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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 BRIMONIDINE Cause Drug dose omission? 50 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 50 reports of Drug dose omission have been filed in association with BRIMONIDINE (BRIMONIDINE TARTRATE). This represents 0.4% of all adverse event reports for BRIMONIDINE.

50
Reports of Drug dose omission with BRIMONIDINE
0.4%
of all BRIMONIDINE reports
0
Deaths
5
Hospitalizations

How Dangerous Is Drug dose omission From BRIMONIDINE?

Of the 50 reports, 5 (10.0%) required hospitalization.

Is Drug dose omission Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for BRIMONIDINE. However, 50 reports have been filed with the FAERS database.

What Other Side Effects Does BRIMONIDINE Cause?

Treatment failure (2,849) Drug ineffective (1,402) Eye irritation (950) Ocular hyperaemia (917) Hypersensitivity (629) Erythema (604) Eye pain (560) Vision blurred (542) Headache (492) Dry eye (490)

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 BRIMONIDINE Alternatives Have Lower Drug dose omission Risk?

BRIMONIDINE vs BRIMONIDINE\BRINZOLAMIDE BRIMONIDINE vs BRIMONIDINE\TIMOLOL BRIMONIDINE vs BRINTELLIX BRIMONIDINE vs BRINZOLAMIDE BRIMONIDINE vs BRINZOLAMIDE\TIMOLOL

Related Pages

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