Does BRIMONIDINE Cause Product complaint? 18 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 18 reports of Product complaint have been filed in association with BRIMONIDINE (BRIMONIDINE TARTRATE). This represents 0.2% of all adverse event reports for BRIMONIDINE.
18
Reports of Product complaint with BRIMONIDINE
0.2%
of all BRIMONIDINE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product complaint From BRIMONIDINE?
Of the 18 reports, 1 (5.6%) required hospitalization.
Is Product complaint Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BRIMONIDINE. However, 18 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 Product complaint?
FLUTICASONE FUROATE\UMECLIDINIUM\VILANTEROL TRIFENATATE (2,417)
ALBUTEROL (2,291)
FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (1,826)
FLUTICASONE\SALMETEROL (1,601)
MEPOLIZUMAB (1,296)
FLUTICASONE (1,112)
UMECLIDINIUM\VILANTEROL TRIFENATATE (1,108)
BELIMUMAB (1,079)
SUMATRIPTAN (718)
NICOTINE (700)
Which BRIMONIDINE Alternatives Have Lower Product complaint Risk?
BRIMONIDINE vs BRIMONIDINE\BRINZOLAMIDE
BRIMONIDINE vs BRIMONIDINE\TIMOLOL
BRIMONIDINE vs BRINTELLIX
BRIMONIDINE vs BRINZOLAMIDE
BRIMONIDINE vs BRINZOLAMIDE\TIMOLOL