664 reports of this reaction
2.4% of all LOPINAVIR AND RITONAVIR reports
#10 most reported adverse reaction
OFF LABEL USE is the #10 most commonly reported adverse reaction for LOPINAVIR AND RITONAVIR, manufactured by AbbVie Inc.. There are 664 FDA adverse event reports linking LOPINAVIR AND RITONAVIR to OFF LABEL USE. This represents approximately 2.4% of all 28,252 adverse event reports for this drug.
Patients taking LOPINAVIR AND RITONAVIR who experience off label use should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
OFF LABEL USE is a less commonly reported adverse event for LOPINAVIR AND RITONAVIR, but still significant enough to appear in the safety profile.
In addition to off label use, the following adverse reactions have been reported for LOPINAVIR AND RITONAVIR:
The following drugs have also been linked to off label use in FDA adverse event reports:
OFF LABEL USE has been reported as an adverse event in 664 FDA reports for LOPINAVIR AND RITONAVIR. This does not prove causation, but indicates an association observed in post-market surveillance data.
OFF LABEL USE accounts for approximately 2.4% of all adverse event reports for LOPINAVIR AND RITONAVIR, making it a notable side effect.
If you experience off label use while taking LOPINAVIR AND 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.