BUPRENORPHINE HYDROCHLORIDE, NALOXONE HYDROCHLORIDE and ANXIETY
1,348 reports of this reaction
2.3% of all BUPRENORPHINE HYDROCHLORIDE, NALOXONE HYDROCHLORIDE reports
#8 most reported adverse reaction
Overview
ANXIETY is the #8 most commonly reported adverse reaction for BUPRENORPHINE HYDROCHLORIDE, NALOXONE HYDROCHLORIDE, manufactured by INDIVIOR INC.. There are 1,348 FDA adverse event reports linking BUPRENORPHINE HYDROCHLORIDE, NALOXONE HYDROCHLORIDE to ANXIETY. This represents approximately 2.3% of all 59,605 adverse event reports for this drug.
Patients taking BUPRENORPHINE HYDROCHLORIDE, NALOXONE HYDROCHLORIDE who experience anxiety should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
Reporting Frequency
ANXIETY1,348 of 59,605 reports
ANXIETY is a less commonly reported adverse event for BUPRENORPHINE HYDROCHLORIDE, NALOXONE HYDROCHLORIDE, but still significant enough to appear in the safety profile.
Other Side Effects of BUPRENORPHINE HYDROCHLORIDE, NALOXONE HYDROCHLORIDE
In addition to anxiety, the following adverse reactions have been reported for BUPRENORPHINE HYDROCHLORIDE, NALOXONE HYDROCHLORIDE:
Does BUPRENORPHINE HYDROCHLORIDE, NALOXONE HYDROCHLORIDE cause ANXIETY?
ANXIETY has been reported as an adverse event in 1,348 FDA reports for BUPRENORPHINE HYDROCHLORIDE, NALOXONE HYDROCHLORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
How common is ANXIETY with BUPRENORPHINE HYDROCHLORIDE, NALOXONE HYDROCHLORIDE?
ANXIETY accounts for approximately 2.3% of all adverse event reports for BUPRENORPHINE HYDROCHLORIDE, NALOXONE HYDROCHLORIDE, making it a notable side effect.
What should I do if I experience ANXIETY while taking BUPRENORPHINE HYDROCHLORIDE, NALOXONE HYDROCHLORIDE?
If you experience anxiety while taking BUPRENORPHINE HYDROCHLORIDE, NALOXONE 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.
Disclaimer: This analysis is based on FDA adverse event reports and is for informational purposes only. Reports do not prove causation. Always consult your healthcare provider.