4,222 reports of this reaction
7.4% of all CINACALCET HYDROCHLORIDE reports
#3 most reported adverse reaction
LABORATORY TEST ABNORMAL is the #3 most commonly reported adverse reaction for CINACALCET HYDROCHLORIDE, manufactured by Amgen Inc. There are 4,222 FDA adverse event reports linking CINACALCET HYDROCHLORIDE to LABORATORY TEST ABNORMAL. This represents approximately 7.4% of all 57,261 adverse event reports for this drug.
Patients taking CINACALCET HYDROCHLORIDE who experience laboratory test abnormal should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
LABORATORY TEST ABNORMAL is moderately reported among CINACALCET HYDROCHLORIDE users, representing a notable but not dominant share of adverse events.
In addition to laboratory test abnormal, the following adverse reactions have been reported for CINACALCET HYDROCHLORIDE:
The following drugs have also been linked to laboratory test abnormal in FDA adverse event reports:
LABORATORY TEST ABNORMAL has been reported as an adverse event in 4,222 FDA reports for CINACALCET HYDROCHLORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
LABORATORY TEST ABNORMAL accounts for approximately 7.4% of all adverse event reports for CINACALCET HYDROCHLORIDE, making it one of the most commonly reported side effect.
If you experience laboratory test abnormal while taking CINACALCET HYDROCHLORIDE, 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.