1,234 reports of this reaction
2.3% of all RITONAVIR reports
#6 most reported adverse reaction
ANHEDONIA is the #6 most commonly reported adverse reaction for RITONAVIR, manufactured by AbbVie Inc.. There are 1,234 FDA adverse event reports linking RITONAVIR to ANHEDONIA. This represents approximately 2.3% of all 53,209 adverse event reports for this drug.
RITONAVIR has an overall safety score of 85 out of 100. Patients taking RITONAVIR who experience anhedonia should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
ANHEDONIA is a less commonly reported adverse event for RITONAVIR, but still significant enough to appear in the safety profile.
In addition to anhedonia, the following adverse reactions have been reported for RITONAVIR:
The following drugs have also been linked to anhedonia in FDA adverse event reports:
ANHEDONIA has been reported as an adverse event in 1,234 FDA reports for RITONAVIR. This does not prove causation, but indicates an association observed in post-market surveillance data.
ANHEDONIA accounts for approximately 2.3% of all adverse event reports for RITONAVIR, making it a notable side effect.
If you experience anhedonia while taking RITONAVIR, 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.