CINACALCET and CALCIPHYLAXIS

139 reports of this reaction

1.9% of all CINACALCET reports

#9 most reported adverse reaction

Overview

CALCIPHYLAXIS is the #9 most commonly reported adverse reaction for CINACALCET, manufactured by Amneal Pharmaceuticals LLC. There are 139 FDA adverse event reports linking CINACALCET to CALCIPHYLAXIS. This represents approximately 1.9% of all 7,231 adverse event reports for this drug.

Patients taking CINACALCET who experience calciphylaxis 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

CALCIPHYLAXIS139 of 7,231 reports

CALCIPHYLAXIS is a less commonly reported adverse event for CINACALCET, but still significant enough to appear in the safety profile.

Other Side Effects of CINACALCET

In addition to calciphylaxis, the following adverse reactions have been reported for CINACALCET:

Other Drugs Associated with CALCIPHYLAXIS

The following drugs have also been linked to calciphylaxis in FDA adverse event reports:

FERROUS FUMARATE, FOLIC ACID

Frequently Asked Questions

Does CINACALCET cause CALCIPHYLAXIS?

CALCIPHYLAXIS has been reported as an adverse event in 139 FDA reports for CINACALCET. This does not prove causation, but indicates an association observed in post-market surveillance data.

How common is CALCIPHYLAXIS with CINACALCET?

CALCIPHYLAXIS accounts for approximately 1.9% of all adverse event reports for CINACALCET, making it a notable side effect.

What should I do if I experience CALCIPHYLAXIS while taking CINACALCET?

If you experience calciphylaxis while taking CINACALCET, 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.

Related Pages

CINACALCET Full ProfileAll Drugs Causing CALCIPHYLAXISAmneal Pharmaceuticals LLC Drugs
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.