211 reports of this reaction
2.0% of all BRIVARACETAM reports
#9 most reported adverse reaction
PRODUCT AVAILABILITY ISSUE is the #9 most commonly reported adverse reaction for BRIVARACETAM, manufactured by Apotex Corp.. There are 211 FDA adverse event reports linking BRIVARACETAM to PRODUCT AVAILABILITY ISSUE. This represents approximately 2.0% of all 10,449 adverse event reports for this drug.
Patients taking BRIVARACETAM who experience product availability issue should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
PRODUCT AVAILABILITY ISSUE is a less commonly reported adverse event for BRIVARACETAM, but still significant enough to appear in the safety profile.
In addition to product availability issue, the following adverse reactions have been reported for BRIVARACETAM:
The following drugs have also been linked to product availability issue in FDA adverse event reports:
PRODUCT AVAILABILITY ISSUE has been reported as an adverse event in 211 FDA reports for BRIVARACETAM. This does not prove causation, but indicates an association observed in post-market surveillance data.
PRODUCT AVAILABILITY ISSUE accounts for approximately 2.0% of all adverse event reports for BRIVARACETAM, making it a notable side effect.
If you experience product availability issue while taking BRIVARACETAM, 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.