244 reports of this reaction
1.5% of all BUPRENORPHINE HYDROCHLORIDE reports
#11 most reported adverse reaction
WITHDRAWAL SYNDROME is the #11 most commonly reported adverse reaction for BUPRENORPHINE HYDROCHLORIDE, manufactured by BioDelivery Sciences International Inc. There are 244 FDA adverse event reports linking BUPRENORPHINE HYDROCHLORIDE to WITHDRAWAL SYNDROME. This represents approximately 1.5% of all 15,869 adverse event reports for this drug.
Patients taking BUPRENORPHINE HYDROCHLORIDE who experience withdrawal syndrome should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
WITHDRAWAL SYNDROME is a less commonly reported adverse event for BUPRENORPHINE HYDROCHLORIDE, but still significant enough to appear in the safety profile.
In addition to withdrawal syndrome, the following adverse reactions have been reported for BUPRENORPHINE HYDROCHLORIDE:
The following drugs have also been linked to withdrawal syndrome in FDA adverse event reports:
WITHDRAWAL SYNDROME has been reported as an adverse event in 244 FDA reports for BUPRENORPHINE HYDROCHLORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
WITHDRAWAL SYNDROME accounts for approximately 1.5% of all adverse event reports for BUPRENORPHINE HYDROCHLORIDE, making it a notable side effect.
If you experience withdrawal syndrome while taking BUPRENORPHINE HYDROCHLORIDE, 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.