Does PARICALCITOL Cause Complication associated with device? 16 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Complication associated with device have been filed in association with PARICALCITOL (Paricalcitol). This represents 0.2% of all adverse event reports for PARICALCITOL.
16
Reports of Complication associated with device with PARICALCITOL
0.2%
of all PARICALCITOL reports
1
Deaths
16
Hospitalizations
How Dangerous Is Complication associated with device From PARICALCITOL?
Of the 16 reports, 1 (6.3%) resulted in death, 16 (100.0%) required hospitalization, and 3 (18.8%) were considered life-threatening.
Is Complication associated with device Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PARICALCITOL. However, 16 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 Complication associated with device?
ETONOGESTREL (6,047)
COPPER (1,083)
BACLOFEN (525)
TREPROSTINIL (422)
EPOPROSTENOL (399)
LEVONORGESTREL (344)
ADALIMUMAB (269)
CARBIDOPA\LEVODOPA (169)
MACITENTAN (169)
TEDUGLUTIDE (133)
Which PARICALCITOL Alternatives Have Lower Complication associated with device Risk?
PARICALCITOL vs PARITAPREVIR
PARICALCITOL vs PAROXETINE
PARICALCITOL vs PAROXETINE\PAROXETINE
PARICALCITOL vs PAROXETINE\PAROXETINE ANHYDROUS
PARICALCITOL vs PASIREOTIDE