brilinta, manufactured by Rising Pharma Holdings, Inc.. There are 2,259 FDA adverse event reports linking Brilinta to MYOCARDIAL INFARCTION. This represents approximately 5.8% of all 39,143 adverse event reports for this drug.
Patients taking Brilinta who experience myocardial infarction should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
MYOCARDIAL INFARCTION is moderately reported among Brilinta users, representing a notable but not dominant share of adverse events.
In addition to myocardial infarction, the following adverse reactions have been reported for Brilinta:
The following drugs have also been linked to myocardial infarction in FDA adverse event reports:
MYOCARDIAL INFARCTION has been reported as an adverse event in 2,259 FDA reports for Brilinta. This does not prove causation, but indicates an association observed in post-market surveillance data.
MYOCARDIAL INFARCTION accounts for approximately 5.8% of all adverse event reports for Brilinta, making it one of the most commonly reported side effect.
If you experience myocardial infarction while taking Brilinta, 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.