3,199 reports of this reaction
2.4% of all SOMATROPIN reports
#9 most reported adverse reaction
POOR QUALITY DEVICE USED is the #9 most commonly reported adverse reaction for SOMATROPIN, manufactured by Pfizer Laboratories Div Pfizer Inc. There are 3,199 FDA adverse event reports linking SOMATROPIN to POOR QUALITY DEVICE USED. This represents approximately 2.4% of all 133,576 adverse event reports for this drug.
SOMATROPIN has an overall safety score of 78 out of 100. Patients taking SOMATROPIN who experience poor quality device used should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
POOR QUALITY DEVICE USED is a less commonly reported adverse event for SOMATROPIN, but still significant enough to appear in the safety profile.
In addition to poor quality device used, the following adverse reactions have been reported for SOMATROPIN:
The following drugs have also been linked to poor quality device used in FDA adverse event reports:
POOR QUALITY DEVICE USED has been reported as an adverse event in 3,199 FDA reports for SOMATROPIN. This does not prove causation, but indicates an association observed in post-market surveillance data.
POOR QUALITY DEVICE USED accounts for approximately 2.4% of all adverse event reports for SOMATROPIN, making it a notable side effect.
If you experience poor quality device used while taking SOMATROPIN, 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.