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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 Product label issue? 15 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 15 reports of Product label issue have been filed in association with BRIMONIDINE (BRIMONIDINE TARTRATE). This represents 0.1% of all adverse event reports for BRIMONIDINE.

15
Reports of Product label issue with BRIMONIDINE
0.1%
of all BRIMONIDINE reports
0
Deaths
0
Hospitalizations

How Dangerous Is Product label issue From BRIMONIDINE?

Of the 15 reports.

Is Product label issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for BRIMONIDINE. However, 15 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 label issue?

RIVAROXABAN (379) ACETAMINOPHEN (276) GUSELKUMAB (177) USTEKINUMAB (164) DIMETHICONE\LOPERAMIDE (154) CETIRIZINE (138) IBUPROFEN (99) GOLIMUMAB (76) POLYETHYLENE GLYCOL 3350 (76) FENTANYL (72)

Which BRIMONIDINE Alternatives Have Lower Product label issue 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 Product label issue Reports All Drugs Causing Product label issue BRIMONIDINE Demographics