Does DORZOLAMIDE Cause Product container issue? 51 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 51 reports of Product container issue have been filed in association with DORZOLAMIDE (DORZOLAMIDE HYDROCHLORIDE TIMOLOL MALEATE). This represents 1.3% of all adverse event reports for DORZOLAMIDE.
51
Reports of Product container issue with DORZOLAMIDE
1.3%
of all DORZOLAMIDE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product container issue From DORZOLAMIDE?
Of the 51 reports.
Is Product container issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DORZOLAMIDE. However, 51 reports have been filed with the FAERS database.
What Other Side Effects Does DORZOLAMIDE Cause?
Treatment failure (1,861)
Drug ineffective (436)
Hypersensitivity (288)
Eye irritation (278)
Eye pain (139)
Ocular hyperaemia (138)
Intraocular pressure increased (121)
Vision blurred (118)
Drug hypersensitivity (112)
Off label use (81)
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 DORZOLAMIDE Alternatives Have Lower Product container issue Risk?
DORZOLAMIDE vs DORZOLAMIDE\TIMOLOL
DORZOLAMIDE vs DOSTARLIMAB
DORZOLAMIDE vs DOSTARLIMAB-GXLY
DORZOLAMIDE vs DOTATATE GALLIUM GA-68
DORZOLAMIDE vs DOTHIEPIN