Does BRINZOLAMIDE Cause Product container issue? 31 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 31 reports of Product container issue have been filed in association with BRINZOLAMIDE (BRINZOLAMIDE). This represents 0.8% of all adverse event reports for BRINZOLAMIDE.
31
Reports of Product container issue with BRINZOLAMIDE
0.8%
of all BRINZOLAMIDE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product container issue From BRINZOLAMIDE?
Of the 31 reports.
Is Product container issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BRINZOLAMIDE. However, 31 reports have been filed with the FAERS database.
What Other Side Effects Does BRINZOLAMIDE Cause?
Treatment failure (1,424)
Eye pain (333)
Dyspnoea (306)
Drug ineffective (301)
Dizziness (294)
Blindness (278)
Vision blurred (274)
Ocular discomfort (244)
Headache (241)
Fall (234)
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)
BRIMONIDINE (121)
ACETAMINOPHEN (118)
Which BRINZOLAMIDE Alternatives Have Lower Product container issue Risk?
BRINZOLAMIDE vs BRINZOLAMIDE\TIMOLOL
BRINZOLAMIDE vs BRIVARACETAM
BRINZOLAMIDE vs BRIVUDINE
BRINZOLAMIDE vs BRODALUMAB
BRINZOLAMIDE vs BROLUCIZUMAB