Does BRIMONIDINE Cause Product quality issue? 388 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 388 reports of Product quality issue have been filed in association with BRIMONIDINE (BRIMONIDINE TARTRATE). This represents 3.3% of all adverse event reports for BRIMONIDINE.
388
Reports of Product quality issue with BRIMONIDINE
3.3%
of all BRIMONIDINE reports
0
Deaths
3
Hospitalizations
How Dangerous Is Product quality issue From BRIMONIDINE?
Of the 388 reports, 3 (0.8%) required hospitalization.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BRIMONIDINE. However, 388 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 quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which BRIMONIDINE Alternatives Have Lower Product quality issue Risk?
BRIMONIDINE vs BRIMONIDINE\BRINZOLAMIDE
BRIMONIDINE vs BRIMONIDINE\TIMOLOL
BRIMONIDINE vs BRINTELLIX
BRIMONIDINE vs BRINZOLAMIDE
BRIMONIDINE vs BRINZOLAMIDE\TIMOLOL