Does TIMOLOL Cause Product administration error? 15 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 15 reports of Product administration error have been filed in association with TIMOLOL (Timoptic). This represents 0.2% of all adverse event reports for TIMOLOL.
15
Reports of Product administration error with TIMOLOL
0.2%
of all TIMOLOL reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product administration error From TIMOLOL?
Of the 15 reports.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TIMOLOL. However, 15 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 administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which TIMOLOL Alternatives Have Lower Product administration error Risk?
TIMOLOL vs TIMOLOL\TRAVOPROST
TIMOLOL vs TINIDAZOLE
TIMOLOL vs TINZAPARIN
TIMOLOL vs TIOCONAZOLE
TIMOLOL vs TIOPRONIN