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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 storage error? 109 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 109 reports of Product storage error have been filed in association with BRIMONIDINE (BRIMONIDINE TARTRATE). This represents 0.9% of all adverse event reports for BRIMONIDINE.

109
Reports of Product storage error with BRIMONIDINE
0.9%
of all BRIMONIDINE reports
0
Deaths
6
Hospitalizations

How Dangerous Is Product storage error From BRIMONIDINE?

Of the 109 reports, 6 (5.5%) required hospitalization.

Is Product storage error Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for BRIMONIDINE. However, 109 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 storage error?

INSULIN GLARGINE (7,743) EVOLOCUMAB (6,606) ETANERCEPT (3,653) DENOSUMAB (3,621) ERENUMAB-AOOE (2,958) DUPILUMAB (2,631) ALBUTEROL (2,474) ABATACEPT (2,101) DARBEPOETIN ALFA (1,619) INSULIN LISPRO (1,448)

Which BRIMONIDINE Alternatives Have Lower Product storage error 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 storage error Reports All Drugs Causing Product storage error BRIMONIDINE Demographics