Does TIMOLOL Cause Product dose omission? 13 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Product dose omission have been filed in association with TIMOLOL (Timoptic). This represents 0.2% of all adverse event reports for TIMOLOL.
13
Reports of Product dose omission with TIMOLOL
0.2%
of all TIMOLOL reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product dose omission From TIMOLOL?
Of the 13 reports, 1 (7.7%) required hospitalization.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TIMOLOL. However, 13 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 dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which TIMOLOL Alternatives Have Lower Product dose omission Risk?
TIMOLOL vs TIMOLOL\TRAVOPROST
TIMOLOL vs TINIDAZOLE
TIMOLOL vs TINZAPARIN
TIMOLOL vs TIOCONAZOLE
TIMOLOL vs TIOPRONIN