22,330 reports of this reaction
1.5% of all ADALIMUMAB reports
#14 most reported adverse reaction
INCORRECT DOSE ADMINISTERED is the #14 most commonly reported adverse reaction for ADALIMUMAB, manufactured by AbbVie Inc.. There are 22,330 FDA adverse event reports linking ADALIMUMAB to INCORRECT DOSE ADMINISTERED. This represents approximately 1.5% of all 1,482,766 adverse event reports for this drug.
Patients taking ADALIMUMAB who experience incorrect dose administered should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
INCORRECT DOSE ADMINISTERED is a less commonly reported adverse event for ADALIMUMAB, but still significant enough to appear in the safety profile.
In addition to incorrect dose administered, the following adverse reactions have been reported for ADALIMUMAB:
The following drugs have also been linked to incorrect dose administered in FDA adverse event reports:
INCORRECT DOSE ADMINISTERED has been reported as an adverse event in 22,330 FDA reports for ADALIMUMAB. This does not prove causation, but indicates an association observed in post-market surveillance data.
INCORRECT DOSE ADMINISTERED accounts for approximately 1.5% of all adverse event reports for ADALIMUMAB, making it a notable side effect.
If you experience incorrect dose administered while taking ADALIMUMAB, 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.