224 reports of this reaction
3.2% of all ATAZANAVIR SULFATE reports
#5 most reported adverse reaction
LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES is the #5 most commonly reported adverse reaction for ATAZANAVIR SULFATE, manufactured by Aurobindo Pharma Limited. There are 224 FDA adverse event reports linking ATAZANAVIR SULFATE to LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES. This represents approximately 3.2% of all 6,992 adverse event reports for this drug.
Patients taking ATAZANAVIR SULFATE who experience loss of personal independence in daily activities should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES is moderately reported among ATAZANAVIR SULFATE users, representing a notable but not dominant share of adverse events.
In addition to loss of personal independence in daily activities, the following adverse reactions have been reported for ATAZANAVIR SULFATE:
The following drugs have also been linked to loss of personal independence in daily activities in FDA adverse event reports:
LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES has been reported as an adverse event in 224 FDA reports for ATAZANAVIR SULFATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES accounts for approximately 3.2% of all adverse event reports for ATAZANAVIR SULFATE, making it a notable side effect.
If you experience loss of personal independence in daily activities while taking ATAZANAVIR SULFATE, 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.