83 reports of this reaction
2.3% of all CISATRACURIUM BESYLATE reports
#8 most reported adverse reaction
RHABDOMYOLYSIS is the #8 most commonly reported adverse reaction for CISATRACURIUM BESYLATE, manufactured by Fresenius Kabi USA, LLC. There are 83 FDA adverse event reports linking CISATRACURIUM BESYLATE to RHABDOMYOLYSIS. This represents approximately 2.3% of all 3,661 adverse event reports for this drug.
Patients taking CISATRACURIUM BESYLATE who experience rhabdomyolysis should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
RHABDOMYOLYSIS is a less commonly reported adverse event for CISATRACURIUM BESYLATE, but still significant enough to appear in the safety profile.
In addition to rhabdomyolysis, the following adverse reactions have been reported for CISATRACURIUM BESYLATE:
The following drugs have also been linked to rhabdomyolysis in FDA adverse event reports:
RHABDOMYOLYSIS has been reported as an adverse event in 83 FDA reports for CISATRACURIUM BESYLATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
RHABDOMYOLYSIS accounts for approximately 2.3% of all adverse event reports for CISATRACURIUM BESYLATE, making it a notable side effect.
If you experience rhabdomyolysis while taking CISATRACURIUM BESYLATE, 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.