HYDROCODONE BITARTRATE AND ACETAMINOPHEN and ANXIETY
4,193 reports of this reaction
2.7% of all HYDROCODONE BITARTRATE AND ACETAMINOPHEN reports
#6 most reported adverse reaction
Overview
ANXIETY is the #6 most commonly reported adverse reaction for HYDROCODONE BITARTRATE AND ACETAMINOPHEN, manufactured by Amneal Pharmaceuticals LLC. There are 4,193 FDA adverse event reports linking HYDROCODONE BITARTRATE AND ACETAMINOPHEN to ANXIETY. This represents approximately 2.7% of all 153,212 adverse event reports for this drug.
Patients taking HYDROCODONE BITARTRATE AND ACETAMINOPHEN 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
ANXIETY4,193 of 153,212 reports
ANXIETY is a less commonly reported adverse event for HYDROCODONE BITARTRATE AND ACETAMINOPHEN, but still significant enough to appear in the safety profile.
Other Side Effects of HYDROCODONE BITARTRATE AND ACETAMINOPHEN
In addition to anxiety, the following adverse reactions have been reported for HYDROCODONE BITARTRATE AND ACETAMINOPHEN:
Does HYDROCODONE BITARTRATE AND ACETAMINOPHEN cause ANXIETY?
ANXIETY has been reported as an adverse event in 4,193 FDA reports for HYDROCODONE BITARTRATE AND ACETAMINOPHEN. This does not prove causation, but indicates an association observed in post-market surveillance data.
How common is ANXIETY with HYDROCODONE BITARTRATE AND ACETAMINOPHEN?
ANXIETY accounts for approximately 2.7% of all adverse event reports for HYDROCODONE BITARTRATE AND ACETAMINOPHEN, making it a notable side effect.
What should I do if I experience ANXIETY while taking HYDROCODONE BITARTRATE AND ACETAMINOPHEN?
If you experience anxiety while taking HYDROCODONE BITARTRATE AND ACETAMINOPHEN, 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.