Does BRIMONIDINE Cause Off label use? 186 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 186 reports of Off label use have been filed in association with BRIMONIDINE (BRIMONIDINE TARTRATE). This represents 1.6% of all adverse event reports for BRIMONIDINE.
186
Reports of Off label use with BRIMONIDINE
1.6%
of all BRIMONIDINE reports
3
Deaths
14
Hospitalizations
How Dangerous Is Off label use From BRIMONIDINE?
Of the 186 reports, 3 (1.6%) resulted in death, 14 (7.5%) required hospitalization, and 6 (3.2%) were considered life-threatening.
Is Off label use Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BRIMONIDINE. However, 186 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 Off label use?
RITUXIMAB (39,751)
INFLIXIMAB (34,801)
DENOSUMAB (34,612)
METHOTREXATE (24,020)
VEDOLIZUMAB (21,017)
ETANERCEPT (20,178)
TOCILIZUMAB (18,256)
PREDNISONE (17,867)
LENALIDOMIDE (17,017)
ADALIMUMAB (16,417)
Which BRIMONIDINE Alternatives Have Lower Off label use Risk?
BRIMONIDINE vs BRIMONIDINE\BRINZOLAMIDE
BRIMONIDINE vs BRIMONIDINE\TIMOLOL
BRIMONIDINE vs BRINTELLIX
BRIMONIDINE vs BRINZOLAMIDE
BRIMONIDINE vs BRINZOLAMIDE\TIMOLOL