Skip to content
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 product storage? 6 Reports in FDA Database

Visibly Younger Skin in Weeks

Synevra Lift & Lock — Swiss peptide serum + nutrients. 60-day money-back guarantee.

Discover Synevra

According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Incorrect product storage have been filed in association with BRIMONIDINE (BRIMONIDINE TARTRATE). This represents 0.1% of all adverse event reports for BRIMONIDINE.

6
Reports of Incorrect product storage with BRIMONIDINE
0.1%
of all BRIMONIDINE reports
0
Deaths
0
Hospitalizations

How Dangerous Is Incorrect product storage From BRIMONIDINE?

Of the 6 reports.

Is Incorrect product storage Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for BRIMONIDINE. However, 6 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 product storage?

ETANERCEPT (2,149) INSULIN LISPRO (1,114) ABATACEPT (583) TERIPARATIDE (573) ADALIMUMAB (476) GOLIMUMAB (392) INSULIN GLARGINE (341) INSULIN HUMAN (336) USTEKINUMAB (299) ERYTHROPOIETIN (268)

Which BRIMONIDINE Alternatives Have Lower Incorrect product storage 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 product storage Reports All Drugs Causing Incorrect product storage BRIMONIDINE Demographics