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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 ALIROCUMAB Cause Device failure? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Device failure have been filed in association with ALIROCUMAB (Praluent). This represents 0.0% of all adverse event reports for ALIROCUMAB.

5
Reports of Device failure with ALIROCUMAB
0.0%
of all ALIROCUMAB reports
0
Deaths
3
Hospitalizations

How Dangerous Is Device failure From ALIROCUMAB?

Of the 5 reports, 3 (60.0%) required hospitalization.

Is Device failure Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ALIROCUMAB. However, 5 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 Device failure?

EPINEPHRINE (1,344) SOMATROPIN (1,141) PEGFILGRASTIM (829) TREPROSTINIL (713) BACLOFEN (691) BUDESONIDE\FORMOTEROL (686) ETANERCEPT (576) GOLIMUMAB (487) LEVONORGESTREL (332) ACLIDINIUM (304)

Which ALIROCUMAB Alternatives Have Lower Device failure Risk?

ALIROCUMAB vs ALISKIREN ALIROCUMAB vs ALISKIREN HEMIFUMARATE ALIROCUMAB vs ALISKIREN\HYDROCHLOROTHIAZIDE ALIROCUMAB vs ALIZAPRIDE ALIROCUMAB vs ALLANTOIN

Related Pages

ALIROCUMAB Full Profile All Device failure Reports All Drugs Causing Device failure ALIROCUMAB Demographics