Does PARICALCITOL Cause Haemoglobin decreased? 38 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 38 reports of Haemoglobin decreased have been filed in association with PARICALCITOL (Paricalcitol). This represents 0.6% of all adverse event reports for PARICALCITOL.
38
Reports of Haemoglobin decreased with PARICALCITOL
0.6%
of all PARICALCITOL reports
4
Deaths
29
Hospitalizations
How Dangerous Is Haemoglobin decreased From PARICALCITOL?
Of the 38 reports, 4 (10.5%) resulted in death, 29 (76.3%) required hospitalization, and 1 (2.6%) were considered life-threatening.
Is Haemoglobin decreased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PARICALCITOL. However, 38 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 Haemoglobin decreased?
LENALIDOMIDE (4,031)
RUXOLITINIB (3,297)
ECULIZUMAB (3,028)
ADALIMUMAB (2,459)
CLOZAPINE (2,396)
RITUXIMAB (1,803)
APIXABAN (1,779)
NIRAPARIB (1,759)
METHOTREXATE (1,754)
RIBAVIRIN (1,753)
Which PARICALCITOL Alternatives Have Lower Haemoglobin decreased Risk?
PARICALCITOL vs PARITAPREVIR
PARICALCITOL vs PAROXETINE
PARICALCITOL vs PAROXETINE\PAROXETINE
PARICALCITOL vs PAROXETINE\PAROXETINE ANHYDROUS
PARICALCITOL vs PASIREOTIDE