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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 BRILINTA Cause Device occlusion? 16 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Device occlusion have been filed in association with BRILINTA. This represents 2.7% of all adverse event reports for BRILINTA.

16
Reports of Device occlusion with BRILINTA
2.7%
of all BRILINTA reports
1
Deaths
12
Hospitalizations

How Dangerous Is Device occlusion From BRILINTA?

Of the 16 reports, 1 (6.3%) resulted in death, 12 (75.0%) required hospitalization, and 2 (12.5%) were considered life-threatening.

Is Device occlusion Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for BRILINTA. However, 16 reports have been filed with the FAERS database.

What Other Side Effects Does BRILINTA Cause?

Dyspnoea (97) Thrombosis in device (50) Myocardial infarction (49) Death (40) Off label use (40) Coronary artery occlusion (37) Gastrointestinal haemorrhage (30) Acute myocardial infarction (23) Fatigue (23) Weight decreased (23)

What Other Drugs Cause Device occlusion?

PEGFILGRASTIM (3,239) CARBIDOPA\LEVODOPA (1,464) SOMATROPIN (823) LEUPROLIDE (786) EPOPROSTENOL (580) TREPROSTINIL (458) ALBUTEROL (431) MEDROXYPROGESTERONE (284) BACLOFEN (254) LEVODOPA (224)

Which BRILINTA Alternatives Have Lower Device occlusion Risk?

BRILINTA vs BRILIQUE BRILINTA vs BRIMONIDINE BRILINTA vs BRIMONIDINE\BRINZOLAMIDE BRILINTA vs BRIMONIDINE\TIMOLOL BRILINTA vs BRINTELLIX

Related Pages

BRILINTA Full Profile All Device occlusion Reports All Drugs Causing Device occlusion BRILINTA Demographics