Does DORZOLAMIDE Cause Product storage error? 23 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 23 reports of Product storage error have been filed in association with DORZOLAMIDE (DORZOLAMIDE HYDROCHLORIDE TIMOLOL MALEATE). This represents 0.6% of all adverse event reports for DORZOLAMIDE.
23
Reports of Product storage error with DORZOLAMIDE
0.6%
of all DORZOLAMIDE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product storage error From DORZOLAMIDE?
Of the 23 reports.
Is Product storage error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DORZOLAMIDE. However, 23 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 storage error?
INSULIN GLARGINE (7,743)
EVOLOCUMAB (6,606)
ETANERCEPT (3,653)
DENOSUMAB (3,621)
ERENUMAB-AOOE (2,958)
DUPILUMAB (2,631)
ALBUTEROL (2,474)
ABATACEPT (2,101)
DARBEPOETIN ALFA (1,619)
INSULIN LISPRO (1,448)
Which DORZOLAMIDE Alternatives Have Lower Product storage error Risk?
DORZOLAMIDE vs DORZOLAMIDE\TIMOLOL
DORZOLAMIDE vs DOSTARLIMAB
DORZOLAMIDE vs DOSTARLIMAB-GXLY
DORZOLAMIDE vs DOTATATE GALLIUM GA-68
DORZOLAMIDE vs DOTHIEPIN