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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does PARICALCITOL Cause Condition aggravated? 32 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 32 reports of Condition aggravated have been filed in association with PARICALCITOL (Paricalcitol). This represents 0.5% of all adverse event reports for PARICALCITOL.

32
Reports of Condition aggravated with PARICALCITOL
0.5%
of all PARICALCITOL reports
22
Deaths
11
Hospitalizations

How Dangerous Is Condition aggravated From PARICALCITOL?

Of the 32 reports, 22 (68.8%) resulted in death, 11 (34.4%) required hospitalization.

Is Condition aggravated 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 Condition aggravated?

TOFACITINIB (16,925) INFLIXIMAB (16,616) DUPILUMAB (16,459) ETANERCEPT (15,897) METHOTREXATE (14,938) ADALIMUMAB (13,527) PREDNISONE (10,751) INFLIXIMAB-DYYB (10,275) HYDROXYCHLOROQUINE (8,848) RITUXIMAB (8,627)

Which PARICALCITOL Alternatives Have Lower Condition aggravated Risk?

PARICALCITOL vs PARITAPREVIR PARICALCITOL vs PAROXETINE PARICALCITOL vs PAROXETINE\PAROXETINE PARICALCITOL vs PAROXETINE\PAROXETINE ANHYDROUS PARICALCITOL vs PASIREOTIDE

Related Pages

PARICALCITOL Full Profile All Condition aggravated Reports All Drugs Causing Condition aggravated PARICALCITOL Demographics