Does PARICALCITOL Cause Device related sepsis? 32 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 32 reports of Device related sepsis have been filed in association with PARICALCITOL (Paricalcitol). This represents 0.5% of all adverse event reports for PARICALCITOL.
32
Reports of Device related sepsis with PARICALCITOL
0.5%
of all PARICALCITOL reports
26
Deaths
8
Hospitalizations
How Dangerous Is Device related sepsis From PARICALCITOL?
Of the 32 reports, 26 (81.3%) resulted in death, 8 (25.0%) required hospitalization, and 1 (3.1%) were considered life-threatening.
Is Device related sepsis Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PARICALCITOL. However, 32 reports have been filed with the FAERS database.
What Other Side Effects Does PARICALCITOL Cause?
Death (1,801)
Myocardial infarction (419)
Cardio-respiratory arrest (396)
Cardiac disorder (384)
Sepsis (277)
Infarction (233)
Cardiac failure (192)
Cerebrovascular accident (181)
Respiratory arrest (174)
General physical health deterioration (144)
What Other Drugs Cause Device related sepsis?
TEDUGLUTIDE (226)
TREPROSTINIL (225)
CYCLOPHOSPHAMIDE (130)
RITUXIMAB (113)
EPOPROSTENOL (89)
CYCLOSPORINE (82)
METHYLPREDNISOLONE (82)
BORTEZOMIB (79)
MACITENTAN (55)
DEXAMETHASONE (53)
Which PARICALCITOL Alternatives Have Lower Device related sepsis Risk?
PARICALCITOL vs PARITAPREVIR
PARICALCITOL vs PAROXETINE
PARICALCITOL vs PAROXETINE\PAROXETINE
PARICALCITOL vs PAROXETINE\PAROXETINE ANHYDROUS
PARICALCITOL vs PASIREOTIDE