1,168 reports of this reaction
1.4% of all INSULIN HUMAN reports
#12 most reported adverse reaction
WRONG TECHNIQUE IN PRODUCT USAGE PROCESS is the #12 most commonly reported adverse reaction for INSULIN HUMAN, manufactured by Eli Lilly and Company. There are 1,168 FDA adverse event reports linking INSULIN HUMAN to WRONG TECHNIQUE IN PRODUCT USAGE PROCESS. This represents approximately 1.4% of all 82,903 adverse event reports for this drug.
Patients taking INSULIN HUMAN who experience wrong technique in product usage process should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
WRONG TECHNIQUE IN PRODUCT USAGE PROCESS is a less commonly reported adverse event for INSULIN HUMAN, but still significant enough to appear in the safety profile.
In addition to wrong technique in product usage process, the following adverse reactions have been reported for INSULIN HUMAN:
The following drugs have also been linked to wrong technique in product usage process in FDA adverse event reports:
WRONG TECHNIQUE IN PRODUCT USAGE PROCESS has been reported as an adverse event in 1,168 FDA reports for INSULIN HUMAN. This does not prove causation, but indicates an association observed in post-market surveillance data.
WRONG TECHNIQUE IN PRODUCT USAGE PROCESS accounts for approximately 1.4% of all adverse event reports for INSULIN HUMAN, making it a notable side effect.
If you experience wrong technique in product usage process while taking INSULIN HUMAN, 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.