1,015 reports of this reaction
3.4% of all RALTEGRAVIR reports
#3 most reported adverse reaction
DEPRESSION is the #3 most commonly reported adverse reaction for RALTEGRAVIR, manufactured by Merck Sharp & Dohme LLC. There are 1,015 FDA adverse event reports linking RALTEGRAVIR to DEPRESSION. This represents approximately 3.4% of all 29,953 adverse event reports for this drug.
Patients taking RALTEGRAVIR who experience depression should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DEPRESSION is moderately reported among RALTEGRAVIR users, representing a notable but not dominant share of adverse events.
In addition to depression, the following adverse reactions have been reported for RALTEGRAVIR:
The following drugs have also been linked to depression in FDA adverse event reports:
DEPRESSION has been reported as an adverse event in 1,015 FDA reports for RALTEGRAVIR. This does not prove causation, but indicates an association observed in post-market surveillance data.
DEPRESSION accounts for approximately 3.4% of all adverse event reports for RALTEGRAVIR, making it one of the most commonly reported side effect.
If you experience depression while taking RALTEGRAVIR, 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.