48,309 reports of this reaction
3.2% of all Humira reports
#3 most reported adverse reaction
ARTHRALGIA is the #3 most commonly reported adverse reaction for Humira, manufactured by AbbVie Inc.. There are 48,309 FDA adverse event reports linking Humira to ARTHRALGIA. This represents approximately 3.2% of all 1,495,215 adverse event reports for this drug.
Patients taking Humira who experience arthralgia should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
ARTHRALGIA is moderately reported among Humira users, representing a notable but not dominant share of adverse events.
In addition to arthralgia, the following adverse reactions have been reported for Humira:
The following drugs have also been linked to arthralgia in FDA adverse event reports:
ARTHRALGIA has been reported as an adverse event in 48,309 FDA reports for Humira. This does not prove causation, but indicates an association observed in post-market surveillance data.
ARTHRALGIA accounts for approximately 3.2% of all adverse event reports for Humira, making it one of the most commonly reported side effect.
If you experience arthralgia while taking Humira, 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.