Does PARICALCITOL Cause Device issue? 28 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 28 reports of Device issue have been filed in association with PARICALCITOL (Paricalcitol). This represents 0.4% of all adverse event reports for PARICALCITOL.
28
Reports of Device issue with PARICALCITOL
0.4%
of all PARICALCITOL reports
3
Deaths
25
Hospitalizations
How Dangerous Is Device issue From PARICALCITOL?
Of the 28 reports, 3 (10.7%) resulted in death, 25 (89.3%) required hospitalization, and 2 (7.1%) were considered life-threatening.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PARICALCITOL. However, 28 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 issue?
ADALIMUMAB (17,630)
SOMATROPIN (5,131)
PEGFILGRASTIM (5,071)
ETANERCEPT (4,143)
INSULIN GLARGINE (3,175)
EXENATIDE (2,862)
LEVONORGESTREL (2,623)
CARBIDOPA\LEVODOPA (2,574)
GOLIMUMAB (1,827)
USTEKINUMAB (1,716)
Which PARICALCITOL Alternatives Have Lower Device issue Risk?
PARICALCITOL vs PARITAPREVIR
PARICALCITOL vs PAROXETINE
PARICALCITOL vs PAROXETINE\PAROXETINE
PARICALCITOL vs PAROXETINE\PAROXETINE ANHYDROUS
PARICALCITOL vs PASIREOTIDE