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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 Drug dose omission? 19 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 19 reports of Drug dose omission have been filed in association with BRILINTA. This represents 3.3% of all adverse event reports for BRILINTA.

19
Reports of Drug dose omission with BRILINTA
3.3%
of all BRILINTA reports
5
Deaths
11
Hospitalizations

How Dangerous Is Drug dose omission From BRILINTA?

Of the 19 reports, 5 (26.3%) resulted in death, 11 (57.9%) required hospitalization, and 3 (15.8%) were considered life-threatening.

Is Drug dose omission Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for BRILINTA. However, 19 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 Drug dose omission?

ETANERCEPT (10,871) CINACALCET (8,683) EVOLOCUMAB (4,914) ADALIMUMAB (3,993) INSULIN LISPRO (3,063) GOLIMUMAB (2,652) TERIPARATIDE (2,616) APREMILAST (2,466) ALBUTEROL (2,309) FLUTICASONE\SALMETEROL (2,153)

Which BRILINTA Alternatives Have Lower Drug dose omission Risk?

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

Related Pages

BRILINTA Full Profile All Drug dose omission Reports All Drugs Causing Drug dose omission BRILINTA Demographics