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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 Incorrect dose administered? 122 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 122 reports of Incorrect dose administered have been filed in association with BRIMONIDINE (BRIMONIDINE TARTRATE). This represents 1.0% of all adverse event reports for BRIMONIDINE.

122
Reports of Incorrect dose administered with BRIMONIDINE
1.0%
of all BRIMONIDINE reports
0
Deaths
2
Hospitalizations

How Dangerous Is Incorrect dose administered From BRIMONIDINE?

Of the 122 reports, 2 (1.6%) required hospitalization.

Is Incorrect dose administered Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for BRIMONIDINE. However, 122 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 Incorrect dose administered?

TIRZEPATIDE (23,301) ADALIMUMAB (14,000) DUPILUMAB (9,907) RANITIDINE (9,337) INSULIN LISPRO (8,318) ACETAMINOPHEN (5,316) DULAGLUTIDE (5,207) SECUKINUMAB (4,524) INSULIN GLARGINE (3,070) SOMATROPIN (2,772)

Which BRIMONIDINE Alternatives Have Lower Incorrect dose administered 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 Incorrect dose administered Reports All Drugs Causing Incorrect dose administered BRIMONIDINE Demographics