Does TIMOLOL Cause Product container issue? 76 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 76 reports of Product container issue have been filed in association with TIMOLOL (Timoptic). This represents 1.0% of all adverse event reports for TIMOLOL.
76
Reports of Product container issue with TIMOLOL
1.0%
of all TIMOLOL reports
0
Deaths
2
Hospitalizations
How Dangerous Is Product container issue From TIMOLOL?
Of the 76 reports, 2 (2.6%) required hospitalization.
Is Product container issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TIMOLOL. However, 76 reports have been filed with the FAERS database.
What Other Side Effects Does TIMOLOL Cause?
Treatment failure (3,690)
Drug ineffective (684)
Hypersensitivity (526)
Eye irritation (421)
Ocular hyperaemia (262)
Intraocular pressure increased (231)
Eye pain (229)
Eye pruritus (228)
Vision blurred (212)
Dizziness (201)
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 TIMOLOL Alternatives Have Lower Product container issue Risk?
TIMOLOL vs TIMOLOL\TRAVOPROST
TIMOLOL vs TINIDAZOLE
TIMOLOL vs TINZAPARIN
TIMOLOL vs TIOCONAZOLE
TIMOLOL vs TIOPRONIN