2.0% of all TACROLIMUS EXTENDED RELEASE CAPSULES reports
#9 most reported adverse reaction
Overview
PYREXIA is the #9 most commonly reported adverse reaction for TACROLIMUS EXTENDED RELEASE CAPSULES, manufactured by Astellas Pharma US, Inc.. There are 3,690 FDA adverse event reports linking TACROLIMUS EXTENDED RELEASE CAPSULES to PYREXIA. This represents approximately 2.0% of all 181,869 adverse event reports for this drug.
TACROLIMUS EXTENDED RELEASE CAPSULES has an overall safety score of 92 out of 100. Patients taking TACROLIMUS EXTENDED RELEASE CAPSULES who experience pyrexia should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
Reporting Frequency
PYREXIA3,690 of 181,869 reports
PYREXIA is a less commonly reported adverse event for TACROLIMUS EXTENDED RELEASE CAPSULES, but still significant enough to appear in the safety profile.
Other Side Effects of TACROLIMUS EXTENDED RELEASE CAPSULES
In addition to pyrexia, the following adverse reactions have been reported for TACROLIMUS EXTENDED RELEASE CAPSULES:
Does TACROLIMUS EXTENDED RELEASE CAPSULES cause PYREXIA?
PYREXIA has been reported as an adverse event in 3,690 FDA reports for TACROLIMUS EXTENDED RELEASE CAPSULES. This does not prove causation, but indicates an association observed in post-market surveillance data.
How common is PYREXIA with TACROLIMUS EXTENDED RELEASE CAPSULES?
PYREXIA accounts for approximately 2.0% of all adverse event reports for TACROLIMUS EXTENDED RELEASE CAPSULES, making it a notable side effect.
What should I do if I experience PYREXIA while taking TACROLIMUS EXTENDED RELEASE CAPSULES?
If you experience pyrexia while taking TACROLIMUS EXTENDED RELEASE CAPSULES, 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.
Disclaimer: This analysis is based on FDA adverse event reports and is for informational purposes only. Reports do not prove causation. Always consult your healthcare provider.