Does BRIMONIDINE\TIMOLOL Cause Product packaging quantity issue? 51 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 51 reports of Product packaging quantity issue have been filed in association with BRIMONIDINE\TIMOLOL. This represents 2.0% of all adverse event reports for BRIMONIDINE\TIMOLOL.
51
Reports of Product packaging quantity issue with BRIMONIDINE\TIMOLOL
2.0%
of all BRIMONIDINE\TIMOLOL reports
0
Deaths
2
Hospitalizations
How Dangerous Is Product packaging quantity issue From BRIMONIDINE\TIMOLOL?
Of the 51 reports, 2 (3.9%) required hospitalization.
Is Product packaging quantity issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BRIMONIDINE\TIMOLOL. However, 51 reports have been filed with the FAERS database.
What Other Side Effects Does BRIMONIDINE\TIMOLOL Cause?
Eye irritation (332)
Ocular hyperaemia (328)
Intraocular pressure increased (211)
Eye pain (200)
Eye pruritus (156)
Drug ineffective (154)
Accidental exposure to product (148)
Vision blurred (136)
Dizziness (119)
Hypersensitivity (114)
What Other Drugs Cause Product packaging quantity issue?
LEUPROLIDE (523)
ALBUTEROL (431)
BUDESONIDE\FORMOTEROL (301)
FENTANYL (286)
BUPRENORPHINE (225)
CYCLOSPORINE (206)
ESTRADIOL (201)
BIMATOPROST (177)
RIVAROXABAN (174)
EXENATIDE (154)
Which BRIMONIDINE\TIMOLOL Alternatives Have Lower Product packaging quantity issue Risk?
BRIMONIDINE\TIMOLOL vs BRINTELLIX
BRIMONIDINE\TIMOLOL vs BRINZOLAMIDE
BRIMONIDINE\TIMOLOL vs BRINZOLAMIDE\TIMOLOL
BRIMONIDINE\TIMOLOL vs BRIVARACETAM
BRIMONIDINE\TIMOLOL vs BRIVUDINE