Does BRIMONIDINE Cause Product container issue? 121 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 121 reports of Product container issue have been filed in association with BRIMONIDINE (BRIMONIDINE TARTRATE). This represents 1.0% of all adverse event reports for BRIMONIDINE.
121
Reports of Product container issue with BRIMONIDINE
1.0%
of all BRIMONIDINE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product container issue From BRIMONIDINE?
Of the 121 reports.
Is Product container issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BRIMONIDINE. However, 121 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 container issue?
CYCLOSPORINE (910)
MINOXIDIL (556)
MOMETASONE FUROATE (450)
FORMOTEROL\MOMETASONE FUROATE (375)
LIFITEGRAST (244)
ALBUTEROL (192)
LATANOPROST (158)
CARBOXYMETHYLCELLULOSE\GLYCERIN (123)
ACETAMINOPHEN (118)
CALCIUM\DEXTROSE\MAGNESIUM\SODIUM\SODIUM (102)
Which BRIMONIDINE Alternatives Have Lower Product container issue Risk?
BRIMONIDINE vs BRIMONIDINE\BRINZOLAMIDE
BRIMONIDINE vs BRIMONIDINE\TIMOLOL
BRIMONIDINE vs BRINTELLIX
BRIMONIDINE vs BRINZOLAMIDE
BRIMONIDINE vs BRINZOLAMIDE\TIMOLOL