The most commonly reported side effects of paricalcitol include death, cardiac disorder, and myocardial infarction, based on 14,218 FDA adverse event reports from 2004 to 2025.
Percentages show how often each reaction appears relative to total reports for paricalcitol.
These are voluntary reports and do not establish that paricalcitol caused these reactions.
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Other drugs that appear in adverse event reports alongside paricalcitol. Drugs flagged as a suspected cause appear in the first column. Drugs taken at the same time but not suspected appear in the second.
Also suspected
Taken alongside
Co-occurrence in adverse event reports does not establish a drug interaction. Patients often take multiple medications, and these lists reflect prescribing patterns rather than causal relationships. Consult a healthcare provider about potential drug interactions.
43.0% of paricalcitol adverse event reports involve female patients and 53.8% involve male patients. The largest age group is adult at 57%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking paricalcitol when the adverse event was reported.
Showing 15 of 154 indications
Paricalcitol is sold under the brand name Paricalcitol.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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