Does TIMOLOL Cause Product complaint? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Product complaint have been filed in association with TIMOLOL (Timoptic). This represents 0.1% of all adverse event reports for TIMOLOL.
7
Reports of Product complaint with TIMOLOL
0.1%
of all TIMOLOL reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product complaint From TIMOLOL?
Of the 7 reports.
Is Product complaint Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TIMOLOL. However, 7 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 complaint?
FLUTICASONE FUROATE\UMECLIDINIUM\VILANTEROL TRIFENATATE (2,417)
ALBUTEROL (2,291)
FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (1,826)
FLUTICASONE\SALMETEROL (1,601)
MEPOLIZUMAB (1,296)
FLUTICASONE (1,112)
UMECLIDINIUM\VILANTEROL TRIFENATATE (1,108)
BELIMUMAB (1,079)
SUMATRIPTAN (718)
NICOTINE (700)
Which TIMOLOL Alternatives Have Lower Product complaint Risk?
TIMOLOL vs TIMOLOL\TRAVOPROST
TIMOLOL vs TINIDAZOLE
TIMOLOL vs TINZAPARIN
TIMOLOL vs TIOCONAZOLE
TIMOLOL vs TIOPRONIN