Does ALIROCUMAB Cause Condition aggravated? 451 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 451 reports of Condition aggravated have been filed in association with ALIROCUMAB (Praluent). This represents 2.0% of all adverse event reports for ALIROCUMAB.
451
Reports of Condition aggravated with ALIROCUMAB
2.0%
of all ALIROCUMAB reports
6
Deaths
47
Hospitalizations
How Dangerous Is Condition aggravated From ALIROCUMAB?
Of the 451 reports, 6 (1.3%) resulted in death, 47 (10.4%) required hospitalization, and 11 (2.4%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALIROCUMAB. However, 451 reports have been filed with the FAERS database.
What Other Side Effects Does ALIROCUMAB Cause?
Myalgia (1,571)
Product dose omission (1,354)
Injection site pain (1,220)
Muscle spasms (1,113)
Arthralgia (993)
Fatigue (922)
Pain (892)
Pain in extremity (888)
Product dose omission issue (864)
Injection site bruising (821)
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 ALIROCUMAB Alternatives Have Lower Condition aggravated Risk?
ALIROCUMAB vs ALISKIREN
ALIROCUMAB vs ALISKIREN HEMIFUMARATE
ALIROCUMAB vs ALISKIREN\HYDROCHLOROTHIAZIDE
ALIROCUMAB vs ALIZAPRIDE
ALIROCUMAB vs ALLANTOIN