Does BRIMONIDINE Cause Expired product administered? 96 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 96 reports of Expired product administered have been filed in association with BRIMONIDINE (BRIMONIDINE TARTRATE). This represents 0.8% of all adverse event reports for BRIMONIDINE.
96
Reports of Expired product administered with BRIMONIDINE
0.8%
of all BRIMONIDINE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Expired product administered From BRIMONIDINE?
Of the 96 reports, 1 (1.0%) required hospitalization.
Is Expired product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BRIMONIDINE. However, 96 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 Expired product administered?
POLYETHYLENE GLYCOL 3350 (1,637)
NAPROXEN (1,305)
ALBUTEROL (1,233)
LORATADINE (1,095)
MINOXIDIL (982)
ACETAMINOPHEN (797)
INSULIN LISPRO (770)
FLUTICASONE\SALMETEROL (753)
CETIRIZINE (714)
DICLOFENAC (714)
Which BRIMONIDINE Alternatives Have Lower Expired product administered Risk?
BRIMONIDINE vs BRIMONIDINE\BRINZOLAMIDE
BRIMONIDINE vs BRIMONIDINE\TIMOLOL
BRIMONIDINE vs BRINTELLIX
BRIMONIDINE vs BRINZOLAMIDE
BRIMONIDINE vs BRINZOLAMIDE\TIMOLOL